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Cay10005033-10
CAS: 298186-​80-​8
S1P3 receptor antagonist Erklärungen der Abkürzungen ansehen.
CAY10444 is a selective antagonist of S1P binding to the S1P3 receptor, blocking the calcium increase in HeLa cells by about 40% when present at 10 µM.
MW: 287 D
Formula: C15H29NO2S
Purity: >98%
Cayman
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10 mg

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84 €

Cay10005033-25
CAS: 298186-​80-​8
S1P3 receptor antagonist Erklärungen der Abkürzungen ansehen.
CAY10444 is a selective antagonist of S1P binding to the S1P3 receptor, blocking the calcium increase in HeLa cells by about 40% when present at 10 µM.
MW: 287 D
Formula: C15H29NO2S
Purity: >98%
Cayman
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25 mg

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198 €

Cay10005033-5
CAS: 298186-​80-​8
S1P3 receptor antagonist Erklärungen der Abkürzungen ansehen.
CAY10444 is a selective antagonist of S1P binding to the S1P3 receptor, blocking the calcium increase in HeLa cells by about 40% when present at 10 µM.
MW: 287 D
Formula: C15H29NO2S
Purity: >98%
Cayman
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5 mg

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44 €

Cay10005033-50
CAS: 298186-​80-​8
S1P3 receptor antagonist Erklärungen der Abkürzungen ansehen.
CAY10444 is a selective antagonist of S1P binding to the S1P3 receptor, blocking the calcium increase in HeLa cells by about 40% when present at 10 µM.
MW: 287 D
Formula: C15H29NO2S
Purity: >98%
Cayman
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50 mg

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353 €

Cay10005633-1
CAS: 1177195-​52-​6
Capsaicin receptor antagonist Erklärungen der Abkürzungen ansehen.
Capsaicin signals are transduced by a heat-​activated ion channel, the vanilloid receptor 1 (VR1), or transient receptor potential vanilloid 1 (TRPV1). CAY10448 is an iodinated nonivamide, a potent capsaicin receptor antagonist with an IC50 of approximatel ... mehr
MW: 433 D
Formula: C18H28INO3
Purity: >98%
Cayman
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1 mg

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19 €

Cay10005633-10
CAS: 1177195-​52-​6
Capsaicin receptor antagonist Erklärungen der Abkürzungen ansehen.
Capsaicin signals are transduced by a heat-​activated ion channel, the vanilloid receptor 1 (VR1), or transient receptor potential vanilloid 1 (TRPV1). CAY10448 is an iodinated nonivamide, a potent capsaicin receptor antagonist with an IC50 of approximatel ... mehr
MW: 433 D
Formula: C18H28INO3
Purity: >98%
Cayman
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10 mg

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148 €

Cay10005633-5
CAS: 1177195-​52-​6
Capsaicin receptor antagonist Erklärungen der Abkürzungen ansehen.
Capsaicin signals are transduced by a heat-​activated ion channel, the vanilloid receptor 1 (VR1), or transient receptor potential vanilloid 1 (TRPV1). CAY10448 is an iodinated nonivamide, a potent capsaicin receptor antagonist with an IC50 of approximatel ... mehr
MW: 433 D
Formula: C18H28INO3
Purity: >98%
Cayman
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5 mg

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84 €

Cay10005633-50
CAS: 1177195-​52-​6
Capsaicin receptor antagonist Erklärungen der Abkürzungen ansehen.
Capsaicin signals are transduced by a heat-​activated ion channel, the vanilloid receptor 1 (VR1), or transient receptor potential vanilloid 1 (TRPV1). CAY10448 is an iodinated nonivamide, a potent capsaicin receptor antagonist with an IC50 of approximatel ... mehr
MW: 433 D
Formula: C18H28INO3
Purity: >98%
Cayman
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50 mg

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650 €

Cay10006794-100
CAS: 88840-​02-​2
IP3 receptor antagonist Erklärungen der Abkürzungen ansehen.
Xestospongins are marine natural products . Xestospongin A antagonizes the calcium-​releasing action of inositol-​1,4,5-​triphosphate at the receptor level in cerebral microsomes, with an IC50 of 2.5 µM. It is thus about ten times less potent than Xestospong ... mehr
MW: 446 D
Formula: C28H50N2O2
Purity: >90%
Cayman
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100 µg

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364 €

Cay10006794-250
CAS: 88840-​02-​2
IP3 receptor antagonist Erklärungen der Abkürzungen ansehen.
Xestospongins are marine natural products . Xestospongin A antagonizes the calcium-​releasing action of inositol-​1,4,5-​triphosphate at the receptor level in cerebral microsomes, with an IC50 of 2.5 µM. It is thus about ten times less potent than Xestospong ... mehr
MW: 446 D
Formula: C28H50N2O2
Purity: >90%
Cayman
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250 µg

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862 €

Cay10006797-100
CAS: 123000-​02-​2
IP3 receptor antagonist Erklärungen der Abkürzungen ansehen.
Xestospongins and araguspongins are marine natural products. Araguspongin B antagonizes the calcium-​releasing action of inositol 1,4,5-​triphosphate at the receptor level in cerebral microsomes, with an IC50 of 0.6 µM. It is nearly as potent as xestospong ... mehr
MW: 447 D
Formula: C28H51N2O2
Purity: >90%
Cayman
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100 µg

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370 €

Cay10006797-250
CAS: 123000-​02-​2
IP3 receptor antagonist Erklärungen der Abkürzungen ansehen.
Xestospongins and araguspongins are marine natural products. Araguspongin B antagonizes the calcium-​releasing action of inositol 1,4,5-​triphosphate at the receptor level in cerebral microsomes, with an IC50 of 0.6 µM. It is nearly as potent as xestospongi ... mehr
MW: 447 D
Formula: C28H51N2O2
Purity: >90%
Cayman
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250 µg

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879 €

Cay10007565-1
CAS: 4671-​75-​4
LPA receptor antagonist Erklärungen der Abkürzungen ansehen.
Tetradecyl phosphonate is a pan-antagonist of LPA1, LPA2, and LPA3 receptors with IC50 values for inhibition of LPA-induced calcium mobilization of 10 µM, 5.5 µM, and 3.1 µM, respectively.
MW: 278 D
Formula: C14H31O3P
Purity: >98%
Cayman
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1 g

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68 €

Cay10007565-100
CAS: 4671-​75-​4
LPA receptor antagonist Erklärungen der Abkürzungen ansehen.
Tetradecyl phosphonate is a pan-antagonist of LPA1, LPA2, and LPA3 receptors with IC50 values for inhibition of LPA-induced calcium mobilization of 10 µM, 5.5 µM, and 3.1 µM, respectively.
MW: 278 D
Formula: C14H31O3P
Purity: >98%
Cayman
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100 mg

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17 €

Cay10007565-500
CAS: 4671-​75-​4
LPA receptor antagonist Erklärungen der Abkürzungen ansehen.
Tetradecyl phosphonate is a pan-antagonist of LPA1, LPA2, and LPA3 receptors with IC50 values for inhibition of LPA-induced calcium mobilization of 10 µM, 5.5 µM, and 3.1 µM, respectively.
MW: 278 D
Formula: C14H31O3P
Purity: >98%
Cayman
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500 mg

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41 €

Cay10008282-1
CAS: 107753-​78-​6
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Zafirlukast is a potent, selective CysLT1 receptor antagonist sold under the trade name Accolate for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. It binds to the human CysLT1 and CysLT2 receptors with IC50 values ... mehr
MW: 575 D
Formula: C31H33N3O6S
Purity: >97%
Cayman
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1 g

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974 €

Cay10008282-10
CAS: 107753-​78-​6
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Zafirlukast is a potent, selective CysLT1 receptor antagonist sold under the trade name Accolate for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. It binds to the human CysLT1 and CysLT2 receptors with IC50 values ... mehr
MW: 575 D
Formula: C31H33N3O6S
Purity: >97%
Cayman
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10 mg

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16 €

Cay10008282-100
CAS: 107753-​78-​6
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Zafirlukast is a potent, selective CysLT1 receptor antagonist sold under the trade name Accolate for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. It binds to the human CysLT1 and CysLT2 receptors with IC50 values ... mehr
MW: 575 D
Formula: C31H33N3O6S
Purity: >97%
Cayman
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100 mg

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130 €

Cay10008282-500
CAS: 107753-​78-​6
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Zafirlukast is a potent, selective CysLT1 receptor antagonist sold under the trade name Accolate for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. It binds to the human CysLT1 and CysLT2 receptors with IC50 values ... mehr
MW: 575 D
Formula: C31H33N3O6S
Purity: >97%
Cayman
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500 mg

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568 €

Cay10008318-10
CAS: 151767-​02-​1
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Montelukast (sodium salt) is a potent, selective CysLT1 receptor antagonist sold under the trade name Singulair for the treatment of asthma as well as for the symptoms associated with allergic rhinitis.
MW: 608 D
Formula: C35H35ClNO3S .Na
Purity: >98%
Cayman
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10 mg

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16 €

Cay10008318-100
CAS: 151767-​02-​1
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Montelukast (sodium salt) is a potent, selective CysLT1 receptor antagonist sold under the trade name Singulair for the treatment of asthma as well as for the symptoms associated with allergic rhinitis.
MW: 608 D
Formula: C35H35ClNO3S .Na
Purity: >98%
Cayman
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100 mg

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130 €

Cay10008318-50
CAS: 151767-​02-​1
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Montelukast (sodium salt) is a potent, selective CysLT1 receptor antagonist sold under the trade name Singulair for the treatment of asthma as well as for the symptoms associated with allergic rhinitis.
MW: 608 D
Formula: C35H35ClNO3S .Na
Purity: >98%
Cayman
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50 mg

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73 €

Cay10008318-500
CAS: 151767-​02-​1
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Montelukast (sodium salt) is a potent, selective CysLT1 receptor antagonist sold under the trade name Singulair for the treatment of asthma as well as for the symptoms associated with allergic rhinitis.
MW: 608 D
Formula: C35H35ClNO3S .Na
Purity: >98%
Cayman
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500 mg

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568 €

Cay10008319-1
CAS: 103177-​37-​3
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Pranlukast (ONO-1078) is a potent, selective and orally active CysLT1 receptor antagonist.
MW: 481 D
Formula: C27H23N5O4
Purity: >98%
Cayman
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1 g

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974 €

Cay10008319-10
CAS: 103177-​37-​3
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Pranlukast (ONO-1078) is a potent, selective and orally active CysLT1 receptor antagonist.
MW: 481 D
Formula: C27H23N5O4
Purity: >98%
Cayman
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10 mg

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16 €

Cay10008319-100
CAS: 103177-​37-​3
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Pranlukast (ONO-1078) is a potent, selective and orally active CysLT1 receptor antagonist.
MW: 481 D
Formula: C27H23N5O4
Purity: >98%
Cayman
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100 mg

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130 €

Cay10008319-500
CAS: 103177-​37-​3
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Pranlukast (ONO-1078) is a potent, selective and orally active CysLT1 receptor antagonist.
MW: 481 D
Formula: C27H23N5O4
Purity: >98%
Cayman
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500 mg

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568 €

Cay10008640-1 Asthma Treatment Standard Set
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
The Asthma Treatment Standard Set contains three potent, selective Cysteinyl Leukotriene (CysLT) 1 receptor antagonists (10 mg each) currently used clinically for the treatment of asthma: Zafirlukast, Montelukast (sodium salt) and Pranlukast, sold under t ... mehr
Cayman
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1 each

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71 €

Cay10009162-1
CAS: 439288-​66-​1
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
The effects of prostaglandin E2 (PGE2) are transduced by at least four distinct receptors designated EP1, EP2, EP3, and EP4. GW 627368X is a potent and selective competitive antagonist of the EP4 receptor with additional human TP receptor affinity. In com ... mehr
MW: 544 D
Formula: C30H28N2O6S
Purity: >96%
Cayman
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1 mg

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53 €

Cay10009162-10
CAS: 439288-​66-​1
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
The effects of prostaglandin E2 (PGE2) are transduced by at least four distinct receptors designated EP1, EP2, EP3, and EP4. GW 627368X is a potent and selective competitive antagonist of the EP4 receptor with additional human TP receptor affinity. In com ... mehr
MW: 544 D
Formula: C30H28N2O6S
Purity: >96%
Cayman
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10 mg

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427 €

Cay10009162-25
CAS: 439288-​66-​1
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
The effects of prostaglandin E2 (PGE2) are transduced by at least four distinct receptors designated EP1, EP2, EP3, and EP4. GW 627368X is a potent and selective competitive antagonist of the EP4 receptor with additional human TP receptor affinity. In com ... mehr
MW: 544 D
Formula: C30H28N2O6S
Purity: >96%
Cayman
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25 mg

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934 €

Cay10009162-5
CAS: 439288-​66-​1
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
The effects of prostaglandin E2 (PGE2) are transduced by at least four distinct receptors designated EP1, EP2, EP3, and EP4. GW 627368X is a potent and selective competitive antagonist of the EP4 receptor with additional human TP receptor affinity. In com ... mehr
MW: 544 D
Formula: C30H28N2O6S
Purity: >96%
Cayman
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5 mg

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240 €

Cay10009458-1
CAS: 383150-​41-​2
S1P2 receptor antagonist Erklärungen der Abkürzungen ansehen.
JTE-​013 is a potent, selective sphingosine-​1-​phosphate 2 (S1P2) receptor antagonist that binds to the human and rat receptors with IC50 values of 17 and 22 nM, respectively, (IC50 values >10 µM for human S1P1 and S1P3). It reverses the inhibitory effects ... mehr
MW: 408 D
Formula: C17H19Cl2N7O
Purity: >98%
Cayman
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1 mg

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22 €

Cay10009458-10
CAS: 383150-​41-​2
S1P2 receptor antagonist Erklärungen der Abkürzungen ansehen.
JTE-​013 is a potent, selective sphingosine-​1-​phosphate 2 (S1P2) receptor antagonist that binds to the human and rat receptors with IC50 values of 17 and 22 nM, respectively, (IC50 values >10 µM for human S1P1 and S1P3). It reverses the inhibitory effects ... mehr
MW: 408 D
Formula: C17H19Cl2N7O
Purity: >98%
Cayman
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10 mg

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176 €

Cay10009458-5
CAS: 383150-​41-​2
S1P2 receptor antagonist Erklärungen der Abkürzungen ansehen.
JTE-​013 is a potent, selective sphingosine-​1-​phosphate 2 (S1P2) receptor antagonist that binds to the human and rat receptors with IC50 values of 17 and 22 nM, respectively, (IC50 values >10 µM for human S1P1 and S1P3). It reverses the inhibitory effects ... mehr
MW: 408 D
Formula: C17H19Cl2N7O
Purity: >98%
Cayman
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5 mg

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100 €

Cay10009458-50
CAS: 383150-​41-​2
S1P2 receptor antagonist Erklärungen der Abkürzungen ansehen.
JTE-​013 is a potent, selective sphingosine-​1-​phosphate 2 (S1P2) receptor antagonist that binds to the human and rat receptors with IC50 values of 17 and 22 nM, respectively, (IC50 values >10 µM for human S1P1 and S1P3). It reverses the inhibitory effects ... mehr
MW: 408 D
Formula: C17H19Cl2N7O
Purity: >98%
Cayman
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50 mg

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771 €

Cay10010024-1
CAS: 117423-​74-​2
BLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from the 5-​lipoxygenase (5-​LO) pathway of arachidonic acid metabolism and is an important mediator of the inflammatory process. The benzophenone dicarboxylic acid derivative LY223982 is a potent BLT1 ... mehr
MW: 502 D
Formula: C30H30O7
Purity: >98%
Cayman
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1 mg

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24 €

Cay10010024-10
CAS: 117423-​74-​2
BLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from the 5-​lipoxygenase (5-​LO) pathway of arachidonic acid metabolism and is an important mediator of the inflammatory process. The benzophenone dicarboxylic acid derivative LY223982 is a potent BLT1 ... mehr
MW: 502 D
Formula: C30H30O7
Purity: >98%
Cayman
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10 mg

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195 €

Cay10010024-25
CAS: 117423-​74-​2
BLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from the 5-​lipoxygenase (5-​LO) pathway of arachidonic acid metabolism and is an important mediator of the inflammatory process. The benzophenone dicarboxylic acid derivative LY223982 is a potent BLT1 ... mehr
MW: 502 D
Formula: C30H30O7
Purity: >98%
Cayman
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25 mg

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427 €

Cay10010024-5
CAS: 117423-​74-​2
BLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Leukotriene B4 (LTB4) is a dihydroxy fatty acid derived from the 5-​lipoxygenase (5-​LO) pathway of arachidonic acid metabolism and is an important mediator of the inflammatory process. The benzophenone dicarboxylic acid derivative LY223982 is a potent BLT1 ... mehr
MW: 502 D
Formula: C30H30O7
Purity: >98%
Cayman
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5 mg

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110 €

Cay10010396-1
CAS: 945716-​28-​9
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
TPalpha and TPbeta are two isoforms of the human TP receptor, the G protein-​coupled receptor (GPCR) that mediates the actions of thromboxane A2 (TXA2). Although their distinct physiological functions have not been fully elucidated, TPbeta is believed to b ... mehr
MW: 423 D
Formula: C18H21N3O7S
Purity: >98%
Cayman
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1 mg

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42 €

Cay10010396-10
CAS: 945716-​28-​9
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
TPalpha and TPbeta are two isoforms of the human TP receptor, the G protein-​coupled receptor (GPCR) that mediates the actions of thromboxane A2 (TXA2). Although their distinct physiological functions have not been fully elucidated, TPbeta is believed to b ... mehr
MW: 423 D
Formula: C18H21N3O7S
Purity: >98%
Cayman
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10 mg

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334 €

Cay10010396-5
CAS: 945716-​28-​9
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
TPalpha and TPbeta are two isoforms of the human TP receptor, the G protein-​coupled receptor (GPCR) that mediates the actions of thromboxane A2 (TXA2). Although their distinct physiological functions have not been fully elucidated, TPbeta is believed to b ... mehr
MW: 423 D
Formula: C18H21N3O7S
Purity: >98%
Cayman
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5 mg

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188 €

Cay10010396-50
CAS: 945716-​28-​9
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
TPalpha and TPbeta are two isoforms of the human TP receptor, the G protein-​coupled receptor (GPCR) that mediates the actions of thromboxane A2 (TXA2). Although their distinct physiological functions have not been fully elucidated, TPbeta is believed to b ... mehr
MW: 423 D
Formula: C18H21N3O7S
Purity: >98%
Cayman
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50 mg

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1462 €

Cay10010470-1
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of prostaglandin F2alpha (PGF2alpha) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-​1 carboxyl group has been modified to an N-​ethyl amide. ... mehr
MW: 429 D
Formula: C26H36FNO3
Purity: >98%
Cayman
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1 mg

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71 €

Cay10010470-10
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of prostaglandin F2alpha (PGF2alpha) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-​1 carboxyl group has been modified to an N-​ethyl amide. ... mehr
MW: 429 D
Formula: C26H36FNO3
Purity: >98%
Cayman
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10 mg

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566 €

Cay10010470-25
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of prostaglandin F2alpha (PGF2alpha) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-​1 carboxyl group has been modified to an N-​ethyl amide. ... mehr
MW: 429 D
Formula: C26H36FNO3
Purity: >98%
Cayman
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25 mg

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1239 €

Cay10010470-5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of prostaglandin F2alpha (PGF2alpha) which acts as a potent and selective antagonist at the FP receptor. AL 8810 ethyl amide is an analog of AL 8810 in which the C-​1 carboxyl group has been modified to an N-​ethyl amide. ... mehr
MW: 429 D
Formula: C26H36FNO3
Purity: >98%
Cayman
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5 mg

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319 €

Cay10010484-0.1
CAS: 122055-​58-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Eicosadienoic acid (5Z,14Z) is a novel omega-​6 C20:2 fatty acid. The more common eicosadienoic acid 11Z,14Z) competitively inhibits inosine 5-​monophosphate dehydrogenase (Ki = 3.1 µM) and inhibits the binding of LTB4 to its receptor on neutrophils (Ki = 3 ... mehr
MW: 308 D
Formula: C20H36O2
Purity: >98%
Cayman
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100 µg

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79 €

Cay10010484-0.5
CAS: 122055-​58-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Eicosadienoic acid (5Z,14Z) is a novel omega-​6 C20:2 fatty acid. The more common eicosadienoic acid 11Z,14Z) competitively inhibits inosine 5-​monophosphate dehydrogenase (Ki = 3.1 µM) and inhibits the binding of LTB4 to its receptor on neutrophils (Ki = 3 ... mehr
MW: 308 D
Formula: C20H36O2
Purity: >98%
Cayman
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500 µg

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355 €

Cay10010484-1
CAS: 122055-​58-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Eicosadienoic acid (5Z,14Z) is a novel omega-​6 C20:2 fatty acid. The more common eicosadienoic acid 11Z,14Z) competitively inhibits inosine 5-​monophosphate dehydrogenase (Ki = 3.1 µM) and inhibits the binding of LTB4 to its receptor on neutrophils (Ki = 3 ... mehr
MW: 308 D
Formula: C20H36O2
Purity: >98%
Cayman
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1 mg

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631 €

Cay10011565-1
CAS: 147776-​06-​5
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) exerts its effects through four separate G coupled-​protein receptors (EP1-​4). L-​161,982 is a potent and selective EP4 receptor antagonist. It demonstrates selective binding to human EP4 receptors with a Ki value of 0.024 µM compare ... mehr
MW: 654 D
Formula: C32H29F3N4O4S2
Purity: >96%
Cayman
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1 mg

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31 €

Cay10011565-10
CAS: 147776-​06-​5
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) exerts its effects through four separate G coupled-​protein receptors (EP1-​4). L-​161,982 is a potent and selective EP4 receptor antagonist. It demonstrates selective binding to human EP4 receptors with a Ki value of 0.024 µM compare ... mehr
MW: 654 D
Formula: C32H29F3N4O4S2
Purity: >96%
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Cay10011565-5
CAS: 147776-​06-​5
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) exerts its effects through four separate G coupled-​protein receptors (EP1-​4). L-​161,982 is a potent and selective EP4 receptor antagonist. It demonstrates selective binding to human EP4 receptors with a Ki value of 0.024 µM compare ... mehr
MW: 654 D
Formula: C32H29F3N4O4S2
Purity: >96%
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142 €

Cay10011565-50
CAS: 147776-​06-​5
EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) exerts its effects through four separate G coupled-​protein receptors (EP1-​4). L-​161,982 is a potent and selective EP4 receptor antagonist. It demonstrates selective binding to human EP4 receptors with a Ki value of 0.024 µM compare ... mehr
MW: 654 D
Formula: C32H29F3N4O4S2
Purity: >96%
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1096 €

Cay10012539-1
CAS: 916046-​55-​4
CRTH2receptor antagonist, DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G protein-​coupled receptors, designated DP1 and CRTH2/DP2. In humans, CRTH2/DP2 is expressed on Th2 cells, eosinophils, and basophils where it mediates the ch ... mehr
MW: 416 D
Formula: C20H14ClFN2O5
Purity: >98%
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63 €

Cay10012539-10
CAS: 916046-​55-​4
CRTH2receptor antagonist, DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G protein-​coupled receptors, designated DP1 and CRTH2/DP2. In humans, CRTH2/DP2 is expressed on Th2 cells, eosinophils, and basophils where it mediates the ch ... mehr
MW: 416 D
Formula: C20H14ClFN2O5
Purity: >98%
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501 €

Cay10012539-5
CAS: 916046-​55-​4
CRTH2receptor antagonist, DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G protein-​coupled receptors, designated DP1 and CRTH2/DP2. In humans, CRTH2/DP2 is expressed on Th2 cells, eosinophils, and basophils where it mediates the ch ... mehr
MW: 416 D
Formula: C20H14ClFN2O5
Purity: >98%
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282 €

Cay10012539-50
CAS: 916046-​55-​4
CRTH2receptor antagonist, DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G protein-​coupled receptors, designated DP1 and CRTH2/DP2. In humans, CRTH2/DP2 is expressed on Th2 cells, eosinophils, and basophils where it mediates the ch ... mehr
MW: 416 D
Formula: C20H14ClFN2O5
Purity: >98%
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2192 €

Cay10023-1
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of PGF2alpha which acts as a potent and selective antagonist at the FP receptor. (S)-​AL 8810 is the C-​15 epimer of AL 8810, having the inverse, (S), or natural configuration at C-​15 relative to AL 8810, which is 15-​(R). ... mehr
MW: 402 D
Formula: C24H31O4F
Purity: >98%
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55 €

Cay10023-10
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of PGF2alpha which acts as a potent and selective antagonist at the FP receptor. (S)-​AL 8810 is the C-​15 epimer of AL 8810, having the inverse, (S), or natural configuration at C-​15 relative to AL 8810, which is 15-​(R). ... mehr
MW: 402 D
Formula: C24H31O4F
Purity: >98%
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436 €

Cay10023-5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11beta-​fluoro analog of PGF2alpha which acts as a potent and selective antagonist at the FP receptor. (S)-​AL 8810 is the C-​15 epimer of AL 8810, having the inverse, (S), or natural configuration at C-​15 relative to AL 8810, which is 15-​(R). ... mehr
MW: 402 D
Formula: C24H31O4F
Purity: >98%
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246 €

Cay10029-1
CAS: 115104-​28-​4
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
The cysteinyl leukotrienes (CysLTs), leukotriene (LTC4), LTD4, and LTE4, mediate their actions through two distinct G-​protein coupled receptors. LTD4 is the preferred ligand for the cysLT1 receptor, whereas LTC4 and LTD4 bind with approximately equal affi ... mehr
MW: 515 D
Formula: C26H27ClN2O3S2
Purity: >95%
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29 €

Cay10029-10
CAS: 115104-​28-​4
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
The cysteinyl leukotrienes (CysLTs), leukotriene (LTC4), LTD4, and LTE4, mediate their actions through two distinct G-​protein coupled receptors. LTD4 is the preferred ligand for the cysLT1 receptor, whereas LTC4 and LTD4 bind with approximately equal affi ... mehr
MW: 515 D
Formula: C26H27ClN2O3S2
Purity: >95%
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114 €

Cay10029-5
CAS: 115104-​28-​4
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
The cysteinyl leukotrienes (CysLTs), leukotriene (LTC4), LTD4, and LTE4, mediate their actions through two distinct G-​protein coupled receptors. LTD4 is the preferred ligand for the cysLT1 receptor, whereas LTC4 and LTD4 bind with approximately equal affi ... mehr
MW: 515 D
Formula: C26H27ClN2O3S2
Purity: >95%
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65 €

Cay10029-50
CAS: 115104-​28-​4
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
The cysteinyl leukotrienes (CysLTs), leukotriene (LTC4), LTD4, and LTE4, mediate their actions through two distinct G-​protein coupled receptors. LTD4 is the preferred ligand for the cysLT1 receptor, whereas LTC4 and LTD4 bind with approximately equal affi ... mehr
MW: 515 D
Formula: C26H27ClN2O3S2
Purity: >95%
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508 €

Cay10113-1
CAS: 208114-​93-​6
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of prostaglandin F2.alpha. (PGF2.alpha.) which acts as a potent and selective antagonist at the FP receptor.
MW: 444 D
Formula: C27H37FO4
Purity: >98%
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63 €

Cay10113-10
CAS: 208114-​93-​6
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of prostaglandin F2.alpha. (PGF2.alpha.) which acts as a potent and selective antagonist at the FP receptor.
MW: 444 D
Formula: C27H37FO4
Purity: >98%
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501 €

Cay10113-5
CAS: 208114-​93-​6
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of prostaglandin F2.alpha. (PGF2.alpha.) which acts as a potent and selective antagonist at the FP receptor.
MW: 444 D
Formula: C27H37FO4
Purity: >98%
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5 mg

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282 €

Cay10113-50
CAS: 208114-​93-​6
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of prostaglandin F2.alpha. (PGF2.alpha.) which acts as a potent and selective antagonist at the FP receptor.
MW: 444 D
Formula: C27H37FO4
Purity: >98%
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2192 €

Cay10156-1
CAS: 116649-​85-​5
DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G-​protein coupled receptors, designated DP1 and DP2/CRTH2. BAY-​u3405 (Ramatroban) is an approved human medication for the treatment of allergic rhinitis that ... mehr
MW: 416 D
Formula: C21H21FN2O4S
Purity: >98%
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1 mg

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20 €

Cay10156-10
CAS: 116649-​85-​5
DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G-​protein coupled receptors, designated DP1 and DP2/CRTH2. BAY-​u3405 (Ramatroban) is an approved human medication for the treatment of allergic rhinitis that ... mehr
MW: 416 D
Formula: C21H21FN2O4S
Purity: >98%
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158 €

Cay10156-5
CAS: 116649-​85-​5
DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G-​protein coupled receptors, designated DP1 and DP2/CRTH2. BAY-​u3405 (Ramatroban) is an approved human medication for the treatment of allergic rhinitis that ... mehr
MW: 416 D
Formula: C21H21FN2O4S
Purity: >98%
Cayman
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89 €

Cay10156-50
CAS: 116649-​85-​5
DP2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The biological effects of prostaglandin D2 (PGD2) are transduced by at least two 7-​transmembrane G-​protein coupled receptors, designated DP1 and DP2/CRTH2. BAY-​u3405 (Ramatroban) is an approved human medication for the treatment of allergic rhinitis that ... mehr
MW: 416 D
Formula: C21H21FN2O4S
Purity: >98%
Cayman
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690 €

Cay14070-1
CAS: 216158-​34-​8
EP1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) initiates its cellular effects by activating one of four E prostanoid (EP) receptors, EP1-​4. ONO-​8711 is a potent and selective competitive antagonist of the EP1 receptor (Ki = 0.6 and 1.7 nM for human and mouse EP1, respectively, ... mehr
MW: 439 D
Formula: C22H30ClNO4S
Purity: >98%
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1 mg

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87 €

Cay14070-10
CAS: 216158-​34-​8
EP1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) initiates its cellular effects by activating one of four E prostanoid (EP) receptors, EP1-​4. ONO-​8711 is a potent and selective competitive antagonist of the EP1 receptor (Ki = 0.6 and 1.7 nM for human and mouse EP1, respectively, ... mehr
MW: 439 D
Formula: C22H30ClNO4S
Purity: >98%
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549 €

Cay14070-25
CAS: 216158-​34-​8
EP1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) initiates its cellular effects by activating one of four E prostanoid (EP) receptors, EP1-​4. ONO-​8711 is a potent and selective competitive antagonist of the EP1 receptor (Ki = 0.6 and 1.7 nM for human and mouse EP1, respectively, ... mehr
MW: 439 D
Formula: C22H30ClNO4S
Purity: >98%
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979 €

Cay14070-5
CAS: 216158-​34-​8
EP1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Prostaglandin E2 (PGE2) initiates its cellular effects by activating one of four E prostanoid (EP) receptors, EP1-​4. ONO-​8711 is a potent and selective competitive antagonist of the EP1 receptor (Ki = 0.6 and 1.7 nM for human and mouse EP1, respectively, ... mehr
MW: 439 D
Formula: C22H30ClNO4S
Purity: >98%
Cayman
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5 mg

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343 €

Cay14532-1
CAS: 105219-​56-​5
PAF receptor antagonist Erklärungen der Abkürzungen ansehen.
Platelet-​activating factor (PAF) is a biologically active phospholipid that activates platelets, polymorphonuclear leukocytes, monocytes, and macrophages. PAF also increases vascular permeability, decreases cardiac output, induces hypotension, stimulates ... mehr
MW: 456 D
Formula: C22H22ClN5O2S
Purity: >98%
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1 mg

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46 €

Cay14532-5
CAS: 105219-​56-​5
PAF receptor antagonist Erklärungen der Abkürzungen ansehen.
Platelet-​activating factor (PAF) is a biologically active phospholipid that activates platelets, polymorphonuclear leukocytes, monocytes, and macrophages. PAF also increases vascular permeability, decreases cardiac output, induces hypotension, stimulates ... mehr
MW: 456 D
Formula: C22H22ClN5O2S
Purity: >98%
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5 mg

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116 €

Cay16032-1
CAS: 68192-​15-​4
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 381 D
Formula: C22H39NO4
Purity: >98%
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1 mg

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60 €

Cay16032-10
CAS: 68192-​15-​4
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 381 D
Formula: C22H39NO4
Purity: >98%
Cayman
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10 mg

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483 €

Cay16032-5
CAS: 68192-​15-​4
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 381 D
Formula: C22H39NO4
Purity: >98%
Cayman
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5 mg

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271 €

Cay16033-1
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 367 D
Formula: C22H41NO3
Purity: >98%
Cayman
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44 €

Cay16033-10
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 367 D
Formula: C22H41NO3
Purity: >98%
Cayman
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10 mg

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353 €

Cay16033-5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
PGF2.alpha. dimethyl amide is a weak FP receptor antagonist. In gerbil colon, PGF2.alpha. dimethyl amide at a dose of 3.2 µg/ml inhibits the contractile effects of PGF2.alpha. (at 6 ng/ml) by 50%.
MW: 367 D
Formula: C22H41NO3
Purity: >98%
Cayman
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5 mg

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198 €

Cay16735-1
CAS: 246246-​19-​5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of PGF2.alpha. which acts as a potent and selective antagonist at the FP receptor.
MW: 402 D
Formula: C24H31O4F
Purity: >98%
Cayman
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1 mg

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97 €

Cay16735-10
CAS: 246246-​19-​5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of PGF2.alpha. which acts as a potent and selective antagonist at the FP receptor.
MW: 402 D
Formula: C24H31O4F
Purity: >98%
Cayman
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10 mg

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780 €

Cay16735-25
CAS: 246246-​19-​5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of PGF2.alpha. which acts as a potent and selective antagonist at the FP receptor.
MW: 402 D
Formula: C24H31O4F
Purity: >98%
Cayman
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25 mg

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1705 €

Cay16735-5
CAS: 246246-​19-​5
FP receptor antagonist Erklärungen der Abkürzungen ansehen.
AL 8810 is an 11.beta.-fluoro analog of PGF2.alpha. which acts as a potent and selective antagonist at the FP receptor.
MW: 402 D
Formula: C24H31O4F
Purity: >98%
Cayman
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5 mg

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438 €

Cay19021-1
CAS: 133538-​58-​6
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
I-SAP is a high affinity TP receptor antagonist. At physiologic pH, I-SAP produces platelet shape change, but not aggregation, with an EC50 value of 9.7 nM.
MW: 531 D
Formula: C22H30INO4S
Purity: >98%
Cayman
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1 mg

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548 €

Cay19021-100
CAS: 133538-​58-​6
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
I-SAP is a high affinity TP receptor antagonist. At physiologic pH, I-SAP produces platelet shape change, but not aggregation, with an EC50 value of 9.7 nM.
MW: 531 D
Formula: C22H30INO4S
Purity: >98%
Cayman
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100 µg

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68 €

Cay19021-500
CAS: 133538-​58-​6
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
I-SAP is a high affinity TP receptor antagonist. At physiologic pH, I-SAP produces platelet shape change, but not aggregation, with an EC50 value of 9.7 nM.
MW: 531 D
Formula: C22H30INO4S
Purity: >98%
Cayman
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500 µg

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309 €

Cay19023-1
TP receptor antagonist, EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Thromboxane (TXA2) activates the T prostanoid (TP) receptor. Prostaglandin E2 (PGE2) activates four E prostanoid (EP) receptors, EP1-​4. AH-​23848 is a dual antagonist of TP and EP4 receptors. It originally was found to inhibit TXA2-​induced platelet aggrega ... mehr
MW: 1.011 D
Formula: (C29H34NO5)2 Ca2 ? xH2O
Purity: >90%
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75 €

Cay19023-10
TP receptor antagonist, EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Thromboxane (TXA2) activates the T prostanoid (TP) receptor. Prostaglandin E2 (PGE2) activates four E prostanoid (EP) receptors, EP1-​4. AH-​23848 is a dual antagonist of TP and EP4 receptors. It originally was found to inhibit TXA2-​induced platelet aggrega ... mehr
MW: 1.011 D
Formula: (C29H34NO5)2 Ca2 ? xH2O
Purity: >90%
Cayman
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10 mg

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603 €

Cay19023-5
TP receptor antagonist, EP4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Thromboxane (TXA2) activates the T prostanoid (TP) receptor. Prostaglandin E2 (PGE2) activates four E prostanoid (EP) receptors, EP1-​4. AH-​23848 is a dual antagonist of TP and EP4 receptors. It originally was found to inhibit TXA2-​induced platelet aggrega ... mehr
MW: 1.011 D
Formula: (C29H34NO5)2 Ca2 ? xH2O
Purity: >90%
Cayman
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5 mg

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340 €

Cay19025-1
CAS: 98672-​91-​4
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
SQ 29,548 is a highly selective TP receptor antagonist which binds to the human recombinant TP receptor with a Ki of 4.1 nm. It inhibits the aggregation of washed human platelets induced by U-​46619 with an IC50 of 0.06 µM. It antagonizes U-​46619 induced c ... mehr
MW: 387 D
Formula: C21H29N3O4
Purity: >99%
Cayman
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1 mg

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68 €

Cay19025-10
CAS: 98672-​91-​4
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
SQ 29,548 is a highly selective TP receptor antagonist which binds to the human recombinant TP receptor with a Ki of 4.1 nm. It inhibits the aggregation of washed human platelets induced by U-​46619 with an IC50 of 0.06 µM. It antagonizes U-​46619 induced c ... mehr
MW: 387 D
Formula: C21H29N3O4
Purity: >99%
Cayman
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10 mg

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548 €

Cay19025-100
CAS: 98672-​91-​4
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
SQ 29,548 is a highly selective TP receptor antagonist which binds to the human recombinant TP receptor with a Ki of 4.1 nm. It inhibits the aggregation of washed human platelets induced by U-​46619 with an IC50 of 0.06 µM. It antagonizes U-​46619 induced c ... mehr
MW: 387 D
Formula: C21H29N3O4
Purity: >99%
Cayman
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100 mg

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4106 €

Cay19025-5
CAS: 98672-​91-​4
TP receptor antagonist Erklärungen der Abkürzungen ansehen.
SQ 29,548 is a highly selective TP receptor antagonist which binds to the human recombinant TP receptor with a Ki of 4.1 nm. It inhibits the aggregation of washed human platelets induced by U-​46619 with an IC50 of 0.06 µM. It antagonizes U-​46619 induced c ... mehr
MW: 387 D
Formula: C21H29N3O4
Purity: >99%
Cayman
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5 mg

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309 €

Cay20112-100
CAS: 877459-​63-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LTB4 ethanolamide (LTB4-EA) is a theoretical 5-LO metabolite of arachidonoyl ethanolamide (AEA). In CHO cells transfected with human BLTR1, LTB4-EA was a potent antagonist with about three times greater affinity for the receptor than LTB4
MW: 379 D
Formula: C22H37NO4
Purity: >97%
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100 µg

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467 €

Cay20112-25
CAS: 877459-​63-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LTB4 ethanolamide (LTB4-EA) is a theoretical 5-LO metabolite of arachidonoyl ethanolamide (AEA). In CHO cells transfected with human BLTR1, LTB4-EA was a potent antagonist with about three times greater affinity for the receptor than LTB4
MW: 379 D
Formula: C22H37NO4
Purity: >97%
Cayman
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25 µg

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130 €

Cay20112-50
CAS: 877459-​63-​7
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LTB4 ethanolamide (LTB4-EA) is a theoretical 5-LO metabolite of arachidonoyl ethanolamide (AEA). In CHO cells transfected with human BLTR1, LTB4-EA was a potent antagonist with about three times greater affinity for the receptor than LTB4
MW: 379 D
Formula: C22H37NO4
Purity: >97%
Cayman
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50 µg

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247 €

Cay20150-100
CAS: 114616-​11-​4
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
14,15-dehydro LTB4 is a LTB4 receptor antagonist that has a higher binding affinity for BLT1.
MW: 334 D
Formula: C20H30O4
Purity: >97%
Cayman
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100 µg

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467 €

Cay20150-25
CAS: 114616-​11-​4
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
14,15-dehydro LTB4 is a LTB4 receptor antagonist that has a higher binding affinity for BLT1.
MW: 334 D
Formula: C20H30O4
Purity: >97%
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25 µg

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130 €

Cay20150-50
CAS: 114616-​11-​4
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
14,15-dehydro LTB4 is a LTB4 receptor antagonist that has a higher binding affinity for BLT1.
MW: 334 D
Formula: C20H30O4
Purity: >97%
Cayman
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50 µg

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247 €

Cay60950-1
CAS: 116673-​45-​1
PAF receptor antagonist Erklärungen der Abkürzungen ansehen.
trans-BTP Dioxolane is a PAF receptor antagonist. This compound demonstrates competitive antagonism of PAF in a rabbit washed platelet assay (Ki = 0.3 µM).
MW: 406 D
Formula: C21H26O8
Purity: >98%
Cayman
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1 mg

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41 €

Cay60950-10
CAS: 116673-​45-​1
PAF receptor antagonist Erklärungen der Abkürzungen ansehen.
trans-BTP Dioxolane is a PAF receptor antagonist. This compound demonstrates competitive antagonism of PAF in a rabbit washed platelet assay (Ki = 0.3 µM).
MW: 406 D
Formula: C21H26O8
Purity: >98%
Cayman
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10 mg

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306 €

Cay60950-5
CAS: 116673-​45-​1
PAF receptor antagonist Erklärungen der Abkürzungen ansehen.
trans-BTP Dioxolane is a PAF receptor antagonist. This compound demonstrates competitive antagonism of PAF in a rabbit washed platelet assay (Ki = 0.3 µM).
MW: 406 D
Formula: C21H26O8
Purity: >98%
Cayman
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5 mg

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172 €

Cay70705-100
CAS: 119477-​85-​9
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
U-75302 is an LTB4 receptor antagonist with a Ki of 159 nM on guinea pig lung membranes. This activity is specific for the BLT1 receptor. U-75302 does not antagonize the binding of [3H]-LTB4 to the human BLT2 receptor.
MW: 361 D
Formula: C22H35NO3
Purity: >98%
Cayman
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100 µg

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119 €

Cay70705-50
CAS: 119477-​85-​9
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
U-75302 is an LTB4 receptor antagonist with a Ki of 159 nM on guinea pig lung membranes. This activity is specific for the BLT1 receptor. U-75302 does not antagonize the binding of [3H]-LTB4 to the human BLT2 receptor.
MW: 361 D
Formula: C22H35NO3
Purity: >98%
Cayman
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50 µg

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63 €

Cay70705-500
CAS: 119477-​85-​9
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
U-75302 is an LTB4 receptor antagonist with a Ki of 159 nM on guinea pig lung membranes. This activity is specific for the BLT1 receptor. U-75302 does not antagonize the binding of [3H]-LTB4 to the human BLT2 receptor.
MW: 361 D
Formula: C22H35NO3
Purity: >98%
Cayman
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500 µg

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501 €

Cay70710-10
CAS: 88107-​10-​2
LTD4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LY171883 is a selective, potent, orally active antagonist of the leukotriene D4 receptor.
MW: 318 D
Formula: C16H22N4O3
Purity: >98%
Cayman
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10 mg

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71 €

Cay70710-100
CAS: 88107-​10-​2
LTD4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LY171883 is a selective, potent, orally active antagonist of the leukotriene D4 receptor.
MW: 318 D
Formula: C16H22N4O3
Purity: >98%
Cayman
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100 mg

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520 €

Cay70710-5
CAS: 88107-​10-​2
LTD4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LY171883 is a selective, potent, orally active antagonist of the leukotriene D4 receptor.
MW: 318 D
Formula: C16H22N4O3
Purity: >98%
Cayman
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5 mg

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37 €

Cay70710-50
CAS: 88107-​10-​2
LTD4 receptor antagonist Erklärungen der Abkürzungen ansehen.
LY171883 is a selective, potent, orally active antagonist of the leukotriene D4 receptor.
MW: 318 D
Formula: C16H22N4O3
Purity: >98%
Cayman
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50 mg

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297 €

Cay70715-1
CAS: 117690-​79-​6
BTL2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The tetrazole LY255283 is a competitive antagonist of the BLT2 receptor.
MW: 360 D
Formula: C19H28N4O3
Purity: >98%
Cayman
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1 mg

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22 €

Cay70715-10
CAS: 117690-​79-​6
BTL2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The tetrazole LY255283 is a competitive antagonist of the BLT2 receptor.
MW: 360 D
Formula: C19H28N4O3
Purity: >98%
Cayman
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10 mg

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132 €

Cay70715-25
CAS: 117690-​79-​6
BTL2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The tetrazole LY255283 is a competitive antagonist of the BLT2 receptor.
MW: 360 D
Formula: C19H28N4O3
Purity: >98%
Cayman
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25 mg

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248 €

Cay70715-5
CAS: 117690-​79-​6
BTL2 receptor antagonist Erklärungen der Abkürzungen ansehen.
The tetrazole LY255283 is a competitive antagonist of the BLT2 receptor.
MW: 360 D
Formula: C19H28N4O3
Purity: >98%
Cayman
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5 mg

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88 €

Cay70720-1
CAS: 115103-​85-​0
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
MK 571 is a selective, orally active CysLT1 receptor antagonist. It blocks the binding of LTD4, but not LTC4, to human and guinea pig lung membranes.
MW: 537 D
Formula: C26H26ClN2O3S2 · Na
Purity: >95%
Cayman
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1 mg

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29 €

Cay70720-10
CAS: 115103-​85-​0
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
MK 571 is a selective, orally active CysLT1 receptor antagonist. It blocks the binding of LTD4, but not LTC4, to human and guinea pig lung membranes.
MW: 537 D
Formula: C26H26ClN2O3S2 · Na
Purity: >95%
Cayman
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10 mg

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102 €

Cay70720-5
CAS: 115103-​85-​0
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
MK 571 is a selective, orally active CysLT1 receptor antagonist. It blocks the binding of LTD4, but not LTC4, to human and guinea pig lung membranes.
MW: 537 D
Formula: C26H26ClN2O3S2 · Na
Purity: >95%
Cayman
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5 mg

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58 €

Cay70720-50
CAS: 115103-​85-​0
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
MK 571 is a selective, orally active CysLT1 receptor antagonist. It blocks the binding of LTD4, but not LTC4, to human and guinea pig lung membranes.
MW: 537 D
Formula: C26H26ClN2O3S2 · Na
Purity: >95%
Cayman
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50 mg

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435 €

Cay70770-100
CAS: 154978-​38-​8
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
BAY-u9773 is a non-selective antagonist of the CysLT receptors, having about the same IC50 (20-80 nM) for the inhibition of LT responses in a variety of tissue preparations containing either/or both receptors.
MW: 472 D
Formula: C27H36O5S
Purity: >95%
Cayman
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100 µg

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193 €

Cay70770-25
CAS: 154978-​38-​8
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
BAY-u9773 is a non-selective antagonist of the CysLT receptors, having about the same IC50 (20-80 nM) for the inhibition of LT responses in a variety of tissue preparations containing either/or both receptors.
MW: 472 D
Formula: C27H36O5S
Purity: >95%
Cayman
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25 µg

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53 €

Cay70770-50
CAS: 154978-​38-​8
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
BAY-u9773 is a non-selective antagonist of the CysLT receptors, having about the same IC50 (20-80 nM) for the inhibition of LT responses in a variety of tissue preparations containing either/or both receptors.
MW: 472 D
Formula: C27H36O5S
Purity: >95%
Cayman
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50 µg

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101 €

Cay70770-500
CAS: 154978-​38-​8
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
BAY-u9773 is a non-selective antagonist of the CysLT receptors, having about the same IC50 (20-80 nM) for the inhibition of LT responses in a variety of tissue preparations containing either/or both receptors.
MW: 472 D
Formula: C27H36O5S
Purity: >95%
Cayman
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500 µg

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854 €

Cay9000629-10
CAS: 1002100-​44-​8
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Oleoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, reducin ... mehr
Cayman
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10 mg

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73 €

Cay9000629-100
CAS: 1002100-​44-​8
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Oleoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, reducin ... mehr
Cayman
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100 mg

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536 €

Cay9000629-5
CAS: 1002100-​44-​8
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Oleoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, reducin ... mehr
Cayman
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5 mg

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38 €

Cay9000629-50
CAS: 1002100-​44-​8
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Oleoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, reducin ... mehr
Cayman
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50 mg

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306 €

Cay9000630-1
CAS: 212707-​51-​2
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Palmitoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, redu ... mehr
Cayman
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1 mg

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61 €

Cay9000630-10
CAS: 212707-​51-​2
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Palmitoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, redu ... mehr
Cayman
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10 mg

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492 €

Cay9000630-25
CAS: 212707-​51-​2
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Palmitoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, redu ... mehr
Cayman
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25 mg

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1076 €

Cay9000630-5
CAS: 212707-​51-​2
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Palmitoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel, redu ... mehr
Cayman
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5 mg

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277 €

Cay9000631-1
CAS: 67964-​87-​8
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Stearoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid-​type 1 (TRPV1) channel, ... mehr
Cayman
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1 mg

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61 €

Cay9000631-10
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Stearoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid-​type 1 (TRPV1) channel, ... mehr
Cayman
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10 mg

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492 €

Cay9000631-25
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Stearoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid-​type 1 (TRPV1) channel, ... mehr
Cayman
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25 mg

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1076 €

Cay9000631-5
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Stearoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid-​type 1 (TRPV1) channel, ... mehr
Cayman
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5 mg

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277 €

Cay9000639-10
CAS: 283601-​58-​1
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Docosahexaenoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel ... mehr
Cayman
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10 mg

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73 €

Cay9000639-100
CAS: 283601-​58-​1
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Docosahexaenoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel ... mehr
Cayman
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100 mg

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536 €

Cay9000639-5
CAS: 283601-​58-​1
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Docosahexaenoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel ... mehr
Cayman
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5 mg

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38 €

Cay9000639-50
CAS: 283601-​58-​1
FAAH / TRPV1 antagonist, pain studies Erklärungen der Abkürzungen ansehen.
Docosahexaenoyl serotonin is a hybrid molecule patterned after arachidonoyl serotonin (Catalog No. Cay70665). Arachidonoyl serotonin is a dual antagonist of fatty acid amide hydrolase (FAAH) and the transient receptor potential vanilloid 1 (TRPV1) channel ... mehr
Cayman
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50 mg

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306 €

Cay9000738-1
CAS: 31450-​14-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma-​Linolenic acid (GLA) is an omega-​6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak leukotriene B4 (LTB4) receptor antagonist, inhibiting [3H]-​LTB4 binding to porcine neutrophil membranes with a ... mehr
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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1 g

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325 €

Cay9000738-100
CAS: 31450-​14-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma-​Linolenic acid (GLA) is an omega-​6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak leukotriene B4 (LTB4) receptor antagonist, inhibiting [3H]-​LTB4 binding to porcine neutrophil membranes with a ... mehr
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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100 mg

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44 €

Cay9000738-250
CAS: 31450-​14-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma-​Linolenic acid (GLA) is an omega-​6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak leukotriene B4 (LTB4) receptor antagonist, inhibiting [3H]-​LTB4 binding to porcine neutrophil membranes with a ... mehr
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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250 mg

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104 €

Cay9000738-50
CAS: 31450-​14-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma-​Linolenic acid (GLA) is an omega-​6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak leukotriene B4 (LTB4) receptor antagonist, inhibiting [3H]-​LTB4 binding to porcine neutrophil membranes with a ... mehr
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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50 mg

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23 €

Cay90220-1
CAS: 506-​26-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma.-Linolenic acid (GLA) is an .omega.-6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak LTB4 receptor antagonist
MW: 278 D
Formula: C18H30O2
Purity: >98%
Cayman
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1 g

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325 €

Cay90220-100
CAS: 506-​26-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma.-Linolenic acid (GLA) is an .omega.-6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak LTB4 receptor antagonist
MW: 278 D
Formula: C18H30O2
Purity: >98%
Cayman
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100 mg

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44 €

Cay90220-250
CAS: 506-​26-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma.-Linolenic acid (GLA) is an .omega.-6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak LTB4 receptor antagonist
MW: 278 D
Formula: C18H30O2
Purity: >98%
Cayman
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250 mg

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104 €

Cay90220-50
CAS: 506-​26-​3
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
gamma.-Linolenic acid (GLA) is an .omega.-6 fatty acid which can be elongated to arachidonic acid for endogenous eicosanoid synthesis. It is a weak LTB4 receptor antagonist
MW: 278 D
Formula: C18H30O2
Purity: >98%
Cayman
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50 mg

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23 €

Cay90230-10
CAS: 1783-​84-​2
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Dihomo-.gamma.-Linolenic acid (DGLA) is an .omega.-6 essential fatty acid especially abundant in primrose seed oil. DGLA is a weak antagonist of the LTB4 receptor with a Ki of about 1 µM.
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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10 mg

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23 €

Cay90230-100
CAS: 1783-​84-​2
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Dihomo-.gamma.-Linolenic acid (DGLA) is an .omega.-6 essential fatty acid especially abundant in primrose seed oil. DGLA is a weak antagonist of the LTB4 receptor with a Ki of about 1 µM.
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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100 mg

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186 €

Cay90230-50
CAS: 1783-​84-​2
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Dihomo-.gamma.-Linolenic acid (DGLA) is an .omega.-6 essential fatty acid especially abundant in primrose seed oil. DGLA is a weak antagonist of the LTB4 receptor with a Ki of about 1 µM.
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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50 mg

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104 €

Cay90230-500
CAS: 1783-​84-​2
LTB4 receptor antagonist Erklärungen der Abkürzungen ansehen.
Dihomo-.gamma.-Linolenic acid (DGLA) is an .omega.-6 essential fatty acid especially abundant in primrose seed oil. DGLA is a weak antagonist of the LTB4 receptor with a Ki of about 1 µM.
MW: 306 D
Formula: C20H34O2
Purity: >98%
Cayman
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500 mg

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812 €

SIH-361-10MG
CAS: 107753-​78-​6
CysLT1 receptor antagonist Erklärungen der Abkürzungen ansehen.
Zafirlukast is a potent, selective CysLT1 receptor antagonist sold under the trade name Accolate for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. It binds to the human CysLT1 and CysLT2 receptors with IC50 values ... mehr
MW: 575 D
Formula: C31H33N3O6S
StressMarq
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10 mg

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105 €



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