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SIH-252-25MG LY 294002
CAS: 154447-​36-​6
PI 3-​Kinase inhibitor Erklärungen der Abkürzungen ansehen.
LY294002 is a potent inhibitor of PI3Ks. It inhibits proliferation and induces apoptosis in human colon cancer cells in vitro and in vivo.
MW: 343 D
Formula: C19H17NO3 - HCl
Purity: >99%
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25 mg

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461 €

SIH-252-5MG LY 294002
CAS: 154447-​36-​6
PI 3-​Kinase inhibitor Erklärungen der Abkürzungen ansehen.
LY294002 is a potent inhibitor of PI3Ks. It inhibits proliferation and induces apoptosis in human colon cancer cells in vitro and in vivo.
MW: 343 D
Formula: C19H17NO3 - HCl
Purity: >99%
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5 mg

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114 €

SIH-256-10MG Lovastatin
CAS: 75330-​75-​5
HMG-​CoA reductase inhibitor Erklärungen der Abkürzungen ansehen.
Lovastatin is a member of the drug class of statins, used for lowering cholersterol, thereby preventing cardiovascular disease. They have a powerful inhibitory effect on HMG-CoA reducatse .
MW: 404 D
Formula: C24H36O5
Purity: >99%
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10 mg

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58 €

SIH-256-50MG Lovastatin
CAS: 75330-​75-​5
HMG-​CoA reductase inhibitor Erklärungen der Abkürzungen ansehen.
Lovastatin is a member of the drug class of statins, used for lowering cholersterol, thereby preventing cardiovascular disease. They have a powerful inhibitory effect on HMG-CoA reducatse .
MW: 404 D
Formula: C24H36O5
Purity: >99%
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50 mg

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241 €

SIH-327-1MG Lactacystin
CAS: 133343-​34-​7
Proteasome inhibitor Erklärungen der Abkürzungen ansehen.
Specific inhibitor of three proteolytic activities of the proteasome. Chymotrypsin-like activity is inhibited most potently followed by trypsin-like activity. Peptidyl-glutamyl peptide hydrolytic activity is relatively weak.
MW: 376 D
Formula: C15H24N2O7
Purity: >98%
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1 mg

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763 €

SIH-327-200UG Lactacystin
CAS: 133343-​34-​7
Proteasome inhibitor Erklärungen der Abkürzungen ansehen.
Specific inhibitor of three proteolytic activities of the proteasome. Chymotrypsin-like activity is inhibited most potently followed by trypsin-like activity. Peptidyl-glutamyl peptide hydrolytic activity is relatively weak.
MW: 376 D
Formula: C15H24N2O7
Purity: >98%
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200 µg

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260 €

SIH-332-10MG LDN-​57444
CAS: 668467-​91-​2
DUB inhibitor Erklärungen der Abkürzungen ansehen.
Inhibits ubiquitin C-terminal hydrolase (UCH-L1). Decreases proteasome activity and increases levels of ubiquitinated proteins. Induces apoptosis. Causes dramatic alterations in synaptic protein distribution and spine morphology in vivo. Cell permeable.
MW: 397 D
Formula: C17H11Cl3N2O3
Purity: >98%
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10 mg

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139 €

SIH-332-50MG LDN-​57444
CAS: 668467-​91-​2
DUB inhibitor Erklärungen der Abkürzungen ansehen.
Inhibits ubiquitin C-terminal hydrolase (UCH-L1). Decreases proteasome activity and increases levels of ubiquitinated proteins. Induces apoptosis. Causes dramatic alterations in synaptic protein distribution and spine morphology in vivo. Cell permeable.
MW: 397 D
Formula: C17H11Cl3N2O3
Purity: >98%
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50 mg

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559 €

SIH-368-50MG
CAS: 75706-​12-​6
Immunosupressant Erklärungen der Abkürzungen ansehen.
Leflunomide is an Immuno-​suppressant, it inhibits de novo synthesis of pyrimidine nucleotides and the activity of the protein kinase. It is a part of the known 'disease-​modifying anti-​rheumatic drugs' (DMARD). It has been suggested that leflunomide modula ... mehr
MW: 270 D
Formula: C12H9F3N2O2
Purity: >98%
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50 mg

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58 €

SIH-403-25MG
CAS: 22556-​62-​3
Autophagy inhibitor Erklärungen der Abkürzungen ansehen.
Oleoyl-​lysophosphatidic acid is an endogenous agonist of the lysophospholipid receptors LPA1 and LPA2. It has been shown to induce cellular functions such as cell proliferation and migration, and ICAM-​1, IL-​8 and MCP-​1 expression. Lysophosphatidic acid ... mehr
MW: 436 D
Formula: C21H41O7P
Purity: >96%
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25 mg

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294 €


 

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