| 232 Treffer |
| ART-NR | PRODUKT | HERSTELLER | MENGE | PREIS |
| Cay81500-10 |
iNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
10 mg |
16 €
|
| Cay81500-100 |
iNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
100 mg |
130 €
|
| Cay81500-25 |
iNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
25 mg |
38 €
|
| Cay81500-50 |
iNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
50 mg |
73 €
|
| Cay81510-10 |
CAS: 157254-60-9 iNOS inhibitor, nNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
10 mg |
14 €
|
| Cay81510-100 |
CAS: 157254-60-9 iNOS inhibitor, nNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
100 mg |
111 €
|
| Cay81510-50 |
CAS: 157254-60-9 iNOS inhibitor, nNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
50 mg |
63 €
|
| Cay81510-500 |
CAS: 157254-60-9 iNOS inhibitor, nNOS inhibitor MW: 444 D Formula: C12H18N4S2 . 2HBr Purity: >98% |
Cayman |
500 mg |
487 €
|
| Cay81520-10 |
CAS: 214358-33-5 iNOS inhibitor 1400W is a potent, selective inhibitor of iNOS. Using purified human iNOS, nNOS, and eNOS, 1400W exhibits Ki values of 7 nM, 2 µM, and 50 µM, respectively. MW: 250 D Formula: C10H15N3 · 2HCl Purity: >98% |
Cayman |
10 mg |
93 €
|
| Cay81520-100 |
CAS: 180001-34-7 iNOS inhibitor 1400W is a potent, selective inhibitor of iNOS. Using purified human iNOS, nNOS, and eNOS, 1400W exhibits Ki values of 7 nM, 2 µM, and 50 µM, respectively. MW: 250 D Formula: C10H15N3 · 2HCl Purity: >98% |
Cayman |
100 mg |
682 €
|
| Cay81520-5 |
CAS: 180001-34-7 iNOS inhibitor 1400W is a potent, selective inhibitor of iNOS. Using purified human iNOS, nNOS, and eNOS, 1400W exhibits Ki values of 7 nM, 2 µM, and 50 µM, respectively. MW: 250 D Formula: C10H15N3 · 2HCl Purity: >98% |
Cayman |
5 mg |
49 €
|
| Cay81520-50 |
CAS: 180001-34-7 iNOS inhibitor 1400W is a potent, selective inhibitor of iNOS. Using purified human iNOS, nNOS, and eNOS, 1400W exhibits Ki values of 7 nM, 2 µM, and 50 µM, respectively. MW: 250 D Formula: C10H15N3 · 2HCl Purity: >98% |
Cayman |
50 mg |
390 €
|
| AG-CR1-0018-M005 |
CAS: 214358-33-5 iNOS inhibitor A slow, tight binding and highly selective inhibitor of iNOS (inducible nitric oxide synthase/NOS II) (Kd &le, 7 nM), Weak and reversible inhibition of nNOS (neuronal nitric oxide synthase/NOS I) (Ki &le, 2) and eNOS (endothelial nitric oxide synthase/NOS ... mehr MW: 250 D Formula: C10H15N3 . 2HCl Purity: >98% |
Adipogen |
5 mg |
55 €
|
| AG-CR1-0018-M025 |
CAS: 214358-33-5 iNOS inhibitor A slow, tight binding and highly selective inhibitor of iNOS (inducible nitric oxide synthase/NOS II) (Kd &le, 7 nM), Weak and reversible inhibition of nNOS (neuronal nitric oxide synthase/NOS I) (Ki &le, 2) and eNOS (endothelial nitric oxide synthase/NOS ... mehr MW: 250 D Formula: C10H15N3 . 2HCl Purity: >98% |
Adipogen |
25 mg |
220 €
|
| AG-CR1-0018-M100 |
CAS: 214358-33-5 iNOS inhibitor A slow, tight binding and highly selective inhibitor of iNOS (inducible nitric oxide synthase/NOS II) (Kd &le, 7 nM), Weak and reversible inhibition of nNOS (neuronal nitric oxide synthase/NOS I) (Ki &le, 2) and eNOS (endothelial nitric oxide synthase/NOS ... mehr MW: 250 D Formula: C10H15N3 . 2HCl Purity: >98% |
Adipogen |
100 mg |
660 €
|
| BVT-0244-C100 |
CAS: 75747-14-7 Hsp90 inhibitor Potent, less toxic analog of geldanamycin, Inhibits the essential ATPase activity of HSP90, Telomerase activity inhibitor, Apoptosis inducer, Antitumor compound. Semi-synthetic derivative from geldanamycin. MW: 585 D Formula: C31H43N3O8 Purity: >98% |
Adipogen |
100 µg |
60 €
|
| BVT-0244-M001 |
CAS: 75747-14-7 Hsp90 inhibitor Potent, less toxic analog of geldanamycin, Inhibits the essential ATPase activity of HSP90, Telomerase activity inhibitor, Apoptosis inducer, Antitumor compound. Semi-synthetic derivative from geldanamycin. MW: 585 D Formula: C31H43N3O8 Purity: >98% |
Adipogen |
1 mg |
110 €
|
| Cay11039-1 |
CAS: 75747-14-7 Hsp90 inhibitor Geldanamycin (Item No. Cay13355) is a potent inhibitor of Hsp90 that exhibits severe hepatotoxicity when used in vivo. 17-AAG is an analog of geldanamycin which has potent in vivo activity and reduced toxicity. Like other Hsp90 inhibitors, 17-AAG has dive ... mehr MW: 585 D Formula: C31H43N3O8 Purity: >98% |
Cayman |
1 mg |
139 €
|
| Cay11039-100 |
CAS: 75747-14-7 Hsp90 inhibitor Geldanamycin (Item No. Cay13355) is a potent inhibitor of Hsp90 that exhibits severe hepatotoxicity when used in vivo. 17-AAG is an analog of geldanamycin which has potent in vivo activity and reduced toxicity. Like other Hsp90 inhibitors, 17-AAG has dive ... mehr MW: 585 D Formula: C31H43N3O8 Purity: >98% |
Cayman |
100 µg |
35 €
|
| SIH-100A |
17-AAG CAS: 75747-14-7 Hsp90 inhibitor Geldanamycin (GA), a benzoquinone ansamycin antibiotic, interferes with the action of Hsp90 leading to degradation of Hsp90 client proteins. GA itself however has undesirable properties such as poor aqueous solubility and liver toxicity, therefore, numero ... mehr MW: 585 D Formula: C31H43N3O8 Purity: 98% |
StressMarq |
1 mg |
210 €
|
|
VB2136 |
CAS: 75747-14-7 Inhibitor of Hsp90 chaperone activity Inhibitor of Hsp90 chaperone activity. Geldanamycin analogue. Autophagy activator. Solubility: DMSO (100 mM). Appearance: Appearance: White crystalline solid. MW: 586 D Formula: C31H43N3O8 |
Vivabioscience |
1 mg |
161 €
|
| Cay11036-1 |
CAS: 467214-20-6 Angiogenesis inhibitor, Heat shock protein 90 ( HSP90 ) inhibitor Less toxic, more potent synthetic derivative of geldanamycin, Angiogenesis inhibitor, Heat shock protein 90 (HSP90) inhibitor, Apoptosis inducer, Shows higher antitumor activity than 17-AAG. Semi-synthetic derivative from geldanamycin. MW: 616 D Formula: C32H48N4O8 Purity: >98% |
Cayman |
1 mg |
32 €
|
|
Cay11036-10 |
CAS: 467214-20-6 Angiogenesis inhibitor, Heat shock protein 90 ( HSP90 ) inhibitor Less toxic, more potent synthetic derivative of geldanamycin, Angiogenesis inhibitor, Heat shock protein 90 (HSP90) inhibitor, Apoptosis inducer, Shows higher antitumor activity than 17-AAG. Semi-synthetic derivative from geldanamycin. MW: 616 D Formula: C32H48N4O8 Purity: >98% |
Cayman |
10 mg |
160 €
|
|
Cay11036-5 |
CAS: 467214-20-6 Angiogenesis inhibitor, Heat shock protein 90 ( HSP90 ) inhibitor Less toxic, more potent synthetic derivative of geldanamycin, Angiogenesis inhibitor, Heat shock protein 90 (HSP90) inhibitor, Apoptosis inducer, Shows higher antitumor activity than 17-AAG. Semi-synthetic derivative from geldanamycin. MW: 616 D Formula: C32H48N4O8 Purity: >98% |
Cayman |
5 mg |
103 €
|
| LKT-D4802.1 |
CAS: 467214-20-6 Hsp90 inhibitor A novel heat shock protein 90 inhibitor that enhances radiosensitization of MiaPaCa tumor cells. MW: 616 D |
LKT |
1 mg |
55 €
|
|
LKT-D4802.10 |
CAS: 467214-20-6 Hsp90 inhibitor A novel heat shock protein 90 inhibitor that enhances radiosensitization of MiaPaCa tumor cells. MW: 616 D |
LKT |
10 mg |
188 €
|
| LKT-D4802.5 |
CAS: 467214-20-6 Hsp90 inhibitor A novel heat shock protein 90 inhibitor that enhances radiosensitization of MiaPaCa tumor cells. MW: 616 D |
LKT |
5 mg |
107 €
|
| SIH-114A |
17-DMAG CAS: 30562-34-6 Hsp90 inhibitor 17-DMAG is a water soluble & cell-permeable analog of Geldanamycin and 17-AAG . It binds to the APTase site of human Hsp90a with high affinity, has cytotoxic activity against many cancer cell lines , and acts as angiogenesis inhibitor . This Hsp90 inhibit ... mehr MW: 616 D Formula: C32H48N4O8 Purity: 98% |
StressMarq |
1 mg |
210 €
|
|
VB2342 |
CAS: 150270-08-9 Inhibitor of Hsp90 chaperone activity Inhibitor of Hsp90 chaperone activity. Geldanamycin analogue. Autophagy activator. Solubility: DMSO (30 mg/ml), ethanol (10 mg/ml). Appearance: Appearance: Purple powder. MW: 617 D Formula: C32H48N4O8 |
Vivabioscience |
1 mg |
201 €
|
| SIH-115A |
17-GMB-APA-GA Hsp90 inhibitor An analog of geldanamycin containing a maleimido moiety suitable for preparation of geldanamycin immunoconjugates. MW: 767 D Formula: C39H53N5O11 Purity: 98% |
StressMarq |
1 mg |
234 €
|
| Cay81015-10 |
CAS: 165383-72-2 NOS inhibitor MW: 171 D Formula: C6H12N2 . C2H3O2 Purity: >98% |
Cayman |
10 mg |
63 €
|
| Cay81015-25 |
CAS: 165383-72-2 NOS inhibitor MW: 171 D Formula: C6H12N2 . C2H3O2 Purity: >98% |
Cayman |
25 mg |
139 €
|
| Cay81015-5 |
CAS: 165383-72-2 NOS inhibitor MW: 171 D Formula: C6H12N2 . C2H3O2 Purity: >98% |
Cayman |
5 mg |
35 €
|
| Cay81015-50 |
CAS: 165383-72-2 NOS inhibitor MW: 171 D Formula: C6H12N2 . C2H3O2 Purity: >98% |
Cayman |
50 mg |
191 €
|
| Cay81345-100 |
CAS: 74209-34-0 nNOS inhibitor MW: 242 D Formula: C7H4BrN3O2 Purity: >98% |
Cayman |
100 mg |
145 €
|
| Cay81345-250 |
CAS: 74209-34-0 nNOS inhibitor MW: 242 D Formula: C7H4BrN3O2 Purity: >98% |
Cayman |
250 mg |
345 €
|
| Cay81345-50 |
CAS: 74209-34-0 nNOS inhibitor MW: 242 D Formula: C7H4BrN3O2 Purity: >98% |
Cayman |
50 mg |
77 €
|
| Cay81345-500 |
CAS: 74209-34-0 nNOS inhibitor MW: 242 D Formula: C7H4BrN3O2 Purity: >98% |
Cayman |
500 mg |
612 €
|
| Cay81340-100 |
CAS: 2942-42-9 NOS inhibitor MW: 163 D Formula: C7H5N3O2 Purity: >98% |
Cayman |
100 mg |
68 €
|
| Cay81340-250 |
CAS: 2942-42-9 NOS inhibitor MW: 163 D Formula: C7H5N3O2 Purity: >98% |
Cayman |
250 mg |
162 €
|
| Cay81340-50 |
CAS: 2942-42-9 NOS inhibitor MW: 163 D Formula: C7H5N3O2 Purity: >98% |
Cayman |
50 mg |
36 €
|
| Cay81340-500 |
CAS: 2942-42-9 NOS inhibitor MW: 163 D Formula: C7H5N3O2 Purity: >98% |
Cayman |
500 mg |
288 €
|
| LKT-N3278.1 |
CAS: 2942-42-9 nNOS inhibitor A neuronal nitric oxide synthase (nNOS) inhibitor. It enhances amphetamine-evoked release, and kainic acid induced cholinergic neurotoxicity in the rat striatum. MW: 163 D Purity: >98% |
LKT |
1 g |
114 €
|
| LKT-N3278.5 |
CAS: 2942-42-9 nNOS inhibitor A neuronal nitric oxide synthase (nNOS) inhibitor. It enhances amphetamine-evoked release, and kainic acid induced cholinergic neurotoxicity in the rat striatum. MW: 163 D Purity: >98% |
LKT |
5 g |
378 €
|
| LKT-N3278.500 |
CAS: 2942-42-9 nNOS inhibitor A neuronal nitric oxide synthase (nNOS) inhibitor. It enhances amphetamine-evoked release, and kainic acid induced cholinergic neurotoxicity in the rat striatum. MW: 163 D Purity: >98% |
LKT |
500 mg |
85 €
|
| Cay80340-10 |
CAS: 73477-53-9 nNOS inhibitor MW: 189 D Formula: C6H11N3O4 Purity: >98% |
Cayman |
10 mg |
46 €
|
| Cay80340-100 |
CAS: 73477-53-9 nNOS inhibitor MW: 189 D Formula: C6H11N3O4 Purity: >98% |
Cayman |
100 mg |
341 €
|
| Cay80340-5 |
CAS: 73477-53-9 nNOS inhibitor MW: 189 D Formula: C6H11N3O4 Purity: >98% |
Cayman |
5 mg |
24 €
|
| Cay80340-50 |
CAS: 73477-53-9 nNOS inhibitor MW: 189 D Formula: C6H11N3O4 Purity: >98% |
Cayman |
50 mg |
195 €
|
| Cay81530-10 |
CAS: 1937-19-5 iNOS inhibitor MW: 110 D Formula: CH6N4 . HCl Purity: >98% |
Cayman |
10 g |
12 €
|
| Cay81530-100 |
CAS: 1937-19-5 iNOS inhibitor MW: 110 D Formula: CH6N4 . HCl Purity: >98% |
Cayman |
100 g |
93 €
|
| Cay81530-25 |
CAS: 1937-19-5 iNOS inhibitor MW: 110 D Formula: CH6N4 . HCl Purity: >98% |
Cayman |
25 g |
28 €
|
| Cay81530-50 |
CAS: 1937-19-5 iNOS inhibitor MW: 110 D Formula: CH6N4 . HCl Purity: >98% |
Cayman |
50 g |
52 €
|
| Cay81010-10 |
CAS: 21463-31-0 iNOS inhibitor MW: 166 D Formula: C5H10N2S . HCl Purity: >98% |
Cayman |
10 mg |
85 €
|
| Cay81010-100 |
CAS: 21463-31-0 iNOS inhibitor MW: 166 D Formula: C5H10N2S . HCl Purity: >98% |
Cayman |
100 mg |
677 €
|
| Cay81010-50 |
CAS: 21463-31-0 iNOS inhibitor MW: 166 D Formula: C5H10N2S . HCl Purity: >98% |
Cayman |
50 mg |
382 €
|
| Cay81010-500 |
CAS: 21463-31-0 iNOS inhibitor MW: 166 D Formula: C5H10N2S . HCl Purity: >98% |
Cayman |
500 mg |
2964 €
|
| D4015-08F1.100 |
IF Involved in the unfolded protein response (UPR) during ER stress. Co-chaperone of HSPA8/HSC70, it stimulates its ATPase activity. May inhibit both the autophosphorylation of EIF2AK2/PKR and the ability of EIF2AK2 to catalyze phosphorylation of the EIF2A. ... mehr Mouse IgG2a SR: human Immunogen: Recombinant protein corresponding to aa1-235 of human DNAJC3. |
USBio |
100 µg |
535 €
|
|
H1830-49H.100 |
WB, IHC Mouse IgG SR: human Immunogen: Partially purified inhibitor of actin polymerization (IAP) protein from Turkey Gizzard smooth muscle |
USBio |
100 µg |
522 €
|
|
H1830-49J.100 |
WB, IP, IHC, ICC, IF Mouse IgG1 SR: human Immunogen: Partially purified inhibitor of actin polymerization (IAP) protein from turkey gizzard smooth muscle. |
USBio |
100 µg |
427 €
|
|
N7100-68D.100 |
ELISA, WB, IHC Does not seem to have NDK kinase activity. Confers protection from cell death by Bax and alters the cellular levels of several antioxidant enzymes including Gpx5. May play a role in spermiogenesis by increasing the ability of late-stage spermatids to elim ... mehr Rabbit IgG SR: human, mouse Immunogen: Synthetic peptide selected from the center region of human NME5 (KLH). |
USBio |
100 µg |
417 €
|
|
WA-AJ1575a |
WB 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Protein function: Involved in the unfolded protein response (UPR) during ER stress. Co-chaperone of HSPA8/HSC70, it stimulates its ATPase activity. May inhibit both ... mehr MW: 58 kD Rabbit SR: human |
Abgent |
100 µl |
380 €
|
|
A300-910A |
WB, IP Stress-activated map kinase-interacting protein 1 (Sin1) is highly similar to the yeast stress- activated protein kinase SIN1. Sin1 is an essential mTORC2 subunit that is required to act as the PDK2 that phosphorylates Akt/PKB at Ser 473. Sin1 has been i ... mehr Rabbit IgG SR: human, mouse Immunogen: synthetic peptide. The epitope recognized by A300-910A maps to a region between residue 470 and the C-terminus (residue 522) of human stress-activated map kinase interacting protein 1 using the numbering given in entry NP_001006618.1 (GeneID 79109). |
Bethyl |
100 µl |
343 €
|
| IHC-00183 |
IHC Stress-activated map kinase-interacting protein 1 (Sin1) is highly similar to the yeast stress- activated protein kinase SIN1. Sin1 is an essential mTORC2 subunit that is required to act as the PDK2 that phosphorylates Akt/PKB at Ser 473. Sin1 has been i ... mehr Rabbit IgG SR: human, mouse Immunogen: synthetic peptide. The epitope recognized by IHC-00183 maps to a region between residues 470 and the C-terminus (residue 522) of human stress-activated map kinase interacting protein 1 using the numbering given in entry NP_001006618.1 (GeneID 79109). |
Bethyl |
100 µl |
399 €
|
| S300-910 |
IP Rabbit anti-Sin1 affinity purified antibodies were coupled to agarose beads using a cyanogen bromide method. Rabbit IgG SR: human, mouse Immunogen: synthetic peptide |
Bethyl |
100 µg |
360 €
|
| Cay11976-1 |
CAS: 498-02-2 NADPH oxidase inhibitor Apocynin is a compound isolated from the traditional medicinal plant P. kurroa and structurally related to vanillin that acts as an inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity. Upon oxidation by myeloperoxidase, apocy ... mehr MW: 166 D Formula: C9H10O3 Purity: >98% |
Cayman |
1 g |
37 €
|
| Cay11976-10 |
CAS: 498-02-2 NADPH oxidase inhibitor Apocynin is a compound isolated from the traditional medicinal plant P. kurroa and structurally related to vanillin that acts as an inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity. Upon oxidation by myeloperoxidase, apocy ... mehr MW: 166 D Formula: C9H10O3 Purity: >98% |
Cayman |
10 g |
297 €
|
| Cay11976-5 |
CAS: 498-02-2 NADPH oxidase inhibitor Apocynin is a compound isolated from the traditional medicinal plant P. kurroa and structurally related to vanillin that acts as an inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity. Upon oxidation by myeloperoxidase, apocy ... mehr MW: 166 D Formula: C9H10O3 Purity: >98% |
Cayman |
5 g |
167 €
|
| Cay10012694-1 |
CAS: 1012788-65-6 Hsp90 chaperone inhibitor CAY10607 binds the N-terminal domain of Hsp90, efficiently displacing geldanamycin from the ATP binding site. In addition, it inhibits the proliferation of several cancer cell lines. MW: 389 D Formula: C19H20ClN3O4 Purity: >98% |
Cayman |
1 mg |
114 €
|
| Cay10012694-10 |
CAS: 1012788-65-6 Hsp90 chaperone inhibitor CAY10607 binds the N-terminal domain of Hsp90, efficiently displacing geldanamycin from the ATP binding site. In addition, it inhibits the proliferation of several cancer cell lines. MW: 389 D Formula: C19H20ClN3O4 Purity: >98% |
Cayman |
10 mg |
899 €
|
| Cay10012694-25 |
CAS: 1012788-65-6 Hsp90 chaperone inhibitor CAY10607 binds the N-terminal domain of Hsp90, efficiently displacing geldanamycin from the ATP binding site. In addition, it inhibits the proliferation of several cancer cell lines. MW: 389 D Formula: C19H20ClN3O4 Purity: >98% |
Cayman |
25 mg |
1989 €
|
| Cay10012694-5 |
CAS: 1012788-65-6 Hsp90 chaperone inhibitor CAY10607 binds the N-terminal domain of Hsp90, efficiently displacing geldanamycin from the ATP binding site. In addition, it inhibits the proliferation of several cancer cell lines. MW: 389 D Formula: C19H20ClN3O4 Purity: >98% |
Cayman |
5 mg |
512 €
|
| Cay10012591-10 |
CAS: 171009-07-7 Hsp90 inhibitor CCT018159 inhibits the ATPase activity of Hsp90 with IC50 values of 3.2 and 6.6 µM for human Hsp90beta and yeast Hsp90, respectively. At concentrations up to 100 µM, CCT018159 does not inhibit human Hsp72 ATPase or topoisomerase II. MW: 352 D Formula: C20H20N2O4 Purity: >98% |
Cayman |
10 mg |
121 €
|
| Cay10012591-5 |
CAS: 171009-07-7 Hsp90 inhibitor CCT018159 inhibits the ATPase activity of Hsp90 with IC50 values of 3.2 and 6.6 µM for human Hsp90beta and yeast Hsp90, respectively. At concentrations up to 100 µM, CCT018159 does not inhibit human Hsp72 ATPase or topoisomerase II. MW: 352 D Formula: C20H20N2O4 Purity: >98% |
Cayman |
5 mg |
68 €
|
| Cay10012591-50 |
CAS: 171009-07-7 Hsp90 inhibitor CCT018159 inhibits the ATPase activity of Hsp90 with IC50 values of 3.2 and 6.6 µM for human Hsp90beta and yeast Hsp90, respectively. At concentrations up to 100 µM, CCT018159 does not inhibit human Hsp72 ATPase or topoisomerase II. MW: 352 D Formula: C20H20N2O4 Purity: >98% |
Cayman |
50 mg |
528 €
|
| SIH-333-10MG |
Celastrol CAS: 34157-83-0 Proteasome inhibitor Displays potent antioxidant and anti-inflammatory activity. It induces heat shock response and cytoprotection in various cells. It inhibits 20S proteasome chymotrypsin activity. Cell permeable. MW: 450 D Formula: C29H38O4 Purity: >98% |
StressMarq |
10 mg |
182 €
|
| SIH-333-50MG |
Celastrol CAS: 34157-83-0 Proteasome inhibitor Displays potent antioxidant and anti-inflammatory activity. It induces heat shock response and cytoprotection in various cells. It inhibits 20S proteasome chymotrypsin activity. Cell permeable. MW: 450 D Formula: C29H38O4 Purity: >98% |
StressMarq |
50 mg |
679 €
|
| Cay10009081-10 |
CAS: 69839-83-4 Ribonucleotide reductase inhibitor Didox is a simple, synthetic antioxidant. It increases the radiosensitivity of cancer cells by inhibition of ribonucleotide reductase, resulting in a reduction of bcl-2 mediated resistance to apoptosis. MW: 169 D Formula: C7H7NO4 Purity: >98% |
Cayman |
10 mg |
121 €
|
| Cay10009081-5 |
CAS: 69839-83-4 Ribonucleotide reductase inhibitor Didox is a simple, synthetic antioxidant. It increases the radiosensitivity of cancer cells by inhibition of ribonucleotide reductase, resulting in a reduction of bcl-2 mediated resistance to apoptosis. MW: 169 D Formula: C7H7NO4 Purity: >98% |
Cayman |
5 mg |
68 €
|
| Cay10009081-50 |
CAS: 69839-83-4 Ribonucleotide reductase inhibitor Didox is a simple, synthetic antioxidant. It increases the radiosensitivity of cancer cells by inhibition of ribonucleotide reductase, resulting in a reduction of bcl-2 mediated resistance to apoptosis. MW: 169 D Formula: C7H7NO4 Purity: >98% |
Cayman |
50 mg |
528 €
|
| Cay81050-10 |
CAS: 4673-26-1 iNOS inhibitor, eNOS inhibitor Diphenyleneiodonium (DPI) is an irreversible inhibitor of iNOS and eNOS with IC50 values of 50 nM and 0.3 µM, respectively. This inhibition is potent, irreversible, and time and temperature dependent. MW: 314 D Formula: C12H8I · Cl Purity: >99% |
Cayman |
10 mg |
65 €
|
| Cay81050-100 |
CAS: 4673-26-1 iNOS inhibitor, eNOS inhibitor Diphenyleneiodonium (DPI) is an irreversible inhibitor of iNOS and eNOS with IC50 values of 50 nM and 0.3 µM, respectively. This inhibition is potent, irreversible, and time and temperature dependent. MW: 314 D Formula: C12H8I · Cl Purity: >99% |
Cayman |
100 mg |
487 €
|
| Cay70530-100 |
CAS: 60940-34-3 COX inhibitor, LO inhibitor The glutathione peroxidase-like activity of ebselen inhibits cyclooxygenase and lipoxygenases at micromolar concentrations. MW: 274 D Formula: C13H9NOSe Purity: >99% |
Cayman |
100 mg |
292 €
|
| Cay70530-50 |
CAS: 60940-34-3 COX inhibitor, LO inhibitor The glutathione peroxidase-like activity of ebselen inhibits cyclooxygenase and lipoxygenases at micromolar concentrations. MW: 274 D Formula: C13H9NOSe Purity: >99% |
Cayman |
50 mg |
167 €
|
| Cay10012088-10 |
CAS: 150403-97-7 NOS inhibitor Ethyl-L-NIO, the saturated analog of vinyl-L-NIO, is a modestly selective NOS inhibitor. The Ki values for inhibition of nNOS, eNOS, and iNOS by ethyl-L-NIO are 5.3, 18, and 12 µM, respectively. MW: 237 D Formula: C9H19N3O2 · HCl Purity: >95% |
Cayman |
10 mg |
95 €
|
| Cay10012088-100 |
CAS: 150403-97-7 NOS inhibitor Ethyl-L-NIO, the saturated analog of vinyl-L-NIO, is a modestly selective NOS inhibitor. The Ki values for inhibition of nNOS, eNOS, and iNOS by ethyl-L-NIO are 5.3, 18, and 12 µM, respectively. MW: 237 D Formula: C9H19N3O2 · HCl Purity: >95% |
Cayman |
100 mg |
698 €
|
| Cay10012088-50 |
CAS: 150403-97-7 NOS inhibitor Ethyl-L-NIO, the saturated analog of vinyl-L-NIO, is a modestly selective NOS inhibitor. The Ki values for inhibition of nNOS, eNOS, and iNOS by ethyl-L-NIO are 5.3, 18, and 12 µM, respectively. MW: 237 D Formula: C9H19N3O2 · HCl Purity: >95% |
Cayman |
50 mg |
399 €
|
| SIH-111A |
Geldanamycin CAS: 30562-34-6 Hsp90 inhibitor Geldanamycin is a benzoquinoid ansamycin produced by Streptomyces hygroscopicus. It binds specifically to Cellular & Oxid. Stress protein HSP90 and downregulates target proteins including tyrosine kinases, steroid receptors, transcription factors and cell ... mehr MW: 560 D Formula: C29H40N2O9 Purity: >95% |
StressMarq |
1 mg |
107 €
|
| SIH-111B |
Geldanamycin CAS: 30562-34-6 Hsp90 inhibitor Geldanamycin is a benzoquinoid ansamycin produced by Streptomyces hygroscopicus. It binds specifically to Cellular & Oxid. Stress protein HSP90 and downregulates target proteins including tyrosine kinases, steroid receptors, transcription factors and cell ... mehr MW: 561 D Formula: C29H40N2O10 Purity: >95% |
StressMarq |
5 mg |
414 €
|
|
VB2138 |
CAS: 30562-34-6 Inhibitor of Hsp90 chaperone activity Inhibitor of Hsp90 chaperone activity. Autophagy activator. Solubility: DMSO. Appearance: Appearance: White crystalline solid. MW: 561 D Formula: C29H40N2O9 |
Vivabioscience |
1 mg |
117 €
|
| SIH-112A |
Geldanamycin-Biotin CAS: 30562-34-6 Hsp90 inhibitor Geldanamycin is a benzoquinoid ansamycin produced by Streptomyces hygroscopicus. It binds specifically to Cellular & Oxid. Stress protein HSP90 and downregulates target proteins including tyrosine kinases, steroid receptors, transcription factors and cell ... mehr MW: 560 D Formula: C55H87N7O17S Purity: 98% |
StressMarq |
1 mg |
216 €
|
| SIH-113A |
Geldanamycin-FITC CAS: 30562-34-6 Hsp90 inhibitor Geldanamycin is a benzoquinoid ansamycin produced by Streptomyces hygroscopicus. It binds specifically to Cellular & Oxid. Stress protein HSP90 and downregulates target proteins including tyrosine kinases, steroid receptors, transcription factors and cell ... mehr MW: 560 D Formula: C55H63N5O13S Purity: 98% |
StressMarq |
1 mg |
234 €
|
| SIH-116A |
Herbimycin A CAS: 70563-58-5 Hsp90 inhibitor Herbimycin A, a benzoquinoid ansamycin antibiotic, irreversibly and selectively inhibits tyrosine kinases by reacting with thiol groups. It is effective on Src, Yes, Fps, Ros, Abl and ErbB oncogene products and inhibits thrombin-induced tyrosine phosphory ... mehr MW: 574 D Formula: C30H42N2O9 Purity: 98% |
StressMarq |
100 µg |
174 €
|
| SIH-116B |
Herbimycin A CAS: 70563-58-5 Hsp90 inhibitor Herbimycin A, a benzoquinoid ansamycin antibiotic, irreversibly and selectively inhibits tyrosine kinases by reacting with thiol groups. It is effective on Src, Yes, Fps, Ros, Abl and ErbB oncogene products and inhibits thrombin-induced tyrosine phosphory ... mehr MW: 575 D Formula: C30H42N2O10 Purity: 98% |
StressMarq |
1 mg |
959 €
|
| BPS-50285 |
ELISA, WB, inhibitor screening Active human Heat Shock Protein 40 (GenBank Accession No. NM_006145), full length with C-terminal His tag, MW = 38.5 kDa, expressed in an E. coli expression system. MW: 38 kD Purity: >90% |
BPS |
100 µg |
408 €
|
| BPS-50287 |
Enzyme kinetics, inhibitor screening Human Heat Shock Protein 70 (GenBank Accession No. NM_005345), amino-acids 2-641 with C-terminal His tag, MW = 71 kDa, expressed in E. coli. MW: 71 kD Purity: >80% |
BPS |
200 µg |
375 €
|
| BPS-50290 |
Enzyme kinetics, inhibitor screening Active human Heat Shock Protein 90 alpha (GenBank Accession No. NM_005348), full length with C-terminal His tag, MW = 85.5 kDa, expressed in an E. coli expression system. MW: 85 kD Purity: >80% |
BPS |
200 µg |
375 €
|
| BPS-50293 |
Enzyme kinetics, inhibitor screening, HTS The Hsp90alpha Assay Kit is designed for identification of Hsp90alpha inhibitors using fluorescence polarization. The assay is based on the competition of fluorescently labeled geldanamycin for binding to purified recombinant Hsp90alpha. Hsp90alpha is a m ... mehr |
BPS |
100 rxns |
440 €
|
| BPS-50298 |
Enzyme kinetics, inhibitor screening, HTS The Hsp90alpha Assay Kit is designed for identification of Hsp90alpha inhibitors using fluorescence polarization. The assay is based on the competition of fluorescently labeled geldanamycin for binding to purified recombinant Hsp90alpha. Hsp90alpha is a m ... mehr |
BPS |
400 rxns |
924 €
|
| BPS-50292 |
Enzyme kinetics, inhibitor screening Active human Heat Shock Protein 90 beta (GenBank Accession No. AY359878), full length with C-terminal His tag, MW = 83 kDa, expressed in an E. coli expression system. MW: 83 kD Purity: >95% |
BPS |
200 µg |
375 €
|
| BPS-50294 |
Enzyme kinetics, inhibitor screening, HTS The Hsp90beta Assay Kit is designed for identification of Hsp90beta inhibitors using fluorescence polarization. The assay is based on the competition of fluorescently labeled geldanamycin for binding to purified recombinant Hsp90beta. Hsp90beta is a m ... mehr |
BPS |
100 rxns |
440 €
|
| BPS-50299 |
Enzyme kinetics, inhibitor screening, HTS The Hsp90beta Assay Kit is designed for identification of Hsp90beta inhibitors using fluorescence polarization. The assay is based on the competition of fluorescently labeled geldanamycin for binding to purified recombinant Hsp90beta. Hsp90beta is a m ... mehr |
BPS |
400 rxns |
924 €
|
| SPR-102A |
WB control, Chaperone assays, Inhibitor / binding assays, ELISA reference standard Recombinant Hsp90beta clones from a human cDNA library expressed in Hi5 cells using baculovirus expression, native sequence with no tags |
StressMarq |
50 µg |
155 €
|
| SPR-102B |
WB control, Chaperone assays, Inhibitor / binding assays, ELISA reference standard Recombinant Hsp90beta clones from a human cDNA library expressed in Hi5 cells using baculovirus expression, native sequence with no tags |
StressMarq |
100 µg |
262 €
|
| SPR-102C |
WB control, Chaperone assays, Inhibitor / binding assays, ELISA reference standard Recombinant Hsp90beta clones from a human cDNA library expressed in Hi5 cells using baculovirus expression, native sequence with no tags |
StressMarq |
200 µg |
369 €
|
| BVT-0262-C500 |
CAS: 213137-53-2 NOS inhibitor Pyridone metabolite, Nitric oxide synthase (NOS) inhibitor, showing selectivity for eNOS (NOS III) versus nNOS (NOS I), Thaxtomine biosynthesis inhibitor, Mitochondrial electron transport chain inhibitor. Isolated from Streptomyces bottropensis. MW: 303 D Formula: C19H29NO2 Purity: >98% |
Adipogen |
500 µg |
160 €
|
| BVT-0262-M001 |
CAS: 213137-53-2 NOS inhibitor Pyridone metabolite, Nitric oxide synthase (NOS) inhibitor, showing selectivity for eNOS (NOS III) versus nNOS (NOS I), Thaxtomine biosynthesis inhibitor, Mitochondrial electron transport chain inhibitor. Isolated from Streptomyces bottropensis. MW: 303 D Formula: C19H29NO2 Purity: >98% |
Adipogen |
1 mg |
240 €
|
| BVT-0262-M005 |
CAS: 213137-53-2 NOS inhibitor Pyridone metabolite, Nitric oxide synthase (NOS) inhibitor, showing selectivity for eNOS (NOS III) versus nNOS (NOS I), Thaxtomine biosynthesis inhibitor, Mitochondrial electron transport chain inhibitor. Isolated from Streptomyces bottropensis. MW: 303 D Formula: C19H29NO2 Purity: >98% |
Adipogen |
5 mg |
720 €
|
| Cay10011724-10 |
iNOS inhibitor ENIPO is a potent, selective inhibitor of iNOS. The Ki values for inhibition of iNOS, nNOS, and eNOS by ENIPO are 17, 10.3 and 58.2 µM, respectively, as determined using initial rate binding kinetics. MW: 249 D Formula: C10H19N3O2 · HCl Purity: >90% |
Cayman |
10 mg |
113 €
|
| Cay10011724-25 |
iNOS inhibitor ENIPO is a potent, selective inhibitor of iNOS. The Ki values for inhibition of iNOS, nNOS, and eNOS by ENIPO are 17, 10.3 and 58.2 µM, respectively, as determined using initial rate binding kinetics. MW: 249 D Formula: C10H19N3O2 · HCl Purity: >90% |
Cayman |
25 mg |
267 €
|
| Cay10011724-5 |
iNOS inhibitor ENIPO is a potent, selective inhibitor of iNOS. The Ki values for inhibition of iNOS, nNOS, and eNOS by ENIPO are 17, 10.3 and 58.2 µM, respectively, as determined using initial rate binding kinetics. MW: 249 D Formula: C10H19N3O2 · HCl Purity: >90% |
Cayman |
5 mg |
59 €
|
| Cay10011724-50 |
iNOS inhibitor ENIPO is a potent, selective inhibitor of iNOS. The Ki values for inhibition of iNOS, nNOS, and eNOS by ENIPO are 17, 10.3 and 58.2 µM, respectively, as determined using initial rate binding kinetics. MW: 249 D Formula: C10H19N3O2 · HCl Purity: >90% |
Cayman |
50 mg |
473 €
|
| Cay10010252-10 |
CAS: 150403-96-6 NOS inhibitor L-N5-(1-iminopropyl) Ornithine (hydrochloride) is a competitive NOS inhibitor that competes with L-arginine for the amino acid binding site. It is a more potent inhibitor of nNOS (Ki = 3.0 µM) than eNOS (Ki = 10.0 µM) or iNOS (Ki = 9.5 µM). MW: 225 D Formula: C8H19N3O2 . HCl Purity: >98% |
Cayman |
10 mg |
113 €
|
| Cay10010252-25 |
CAS: 150403-96-6 NOS inhibitor L-N5-(1-iminopropyl) Ornithine (hydrochloride) is a competitive NOS inhibitor that competes with L-arginine for the amino acid binding site. It is a more potent inhibitor of nNOS (Ki = 3.0 µM) than eNOS (Ki = 10.0 µM) or iNOS (Ki = 9.5 µM). MW: 225 D Formula: C8H19N3O2 . HCl Purity: >98% |
Cayman |
25 mg |
267 €
|
| Cay10010252-5 |
CAS: 150403-96-6 NOS inhibitor L-N5-(1-iminopropyl) Ornithine (hydrochloride) is a competitive NOS inhibitor that competes with L-arginine for the amino acid binding site. It is a more potent inhibitor of nNOS (Ki = 3.0 µM) than eNOS (Ki = 10.0 µM) or iNOS (Ki = 9.5 µM). MW: 225 D Formula: C8H19N3O2 . HCl Purity: >98% |
Cayman |
5 mg |
59 €
|
| Cay10010252-50 |
CAS: 150403-96-6 NOS inhibitor L-N5-(1-iminopropyl) Ornithine (hydrochloride) is a competitive NOS inhibitor that competes with L-arginine for the amino acid binding site. It is a more potent inhibitor of nNOS (Ki = 3.0 µM) than eNOS (Ki = 10.0 µM) or iNOS (Ki = 9.5 µM). MW: 225 D Formula: C8H19N3O2 . HCl Purity: >98% |
Cayman |
50 mg |
473 €
|
| Cay80210-1 |
CAS: 51298-62-5 NOS inhibitor MW: 269 D Formula: C7H15N5O4 . HCl Purity: >99% |
Cayman |
1 g |
12 €
|
| Cay80210-10 |
CAS: 51298-62-5 NOS inhibitor MW: 269 D Formula: C7H15N5O4 . HCl Purity: >99% |
Cayman |
10 g |
93 €
|
| Cay80210-5 |
CAS: 51298-62-5 NOS inhibitor MW: 269 D Formula: C7H15N5O4 . HCl Purity: >99% |
Cayman |
5 g |
48 €
|
| Cay80210-50 |
CAS: 51298-62-5 NOS inhibitor MW: 269 D Formula: C7H15N5O4 . HCl Purity: >99% |
Cayman |
50 g |
399 €
|
| Cay80310-100 |
CAS: 159190-45-1 INOS inhibitor L-NIL is a relatively selective inhibitor of iNOS. It exhibits IC50 values of 3.3 and 92 µM for iNOS (murine) and nNOS (rat). MW: 260 D Formula: C8H17N3O2 · 2HCl Purity: >95% |
Cayman |
100 mg |
146 €
|
| Cay80310-50 |
CAS: 159190-45-1 iNOS inhibitor L-NIL is a relatively selective inhibitor of iNOS. It exhibits IC50 values of 3.3 and 92 µM for iNOS (murine) and nNOS (rat). MW: 260 D Formula: C8H17N3O2 · 2HCl Purity: >95% |
Cayman |
50 mg |
84 €
|
| Cay80320-100 |
CAS: 36889-13-1 NOS inhibitor L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (bovine), and iNOS (murine) are 1.7, 3.9, and 3.9 µM, respectively. MW: 246 D Formula: C7H15N3O2 · 2HCl Purity: >95% |
Cayman |
100 mg |
195 €
|
| Cay80320-50 |
CAS: 36889-13-1 NOS inhibitor L-NIO is a non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (bovine), and iNOS (murine) are 1.7, 3.9, and 3.9 µM, respectively. MW: 246 D Formula: C7H15N3O2 · 2HCl Purity: >95% |
Cayman |
50 mg |
111 €
|
| Cay10005031-100 |
CAS: 53308-83-1 NOS inhibitor L-NMMA is the archetypal competitive NOS inhibitor to which other inhibitors are often compared. It is a relatively non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (human), and iNOS (murine) are approximately 0.18, 0.4, and ... mehr MW: 248 D Formula: C7H16N4O2 . C2H4O2 Purity: >99% |
Cayman |
100 mg |
195 €
|
| Cay10005031-25 |
CAS: 53308-83-1 NOS inhibitor L-NMMA is the archetypal competitive NOS inhibitor to which other inhibitors are often compared. It is a relatively non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (human), and iNOS (murine) are approximately 0.18, 0.4, and ... mehr MW: 248 D Formula: C7H16N4O2 . C2H4O2 Purity: >99% |
Cayman |
25 mg |
63 €
|
| Cay10005031-5 |
CAS: 53308-83-1 NOS inhibitor L-NMMA is the archetypal competitive NOS inhibitor to which other inhibitors are often compared. It is a relatively non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (human), and iNOS (murine) are approximately 0.18, 0.4, and ... mehr MW: 248 D Formula: C7H16N4O2 . C2H4O2 Purity: >99% |
Cayman |
5 mg |
14 €
|
| Cay10005031-50 |
CAS: 53308-83-1 NOS inhibitor L-NMMA is the archetypal competitive NOS inhibitor to which other inhibitors are often compared. It is a relatively non-selective inhibitor of all NOS isoforms. The Ki values for nNOS (rat), eNOS (human), and iNOS (murine) are approximately 0.18, 0.4, and ... mehr MW: 248 D Formula: C7H16N4O2 . C2H4O2 Purity: >99% |
Cayman |
50 mg |
111 €
|
| Cay80200-10 |
NOS inhibitor MW: 756 D Formula: 3[C7H16N4O2] . C6H8O7 Purity: >99% |
Cayman |
10 mg |
32 €
|
| Cay80200-100 |
NOS inhibitor MW: 756 D Formula: 3[C7H16N4O2] . C6H8O7 Purity: >99% |
Cayman |
100 mg |
260 €
|
| Cay80200-25 |
NOS inhibitor MW: 756 D Formula: 3[C7H16N4O2] . C6H8O7 Purity: >99% |
Cayman |
25 mg |
78 €
|
| Cay80200-50 |
NOS inhibitor MW: 756 D Formula: 3[C7H16N4O2] . C6H8O7 Purity: >99% |
Cayman |
50 mg |
146 €
|
| AG-CR1-3578-G001 |
CAS: 53308-83-1 NOS inhibitor Synthetic. Endothelium-derived relaxing factor inhibitor. Inhibits the generation of NO from arginine. Competitive, irreversible non-selective inhibitor of all three NOS I, II, and III isoforms (eNOS, iNOS and nNOS). Inhibits the synthesis of nitric oxide ... mehr MW: 248 D Formula: C7H16N4O2 . CH3COOH |
Adipogen |
1 g |
429 €
|
| AG-CR1-3578-M005 |
CAS: 53308-83-1 NOS inhibitor Synthetic. Endothelium-derived relaxing factor inhibitor. Inhibits the generation of NO from arginine. Competitive, irreversible non-selective inhibitor of all three NOS I, II, and III isoforms (eNOS, iNOS and nNOS). Inhibits the synthesis of nitric oxide ... mehr MW: 248 D Formula: C7H16N4O2 . CH3COOH |
Adipogen |
5 mg |
22 €
|
| AG-CR1-3578-M025 |
CAS: 53308-83-1 NOS inhibitor Synthetic. Endothelium-derived relaxing factor inhibitor. Inhibits the generation of NO from arginine. Competitive, irreversible non-selective inhibitor of all three NOS I, II, and III isoforms (eNOS, iNOS and nNOS). Inhibits the synthesis of nitric oxide ... mehr MW: 248 D Formula: C7H16N4O2 . CH3COOH |
Adipogen |
25 mg |
60 €
|
| AG-CR1-3578-M100 |
CAS: 53308-83-1 NOS inhibitor Synthetic. Endothelium-derived relaxing factor inhibitor. Inhibits the generation of NO from arginine. Competitive, irreversible non-selective inhibitor of all three NOS I, II, and III isoforms (eNOS, iNOS and nNOS). Inhibits the synthesis of nitric oxide ... mehr MW: 248 D Formula: C7H16N4O2 . CH3COOH |
Adipogen |
100 mg |
198 €
|
| Cay80220-50 |
CAS: 2149-70-4 NOS inhibitor L-NNA is a competitive inhibitor of nitric oxide synthase (NOS) with selectivity for the neuronal and endothelial isoforms of the enzyme. L-NNA inhibits nNOS, eNOS, and iNOS. MW: 219 D Formula: C6H13N5O4 Purity: >99% |
Cayman |
50 g |
399 €
|
| Cay80580-10 |
CAS: 212051-53-1 NOS inhibitor L-Thiocitrulline is a competitive inhibitor of nitric oxide synthase. The Ki values for the neuronal (rat) and inducible (rat aortic smooth muscle) isoforms of nitric oxide synthase were found to be 0.06 µM and 3.6 µM, respectively. The IC50 value for i ... mehr MW: 264 D Formula: C6H13N3O2S . 2HCl Purity: >98% |
Cayman |
10 mg |
38 €
|
| Cay80580-100 |
CAS: 212051-53-1 NOS inhibitor L-Thiocitrulline is a competitive inhibitor of nitric oxide synthase. The Ki values for the neuronal (rat) and inducible (rat aortic smooth muscle) isoforms of nitric oxide synthase were found to be 0.06 µM and 3.6 µM, respectively. The IC50 value for i ... mehr MW: 264 D Formula: C6H13N3O2S . 2HCl Purity: >98% |
Cayman |
100 mg |
299 €
|
| Cay80580-50 |
CAS: 212051-53-1 NOS inhibitor L-Thiocitrulline is a competitive inhibitor of nitric oxide synthase. The Ki values for the neuronal (rat) and inducible (rat aortic smooth muscle) isoforms of nitric oxide synthase were found to be 0.06 µM and 3.6 µM, respectively. The IC50 value for i ... mehr MW: 264 D Formula: C6H13N3O2S . 2HCl Purity: >98% |
Cayman |
50 mg |
173 €
|
| Cay80580-500 |
CAS: 212051-53-1 NOS inhibitor L-Thiocitrulline is a competitive inhibitor of nitric oxide synthase. The Ki values for the neuronal (rat) and inducible (rat aortic smooth muscle) isoforms of nitric oxide synthase were found to be 0.06 µM and 3.6 µM, respectively. The IC50 value for i ... mehr MW: 264 D Formula: C6H13N3O2S . 2HCl Purity: >98% |
Cayman |
500 mg |
1340 €
|
| Cay10009645-10 |
CAS: 4373-41-5 NO production inhibitor Maslinic acid has been found to attenuate intracellular oxidative stress via inhibition of NO and H2O2 production and reduction of pro-inflammatory cytokine generation. MW: 472 D Formula: C30H48O4 Purity: >98% |
Cayman |
10 mg |
195 €
|
| Cay10009645-25 |
CAS: 4373-41-5 NO production inhibitor Maslinic acid has been found to attenuate intracellular oxidative stress via inhibition of NO and H2O2 production and reduction of pro-inflammatory cytokine generation. MW: 472 D Formula: C30H48O4 Purity: >98% |
Cayman |
25 mg |
427 €
|
| Cay10009645-5 |
CAS: 4373-41-5 NO production inhibitor Maslinic acid has been found to attenuate intracellular oxidative stress via inhibition of NO and H2O2 production and reduction of pro-inflammatory cytokine generation. MW: 472 D Formula: C30H48O4 Purity: >98% |
Cayman |
5 mg |
110 €
|
| Cay81020-10 |
CAS: 3979-00-8 iNOS inhibitor MEG is a selective iNOS inhibitor and scavenger of peroxynitrite. The EC50 values for inhibition of iNOS (LPS-treated rat lung), eNOS (bovine endothelial), and nNOS (rat brain) are 11.5, 110, and 60 µM, respectively. MW: 336 D Formula: (C3H9N3S)2 · H2SO4 Purity: >98% |
Cayman |
10 mg |
122 €
|
| Cay81020-100 |
CAS: 3979-00-8 iNOS inhibitor MEG is a selective iNOS inhibitor and scavenger of peroxynitrite. The EC50 values for inhibition of iNOS (LPS-treated rat lung), eNOS (bovine endothelial), and nNOS (rat brain) are 11.5, 110, and 60 µM, respectively. MW: 336 D Formula: (C3H9N3S)2 · H2SO4 Purity: >98% |
Cayman |
100 mg |
893 €
|
| Cay700167-1 |
MPO inhibitor MPO inhibitor |
Cayman |
1 each |
13 €
|
| Cay700170-2 |
MPO inhibitor screening Cayman's MPO Inhibitor Screening Assay provides convenient fluorescence-based methods for screening inhibitors to both the chlorination and peroxidation activities of MPO. The chlorination assay utilizes the non-fluorescent 2-[6-(4-aminophenoxy)-3-oxo-3H- ... mehr |
Cayman |
192 wells |
254 €
|
| Cay13570-10 |
CAS: 186545-76-6 iNOS inhibitor Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylaceta ... mehr MW: 229 D Formula: C9H12N2 . HBr Purity: >98% |
Cayman |
10 mg |
115 €
|
| Cay13570-100 |
CAS: 186545-76-6 iNOS inhibitor Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylaceta ... mehr MW: 229 D Formula: C9H12N2 . HBr Purity: >98% |
Cayman |
100 mg |
844 €
|
| Cay13570-5 |
CAS: 186545-76-6 iNOS inhibitor Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylaceta ... mehr MW: 229 D Formula: C9H12N2 . HBr Purity: >98% |
Cayman |
5 mg |
60 €
|
| Cay13570-50 |
CAS: 186545-76-6 iNOS inhibitor Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylaceta ... mehr MW: 229 D Formula: C9H12N2 . HBr Purity: >98% |
Cayman |
50 mg |
483 €
|
| Cay80587-10 |
CAS: 137361-05-8 nNOS inhibitor MW: 216 D Formula: C9H20N4O2 Purity: >98% |
Cayman |
10 mg |
95 €
|
| Cay80587-100 |
CAS: 137361-05-8 nNOS inhibitor MW: 216 D Formula: C9H20N4O2 Purity: >98% |
Cayman |
100 mg |
698 €
|
| Cay80587-5 |
CAS: 137361-05-8 nNOS inhibitor MW: 216 D Formula: C9H20N4O2 Purity: >98% |
Cayman |
5 mg |
50 €
|
| Cay80587-50 |
CAS: 137361-05-8 nNOS inhibitor MW: 216 D Formula: C9H20N4O2 Purity: >98% |
Cayman |
50 mg |
399 €
|
|
Cay14173-1 |
CAS: 480-41-1 CYP3A4 inhibitor Naringenin is a citrus-derived flavonoid that inhibits CYP3A4 activity in human liver microsomes (IC50s = 139-188 µM). At 100 mg/kg/day, naringenin selectively inhibits the transcription of Smad3 and directly down-regulates TGF-beta1, significantly reduc ... mehr MW: 272 D Formula: C15H12O5 Purity: >98% |
Cayman |
1 g |
29 €
|
|
Cay14173-10 |
CAS: 480-41-1 CYP3A4 inhibitor Naringenin is a citrus-derived flavonoid that inhibits CYP3A4 activity in human liver microsomes (IC50s = 139-188 µM). At 100 mg/kg/day, naringenin selectively inhibits the transcription of Smad3 and directly down-regulates TGF-beta1, significantly reduc ... mehr MW: 272 D Formula: C15H12O5 Purity: >98% |
Cayman |
10 g |
125 €
|
|
Cay14173-5 |
CAS: 480-41-1 CYP3A4 inhibitor Naringenin is a citrus-derived flavonoid that inhibits CYP3A4 activity in human liver microsomes (IC50s = 139-188 µM). At 100 mg/kg/day, naringenin selectively inhibits the transcription of Smad3 and directly down-regulates TGF-beta1, significantly reduc ... mehr MW: 272 D Formula: C15H12O5 Purity: >98% |
Cayman |
5 g |
102 €
|
| Cay80230-50 |
CAS: 220805-22-1 NOS inhibitor NG,NG-dimethyl-L-Arginine (ADMA) is an endogenous nitric oxide synthase inhibitor. ADMA concentrations increase in several disease states including renal failure, muscular dystrophy, hypercholesterolemia, and pregnancy with preeclampsia. MW: 275 D Formula: C8H18N4O2 · 2HCl Purity: >98% |
Cayman |
50 mg |
176 €
|
| Cay10554-10 |
NOS inhibitor NG-amino-L-Arginine inhibits nNOS, iNOS, and eNOS with Ki values of 0.3, 3, and 2.5 µM, respectively. Inhibition is mediated by covalent alteration of the heme prosthetic group leading to inactivation of the enzyme. NG-amino-L-Arginine can be used both i ... mehr MW: 225 D Formula: C6H15NSO2 - HCl Purity: >97% |
Cayman |
10 mg |
90 €
|
| Cay10554-25 |
NOS inhibitor NG-amino-L-Arginine inhibits nNOS, iNOS, and eNOS with Ki values of 0.3, 3, and 2.5 µM, respectively. Inhibition is mediated by covalent alteration of the heme prosthetic group leading to inactivation of the enzyme. NG-amino-L-Arginine can be used both i ... mehr MW: 225 D Formula: C6H15NSO2 - HCl Purity: >97% |
Cayman |
25 mg |
215 €
|
| Cay10554-5 |
NOS inhibitor NG-amino-L-Arginine inhibits nNOS, iNOS, and eNOS with Ki values of 0.3, 3, and 2.5 µM, respectively. Inhibition is mediated by covalent alteration of the heme prosthetic group leading to inactivation of the enzyme. NG-amino-L-Arginine can be used both i ... mehr MW: 225 D Formula: C6H15NSO2 - HCl Purity: >97% |
Cayman |
5 mg |
48 €
|
| Cay10554-50 |
NOS inhibitor NG-amino-L-Arginine inhibits nNOS, iNOS, and eNOS with Ki values of 0.3, 3, and 2.5 µM, respectively. Inhibition is mediated by covalent alteration of the heme prosthetic group leading to inactivation of the enzyme. NG-amino-L-Arginine can be used both i ... mehr MW: 225 D Formula: C6H15NSO2 - HCl Purity: >97% |
Cayman |
50 mg |
380 €
|
| N2577-04M.5 | Nitric Oxide Synthase (NOS) Inhibitor HP-228 [Nle4-Acetyl, Gln5, D-Phe7, D-Trp9]-a-MSH (4-10) amide |
USBio |
5 mg |
399 €
|
| Cay10006861-10 |
CAS: 189302-40-7 Arginase inhibitor nor-NOHA is a potent, reversible inhibitor of rat liver arginase with a Ki value of 0.5 µM, which is 20-fold lower than the Ki of 10 µM observed for NOHA. MW: 176 D Formula: C5H12N4O3 Purity: >97% |
Cayman |
10 mg |
158 €
|
| Cay10006861-5 |
CAS: 189302-40-7 Arginase inhibitor nor-NOHA is a potent, reversible inhibitor of rat liver arginase with a Ki value of 0.5 µM, which is 20-fold lower than the Ki of 10 µM observed for NOHA. MW: 176 D Formula: C5H12N4O3 Purity: >97% |
Cayman |
5 mg |
89 €
|
| Cay10006861-50 |
CAS: 189302-40-7 Arginase inhibitor nor-NOHA is a potent, reversible inhibitor of rat liver arginase with a Ki value of 0.5 µM, which is 20-fold lower than the Ki of 10 µM observed for NOHA. MW: 176 D Formula: C5H12N4O3 Purity: >97% |
Cayman |
50 mg |
690 €
|
| BPS-70015 |
Enzyme kinetics, inhibitor screening, selectivity profiling Human nitric oxide synthase 2 (NOS2) or inducible NOS (iNOS) (GenBank Accession No. NM_000625), amino acids 2 - 1153 (end) with N-terminal His-Flag tag, MW= 133 kDa, expressed in a baculovirus infected Sf9 cell expression system. MW: 133 kD Purity: >95% |
BPS |
10 µg |
440 €
|
| BPS-70018 |
Enzyme kinetics, inhibitor screening, selectivity profiling Human nitric oxide synthase 3 (NOS3), also known as endothelial NOS (eNOS), (GenBank Accession No. NM_000603), amino acids 2 ? 1203 (end) with N-terminal His-Flag tag, MW= 135 kDa, expressed in a baculovirus infected Sf9 cell expression system. MW: 135 kD Purity: >71% |
BPS |
10 µg |
440 €
|
| Cay10012698-10 |
CAS: 747412-49-3 Hsp90 Inhibitor Hsp90 is a molecular chaperone of many different kinases, transcription factors, and hormone receptors involved in signal transduction, cell cycle regulation, and apoptosis. In addition to its important function in normal cell homeostasis, a high affinity ... mehr MW: 465 D Formula: C26H31N3O5 Purity: >98% |
Cayman |
10 mg |
232 €
|
| Cay10012698-5 |
CAS: 747412-49-3 Hsp90 Inhibitor Hsp90 is a molecular chaperone of many different kinases, transcription factors, and hormone receptors involved in signal transduction, cell cycle regulation, and apoptosis. In addition to its important function in normal cell homeostasis, a high affinity ... mehr MW: 465 D Formula: C26H31N3O5 Purity: >98% |
Cayman |
5 mg |
145 €
|
| BPS-70011 |
Enzyme kinetics, inhibitor screening Peroxiredoxin 2, full length (Gene bank accession number NM_005809) with N-terminal HIS tag, MW=22.7 kDa, expressed in Baculovirus infected Sf9 cell expression system. Specific Activity: 149 pmol/min/ug. 3.45 µg of PRDX2 was incubated in 50 mM Hepes (pH ... mehr MW: 22 kD Purity: >80% |
BPS |
100 µg |
440 €
|
| SIH-325-10MG |
Pifithrin mu CAS: 64984-31-2 Hsp70 inhibitor Selectively interacts with HSP70 and disrupts its association with co-chaperones and substrate proteins. It induces apoptosis and is cell permeable. Also, inhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and B ... mehr MW: 181 D Formula: C8H7NO2S Purity: >99% |
StressMarq |
10 mg |
53 €
|
| SIH-325-50MG |
Pifithrin mu CAS: 64984-31-2 Hsp70 inhibitor Selectively interacts with HSP70 and disrupts its association with co-chaperones and substrate proteins. It induces apoptosis and is cell permeable. Also, inhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and B ... mehr MW: 181 D Formula: C8H7NO2S Purity: >99% |
StressMarq |
50 mg |
197 €
|
| Cay11450-1 |
CAS: 1202865-65-3 HSP90 inhibitor The heat shock protein 90 (HSP90) family of proteins are molecular chaperones involved in folding, activation, maturation, and assembly of different proteins, including the mediators of signal transduction and cell cycle progression. A class of inhibitors ... mehr MW: 512 D Formula: C18H21IN6O2S XH2O Purity: >98% |
Cayman |
1 mg |
41 €
|
| Cay11450-10 |
CAS: 1202865-65-3 HSP90 inhibitor The heat shock protein 90 (HSP90) family of proteins are molecular chaperones involved in folding, activation, maturation, and assembly of different proteins, including the mediators of signal transduction and cell cycle progression. A class of inhibitors ... mehr MW: 512 D Formula: C18H21IN6O2S XH2O Purity: >98% |
Cayman |
10 mg |
325 €
|
| Cay11450-5 |
CAS: 1202865-65-3 HSP90 inhibitor The heat shock protein 90 (HSP90) family of proteins are molecular chaperones involved in folding, activation, maturation, and assembly of different proteins, including the mediators of signal transduction and cell cycle progression. A class of inhibitors ... mehr MW: 512 D Formula: C18H21IN6O2S XH2O Purity: >98% |
Cayman |
5 mg |
183 €
|
|
Cay14192-1 |
CAS: 141400-58-0 Trx1 inhibitor PX 12 is a competitive, irreversible inhibitor of thioredoxin 1 (Trx1), acting by binding to Cys73 of this enzyme. As Trx1 is overexpressed in certain cancers, PX 12 is effective in suppressing the growth of cancer cells, with growth inhibition in a panel ... mehr MW: 188 D Formula: C7H12N2S2 Purity: >98% |
Cayman |
1 mg |
41 €
|
|
Cay14192-10 |
CAS: 141400-58-0 Trx1 inhibitor PX 12 is a competitive, irreversible inhibitor of thioredoxin 1 (Trx1), acting by binding to Cys73 of this enzyme. As Trx1 is overexpressed in certain cancers, PX 12 is effective in suppressing the growth of cancer cells, with growth inhibition in a panel ... mehr MW: 188 D Formula: C7H12N2S2 Purity: >98% |
Cayman |
10 mg |
203 €
|
|
Cay14192-5 |
CAS: 141400-58-0 Trx1 inhibitor PX 12 is a competitive, irreversible inhibitor of thioredoxin 1 (Trx1), acting by binding to Cys73 of this enzyme. As Trx1 is overexpressed in certain cancers, PX 12 is effective in suppressing the growth of cancer cells, with growth inhibition in a panel ... mehr MW: 188 D Formula: C7H12N2S2 Purity: >98% |
Cayman |
5 mg |
122 €
|
| LKT-P9770.1 |
CAS: 144314-68-1 Lipid peroxidation inhibitor Inhibits lipid peroxidation by scavenging free radicals. MW: 247 D Purity: >98% |
LKT |
1 mg |
318 €
|
| AG-CN2-0021-M001 |
CAS: 12772-57-5 COX-2 inhibitor, HSP90 inhibitor Isolated from Gilmaniella sp. Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1 expression ... mehr MW: 364 D Formula: C18H17ClO6 Purity: >99% |
Adipogen |
1 mg |
99 €
|
| AG-CN2-0021-M005 |
CAS: 12772-57-5 COX-2 inhibitor, HSP90 inhibitor Isolated from Gilmaniella sp. Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1 expression ... mehr MW: 364 D Formula: C18H17ClO6 Purity: >99% |
Adipogen |
5 mg |
396 €
|
| Cay13089-1 |
CAS: 12772-57-5 Hsp90 inhibitor Radicicol is a natural product with antibiotic, antifungal, and antimalarial properties. It binds and inhibits heat shock protein 90 (Hsp90) with nanomolar affinity. MW: 364 D Formula: C18H17ClO6 Purity: >98% |
Cayman |
1 mg |
75 €
|
| Cay13089-5 |
CAS: 12772-57-5 Hsp90 inhibitor Radicicol is a natural product with antibiotic, antifungal, and antimalarial properties. It binds and inhibits heat shock protein 90 (Hsp90) with nanomolar affinity. MW: 364 D Formula: C18H17ClO6 Purity: >98% |
Cayman |
5 mg |
334 €
|
| SIH-117A |
Radicicol CAS: 12772-57-5 Hsp90 inhibitor Radicicol inhibits src (IC50=0.27?M) and src-like kinases, leading to hypophosphorylation of retinoblastoma tumor suppressor protein. It causes morphological reversion of ras-transformed cells and leads to selective depletion of Raf kinase. It also displa ... mehr MW: 364 D Formula: C18H17CIO6 Purity: 97% |
StressMarq |
1 mg |
143 €
|
| Cay81005-1 |
CAS: 56-10-0 NOS inhibitor MW: 281 D Formula: C3H9N3S . 2HBr Purity: >98% |
Cayman |
1 g |
162 €
|
| Cay81005-100 |
CAS: 56-10-0 NOS inhibitor MW: 281 D Formula: C3H9N3S . 2HBr Purity: >98% |
Cayman |
100 mg |
22 €
|
| Cay81005-50 |
CAS: 56-10-0 NOS inhibitor MW: 281 D Formula: C3H9N3S . 2HBr Purity: >98% |
Cayman |
50 mg |
12 €
|
| Cay81005-500 |
CAS: 56-10-0 NOS inhibitor MW: 281 D Formula: C3H9N3S . 2HBr Purity: >98% |
Cayman |
500 mg |
93 €
|
| Cay81275-1 |
CAS: 1071-37-0 NOS inhibitor MW: 185 D Formula: C3H8N2S . HBr Purity: >98% |
Cayman |
1 g |
195 €
|
| Cay81275-100 |
CAS: 1071-37-0 NOS inhibitor MW: 185 D Formula: C3H8N2S . HBr Purity: >98% |
Cayman |
100 mg |
27 €
|
| Cay81275-50 |
CAS: 1071-37-0 NOS inhibitor MW: 185 D Formula: C3H8N2S . HBr Purity: >98% |
Cayman |
50 mg |
14 €
|
| Cay81275-500 |
CAS: 1071-37-0 NOS inhibitor MW: 185 D Formula: C3H8N2S . HBr Purity: >98% |
Cayman |
500 mg |
111 €
|
| Cay81280-10 |
CAS: 163490-78-6 nNOS inhibitor MW: 284 D Formula: C10H11F3N2S . HCl Purity: >98% |
Cayman |
10 mg |
113 €
|
| Cay81280-100 |
CAS: 163490-78-6 nNOS inhibitor MW: 284 D Formula: C10H11F3N2S . HCl Purity: >98% |
Cayman |
100 mg |
828 €
|
| Cay81280-5 |
CAS: 163490-78-6 nNOS inhibitor MW: 284 D Formula: C10H11F3N2S . HCl Purity: >98% |
Cayman |
5 mg |
59 €
|
| Cay81280-50 |
CAS: 163490-78-6 nNOS inhibitor MW: 284 D Formula: C10H11F3N2S . HCl Purity: >98% |
Cayman |
50 mg |
473 €
|
| Cay81290-1 |
CAS: 4269-97-0 NOS inhibitor MW: 199 D Formula: C4H10N2S . HBr Purity: >98% |
Cayman |
1 g |
438 €
|
| Cay81290-100 |
CAS: 4269-97-0 NOS inhibitor MW: 199 D Formula: C4H10N2S . HBr Purity: >98% |
Cayman |
100 mg |
59 €
|
| Cay81290-50 |
CAS: 4269-97-0 NOS inhibitor MW: 199 D Formula: C4H10N2S . HBr Purity: >98% |
Cayman |
50 mg |
31 €
|
| Cay81290-500 |
CAS: 4269-97-0 NOS inhibitor MW: 199 D Formula: C4H10N2S . HBr Purity: >98% |
Cayman |
500 mg |
251 €
|
| Cay81300-1 |
CAS: 867-44-7 NOS inhibitor MW: 278 D Formula: 2(C2H6N2S) . H2SO4 Purity: >98% |
Cayman |
1 g |
179 €
|
| Cay81300-100 |
CAS: 867-44-7 NOS inhibitor MW: 278 D Formula: 2(C2H6N2S) . H2SO4 Purity: >98% |
Cayman |
100 mg |
24 €
|
| Cay81300-50 |
CAS: 867-44-7 NOS inhibitor MW: 278 D Formula: 2(C2H6N2S) . H2SO4 Purity: >98% |
Cayman |
50 mg |
13 €
|
| Cay81300-500 |
CAS: 867-44-7 NOS inhibitor MW: 278 D Formula: 2(C2H6N2S) . H2SO4 Purity: >98% |
Cayman |
500 mg |
99 €
|
| Cay80585-10 |
CAS: 209589-59-3 NOS inhibitor S-methyl-L-Thiocitrulline is a potent NOS inhibitor with selectivity toward the neuronal isoform compared to eNOS and iNOS. For human enzymes, it exhibits Ki values of 1.2, 11, and 40 nM for nNOS, eNOS, and iNOS, respectively. MW: 278 D Formula: C7H15N3O2S . 2HCl Purity: >97% |
Cayman |
10 mg |
46 €
|
| Cay80585-100 |
CAS: 209589-59-3 NOS inhibitor S-methyl-L-Thiocitrulline is a potent NOS inhibitor with selectivity toward the neuronal isoform compared to eNOS and iNOS. For human enzymes, it exhibits Ki values of 1.2, 11, and 40 nM for nNOS, eNOS, and iNOS, respectively. MW: 278 D Formula: C7H15N3O2S . 2HCl Purity: >97% |
Cayman |
100 mg |
341 €
|
| Cay80585-5 |
CAS: 209589-59-3 NOS inhibitor S-methyl-L-Thiocitrulline is a potent NOS inhibitor with selectivity toward the neuronal isoform compared to eNOS and iNOS. For human enzymes, it exhibits Ki values of 1.2, 11, and 40 nM for nNOS, eNOS, and iNOS, respectively. MW: 278 D Formula: C7H15N3O2S . 2HCl Purity: >97% |
Cayman |
5 mg |
24 €
|
| Cay80585-50 |
CAS: 209589-59-3 NOS inhibitor S-methyl-L-Thiocitrulline is a potent NOS inhibitor with selectivity toward the neuronal isoform compared to eNOS and iNOS. For human enzymes, it exhibits Ki values of 1.2, 11, and 40 nM for nNOS, eNOS, and iNOS, respectively. MW: 278 D Formula: C7H15N3O2S . 2HCl Purity: >97% |
Cayman |
50 mg |
195 €
|
| BPS-50284 |
enzyme kinetics, inhibitor screening Human Sestrin1, also known as p53-regulated protein PA26 (GenBank Accession No. NM_014454), full length, a.a. 2-551(end), with N-terminal FLAG-tag, MW=65 kDa, expressed in Sf9 insect cells via a baculovirus expression system. Application: Useful for the MW: 65 kD |
BPS |
50 µg |
418 €
|
| BPS-50286 |
enzyme kinetics, inhibitor screening Human Sestrin2, also known as hypoxia induced gene 95 (GenBank Accession No. NM_031459), full length, a.a. 2-480(end), with N-terminal FLAG-tag, MW=55 kDa, expressed in Sf9 insect cells via a baculovirus expression system.Application: Useful for the stud MW: 55 kD |
BPS |
50 µg |
418 €
|
| Cay11882-1 |
CAS: 64506-49-6 NO inhibitor Sofalcone is an anti-ulcer chalcone derivative. It blocks inflammation by suppressing the production of nitric oxide, TNF-alpha, and MCP-1 while inducing the expression of heme oxygenase-1 when given at 10-20 µM. Sofalcone (20-50 µM) induces VEGF expres ... mehr MW: 450 D Formula: C27H30O6 Purity: >98% |
Cayman |
1 g |
130 €
|
| Cay11882-500 |
CAS: 64506-49-6 NO inhibitor Sofalcone is an anti-ulcer chalcone derivative. It blocks inflammation by suppressing the production of nitric oxide, TNF-alpha, and MCP-1 while inducing the expression of heme oxygenase-1 when given at 10-20 µM. Sofalcone (20-50 µM) induces VEGF expres ... mehr MW: 450 D Formula: C27H30O6 Purity: >98% |
Cayman |
500 mg |
199 €
|
| Cay81310-100 |
CAS: 25371-96-4 iNOS inhibitor, nNOS inhibitor MW: 212 D Formula: C10H7N2F3 Purity: >98% |
Cayman |
100 mg |
57 €
|
| Cay81310-250 |
CAS: 25371-96-4 iNOS inhibitor, nNOS inhibitor MW: 212 D Formula: C10H7N2F3 Purity: >98% |
Cayman |
250 mg |
136 €
|
| Cay81310-50 |
CAS: 25371-96-4 iNOS inhibitor, nNOS inhibitor MW: 212 D Formula: C10H7N2F3 Purity: >98% |
Cayman |
50 mg |
30 €
|
| Cay81310-500 |
CAS: 25371-96-4 iNOS inhibitor, nNOS inhibitor MW: 212 D Formula: C10H7N2F3 Purity: >98% |
Cayman |
500 mg |
241 €
|
| Cay10009094-1 |
TrxR inhibitor TrxR inhibitor |
Cayman |
1 each |
13 €
|
| Cay13131-1 |
CAS: 940289-57-6 Hsp90 inhibitor The heat shock proteins (Hsps) act as molecular chaperones. Hsp90 is an abundant protein with roles in protein folding, cell signaling, and cancer. VER-49009 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 47 nM. It produces a cellular ... mehr MW: 387 D Formula: C19H18ClN3O4 Purity: >98% |
Cayman |
1 mg |
181 €
|
| Cay13131-10 |
CAS: 940289-57-6 Hsp90 inhibitor The heat shock proteins (Hsps) act as molecular chaperones. Hsp90 is an abundant protein with roles in protein folding, cell signaling, and cancer. VER-49009 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 47 nM. It produces a cellular ... mehr MW: 387 D Formula: C19H18ClN3O4 Purity: >98% |
Cayman |
10 mg |
1332 €
|
| Cay13131-5 |
CAS: 940289-57-6 Hsp90 inhibitor The heat shock proteins (Hsps) act as molecular chaperones. Hsp90 is an abundant protein with roles in protein folding, cell signaling, and cancer. VER-49009 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 47 nM. It produces a cellular ... mehr MW: 387 D Formula: C19H18ClN3O4 Purity: >98% |
Cayman |
5 mg |
761 €
|
| Cay13131-500 |
CAS: 940289-57-6 Hsp90 inhibitor The heat shock proteins (Hsps) act as molecular chaperones. Hsp90 is an abundant protein with roles in protein folding, cell signaling, and cancer. VER-49009 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 47 nM. It produces a cellular ... mehr MW: 387 D Formula: C19H18ClN3O4 Purity: >98% |
Cayman |
500 µg |
95 €
|
| Cay13132-1 |
CAS: 747413-08-7 Hsp90 inhibitor VER-50589 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM. It produces a mean cellular antiproliferative GI50 value of 78 nM when tested against a human cancer cell line panel. Consistent with inhibition of Hsp90, VER-50589 induce ... mehr MW: 388 D Formula: C19H17ClN2O5 Purity: >98% |
Cayman |
1 mg |
181 €
|
| Cay13132-5 |
CAS: 747413-08-7 Hsp90 inhibitor VER-50589 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM. It produces a mean cellular antiproliferative GI50 value of 78 nM when tested against a human cancer cell line panel. Consistent with inhibition of Hsp90, VER-50589 induce ... mehr MW: 388 D Formula: C19H17ClN2O5 Purity: >98% |
Cayman |
5 mg |
761 €
|
| Cay13132-500 |
CAS: 747413-08-7 Hsp90 inhibitor VER-50589 is an isoxazole compound that inhibits Hsp90 with an IC50 value of 21 nM. It produces a mean cellular antiproliferative GI50 value of 78 nM when tested against a human cancer cell line panel. Consistent with inhibition of Hsp90, VER-50589 induce ... mehr MW: 388 D Formula: C19H17ClN2O5 Purity: >98% |
Cayman |
500 µg |
95 €
|
| Cay80330-10 |
CAS: 728944-69-2 nNOS inhibitor Vinyl-L-NIO is a potent, selective inhibitor of nNOS. The Ki values for inhibition of nNOS, eNOS, and iNOS by vinyl-L-NIO are 100 nM, 12 and 60 µM, respectively, as determined using initial rate measurements. MW: 235 D Formula: C9H17N3O2 · HCl Purity: >98% |
Cayman |
10 mg |
95 €
|
| Cay80330-100 |
CAS: 728944-69-2 nNOS inhibitor Vinyl-L-NIO is a potent, selective inhibitor of nNOS. The Ki values for inhibition of nNOS, eNOS, and iNOS by vinyl-L-NIO are 100 nM, 12 and 60 µM, respectively, as determined using initial rate measurements. MW: 235 D Formula: C9H17N3O2 · HCl Purity: >98% |
Cayman |
100 mg |
698 €
|
| Cay80330-50 |
CAS: 728944-69-2 nNOS inhibitor Vinyl-L-NIO is a potent, selective inhibitor of nNOS. The Ki values for inhibition of nNOS, eNOS, and iNOS by vinyl-L-NIO are 100 nM, 12 and 60 µM, respectively, as determined using initial rate measurements. MW: 235 D Formula: C9H17N3O2 · HCl Purity: >98% |
Cayman |
50 mg |
399 €
|
| BVT-0365-C500 |
CAS: 1685-91-2 iNOS inhibitor Genotoxic mycotoxin, Antitumor compound, Potent iNOS (NOSII) inhibitor, Interferes with cellular respiratory processes. Isolated from Penicillium citreo-viride. MW: 574 D Formula: C30H22O12 Purity: >97% |
Adipogen |
500 µg |
120 €
|
| BVT-0365-M001 |
CAS: 1685-91-2 iNOS inhibitor Genotoxic mycotoxin, Antitumor compound, Potent iNOS (NOSII) inhibitor, Interferes with cellular respiratory processes. Isolated from Penicillium citreo-viride. MW: 574 D Formula: C30H22O12 Purity: >97% |
Adipogen |
1 mg |
200 €
|