Name | Description | Size | Catalog # | |
---|---|---|---|---|
ATX-II | ATX-II potently modulates voltage-gated Na+ channel gating kinetics by del… | 5 mg | STA-700 | More Info |
ATX-II | ATX-II potently modulates voltage-gated Na+ channel gating kinetics by del… | 5 x 0.1 mg | STA-700 | More Info |
ATX-II | ATX-II potently modulates voltage-gated Na+ channel gating kinetics by del… | 5 x 50 µg | STA-700 | More Info |
ATX-II | ATX-II potently modulates voltage-gated Na+ channel gating kinetics by del… | 50 µg | STA-700 | More Info |
Avosentan | Avosentan is a selective antagonist of ET-A endothelin receptors, shown to… | 10 mg | A-355 | More Info |
Avosentan | Avosentan is a selective antagonist of ET-A endothelin receptors, shown to… | 25 mg | A-355 | More Info |
Avosentan | Avosentan is a selective antagonist of ET-A endothelin receptors, shown to… | 5 mg | A-355 | More Info |
Avosentan | Avosentan is a selective antagonist of ET-A endothelin receptors, shown to… | 50 mg | A-355 | More Info |
AZ11645373 | AZ11645373 is a potent and selective antagonist of human P2X7 purinergic r… | 10 mg | A-395 | More Info |
AZ11645373 | AZ11645373 is a potent and selective antagonist of human P2X7 purinergic r… | 25 mg | A-395 | More Info |
AZ11645373 | AZ11645373 is a potent and selective antagonist of human P2X7 purinergic r… | 5 mg | A-395 | More Info |
AZ11645373 | AZ11645373 is a potent and selective antagonist of human P2X7 purinergic r… | 50 mg | A-395 | More Info |
Azasetron | Azasetron is a potent and selective 5-HT3 channel blocker with Ki ~2.9 nM1… | 10 mg | A-240 | More Info |
Azasetron | Azasetron is a potent and selective 5-HT3 channel blocker with Ki ~2.9 nM1… | 25 mg | A-240 | More Info |
Azasetron | Azasetron is a potent and selective 5-HT3 channel blocker with Ki ~2.9 nM1… | 5 mg | A-240 | More Info |
Azasetron | Azasetron is a potent and selective 5-HT3 channel blocker with Ki ~2.9 nM1… | 50 mg | A-240 | More Info |
Azasetron hydrochloride | Azasetron hydrochloride is a potent 5-HT3 channel blocker with a Ki ~2.9 n… | 10 mg | Y-100 | More Info |
Azasetron hydrochloride | Azasetron hydrochloride is a potent 5-HT3 channel blocker with a Ki ~2.9 n… | 25 mg | Y-100 | More Info |
Azasetron hydrochloride | Azasetron hydrochloride is a potent 5-HT3 channel blocker with a Ki ~2.9 n… | 5 mg | Y-100 | More Info |
Azasetron hydrochloride | Azasetron hydrochloride is a potent 5-HT3 channel blocker with a Ki ~2.9 n… | 50 mg | Y-100 | More Info |
AZD-1332 | AZD-1332 is a potent, selective, and orally bioavailable inhibitor of tyro… | 10 mg | A-495 | More Info |
AZD-1332 | AZD-1332 is a potent, selective, and orally bioavailable inhibitor of tyro… | 25 mg | A-495 | More Info |
AZD-1332 | AZD-1332 is a potent, selective, and orally bioavailable inhibitor of tyro… | 5 mg | A-495 | More Info |
AZD-1332 | AZD-1332 is a potent, selective, and orally bioavailable inhibitor of tyro… | 50 mg | A-495 | More Info |
AZD-9056 hydrochloride | AZD-9056 is a potent and selective, orally bioavailable antagonist of the… | 1 mg | A-425 | More Info |
AZD-9056 hydrochloride | AZD-9056 is a potent and selective, orally bioavailable antagonist of the… | 10 mg | A-425 | More Info |
AZD-9056 hydrochloride | AZD-9056 is a potent and selective, orally bioavailable antagonist of the… | 25 mg | A-425 | More Info |
AZD-9056 hydrochloride | AZD-9056 is a potent and selective, orally bioavailable antagonist of the… | 5 mg | A-425 | More Info |
AZ 10606120 dihydrochloride | AZ 10606120 dihydrochloride is a potent and selective non-competitive anta… | 10 mg | A-405 | More Info |
AZ 10606120 dihydrochloride | AZ 10606120 dihydrochloride is a potent and selective non-competitive anta… | 25 mg | A-405 | More Info |
AZ 10606120 dihydrochloride | AZ 10606120 dihydrochloride is a potent and selective non-competitive anta… | 5 mg | A-405 | More Info |
AZ 10606120 dihydrochloride | AZ 10606120 dihydrochloride is a potent and selective non-competitive anta… | 50 mg | A-405 | More Info |
Azelnidipine | 0.3-1 µM inhibited guinea-pig vascular smooth muscle1. Synthetic. Pu… | 10 mg | A-135 | More Info |
Azelnidipine | 0.3-1 µM inhibited guinea-pig vascular smooth muscle1. Synthetic. Pu… | 25 mg | A-135 | More Info |
Azelnidipine | 0.3-1 µM inhibited guinea-pig vascular smooth muscle1. Synthetic. Pu… | 5 mg | A-135 | More Info |
Azelnidipine | 0.3-1 µM inhibited guinea-pig vascular smooth muscle1. Synthetic. Pu… | 50 mg | A-135 | More Info |
Azemiopsin | Azemiopsin blocks the adult form (α1/β1/ε/δ) as w… | 0.1 mg | STA-100 | More Info |
Azemiopsin | Azemiopsin blocks the adult form (α1/β1/ε/δ) as w… | 0.5 mg | STA-100 | More Info |
Azemiopsin | Azemiopsin blocks the adult form (α1/β1/ε/δ) as w… | 1 mg | STA-100 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 1 g | A-245 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 10 mg | A-245 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 100 mg | A-245 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 250 mg | A-245 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 50 mg | A-245 | More Info |
Azilsartan | Azilsartan is an angiotensin II type 1 receptor antagonist. The physiologi… | 500 mg | A-245 | More Info |
BAPTA-AM | Ca2+ chelator (negative control). Purity ≥90%. MW: 764.68 | 2 mg | B-180 | More Info |
BCTC | BCTC is a potent and selective antagonist of TRPV1 channels, shown to inhi… | 10 mg | B-110 | More Info |
BCTC | BCTC is a potent and selective antagonist of TRPV1 channels, shown to inhi… | 25 mg | B-110 | More Info |
BCTC | BCTC is a potent and selective antagonist of TRPV1 channels, shown to inhi… | 50 mg | B-110 | More Info |
BDNF Basic Research Pack | All You Need for BDNF Research | 9 vials | ESB-600 | More Info |
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