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erastin

Chemical Information M.Wt 547.04 Storage Please store the product under th...

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VX809

Chemical Information M.Wt 452.41 Storage Please store the product under th...

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VX661

Chemical Information M.Wt 520.5 Storage Please store the product under the...

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PPQ-102

Chemical Information M.Wt 438.48 Storage Please store the product under th...

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KPT-330

Chemical Information Download Selinexor (KPT-330) SDF Molecular Weight (MW) 443.31 ...

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Tariquidar (XR 9576)

Tariquidar (XR-9576) is a P-glycoprotein inhibitor undergoing research as an adjuvant against multidrug resistance in cancer. Tariquidar non-competiti...

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Bafilomycin A1

Bafilomycin A1 is a highly potent vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. Bafilomycin A1 is selective for v-ATPase over other ATP hydrolyzi...

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TAK 438

TAK-438 is a novel potassium-competitive acid blocker (P-CAB) type antisecretory agent that reversibly inhibits gastric H+,K+-ATPase with IC50 of 19 n...

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AMG 073

AMG-073 HCl (Cinacalcet hydrochloride) represents a new class of compounds for the treatment of hyperparathyroidism known as calcimimetics, which redu...

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Azelnidipine

Azelnidipine is a novel dihydropyridine derivative, a L-type calcium channel blocker, and an antihypertensive. Acute administration of azelnidipine pr...

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Dapagliflozin (BMS 512148)

Dapagliflozin (BMS-512148) is a potent and selective sodium-glucose transport proteins (SGLT2) inhibitor with EC50 of 1.1 nM. SGLT2 is responsible for...

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Canagliflozin (JNJ 28431754)

Canagliflozin (JNJ-28431754) is a highly potent and selective subtype 2 sodium-glucose transport protein (SGLT2) inhibitor for CHO- hSGLT2, CHO- rSGLT...

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VX 770 (Ivacaftor)

Ivacaftor (VX-770) is a CFTR potentiator with an IC50 of 43 ± 38 nM. In recombinant cells Ivacaftor (VX770) increased CFTR channel open probabi...

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Clevidipine (Cleviprex)

Clevidipine (Cleviprex) is a dihydropyridine calcium channel blocker indicated for the reduction of blood pressure when oral therapy is not feasible o...

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Valspodar (PSC 833)

Valspodar (PSC-833, SDZ PSC-833) inhibits p-glycoprotein, the multidrug resistance efflux pump, thereby restoring the retention and activity of some d...

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EGT 1442

EGT1442 is a potent and selective SGLT2 inhibitor. The IC50 values for EGT-1442 against human SGLT1 and SGLT2 are 5.6μM and 2nM, respectively. Sodi...

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