Catalog |
name |
Description |
price |
R-C-510 |
A-803467 cas:944261-79-4 |
A 803467 is a selective blocker of NaV1.8 channels(IC50 values are 8,2450,6740, 7340 and 7380 nM for hNaV1.8,hNaV1.3,hNaV1.7,hNaV1.5 and hNaV1.2 channels respectively). |
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R-C-524 |
Vonoprazan Fumarate (TAK-438) |
Vonoprazan Fumarate (TAK-438) is a novel P-CAB(potassium-competitive acid blocker)that reversibly inhibits H+/K+,ATPase with IC50 of 19 nM (pH 6.5), controls gastric acid secretion. |
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R-C-575 |
Emtricitabine cas:143491-57-0 |
Emtricitabine is a nucleoside reverse transcriptase inhibitor(NRTI) with an EC50 of 0.01 µM in PBMC cell.It is an antiviral drug for the treatment of HIV infection. |
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R-C-601 |
Rabeprazole sodium cas:117976-90-6 |
Rabeprazole sodium (LY307640 sodium)is a second-generation proton pump inhibitor(PPI)that irreversibly inactivates gastric H+/K+-ATPase.Rabeprazole sodium induces apoptosis.Rabeprazole sodium acts as an uridine nucleoside ribohydrolase(UNH)inhibitor with an IC50 of 0.3 μM.Rabeprazole sodium can be used for the research of gastric ulcerations and gastroesophageal reflux. |
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R-C-603 |
vx809 cas:936727-05-8 |
VX-80(Lumacaftor,VRT 826809) acts to correct CFTR mutations common in cystic fibrosis by increasing mutant CFTR (F508del-CFTR)maturation,EC50 of 0.1 μM in fisher rat thyroid cells. |
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R-C-614 |
Rostafuroxin(PST2238) cas:156722-18-8 |
Rostafuroxin(PST 2238),a digitoxigenin derivative,is an orally active and potent Na+,K+-ATPase(ATP1A1)antognist.Rostafuroxin binds specifically to the ATP1A1 extracellular domain and blocks respiratory syncytial virus(RSV)-triggered EGFR Tyr845 phosphorylation.Rostafuroxin has antihypertensive and anti-RSV activity. |
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R-C-654 |
tariquidar cas:206873-63-4 |
Tariquidar(XR9576)is a potent and selective noncompetitive inhibitor of P-glycoprotein with Kd of 5.1 nM in CHrB30 cell line,reverses drug resistance in MDR cell Lines. |
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R-C-744 |
AZD628 CAS No. : 942436-93-3 |
AZD-6280 is a selective GABAA(α2/3) receptor modulator,used for treatment of generalized anxiety disorder. |
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R-C-753 |
CVT-10216 cas:1005334-57-5 |
CVT-10216 is a highly selective,reversible aldehyde dehydrogenase-2(ALDH-2)inhibitor with an IC50 of 29 nM.CVT-10216 also has inhibitory effect of ALDH-1 with an IC50 of 1.3 μM.CVT-10216 can reduce excessive alcohol drinking in alcohol-preferring rats and exhibit anxiolytic effects. |
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R-C-757 |
KPT185 cas:133315-73-7 |
KPT185 is a selective CRM1 inhibitor.KPT-185 significantly inhibits leukemia cell proliferation with IC50 ranging from 100 nM to 500 nM,and induces cell-cycle arrest and apoptosis of AML cell lines and primary AML blasts. |
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