| 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). | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |
| 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. | price> |

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