Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 80317 | (2R,4R)-1-tert-Butyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride | 1217474-04-8 | 97% | -1-tert-Butyl2-methyl4-aminopyrrolidine-12-dicarboxylatehydrochloride-cas-1217474-04-8.png) |
| Coming soon! | ||||
| 73101 | RVX-208 | 1044870-39-4 | 97% |  |
| RVX-208(RVX 000222) is a small molecule that increases apolipoprotein A-I and high-de | ||||
| 52825 | RU 58841 | 154992-24-2 | 98% |  |
| RU 58841 is a specific androgen receptor antagonist or anti-androgen; RU 58841 has a | ||||
| 52814 | (R)-Oxiracetam | 68252-28-8 | 98% | -Oxiracetam-cas-68252-28-8.png) |
| (R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (IS | ||||
| 52807 | Rabusertib(LY2603618) | 911222-45-2 | 98% |  |
| LY2603618(IC-83) is a potent and selective small molecule inhibitor of Chk1 protein k | ||||
| 52736 | RKI-1447 | 1342278-01-6 | 98% |  |
| RKI-1447 is a potent small molecule inhibitor of ROCK1 and ROCK2. | ||||
| 52722 | Regorafenib | 755037-03-7 | 98% |  |
| Regorafenib (BAY 73-4506) is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDG | ||||
| 52706 | RN486 | 1242156-23-5 | 98% | |
| RN486 is a selective Btk inhibitor with an IC50 Value of 4.0 nM. | ||||
| 52612 | Raltegravir potassium sal | 871038-72-1 | 98% |  |
| Raltegravir potassium salt(MK0518 potassium salt) is a potent integrase (IN) inhibito | ||||
| 52602 | Ramelteon | 196597-26-9 | 98% |  |
| Ramelteon (TAK-375; Rozerem)is a melatonin receptor agonist with both high affinity f | ||||
| 52826 | Ro3280 | 1062243-51-9 | 98% |  |
| RO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 | ||||
| 52580 | Ro-3306 | 872573-93-8 | 98% |  |
| Ro-3306 is a potent and selective inhibitor of CDK1 with Ki value of 35 nM for CDK1/c | ||||
| 52570 | Roscovitine | 186692-46-6 | 98% |  |
| Roscovitine (Seliciclib, CYC202) is a potent and selective CDK inhibitor for Cdc2, CD | ||||
| 52526 | RITA | 213261-59-7 | 98% |  |
| RITA(NSC 652287) induced both DNA-protein and DNA-DNA cross-links with no detectable | ||||
| 52515 | Reversine | 656820-32-5 | 98% |  |
| Reversine, a small synthetic purine analogue (2,6-disubstituted purine), is a potent | ||||
| 52501 | RG108 | 48208-26-0 | 98% |  |
| RG108 is a non-nucleoside inhibitor of DNA methyltransferase with IC50 of 115 nM. | ||||
| 51501 | Ro 61-8048 | 199666-03-0 | 98% |  |
| Ro 61-8048 is a potent and selective inhibitors of kynurenine hydroxylase with IC50 o | ||||
| 52204 | Rostafuroxin | 156722-18-8 | 98% |  |
| Rostafuroxin(PST 2238) is a antihypertensive compound; Na,K-ATPase antognist;displace | ||||
| 52104 | Rocilinostat (ACY-1215) | 1316214-52-4 | 98% | -cas-1316214-52-4.png) |
| Rocilinostat (ACY-1215) is a selectiveHDAC6inhibitor withIC50of 5 nM. It is >10-fo | ||||
| 52009 | Rucaparib(AG-014699,PF-01367338) | 459868-92-9 | 98% | -cas-459868-92-9.png) |
| Rucaparib (AG-014699, PF-01367338) is an inhibitor ofPARPwithKiof 1.4 nM for PARP1, a | ||||
| 52010 | Rigosertib sodium | 1225497-78-8 | 98% |  |
| Rigosertib (ON-01910) is a non-ATP-competitive inhibitor ofPLK1withIC50of 9 nM. It sh | ||||
| 51911 | Ribociclib (LEE011) | 1211441-98-3 | 98% | -cas-1211441-98-3.png) |
| Ribociclib (LEE011) is an orally available, and highly specificCDK4/6inhibitor. Phase | ||||
| 51609 | R788 (Fostamatinib) Disodium | 1025687-58-4 | 98% | Disodium-cas-1025687-58-4.png) |
| R788 (Fostamatinib) disodium, a prodrug of the active metabolite R406, is aSykinhibit | ||||