产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 52809 | Montelukast sodium | 151767-02-1 | 98% |  |
| Montelukast Sodium(Singulair) is a potent, selective, anti-inflammatory CysLT1 recept | ||||
| 52774 | MEK162 | 606143-89-9 | 98% |  |
| MEK162(ARRY-438162; ARRY-162) is a potent inhibitor of MEK1/2 with IC50 of 12 nM. | ||||
| 52749 | MLN9708 | 1201902-80-8 | 98% |  |
| MLN9708 immediately hydrolyzed to MLN2238, which is an N-capped dipeptidyl leucine bo | ||||
| 52742 | ML347 | 1062368-49-3 | 98% |  |
| ML347(DN193719) is a highly selective ALK1/ALK2 inhibitor with IC50s of 46/32 nM; sho | ||||
| 52582 | MLS-2052 | 667463-62-9 | 98% |  |
| 6-BIO(6-Bromoindirubin-3'-oxime) is a potent and selective inhibitor of GSK-3 and | ||||
| 52827 | MLN0905 | 1228960-69-7 | 98% |  |
| MLN0905 is a small-molecule and potent inhibitor of PLK1 with IC50 of 2 nM. | ||||
| 51505 | MK 2206 | 1032350-13-2 | 98% |  |
| MK-2206 (Merck, Whitehouse Station, NJ) is an investigational oral allosteric AKT inh | ||||
| 52554 | ML161 | 423735-93-7 | 98% |  |
| ML-161 is an allosteric inhibitor ofPAR1withIC50of 0.26 M. | ||||
| 52545 | MDL-29951 | 130798-51-5 | 98% |  |
| MDL-29951 is a novel glycine antagonist of NMDA receptor activation (Ki=0.14 mM, [3H] | ||||
| 52542 | Meisoindigo | 97207-47-1 | 98% |  |
| Meisoindigo(Natura-; N-Methylisoindigotin; Dian III), a derivative of Indigo naturali | ||||
| 52525 | 3-Methyladenine (3-MA) | 5142-23-4 | 98% | -cas-5142-23-4.png) |
| 3-Methyladenine is a selective PI3K inhibitor forVps34andPI3KwithIC50of 25 M and 60 M | ||||
| 52510 | Mdivi-1 | 338967-87-6 | 98% |  |
| Mdivi-1 is a selective cell-permeable inhibitor of mitochondrial division DRP1 (dynam | ||||
| 52219 | MHY1485 | 326914-06-1 | 98% | |
| MHY1485 is a mTOR activator; inhibits the autophagic process by inhibition of fusion | ||||
| 52317 | MS436 | 1395084-25-9 | 98% |  |
| MS436 is a diazobenzene-based small-molecule inhibitor for the BRD4 bromodomains with | ||||
| 52101 | Motesanib Diphosphate (AMG-706) | 857876-30-3 | 98% | -cas-857876-30-3.png) |
| Motesanib Diphosphate (AMG-706) is a potent ATP-competitive inhibitor ofVEGFR1/2/3wit | ||||