Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 16062701 | AM-580 | 102121-60-8 | 98% by HPLC |  |
| AM-580 is a potent RARalpha agonist. AM580 has powerful and selective cyto-differenti | ||||
| 16062401 | Aurora A Inhibitor I | 1158838-45-9 | 98% by H PLC |  |
| Aurora A Inhibitor I | ||||
| 16062104 | AN-2718 | 174672-06-1 | 98% by HPLC |  |
| AN-2718 | ||||
| 16062102 | AZ7371 | 1494675-86-3 | 98% by HPLC |  |
| AZ7371 is a a novel non-covalent DprE1 inhibitor | ||||
| 16062001 | Amcinafide | 7332-27-6 | 98% by HPLC |  |
| Amcinafide | ||||
| 33001 | AZD-3965 | 1448671-31-5 | 98% |  |
| AZD3965 is a selective inhibitor of monocarboxylate transporter 1 (MCT1) with a bindi | ||||
| 022201 | AVN944 | 297730-17-7 | 98% |  |
| AVN944 is an orally available, synthetic small molecule with potential antineoplastic | ||||
| 021801 | Arry-380 | 937265-83-3 | 98% |  |
| ARRY-380 is a potent and selective HER2 inhibitor with IC50 of 8 nM, equipotent again | ||||
| 012603 | A-1331852 | 1430844-80-6 | 98% |  |
| Coming soon! | ||||
| 012602 | A-1155463 | 1235034-55-5 | 98% |  |
| A-1155463 is a highly potent and selective BCL-XL inhibitor. | ||||
| 011919 | AH13205 | 148436-63-9 | 98% |  |
| Coming soon! | ||||
| 011918 | Alofanib | 1612888-66-0 | 98% |  |
| Alofanib is a potential small molecule kinase inhibitor with potential anticancer act | ||||
| 011913 | AS 602801 | 848344-36-5 | 98% |  |
| AS 602801 is a novel, orally active inhibitor of JNK. | ||||
| 011911 | AMG232 | 1352066-68-2 | 98% |  |
| AMG232 is an extremely potent MDM2 inhibitor (SPR KD = 0.045 nM, SJSA-1 EdU IC50 = 9. | ||||
| 011905 | Afdx 384 | 118290-27-0 | 98% |  |
| Coming soon! | ||||
| 011813 | Avoralstat | 918407-35-9 | 95.0% |  |
| Avoralstat (formerly BCX4161) is a potent small-molecule oral plasma kallikrein inhib | ||||
| 01181 | AMG-337 | 1173699-31-4 | 98% |  |
| AMG-337 is a potent and highly selective small molecule ATP-competitive MET kinase in | ||||
| 011811 | Afuresertib | 1047644-62-1 | 98% |  |
| Afuresertib is a potent pan-AKT inhibitor that demonstrated synergy with bortezomib i | ||||
| 011803 | AMG 900 | 945595-80-2 | 98% |  |
| AMG 900 is a potent and highly selective pan-Aurora kinases inhibitor for Aurora A/B/ | ||||
| 011802 | APTO-253 | 1422731-37-0 | 98% |  |
| APTO-253 is a small molecule inhibitor of human metal-regulatory transcription factor | ||||
| 011302 | AC-55541 | 916170-19-9 | 98% |  |
| AC-55541 is a novel small-molecule protease-activated receptor 2(PAR2) agonist. | ||||
| 011120 | AZ 628 | 878739-06-1 | 98% |  |
| AZ628 is a new pan-Raf inhibitor for BRAF, BRAFV600E, and c-Raf-1 with IC50 of 105 nM | ||||
| 011117 | AZD-5582 | 1258392-53-8 | 98% |  |
| AZD5582 is a potent IAP inhibitor, which is a dimeric compound based on the AVPI moti | ||||
| 011111 | Arbidol hydrochloride | 131707-23-8 | 98% |  |
| Arbidol is an broad-spectrum antiviral chemical agent which can inhibit cell entry of | ||||
| 011108 | APY29 | 1216665-49-4 | 98% |  |
| APY29 is an allosteric modulator of IRE1; inhibits IRE1 autophosphorylation (IC50 = 2 | ||||
| 011107 | AMG-47a | 882663-88-9 | 98% |  |
| AMG-47a is a potent inhibitor of Lck and T cell proliferation. | ||||
| 011104 | ARQ-736 | 1228237-57-7 | 98% |  |
| ARQ 736 is a potent and selective BRAF inhibitor. | ||||
| 010820 | AZD4547 | 1035270-39-3 | 98% |  |
| AZD4547 is a novel selective FGFR inhibitor targeting FGFR1/2/3 with IC50 of 0.2 nM/2 | ||||
| 010816 | AZD-1480 | 935666-88-9 | 98% |  |
| AZD1480 is a novel ATP-competitive JAK2 inhibitor with IC50 of 0.26 nM, selectivity a | ||||
| 010809 | AZD8330 | 869357-68-6 | 98% |  |
| AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 n | ||||