编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
16070910 | ARS-853 | 1629268-00-3 | 98% by HPLC | |
ARS-853 is a selective, covalent inhibitor of KRAS-G12C that inhibits mutant KRAS dri | ||||
16070810 | Asunaprevir | 630420-16-5 | 98% by HPLC | |
Asunaprevir, also known as BMS-650032, is an inhibitor of the hepatitis C virus enzym | ||||
92801 | AZD2281(Olaparib) | 763113-22-0 | 98% by HPLC | |
Olaparib (AZD-2281, trade name Lynparza) is an FDA-approved targeted therapy for canc | ||||
16070801 | AZ91498 | 773871-93-5 | 98% by HPLC | |
AZ91498 | ||||
16070701 | A-769662 | 844499-71-4 | 98% by HPLC | |
A-769662 is a potent, reversible AMP-activated protein kinase (AMPK) activator with a | ||||
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(前身为BCX4161)是一种有效的小分子口服血浆激肽释放酶 | ||||
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 |