Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
16071413 | Acalisib | 870281-34-8 | 98% by HPLC | ![]() |
Acalisib, also known as GS-9820, is an inhibitor of the beta and delta isoforms of th | ||||
16071301 | AZD8330 | 1204531-17-8 | 98% by HPLC | ![]() |
AZD8330 | ||||
16071109 | AZD-4547 | 1394854-62-6 | 98% by HPLC | ![]() |
AZD-4547 | ||||
16071104 | Apaziquone | 114560-48-4 | 98% by HPLC | ![]() |
Apaziquone, also known as EO9, EOquin, is a n indolequinone bioreductive prodrug and | ||||
16071021 | AF-353 | 865305-30-2 | 98% by HPLC | ![]() |
AF-353 is a novel, potent and orally bioavailable P2X3/P2X2/3 receptor antagonist, in | ||||
16071001 | AMG-517 | 659730-32-2 | 98% by HPLC | ![]() |
AMG 517 is a potent and selective TRPV1 antagonist, and antagonizes capsaicin, proton | ||||
16070919 | ascorbic acid | 89924-69-6 | 98% by HPLC | ![]() |
(2R)-2-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxy-2H-furan-5-one | ||||
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 (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 | ||||
011803 | AMG 900 | 945595-80-2 | 98% | ![]() |
AMG 900 is a potent and highly selective pan-Aurora kinases inhibitor for Aurora A/B/ |
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