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Cas Index 8

• 850879-09-3 | Amuvatinib (Catalog# : 123016)Amuvatinib is a potent and multi-targeted inhibitor of c-Kit, PDGFR and Flt3 with IC5
• 897383-62-9 | AST-1306 (Catalog# : 122926)AST-1306 is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and
• 897732-93-3 | APD597 (Catalog# : 121804)APD597 is a potent and selective GPR119 agonist, which is potential useful for the tr
• 80460-73-7 | 4-Aminobenzeneboronic Acid Hydrochloride (Catalog# : 120701)Coming soon!
• 802904-66-1 | AZD1981 (Catalog# : 102604)AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 fro
• 896466-04-9 | AT9283 (Catalog# : 52769)AT9283 is a small molecule a multi-targeted inhibitor with IC50s of 4, 1.2, 1.1 and a
• 85650-56-2 | Asenapine maleate (Catalog# : 52767)Asenapine maleate(Org 5222 maleate) inhibits adrenergic receptor (1, 2A, 2B, 2C) with
• 850649-62-6 | Alogliptin Benzoate (Catalog# : 52741)Alogliptin benzoate(SYR 322) is a potent, selective inhibitor of DPP-4 with IC50 of &
• 850140-72-6 | Afatinib (Catalog# : 52719)Afatinib (BIBW2992) irreversibly inhibits EGFR/HER2 including EGFR(wt), EGFR(L858R),
• 852808-04-9 | ABT-737 (Catalog# : 52640)ABT-737 is a BH3 mimetic inhibitor ofBcl-xL,Bcl-2andBcl-wwithEC50of 78.7 nM, 30.3 nM
• 860352-01-8 | AZD-7762 (Catalog# : 52638)AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM; equally potent
• 844442-38-2 | AT7519 (Catalog# : 52314)AT7519 is a multi-CDKinhibitor for CDK1, 2, 4, 6 and 9 withIC50of 10-210 nM. It is le
• 89796-99-6 | Aceclofenac (Catalog# : 51914)Aceclofenac is a non-steroidal anti-inflammatory drug (NSAID) analog of Diclofenac.
• 866086-05-7 | BI 44370 (Catalog# : 26A043)BI 44370 was developed as a calcitonin gene-related peptide(CGRP)receptor antagonist
• 886372-53-8 | 4-Bromo-6-methylpyridine-2-carbonitrile (Catalog# : 171653)4-Bromo-6-methylpyridine-2-carbonitrile, CAS 886372-53-8
• 885280-42-2 | 6-BENZYLOXY-3,4-DIHYDRO-1H-NAPHTHALEN-2-ONE (Catalog# : 20372)
• 887650-05-7 | Bafetinib (Catalog# : 2021221)Bafetinib, also known as INNO-406 and NS187, is an orally bioavailable 2-phenylaminop
• 893397-44-9 | BMS-688521 (Catalog# : 1811281)BMS-688521 is a small molecule antagonist of leukocyte function associated antigen-1
• 890405-51-3 | 3BDO (Catalog# : 186232)3BDO, a butyrolactone derivative, could target FKBP1A and activate the mTOR signaling
• 83314-01-6 | Bryostatin 1 (Catalog# : 18573)Bryostatin 1 is a potent Protein Kinase C modulator isolated from the bryozoan Bugula
• 850717-64-5 | BX-517 (Catalog# : 1791314)BX-517, also known as PDK1 inhibitor2, is a potent and selective PDK1 inhibitor.
• 882405-89-2 | BBT-594 (Catalog# : 179133)BBT594, also known as NVP-BBT594, is potent and selective RET and JAK2 inhibitor. NVP
• 863029-99-6 | Balamapimod (Catalog# : 2017822)Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be p
• 848695-25-0 | BIIB021 (Catalog# : 16122868)BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
• 890128-81-1 | BFH772 (Catalog# : 16122778)BFH772 is a novel potent oral VEGFR2 inhibitor, targeting VEGFR2 kinase with IC50 of
• 883065-90-5 | BI-78D3 (Catalog# : 16122776)BI-78D3 is a competitive JNK inhibitor with IC50 of 280nM that displays > 100 fold
• 861875-60-7 | BAW2881 (NVP-BAW2881) (Catalog# : 16122733)BAW2881 (NVP-BAW2881) is a novel vascular endothelial growth factor (VEGF) receptor t
• 865783-99-9 | Briciclib (Catalog# : 611917)Briciclib is a small molecule that suppresses cyclin D1 accumulation in cancer cells.
• 859853-30-8 | BMS-690514 (Catalog# : 011102)BMS-690514 is a potent and selective inhibitor of epidermal growth factor receptor (E
• 859212-16-1 | Bafetinib (Catalog# : 122947)Bafetinib is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM/19