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Cas号索引 1

• 1220327-45-6 | (3aR,5R)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole (Catalog# : 91803)Coming soon!
• 1626387-80-1 | AZD3759 (Catalog# : 901301)AZD3759 isan orally available inhibitor of the epidermal growth factor receptor (EGFR
• 1664-54-6 | 3-(3-Aminophenyl)propanoic acid (Catalog# : 90607)Coming soon!
• 1035229-35-6 | 8-(2-aminoethyl)-5-hydroxy-4H-1,4-benzoxazin-3-one,hydrochloride (Catalog# : 82801)Coming soon!
• 173334-57-1 | Aliskiren (Catalog# : 82708)Aliskiren(CGP 60536) is a direct renin inhibitor with IC50 of 1.5 nM.
• 154229-19-3 | Abiraterone (Catalog# : 82706)Abiraterone is a potent steroidal cytochrome P450 17alpha-hydroxylase-17,20-lyase (CY
• 1594092-37-1 | AZ191 (Catalog# : 82405)AZ191 selectively inhibits DYRK1B serine/threonine kinase activity with no effect on
• 120278-07-1 | 4-Amino-Piperidine-1-Carboxylic Acid Benzyl Ester (Catalog# : 81805)Coming soon!
• 1351522-04-7 | AC710 (Catalog# : 80702)AC710 is a potent, selective PDGFR-family kinases inhibitor with Kd values of 0.6 nM/
• 19229-57-3 | ALPHA-BENZYL-4,6-O-BENZYLIDENE-MURAMIC ACID (Catalog# : 80302)Coming soon
• 1009298-59-2 | AZD2014(Vistusertib) (Catalog# : 71804)AZD2014is a potent (IC50 2.81 nM), selective (inactive against 220 other kinases) inh
• 1639042-08-2 | AZD9496 (Catalog# : 71802)1) Sponsor:AstraZeneca2) Phase:Phase 13)AZD9496 is a novel, oral selective oestrogen
• 1217486-61-7 | Alpelisib(BYL719) (Catalog# : 62504)NVP-BYL719 is novel and specific PI3K inhibitor.NVP-BYL719 has displayed promising re
• 1032754-93-0 | Apitolisib(GDC-0980,RG7422) (Catalog# : 62503)Apitolisib(GDC-0980,RG7422) is a dual PI3K/mTOR inhibitor.GDC-0980 was potent across
• 198904-31-3 | Atazanavir (Catalog# : 61005)Atazanavir(BMS-232632) is an highly potent HIV-1 protease inhibitor.
• 1202757-89-8 | AVL-292 (Catalog# : 52770)AVL-292 is a covalent, highly selective, orally active small molecule inhibitor of Bt
• 1197958-12-5 | AP26113 (Catalog# : 52766)AP26113 is a potent and selective active inhibitor of anaplastic lymphoma kinase(ALK)
• 1228690-36-5 | AM095 free acid (Catalog# : 52765)AM095 is a potent LPA1 receptor antagonist with IC50 values of 0.98 and 0.73 M for re
• 1232221-74-7 | APY0201 (Catalog# : 52759)APY0201 is a potent, highly selective, ATP-competitive PIKfyve inhibitor (IC50=5.2 nM
• 1256094-72-0 | AI-10-49 (Catalog# : 52757)AI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBF-SMM
• 1233339-22-4 | AZ20 (Catalog# : 52734)AZ20 is a potent and selective inhibitor of ATR with an IC50 of 5 nM; 8-fold selectiv
• 1608125-21-8 | AMG-319 (Catalog# : 52026)AMG 319 is an investigational, highly selective, small molecule inhibitor of PI3K tha
• 1401033-86-0 | AMG-925 (Catalog# : 51614)AMG-925 is a potent and orally bioavailable dual inhibitor of CDK4 and FLT3, includin
• 1028486-01-2 | Alisertib(MLN8237) (Catalog# : 52587)Alisertib (MLN8237) is a selective Aurora A inhibitor with IC50 of 1.2 nM; has >20
• 1002304-34-8 | AMG-208 (Catalog# : 52585)AMG-208 is a potent small molecular c-Met inhibitor with an IC50 of 9.3 nM.
• 1432660-47-3 | AGI-6780 (Catalog# : 52547)AGI-6780 is the first highly potent and selective small molecule inhibitor of isocitr
• 1177827-73-4 | AP-III-a4 (Catalog# : 52538)ENOblock(AP-III-a4) is a novel small molecule which is the first, nonsubstrate analog
• 188116-07-6 | AWD 131-138 (Catalog# : 52533)AWD 131-138(Imepitoin) is a new low-affinity partial benzodiazepine receptor agonist
• 154235-83-3 | Ampalex (Catalog# : 52524)Ampalex (Ampakine CX516; CX516; BDP 12) is an ampakine and nootropic that acts as an
• 118409-57-7 | AG 18 (Catalog# : 52504)AG-18(RG-50810; Tyrphostin A23) inhibits EGFR with IC50 of 40 M.