Search By Initial

Cas Index 9

• 919783-22-5 | AZD-1656 (Catalog# : 24070)AZD-1656 is a glucokinase (GK) activator potentially for the treatment of type 2 diab
• 951884-75-6 | 2-Amino-5-bromo-4-methoxy-3-pyridinecarbonitrile (Catalog# : 20424)
• 952753-59-2 | 2-amino-4-(4-fluorophenyl)thiazole-5-carbonitrile (Catalog# : 20400)
• 958295-17-5 | AGN 196996 (Catalog# : 226191)AGN 196996 is a potent and selective RARα antagonist with Ki value of 2 nM; little b
• 96566-25-5 (free acid) | Ablukast (Catalog# : 20319)Ablukast is a leuktriene receptor antagonist that acts as an anti-asthmatic.
• 959850-74-9 | AP1189 acetate (Catalog# : 2105071)AP1189 is a melanocortin receptor agonist on MC1 and MC3 receptors.
• 932372-01-5 | Asapiprant (Catalog# : 2051515)Asapiprant is a potent and selective DP1 receptor antagonist, with a Ki of 0.44 nM. A
• 942507-42-8 | AZ304 (Catalog# : 19363)AZ304 is an ATP-competitive dual BRAF kinase inhibitor, potently inhibits wild type B
• 913548-29-5 | AR-9281 (Catalog# : 191146)AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment
• 949164-09-4 | ALX 1393 (Catalog# : 185213)ALX 1393 is a glycine transporter-2 inhibitor.
• 919486-40-1 | AS-1517499 (Catalog# : 185187)AS-1517499 is a potent and selective STAT6 inhibitor.
• 943764-99-6 | Acebilustat (Catalog# : 179159)Acebilustat, also known as ZK322, is a potent and selective leukotriene A4 hydrolase
• 924641-59-8 | AZD-5597 (Catalog# : 16122865)AZD-5597 is potent CDK inhibitor with in vitro anti-proliferative effects against a r
• 942398-84-7 | Amiselimod HCl (Catalog# : 16122856)Amiselimod, also known as MT1303, is a potent and selective immunosuppressant and sph
• 9087-70-1 | Aprotinin (Catalog# : 16122761)Aprotinin is a small protein serine protease inhibitor, used to reduce perioperative
• 959746-77-1 | A-836339 (Catalog# : 6111107)A-836339 is a cannabinoid CB2 receptor-selective agonist; exhibits high potencies at
• 900515-16-4 | AS-252424 (Catalog# : 160926012)AS-252424 is a potent and selective small-molecule PI3Kgamma inhibitor. Oral administ
• 937265-83-3 | Arry-380 (Catalog# : 021801)ARRY-380 is a potent and selective HER2 inhibitor with IC50 of 8 nM, equipotent again
• 918407-35-9 | Avoralstat (Catalog# : 011813)Avoralstat (formerly BCX4161) is a potent small-molecule oral plasma kallikrein inhib
• 945595-80-2 | AMG 900 (Catalog# : 011803)AMG 900 is a potent and highly selective pan-Aurora kinases inhibitor for Aurora A/B/
• 916170-19-9 | AC-55541 (Catalog# : 011302)AC-55541 is a novel small-molecule protease-activated receptor 2(PAR2) agonist.
• 935666-88-9 | AZD-1480 (Catalog# : 010816)AZD1480 is a novel ATP-competitive JAK2 inhibitor with IC50 of 0.26 nM, selectivity a
• 935881-37-1 | AR-42 (Catalog# : 123009)AR-42 is a novel, oral cancer therapy currently in early clinical development.
• 934162-61-5 | A-966492 (Catalog# : 123006)A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 nM and 1.5 n
• 90779-69-4 | Atosiban acetate (Catalog# : 122931)Atosiban is a nonapeptide, desamino-oxytocin analogue, and a competitive vasopressin/
• 909910-43-6 | A 83-01 (Catalog# : 122843)A 83-01 is a selective inhibitor of TGF- type I receptor ALK5 kinase, type I activin/
• 924416-43-3 | AdipoRon (Catalog# : 122822)AdipoRon is a novel small-molecule AdipoR agonist; binds to both AdipoR1(Kd= 1.8 uM)
• 90141-22-3 | AT-101 (Catalog# : 121434)AT-101 is the orally bioavailable the R-(-) enantiomer of gossypol with potential ant
• 939805-30-8 | ACTB-1003 (Catalog# : 102619)ACTB-1003 is a potent inhibitor of FGFR1 with IC50 <10 nM in FGFR-1 biochemical as
• 902135-91-5 | AT7519 Hydrochloride (Catalog# : 82702)AT7519 hydrochloride is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10