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Cas Index 2

• 2416874-75-2 | KB-0742 dihydrochloride (Catalog# : 24020)KB-0742 is a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of CDK9
• 2082765-42-0 | KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) (Catalog# : 20641)KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) is a small molecule inhibitor of protein
• 2446480-97-1 | KSQ-4279 (Catalog# : 20472)KSQ-4279 is a USP1 and PARP inhibitor. KSQ-4279 showed anti-proliferative effects in
• 2226664-93-1 | KY19382 (Catalog# : L20334)KY19382 is an orally active dual inhibitor of CXXC5-DVL and GSK3β
• 228559-41-9 | Ki8751 (Catalog# : 17022703)Ki8751 is a potent, selective inhibitor of VEGFR-2 tyrosine kinase (IC50 = 0.9 nM). D
• 286370-15-8 | KRN 633 (Catalog# : 51912)KRN 633 is an ATP-competitive inhibitor ofVEGFR1/2/3withIC50of 170 nM/160 nM/125 nM,
• 2688040-45-9 | Lirafugratinib HCl (Catalog# : 24113)Lirafugratinib, also known as RLY-4008, is a tyrosine kinase inhibitor with potential
• 2251753-65-6 | LXH-3-71 (Catalog# : 24107)LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH
• 2834106-06-6 | LTGO-33 (Catalog# : 24103)LTGO-33 is a selective, state-independent, and potent preclinical small molecule NaV1
• 2719793-90-3 | Lunresertib (Catalog# : 24080)Lunresertib, alsop known as RP-6306, is a potent and selective PKMYT1 inhibitor (IC50
• 2495096-26-7 | lartesertib (Catalog# : 24066)Lartesertib (M4076) is a potent inhibitor of serine/threonine protein kinase ATM (ext
• 297180-15-5 | Lipofermata (Catalog# : 24030)Lipofermata is a fatty acid transport protein 2(FATP2)inhibitor. Lipofermata shows fa
• 2568608-48-8 | LY3522348 (Catalog# : 20577)
• 244240-24-2 | LFM-A13 (Catalog# : 20438)LFM-A13 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). LF
• 2375815-63-5 | LY-3475070 (Catalog# : 21244)LY-3475070 is a potent and selective CD73 Inhibitor with IC50 of 28 nM. LY3475070 Alo
• 2097938-59-3 | Lerociclib HCl (G1T38 HCl) (Catalog# : 2073106)Lerociclib HCl (G1T38)is a novel, selective,differentiated oral CDK4/6 inhibitor with
• 2055050-87-6 | LAU159 (Catalog# : 2071505)LAU159 is a potent modulator of α6β3γ2 GABAA receptor.
• 294623-49-7 | L006235 (Catalog# : 2061307)L006235 is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays
• 2274819-46-2 | LUT-014 (Catalog# : 2042701)LUT-014 is a B-Raf Inhibitor. Leveraging the paradoxical effect of B-Raf Inhibitors,
• 2135600-76-7 | LSZ102 (Catalog# : 2041502)LSZ102 is a potent ERα antagonist and degrader. LSZ102 showed ERα degradation IC50
• 2173037-97-1 | LY2794193 (Catalog# : 193262)LY2794193 is a highly potent and selective mGlu3 receptor agonist.
• 2166616-75-5 | LY-3381916 (Catalog# : 193123)LY-3381916 is a potent, selective and brain penetrated inhibitor of IDO1 activity, bi
• 245075-84-7 | LR-90 (Catalog# : 19364)LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory res
• 2222755-14-6 | LOXO-292 (Catalog# : 192195)LOXO-292 (ARRY-192) is an oral and selective investigational drug in clinical develop
• 292632-98-5 | L685458 (Catalog# : 186156)L685458 is a potent and selective γ -secretase inhibitor.
• 2097002-61-2 | LOXO-195 (Catalog# : 185212)LOXO-195 is a potent and selective TRK inhibitor capable of addressing potential mech
• 2088939-99-3 | LYN-1604 (Catalog# : 18493)LYN-1604 is a novel activator of ULK1, inducing cell death involved in ATF3, RAD21, a
• 226929-39-1 | LB42708 (Catalog# : 18443)LB42708 is a potent, orally active and selective nonpeptidic farnesyltransferase inhi
• 2040291-27-6 | LLY-283 (Catalog# : 184314)LLY-283 is a potent and selective SAM-competitive chemical probe for PRMT5.
• 231277-92-2 | Lapatinib (Catalog# : 17022807)Lapatinib(GW-572016) is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 n