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Cas Index 1

• 1627710-50-2 | LJH685 (Catalog# : 16070903)LJH685 is a potent pan-RSKinhibitor withIC50of 6 nM, 5 nM and 4 nM for RSK1, RSK2, an
• 1137608-69-5 | LX1606 (Hippurate) (Catalog# : 16062301)LX1606 is an orally bioavailable, small-molecule, tryptophan hydroxylase (TPH) inhibi
• 1165910-22-4 | LGD-4033(Ligandrol) (Catalog# : 030907)LGD-4033, also known as VK5211 and Ligandrol, is an investigational selective androge
• 191471-52-0 | LY-379268 (Catalog# : 011904)Coming soon!
• 1350636-82-6 | Lefamulin acetate (Catalog# : 011808)Coming soon!
• 1061337-51-6 | Lefamulin (Catalog# : 011807)Coming soon!
• 111358-88-4 | Lestaurtinib (Catalog# : 010815)Lesraurtinib is an orally bioavailable indolocarbazole derivative with antineoplastic
• 1192189-69-7 | LX7101 (Catalog# : 010802)LX7101 is a potent inhibitor of LIMK1/2, ROCK2 and PKA, with IC50 of 24/1.6, 10, and
• 1082949-67-4 | LY2584702 free base (Catalog# : 122909)LY2584702 is an orally available inhibitor of p70S6K signaling; inhibits p70S6K and p
• 1082949-68-5 | LY2584702 tosylate (Catalog# : 122907)LY-2584702 tosylate salt is an orally available inhibitor of p70S6K signaling; inhibi
• 1062368-62-0 | LDN193189 Hydrochloride (Catalog# : 122830)LDN193189 Hydrochloride is a selective BMP signaling inhibitor, inhibits the transcri
• 1005342-46-0 | LCL161 (Catalog# : 122820)LCL161 is an orally bioavailable SMAC mimetic and inhibitor of Inhibitor of Apoptosis
• 1234703-40-2 | LY2608204 (Catalog# : 122218)LY2608204 is a activator of glucokinase (GK) with EC50 of 42 nM.
• 1194044-20-6 | LY2811376 (Catalog# : 121435)LY2811376 is a BACE1 inhibitor with marked Ab-lowering effects in animal models.
• 1262036-50-9 | LY2886721 (Catalog# : 121427)LY2886721 is an BACE inhibitor used for the treatment of Alzheimer's Disease.
• 1418033-25-6 | LMK 235 (Catalog# : 120422)LMK 235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor, which demons
• 1308256-94-1 | LHW090-A7 (Catalog# : 91810)Coming soon!
• 1234480-84-2 | LRRK2-IN-1 (Catalog# : 81001)LRRK2-IN-1 is a cell-permeable, ATP competitive, potent, and selective LRRK2 inhibito
• 1254473-64-7 | LY2874455 (Catalog# : 71801)1) Sponsor: Eli Lilly and Company.2) Phase:Phase 12) LY2874455 is potent, selective,
• 1032900-25-6 | LDK378 (Catalog# : 52806)LDK378(Ceritinib) is potent inhibitor against ALK with IC50 of 0.2 nM, shows 40- and
• 1062368-24-4 | LDN193189 (Catalog# : 52733)LDN193189(DM 3189) is a selective BMP signaling inhibitor, inhibits the transcription
• 1627503-67-6 | LDN-214117 (Catalog# : 52707)LDN-214117 is a potent and selective ALK2 inhibitor with IC50 of 22 nM; > 100 fold
• 1432597-26-6 | LDN-212854 (Catalog# : 52588)LDN-212854 is a potent and selectiveBMP receptorinhibitor with IC50 of 1.3 nM for ALK
• 1026680-07-8 | LB-100 (Catalog# : 52511)LB-100 is a small-molecular protein phosphatase 2A(PP2A)inhibitor with IC50 of 0.85 M
• 154447-36-6 | LY294002 (Catalog# : 52309)LY294002 is the first synthetic molecule known to inhibitPI3K//withIC50of 0.5 M/0.57
• 1398568-47-2 | Milademetan free base (Catalog# : 20529)Milademetan, also known as DS-3032b or DS-3032, is a potent and selective MDM2 inhibi
• 1424371-93-6 | MK-8189 (Catalog# : 20503)MK-8189 is a Highly Potent and Selective PDE10A Inhibitor for the Treatment of Schizo
• 1933460-19-5 | Mitiperstat (Catalog# : 20457)Mitiperstat is a myeloperoxidase inhibitor.
• 129047-38-7 | 3-METHOXY-4-[(4-METHOXYBENZYL)OXY]BENZENECARBALDEHYDE (Catalog# : 20398)
• 1032570-74-3 | 7-methoxy-8-[3-(4-morpholinyl)propoxy]-Imidazo[1,2-c]quinazolin-5-amine (Catalog# : 20394)