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• 182431-12-5 | Lomitapide free base (Catalog# : 16123035)Lomitapide is a MTP inhibitor. Lomitapid is a novel agent for the treatment of homozy
• 106400-81-1 | Lometrexol disodium (Catalog# : 16123034)Lometrexol is a folate analog antimetabolite with antineoplastic activity. As the 6R
• 1243244-14-5 | LGK974 (WNT974) (Catalog# : 16123033)LGK974, aslo known as is a selective and orally bioavailable Porcupine (PORCN) inhibi
• 1256388-51-8 | Ledipasvir (GS5885) (Catalog# : 16122765)Ledipasvir (GS5885) is a HCV NS5A polymerase inhibitor, used for the treatment of hep
• 1793053-37-8 | LLY-507 (Catalog# : 16122739)LLY-507 is a cell-active, potent, and selective inhibitor of protein-lysine Methyltra
• 1621862-70-1 | Lirametostat ( CPI-1205 ) (Catalog# : 16122736)Lirametostat ( CPI-1205 ) 是一种有效的、选择性的、辅助因子竞争性的
• 159182-43-1 | L755507 (Catalog# : 16122732)L-755,507 is characterized as a potent and selective 3 adrenergic receptor partial ag
• 169939-93-9 | LY333531 (Catalog# : 16122722)LY333531 is a -specific protein kinase C inhibitor. It competitively and reversibly i
• 1243329-97-6 | Lenalidomide hydrochloride (Catalog# : 6111410)Lenalidomide (Revlimid, CC-5013) is a TNF- secretion inhibitor with IC50 of 13 nM
• 1223405-08-0 | LOXO-101 (Catalog# : 61123)LOXO-101 is an oral potent and selective ATP-competitive inhibitor of tropomyosin rec
• 1017606-66-4 | LPA2 antagonist 1 (Catalog# : 61120)LPA2 antagonist 1 is a selective inhibitor of LPA2 activity in with IC50 17 nM in vit
• 154447-38-8 | LY 303511 (Catalog# : 611818)LY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit
• 1386874-06-1 | LY3023414 (Catalog# : 611808)LY3023414 is an oral ATP competitive inhibitor of the class I PI3K isoforms, mTOR and
• 1025967-78-5 | Lifitegrast (Catalog# : 16071412)Lifitegrast, also known as SAR-1118, is an LFA-1 antagonist intended for the treatmen
• 193275-84-2 | Lonafarnib (Catalog# : 16071008)Lonafarnib is a farnesyl transferase inhibitor. Structurely, it is also a synthetic t
• 1627709-94-7 | LJI308 (Catalog# : 16070904)LJI308 is a potent, and pan-RSK(p90 ribosomal S6 kinase) inhibitor withIC50of 6 nM, 4
• 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.