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Cas Index 8

• 819812-04-9 | KW-2478 (Catalog# : 121431)KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti
• 849776-05-2 | Ladarixin (Catalog# : 24039)Ladarixin (DF-2156 ; DF-2156A) is an orally active, allosteric non-competitive and du
• 878672-00-5 | Lesinurad (Catalog# : 17022706)Lesinurad(RDEA594), once-daily inhibitor of URAT1, is a transporter in the kidney tha
• 892128-60-8 | LY2334737 (Catalog# : 16123040)LY2334737 is an orally available valproic acid ester of gemcitabine, a broad-spectrum
• 847871-99-2 | Lenalidomide hemihydrate (Catalog# : 6111409)Lenalidomide (Revlimid, CC-5013) is a TNF- secretion inhibitor with IC50 of 13 nM.Len
• 867160-71-2 | Linsitinib (Catalog# : 010819)Linsitinib is highly potent, orally efficacious and highly selective, dual ATP-compet
• 862507-23-1 | LY2228820 (Catalog# : 122509)LY2228820 is a novel and potent p38MAPK inhibitor (the IC50 for p38MAPK and p38MAPK w
• 891016-02-7 | ML-SI3 (Catalog# : 20287)ML-SI3 is a chemical compound which acts as an "antagonist" (i.e. channel b
• 838810-96-1 | MAC-545496 (Catalog# : 2071611)MAC-545496 is potent GraR inhibitor (glycopeptide-resistance-associated protein R). M
• 877636-42-5 | ML221 (Catalog# : 19311)ML221 is an antagonist of the apelin (APJ) receptor.
• 869901-69-9 | MK-2048 (Catalog# : 181251)MK-2048 is a a second-generation HIV-1 integrase inhibitor.
• 847163-28-4 | ML 351 (Catalog# : 1811282)ML 351 is a selective 12/15 LOX inhibitor that is active in vivo.
• 869363-13-3 | MLN8054 (Catalog# : 18742)MLN8054 is an aurora kinase inhibitor MLN8054, which is an orally bioavailable, highl
• 825658-06-8 | ML335 (Catalog# : 184216)ML335是一种有效的、选择性的TREK-1/2激活剂。ML335是一种用于OPRM1-O
• 846557-71-9 | ML-385 (Catalog# : 179119)ML-385 is a potent and selective NRF2 inhibitor (Nrf2; IC50 = 1.9 μM) . ML-385 selec
• 878978-76-8 | ML-098 (Catalog# : 17030910)ML-098, also known as CID-7345532, is an activator of the GTP-binding protein Rab7 (E
• 899713-86-1 | ML348 (Catalog# : 17030712)ML348, also known as CID 3238952; SID 160654487, is a reversible LYPLA1 inhibitor wit
• 863971-19-1 | Mafodotin (Catalog# : 16122831)Mafodotin, also known as mc-MMAF and SGD-1269 or Maleimidocaproyl monomethylauristati
• 862189-95-5 | Mirodenafil (Catalog# : 030904)Coming soon!
• 897657-95-3 | MSX-122 (Catalog# : 011906)MSX-122 is a n orally bioavailable inhibitor of CXCR4 with potential antineoplastic a
• 852536-39-1 | ME-143 (Catalog# : 011902)ME -143 is a derivative of triphendiol and is a highly potent, pan acting ant-cancer.
• 86347-15-1 | Medetomidine hydrochloride (Catalog# : 010606)Medetomidine Hydrochloride is an agonist of adrenergic alpha-2 receptor, which is use
• 870005-19-9 | MK-2048 (Catalog# : 010424)MK-2048 is a second generation integrase inhibitor, intended to be used against HIV i
• 885325-71-3 | MK8745 (Catalog# : 122819)MK-8745 is a novel Aurora-A specific inhibitor. MK8745 induced apoptotic cell death i
• 875337-44-3 | MGCD-265-analog (Catalog# : 111013)MGCD-265-analog is a tyrosine kinase inhibitor that selectively targets MET and Axl.M
• 88191-84-8 | MDL 28170 (Catalog# : 102610)MDL 28170 is a potent, cell-permeable, and selective inhibitor of calpain and catheps
• 85278-24-6 | MDL72274(HCl) (Catalog# : 90301A)MDL72274 is a specific semicarbazide-sensitive amine oxidase (SSAO) inhibitor.
• 857876-30-3 | Motesanib Diphosphate (AMG-706) (Catalog# : 52101)Motesanib Diphosphate (AMG-706) is a potent ATP-competitive inhibitor ofVEGFR1/2/3wit
• 81624-55-7 | NSC348884 (Catalog# : 20487)NSC348884 is a nucleophosmin inhibitor. NSC348884 also disrupts oligomer formation an
• 83366-66-9 | Nefazodone (Catalog# : 20463)Nefazodone is an antidepressant. Its chemical structure is unrelated to selective ser