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Cas号索引 8

• 819812-04-9 | KW-2478 (Catalog# : 121431)KW-2478 是一种针对人类热休克蛋白 90 (Hsp90) 的药物，具有潜在的抗
• 849776-05-2 | Ladarixin (Catalog# : 24039)Ladarixin（DF-2156；DF-2156A）是一种口服活性、变构非竞争性和双CXCR
• 878672-00-5 | 雷西那德 (Catalog# : 17022706)雷西那德(RDEA594),是URAT1的一日一次抑制剂，是肾脏中调节尿酸排泄
• 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是apelin (APJ)受体的拮抗剂。
• 869901-69-9 | MK-2048 (Catalog# : 181251)MK-2048是第二代HIV-1整合酶抑制剂。
• 847163-28-4 | ML 351 (Catalog# : 1811282)ML 351是一种选择性的12/15 LOX抑制剂，在体内具有活性。
• 869363-13-3 | MLN8054 (Catalog# : 18742)MLN8054是一种MLN8054的极光激酶抑制剂，它是一种口服的生物活性药
• 825658-06-8 | ML335 (Catalog# : 184216)ML335 is a potent and selective TREK-1/2 Activator. ML335 is an agonist for OPRM1-OPR
• 846557-71-9 | ML-385 (Catalog# : 179119)ML-385是强有力的和有选择性的Nrf2抑制剂（IC50 = 1.9μNrf2；M）。ML-3
• 878978-76-8 | ML-098 (Catalog# : 17030910)ML-098, 也叫 CID- 7345532，是GTP结合蛋白Rab7(EC50 = 77.6 nM)的激活剂。
• 899713-86-1 | ML348 (Catalog# : 17030712)ML348，又称CID 3238952;SID 160654487，是一个可逆的LYPLA1抑制剂，IC50值
• 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-analogis a tyrosine kinase inhibitor that selectively targets MET and Axl.MG
• 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