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Cas号索引 1

• 189453-10-9 | 环氧丙烷D (Catalog# : 186292)环氧丙烷D是从纤维素粘液杆菌中分离出来的一种天然聚酮化合物
• 1628830-21-6 | EZM2302 (Catalog# : 186272)EZM2302是一种有效的，选择性的，可口服的精氨酸甲基转移酶CARM1抑
• 169869-90-3 | 依沙替康甲磺酸盐 (Catalog# : 186271)依沙替康也叫DX 8951，是一种半合成的水溶性喜树碱衍生物，具有
• 164650-44-6 | 艾菲康唑 (Catalog# : 186213)艾菲康唑是一种三唑类抗真菌药。它被批准用于加拿大和美国作为
• 1197194-61-8 | 内昔芬 E-异构体盐酸盐 (Catalog# : 184124)内昔芬 E-异构体是一种他莫昔芬的代谢物和有效的选择性雌激素反
• 1370651-20-9 | Ensartinib ( X396 ) (Catalog# : 184321)Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
• 1914078-41-3 | eCF506 ( 别名：NXP 900 ) (Catalog# : 18382)eCF506靶向一种叫做Src酪氨酸激酶的分子，这是乳腺癌细胞生长和传
• 1632006-28-0 | Esaxerenone (Catalog# : 1710121)Esaxerenone（cs-3150，xl-550）是一种非甾体类抗盐皮质激素Exelixis发现
• 1616391-65-1 | EPZ015666 (Catalog# : 011309)EPZ-015666 是一种强效、选择性的口服生物药，PRMT5抑制剂与Ki为5 nm
• 1346242-81-6 | 厄达替尼(JNJ-42756493) (Catalog# : 651701)Erdafitinib(JNJ-42756493) is a potent and selective panfibroblast growth factor recep
• 13275-31-5 | Ethyl 2-cyclohexyl-2-oxoacetate (Catalog# : 178157)Ethyl 2-cyclohexyl-2-oxoacetate
• 1140964-99-3 | E7449 (Catalog# : 178903)E7449是一种可口服的小分子抑制剂，核酶聚(ADP-核糖)聚合酶(PARP)1和
• 1388651-30-6 | Elenbecestat ( E2609 ) (Catalog# : 2017878)Elenbecestat是一种β-Site淀粉样前体蛋白裂解酶BACE）抑制剂，主要用
• 117091-64-2 | 依托泊苷磷酸酯 (Catalog# : 20178213)依托泊苷磷酸盐是一种半合成足叶草毒素的磷酸盐。
• 1206123-37-6 | Etrasimod (Catalog# : 17031018)Etrasimod，也被称为APD334，是一种多功能S1P1受体的功能拮抗剂，用
• 1849590-01-7 | eFT-508 (Catalog# : 17031010)eFT-508 (eFT508)是一种有效且选择性的MNK1 / 2抑制剂，可能导致肿瘤细
• 1234563-16-6 | 盐酸Epetraborole (Catalog# : 17022806)盐酸Epetraborole是一种新型的leucyl - trna合成酶(LeuRS)抑制剂。
• 1693758-51-8 | Eganelisib ( IPI-549 ) (Catalog# : 711401)Eganelisib (IPI-549) 是一种首创、口服、高选择性 PI3Kγ 抑制剂，单独
• 124750-92-1 | EXP-3174 (Catalog# : 16122943)EXP-3174, also known as Losartan Carboxylic Acid, is a physiologically active metabol
• 179756-85-5 | Eptapirone (Catalog# : 16122941)Eptapirone, also known as F11440, is a potent, selective, high efficacy 5-HT1A recept
• 1349723-93-8 | Elacestrant dihydrochloride (Catalog# : 16122810)Elacestrant dihydrochloride, also known as RAD1901, is an orally available, selective
• 154598-52-4 | Efavirenz (Catalog# : 16122763)Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with ant
• 134381-21-8 | Epoxomicin (Catalog# : 16122762)Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhib
• 1942114-09-1 | EAI045 (Catalog# : 16122734)EAI045 is an allosteric inhibitor that targets selected drug-resistant EGFR mutants b
• 1234479-76-5 | ERK5-IN-1 (Catalog# : 6111502)ERK5-IN-1 exhibits potent inhibition of ERK5 with cellular EC50 values of 0.19 M and
• 1352608-82-2 | EW-7197 (Catalog# : 6111007)EW-7197 is a highly potent, selective, and orally bioavailable TGF- receptor ALK4/ALK
• 1252594-99-2 | ETP-46321 (Catalog# : 611825)ETP-46321 is a potent and orally bioavailable PI3K / inhibitor with IC50 of 2.3/14.2
• 1345675-02-6 | ETP-46464 (Catalog# : 161009015)ATR,Bioactive Small Molecule Alphabetical Index,Bioactive Small Molecules,Cell Biolog
• 1700663-41-7 | EPZ020411 (Catalog# : 16090201)EPZ020411 is a potent and selective inhibitor of PRMT6 with IC50 of 10 nM, has 10 fol
• 1808011-22-4 | EPZ031686 (Catalog# : 16071015)EPZ031686