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Cas号索引 2

• 2883540-92-7 | STX-478 (Catalog# : 20633)STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
• 256414-75-2 | SEW2871 (Catalog# : 20604)SEW2871 is a S1P1 agonist (sphingosine-1-phosphate type 1 receptor agonist). SEW2871
• 2765525-82-2 | STX-721 (Catalog# : 20576)STX-721 is a next-generation, orally delivered therapy, designed with potential best-
• 2648257-56-9 | STC-15 (Catalog# : 20549)STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me
• 2921961-53-5 | (S)-5-fluoro-3-methylbenzo[c][1,2]oxaborol-1(3H)-ol (Catalog# : 20522)
• 2170746-98-0 | Spiro[cyclohexane-1,9'(6'H)-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyrimidine]-7'(8'H)-carboxylic acid, 2'-(methylthio)-6'-oxo-5'-[[(trifluoromethyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester (Catalog# : 20412)
• 2322245-42-9 (free base) | SRI-37330 free base (Catalog# : 1711224)SRI-37330 is a novel inhibitor of TXNIP expression, decreasing glucagon secretion and
• 2370013-12-8 | Sunvozertinib ( DZD 9008 ) (Catalog# : 20369)Sunvozertinib，也称为 DZD9008，是一种口服、强效、不可逆和选择性
• 2102681-49-0 | SHMT-IN-2 抑制剂 (Catalog# : 20368)SHMT-IN-2 是一种丝氨酸羟甲基转移酶 (SHMT) 抑制剂，可有效抑制人
• 2582757-90-0 | Stafia-1 (Catalog# : L20338)
• 2499663-01-1 | STM2457 (Catalog# : 20321)STM2457 is a highly potent and selective first-in-class catalytic inhibitor of METTL3
• 2322245-49-6 | SRI-37330 HCl (Catalog# : 20306)SRI-37330 hydrochloride 是一种新型 TXNIP 表达抑制剂，呈剂量依赖性抑
• 2089251-47-6 | SM-102 (Catalog# : 21252)SM-102 is an ionizable amino lipid that has been used in combination with other lipid
• 287383-59-9 | Scriptaid (Catalog# : 21229)Scriptaid, also known as GCK 1026, is a HDAC inhibitor. Scriptaid protects against tr
• 2301974-60-5 | (S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)- 1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol (Catalog# : 20123103)
• 2351882-11-4 | Spastazoline (Catalog# : 2071521)Spastazoline is a novel inhibitor for aaa+ (atpases associated with diverse cellular
• 296280-56-3 | S26131 (Catalog# : 112592)S26131 is a bioactive chemical.
• 2195361-33-0 | SPL-707 (Catalog# : 193209)SPL-707是第一种选择性口服活性SPPL2a抑制剂。密切相关的酶γ-secret
• 2055757-40-7 | SHP394 (Catalog# : 193122)SHP394是一种有效的口服SHP2抑制剂(IC50 = 23nm)，具有高亲脂性、增强
• 2226517-76-4 | SGC-GAK-1 (Catalog# : 193113)SGC-GAK-1是一种针对atp结合位点的高效选择性GAK激酶探查。
• 2152628-33-4 | Selpercatinib (Catalog# : 192276)Selpercatinib是一种具有抗肿瘤作用的酪氨酸激酶抑制剂。
• 254740-64-2 | Sparsentan (Catalog# : 1812132)Sparsentan, 也称为RE-021, PS433540和DARA-a,是一种日常血管紧张素II和内
• 2134602-45-0 | SR-17018 (Catalog# : 187166)SR17018是一种muo -opioid受体激动剂，EC50为97nm。
• 205678-31-5 | SB-273005 (Catalog# : 186221)SB-273005是一种整合素αvβ3的抑制剂。
• 2097334-20-6 | (S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic acid (Catalog# : 183218)(S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic aci
• 2070015-26-6 | SRT3025 HCl (Catalog# : 17101310)SRT3025是一种可口服的小分子激活SIRT1酶。
• 271576-80-8 | SD-06 (Catalog# : 1791320)SD-06是治疗关节炎的MAPK p38α抑制剂。
• 215543-92-3 | SU5402 (Catalog# : 174191)SU5402是一种纤维母细胞生长因子受体(FGFR)-特异性酪氨酸激酶抑制
• 201677-61-4 | Sivelestat sodium (Catalog# : 16122758)Sivelestat sodium is a competitive inhibitor of human neutrophil elastase, also inhib
• 2070015-29-9 | SJB3-019A (Catalog# : 611930)SJB3-019A is a potent and novel usp1 inhibitor. SJB3-019A (IC50 = 0.0781 uM) was 5 ti