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Cas号索引 2

• 2055050-87-6 | LAU159 (Catalog# : 2071505)LAU159 is a potent modulator of α6β3γ2 GABAA receptor.
• 294623-49-7 | L006235 (Catalog# : 2061307)L006235 is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays
• 2274819-46-2 | LUT-014 (Catalog# : 2042701)LUT-014 is a B-Raf Inhibitor. Leveraging the paradoxical effect of B-Raf Inhibitors,
• 2135600-76-7 | LSZ102 (Catalog# : 2041502)LSZ102 is a potent ERα antagonist and degrader. LSZ102 showed ERα degradation IC50
• 2173037-97-1 | LY2794193 (Catalog# : 193262)LY2794193是一种高效选择性的mGlu3受体激动剂。
• 2166616-75-5 | LY-3381916 (Catalog# : 193123)LY-3381916是一种强效的、选择性的、脑透性的IDO1活性抑制剂，与缺
• 245075-84-7 | LR-90 (Catalog# : 19364)LR-90是一种晚期糖基化终产物(AGE)抑制剂，可抑制人单核细胞的炎
• 2222755-14-6 | LOXO-292 (Catalog# : 192195)LOXO-292 (ARRY-192)是一种口服和临床开发的选择性研究药物，用于治
• 292632-98-5 | L685458 (Catalog# : 186156)L685458是一个强有力的和选择性γ分泌酶抑制剂。
• 2097002-61-2 | LOXO-195 (Catalog# : 185212)LOXO-195是一种有效的选择性TRK抑制剂，能够解决在接受larotrectinib
• 2088939-99-3 | LYN-1604 (Catalog# : 18493)LYN-1604是一种新型的ULK1激活剂，诱导细胞死亡，参与ATF3、RAD21和c
• 226929-39-1 | LB42708 (Catalog# : 18443)LB42708是一种有效的、口服活性和选择性的非肽基转移酶抑制剂(FT
• 2040291-27-6 | LLY-283 (Catalog# : 184314)LLY-283是一种有效、选择的针对PRMT5的SAM-竞争性化学探针。
• 231277-92-2 | 拉帕替尼 (Catalog# : 17022807)拉帕替尼(GW-572016) 是一种有效的EGFR和ErbB2抑制剂，IC50分别为10.8和
• 27262-47-1 | Levobupivacaine free base (Catalog# : 16123031)Levobupivacaine is a local anaesthetic drug belonging to the amino amide group. It is
• 2070014-90-1 | LY 303511 hydrochloride (Catalog# : 611819)LY303511 Hcl, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhi
• 253863-00-2 | L-778123 hydrochloride (Catalog# : 121805)L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and
• 248281-84-7 | Laquinimod (Catalog# : 121506)Laquinimod is an experimental immunomodulator developed by Active Biotech and Teva.
• 244240-24-2 | LFM-A13 (Catalog# : 52206)Selective Bruton's tyrosine kinase (BTK) inhibitor (IC50 = 2.5 M). Also inhibits poli
• 2925324-58-7 | MAT2A-IN-23 (Catalog# : 25210)MAT2A-IN-23 是一种潜在的MTA2A抑制剂。
• 2271348-04-8 | MK256 (Catalog# : 25208)MK256是一种新型CDK8抑制剂，通过下调STAT通路在急性髓系白血病（
• 2957874-18-7 | MAT2A inhibitor 5 (Catalog# : 25204)MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著
• 2750895-97-5 | MTX115325 (Catalog# : 186264)MTX115325是一种强效、选择性、脑渗透性USP30抑制剂，具有良好的类
• 2439277-80-0 | GSK4362676 ( MAT2A-IN-9 ) (Catalog# : 25147)MAT2A-IN-9 ( GSK4362676 )是一种2-氧代喹唑啉衍生物，是一种强效的MAT2
• 2769008-22-0 | MEN-1703 (Catalog# : 25143)
• 228113-66-4 | Maralixibat Chloride (Catalog# : 25126)Maralixibat (also known as SHP625, LUM001, and lopixibat) is an ileal bile acid trans
• 2991818-13-2 | MGD-28 (Catalog# : 25073)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
• 2891709-58-1 | MS6105 (Catalog# : 25039)
• 2763252-25-9 | M3554 (Catalog# : 25017)M3554，一种新型抗GD2抗体药物偶联物。
• 2990506-75-5 | ML353 (Catalog# : 24151)ML353 is a selective ligand of mGlu5 silent allosteric modulator (SAM).