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Cas号索引 2

• 286370-15-8 | KRN 633 (Catalog# : 51912)KRN 633 is an ATP-competitive inhibitor ofVEGFR1/2/3withIC50of 170 nM/160 nM/125 nM,
• 2688040-45-9 | Lirafugratinib HCl (Catalog# : 24113)Lirafugratinib, also known as RLY-4008, is a tyrosine kinase inhibitor with potential
• 2251753-65-6 | LXH-3-71 (Catalog# : 24107)LXH-3-71是一种新型“分子胶”，可诱导PHGDH和DDB1-CUL4泛素连接酶之
• 2834106-06-6 | LTGO-33 (Catalog# : 24103)LTGO-33 is a selective, state-independent, and potent preclinical small molecule NaV1
• 2719793-90-3 | Lunresertib (Catalog# : 24080)Lunresertib, alsop known as RP-6306, is a potent and selective PKMYT1 inhibitor (IC50
• 2495096-26-7 | lartesertib (Catalog# : 24066)Lartesertib (M4076) is a potent inhibitor of serine/threonine protein kinase ATM (ext
• 297180-15-5 | Lipofermata (Catalog# : 24030)Lipofermata is a fatty acid transport protein 2(FATP2)inhibitor. Lipofermata shows fa
• 2568608-48-8 | LY3522348 (Catalog# : 20577)
• 244240-24-2 | LFM-A13 (Catalog# : 20438)LFM-A13 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). LF
• 2375815-63-5 | LY-3475070 (Catalog# : 21244)LY-3475070 is a potent and selective CD73 Inhibitor with IC50 of 28 nM. LY3475070 Alo
• 2097938-59-3 | Lerociclib HCl (G1T38 HCl) (Catalog# : 2073106)Lerociclib HCl (G1T38 dihydrochloride)是一种分化型口服CDK4 / 6抑制剂，对
• 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