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Cas号索引 2

• 218791-21-0 | Imisopasem-manganese(M40403) (Catalog# : 72602)M40403 is a low molecular weight, synthetic manganese containing superoxide dismutase
• 2982787-50-6 | JBI-802 (Catalog# : 24116)
• 2410512-38-6 | JQKD82 (Catalog# : 20285)JQKD82 is a cell-permeable and selective KDM5 inhibitor (MM.1S cells, IC50 = 0.42 uM)
• 2110426-27-0 | JNJ-63576253 (Catalog# : 21250)TRC253, also known as JNJ63576253, is a potent and orally active androgen receptor an
• 2098890-15-2 | JUN90152 (Catalog# : 21247)JUN90152, also known as SMS2-IN-1, is a potent and highly selective sphingomyelin syn
• 2260886-64-2 | JND3229 (Catalog# : 2091904)JND3229 is a New EGFRC797S Mutant Inhibitor with In Vivo Monodrug Efficacy (IC50 = 5.
• 2234281-75-3 | JI051 (Catalog# : 2071526)JI051 is an inhibitor of the cancer-associated transcription factor Hes1 via the PHB2
• 2086772-26-9 | JNJ-64619178 (Catalog# : 193292)JNJ-64619178是一种候选的抗癌药物。
• 259869-55-1 | JWH-133 (Catalog# : 6111109)JWH 133 is a potent CB2 selective agonist with Ki of 3.4 nM, 200-fold selective over
• 202475-60-3 | JANEX-1 (Catalog# : 52220)Janex-1 is a cell-permeable, reversible, potent, ATP-competitive, and specific inhibi
• 2432994-31-3 | KT-474 ( 别名: SAR-444656 ) (Catalog# : 25165)KT-474 (SAR-444656) 是一种口服的 IRAK4 降解诱导剂。
• 2416873-83-9 | KB-0742 (Catalog# : 24040)KB-0742 是一种有效的，选择性的和具有口服活性的 CDK9 抑制剂。
• 2416874-75-2 | KB-0742 dihydrochloride (Catalog# : 24020)KB-0742 是一种有效的、选择性的、口服生物可利用的 CDK9 小分子抑
• 2082765-42-0 | KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) (Catalog# : 20641)KP-302 ( Synonyms: Lucid-21-302 ; Lucid-MS ) 是一种蛋白质精氨酸脱亚胺酶的
• 2446480-97-1 | KSQ-4279 (Catalog# : 20472)KSQ-4279 is a USP1 and PARP inhibitor. KSQ-4279 showed anti-proliferative effects in
• 2226664-93-1 | KY19382 (Catalog# : L20334)KY19382 is an orally active dual inhibitor of CXXC5-DVL and GSK3β
• 228559-41-9 | Ki8751 (Catalog# : 17022703)Ki8751是一种强力的、选择性的VEGFR- 2酪氨酸激酶(IC50 = 0.9 nM)的抑制
• 286370-15-8 | KRN 633 (Catalog# : 51912)KRN 633 is an ATP-competitive inhibitor ofVEGFR1/2/3withIC50of 170 nM/160 nM/125 nM,
• 2833703-74-3 | LOXO-435 (Catalog# : 25080)LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
• 2247995-37-3 | Lazertinib mesylate (Catalog# : 25052)Lazertinib是一种口服的第三代选择性表皮生长因子受体（EGFR）抑制
• 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）是丝氨酸/苏氨酸蛋白激酶ATM的强效抑制剂。
• 297180-15-5 | Lipofermata (Catalog# : 24030)Lipofermata is a fatty acid transport protein 2(FATP2)inhibitor. Lipofermata shows fa
• 2568608-48-8 | LY-3522348 (Catalog# : 20577)LY-3522348是一种酮己糖激酶（KHK）抑制剂.
• 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