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Cas号索引 1

• 1206799-15-6 | Merestinib (LY2801653) (Catalog# : 178905)Merestinib，又名LY2801653，是一种可口服的小分子抑制剂，原癌基因
• 1628317-18-9 | MI-463 (Catalog# : 17031006)MI-463是一种Menin-MLL强力抑制剂，与IC50值15.3 nM相互作用。
• 1221186-53-3 | ML-265 (Catalog# : 17030804)ML265是一个强有力的PKM2活化剂诱导四聚体，降低肿瘤的形成和大小
• 1346528-06-0 | ML241 (Catalog# : 17030714)ML241是一种p97 ATPase有效的选择性抑制剂。ML241抑制p97 ATPase的IC(50)值
• 198821-22-6 | Merimepodib (Catalog# : 17030308)Merimepodib, 也称为VX-497,是有效的口服生物IMPDH抑制剂，它可以抑制
• 1550008-55-3 | ML-264 (Catalog# : 17030302)ML-264是一种Krüppel-like因子5(KLF5)抑制剂，能有效抑制结直肠癌的生
• 1030612-90-8 | MK-8245 (Catalog# : 17030109)MK-8245是一种有效的、以肝脏为靶点的SCD抑制剂，具有临床前抗糖
• 1268454-23-4 | MLN-1117 (Catalog# : 17030101)Serabelisib(又名MLN1117,INK1117,TAK- 117)是一类具有潜在抗肿瘤活性的磷
• 1404437-62-2 | ML-281 (Catalog# : 17022811)ML-281是一种有效的选择性STK33抑制剂(IC50 = 14nm)。与其他STK33抑制剂
• 1502816-23-0 | MS049 (Catalog# : 17021313)MS049是PRMT4和PRMT6的一种有效的选择性抑制剂，IC50分别为34 nM和43 n
• 1313883-00-9 | Miransertib(ARQ 092) (Catalog# : 17021301)ARQ 092是一种新型的口服生物可用性和选择性AKT通路抑制剂，在晚
• 1399840-35-7 | MT-DADMe-ImmA(MTDIA HCl) (Catalog# : 712101)MT-DADMe-ImmA(MTDIA盐酸盐)是一种新型的MTAP抑制剂，具有治疗头颈部和
• 110448-33-4 | ML-7 (Catalog# : 17011107)ML-7是平滑肌肌球蛋白轻链激酶的抑制剂(MLCK)，Ki值为0.3μM。
• 1005264-47-0 | MX69 (Catalog# : 17011105)MX69是一种MDM2/XIAP抑制剂, 用于治疗癌症。
• 115104-28-4 | MK-571 sodium salt (Catalog# : 16123055)MK-571 is a selective, orally active CysLT1 receptor antagonist. It blocks the bindin
• 1445993-26-9 | Mivebresib (Catalog# : 16123052)Mivebresib, also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-cont
• 1198097-97-0 | Mirin (Catalog# : 16123049)Mirin is a Mre11-Rad50-Nbs1 (MRN)-ATM pathway inhibitor.
• 1047953-91-2 | MI-2 (MALT1 inhibitor) (Catalog# : 16123047)MI-2 is a MALT1 inhibitor (IC50 = 5.84 M). MI-2 binds directly to MALT1 and irreversi
• 110044-82-1 | MG-101 (Catalog# : 16123046)MG-101, also known as Calpain Inhibitor I and ALLN, is a calpain inhibitor (IC50 = 0.
• 139504-50-0 | Mertansine (DM1) (Catalog# : 16123045)Mertansine refers to the thiol-containing maytansinoid, DM1 (N2-deacetyl-N2-(3-mercap
• 129831-99-8 | MC-976 (Catalog# : 16122832)MC-976 is an Vitamin D3 derivative.
• 115103-85-0 | MK571 (Catalog# : 161227105)MK-571 is a selective, orally active CysLT1 receptor(Cysteinyl leukotriene receptor)
• 1572414-83-5 | ML323 (Catalog# : 16122790)ML323 is a highly potent and selective USP1-UAF1 inhibitor with IC50 of 76 nM.ML323 i
• 1190378-57-4 | MRT67307 (Catalog# : 16122745)MRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, re
• 1038915-73-9 | MK-4827(Niraparib) tosylate (Catalog# : 16122717)MK-4827(Niraparib) tosylate is a selective inhibitor of PARP1/PARP2 with IC50 of 3.8
• 1227962-62-0 | Marinopyrrole A (Catalog# : 6111403)Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value
• 1338824-21-7 | ML224 (Catalog# : 61116)ML224(NCGC00242364; ANTAG3) is a selective TSHR inverse agonist; inhibits TSH-stimula
• 1189805-51-3 | (±)-Methotrimeprazine D6 (Catalog# : 61114)()-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 d
• 1831110-54-3 | MS023 (Catalog# : 6111012)MS023 is a potent, selective, and cell-active inhibitor of human type I PRMTs with IC
• 100872-83-1 | ML346 (Catalog# : 611940)ML346 is a novel activator of Hsp70 with EC50 of 4600 nM in HeLa cell toxicity assay.