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Cas号索引 1

• 1276110-06-5 | HS-173 (Catalog# : 161009001)HS-173 inhibited the PI3K signaling pathway, and showed anti-proliferative effects on
• 1453097-13-6 | HUHS015 (Catalog# : 16062902)HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo. The bioavailabi
• 156270-06-3 | 1H-Pyrrolo[2,3-B]Pyridine-3-Carboxylic Acid (Catalog# : 032511)Coming soon!
• 1613724-42-7 | HTH-01-015 (Catalog# : 011306)HTH-01-015 is a potent and selective inhibitor of NUAK1 with IC50 of 100 nM, does not
• 162641-16-9 | HQL-79 (Catalog# : 121507)Coming soon!
• 1366302-52-4 | HBED-CC-PSMA ( PSMA-11 ) (Catalog# : 103003)PSMA-11, also known as HBED-CC-PSMA or Psma-hbed-CC, has potential use as a tracer fo
• 143557-99-7 | HBED-CC (Catalog# : 103002)Coming soon!
• 1469338-01-9 | 6H05 (Catalog# : 52732)6H05 is a selective, and allosteric inhibitor of oncogenic mutant K-Ras(G12C
• 173529-46-9 | HMN-214 (Catalog# : 52581)HMN-214(IVX214) is a potent PLK1 inhibitor an average IC50 of 0.12 M.
• 1033836-12-2 | HPGDS inhibitor 1 (Catalog# : 52535)HPGDS inhibitor 1 is a novel and selective Hematopoietic Prostaglandin D Synthase (HP
• 1227948-82-4 | Ifebemtinib (Catalog# : 24092)Ifebemtinib, also known as BI-853520 and IN-10018, is a novel, highly selective PTK2
• 1421936-85-7 | Iclepertin (BI-425809) (Catalog# : 24084)Iclepertin（BI-425809）是一种口服的GlyT-1小分子抑制剂，用于治疗与
• 1221412-23-2 | IMM-H007 (Catalog# : L20336)IMM-H007 is a novel lipid-lowering agent, increasing abca1 protein expression
• 160807-49-8 | Indirubin-3’-oxime (Catalog# : L20330)Indirubin-3’-oxime is a potent inhibitor of glycogen synthase kinase 3β (GSK3β; I
• 1154097-71-8 | IOX4 (Catalog# : 20122401)
• 1034895-42-5 | 9-ING-41 (Catalog# : 2091905)9-ING-41 is a glycogen synthase kinase-3 (GSK-3) inhibitor.
• 1807988-47-1 | IITZ-01 (Catalog# : 2071519)IITZ-01 (Autophagy inhibitor IITZ-01) is a novel potent lysosomotropic autophagy inhi
• 186583-59-5 | 1-iodo-2-methoxy-4-methylbenzene (Catalog# : 2062008)
• 1690176-75-0 | IUN76750 (Catalog# : 2051507)IUN76750 is a PAR-2 signaling pathway inhibitor. IUN76750 has CAS#1690176-75-0, has n
• 1805789-54-1 (HCl) | ICEC0942 HCl (Catalog# : 204305)ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
• 1805833-75-3 (free base) | ICEC0942 free base (Catalog# : 204304)ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
• 1160521-50-5 | ITI-214 (Catalog# : 54192)ITI214 是一种选择性的PDE1抑制剂。
• 1642303-38-5 | ITI-214磷酸盐 (Catalog# : 512193)ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
• 1429179-07-6 | IDH889 (Catalog# : 19319)IDH889是一种有效的选择性IDH1抑制剂。IDH899为IDH (R132H) IC50 = 20 nM;细
• 1584121-99-2 | IT-901 (Catalog# : 186276)IT-901是一个血液恶性肿瘤抑制剂,通过阻断NF-κB-Controlled氧化应激反
• 1234490-83-5 | INX 08189 (Catalog# : 186253)INX 08189 是一种RNA引导的RNA聚合酶(NS5B)抑制剂，可用于丙型肝炎病
• 1820889-23-3 | INCB057643 (Catalog# : 185232)INCB057643是一种BET抑制剂。在卵巢癌中，INCB054329降低了同源重组效
• 1323403-33-3 | Iberdomide (Catalog# : 185216)Iberdomide,也称为CC-220，可用于治疗系统性红斑狼疮。
• 1262238-11-8 | INCB3344 (Catalog# : 185215)INCB3344是CCR2受体的一种有效的选择性拮抗剂，它在结合拮抗的IC(5
• 1668565-74-9 | IDO-IN-2 (Catalog# : 184317)IDO抑制剂1是IDO的有效抑制剂(吲哚胺-(2,3)-二氧合酶)，IC50为3nm。