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Cas号索引 2

• 2244989-34-0 | UCB9608 (Catalog# : 2071516)UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
• 256477-09-5 | UK-371804 (Catalog# : 1791114)UK-371804是强有力和有选择性的优良酶效价uPA（Ki 10 nm）抑制剂和选
• 256476-36-5 | UK-371804 HCl (Catalog# : 17031008)UK-371804是一种有效的选择性尿激酶型等离子体激活剂(uPA)抑制剂，
• 2647442-33-7 | VV116 (Catalog# : 20536)VV116, also known as JT001, is an oral drug candidate of nucleoside analog against SA
• 2649467-58-1 | VX-548 (Catalog# : 20525)
• 2169916-18-9 | VTP-50469 (Catalog# : 20111202)VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being
• 2173134-00-2 | VUN34002 (Catalog# : 2071534)VUN34002, also known as Vanin-1-IN-1 is an inhibitor of vanin-1 enzyme which is a cel
• 23261-20-3 | VAL-083 (Catalog# : 112091)VAL-083 is a bi-functional alkylating agent, with potential antineoplastic activity.
• 2097381-85-4 | VH298 (Catalog# : 18581)VH298是一种有效的VHL抑制剂，通过不同的机制和抒发缺氧反应稳定
• 2095432-65-6 | Verubecestat TFA (Catalog# : 18417)Verubecestat，也被称为MK-8931或SCH 900931，是一种有效的选择性的-分泌
• 235106-62-4 | VP 14637 (Catalog# : 011112)Coming soon!
• 212141-54-3 | Vatalanib (Catalog# : 010434)Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
• 2229025-70-9 | WM 3835 (Catalog# : 20504)WM 3835 is a lysine acetyltransferase HBO1 (KAT7) inhibitor. It reduces H3K14ac level
• 2253985-29-2 | WK500B (Catalog# : 20491)WK500B is a BCL6 inhibitor. WK500B engaged BCL6 inside cells, blocked BCL6 repression
• 2055397-28-7 | WM-1119 (Catalog# : 181181)WM-1119是赖氨酸乙酰转移酶 KAT6A的高效选择性抑制剂，Kd为2nm, WM-11
• 211555-05-4 | WHI-P97 (Catalog# : 185710)WHI-P97是一种JAK3抑制剂。
• 214358-33-5 | 1400W (Catalog# : 17021321)1400W是一种缓慢，紧密结合，具有高度选择性的诱导型一氧化氮合
• 2012607-27-9 | WNK463 (Catalog# : 6111509)WNK463 is a pan-WNK-kinase inhibitor. It potently inhibits the in vitro kinase activi
• 211555-04-3 | WHI-P154 (Catalog# : 73107)WHI-P 154 is a JAK3 inhibitor (IC50 = 1.8 M) that displays no activity at JAK1 or JAK
• 211555-08-7 | WHI-P180 (Catalog# : 52221)WHI-P180 is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0 uM, respective
• 2700286-66-2 | XPW1 (Catalog# : 20659)XPW1 is a potent and selective CDK9 inhibitor with excellent activity against clear c
• 2367004-54-2 | XL092 (Catalog# : 20506)XL092 is an ATP-competitive inhibitor of multiple RTKs including MET, VEGFR2, AXL and
• 2061980-01-4 | XMU-MP-1 (Catalog# : 18579)XMU-MP-1是一种有效且就有选择性的MST1/2抑制剂。
• 284028-89-3 | XAV-939 (Catalog# : 52632)XAV939 is a small molecule and selective Wnt pathway -catenin-mediated transcription
• 2064269-82-3 | YK-029A (Catalog# : 20670)
• 2131223-85-1 | YW2065 (Catalog# : 20494)YW2065 has excellent anti-colorectal cancer effects in vitro and in vivo. YW2065 achi
• 2226534-49-0 | Y06137 (Catalog# : 193193)Y06137是一种有效的选择性BET抑制剂，它与Kd为81 nM的BRD4(1)溴域结合
• 223499-30-7 | YM-58483 (BTP2) (Catalog# : 17109009)YM-58483/BTP2是一种能调节非兴奋细胞(如淋巴细胞)活化的贮藏操作C
• 288250-47-5 | Y-320 (Catalog# : 52516)Y-320 is a new phenylpyrazoleanilide immunomodulator; inhibits IL-17 production by CD
• 2403703-30-8 | Zurletrectinib (Catalog# : 24104)Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic age