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Cas号索引 2

• 212141-54-3 | Vatalanib (Catalog# : 010434)Vatalanib free base is an inhibitor of VEGFR2/KDR with IC50 of 37 nM, less potent aga
• 2630378-05-9 | Wu-5 (Catalog# : 24160)Wu-5 is a USP10 inhibitor that can inhibit FLT3 and AMPK pathways, induce FLT3-ITD de
• 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
• 2595308-10-2 | XRD-0394 (Catalog# : 25042)XRD-0394 is a DNA-PKcs inhibitor. XRD-0394 selectively targets, binds to and inhibits
• 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
• 2225824-53-1 | YTX-465 (Catalog# : 24139)YTX-465 is a SCD inhibitor. YTX-465 strongly reduced fatty desaturation in a concentr
• 2863670-67-9 | YCT529 (Catalog# : 24120)YCT529, an RAR-α inhibitor, is used as a contraceptive, with a 99% effectiveness. YC
• 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
• 2306303-35-3 | ZINC20451377 (Catalog# : 24132)ZINC20451377 is a small molecule that binds to hepatitis B surface antigen (HBsAg) wi
• 210345-04-3 | Z-LEHD-FMK (Catalog# : 24127)Z-LEHD-FMK is a potent, cell-permeable, and irreversible inhibitor of caspase-9. Z-LE
• 210344-98-2 | Z-IETD-FMK (Catalog# : 24126)MDK4982, also known as Z-IETD-FMK, is a potent, cell-permeable, irreversible inhibito
• 210344-95-9 | Z-DEVD-fmk (Catalog# : 24125)Z-DEVD-fmk is a cell-permeable, irreversible inhibitor of caspase-3. Caspase-3 is a c
• 2133852-18-1 | Zastaprazan ( JP-1366 ) (Catalog# : 24123)Zastaprazan，也称为JP-1366，是一种质子泵抑制剂。JP-1366介导对H+/K+-
• 2403703-30-8 | Zurletrectinib (Catalog# : 24104)Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic age
• 2365193-22-0 | Zelasudil (Catalog# : 24014)Zelasudil 是一种有效的、高选择性的口服活性抑制剂，针对 Rho 相关
• 2134675-36-6 | Ziftomenib ( KO-539 ) (Catalog# : 24013)Ziftomenib 是一种口服、有效、选择性的小分子抑制剂，针对 menin 和