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  • abs810646GSK-3787 188591-46-0
    abs810646GSK-3787 188591-46-0

    GSK-3787 188591-46-0 GSK3787 is as a potent and selective antagonist of PPARδ with pIC50 of 6.6.

    更新时间:2026-02-05型号:abs810646访问量:1333
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  • abs810628I-BET151 1300031-49-5
    abs810628I-BET151 1300031-49-5

    I-BET151 1300031-49-5 I-BET151 (GSK1210151A) is a novel selective BET inhibitor for BRD2, BRD3 and BRD4 with IC50 of 0.5 μM, 0.25 μM, and 0.79 μM, respectively.

    更新时间:2026-02-05型号:abs810628访问量:1274
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  • abs810613Omecamtiv mecarbil (CK-1827452) 873697-71-3
    abs810613Omecamtiv mecarbil (CK-1827452) 873697-71-3

    Omecamtiv mecarbil (CK-1827452) 873697-71-3 Omecamtivmecarbil (CK-1827452) is a specific cardiac myosinactivator and a clinical drug for left ventricular systolic heart failure.

    更新时间:2026-02-05型号:abs810613访问量:1222
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  • abs810579JNJ26854165  881202-45-5
    abs810579JNJ26854165 881202-45-5

    JNJ26854165 881202-45-5 JNJ-26854165 (Serdemetan) acts as a HDM2 ubiquitin ligase antagonist and also induces early apoptosis in p53 wild-type cells

    更新时间:2026-02-05型号:abs810579访问量:1247
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  • abs810569TAK-632 1228591-30-7
    abs810569TAK-632 1228591-30-7

    TAK-632 1228591-30-7 TAK-632 is a selective pan-RAF kinase inhibitor with IC50 values of 2.4/1.4 nM for BRAF V600E/c-RAF; 60 fold selectivity over VEGFR.

    更新时间:2026-02-05型号:abs810569访问量:1158
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  • abs810561SC-514 (GK 01140)  354812-17-2
    abs810561SC-514 (GK 01140) 354812-17-2

    SC-514 (GK 01140) 354812-17-2 SC-514 (GK 01140), a small molecule, is a selective inhibitor of IKK-2; does not inhibit other IKK isoforms or other serine-threonine and tyrosine kinases.

    更新时间:2026-02-05型号:abs810561访问量:1134
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  • abs810560AGI5198 1355326-35-0
    abs810560AGI5198 1355326-35-0

    AGI5198 1355326-35-0 AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.

    更新时间:2026-02-05型号:abs810560访问量:1207
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  • abs810559ABT-199 1257044-40-8
    abs810559ABT-199 1257044-40-8

    ABT-199 1257044-40-8 ABT-199 is a Bcl-2-selective inhibitor with Ki of 0.01 nM in cell-free assays, 4800-fold more selective versus Bcl-xL and Bcl-w, and no activity to Mcl-1. Phase 3.

    更新时间:2026-02-05型号:abs810559访问量:1330
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