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  • abs810437Carfilzomib (PR-171) 868540-17-4
    abs810437Carfilzomib (PR-171) 868540-17-4

    Carfilzomib (PR-171) 868540-17-4 Carfilzomib (PR-171) is a proteasome inhibitor with IC50 less than 5 nM.

    更新时间:2026-02-05型号:abs810437访问量:1176
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  • abs810429ONX-0912(Oprozomib) 935888-69-0
    abs810429ONX-0912(Oprozomib) 935888-69-0

    ONX-0912(Oprozomib) 935888-69-0 Oprozomib (ONX 0912) selectively inhibits CT-L activity of 20S proteasome β5/LMP7 with IC50 of 36 nM/82 nM.

    更新时间:2026-02-05型号:abs810429访问量:1036
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  • abs810425LY-364947 396129-53-6
    abs810425LY-364947 396129-53-6

    LY-364947 396129-53-6 LY-364947 is a potent ATP-competitive inhibitor of TGFβR-I with IC50 of 59 nM, shows 7-fold selectivity over TGFβR-II.

    更新时间:2026-02-05型号:abs810425访问量:1051
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  • abs810420aICG-001  780757-88-2;847591-62-2
    abs810420aICG-001 780757-88-2;847591-62-2

    ICG-001 780757-88-2;847591-62-2 ICG-001 is a small-molecule antagonist of b-catenin/TCF-mediated transcription (IC50 = 3 uM) and specifically downregulates the expression of a subset of b-catenin/TCF

    更新时间:2026-02-05型号:abs810420a访问量:1168
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  • abs810410RKI-1447 1342278-01-6
    abs810410RKI-1447 1342278-01-6

    RKI-1447 1342278-01-6 RKI-1447 is a potent small molecule inhibitor of ROCK1 and ROCK2.

    更新时间:2026-02-05型号:abs810410访问量:1110
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  • abs810399IPI-145 1201438-56-3
    abs810399IPI-145 1201438-56-3

    IPI-145 1201438-56-3 Duvelisib is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immuno

    更新时间:2026-02-04型号:abs810399访问量:1200
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  • abs810391AZ3146 1124329-14-1
    abs810391AZ3146 1124329-14-1

    AZ3146 1124329-14-1 AZ3146 is a potent and selective monopolar spindle 1 (Mps1) kinase inhibitor (IC50 = 35 nM); less potent to FAK, JNK1, JNK2, and Kit.

    更新时间:2026-02-04型号:abs810391访问量:1043
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  • abs810374SB525334
    abs810374SB525334

    SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM, is 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.

    更新时间:2025-11-11型号:abs810374访问量:1116
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