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  • abs47028272SU9516 377090-84-1
    abs47028272SU9516 377090-84-1

    SU9516 377090-84-1 SU 9516 is a 3-substituted indolinone CDK inhibitor with IC50 of 22 nM, 40 nM, and 200 nM for CDK2, CDK1, and CDK4, respectively.

    更新时间:2026-01-27型号:abs47028272访问量:823
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  • abs47028271Salirasib 162520-00-5
    abs47028271Salirasib 162520-00-5

    Salirasib 162520-00-5 Salirasib is a potent competitive prenylated protein methyltransferase (PPMTase) inhibitor with Ki of 2.6 μM, which inhibits Ras methylation. Phase 2.

    更新时间:2026-01-27型号:abs47028271访问量:791
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  • abs47028269S-Ruxolitinib  941685-37-6
    abs47028269S-Ruxolitinib 941685-37-6

    S-Ruxolitinib 941685-37-6 S-Ruxolitinib is the chirality of INCB018424, which is the first potent, selective, JAK1/2 inhibitor to enter the clinic with IC50 of 3.3 nM/2.8 nM

    更新时间:2026-01-27型号:abs47028269访问量:898
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  • abs47028268YH239-EE 1364488-67-4
    abs47028268YH239-EE 1364488-67-4

    YH239-EE 1364488-67-4 YH239-EE, the ethyl ester of YH239, is a potent p53-MDM2 antagonist and an apoptosis inducer.

    更新时间:2026-01-27型号:abs47028268访问量:864
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  • abs47028267CX-6258 hydrochloride  1353859-00-3
    abs47028267CX-6258 hydrochloride 1353859-00-3

    CX-6258 hydrochloride 1353859-00-3 CX-6258 hydrochloride is a potent, orally efficacious pan-Pim kinase inhibitor with IC50 of 5 nM, 25 nM and 16 nM for Pim1, Pim2, and Pim3, respectively.

    更新时间:2026-01-27型号:abs47028267访问量:794
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  • abs47028266SB-334867  792173-99-0
    abs47028266SB-334867 792173-99-0

    SB-334867 792173-99-0 SB-334867 is a selective orexin-1 (OX1) receptor antagonist.

    更新时间:2026-01-27型号:abs47028266访问量:807
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  • abs47028265Remodelin hydrobromide  1622921-15-6
    abs47028265Remodelin hydrobromide 1622921-15-6

    Remodelin hydrobromide 1622921-15-6 Remodelin is a potent acetyl-transferase NAT10 inhibitor.

    更新时间:2026-01-27型号:abs47028265访问量:782
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  • abs47028264ENMD-2076 L-(+)-Tartaric acid 1291074-87-7
    abs47028264ENMD-2076 L-(+)-Tartaric acid 1291074-87-7

    ENMD-2076 L-(+)-Tartaric acid 1291074-87-7 ENMD-2076 L-(+)-Tartaric acid is the tartaric acid of ENMD-2076, selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.86 nM

    更新时间:2026-01-27型号:abs47028264访问量:824
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