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  • abs47028296GSK2830371 1404456-53-6
    abs47028296GSK2830371 1404456-53-6

    GSK2830371 1404456-53-6 GSK2830371 is an orally active, allosteric Wip1 phosphatase inhibitor with IC50 of 6 nM.

    更新时间:2026-01-28型号:abs47028296访问量:962
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  • abs47028295Dovitinib (TKI258) Lactate  915769-50-5
    abs47028295Dovitinib (TKI258) Lactate 915769-50-5

    Dovitinib (TKI258) Lactate 915769-50-5 Dovitinib (TKI258) Lactate is the Lactate of Dovitinib, which is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit) with IC50 of 1 nM/2 nM

    更新时间:2026-01-28型号:abs47028295访问量:1076
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  • abs47028294Sitafloxacin Hydrate 163253-35-8
    abs47028294Sitafloxacin Hydrate 163253-35-8

    Sitafloxacin Hydrate 163253-35-8 Sitafloxacin (INN; also called DU-6859a) is a fluoroquinolone antibiotic that shows promise in the treatment of Buruli ulcer.

    更新时间:2026-01-28型号:abs47028294访问量:879
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  • abs47028293Sevelamer HCl 152751-57-0
    abs47028293Sevelamer HCl 152751-57-0

    Sevelamer HCl 152751-57-0 Sevelamer HCl is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.

    更新时间:2026-01-28型号:abs47028293访问量:874
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  • abs47028290Desmethyl Erlotinib  183321-86-0
    abs47028290Desmethyl Erlotinib 183321-86-0

    Desmethyl Erlotinib 183321-86-0 Desmethyl Erlotinib (CP-473420) is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).

    更新时间:2026-01-28型号:abs47028290访问量:857
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  • abs47028288CCT128930 885499-61-6
    abs47028288CCT128930 885499-61-6

    CCT128930 885499-61-6 CCT128930 is a potent, ATP-competitive and selective inhibitor of Akt2 with IC50 of 6 nM, 28-fold greater selectivity for Akt2 than the closely related PKA kinase.

    更新时间:2026-01-28型号:abs47028288访问量:922
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  • abs47028285Idasanutlin (RG-7388) 1229705-06-9
    abs47028285Idasanutlin (RG-7388) 1229705-06-9

    Idasanutlin (RG-7388) 1229705-06-9 Idasanutlin (RG-7388) is a potent and selective p53-MDM2 inhibitor with IC50 of 6 nM.

    更新时间:2026-01-28型号:abs47028285访问量:933
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  • abs47028284NMS-P937 1034616-18-6
    abs47028284NMS-P937 1034616-18-6

    NMS-P937 1034616-18-6 NMS-P937 (NMS1286937) is an orally available, selective Polo-like Kinase 1 (PLK1) inhibitor with IC50 of 2 nM, 5000-fold selectivity over PLK2/PLK3. Phase 1.

    更新时间:2026-01-27型号:abs47028284访问量:884
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