GlpBio

Other Apoptosis

Other Apoptosis(其他细胞凋亡)

Other Apoptosis 相关产品(883)

  • GC14815 structure
    GC14815GMX1778 (CHS828)
    CAS: 200484-11-3
    纯度: >99.00%

    GMX1778 (CHS828) 是一种特异性的烟酰胺磷酸核糖转移酶（NAMPT）抑制剂。

  • GC14817 structure
    GC14817Salermide
    CAS: 1105698-15-4
    纯度: >98.00%

    A sirtuin inhibitor

  • GC14853 structure
    GC14853TC ASK 10
    CAS: 1005775-56-3
    纯度: >99.00%

    A inhibitor of ASK1

  • GC14860 structure
    GC14860Oncrasin 1
    CAS: 75629-57-1
    纯度: >99.50%

    An anticancer agent

  • GC14882 structure
    GC14882Salinomycin
    CAS: 53003-10-4
    纯度: >98.00%

    A selective cancer stem cell inhibitor

  • GC14921 structure
    GC14921CPI-613 (Devimistat)
    CAS: 95809-78-2
    纯度: >98.00%

    An inhibitor of α-ketoglutarate dehydrogenase

  • GC14929 structure
    GC14929Monastrol
    CAS: 254753-54-3;329689-23-8
    纯度: >99.50%

    Monastrol是一种强效且具细胞通透性的有丝分裂驱动蛋白Eg5抑制剂，其 IC 50 为14μM。

  • GC14930 structure
    GC14930Benzbromarone
    CAS: 3562-84-3
    纯度: >99.50%

    An inhibitor of URAT1

  • GC14945 structure
    GC14945Sirtinol
    CAS: 410536-97-9
    纯度: >98.00%

    Inhibitor of sirtuin deacetylases

  • GC14957 structure
    GC14957OSI-930
    CAS: 728033-96-3
    纯度: >98.00%

    A dual inhibitor of Kit and VEGFR2

  • GC14976 structure
    GC14976Lenalidomide (CC-5013)
    CAS: 191732-72-6
    纯度: >99.50%

    Lenalidomide (CC-5013)是thalidomide的4-氨基-谷氨酰类似物，具有更强的效力，且不具有thalidomide相关的镇静和神经病变等神经系统副作用。

  • GC14987 structure
    GC14987GSK-3 Inhibitor IX (BIO)
    CAS: 667463-62-9
    纯度: >99.50%

    GSK-3 Inhibitor IX (BIO)是一种强效、选择性和可逆的糖原合成酶激酶-3（GSK-3）抑制剂，对GSK-3α/β的IC 50 值为5nM。

  • GC14998 structure
    GC14998Rocilinostat (ACY-1215)
    CAS: 1316214-52-4
    纯度: >98.00%

    A selective inhibitor of HDAC6

  • GC15002 structure
    GC15002Sodium Phenylbutyrate
    CAS: 1716-12-7
    纯度: >99.50%

    Sodium Phenylbutyrate是一种组蛋白去乙酰化酶（HDAC）抑制剂。

  • GC15022 structure
    GC15022Vandetanib (ZD6474)
    CAS: 443913-73-3
    纯度: >99.50%

    A multi-kinase inhibitor

  • GC15033 structure
    GC15033Azathioprine
    CAS: 446-86-6
    纯度: >99.50%

    An immunosuppressive purine analog

  • GC15047 structure
    GC15047PHA-793887
    CAS: 718630-59-2
    纯度: >98.00%

    A CDK inhibitor

  • GC15055 structure
    GC15055AZ 628
    CAS: 878739-06-1
    纯度: >99.50%

    A Raf kinase inhibitor

  • GC15083 structure
    GC15083Celastrol
    CAS: 34157-83-0
    纯度: >99.50%

    Celastrol是一种蛋白酶体抑制剂，有效且优先的抑制纯化的20S蛋白酶体，IC 50 为2.5 μM。

  • GC15084 structure
    GC150842-Methoxyestradiol (2-MeOE2)
    CAS: 362-07-2
    纯度: >99.50% / >98.00%

    2-Methoxyestradiol (2-MeOE2/2-Me)是一种HIF-1α抑制剂。

  • GC15089 structure
    GC15089Carfilzomib (PR-171)
    CAS: 868540-17-4
    纯度: >99.00%

    A proteasome inhibitor

  • GC15104 structure
    GC15104(R)-(+)-Etomoxir sodium salt
    CAS: 828934-41-4
    纯度: >99.00%

    (R)-(+)-Etomoxir sodium salt(Etomoxir; ETO)是一种用于代谢和心血管疾病的小分子,经酶转化为活性抑制剂乙托莫西里尔辅酶a (IC50 约为0.01-0.70 µM)后,对CPT-1a和CPT-1b的抑制表现出纳摩尔效价。

  • GC15134 structure
    GC15134Fludarabine Phosphate (Fludara)
    CAS: 75607-67-9
    纯度: >98.00%

    A prodrug form of fludarabine and 2-fluoro-ara-ATP

  • GC15142 structure
    GC15142PD-1/PD-L1 inhibitor 1 (BMS-1)
    CAS: 1675201-83-8
    纯度: >99.50%

    PD-1/PD-L1 inhibitor 1 是一种 PD-1/PD-L1 相互作用抑制剂，IC50 值介于 6 和 100 nM . PD-1/PD-L1 调节细胞信号通路和表观遗传修饰，从而抑制 T 细胞和 B 细胞的增殖和效应子功能。