Metabolism

Metabolism(代谢)

研究方向

Metabolism 相关产品(3072)

  • GC16687 structure
    GC16687(R)-Edelfosine
    CAS: 77286-66-9
    纯度: >98.00% / >99.00%

    (R)-Edelfosine是一种属于具有抗肿瘤和抗寄生虫活性的合成脂质药物。(R)-Edelfosine可通过靶向线粒体和脂筏上的FOF1-ATP合酶,诱导肿瘤细胞发生凋亡样细胞死亡。

  • GC16697 structure
    GC16697fluoro-Dapagliflozin
    CAS: 1181681-43-5

    A potent inhibitor of hSGLT2

  • GC16707 structure
    GC16707Isavuconazole
    CAS: 241479-67-4
    纯度: >98.00%

    A broad-spectrum triazole antifungal agent

  • GC16714 structure
    GC16714PACOCF3
    CAS: 141022-99-3
    纯度: >98.00%

    Antagonizes DP receptor agonist effects

  • GC16733 structure
    GC16733Vildagliptin (LAF-237)
    CAS: 274901-16-5
    纯度: >98.00%

    A DPP-4 inhibitor

  • GC16738 structure
    GC16738Tunicamycin Mixture
    CAS: 11089-65-9
    纯度: >95.00%

    Tunicamycin Mixture是一种同源核苷抗生素的混合物, 可抑制N-糖基化并阻断GlcNAc 磷酸转移酶(GPT)。

  • GC16751 structure
    GC16751Chlorzoxazone
    CAS: 95-25-0
    纯度: >99.50%

    A centrally acting muscle relaxant

  • GC16754 structure
    GC16754Clarithromycin
    CAS: 81103-11-9
    纯度: >98.00%

    Clarithromycin是一种大环内酯类抗生素,通过抑制细菌蛋白质合成发挥作用,与细菌核糖体的50S亚基结合,阻止肽链延长,从而抑制细菌生长。

  • GC16756 structure
    GC16756KT182
    CAS: 1402612-62-7
    纯度: >98.00%

    A potent inhibitor of ABHD6

  • GC16770 structure
    GC16770Arachidonic Acid Leelamide

    A novel fatty acid amide

  • GC16775 structure
    GC16775Rotenone
    CAS: 83-79-4
    纯度: >99.50%

    Rotenone是一种线粒体电子传递链复合物 I 抑制剂,可通过增强线粒体活性氧的产生来诱导细胞凋亡。

  • GC16777 structure
    GC16777YM 511
    CAS: 148869-05-0

    YM 511 是一种高度特异性的非甾体芳香酶抑制剂。

  • GC16816 structure
    GC16816Galloflavin
    CAS: 568-80-9

    An inhibitor of lactate dehydrogenase

  • GC16824 structure
    GC16824Pargyline (hydrochloride)
    CAS: 306-07-0
    纯度: >99.50% / >99.00%

    An irreversible MAO inhibitor

  • GC16849 structure
    GC16849MBCQ
    CAS: 150450-53-6
    纯度: >99.00%

    An inhibitor of PDE5

  • GC16856 structure
    GC16856Avanafil
    CAS: 330784-47-9
    纯度: >98.00% / >99.00%

    A potent and selective PDE5 inhibitor

  • GC16860 structure
    GC16860NCT-502
    CAS: 1542213-00-2
    纯度: >99.00%

    A PHGDH inhibitor

  • GC16868 structure
    GC16868Sulfasalazine
    CAS: 599-79-1
    纯度: >99.00% / >98.00%

    Sulfasalazine是一种磺胺类药物。

  • GC16892 structure
    GC16892XL-888
    CAS: 1149705-71-4
    纯度: >99.50%

    An orally bioavailable Hsp90 inhibitor

  • GC16944 structure
    GC16944SR 1664
    CAS: 1338259-05-4

    An inhibitor of Cdk5-mediated PPARγ phosphorylation

  • GC16951 structure
    GC16951Stiripentol
    CAS: 49763-96-4
    纯度: >99.50%

    An antiepileptic compound

  • GC16966 structure
    GC16966VER 155008
    CAS: 1134156-31-2
    纯度: >99.50%

    VER 155008是一种强效的,源自腺苷的热休克蛋白70(Hsp70)家族抑制剂,对Hsp70、热休克同源蛋白70(Hsc70)和葡萄糖调节蛋白78(Grp78)的IC 50 值分别为0.5μM、2.6μM和2.6μM。

  • GC17003 structure
    GC17003Benzenesulfonamide
    CAS: 98-10-2

    carbonic anhydrase inhibitor

  • GC17013 structure
    GC17013Amidepsine D
    CAS: 79786-34-8

    A diacylglycerol acyltransferase inhibitor