GlpBio

Metabolism

Metabolism(代谢)

研究方向

Metabolism 相关产品(3072)

  • GC13842 structure
    GC13842Ro 20-1724
    CAS: 29925-17-5
    纯度: >98.00% / >95.00%

    Ro 20-1724是一种选择性cAMP特异性磷酸二酯酶（PDE4）抑制剂，IC 50 值为1.930μM。

  • GC13856 structure
    GC13856Dalcetrapib (JTT-705, RO4607381)
    CAS: 211513-37-0
    纯度: >99.00%

    An inhibitor of cholesteryl ester transfer protein

  • GC13912 structure
    GC13912NLG919
    CAS: 1402836-58-1
    纯度: >99.50%

    An IDO pathway inhibitor

  • GC13946 structure
    GC13946SNX-2112
    CAS: 908112-43-6

    SNX-2112是一种强效的合成型热休克蛋白（Hsp 90）抑制剂，IC 50 值为30nM。

  • GC13969 structure
    GC13969GW9662
    CAS: 22978-25-2
    纯度: >99.50% / >98.00%

    GW9662是一种特异性的过氧化物酶体增殖物激活受体-γ(PPAR-γ)抑制剂,其IC50为3.3 nM。

  • GC14038 structure
    GC14038Atorvastatin Calcium
    CAS: 134523-03-8
    纯度: >99.50%

    An HMG-CoA reductase inhibitor

  • GC14061 structure
    GC14061Evacetrapib (LY2484595)
    CAS: 1186486-62-3
    纯度: >99.00%

    A CETP inhibitor

  • GC14226 structure
    GC14226Methazolamide
    CAS: 554-57-4
    纯度: >98.00%

    A carbonic anhydrase inhibitor

  • GC14269 structure
    GC14269Cobicistat (GS-9350)
    CAS: 1004316-88-4
    纯度: >98.00%

    An inhibitor of CYP3A

  • GC14308 structure
    GC14308FK866 (APO866)
    CAS: 658084-64-1
    纯度: >99.50%

    Inhibitor of nicotinamide phosphoribosyltransferase

  • GC14398 structure
    GC14398Siguazodan
    CAS: 115344-47-3
    纯度: >99.00%

    Siguazodan (SKF 94836) 是一种有效的、选择性的、具有口服活性的磷酸二酯酶 III (PDE-III) 抑制剂，IC50 为 117 nM。

  • GC14403 structure
    GC14403WY-14643 (Pirinixic Acid)
    CAS: 50892-23-4
    纯度: >99.50% / >98.00%

    WY-14643 (Pirinixic Acid)是一种高效、具备选择性高亲和力的过氧化物酶体增殖物激活受体α（PPARα）受体激动剂，对小鼠的 PPARα受体的EC 50 为0.63μM，对人的 PPARα受体的EC 50 为5μM。

  • GC14425 structure
    GC14425IDO inhibitor 1
    CAS: 1204669-37-3

    Indoleamine-2,3-dioxygenase inhibitor

  • GC14435 structure
    GC14435Zileuton sodium
    CAS: 118569-21-4

    A reversible inhibitor of 5-lipoxygenase

  • GC14538 structure
    GC14538Pravastatin sodium
    CAS: 81131-70-6
    纯度: >99.00% / >98.00%

    Pravastatin sodium 是一种HMG-CoA可逆的竞争性抑制剂，IC 50 为5.6μM，通常用于高胆固醇血症和冠心病的研究。

  • GC14581 structure
    GC14581JNJ-1661010
    CAS: 681136-29-8
    纯度: >98.50%

    A selective FAAH inhibitor

  • GC14636 structure
    GC14636KW-2478
    CAS: 819812-04-9
    纯度: >98.50%

    An Hsp90 inhibitor

  • GC14673 structure
    GC14673Safinamide Mesylate
    CAS: 202825-46-5
    纯度: >98.00%

    An inhibitor of MAO-B

  • GC14751 structure
    GC14751Malotilate
    CAS: 59937-28-9
    纯度: >99.50%

    A hepatoprotective agent

  • GC14783 structure
    GC14783Trilostane
    CAS: 13647-35-3
    纯度: >99.50%

    A 3β-hydroxysteroid dehydrogenase inhibitor

  • GC14935 structure
    GC14935Capadenoson
    CAS: 544417-40-5
    纯度: >99.00%

    A partial adenosine receptor agonist

  • GC14983 structure
    GC14983GW0742
    CAS: 317318-84-6
    纯度: >98.00%

    A selective agonist of PPARδ

  • GC15077 structure
    GC15077SA 47
    CAS: 792236-07-8
    纯度: >99.00%

    SA 47 是一种选择性强效的脂肪酸酰胺水解酶 (FAAH) 和氨基甲酸酯抑制剂 。

  • GC15094 structure
    GC15094LY2183240
    CAS: 874902-19-9
    纯度: >99.00%

    A potent, competitive inhibitor of anandamide uptake