GlpBio

Metabolism

Metabolism(代谢)

研究方向

Metabolism 相关产品(3072)

  • GC12596 structure
    GC12596Nepicastat (SYN-117) HCl
    CAS: 170151-24-3
    纯度: >98.50%

    An inhibitor of dopamine β-hydroxylase

  • GC12693 structure
    GC12693JZL 195
    CAS: 1210004-12-8
    纯度: >98.00%

    JZL 195是一种具有高效选择性、不可逆的脂肪酸酰胺水解酶（FAAH）和单酰甘油脂肪酶（MAGL）双重抑制剂，IC 50 值分别为2nM和4nM。

  • GC12764 structure
    GC12764Aminophylline
    CAS: 317-34-0
    纯度: >99.50%

    A phosphodiesterase inhibitor and adenosine receptor antagonist

  • GC12771 structure
    GC12771Etazolate hydrochloride
    CAS: 35838-58-5

    PDE-4 inhibitor and selective GABA-A receptor modulator

  • GC12801 structure
    GC12801Rasagiline Mesylate
    CAS: 161735-79-1
    纯度: >99.50%

    An inhibitor of MAO-B

  • GC12808 structure
    GC12808Pimobendan
    CAS: 74150-27-9
    纯度: >99.00%

    An inhibitor of PDE3

  • GC12820 structure
    GC12820T0070907
    CAS: 313516-66-4
    纯度: >99.50%

    T0070907是一种有效的选择性过氧化物酶体增殖物激活受体γ（PPARγ）拮抗剂，IC 50 值为1nM。

  • GC12878 structure
    GC12878MMPX
    CAS: 78033-08-6

    calmodulin-sensitive cyclic GMP phosphodiesterase inhibitor

  • GC12880 structure
    GC12880GSK 2830371
    CAS: 1404456-53-6
    纯度: >98.50%

    An inhibitor of Wip1 phosphatase

  • GC12894 structure
    GC12894Balaglitazone
    CAS: 199113-98-9
    纯度: >99.50%

    A partial agonist of PPARγ

  • GC12919 structure
    GC12919Pralatrexate
    CAS: 146464-95-1
    纯度: >98.00%

    A dihydrofolate reductase inhibitor

  • GC13044 structure
    GC1304417-DMAG (Alvespimycin) HCl
    CAS: 467214-21-7
    纯度: >98.00%

    17-DMAG (Alvespimycin) HCl是一种有效的Hsp90的抑制剂，其IC 50 值为62nM。

  • GC13076 structure
    GC13076Deltarasin
    CAS: 1440898-61-2

    A KRAS inhibitor

  • GC13121 structure
    GC13121Piclamilast
    CAS: 144035-83-6

    A PDE4 inhibitor

  • GC13204 structure
    GC13204Inolitazone
    CAS: 223132-37-4

    Inolitazone 是一种新型的高亲和力 PPARγ 激动剂，其生物活性依赖于 PPARγ，抑制生长的 IC50 为 0.8 nM。

  • GC13414 structure
    GC13414AT13387
    CAS: 912999-49-6
    纯度: >99.50%

    AT13387是一种小分子非安沙霉素类HSP90（热休克蛋白90）抑制剂，其作用机制是通过靶向AKT和ERK信号通路。

  • GC13495 structure
    GC13495Trequinsin hydrochloride
    CAS: 78416-81-6
    纯度: >99.50%

    An inhibitor of PDE3

  • GC13535 structure
    GC13535Fluvastatin
    CAS: 93957-54-1
    纯度: >98.00%

    Fluvastatin是一种亲脂性的3-羟基-3-甲基戊二酰辅酶A（HMG-CoA）还原酶抑制剂，可在多种癌细胞中抑制增殖并诱导凋亡。

  • GC13614 structure
    GC13614Mycophenolate Mofetil
    CAS: 128794-94-5
    纯度: >99.50%

    A prodrug form of mycophenolic acid

  • GC13633 structure
    GC13633Ciprofibrate
    CAS: 52214-84-3
    纯度: >99.50%

    A selective PPARα agonist

  • GC13652 structure
    GC13652Dyphylline
    CAS: 479-18-5
    纯度: >99.00%

    An adenosine receptor antagonist and phosphodiesterase inhibitor

  • GC13657 structure
    GC13657Mesopram
    CAS: 189940-24-7

    PDE4 inhibitor, orally active

  • GC13683 structure
    GC13683Rivaroxaban
    CAS: 366789-02-8
    纯度: >99.50%

    A selective inhibitor of Factor Xa

  • GC13771 structure
    GC13771Canagliflozin
    CAS: 842133-18-0
    纯度: >99.50% / >98.00%

    Canagliflozin是一种用于治疗2型糖尿病的钠葡萄糖共转运体（SGLT2）抑制剂。