Metabolism

Metabolism(代谢)

研究方向

Metabolism 相关产品(3072)

  • GC12962 structure
    GC12962Isatin
    CAS: 91-56-5
    纯度: >98.00%

    Isatin (Indoline-2,3-dione) 是一种有效的单胺氧化酶 (MAO) 抑制剂,IC50 为 3 μM。

  • GC12981 structure
    GC12981OU749
    CAS: 519170-13-9

    Inhibitor of γ-glutamyl transferase

  • GC12992 structure
    GC12992Fluorometholone Acetate
    CAS: 3801-06-7
    纯度: >98.00%

    A synthetic glucocorticoid

  • GC13063 structure
    GC13063N-Benzylpalmitamide
    CAS: 74058-71-2
    纯度: >98.00%

    A long-chain fatty acid amide

  • GC13079 structure
    GC13079Voriconazole
    CAS: 137234-62-9
    纯度: >99.50%

    Voriconazole是一种强效竞争性抑制剂,可抑制CYP2B6(IC 50 =1.71μM)、CYP2C9(IC 50 =3.62μM)、CYP2C19(IC 50 =5.25μM)和CYP3A(IC 50 =2.90μM)。

  • GC13083 structure
    GC13083Siramesine
    CAS: 147817-50-3

    A selective σ 2 receptor agonist

  • GC13124 structure
    GC13124LY2608204
    CAS: 1234703-40-2
    纯度: >98.00%

    An activator of glucokinase

  • GC13130 structure
    GC13130Apixaban
    CAS: 503612-47-3
    纯度: >99.50%

    An inhibitor of Factor Xa

  • GC13139 structure
    GC13139FG-4592 (ASP1517)
    CAS: 808118-40-3
    纯度: >99.50%

    FG-4592 作为一种口服生物可利用的缺氧诱导因子 (HIF) 脯氨酰羟化酶抑制剂,可通过 HIF 介导的转录促进协调性红细胞生成。

  • GC13147 structure
    GC13147AG-221 (Enasidenib)
    CAS: 1446502-11-9
    纯度: >99.50%

    An inhibitor of mutant IDH2

  • GC13262 structure
    GC13262A-771726
    CAS: 163451-81-8
    纯度: >98.00%

    An active metabolite of leflunomide

  • GC13275 structure
    GC13275Ibudilast
    CAS: 50847-11-5
    纯度: >99.50%

    An inhibitor of PDE4

  • GC13276 structure
    GC13276Oleyloxyethyl Phosphorylcholine
    CAS: 84601-19-4

    A PLA 2 inhibitor

  • GC13293 structure
    GC13293LP533401 hcl
    CAS: 1040526-12-2
    纯度: >98.50%

    An inhibitor of gut-derived serotonin biosynthesis

  • GC13307 structure
    GC13307PU-WS13
    CAS: 1454619-14-7
    纯度: >98.00%

    PU-WS13是一种嘌呤支架类Grp94特异性热休克蛋白90(Hsp90)抑制剂。

  • GC13319 structure
    GC133195,8,11-Eicosatriynoic Acid
    CAS: 13488-22-7

    A nonselective inhibitor of lipoxygenases

  • GC13336 structure
    GC13336CBR-5884
    CAS: 681159-27-3
    纯度: >99.00%

    A selective PHGDH inhibitor

  • GC13351 structure
    GC13351VU0359595
    CAS: 1246303-14-9
    纯度: >95.00%

    A selective PLD 1 inhibitor

  • GC13362 structure
    GC13362TOK-001
    CAS: 851983-85-2
    纯度: >99.50%

    A CYP17 inhibitor

  • GC13379 structure
    GC133791-Naphthyl 3,5-dinitrobenzoate
    CAS: 93261-39-3

    A dual inhibitor of 5-LO and mPGES-1

  • GC13444 structure
    GC13444Doxofylline
    CAS: 69975-86-6
    纯度: >99.00%

    A bronchodilator

  • GC13464 structure
    GC13464GSK 2837808A
    CAS: 1445879-21-9
    纯度: >99.00%

    GSK2837808A 是一种选择性的 LDHA (lactate dehydrogenase A) 的抑制剂,对hLDHA和hLDHB的IC50分别为2.6 nM和43 nM.GSK2837808A(10 µM;24-72h)通过促进有氧糖酵解、增殖、细胞周期和细胞凋亡抵抗,阻断了着丝粒蛋白N (CENP-N)过表达对鼻咽癌细胞的影响。

  • GC13470 structure
    GC13470Rhapontigenin
    CAS: 500-65-2
    纯度: >98.00% / >99.50%

    Rhapontigenin(丹叶大黄素)是一种有效的细胞色素P4501A1选择性灭活剂,IC 50 为0.4μM,对P4501A1的选择性分别是P4501A2和P4501B1的400倍和23倍。

  • GC13516 structure
    GC13516AS 1949490
    CAS: 1203680-76-5
    纯度: >98.00%

    A selective SHIP2 inhibitor