Metabolism

Metabolism(代谢)

研究方向

Metabolism 相关产品(3072)

  • GC31299 structure
    GC31299Sch59498
    CAS: 224157-99-7

    Sch59498是一种有效的phosphodiesterase1c(Pde1c)抑制剂。

  • GC31324 structure
    GC31324PTP1B-IN-2
    CAS: 1919853-46-5
    纯度: >99.50%

    A PTP1B inhibitor

  • GC31325 structure
    GC31325Saroglitazar Magnesium
    CAS: 1639792-20-3
    纯度: >98.50%

    Saroglitazarmagnesium是一种新型的过氧化物酶体增殖物活化受体PPAR的激动剂,具有显著PPARα活性和中度PPARγ活性,在HepG2细胞中的EC50值分别为0.65pMand3nM。

  • GC31327 structure
    GC31327Win 58237
    CAS: 158001-76-4

    Win58237是一种phosphodiesterase(PDE)抑制剂,对PDEV有很强的亲和力,Ki值为170nM,具有舒张血管的作用。

  • GC31345 structure
    GC31345Retinol (Vitamin A1)
    CAS: 68-26-8
    纯度: >98.00%

    视黄醇,也称为维生素A 1 ,是维生素A家族中的一种脂溶性维生素,存在于食物中,用作膳食补充剂。

  • GC31350 structure
    GC31350Astaxanthin
    CAS: 472-61-7
    纯度: >98.00%

    Astaxanthin (β-Carotene-4,4'-dione, Trans-Astaxanthin), a xanthophyll carotenoid, is a nutrient with unique cell membrane actions and diverse clinical benefits with excellent safety and tolerability. Astaxanthin, a red dietary carotenoid isolated from Haematococcus pluvialis, is a modulator of PPARγ and a potent antioxidant with antiproliferative, neuroprotective and anti-inflammatory activity.

  • GC31355 structure
    GC31355AA26-9
    CAS: 1312782-34-5
    纯度: >98.00%

    A pan-serine hydrolase inhibitor

  • GC31366 structure
    GC31366Licogliflozin (LIK066)
    CAS: 1291094-73-9
    纯度: >98.00%

    Licogliflozin (LIK066) 是一种钠葡萄糖协同转运蛋白(SGLT1 和 SGLT2)抑制剂。

  • GC31377 structure
    GC31377Tofogliflozin hydrate (CSG-452 hydrate)
    CAS: 1201913-82-7
    纯度: >98.50% / >98.00%

    A potent inhibitor of SGLT2

  • GC31396 structure
    GC31396Raspberry ketone (Frambione)
    CAS: 5471-51-2
    纯度: >99.50%

    Raspberry ketone (p-Hydroxybenzyl acetone, Frambinone, Oxyphenylon, Rheosmin, Rasketone) is a natural phenolic compound that is the primary aroma compound of red raspberries. Raspberry ketone shows cardioprotective action against isoproterenol-induced myocardial infarction in rats, and the effects may be due to its PPAR-α agonistic activity.

  • GC31408 structure
    GC31408Indeglitazar (PPM 204)
    CAS: 835619-41-5
    纯度: >99.50%

    Indeglitazar (PPM 204) (PPM 204) 是一种可口服的 PPAR 泛激动剂,适用于所有三种 PPARα, PPARδ和PPARγ;。

  • GC31422 structure
    GC31422MCH-1 antagonist 1
    CAS: 1039825-68-7

    MCH-1antagonist1是一种有效的黑色素浓缩激素1(MCH-1)拮抗剂,Ki值为2.6nM。MCH-1antagonist1还抑制CYP3A4,IC50为10μM。

  • GC31447 structure
    GC31447CVT-12012
    CAS: 1018675-35-8
    纯度: >98.50%

    A stearoyl-CoA desaturase inhibitor

  • GC31450 structure
    GC31450Naveglitazar racemate
    CAS: 916085-47-7

    Naveglitazarracemate是Naveglitazar的外消旋体。Naveglitazar是过氧化物酶体增殖物激活受体(PPAR)α-γ双重,γ显性激动剂,在动物模型具有降低葡萄糖潜力。

  • GC31451 structure
    GC31451Peliglitazar racemate (BMS 426707-01 racemate)
    CAS: 331744-72-0

    Peliglitazar 外消旋体(BMS 426707-01 外消旋体)是 Peliglitazar 的外消旋体。

  • GC31452 structure
    GC31452AVE-8134
    CAS: 304025-09-0

    AVE-8134是PPARα的有效激动剂,对人体和啮齿类动物的PPARα的EC50值分别为100和3000nM。

  • GC31460 structure
    GC31460CDD3506
    CAS: 197913-15-8
    纯度: >98.00%

    CDD3506可以通过诱导肝CYP3A的活动,来提高高密度脂蛋白胆固醇(HDL)的水平。

  • GC31461 structure
    GC31461Tofogliflozin (CSG452)
    CAS: 903565-83-3

    Tofogliflozin (CSG 452) is a novel sodium-glucose co-transporter 2(SGLT2) inhibitor with IC50 values of 2.9 nM and 8444 nM for hSGLT2 and hSGLT1, respectively.

  • GC31462 structure
    GC31462Arhalofenate (MBX 102)
    CAS: 24136-23-0

    A prodrug form of a PPARγ partial agonist

  • GC31464 structure
    GC31464CDD3505
    CAS: 173865-33-3
    纯度: >98.00%

    CDD3505 is used for elevating high density lipoprotein cholesterol (HDL) by inducing hepatic cytochrome P450IIIA (CYP3A) activity.

  • GC31471 structure
    GC31471GSK376501A
    CAS: 1010412-80-2
    纯度: >99.00%

    GSK376501A是一种选择性的过氧化物酶体增殖物激活受体γ(PPARγ)调节剂。可用于治疗2型糖尿病。

  • GC31479 structure
    GC31479BMS-819881
    CAS: 1197420-05-5

    BMS-819881是一种黑色素浓缩激素受体1(MCHR1)拮抗剂,结合大鼠MCHR1,Ki值为7nM。BMS-819881还有效且选择性地作用于CYP3A4,EC50为13μM.

  • GC31492 structure
    GC31492Vildagliptin dihydrate (LAF237 dihydrate)
    CAS: 2133364-01-7

    A DPP-4 inhibitor

  • GC31497 structure
    GC31497KD-3010
    CAS: 934760-92-6

    KD3010是一种具有口服活性的有效的选择性PPARδ激动剂。