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Others 相关产品(2412)

  • GC13491 structure
    GC13491Mirin
    CAS: 1198097-97-0
    纯度: >99.50%

    Mirin是一种Mre11-Rad50-Nbs1（MRN）复合物抑制剂（IC 50 =12μM），能够抑制Mre11相关的外切酶活性，Mirin可抑制MRN依赖的ATM的激活。通常用于与DNA修复机制相关的癌症的研究。

  • GC13528 structure
    GC13528Zoxazolamine
    CAS: 61-80-3
    纯度: >98.00%

    A skeletal muscle relaxant

  • GC13536 structure
    GC13536Furegrelate (sodium salt)
    CAS: 85666-17-7

    A potent inhibitor of thromboxane synthase

  • GC13538 structure
    GC13538GSK180
    CAS: 1799725-26-0
    纯度: >99.00%

    GSK180 是 kynurenine-3-monooxygenase (KMO) 的选择性、竞争性和强效抑制剂，KMO 是色氨酸代谢的关键酶 (IC50, ~6 nM)，但对色氨酸途径上的其他酶的活性可忽略不计。

  • GC13560 structure
    GC13560Acipimox
    CAS: 51037-30-0
    纯度: >99.00%

    An antilipolytic agent

  • GC13565 structure
    GC13565SHU 9119
    CAS: 168482-23-3
    纯度: >98.00%

    An MC1R agonist and MC4R antagonist

  • GC13566 structure
    GC13566NVP 231
    CAS: 362003-83-6
    纯度: >98.50%

    A potent and reversible inhibitor of ceramide kinase

  • GC13574 structure
    GC13574Amoxapine
    CAS: 14028-44-5
    纯度: >98.50%

    A tetracyclic antidepressant

  • GC13582 structure
    GC13582KHS 101 hydrochloride
    CAS: 1784282-12-7
    纯度: >98.00%

    neuronal differentiation inducer

  • GC13643 structure
    GC13643c-di-AMP
    CAS: 54447-84-6
    纯度: >98.50% / >95.00%

    C-di-AMP是STING(刺激内质网的蛋白)的激动剂,通过与该跨膜蛋白结合,激活TBK3-IRF3信号通路,进而引发I型IFN和TNF的产生。

  • GC13651 structure
    GC13651(Z)-PUGNAc
    CAS: 132489-69-1
    纯度: >95.00% / >98.00%

    (Z)-PUGNAc是一种O-GlcNAc-β-N-乙酰氨基葡萄糖苷酶（O-GlcNAcase）和β-氨基己糖苷酶（β-Hexosaminidase）抑制剂，K i 值分别为46和36nM。

  • GC13710 structure
    GC13710Halobetasol Propionate
    CAS: 66852-54-8
    纯度: >98.00%

    A synthetic glucocorticoid

  • GC13727 structure
    GC13727TC Mps1 12
    CAS: 1206170-62-8
    纯度: >99.00%

    TC Mps1 12 是一种有效的选择性单极纺锤体 1 (Mps1) 抑制剂，IC50 为 6.4 nM。

  • GC13746 structure
    GC13746Fenbufen
    CAS: 36330-85-5
    纯度: >98.50%

    An NSAID

  • GC13760 structure
    GC13760TC HSD 21
    CAS: 330203-01-5

    An inhibitor of 17β-HSD3

  • GC13770 structure
    GC13770Troxipide
    CAS: 30751-05-4
    纯度: >98.00%

    An antiulcerative agent

  • GC13772 structure
    GC13772SC 26196
    CAS: 218136-59-5
    纯度: >98.00%

    SC 26196是一种具有口服活性的Delta6去饱和酶（D6D, FADS2）抑制剂，SC 26196可抑制亚油酸和α-亚麻酸向长链不饱和脂肪酸的转化以调控脂质代谢。

  • GC13782 structure
    GC13782(3S,4S)-3-(Boc-amino)-4-methylpyrrolidine
    CAS: 127199-54-6

    (3S,4S)-3-(Boc-amino)-4-methylpyrrolidine

  • GC13944 structure
    GC13944(5Z)-7-Oxozeaenol
    CAS: 66018-38-0,253863-19-3
    纯度: >99.00%

    A selective TAK1 inhibitor

  • GC13955 structure
    GC13955Enoxolone
    CAS: 471-53-4
    纯度: >99.50% / >98.00%

    An anti-inflammatory and immunomodulatory compound

  • GC13958 structure
    GC13958BPTES
    CAS: 314045-39-1
    纯度: >98.00%

    BPTES是一种高效且选择性的肾型谷氨酰胺酶（GLS）变构抑制剂，已被用作分子探针以确定GLS抑制的治疗潜力。

  • GC13967 structure
    GC13967Tosyllysine Chloromethyl Ketone (hydrochloride)
    CAS: 4272-74-6
    纯度: >98.00%

    A non-selective proteinase inhibitor

  • GC14010 structure
    GC14010Etofibrate
    CAS: 31637-97-5
    纯度: >99.00%

    A hypolipidemic agent

  • GC14147 structure
    GC14147Lactulose
    CAS: 4618-18-2
    纯度: >99.00%

    A synthetic sugar