Ubiquitination/ Proteasome

Ubiquitination/ Proteasome(泛素化/蛋白酶体)

研究方向

Ubiquitination/ Proteasome 相关产品(1292)

  • GC33779 structure
    GC33779Cysteamine (β-Mercaptoethylamine)
    CAS: 60-23-1
    纯度: >95.00%

    2-Aminoethanethiol (cysteamine, β-Mercaptoethylamine, 2-Mercaptoethylamine, Thioethanolamine, Mercaptamine) is a radiation-protective agent that oxidizes in air to form cystamine.

  • GC33833 structure
    GC33833Tetrahydrocurcumin (HZIV 81-2)
    CAS: 36062-04-1

    A metabolite of curcumin with diverse biological activities

  • GC33848 structure
    GC33848Fludrocortisone acetate (9α-Fludrocortisone acetate)
    CAS: 514-36-3
    纯度: >99.50%

    A mineralocorticoid agonist

  • GC34009 structure
    GC34009Nitroprusside disodium dihydrate (Sodium nitroprusside dihydrate)
    CAS: 13755-38-9
    纯度: >99.50% / >99.00%

    Sodium Nitroprusside Dihydrate is a potent vasodilator working through releasing NO spontaneously in blood.

  • GC34010 structure
    GC34010Danshensu (Dan shen suan A)
    CAS: 76822-21-4
    纯度: >98.00%

    丹参素是丹参的一种活性成分,通过激活 Nrf2 信号通路显示出广泛的心血管益处。

  • GC34014 structure
    GC34014Trimetazidine dihydrochloride
    CAS: 13171-25-0
    纯度: >99.50%

    Trimetazidine dihydrochloride是一种亲脂性piperazine衍生物,用于治疗心绞痛。

  • GC34035 structure
    GC34035Meglutol (Dicrotalic acid)
    CAS: 503-49-1
    纯度: >98.00%

    An HMG-CoA reductase inhibitor

  • GC34057 structure
    GC34057TBHQ (tert-Butylhydroquinone)
    CAS: 1948-33-0
    纯度: >99.50%

    TBHQ(tert-Butylhydroquinone)是一种强效的酚类抗氧化剂,能够减轻氧化应激和炎症反应。

  • GC34072 structure
    GC34072Talmapimod (SCIO-469)
    CAS: 309913-83-5
    纯度: >98.00%

    A p38 MAPK inhibitor

  • GC34094 structure
    GC34094Mycro 3
    CAS: 944547-46-0
    纯度: >99.00%

    Mycro 3 is a potent and selective inhibitor of c-Myc in whole cell assays. Mycro 3 also shows weak inhibitory activity against AP-1.

  • GC34096 structure
    GC34096(R)-(-)-Gossypol acetic acid (AT-101 (acetic acid))
    CAS: 866541-93-7
    纯度: >98.00%

    (R)-(-)-Gossypol acetic acid (AT-101 (acetic acid))是一种新型的、具有口服活性的Bcl-2家族蛋白抑制剂,可抑制Bcl-2(K i =260±30nM),Mcl-1(K i =170±10nM)和Bcl-xL(K i =480±40nM)。

  • GC34117 structure
    GC34117SMER18
    CAS: 944153-47-3

    SMER18是Rapamycin的一种小分子增强剂,充当mTOR非依赖性的的自噬诱导剂。

  • GC34173 structure
    GC34173LG-100064
    CAS: 153559-46-7
    纯度: >99.50%

    LG-100064是一种类视黄醇X受体(retinoid-X-receptor(RXR))激动剂,对RXRα,RXRβ和RXRγ的EC50值分别为330nM,200nM和260nM;LG-100064可用于癌症研究。

  • GC34315 structure
    GC34315ULK-101
    CAS: 2443816-45-1
    纯度: >99.50%

    ULK-101是一种选择性的ULK1( IC 50 =1.6nM)抑制剂,还可抑制 ULK2( IC 50 =30nM)的活性。

  • GC34330 structure
    GC34330XRK3F2
    CAS: 2375193-43-2
    纯度: >95.00% / >98.50%

    XRK3F2 is an inhibitor of the p62-ZZ domain that blunts MM-induced Runx2 suppression in vitro, and induces new bone formation and remodeling in the presence of tumor in vivo.

  • GC34390 structure
    GC34390Autocamtide 2, amide
    纯度: >99.00%

    Autocamtide2,amide是钙调蛋白激酶(CaMK)家族实验的底物(100μMfinalconcentration)。

  • GC34532 structure
    GC34532CFTR corrector 2
    CAS: 1628416-28-3
    纯度: >99.50%

    FDL169 is a CFTR corrector that is designed to fix and restore the function of the defective CFTR protein.

  • GC34649 structure
    GC34649LMP7-IN-1
    CAS: 2285330-15-4
    纯度: >98.00%

    LMP7-IN-1 是一种可口服的、有效的、可逆的和高度选择性的免疫蛋白酶体亚基 LMP7 (β5i) 抑制剂。 LMP7-IN-1 对 LMP7 亚基具有高生化 (IC50=3.6 nM) 和细胞 (IC50=3.4 nM) 效力。 LMP7-IN-1 在多发性骨髓瘤异种移植模型中显示出强大的抗肿瘤功效。 LMP7-IN-1 可显着长期抑制肿瘤 LMP7 活性和泛素化蛋白转换,并诱导多发性骨髓瘤细胞凋亡。

  • GC34686 structure
    GC34686Nidufexor
    CAS: 1773489-72-7
    纯度: >98.50%

    An FXR partial agonist

  • GC34745 structure
    GC34745PTI-428
    CAS: 1953130-87-4
    纯度: >99.50%

    PTI-428是一种可增强并稳定囊性纤维化跨膜传导调节因子(CFTR)蛋白功能的特异性调节剂。

  • GC34817 structure
    GC34817Sulfosuccinimidyl oleate sodium
    CAS: 1212012-37-7
    纯度: >95.00% / >98.00%

    Sulfosuccinimidyl oleate sodium是一种不可逆的CD36抑制剂。

  • GC34849 structure
    GC34849UBCS039
    CAS: 358721-70-7
    纯度: >98.50%

    UBCS039 is the first synthetic SIRT6 activator with EC50 of 38 μM,induces a time-dependent activation of autophagy in several human tumor cell lines.

  • GC34862 structure
    GC34862WYC-209
    CAS: 2131803-90-0
    纯度: >99.50%

    WYC-209是一种合成类视黄醇,能抑制恶性小鼠黑色素瘤肿瘤再生细胞(TRC)的增殖,IC50值为0.19μM。WYC-209主要细胞靶点是维甲酸受体(RARs)。

  • GC34918 structure
    GC34918MW-150 dihydrochloride dihydrate
    CAS: 1661020-92-3

    An inhibitor of p38α MAPK