• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

3-Oxo-5β-cholanoic acid

CAS No. 1553-56-6

3-Oxo-5β-cholanoic acid ( Dehydrolithocholic acid | 3-oxoLCA )

产品货号. M26539 CAS No. 1553-56-6

3-Oxo-5β-cholanoic Acid (Dehydrolithocholic Acid) 是一种胆汁酸代谢物,通过直接与关键转录因子 RORγt (Kd: 1.13 μM) 结合来抑制 TH17 细胞的分化。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥242 有现货
10MG ¥392 有现货
25MG ¥605 有现货
50MG ¥830 有现货
100MG ¥1188 有现货
500MG ¥2997 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥199 有现货

生物学信息

  • 产品名称
    3-Oxo-5β-cholanoic acid
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    3-Oxo-5β-cholanoic Acid (Dehydrolithocholic Acid) 是一种胆汁酸代谢物,通过直接与关键转录因子 RORγt (Kd: 1.13 μM) 结合来抑制 TH17 细胞的分化。
  • 产品描述
    3-Oxo-5β-cholanoic acid (Dehydrolithocholic acid) is a bile acid metabolite and inhibits the differentiation of TH17 cells by directly binding to the key transcription factor RORγt (Kd: 1.13 μM).(In Vitro):Treatment with 3-Oxo-5β-cholanoic acid significantly reduced the activity of the RORγt reporter. 3-Oxo-5β-cholanoic acid probably inhibits TH17 cell differentiation by physically interacting with RORγt, and inhibiting its transcriptional activity.(In Vivo):3-Oxo-5β-cholanoic acid (Dehydrolithocholic acid) (0.3% (w/w); p.o.; for 1 week) significantly reduces the percentage of ileal TH17 cells.
  • 体外实验
    Treatment with 3-Oxo-5β-cholanoic acid significantly reduced the activity of the RORγt reporter. These data suggest that 3-Oxo-5β-cholanoic acid probably inhibits TH17 cell differentiation by physically interacting with RORγt, and inhibiting its transcriptional activity.
  • 体内实验
    3-Oxo-5β-cholanoic acid (Dehydrolithocholic acid) (0.3% (w/w); p.o.; for 1 week) significantly reduces the percentage of ileal TH17 cells. Animal Model:B6 Jax mice (with a faecal slurry containing SFB)Dosage:0.3% (w/w)Administration:Gavaged; for 1 week Result:Significantly reduced the percentage of ileal TH17 cells.
  • 同义词
    Dehydrolithocholic acid | 3-oxoLCA
  • 通路
    Nuclear Receptor/Transcription Factor
  • 靶点
    ROR
  • 受体
    KSP
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1553-56-6
  • 分子量
    374.565
  • 分子式
    C24H38O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (266.98 mM)
  • SMILES
    C[C@H](CCC(O)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Christine Lemieux, et al. ARRY-520, a Novel, Highly Selective KSP Inhibitor with Potent Anti-Proliferative Activity. AACR Annual Meeting. 2007.
产品手册
关联产品
  • SR3335

    SR 3335 是 RORα 的选择性反向激动剂,竞争性抑制 25-羟基胆固醇与配体结合域的结合 (Ki: 220 nM)。

  • GSK805

    GSK805 是一种有效的、口服生物可利用的视黄醇相关孤儿受体 γ t (RORγt) 反向激动剂,可与受体的推定配体结合域相互作用,而不会对 DNA 结合产生显着影响。

  • GSK 2981278

    GSK 2981278 (GSK2981278) 是一种有效的、高选择性的 RORγ/RORγt 抑制剂,可有效抑制人外周 T 细胞中 IL-17A 和 IL-22 蛋白的分泌,IC50 为 3.2 nM。