Urolithin A 3,8-二羟基-6H-二苯并[B,D]吡喃-6-酮

CAS 1143-70-0 MFCD20275235

化学结构图

1143-70-0
SMILES: O=c1oc2cc(O)ccc2c2ccc(O)cc12

化学属性

Mol. Weight228
Mol. FormulaC13H8O4
Density
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别名和识别编码

InChIKeyRIUPLDUFZCXCHM-UHFFFAOYSA-N
Chemical NameUrolithin A
Chemical Name Translation3,8-二羟基-6H-二苯并[B,D]吡喃-6-酮
MDL Number
CAS Number1143-70-0
PubChem Substance ID5488186
InChIInChI=1S/C13H8O4/c14-7-1-3-9-10-4-2-8(15)6-12(10)17-13(16)11(9)5-7/h1-6,14-15H
Synonym 3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one urolithin A
EC Number
Beilstein Registry Number
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相关文献及参考

  • [2]. Wang Y, et al. In vitro antiproliferative and antioxidant effects of urolithin A, the colonic metabolite of ellagic acid, on hepatocellular carcinomas HepG2 cells. Toxicol In Vitro. 2015 Aug;29(5):1107-15.
  • [3]. Zhao W, et al. Metabolite of ellagitannins, urolithin A induces autophagy and inhibits metastasis in human sw620colorectal cancer cells. Mol Carcinog. 2018 Feb;57(2):193-200.
  • [4]. Ishimoto H, et al. In vivo anti-inflammatory and antioxidant properties of ellagitannin metabolite urolithin A. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5901-4.
  • [5]. Qiu Z, et al. In vitro antioxidant and antiproliferative effects of ellagic acid and its colonic metabolite, urolithins, on human bladder cancer T24 cells. Food Chem Toxicol. 2013 Sep;59:428-37.
  • [6]. González-Sarrías A, et al. Antiproliferative activity of the ellagic acid-derived gut microbiota isourolithin A and comparison with its urolithin A isomer: the role of cell metabolism.Eur J N

安全信息

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系列性分类


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