Urolithin A 3,8-二羟基-6H-二苯并[B,D]吡喃-6-酮
CAS 1143-70-0 MFCD01143700
化学结构图
SMILES: O=c1oc2cc(O)ccc2c2ccc(O)cc12
化学属性
| Mol. Weight | 228 |
|---|---|
| Mol. Formula | C13H8O4 |
| Density | |
| Boiling Point | |
| Melting Point |
别名和识别编码
| InChIKey | RIUPLDUFZCXCHM-UHFFFAOYSA-N |
|---|---|
| Chemical Name | Urolithin A |
| Chemical Name Translation | 3,8-二羟基-6H-二苯并[B,D]吡喃-6-酮 |
| MDL Number | |
| CAS Number | 1143-70-0 |
| PubChem Substance ID | 5488186 |
| InChI | InChI=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
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