174023-48-4
174023-48-4
Chemical Structure
Isourolithin A
Synonym(s): Iso-uroA
- CAS No.: 174023-48-4
- Formula:C13H8O4
- Molecular Weight:228.20
IUPAC Name: 3,9-dihydroxy-6H-benzo[c]chromen-6-one
InChIKey: WDGSXHQNUPZEHA-UHFFFAOYSA-N
SMILES: O=C1OC=2C=C(O)C=CC2C3=CC(O)=CC=C13
Biological Activity: Isourolithin A (Iso-uroA) is a urolithin metabolite. Isourolithin A induces S-phase and G2/M-phase cell cycle arrest and apoptosis. Isourolithin A can be used for research on colon cancer[1][2].
| Cat. No. | 상품명 | Purity | 제품 설명 | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Isourolithin A | 98.32% | Isourolithin A (Iso-uroA) is a urolithin metabolite. Isourolithin A induces S-phase and G2/M-phase cell cycle arrest and apoptosis. Isourolithin A can be used for research on colon cancer. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Selma MV, et al. Isolation of Human Intestinal Bacteria Capable of Producing the Bioactive Metabolite Isourolithin A from Ellagic Acid. Front Microbiol. 2017 Aug 7;8:1521.
- [2]. 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 Nutr. 2017 Mar;56(2):831-841. [Content Brief]
