2270-20-4
2270-20-4
Chemical Structure
5-Phenylvaleric acid
Synonym(s): 5-Phenylpentanoic acid
- CAS No.: 2270-20-4
- Formula:C11H14O2
- Molecular Weight:178.23
IUPAC Name: 5-phenylpentanoic acid
InChIKey: BYHDDXPKOZIZRV-UHFFFAOYSA-N
SMILES: O=C(CCCCC1=CC=CC=C1)O
Biological Activity: 5-Phenylvaleric acid (5-Phenylpentanoic acid) is a major metabolite produced by the gut microbiota during the metabolism of flavan-3-ols and can serve as a biomarker for flavan-3-ol intake. 5-Phenylvaleric acid can also be used as a raw material for the synthesis of polyhydroxyalkanoates[1][2].
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5-Phenylvaleric acid | 98.0% | 5-Phenylvaleric acid (5-Phenylpentanoic acid) is a major metabolite produced by the gut microbiota during the metabolism of flavan-3-ols and can serve as a biomarker for flavan-3-ol intake. 5-Phenylvaleric acid can also be used as a raw material for the synthesis of polyhydroxyalkanoates. | ||||||||||||||||||||
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5-Phenylvaleric acid (Standard) | ≥98% | 5-Phenylvaleric acid (Standard) is an analytical standard for 5-Phenylvaleric acid (HY-W032915). This product is used for research and analytical applications. 5-Phenylvaleric acid (5-Phenylpentanoic acid) is a major metabolite produced by the gut microbiota during the metabolism of flavan-3-ols and can serve as a biomarker for flavan-3-ol intake. 5-Phenylvaleric acid can also be used as a raw material for the synthesis of polyhydroxyalkanoates. | ||||||||||||||||||||
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5-Phenylvaleric acid-13 | 5-Phenylvaleric acid-d13 (5-Phenylpentanoic acid-d13) is the deuterium labeled 5-Phenylvaleric acid (HY-W032915). 5-Phenylvaleric acid (5-Phenylpentanoic acid) is a major metabolite produced by the gut microbiota during the metabolism of flavan-3-ols and can serve as a biomarker for flavan-3-ol intake. 5-Phenylvaleric acid can also be used as a raw material for the synthesis of polyhydroxyalkanoates. | |||||||||||||||||||||
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References
- [1]. Mena P, et al. Phenyl-γ-valerolactones and phenylvaleric acids, the main colonic metabolites of flavan-3-ols: synthesis, analysis, bioavailability, and bioactivity. Nat Prod Rep. 2019 May 22;36(5):714-752. [Content Brief]
- [2]. Chung DM, et al. Intracellular degradation of two structurally different polyhydroxyalkanoic acids accumulated in Pseudomonas putida and Pseudomonas citronellolis from mixtures of octanoic acid and 5-phenylvaleric acid. Int J Biol Macromol. 2001 Dec 10;29(4-5):243-50. [Content Brief]
