1189708-92-6
Chemical Structure
2-Phenylbutyric acid-d5
- CAS. Nr.: 1189708-92-6
- Formula:C10H7D5O2
- Molecular Weight:169.23
IUPAC Name: (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol-2-13C
InChIKey: OFJWFSNDPCAWDK-ZBJDZAJPSA-N
SMILES: OC(C(C1=CC=CC=C1)C([2H])([2H])C([2H])([2H])[2H])=O
Biological Activity: 2-Phenylbutyric acid-d5 is the deuterated-labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma[1][2][3].
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2-Phenylbutyric acid-d5 | 2-Phenylbutyric acid-d5 is the deuterated-labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | |||||||||||||||||||||
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2-Phenylbutanoic acid (Standard) | ≥98% | 2-Phenylbutanoic acid (Standard) is the analytical standard of 2-Phenylbutanoic acid (HY-W017194). This product is intended for research and analytical applications. 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | ||||||||||||||||||||
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2-Phenylbutanoic acid-d3 | 2-Phenylbutanoic acid-d3 is the deuterated-labeled 2-Phenylbutanoic acid (HY-W017194). 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | |||||||||||||||||||||
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2-Phenylbutanoic acid | 99.90% | 2-Phenylbutanoic acid is a sterically hindered carboxylic acid. 2-Phenylbutanoic acid exhibits anticancer activity through molecular docking interactions with cytochrome P450 proteins. 2-Phenylbutanoic acid can be used in research on malignant lymphoma. | ||||||||||||||||||||
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References
- [1]. Cavallaro PA, et al. Titanium Tetrachloride-Assisted Direct Esterification of Carboxylic Acids. Molecules (Basel, Switzerland). 2024 Feb 08;29(4):777.
- [2]. Kodama K, et al. Application of threo-2-amino-1,2-diphenylethanol as a Resolving Agent for Racemic Carboxylic Acids via Diastereomeric Salt Formation. Chirality. 2026 Sep;38(9):e70149.
- [3]. Raajaraman BR, et al. Influence of acetyl, hydroxy and methyl functional groups on 2‑phenylbutanoic acid by quantum computational, spectroscopic and ligand‑protein docking studies. J Mol Struct. 2019;1188:99‑109.
