Structured Summary
Abstract
A reagent that is highly selective for the modification of arginyl residues. It is used to selectively inhibit various enzymes and acts as an energy transfer inhibitor in photophosphorylation.
Chemical Identity
Chemical Information
- Molecular Formula
- C8H6O2
- Molecular Weight
- 134.13 g/mol
- CAS Registry No.
- 1074-12-0
- IUPAC Name
- 2-oxo-2-phenylacetaldehyde
- InChIKey
- OJUGVDODNPJEEC-UHFFFAOYSA-N
- SMILES
- C1=CC=C(C=C1)C(=O)C=O
- MeSH Unique ID
- D010658
- Source
- PubChem CID 14090
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
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Drug Class
Pharmacological Action
MeSH Record
Aspects Covered
19 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analogs & derivatives, analysis, chemical synthesis, chemistry, classification, economics, history, isolation & purification, metabolism, pharmacokinetics, pharmacology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity.
MeSH Record
History Note
91(80); was see under ALDEHYDES 1980-90
MeSH Record
Previous Indexing
- Aldehydes (1966-1972)
- Glyoxal (1973-1974) /AA (1975-1979)
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. Phenylglyoxal. Medical Subject Headings (MeSH). 2026. Unique ID D010658. http://id.nlm.nih.gov/mesh/2026/D010658
- Phenylglyoxal. In: Wikipedia. https://en.wikipedia.org/wiki/Phenylglyoxal
- Phenylglyoxal. In: Wikidata. https://www.wikidata.org/wiki/Q5934181
- Phenylglyoxal. In: PubChem Compound. CID 14090. https://pubchem.ncbi.nlm.nih.gov/compound/14090