Сложные тиоэфиры
Sign in to savethumb|class=skin-invert-image|right|150px|General structure of a thioester, where R and R' are organyl groups, or H in the case of R. In organic chemistry, thioesters are organosulfur compounds with the molecular structure . They are analogous to carboxylate esters () with the sulfur in the thioester replacing oxygen in the carboxylate ester, as implied by the thio- prefix. They are the product of esterification of a carboxylic acid () with a thiol (). In biochemistry, the best-known thioesters are derivatives of coenzyme A, e.g., acetyl-CoA. The R and R' represent organyl groups, or H in the
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Wikidata facts
- Subclass of
- organosulfur compound
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- Commons category
- Thioesters
- topic's main category
- Category:Thioesters
- SMARTS notation
- [#6][#6](=[OX1])[#16][#6]
Sources (2)
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Article · Русский
Сложные тиоэфиры — органические соединения, содержащие функциональную группу C-S-CO-C и являющиеся сложными эфирами тиолов и карбоновых кислот. Сложные тиоэфиры играют важную роль в биохимических процессах, наиболее известный представитель этого класса — ацетил-CoA.
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