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Names | |
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IUPAC name
(9R,21S)-1-[(2R,3S,4R,5R)-5-
(6-amino-9H-purin-9-yl)-4-hydroxy- 3-(phosphonooxy)tetrahydrofuran-2-yl]- 3,5,9,21-tetrahydroxy-8,8,21-trimethyl- 10,14,19-trioxo-2,4,6-trioxa-18-thia- 11,15-diaza-3,5-diphosphatricosan-23- oic acid 3,5-dioxide |
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Identifiers | |
CAS Number
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3D model (JSmol)
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ChEBI |
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ChemSpider |
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ECHA InfoCard | 100.014.820 |
IUPHAR/BPS
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MeSH | HMG-CoA |
PubChem CID
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InChI
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SMILES
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Properties | |
Chemical formula
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C27H44N7O20P3S |
Molar mass | 911.661 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Y verify (what is YN ?) | |
Infobox references | |
HMG-CoA (or 3-hydroxy-3-methylglutaryl-coenzyme A) is an intermediate in the mevalonate and ketogenesis pathways. It is formed from acetyl CoA and acetoacetyl CoA by HMG-CoA synthase. The researches of Minor J. Coon and Bimal Kumar Bachhawat in the 1950s at University of Illinois led to its discovery.[1][2]
It is also an intermediate in the metabolism of leucine. Its immediate precursor is 3-methylglutaconyl CoA.
HMG-CoA reductase converts it into mevalonic acid.
HMG-CoA lyase breaks it into acetyl CoA and acetoacetate.
Cholesterol and steroid metabolic intermediates
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Mevalonate pathway |
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Non-mevalonate pathway |
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To Cholesterol |
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From Cholesterol (to steroids) |
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Steroid hormones |
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Nonhuman |
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Amino acid metabolism metabolic intermediates
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K→acetyl-CoA |
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G |
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Other |
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==参考
3-ヒドロキシ-3-メチルグルタリル補酵素A、3-ヒドロキシ-3-メチルグルタリルCoA
.