Weight | 130.143 g/mol |
---|---|
Formula | C6H10O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
DL-Mevalonic acid lactone (674-26-0)
mevalonolactone · mevalonic acid lactone · mevalonolactone, (+-)-isomer
Score:
#2523 in Biochemistry
,
#6293 in Chemistry
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- Mevalonolactone inhibits the rate of synthesis and enhances the rate of degradation of 3-hydroxy-3-methylglutaryl coenzyme A reductase in rat hepatocytes. (Journal of Biological Chemistry, 1983)
- Chloroperoxidase as Enantioselective Epoxidation Catalyst: An Efficient Synthesis of (R)-(-)-Mevalonolactone. (Journal of Organic Chemistry, 1996)
- Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof (1988)
- Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (Journal of the American Chemical Society, 1981)
- Cholesterol biosynthesis inhibiting pyrazole analogs of mevalonolactone and its derivatives (1985)
- OnePot Synthesis of Novel Branched Polylactide Through the Copolymerization of Lactide with Mevalonolactone (Macromolecular Rapid Communications, 2001)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - mevalonolactone
- mevalonic acid lactone
- mevalonolactone, (+-)-isomer
- mevalonolactone, (R)-isomer
- mevalonolactone, 3-(14)C-labeled
- mevalonolactone, (S)-isomer
-
SMILESCC1(CCOC(=O)C1)O
-
InChIKeyJYVXNLLUYHCIIH-UHFFFAOYSA-N
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