Biosynthesis of 3-hydroxy-3-methylglutaryl-CoA, 3-hydroxy-3-ethylglutaryl-CoA, mevalonate and homomevalonate by insect corpus allatum and mammalian hepatic tissues
- 1 May 1981
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism
- Vol. 664 (2) , 356-372
- https://doi.org/10.1016/0005-2760(81)90058-8
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Absolute configuration of homomevalonate and 3-hydroxy-3-ethylglutaryl- and 3-hydroxy-3-methylglutaryl CoA, produced by cell-free extracts of insect corpora allata; cautionary note on prediction of absolute stereochemistry based on liquid chromatographic elution order of diastereomeric derivativesJournal of the American Chemical Society, 1979
- Influence of a naturally occurring competing enzymic activity on studies of 3-hydroxy-3-methylglutaryl coenzyme a reductase activityBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1979
- Biosynthesis of juvenile hormone in thececropia moth. labelling pattern from 1-[14C]-propionate through degradation to single carbon atom derivativesHelvetica Chimica Acta, 1975
- Juvenile hormone production by corpora allta of Tenebrio molitor in vitroLife Sciences, 1975
- The identification and biosynthesis of two juvenile hormones from the tobacco budworm moth (Heliothis virescens)Life Sciences, 1975
- Biosynthesis of the homosesquiterpenoid juvenile hormone JH II [methyl (2E,6E,10Z)-10,11 -epoxy-3,7,11-trimethyltridecadienoate] from [5-3H]homomevalonate in Manduca sextaJournal of the Chemical Society, Chemical Communications, 1975
- Substrate Stereochemistry of 3‐Hydroxy‐3‐Methylglutaryl‐Coenzyme A SynthaseEuropean Journal of Biochemistry, 1974
- A High-yield Synthesis ofdl-MevalonolactoneSynthesis, 1974
- Chemical structure and absolute configuration of a juvenile hormone from grasshopper corpora allata in vitroLife Sciences, 1973
- The Isolation of β-Hydroxy-β-methylglutaric Acid from the Seed of Flax (Linum usitatissimum)1Journal of the American Chemical Society, 1954