Mechanism of biosynthesis of squalene from sesquiterpenoids
✍ Scribed by J.W. Cornforth; G. Popják
- Publisher
- Elsevier Science
- Year
- 1959
- Tongue
- French
- Weight
- 292 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
ALTHOUGH farnesyl pyrophosphate (I) has been shown to produce squalene when incubated with yeast cell particles and reduced triphosphopyridine nucleotide, ' the detailed mechanism of this change is still unknown. The two hypotheses previously advanced 192 are incompatible with the new data2 obtained by using hydrogen isotopes to study the biosynthesis of squalene from mevalonic acid.
CH3 -C = CH -CH2 -CH2 -C -CR -CH2 -CH2 -C -CH -CH2 -0P206H3
We now propose an alternative scheme based on the discovery of acid-.
labile derivatives, presumably pyrophosphates, of both nerolidol and farnesol in a liver enzyme system after incubation with mevalonate.3
📜 SIMILAR VOLUMES
Tri¯uoromethyl ketones 1 and 2, have been prepared from trisnorsqualene aldehyde 3. These compounds and their corresponding alcohols 4 and 7 have been found to be good inhibitors of the biosynthesis of cholesterol in HepG2 cells. The inhibition is correlated with a decrease of the HMG-CoA reductase
Various squalene derivatives, including squalene, squalene 2,3-epoxide (monoepoxide, SQME), squalene 2,3;22,23diepoxide (SQDE), 2-aza-2,3-dihydrosqualene (SQN) and 2-aza-2,3-dihydrosqualene N-oxide (SQNO), were studied in chloroform solutions using ID high-resolution mH spectra and ~3C longitudinal