1956
DOI: 10.1021/ja01604a075
|View full text |Cite
|
Sign up to set email alerts
|

The METABOLISM OF Β,γ-Dihydroxy-Β-Methylvaleric ACID BY LIVER HOMOGENATES

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
2
0

Year Published

1959
1959
2008
2008

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 59 publications
(2 citation statements)
references
References 0 publications
0
2
0
Order By: Relevance
“…Since it is now known that only one enantiomorph ofmevalonate is used, and that one-sixth of the radioactivity of this is lost on the way to cholesterol, the yield first reported was, indeed, slightly more than 100 per cent, but the excess would be within experimental error. Soon afterwards, Tavormina and Gibbs 19 showed that radioactivity in the carboxyl group of mevalonate was not incorporated at all into cholesterol, but lost as carbon dioxide during biosyn thesis. To all workers on polyisoprenoid biosynthesis, these discoveries came like an answer to prayer.…”
Section: Mevalonic Acidmentioning
confidence: 99%
“…Since it is now known that only one enantiomorph ofmevalonate is used, and that one-sixth of the radioactivity of this is lost on the way to cholesterol, the yield first reported was, indeed, slightly more than 100 per cent, but the excess would be within experimental error. Soon afterwards, Tavormina and Gibbs 19 showed that radioactivity in the carboxyl group of mevalonate was not incorporated at all into cholesterol, but lost as carbon dioxide during biosyn thesis. To all workers on polyisoprenoid biosynthesis, these discoveries came like an answer to prayer.…”
Section: Mevalonic Acidmentioning
confidence: 99%
“…The original trivial 4 3 rat liver homogenates. [2- 14 C]Mevalonolactone, (±)-2 14 C]bromoacetate 4 5 and found to 1,2 In 1957, [5][6][7] it the C 5 6 mevalonic acid.…”
mentioning
confidence: 99%