Mevalonate: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>David E. Volk
mNo edit summary
mNo edit summary
 
(One intermediate revision by one other user not shown)
Line 5: Line 5:




[[Image:Mevalonate synthesis.jpg|left|thumb|250px|{{#ifexist:Template:Mevalonate synthesis.jpg/credit|{{Mevalonate synthesis.jpg/credit}}<br/>|}}Biosynthesis of mevalonate from HMG CoA.]]
{{Image|Mevalonate synthesis.jpg|left|250px|Biosynthesis of mevalonate from HMG CoA.}}


Its IUPAC chemical name is (3R)-3,5-dihydroxy-3-methylpentanoic acid and its chemical formula is C<sub>6</sub>H<sub>12</sub>O<small>4</small> in the protonated state.
Its IUPAC chemical name is (3R)-3,5-dihydroxy-3-methylpentanoic acid and its chemical formula is C<sub>6</sub>H<sub>12</sub>O<small>4</small> in the protonated state.[[Category:Suggestion Bot Tag]]

Latest revision as of 11:01, 18 September 2024

This article is developing and not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.
Mevalonate.

Mevalonate is a key chemical precursor in the biosynthesis of cholesterol. The statin drugs used to lower cholesterol are HMG-CoA reductase inhibitors that work by inhibiting the synthesis of mevalonate from the reduction of 3-hydroxy-3-methyl-glutaryl CoA (HMG-CoA).


(CC) Image: David E. Volk
Biosynthesis of mevalonate from HMG CoA.

Its IUPAC chemical name is (3R)-3,5-dihydroxy-3-methylpentanoic acid and its chemical formula is C6H12O4 in the protonated state.