Misplaced Pages

Benzoyl-CoA: Difference between revisions

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 00:25, 2 June 2011 editMystBot (talk | contribs)177,678 editsm r2.7.1) (robot Adding: fr:Benzoyl-coenzyme A← Previous edit Revision as of 17:59, 28 December 2011 edit undoDrphilharmonic (talk | contribs)6,066 editsNo edit summaryNext edit →
Line 30: Line 30:
'''Benzoyl-CoA''' is a molecule implied in the activity of the different enzymes ], ], ], ], ], ], ], ], ] and ]. '''Benzoyl-CoA''' is a molecule implied in the activity of the different enzymes ], ], ], ], ], ], ], ], ] and ].


It is a substrate in the formation of ]s in '']'' by ] condensing a molecule of benzoyl-CoA with three ] yielding to ]. This intermediate is subsequently converted by a ], a cytochrome P450 monooxygenase, leading to the formation of ]<ref></ref>. It is a substrate in the formation of ]s in '']'' by ], condensing a molecule of benzoyl-CoA with three ], yielding to ]. This intermediate is subsequently converted by a ], a cytochrome P450 monooxygenase, leading to the formation of ]<ref></ref>.


==References== ==References==

Revision as of 17:59, 28 December 2011

Benzoyl-Coenzyme A
Chemical structure of benzoyl-CoA
Chemical structure of benzoyl-CoA
Names
Other names benzoyl-S-CoA
S-Benzoate coenzyme A
Identifiers
CAS Number
PubChem CID
CompTox Dashboard (EPA)
Properties
Chemical formula C28H36N7O17P3S
Molar mass 867.60 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Benzoyl-CoA is a molecule implied in the activity of the different enzymes 4-hydroxybenzoyl-CoA reductase, benzoyl-CoA reductase, benzoyl-CoA 3-monooxygenase, benzoate-CoA ligase, 2alpha-hydroxytaxane 2-O-benzoyltransferase, anthranilate N-benzoyltransferase, biphenyl synthase, glycine N-benzoyltransferase, ornithine N-benzoyltransferase and phenylglyoxylate dehydrogenase (acylating).

It is a substrate in the formation of xanthonoids in Hypericum androsaemum by benzophenone synthase, condensing a molecule of benzoyl-CoA with three malonyl-CoA, yielding to 2,4,6-trihydroxybenzophenone. This intermediate is subsequently converted by a benzophenone 3′-hydroxylase, a cytochrome P450 monooxygenase, leading to the formation of 2,3′,4,6-tetrahydroxybenzophenone.

References

  1. Alternative pathways of xanthone biosynthesis in cell cultures of Hypericum androsaemum L. Werner Schmidt and Ludger Beerhues, FEBS Letters, Volume 420, Issues 2-3, 29 December 1997, Pages 143-146, doi:10.1016/S0014-5793(97)01507-X
Stub icon

This article about metabolism is a stub. You can help Misplaced Pages by expanding it.

Categories:
Benzoyl-CoA: Difference between revisions Add topic