Geranylgeranyl pyrophosphate: Difference between revisions

Geranylgeranyl pyrophosphate
Identifiers
CAS Number	6699-20-3;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:48861;
ChemSpider	394418 ;
MeSH	geranylgeranyl+pyrophosphate
PubChem CID	447277;
CompTox Dashboard (EPA)	DTXSID90863929 ;
	InChI InChI=1S/C20H36O7P2/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-26-29(24,25)27-28(21,22)23/h9,11,13,15H,6-8,10,12,14,16H2,1-5H3,(H,24,25)(H2,21,22,23)/b18-11+,19-13+,20-15+ Key: OINNEUNVOZHBOX-QIRCYJPOSA-N ; InChI=1/C20H36O7P2/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-26-29(24,25)27-28(21,22)23/h9,11,13,15H,6-8,10,12,14,16H2,1-5H3,(H,24,25)(H2,21,22,23)/b18-11+,19-13+,20-15+ Key: OINNEUNVOZHBOX-QIRCYJPOBR;
	SMILES O=P(O)(O)OP(=O)(O)OC/C=C(/CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)C)C;
Properties
Chemical formula	C20H36O7P2
Molar mass	450.443
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Revision as of 08:29, 9 August 2011

Geranylgeranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. In plants it is also the precursor to carotenoids, gibberellins, tocopherols, and chlorophylls.

It is also a precursor to geranylgeranylated proteins.

This biochemistry article is a stub. You can help Wikipedia by expanding it.

@@ Line 17: / Line 17: @@
 | CASNo = 6699-20-3
 |   PubChem = 447277
+|   ChEBI = 48861
-|   SMILES = O=P(O)(O)OP(=O)(O)OC/C=C(/CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)C)C
+| SMILES = O=P(O)(O)OP(=O)(O)OC/C=C(/CC\C=C(/C)CC\C=C(/C)CC\C=C(/C)C)C
 |   MeSHName = geranylgeranyl+pyrophosphate
   }}