Geranylgeranyl

Geranylgeranyl pyrophosphate

Names
IUPAC name (2E,4E,6E)-3,5,7,11-Tetramethyldodeca-2,4,6,10-tetraene-1-pyrrophosphate
Identifiers
CAS Number	6699-20-3 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:48861 Y
ChemSpider	394418 Y
IUPHAR/BPS	3052
MeSH	geranylgeranyl+pyrophosphate
PubChem CID	447277
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+ Y Key: OINNEUNVOZHBOX-QIRCYJPOSA-N Y 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	450.45 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

Geranylgeranyl pyrophosphate is an intermediate in the biosynthesis of some terpenes and terpenoids. In plants it is also the precursor to carotenoids, gibberellins, , and chlorophylls.

It is also a precursor to geranylgeranylated proteins, which is its primary use in human cells.

In Drosophila, geranylgeranyl pyrophosphate is synthesised by HMG-CoA encoded by the Columbus gene. Geranylgeranyl pyrophosphate is utilised as a chemoattractant for migrating germ cells that have traversed the midgut epithelia. The attractant signal is produced at the gonadal precursors, directing the germ cells to these sites, where they will differentiate into ova (eggs) and spermatozoa (sperm).