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Sigma-Aldrich

Geranyl pyrophosphate lithium salt

≥95.0% (TLC)

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Synonym(s):
(E)-3,7-Dimethyl-2,6-octadien-1-ol trihydrogen pyrophosphate lithium salt, (E)-3,7-Dimethyl-2,6-octadien-1-yl pyrophosphate lithium salt, GPP-Li
Empirical Formula (Hill Notation):
C10H20O7P2 · xLi+
CAS Number:
21141-43-5
Molecular Weight:
314.21 (free acid basis)
Beilstein:
1915690
NACRES:
NA.25

Assay

≥95.0% (TLC)

form

powder

storage temp.

−20°C

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Related Categories

Biochem/physiol Actions

Metabolite in monoterpenoid biosynthesis, substrate for monoterpene synthases.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Charles Burke et al.
The Journal of biological chemistry, 277(5), 3141-3149 (2001-12-26)
Geranyl diphosphate synthase belongs to a subgroup of prenyltransferases, including farnesyl diphosphate synthase and geranylgeranyl diphosphate synthase, that catalyzes the specific formation, from C(5) units, of the respective C(10), C(15), and C(20) precursors of monoterpenes, sesquiterpenes, and diterpenes. Unlike farnesyl
Orapin Ariyawutthiphan et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 11), 1558-1569 (2012-10-24)
In the typical isoprenoid-biosynthesis pathway, condensation of the universal C(5)-unit precursors isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) occurs via the common intermediates prenyl pyrophosphates (C(10)-C(20)). The diversity of isoprenoids reflects differences in chain length, cyclization and further additional modification
Sarah A Holstein et al.
Lipids, 39(4), 293-309 (2004-09-11)
The isoprenoid biosynthetic pathway is the source of a wide array of products. The pathway has been highly conserved throughout evolution, and isoprenoids are some of the most ancient biomolecules ever identified, playing key roles in many life forms. In
F Pont et al.
Analytical chemistry, 73(15), 3562-3569 (2001-08-21)
New phosphorylated microbial metabolites referred to as phosphoantigens activate immune responses in humans. Although these molecules have leading applications in medical research, no direct method allows their rapid and unambiguous structural identification. Here, we interfaced online HPAEC (high performance anion-exchange
Ravi S Singh et al.
BMC molecular biology, 11, 88-88 (2010-11-26)
Geranyl pyrophosphate (GPP) and p-hydroxybenzoate (PHB) are the basic precursors involved in shikonins biosynthesis. GPP is derived from mevalonate (MVA) and/or 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway(s), depending upon the metabolite and the plant system under consideration. PHB, however, is synthesized by
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