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A propos de cet article
Formule empirique (notation de Hill) :
C10H20O7P2 · xLi+
Numéro CAS:
Poids moléculaire :
314.21 (free acid basis)
MDL number:
UNSPSC Code:
85151701
NACRES:
NA.25
Beilstein/REAXYS Number:
1915690
Assay:
≥95.0% (TLC)
Form:
powder
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Laissez-nous vous aiderBiochem/physiol Actions
Metabolite in monoterpenoid biosynthesis, substrate for monoterpene synthases.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
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Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
V G Ladygin
Zhurnal obshchei biologii, 63(4), 299-325 (2002-09-27)
The author discusses the current state of biochemical and genetic aspects of carotenoid biosynthesis in chloroplasts of algae and higher plants. Two ways of biosynthesis of key C5-isoperene units have been considered: 1) from acetate (C2) via mevalonic acid (C6)
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
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 76532-10MG | 04061832405186 |
| 76532-50MG | 04061832405193 |