Isopentenyl pyrophosphate
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Ball-and-stick model of IPP | |
Names | |
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IUPAC name
(hydroxy-(3-methylbut-3-enoxy) phosphoryl)oxyphosphonic acid
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Identifiers | |
358-71-4 ![]() |
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ChEBI | CHEBI:128769 ![]() |
ChemSpider | 13115335 ![]() |
Jmol 3D model | Interactive image |
MeSH | isopentenyl+pyrophosphate |
PubChem | 15983957 |
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Properties | |
C5H12O7P2 | |
Molar mass | 246.092 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Isopentenyl pyrophosphate (IPP, isopentenyl diphosphate, or IDP)[1] is an intermediate in the classical, HMG-CoA reductase pathway (commonly called the mevalonate pathway), and is used by organisms in the biosynthesis of terpenes and terpenoids. IPP is formed from acetyl-CoA via the mevalonate pathway (the "upstream" part), and then is isomerized to dimethylallyl pyrophosphate by the enzyme isopentenyl pyrophosphate isomerase.[2]
![](/w/images/thumb/1/18/Sterol_synthesis.svg/350px-Sterol_synthesis.svg.png)
IPP can be synthesized via the alternative, non-mevalonate pathway of isoprenoid biosynthesis instead, where it is formed from (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate (HMB-PP) by the enzyme HMB-PP reductase (LytB, IspH). The non-mevalonate pathway is utilized by many bacteria, apicomplexan protozoa such as malaria parasites, and the plastids of higher plants.[3]
See also
References
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- ↑ http://pubs.rsc.org/en/Content/ArticleLanding/2014/NP/C3NP70124G#!divAbstract
- ↑ Chang, Wei-chen; Song, Heng; Liu, Hung-wen; Liu, Pinghua "Current development in isoprenoid precursor biosynthesis and regulation" Current Opinion in Chemical Biology, 2013 volume 17, pp. 571-579. doi:10.1016/j.cbpa.2013.06.020
- ↑ Lua error in package.lua at line 80: module 'strict' not found.