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18629

Sigma-Aldrich

Isopentenyl phosphate dilithium salt

≥95.0% (TLC)

Sinonimo/i:

Dilithium isopentenylphosphate, Phosphoric acid mono-(3-methyl-3-butenyl ester) dilithium salt

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About This Item

Formula empirica (notazione di Hill):
C5H9Li2O4P
Numero CAS:
18687-42-8
Peso molecolare:
177.98
Beilstein:
4339123
Numero MDL:
MFCD17215949
Codice UNSPSC:
12352106
ID PubChem:
329751724
NACRES:
NA.25

Livello qualitativo

100

Saggio

≥95.0% (TLC)

Impurezze

≤10.0% water

Temperatura di conservazione

−20°C

Stringa SMILE

[Li+].[Li+].CC(=C)CCOP([O-])([O-])=O

InChI

1S/C5H11O4P.2Li/c1-5(2)3-4-9-10(6,7)8;;/h1,3-4H2,2H3,(H2,6,7,8);;/q;2*+1/p-2
ACAZFVVXIFTWMF-UHFFFAOYSA-L

Categorie correlate

Applicazioni

Isopentenyl phosphate may be used as a substrate to study the characteristics and kinetics of isopentenyl phosphate kinases.

Azioni biochim/fisiol

Isopentenyl monophosphate is phosphorylated into isopentenyl pyrophosphate at very low rates.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335

Classi di pericolo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCBT4347
BCBC1384V
BCBC1384

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Mark F Mabanglo et al.
Biochemistry, 51(4), 917-925 (2011-12-14)
Isopentenyl phosphate kinase (IPK) catalyzes the phosphorylation of isopentenyl phosphate to form the isoprenoid precursor isopentenyl diphosphate in the archaeal mevalonate pathway. This enzyme is highly homologous to fosfomycin kinase (FomA), an antibiotic resistance enzyme found in a few strains
C Donninger et al.
The Biochemical journal, 105(2), 545-547 (1967-11-01)
1. Isopentenol was converted into isopentenyl phosphate with phosphoryl chloride in ether containing pyridine. 2. The isopentenyl phosphate reacted in 2-methylpropan-2-ol-water with morpholine and dicyclohexylcarbodi-imide to give isopentenyl phosphoromorpholidate. 3. The isopentenyl phosphoromorpholidate, with inorganic phosphate in pyridine containing tributylamine
Mark F Mabanglo et al.
ACS chemical biology, 7(7), 1241-1246 (2012-04-27)
Isopentenyl phosphate kinase (IPK) catalyzes the ATP-dependent phosphorylation of isopentenyl phosphate (IP) to form isopentenyl diphosphate (IPP) during biosynthesis of isoprenoid metabolites in Archaea. The structure of IPK from the archeaon Thermoplasma acidophilum (THA) was recently reported and guided the
Mo Chen et al.
Biochemistry, 49(1), 207-217 (2009-11-26)
Archaea synthesize isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), the essential building blocks of isoprenoid compounds, from mevalonate (MVA). However, an analysis of the genomes of several members of the Archaea failed to identify genes for the enzymes required to
Nikki Dellas et al.
ACS chemical biology, 5(6), 589-601 (2010-04-16)
The biosynthesis of isopentenyl diphosphate (IPP) from either the mevalonate (MVA) or the 1-deoxy-d-xylulose 5-phosphate (DXP) pathway provides the key metabolite for primary and secondary isoprenoid biosynthesis. Isoprenoid metabolism plays crucial roles in membrane stability, steroid biosynthesis, vitamin production, protein

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