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Fosmidomycin sodium salt hydrate

SIGMA/F8682 - ≥95% (NMR)

Synonym: (3-(Formylhydroxyamino)propyl)phosphonic acid sodium salt; (3-(N-Hydroxyformamido)propyl)phosphonic acid sodium salt; FR 31564

CAS Number: 66508-53-0 (free base)
Empirical Formula (Hill Notation): C4H10NO5P · xNa+ · yH2O
Molecular Weight: 183.10 (anhydrous free acid basis)
MDL Number: MFCD00865023
Linear Formula: C4H10NO5P · xNa+ · yH2O
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-F8682-5MG 5 mg
$229.00
1/EA
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45-F8682-25MG 25 mg
$883.00
1/EA
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assay ≥95% (NMR)
color white to beige
form powder
InChI 1S/C4H10NO5P/c6-4-5(7)2-1-3-11(8,9)10/h4,7H,1-3H2,(H2,8,9,10)
InChI key GJXWDTUCERCKIX-UHFFFAOYSA-N
Quality Level 100 
SMILES string [P](=O)(O)(O)CCCN(O)C=O
solubility H2O: 20 mg/mL, clear
storage condition desiccated
storage temp. −20°C
Application: Fosmidomycin sodium salt hydrate has been used as an inhibitor of 1-deoxy-D-xylulose 5-phosphate reductoisomerase in a study to determine monotropin carvacrol biosynthesis in Satureja khuzistanica plant.
Biochem/physiol Actions: Fosmidomycin is an inhibitor of 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) (MEP synthase): an antimalarial compound.
Biochem/physiol Actions: Fosmidomycin is an inhibitor of 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) (MEP synthase): an antimalarial compound. 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) is an enzyme involved in the first step in the nonmevalonate pathway for isoprenoid biosynthesis in Gram-negative, Gram-positive bacteria, plants, and the parasite causing the most virulent form of malaria, Plasmodium falciparum (Mammals produce isoprenoids via the mevalonate pathway).
Packaging: 5, 25 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95% (NMR)
Storage Temp. −20°C
UNSPSC 12352200

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