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FR-900098 monosodium salt_Molecular_structure_CAS_73226-73-0)
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FR-900098 monosodium salt

Catalog No. F8307 Name Sigma Aldrich
CAS Number 73226-73-0 Website http://www.sigmaaldrich.com
M. F. C5H11NNaO5P Telephone 1-800-521-8956
M. W. 219.108071 Fax
Purity ≥97% (NMR) Email
Storage desiccated Chembase ID: 154722

SYNONYMS

IUPAC name
sodium hydrogen [3-(N-hydroxyacetamido)propyl]phosphonate
IUPAC Traditional name
sodium hydrogen 3-(N-hydroxyacetamido)propylphosphonate
Synonyms
BRN 2096083
P-[3-(Acetylhydroxyamino)propyl]-phosphonic acid
(3-(Acetylhydroxyamino)propyl)-phosphonic acid

DATABASE IDS

MDL Number MFCD17215926
CAS Number 73226-73-0

PROPERTIES

Empirical Formula (Hill Notation) C5H11NNaO5P
Purity ≥97% (NMR)
Apperance yellow to orange powder
Solubility H2O: ≥20 mg/mL
MSDS Link Download
Storage Condition desiccated
Storage Condition protect from light
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
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). Inhibiton of the enzyme provides alternative to traditional antimalaria therapy. FR-900098 is twice more effective than fosmidomycin against various strains of P. falciparum in vitro and the closely related P. vinckei in mice.
Description (简体中文)
Biochem/physiol Actions
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). Inhibiton of the enzyme provides alternative to traditional antimalaria therapy. FR-900098 is twice more effective than fosmidomycin against various strains of P. falciparum in vitro and the closely related P. vinckei in mice.

REFERENCES