Fosmidomycin sodium salt - ≥95% , CAS No.66508-37-0

CAS: 66508-37-0 Cat. No.: F302004 Molecular Weight: 205.08
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Synonyms
FOSMIDOMYCIN MONOSODIUM SALT [MI] | AKOS030254266 | Fosmidomycin Sodium Salt | (3-(Formylhydroxyamino)propyl)phosphonic acid monosodium salt | DTXSID10216711 | Phosphonic acid, (3-(formylhydroxyamino)propyl)-, monosodium salt | Q27280957 | FR-31564 | sodi
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1mg
F302004-1mg
6
$91.90
5mg
F302004-5mg
5
$366.90
25mg
F302004-25mg
2
$1,099.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial drug, which is active against both Gram-negative and Gram-positive bacteria.

Fosmidomycin is a specific inhibitor of 1-deoxy-d-xylulose 5-phosphate reductoisomerase (DXP). Fosmidomycin is an antibiotic originally isolated from bacteria of the genus Streptomyces.
1-deoxy-d-xylulose 5-phosphate reductoisomerase is an enzyme that interconverts DXP and 2-C-methyl-D-erythritol 4-phosphate (MEP).
Fosmidomycin was active against both Gram-negative and Gram-positive bacteria and the human malarial parasite P. falciparum with the IC50 of 290-370 nM. Fosmidomycin inhibited 1-deoxy-d-xylulose 5-phosphate reductoisomerase in an alternative nonmevalonate pathway for terpenoid biosynthesis with IC50 of 8.2 nM. Fosmidomycin has been shown to possess activity against Plasmodium falciparum in vitro and in the mouse model. In patients with acute uncomplicated Plasmodium falciparum malaria, oral administration of 1,200 mg fosmidomycin every 8 h for 7 days was effective in curing uncomplicated Plasmodiumfalciparum malaria in humans. Fosmidomycin was an effective and safe antimalarial drug. The treatment was well tolerated and showed a fast parasite and fever clearance.

Specifications

Synonyms
FOSMIDOMYCIN MONOSODIUM SALT [MI] | AKOS030254266 | Fosmidomycin Sodium Salt | (3-(Formylhydroxyamino)propyl)phosphonic acid monosodium salt | DTXSID10216711 | Phosphonic acid, (3-(formylhydroxyamino)propyl)-, monosodium salt | Q27280957 | FR-31564 | sodi
Specifications & Purity
≥95%
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥95%
Names and Identifiers
Pubchem Sid488195110
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195110
Canonical SmilesC(CN(C=O)O)CP(=O)(O)[O-].[Na+]
IUPAC Namesodium;3-[formyl(hydroxy)amino]propyl-hydroxyphosphinate
InChIKeyZZPUYRHMTGOTEU-UHFFFAOYSA-M
INCHI1S/C4H10NO5P.Na/c6-4-5(7)2-1-3-11(8,9)10;/h4,7H,1-3H2,(H2,8,9,10);/q;+1/p-1
Isomeric SMILES C(CN(C=O)O)CP(=O)(O)[O-].[Na+]
Molecular Weight 205.08
Reaxy-Rn 4729075
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4729075&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassOrganic phosphonic acids and derivatives
SubclassOrganic phosphonic acids
Intermediate Tree Nodes Not available
Direct ParentOrganic phosphonic acids
Alternative Parents Hydroxamic acids  Organophosphorus compounds  Organonitrogen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Organic cations  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organophosphonic acid - Hydroxamic acid - Carboxylic acid derivative - Organic alkali metal salt - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic cation - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MTARC1 Tbio Mitochondrial amidoxime-reducing component 1 (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
dxr 1-deoxyxylulose-5-phosphate reductoisomerase (147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dxr 1-deoxy-D-xylulose 5-phosphate reductoisomerase (191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DXR 1-deoxy-D-xylulose 5-phosphate reductoisomerase, apicoplastic (44 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDateItem
E2310207Certificate of AnalysisFeb 04, 2026 F302004
E2310214Certificate of AnalysisFeb 04, 2026 F302004
E2310218Certificate of AnalysisFeb 04, 2026 F302004
E2310226Certificate of AnalysisFeb 04, 2026 F302004
E2231250Certificate of AnalysisMar 04, 2025 F302004
E2231463Certificate of AnalysisMar 04, 2025 F302004
E2310206Certificate of AnalysisOct 29, 2022 F302004
E2310223Certificate of AnalysisOct 29, 2022 F302004
E2231238Certificate of AnalysisMar 29, 2022 F302004
Chemical and Physical Properties
Solubility≤5mg/ml in PBS, pH 7.2
Molecular Weight205.080 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass205.012 Da
Monoisotopic Mass205.012 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count12
Formal Charge0
Complexity177.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Solution Calculators
Reviews

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