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Fosmidomycin sodium salt - >95.0%, high purity , CAS No.66508-37-0

    Grade & Purity:
  • ≥95%
In stock
Item Number
F302004
Grouped product items
SKU Size
Availability
Price Qty
F302004-1mg
1mg
6
$33.90
F302004-5mg
5mg
5
$137.90
F302004-25mg
25mg
2
$543.90

Basic Description

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 Temp 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.
Product Description

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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Organic phosphonic acids and derivatives
Subclass Organic phosphonic acids
Intermediate Tree Nodes Not available
Direct Parent Organic phosphonic acids
Alternative Parents Hydroxamic acids  Organophosphorus compounds  Organonitrogen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Organic cations  
Molecular Framework Aliphatic 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
Description This compound belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid.
External Descriptors Not available

Associated Targets(Human)

Homo sapiens (32628 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MRC5 (9203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HeLa (62764 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MTARC1 Tbio Mitochondrial amidoxime-reducing component 1 (51 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

dxr 1-deoxyxylulose-5-phosphate reductoisomerase (147 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
dxr 1-deoxy-D-xylulose 5-phosphate reductoisomerase (191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DXR 1-deoxy-D-xylulose 5-phosphate reductoisomerase, apicoplastic (44 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488195110
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195110
IUPAC Name sodium;3-[formyl(hydroxy)amino]propyl-hydroxyphosphinate
INCHI InChI=1S/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
InChIKey ZZPUYRHMTGOTEU-UHFFFAOYSA-M
Smiles C(CN(C=O)O)CP(=O)(O)[O-].[Na+]
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=

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 Number Certificate Type Date Item
E2231250 Certificate of Analysis Mar 04, 2025 F302004
E2231463 Certificate of Analysis Mar 04, 2025 F302004
E2310206 Certificate of Analysis Oct 29, 2022 F302004
E2310223 Certificate of Analysis Oct 29, 2022 F302004
E2310226 Certificate of Analysis Oct 29, 2022 F302004
E2310218 Certificate of Analysis Oct 29, 2022 F302004
E2310207 Certificate of Analysis Oct 29, 2022 F302004
E2310214 Certificate of Analysis Oct 29, 2022 F302004
E2231238 Certificate of Analysis Mar 29, 2022 F302004

Chemical and Physical Properties

Solubility ≤5mg/ml in PBS, pH 7.2
Molecular Weight 205.080 g/mol
XLogP3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 4
Exact Mass 205.012 Da
Monoisotopic Mass 205.012 Da
Topological Polar Surface Area 101.000 Ų
Heavy Atom Count 12
Formal Charge 0
Complexity 177.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

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