Date published: 2026-5-13

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Fosmidomycin Sodium Salt (CAS 66508-37-0)

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Alternate Names:
3-(N-Formyl-N-hydroxyamino)propyl Phosphonic Acid Sodium Salt
Application:
Fosmidomycin Sodium Salt is a gram-negative and gram-positive antibiotic
CAS Number:
66508-37-0
Purity:
≥90%
Molecular Weight:
205.08
Molecular Formula:
C4H9NNaO5P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Fosmidomycin Sodium Salt, carrying the CAS number 66508-37-0, is a derivative of fosmidomycin, a phosphonic acid antibiotic that has been extensively utilized in biochemical research for its unique mode of action against the enzyme 1-deoxy-D-xylulose 5-phosphate (DXP) reductoisomerase. This enzyme is a key component in the non-mevalonate pathway of isoprenoid biosynthesis, which is crucial for the production of terpenoids and isoprenoids in various bacteria and plants. Fosmidomycin Sodium Salt inhibits DXP reductoisomerase by mimicking the natural substrate of the enzyme, thereby blocking the pathway and disrupting the synthesis of essential metabolites derived from isoprenoids. This specific inhibition has made it a valuable tool in the study of the non-mevalonate pathway, providing insights into a critical metabolic route that differs from the mevalonate pathway found in humans and other higher organisms. Researchers employ Fosmidomycin Sodium Salt to explore the fundamental aspects of this pathway, investigating its role in cellular metabolism and the potential effects of its disruption. Such studies are pivotal in understanding metabolic diversity and the evolutionary aspects of metabolic pathways. Additionally, the use of this chemical in research aids in examining how organisms adapt to the inhibition of crucial biosynthetic pathways and can shed light on potential targets for controlling harmful bacterial growth.


Fosmidomycin Sodium Salt (CAS 66508-37-0) References

  1. Induction of de novo volatile terpene biosynthesis via cytosolic and plastidial pathways by methyl jasmonate in foliage of Vitis vinifera L.  |  Hampel, D., et al. 2005. J Agric Food Chem. 53: 2652-7. PMID: 15796607
  2. Biosynthesis of mono- and sesquiterpenes in strawberry fruits and foliage: 2H labeling studies.  |  Hampel, D., et al. 2006. J Agric Food Chem. 54: 1473-8. PMID: 16478276
  3. Effects of fosmidomycin on plant photosynthesis as measured by gas exchange and chlorophyll fluorescence.  |  Possell, M., et al. 2010. Photosynth Res. 104: 49-59. PMID: 19915954
  4. The isolation and characterization of the vitamin D-binding protein from rat serum.  |  Bouillon, R., et al. 1978. J Biol Chem. 253: 4426-31. PMID: 207701
  5. Different roles of the mevalonate and methylerythritol phosphate pathways in cell growth and tanshinone production of Salvia miltiorrhiza hairy roots.  |  Yang, D., et al. 2012. PLoS One. 7: e46797. PMID: 23209548
  6. Involvement of abscisic acid and salicylic acid in signal cascade regulating bacterial endophyte-induced volatile oil biosynthesis in plantlets of Atractylodes lancea.  |  Wang, XM., et al. 2015. Physiol Plant. 153: 30-42. PMID: 24862990
  7. Inhibition of bacterial isoprenoid synthesis by fosmidomycin, a phosphonic acid-containing antibiotic.  |  Shigi, Y. 1989. J Antimicrob Chemother. 24: 131-45. PMID: 2676937
  8. Isoprenoid alcohols utilization by malaria parasites.  |  Bofill Verdaguer, I., et al. 2022. Front Chem. 10: 1035548. PMID: 36531309
  9. In vitro and in vivo antibacterial activity of FR-31564, a phosphonic acid antimicrobial agent.  |  Neu, HC. and Kamimura, T. 1981. Antimicrob Agents Chemother. 19: 1013-23. PMID: 7271270
  10. Antibiotic-modified ionic liquids-assisted preparation of biomedical silver NPs with antibacterial, anti-colon cancer, antioxidant, cytotoxicity, and antifungal activity.  |  Amasha and Reda Hassan Huseen, et al. 2023. Inorganic Chemistry Communications. 149: 110375.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Fosmidomycin Sodium Salt, 10 mg

sc-207701
10 mg
$700.00