Date published: 2026-5-20

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Iclaprim (CAS 192314-93-5)

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Application:
Iclaprim is a compound with antibacterial properties
CAS Number:
192314-93-5
Molecular Weight:
354.40
Molecular Formula:
C19H22N4O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Iclaprim, bearing the CAS number 192314-93-5, is a diaminopyrimidine antibiotic that has been actively employed in research to explore its unique mechanism of action and its potential role in combating bacterial growth through inhibition of folate metabolism. Specifically, Iclaprim functions by selectively inhibiting bacterial dihydrofolate reductase (DHFR), an enzyme critical for the thymidine and purine synthesis necessary for DNA replication and cell division. This inhibition disrupts the folate cycle, thereby preventing the bacteria from synthesizing the DNA, RNA, and proteins essential for their growth and multiplication. Iclaprim′s high affinity for bacterial DHFR, compared to its affinity for mammalian DHFR, makes it a particularly interesting subject in the study of selective toxicity and bacterial resistance mechanisms. In research contexts, Iclaprim has been notably useful in detailed studies of bacterial resistance development, particularly in how mutations in the DHFR gene may confer resistance to dihydrofolate reductase inhibitors. Additionally, due to its unique mechanism and potent activity against a wide range of Gram-positive pathogens, Iclaprim has been utilized in studies aiming to understand cross-resistance patterns with other antibiotics and in investigations of synergistic effects when used in combination with other antimicrobial agents. These research efforts contribute significantly to the broader scientific understanding of microbial pathogenesis and resistance.


Iclaprim (CAS 192314-93-5) References

  1. Efficacy evaluation of iclaprim in a neutropenic rat lung infection model with methicillin-resistant Staphylococcus aureus entrapped in alginate microspheres.  |  Huang, DB., et al. 2018. Eur J Clin Microbiol Infect Dis. 37: 673-678. PMID: 29222698
  2. Surveillance of iclaprim activity: In vitro susceptibility of gram-positive pathogens collected from 2012 to 2014 from the United States, Asia Pacific, Latin American and Europe.  |  Huang, DB., et al. 2018. Diagn Microbiol Infect Dis. 90: 329-334. PMID: 29306582
  3. Surveillance of iclaprim activity: in vitro susceptibility of Gram-positive skin infection pathogens collected from 2015 to 2016 from North America and Europe.  |  Huang, DB., et al. 2019. Diagn Microbiol Infect Dis. 93: 154-158. PMID: 30266399
  4. Iclaprim activity against wild-type and corresponding thymidine kinase-deficient Staphylococcus aureus in a mouse protection model.  |  Huang, DB., et al. 2019. Eur J Clin Microbiol Infect Dis. 38: 409-412. PMID: 30483998
  5. The effects of iclaprim on exotoxin production in methicillin-resistant and vancomycin-intermediate Staphylococcus aureus.  |  Bryant, AE., et al. 2019. J Med Microbiol. 68: 456-466. PMID: 30676310
  6. Worldwide surveillance of Iclaprim activity: In Vitro susceptibility of gram-positive pathogens collected from patients with skin and skin structure infections from 2013 to 2017.  |  Huang, DB., et al. 2020. Diagn Microbiol Infect Dis. 97: 115013. PMID: 32081524
  7. Evaluation of in vitro activity of iclaprim in combination with other antimicrobials against pulmonary pathogens: a pilot study.  |  Huang, DB., et al. 2019. Access Microbiol. 1: e000027. PMID: 32974519
  8. In vitro activity of iclaprim and comparator agents against Listeria monocytogenes clinical isolates from 2012 to 2018.  |  Huang, DB., et al. 2021. J Glob Antimicrob Resist. 25: 14-17. PMID: 33662644
  9. Iclaprim mesylate displaying a hydrogen-bonded mol-ecular tape.  |  Neuner, S., et al. 2023. Acta Crystallogr E Crystallogr Commun. 79: 24-27. PMID: 36628360

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Iclaprim, 25 mg

sc-215166
25 mg
$10000.00