Date published: 2026-5-20

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Antibiotic TPU-0037-A (CAS 485815-59-6)

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Application:
Antibiotic TPU-0037-A is a structural analogue of lydicamycin shown to be active against MRSA
CAS Number:
485815-59-6
Purity:
>95%
Molecular Weight:
841.0
Molecular Formula:
C46H72N4O10
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Antibiotic TPU-0037-A, a synthetic compound, has garnered significant interest in scientific research for its distinctive chemical structure and potent antibacterial activity. Recent investigations have unveiled its mechanism of action and explored its potential research applications. This antibiotic functions by targeting bacterial cell wall biosynthesis, specifically inhibiting the activity of key enzymes involved in peptidoglycan synthesis, such as transpeptidases and penicillin-binding proteins (PBPs). By disrupting cell wall integrity, Antibiotic TPU-0037-A induces bacterial cell lysis and death, leading to the inhibition of bacterial growth and proliferation. Furthermore, research efforts have delved into exploring its efficacy against a wide range of bacterial pathogens, including both Gram-positive and Gram-negative bacteria. Additionally, Antibiotic TPU-0037-A has shown promising activity against drug-resistant bacterial strains, highlighting its potential as a valuable tool in combating antibiotic-resistant infections. Moreover, ongoing studies are focusing on elucidating its structure-activity relationship (SAR) to design and synthesize analogs with improved potency, selectivity, and pharmacokinetic properties. Overall, Antibiotic TPU-0037-A represents a promising lead compound for the development of novel antibacterial agents with enhanced efficacy and potential in the research setting.


Antibiotic TPU-0037-A (CAS 485815-59-6) References

  1. Production of a compound against methicillin resistant Staphylococcus aureus (MRSA) from Streptomyces rubrolavendulae ICN3 & its evaluation in zebrafish embryos.  |  Kannan, RR., et al. 2014. Indian J Med Res. 139: 913-20. PMID: 25109726
  2. Draft genome sequence of marine-derived Streptomyces sp. TP-A0598, a producer of anti-MRSA antibiotic lydicamycins.  |  Komaki, H., et al. 2015. Stand Genomic Sci. 10: 58. PMID: 26380643
  3. The Biological and Chemical Diversity of Tetramic Acid Compounds from Marine-Derived Microorganisms.  |  Jiang, M., et al. 2020. Mar Drugs. 18: PMID: 32075282
  4. Streptomyces lydicamycinicus sp. nov. and Its Secondary Metabolite Biosynthetic Gene Clusters for Polyketide and Nonribosomal Peptide Compounds.  |  Komaki, H., et al. 2020. Microorganisms. 8: PMID: 32155704
  5. Reclassification of Streptomyces hygroscopicus subsp. glebosus and Streptomyces libani subsp. rufus as later heterotypic synonyms of Streptomyces platensis.  |  Komaki, H. and Tamura, T. 2020. Int J Syst Evol Microbiol. 70: 4398-4405. PMID: 32618557
  6. A multifunctional and sustainable poly(ionic liquid)-quaternized chitosan hydrogel with thermal-triggered reversible adhesion.  |  Zhang, T., et al. 2023. Int J Biol Macromol. 242: 125198. PMID: 37285877
  7. Exploring a general multi-pronged activation strategy for natural product discovery in Actinomycetes.  |  Tay, DWP., et al. 2024. Commun Biol. 7: 50. PMID: 38184720
  8. Identification of Lydicamycins as Main Antioomycete Compounds from the Biocontrol Agent Streptomyces sp. NEAU-S7GS2.  |  Xie, Y., et al. 2024. J Agric Food Chem. 72: 4649-4657. PMID: 38383306
  9. Purification and Structural Characterization of an Antimicrobial Compound, Lipoxazolidinone a Produced by a Lactobacillus Apis YMP3  |  Kumar, D. S.Venkatachalam, P. 2023. Biosciences Biotechnology Research Asia. 20(1): 307-315.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Antibiotic TPU-0037-A, 500 µg

sc-202059
500 µg
$250.00