Date published: 2026-5-24

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Platencin (CAS 869898-86-2)

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Application:
Platencin is a potent antibiotic that targets FabF and FabH proteins
CAS Number:
869898-86-2
Purity:
>99%
Molecular Weight:
425.2
Molecular Formula:
C24H27NO6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Platencin, a natural product derived from Streptomyces platensis, has emerged as a significant compound in scientific research for its potent antibacterial activity and unique mechanism of action. Studies have explaind that Platencin targets bacterial fatty acid synthesis by inhibiting the enzyme FabF, also known as β-ketoacyl-acyl carrier protein synthase II (KAS II), which catalyzes the elongation of fatty acids in the bacterial cell membrane. By disrupting this essential metabolic pathway, Platencin interferes with bacterial membrane integrity and function, ultimately leading to bacterial cell death. Research has further explored the structural features of Platencin and its binding interactions with FabF, providing insights into its mechanism of action and potential for structure-based drug design. Additionally, Platencin has been investigated for its efficacy against various bacterial pathogens, including multidrug-resistant strains, highlighting its potential as a lead compound for the development of novel antibiotics. Furthermore, Platencin has served as a valuable tool in chemical biology research, facilitating the study of fatty acid metabolism and its implications for bacterial physiology and pathogenesis. Overall, Platencin represents a promising candidate for further exploration in antibacterial drug discovery and as a tool for investigating bacterial lipid metabolism.


Platencin (CAS 869898-86-2) References

  1. Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties.  |  Wang, J., et al. 2007. Proc Natl Acad Sci U S A. 104: 7612-6. PMID: 17456595
  2. Discovery and syntheses of 'superbug challengers'-platensimycin and platencin.  |  Palanichamy, K. and Kaliappan, KP. 2010. Chem Asian J. 5: 668-703. PMID: 20209576
  3. Syntheses and antibacterial properties of iso-platencin, Cl-iso-platencin and Cl-platencin: identification of a new lead structure.  |  Tiefenbacher, K., et al. 2010. Chemistry. 16: 9616-22. PMID: 20486112
  4. Stereoselective functionalization of platensimycin and platencin by sulfa-Michael/aldol reactions.  |  Qiu, L., et al. 2019. Org Biomol Chem. 17: 4261-4272. PMID: 30816397
  5. Structural characterization of β-ketoacyl ACP synthase I bound to platencin and fragment screening molecules at two substrate binding sites.  |  Patterson, EI., et al. 2020. Proteins. 88: 47-56. PMID: 31237717
  6. Characterization and Crystal Structure of a Nonheme Diiron Monooxygenase Involved in Platensimycin and Platencin Biosynthesis.  |  Dong, LB., et al. 2019. J Am Chem Soc. 141: 12406-12412. PMID: 31291107
  7. Novel Targets for Antimicrobials.  |  Gupta, S., et al. 2020. Turk J Pharm Sci. 17: 565-575. PMID: 33177939
  8. Semisynthesis and Biological Evaluation of Platencin Thioether Derivatives: Dual FabF and FabH Inhibitors against MRSA.  |  Li, Y., et al. 2021. ACS Med Chem Lett. 12: 433-442. PMID: 33738071
  9. Computational Study of the C5-Hydroxylation Mechanism Catalyzed by the Diiron Monooxygenase PtmU3 as Part of the Platensimycin Biosynthesis.  |  Zhang, S., et al. 2021. Inorg Chem. 60: 17783-17796. PMID: 34762413
  10. Development of platensimycin, platencin, and platensilin overproducers by biosynthetic pathway engineering and fermentation medium optimization.  |  Fluegel, LL., et al. 2024. J Ind Microbiol Biotechnol. 51: PMID: 38262768

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Platencin, 100 µg

sc-202291
100 µg
$612.00