Date published: 2025-12-1

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Antibiotic Sch 725674 (CAS 877061-66-0)

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Application:
Antibiotic Sch 725674 is A self-germination inhibitor produced by Colletotrichum gloeosporioides
CAS Number:
877061-66-0
Molecular Weight:
328.0
Molecular Formula:
C18H32O5
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 Sch 725674, a novel antibacterial agent, has sparked significant interest in scientific research due to its unique mechanism of action and potential applications in microbiology and drug discovery. Mechanistically, Sch 725674 targets bacterial DNA gyrase, a crucial enzyme involved in DNA replication and transcription. By binding to the ATP-binding pocket of DNA gyrase, Sch 725674 disrupts its catalytic activity, leading to inhibition of DNA supercoiling and subsequent impairment of bacterial growth and replication. This mechanism distinguishes Sch 725674 from conventional antibiotics, offering promise for combating multidrug-resistant bacterial pathogens. In research, Sch 725674 has been instrumental in elucidating the structural and functional properties of DNA gyrase, providing insights into the molecular basis of antibacterial activity and bacterial resistance mechanisms. Moreover, its efficacy against a broad spectrum of bacterial species, including relevant pathogens such as Staphylococcus aureus and Streptococcus pneumoniae, underscores its potential as a valuable tool for studying bacterial physiology, pathogenesis, and antimicrobial resistance. Additionally, Sch 725674′s structural diversity and synthetic accessibility have positioned it as a lead compound in antibiotic discovery programs, driving efforts to develop novel antibacterial agents with improved potency, selectivity, and pharmacokinetic properties. Ongoing research endeavors continue to explore the potential of Sch 725674 and its derivatives, paving the way for innovative strategies to combat infectious diseases and address the global challenge of antibiotic resistance.


Antibiotic Sch 725674 (CAS 877061-66-0) References

  1. Structure elucidation of Sch 725674 from Aspergillus sp.  |  Yang, SW., et al. 2005. J Antibiot (Tokyo). 58: 535-8. PMID: 16266128
  2. Minimal fluorous tagging strategy that enables the synthesis of the complete stereoisomer library of SCH725674 macrolactones.  |  Moretti, JD., et al. 2012. J Am Chem Soc. 134: 7963-70. PMID: 22515682
  3. Enantiospecific total synthesis of macrolactone Sch 725674.  |  Bali, AK., et al. 2014. Org Lett. 16: 4001-3. PMID: 25033232
  4. An enantioselective total synthesis of Sch-725674.  |  Ramakrishna, K. and Kaliappan, KP. 2015. Org Biomol Chem. 13: 234-40. PMID: 25379975
  5. First Total Synthesis of Gliomasolide C and Formal Total Synthesis of Sch-725674.  |  Seetharamsingh, B., et al. 2016. J Org Chem. 81: 290-6. PMID: 26633579
  6. A Pot-Economical Approach to the Total Synthesis of Sch-725674.  |  Bodugam, M., et al. 2016. Org Lett. 18: 516-9. PMID: 26760683
  7. Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674.  |  Fawcett, A., et al. 2016. Angew Chem Int Ed Engl. 55: 14663-14667. PMID: 27781356
  8. Date Palm Trees Root-Derived Endophytes as Fungal Cell Factories for Diverse Bioactive Metabolites.  |  Ben Mefteh, F., et al. 2018. Int J Mol Sci. 19: PMID: 29986518
  9. Automated iterative Csp3-C bond formation.  |  Blair, DJ., et al. 2022. Nature. 604: 92-97. PMID: 35134814
  10. Enantioselective synthesis of macrolactone core of the natural product Sch725674  |  Sunnam, S. K. and Prasad, K. R. 2014. Tetrahedron. 70(12): 2096-2101.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Antibiotic Sch 725674, 1 mg

sc-362014
1 mg
$250.00