Date published: 2026-5-27

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Nodusmicin (CAS 76265-48-0)

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Application:
Nodusmicin is a potent antibiotic against aerobic and anaerobic bacteria
CAS Number:
76265-48-0
Purity:
≥99%
Molecular Weight:
422.51
Molecular Formula:
C23H34O7
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Nodusmicin, a member of the ansamycin antibiotic family, has been a subject of significant scientific research interest due to its distinctive mechanism of action and potential applications in various research fields. Mechanistically, nodusmicin exerts its antimicrobial activity by selectively inhibiting DNA gyrase, a key enzyme involved in bacterial DNA replication and transcription. By binding to the DNA gyrase enzyme-DNA complex, nodusmicin interferes with its catalytic activity, thereby preventing the supercoiling of bacterial DNA and inhibiting bacterial growth. This mechanism of action distinguishes nodusmicin from other antibiotics and renders it effective against a broad spectrum of gram-positive and gram-negative bacteria. In research, nodusmicin has been instrumental in elucidating the structural and functional properties of DNA gyrase, offering insights into the molecular mechanisms of antibiotic action and bacterial resistance. Moreover, nodusmicin has been utilized as a tool in microbiological studies to investigate DNA replication, transcription, and DNA-protein interactions. Additionally, nodusmicin and its derivatives have been explored for their potential applications in drug discovery programs targeting bacterial infections and antibiotic resistance. Ongoing research endeavors continue to explore the diverse research applications of nodusmicin, providing promising avenues for understanding bacterial biology and developing novel antimicrobial strategies.


Nodusmicin (CAS 76265-48-0) References

  1. Stereostructure of luminamicin, an anaerobic antibiotic, via molecular dynamics, NMR spectroscopy, and the modified Mosher method.  |  Gouda, H., et al. 2005. Proc Natl Acad Sci U S A. 102: 18286-91. PMID: 16344486
  2. Biosynthetic origin of the carbon skeleton and oxygen atoms of the LL-F28249 alpha, a potent antiparasitic macrolide.  |  Tsou, HR., et al. 1989. J Antibiot (Tokyo). 42: 398-406. PMID: 2708133
  3. The Nargenicin Family of Oxa-Bridged Macrolide Antibiotics.  |  Pidot, SJ. and Rizzacasa, MA. 2020. Chemistry. 26: 2780-2792. PMID: 31667915
  4. Coloradocin, an antibiotic from a new Actinoplanes. II. Identity with luminamicin and elucidation of structure.  |  Rasmussen, RR., et al. 1987. J Antibiot (Tokyo). 40: 1383-93. PMID: 3680004
  5. Synthesis of 18-deoxynargenicin A1 (antibiotic 367c) from nargenicin A1.  |  Magerlein, BJ. and Reid, RJ. 1982. J Antibiot (Tokyo). 35: 254-5. PMID: 7076571
  6. Studies of an intramolecular Diels-Alder approach to the nargenicins: involvement of boatlike transition states in the cyclizations of substituted 1, 7, 9-decatrien-3-ones  |  Coe, J. W. and Roush, W. R. 1989. The Journal of Organic Chemistry. 54(4): 915-930.
  7. Nargenicin biosynthesis. Incorporation of polyketide chain elongation intermediates and support for a proposed intramolecular Diels-Alder cyclization  |  Cane, D. E., et al. 1993. Journal of the American Chemical Society. 115(2): 527-535.
  8. Studies on the synthesis of nargenicin A1: Highly stereoselective synthesis of the complete carbon framework via the transannular diels− alder reaction of an 18-membered macrolide  |  Roush, W. R., et al. 1996. Journal of the American Chemical Society. 118(32): 7502-7512.
  9. Synthesis of the decalin subunit of coloradocin  |  Gössinger, E., et al. 2000. Tetrahedron. 56(14): 2007-2014.
  10. Formation of the compounds with an epoxychromene framework: role of the methoxy groups  |  Mikhalchenko, O. S.Korchagina, D. V. and Volcho, K. P.Salakhutdinov, N. F. 2014. Helvetica Chimica Acta. 97(10): 1406-1421.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Nodusmicin, 1 mg

sc-362771
1 mg
$208.00