Date published: 2026-5-7

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Hormaomycin (CAS 92092-69-8)

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CAS Number:
92092-69-8
Purity:
≥98%
Molecular Weight:
1129.7
Molecular Formula:
C55H69N10O14Cl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Hormaomycin exhibits a unique mechanism of action; it interferes with bacterial communication systems, particularly those involving quorum sensing, which bacteria use to regulate gene expression in response to population density. By modulating these signaling pathways, Hormaomycin affects various bacterial behaviors, including biofilm formation and sporulation. Studies have employed techniques like gene expression analysis and microbial culture assays to investigate these effects in detail, providing insights into how Hormaomycin influences microbial community dynamics. Additionally, Hormaomycin has been studied for its ability to inhibit bacterial proteases, enzymes that play crucial roles in protein degradation and processing. This inhibition is significant because it potentially disrupts normal bacterial metabolism and physiology. Research in this area typically involves enzymatic assays and inhibitor studies to explain the interaction between Hormaomycin and target enzymes. The compound′s role in promoting the production of secondary metabolites in producing organisms has also been a subject of investigation. This involves exploring how Hormaomycin triggers chemical defense mechanisms within Streptomyces, which may be crucial for competitive interactions within microbial communities.


Hormaomycin (CAS 92092-69-8) References

  1. First total synthesis of hormaomycin, a naturally occurring depsipeptide with interesting biological activities.  |  Zlatopolskiy, BD. and de Meijere, A. 2004. Chemistry. 10: 4718-27. PMID: 15372657
  2. The structure of hormaomycin and one of its all-peptide aza-analogues in solution: syntheses and biological activities of new hormaomycin analogues.  |  Reinscheid, UM., et al. 2005. Chemistry. 11: 2929-45. PMID: 15754385
  3. Effect of the solvent on the conformation of a depsipeptide: NMR-derived solution structure of hormaomycin in DMSO from residual dipolar couplings in a novel DMSO-compatible alignment medium.  |  Reinscheid, UM., et al. 2006. Chembiochem. 7: 287-96. PMID: 16416488
  4. Use of a halogenase of hormaomycin biosynthesis for formation of new clorobiocin analogues with 5-chloropyrrole moieties.  |  Heide, L., et al. 2008. Chembiochem. 9: 1992-9. PMID: 18655076
  5. Formal synthesis of belactosin A and hormaomycin via a diastereoselective intramolecular cyclopropanation of an alpha-nitro diazoester.  |  Vanier, SF., et al. 2010. Org Lett. 12: 672-5. PMID: 20055454
  6. Insights into the biosynthesis of hormaomycin, an exceptionally complex bacterial signaling metabolite.  |  Höfer, I., et al. 2011. Chem Biol. 18: 381-91. PMID: 21439483
  7. Manipulation of regulatory genes reveals complexity and fidelity in hormaomycin biosynthesis.  |  Cai, X., et al. 2013. Chem Biol. 20: 839-46. PMID: 23790494
  8. Tearing down to build up: Metalloenzymes in the biosynthesis lincomycin, hormaomycin and the pyrrolo [1,4]benzodiazepines.  |  Colabroy, KL. 2016. Biochim Biophys Acta. 1864: 724-737. PMID: 26963649
  9. New Concept of the Biosynthesis of 4-Alkyl-L-Proline Precursors of Lincomycin, Hormaomycin, and Pyrrolobenzodiazepines: Could a γ-Glutamyltransferase Cleave the C-C Bond?  |  Jiraskova, P., et al. 2016. Front Microbiol. 7: 276. PMID: 27014201
  10. Biosynthesis and incorporation of an alkylproline-derivative (APD) precursor into complex natural products.  |  Janata, J., et al. 2018. Nat Prod Rep. 35: 257-289. PMID: 29517100

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hormaomycin, 500 µg

sc-364113
500 µg
$390.00

Hormaomycin, 1 mg

sc-364113A
1 mg
$640.00