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Verdamicin

Base Information
  • Chemical Name:Verdamicin
  • CAS No.:49863-48-1
  • Molecular Formula:C20H39N5O7
  • Molecular Weight:461.553
  • Hs Code.:
  • Wikipedia:Verdamicin
  • Mol file:49863-48-1.mol
Verdamicin

Synonyms:verdamicin

Suppliers and Price of Verdamicin
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • VERDAMICIN 95.00%
  • 5MG
  • $ 495.97
Total 4 raw suppliers
Chemical Property of Verdamicin
Chemical Property:
  • Vapor Pressure:2.95E-21mmHg at 25°C 
  • Boiling Point:677.3°Cat760mmHg 
  • Flash Point:363.4°C 
  • Density:1.36g/cm3 
  • XLogP3:-4.7
  • Hydrogen Bond Donor Count:8
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:6
  • Exact Mass:461.28494860
  • Heavy Atom Count:32
  • Complexity:672
Purity/Quality:

99% *data from raw suppliers

VERDAMICIN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C1=CCC(C(O1)OC2C(CC(C(C2O)OC3C(C(C(CO3)(C)O)NC)O)N)N)N)N
Refernces

Biotransformation of sisomicin and verdamicin by Micromonospora sagamiensis

10.1080/00021369.1982.10865090

The research investigates the biotransformation of sisomicin and verdamicin by Micromonospora sagamiensis. The study found that the resting cells of a 2-deoxystreptamine idiotrophic mutant of M. sagamiensis could transform sisomicin into gentamicin CIa and sagamicin, while verdamicin was transformed into gentamicin C2a, C2, and then CI. The biotransformation products were isolated using ion exchange and carbon column chromatographic procedures and identified through various analytical techniques. The study also compared the biotransformation capabilities of other Micromonospora species, such as M. zionensis and M. inyoensis, and found that they lacked the (4',5')-reduction activity present in M. sagamiensis. Instead, M. zionensis transformed sisomicin into antibiotic G-52 and verdamicin into a new antibiotic, VF3-1, which was suggested to be 6'-N-methylverdamicin based on chromatographic and mass spectrum data. The findings provide insights into the biosynthetic pathways of these antibiotics and their potential for further development.

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