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CID 15559221

Base Information
  • Chemical Name:CID 15559221
  • CAS No.:23152-29-6
  • Molecular Formula:C43H49N7O10
  • Molecular Weight:823.903
  • Hs Code.:2941900000
  • European Community (EC) Number:245-462-6
  • ChEMBL ID:CHEMBL3182997
  • Metabolomics Workbench ID:109854
  • NCI Thesaurus Code:C1296
  • Wikipedia:Virginiamycin_S1
  • Mol file:23152-29-6.mol
CID 15559221

Synonyms:dihydrovirginiamycin S1;staphylomycin S1;virginiamycin factor S1;virginiamycin S1

Suppliers and Price of CID 15559221
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
  • Usbiological
  • Virginiamycin S1
  • 5mg
  • $ 523.00
  • Usbiological
  • Virginiamycin Complex
  • 5mg
  • $ 523.00
  • TRC
  • Virginiamycin S1
  • 1mg
  • $ 255.00
  • Sigma-Aldrich
  • Virginiamycin S1 ≥99% (HPLC)
  • 5mg
  • $ 384.00
  • ChemScene
  • Virginiamycin S1
  • 10mg
  • $ 960.00
  • ChemScene
  • Virginiamycin S1
  • 5mg
  • $ 600.00
  • Cayman Chemical
  • Virginiamycin S1 ≥99%
  • 25mg
  • $ 998.00
  • Cayman Chemical
  • Virginiamycin S1 ≥99%
  • 5mg
  • $ 285.00
  • Apolloscientific
  • Virginiamycin S1
  • 10mg
  • $ 535.00
  • Apolloscientific
  • Virginiamycin S1
  • 1mg
  • $ 95.00
Total 13 raw suppliers
Chemical Property of CID 15559221
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:240-242° 
  • Boiling Point:1182.9°Cat760mmHg 
  • Flash Point:669.2°C 
  • PSA:224.72000 
  • Density:1.4g/cm3 
  • LogP:2.06620 
  • Storage Temp.:?20°C 
  • Solubility.:methanol: soluble5mg/mL 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:6
  • Exact Mass:823.35409079
  • Heavy Atom Count:60
  • Complexity:1620
Purity/Quality:

97% *data from raw suppliers

Virginiamycin S1 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCC1C(=O)N2CCCC2C(=O)N(C(C(=O)N3CCC(=O)CC3C(=O)NC(C(=O)OC(C(C(=O)N1)NC(=O)C4=C(C=CC=N4)O)C)C5=CC=CC=C5)CC6=CC=CC=C6)C
  • Isomeric SMILES:CC[C@@H]1C(=O)N2CCC[C@H]2C(=O)N([C@H](C(=O)N3CCC(=O)CC3C(=O)N[C@H](C(=O)OC([C@@H](C(=O)N1)NC(=O)C4=C(C=CC=N4)O)C)C5=CC=CC=C5)CC6=CC=CC=C6)C
  • Uses Virginiamycin complex is defined as a mixture of 75% ostreogrycin A (virginamycin M1) and 25% virginiamycin S1, together with the less abundant S analogues. As the two major components have quite different solubilities, these proportions are not readily achieved or used. BioAustralis has isolated and re-combined the individual components to provide the defined components of virginiamycin complex. The composition of the complex is important as Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A. Virginiamycin S1 is one of a family of depsipeptide antibiotics co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A. Virginiamycin S1 is a main component of virginiamycin preparations.
Technology Process of CID 15559221

There total 14 articles about CID 15559221 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
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