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Technology Process of Venturicidin A

Venturicidin A

Base Information
  • Chemical Name:Venturicidin A
  • CAS No.:33538-71-5
  • Molecular Formula:C41H67 N O11
  • Molecular Weight:749.97
  • Hs Code.:2941900000
  • European Community (EC) Number:251-568-3
  • UNII:46L30W9XBB
  • DSSTox Substance ID:DTXSID201317371
  • Wikidata:Q76415010
  • Metabolomics Workbench ID:112950
  • ChEMBL ID:CHEMBL4848659
  • Mol file:33538-71-5.mol
Venturicidin A

Synonyms:venturicidin A

Suppliers and Price of Venturicidin A
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
  • TRC
  • VenturicidinA
  • 1mg
  • $ 635.00
  • Cayman Chemical
  • Venturicidin A ≥95%
  • 1mg
  • $ 125.00
  • Cayman Chemical
  • Venturicidin A ≥95%
  • 5mg
  • $ 405.00
  • ApexBio Technology
  • VenturicidinA
  • 5mg
  • $ 1005.00
  • ApexBio Technology
  • VenturicidinA
  • 1mg
  • $ 249.00
  • American Custom Chemicals Corporation
  • VENTURICIDIN A 95.00%
  • 5MG
  • $ 504.09
  • American Custom Chemicals Corporation
  • VENTURICIDIN A 95.00%
  • 1MG
  • $ 372.75
  • Adipogen Life Sciences
  • VenturicidinA ≥98%(1H-NMR,HPLC)
  • 1 mg
  • $ 120.00
Total 5 raw suppliers
Chemical Property of Venturicidin A
Chemical Property:
  • Melting Point:145-147°; mp 140-142° 
  • Boiling Point:874.9°Cat760mmHg 
  • PKA:11.80±0.70(Predicted) 
  • Flash Point:482.9°C 
  • PSA：184.07000 
  • Density:1.16g/cm3 
  • LogP:6.74440 
  • Storage Temp.:2-8°C 
  • XLogP3:5
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:11
  • Exact Mass:749.47141195
  • Heavy Atom Count:53
  • Complexity:1310
Purity/Quality:

99% *data from raw suppliers

VenturicidinA *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:CCC(=O)C(C)C(C(C)CC(C)C1C(CC(C=CC(CCCC=C(C2C(=CCC(O2)(CC(=O)O1)O)C)C)OC3CC(C(C(O3)C)O)OC(=O)N)C)C)O
  • Isomeric SMILES:CCC(=O)[C@@H](C)[C@H]([C@H](C)C[C@@H](C)[C@@H]1[C@@H](C[C@H](/C=C/[C@@H](CCC/C=C(/[C@@H]2C(=CC[C@@](O2)(CC(=O)O1)O)C)\C)O[C@H]3C[C@H]([C@@H]([C@H](O3)C)O)OC(=O)N)C)C)O
  • Description Venturicidin A is a macrolide antibiotic isolated from strains of Streptomyces. It is active against fungi in the genus Venturia which cause apple scab, as well as other fungi, but not against higher plants. Venturicidin A is also cytotoxic against trypanosomes (IC50 = 120-540 ng/ml) while being more than 25,000 times less effective against mammalian cells. It inhibits bacterial and mitochondrial ATP synthases.
  • Uses The macrolide antibiotic, Venturicidin A, isolated from a Streptomyces sp., is a potent inhibitor of mitochondrial ATP synthase complex acting on the F0 membrane sector. Venturicidin A was originally isolated as an antifungal agent. Venturicidin A is an antibiotic and potent inhibitor of mitochondrial ATP synthase.
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