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Asukamycin

Base Information
  • Chemical Name:Asukamycin
  • CAS No.:61116-33-4
  • Molecular Formula:C31H34 N2 O7
  • Molecular Weight:546.62
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401318456
  • Nikkaji Number:J575.853J
  • Wikidata:Q25419435
  • Metabolomics Workbench ID:52714
  • Mol file:61116-33-4.mol
Asukamycin

Synonyms:asukamycin

Suppliers and Price of Asukamycin
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
  • Cayman Chemical
  • Asukamycin ≥95%
  • 500μg
  • $ 323.00
  • Cayman Chemical
  • Asukamycin ≥95%
  • 2.5mg
  • $ 809.00
  • American Custom Chemicals Corporation
  • ASUKAMYCIN 95.00%
  • 5MG
  • $ 499.76
Total 8 raw suppliers
Chemical Property of Asukamycin
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:910°C at 760 mmHg 
  • PKA:3.80±0.30(Predicted) 
  • Flash Point:504.1°C 
  • PSA:145.33000 
  • Density:1.32g/cm3 
  • LogP:4.01570 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:10
  • Exact Mass:546.23660143
  • Heavy Atom Count:40
  • Complexity:1270
Purity/Quality:

97% *data from raw suppliers

Asukamycin ≥95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC(CC1)C=CC=CC=CC(=O)NC2=CC(C3C(C2=O)O3)(C=CC=CC=CC(=O)NC4=C(CCC4=O)O)O
  • Isomeric SMILES:C1CCC(CC1)/C=C/C=C/C=C/C(=O)NC2=C[C@]([C@H]3[C@@H](C2=O)O3)(/C=C/C=C/C=C/C(=O)NC4=C(CCC4=O)O)O
  • Uses Asukamycin is an unusual trienoic acid amide metabolite produced by Streptomyces nodosus, reported by Omura and colleagues at the Kitasato Institute, Japan, in 1976. Asukamycin belongs to the manumycin class that comprises two trienoic acid amides pivoted on a central cyclohexenone ring to give the molecule an unprecedented angular geometry. Asukamycin is active against Gram positive bacteria, tumor cell lines and protozoans, notably coccidia. Asukamycin’s cell toxicity is accompanied by activation of Caspases 3 and 8.
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