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ANTIBIOTIC MYC-8003

Base Information Edit
  • Chemical Name:ANTIBIOTIC MYC-8003
  • CAS No.:50935-71-2
  • Molecular Formula:C43H60N2O12
  • Molecular Weight:796.956
  • Hs Code.:
  • Mol file:50935-71-2.mol
ANTIBIOTIC MYC-8003

Synonyms:(2R)-N-[(2E,4E,6R)-7-[(2S,5R)-3,4-dihydroxy-5-[(1E,3E,5E)-7-(2-hydroxy-4-oxo-1H-pyridin-3-yl)-6-methyl-7-oxo-hepta-1,3,5-trienyl]oxolan-2-yl]-6-methoxy-5-methyl-octa-2,4-dienyl]-2-[2,3,4-trihydroxy-5,5-dimethyl-6-[(1E,3Z)-penta-1,3-dienyl]oxan-2-yl]butanamide;2H-Pyran-2-acetamide,N-[7-[(2E,4E,6S,7R)- 5-[(1E,2E,5E)-7-(1,2-dihydro-4-hydroxy-2- oxo-3-pyridinyl)-6-methyl-7-oxo-1,3,5- heptatrienyl]tetrahydro-3,4-dihydroxy-2- furanyl]-6-methoxy-5-methyl-2,4- octadienyl]-R-ethyltetrahydro-2,3,4- trihydroxy-5,5-dimethyl-6-[(1E,3E)-1,3- pentadienyl]-,(RS,2R,3R,4R,6S)-;2H-Pyran-2-acetamide, N-[7-[5-[7-(1, 2-dihydro-4-hydroxy-2-oxo-3-pyridinyl)-6-methyl-7-oxo-1,3, 5-heptatrienyl]tetrahydro-3, 4-dihydroxy-2-furanyl]-6-methoxy-5-methyl-2, 4-octadienyl]-.alpha.-ethyltetrahydro-2,3,4-trihydroxy-5, 5-dimethyl-6-(1,3-pentadienyl)-;MOCIMYCIN;(2S)-N-[(2E,4E,6S,7R)-7-[(2S,3R,4S,5R)-3,4-dihydroxy-5-[(1E,3E,5E)-7-(2-hydroxy-4-oxo-1H-pyridin-3-yl)-6-methyl-7-oxo-hepta-1,3,5-trienyl]oxolan-2-yl]-6-methoxy-5-methyl-octa-2,4-dienyl]-2-[(2R,3R,4R,6S)-2,3,4-trihydroxy-5,5-dimethyl-6-[(1E,3E)-penta-1,3-dienyl]oxan-2-yl]butanamide;Kirromycin;Delvomycin;

Suppliers and Price of ANTIBIOTIC MYC-8003
Supply Marketing:Edit
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
  • Kirromycin
  • 1mg
  • $ 392.00
  • TRC
  • Kirromycin from Streptomyces collinus
  • 5mg
  • $ 620.00
  • Sigma-Aldrich
  • Kirromycin from Streptomyces collinus ≥90% (HPLC)
  • 5mg
  • $ 867.00
  • Cayman Chemical
  • Kirromycin
  • 1mg
  • $ 568.00
  • American Custom Chemicals Corporation
  • KIRROMYCIN 95.00%
  • 5MG
  • $ 500.65
  • Adipogen Life Sciences
  • Kirromycin ≥96%(HPLC)
  • 1 mg
  • $ 170.00
Total 12 raw suppliers
Chemical Property of ANTIBIOTIC MYC-8003 Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.621 
  • Boiling Point:936°C at 760 mmHg 
  • Flash Point:519.9°C 
  • PSA:228.10000 
  • Density:1.279g/cm3 
  • LogP:3.46570 
  • Storage Temp.:−20°C 
  • Solubility.:methanol: soluble1.90-2.10mg/mL, clear, yellow 
Purity/Quality:

99.3% *data from raw suppliers

Kirromycin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38-66 
  • Safety Statements: 26-36 
MSDS Files:

Total 1 MSDS from other Authors

Useful:
  • Description Kirromycin is an antibiotic originally isolated from Streptomyces and an inhibitor of protein biosynthesis. It inhibits isoleucine incorporation, polyphenylalanine synthesis, and growth of B. brevis. Kirromycin inhibits elongation factor Tu-dependent peptidyl transfer activity in E. coli.
  • Uses Kirromycin from Streptomyces collinus is an antibiotic inhibitor of protein synthesis.
Technology Process of ANTIBIOTIC MYC-8003

There total 1 articles about ANTIBIOTIC MYC-8003 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:

Reference yield:

Guidance literature:
Guidance literature:
Multi-step reaction with 3 steps
1: 87 percent / dioxane / 22 h / 35 °C
2: 50 percent / triethylamine / dimethylformamide / 1 h / 0 - 20 °C
3: 760 mg / sodium metaperiodate; ammonium acetate / H2O; dioxane; methanol
With ammonium acetate; sodium periodate; triethylamine; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; 1: amidic cleavage / 2: Addition / 3: Oxidation;
DOI:10.7164/antibiotics.49.1249
Guidance literature:
Multi-step reaction with 4 steps
1: 87 percent / dioxane / 22 h / 35 °C
2: 50 percent / triethylamine / dimethylformamide / 1 h / 0 - 20 °C
3: 760 mg / sodium metaperiodate; ammonium acetate / H2O; dioxane; methanol
4: 73 percent / sodium borohydride / ethanol / 0.75 h / 0 °C
With ammonium acetate; sodium tetrahydroborate; sodium periodate; triethylamine; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; 1: amidic cleavage / 2: Addition / 3: Oxidation / 4: Reduction;
DOI:10.7164/antibiotics.49.1249
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