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N-(3-amino-3-oxoprop-1-en-2-yl)-2-[21-ethylidene-9,30-dihydroxy-18-(1-hydroxyethyl)-40-methyl-16,19,26,31,42,46-hexaoxo-32-oxa-3,13,23,43,49-pentathia-7,17,20,27,45,51,52,53,54,55-decazanonacyclo[26.16.6.12,5.112,15.122,25.138,41.147,50.06,11.034,39]pentapentaconta-2(55),4,6,8,10,12(54),14,22(53),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide

Base Information Edit
  • Chemical Name:N-(3-amino-3-oxoprop-1-en-2-yl)-2-[21-ethylidene-9,30-dihydroxy-18-(1-hydroxyethyl)-40-methyl-16,19,26,31,42,46-hexaoxo-32-oxa-3,13,23,43,49-pentathia-7,17,20,27,45,51,52,53,54,55-decazanonacyclo[26.16.6.12,5.112,15.122,25.138,41.147,50.06,11.034,39]pentapentaconta-2(55),4,6,8,10,12(54),14,22(53),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide
  • CAS No.:56377-79-8
  • Molecular Formula:C51H43N13O12S6
  • Molecular Weight:1222.36
  • Hs Code.:
  • European Community (EC) Number:260-138-4
  • Metabolomics Workbench ID:71129
  • NCI Thesaurus Code:C170235
  • Wikidata:Q104193609,Q105196681
  • Wikipedia:Nosiheptide
  • Mol file:56377-79-8.mol
N-(3-amino-3-oxoprop-1-en-2-yl)-2-[21-ethylidene-9,30-dihydroxy-18-(1-hydroxyethyl)-40-methyl-16,19,26,31,42,46-hexaoxo-32-oxa-3,13,23,43,49-pentathia-7,17,20,27,45,51,52,53,54,55-decazanonacyclo[26.16.6.12,5.112,15.122,25.138,41.147,50.06,11.034,39]pentapentaconta-2(55),4,6,8,10,12(54),14,22(53),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide

Synonyms:multhiomycin;nosiheptide

Suppliers and Price of N-(3-amino-3-oxoprop-1-en-2-yl)-2-[21-ethylidene-9,30-dihydroxy-18-(1-hydroxyethyl)-40-methyl-16,19,26,31,42,46-hexaoxo-32-oxa-3,13,23,43,49-pentathia-7,17,20,27,45,51,52,53,54,55-decazanonacyclo[26.16.6.12,5.112,15.122,25.138,41.147,50.06,11.034,39]pentapentaconta-2(55),4,6,8,10,12(54),14,22(53),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide
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
  • Nosiheptide
  • 5mg
  • $ 496.00
  • TRC
  • Nosiheptide
  • 1mg
  • $ 100.00
  • Medical Isotopes, Inc.
  • Nosiheptide
  • 1 mg
  • $ 585.00
  • Medical Isotopes, Inc.
  • Nosiheptide
  • 50 mg
  • $ 2400.00
  • Matrix Scientific
  • Nosiheptide 90%
  • 1g
  • $ 3600.00
  • Matrix Scientific
  • Nosiheptide 90%
  • 250mg
  • $ 1440.00
  • DC Chemicals
  • Nosiheptide >98%
  • 10 mg
  • $ 500.00
  • CSNpharm
  • Nosiheptide
  • 5mg
  • $ 162.00
  • Crysdot
  • Nosiheptide 97%
  • 1g
  • $ 997.00
  • ChemScene
  • Nosiheptide 97.20%
  • 100mg
  • $ 1500.00
Total 63 raw suppliers
Chemical Property of N-(3-amino-3-oxoprop-1-en-2-yl)-2-[21-ethylidene-9,30-dihydroxy-18-(1-hydroxyethyl)-40-methyl-16,19,26,31,42,46-hexaoxo-32-oxa-3,13,23,43,49-pentathia-7,17,20,27,45,51,52,53,54,55-decazanonacyclo[26.16.6.12,5.112,15.122,25.138,41.147,50.06,11.034,39]pentapentaconta-2(55),4,6,8,10,12(54),14,22(53),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide Edit
Chemical Property:
  • Melting Point:310-320° (dec) 
  • Refractive Index:1.698 
  • PKA:1.42±0.60(Predicted) 
  • PSA:552.28000 
  • Density:1.534 g/cm3 
  • LogP:7.28900 
  • Storage Temp.:Sealed in dry,Store in freezer, under -20°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:10
  • Hydrogen Bond Acceptor Count:24
  • Rotatable Bond Count:5
  • Exact Mass:1221.14784090
  • Heavy Atom Count:82
  • Complexity:2510
Purity/Quality:

99% *data from raw suppliers

Nosiheptide *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC=C1C2=NC(=CS2)C(=O)NC3CC(C(=O)OCC4=C5C(=C(C(=O)SCC(C6=NC(=CS6)C7=NC(=C(C=C7C8=NC(=CS8)C(=O)NC(C(=O)N1)C(C)O)O)C9=NC(=CS9)C(=O)NC(=C)C(=O)N)NC(=O)C1=CSC3=N1)NC5=CC=C4)C)O
  • Uses Nosiheptide is an antibacterial item used in feedstock and feed additives for chickens. Nosiheptide is a bicyclic thiopeptide antibiotic produced by several species of actinomycetes, notably Streptomyces, first reported by Japanese researchers in 1970. Unlike other bicyclic thiopeptides such as thiostrepton, the second macrocyclic ring is linked by relatively fragile lactone and thiolactone bridges to the core cyclic peptide. Nosiheptide has broad spectrum antibacterial activity, and has recently demonstrated a prolonged post-antibiotic effect in both nosocomial and community-acquired MRSA compared with vancomycin. Despite its long history in animal health, nosiheptide has not been extensively studied and is regarded as a “lost antibiotic” largely escaping intensive investigation for human application.
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