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An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
http://linked.open...gbank/description
  • A macrolide antibiotic from Streptomyces narbonensis. The drug has antimicrobial activity against a wide spectrum of pathogens. [PubChem] (en)
http://linked.open...generalReferences
  • # Przybylski P, Pyta K, Stefanska J, Brzezinski B, Bartl F: Structure elucidation, complete NMR assignment and PM5 theoretical studies of new hydroxy-aminoalkyl-alpha,beta-unsaturated derivatives of the macrolide antibiotic josamycin. Magn Reson Chem. 2010 Apr;48(4):286-96. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/20186698 (en)
http://linked.open...gy/drugbank/group
  • approved (en)
http://linked.open...ugbank/indication
  • For the treatment of bacterial infections. (en)
sameAs
Title
  • Josamycin (en)
adms:identifier
http://linked.open...mechanismOfAction
  • The mechanism of action of macrolides such as Josamycin is via inhibition of bacterial protein biosynthesis by binding reversibly to the subunit 50S of the bacterial ribosome, thereby inhibiting translocation of peptidyl tRNA. This action is mainly bacteriostatic, but can also be bactericidal in high concentrations. Macrolides tend to accumulate within leukocytes, and are therefore actually transported into the site of infection. (en)
http://linked.open.../drugbank/synonym
  • JM (en)
  • Leucomycin A3 (en)
  • Leucomycin V, 3-acetate 4B-(3-methylbutanoate) (en)
  • Leucomycin V, 3-acetate 4(sup beta)-(3-methylbutanoate) (en)
  • Leucomycin V, 3-acetate 4(sup B)-(3-methylbutanoate) (en)
  • Josamycine (en)
  • Antibiotic yl-704 a3 (en)
  • EN-141 (en)
  • Josamicina (en)
  • Josamycinum (en)
  • Kitasamycin a3 (en)
  • Leucomycin v 3-acetate 4(b)-(3-methylbutanoate) (en)
  • Leucomycin v 3-acetate 4(beta)-(3-methylbutanoate) (en)
  • Leucomycin v 3-acetate 4b-(3-methylbutanoate) (en)
  • Turimycin a5 (en)
  • yl-704 a3 (en)
http://linked.open...ynthesisReference
  • Takashi Osono, Kiruko Moriyama, Keisuke Murakami, Hamao Umezawa, "Process for the production of monopropionyl-josamycin-2." U.S. Patent US4001399, issued January, 1972. (en)
http://linked.open...y/mesh/hasConcept
http://linked.open...ugbank/IUPAC-Name
http://linked.open...gy/drugbank/InChI
http://linked.open...Molecular-Formula
http://linked.open.../Molecular-Weight
http://linked.open...noisotopic-Weight
http://linked.open...y/drugbank/SMILES
http://linked.open.../Water-Solubility
http://linked.open...ogy/drugbank/logP
http://linked.open...ogy/drugbank/logS
http://linked.open...l/drug/hasATCCode
http://linked.open...nd-Acceptor-Count
http://linked.open...-Bond-Donor-Count
http://linked.open...drugbank/InChIKey
http://linked.open...urface-Area--PSA-
http://linked.open...nk/Polarizability
http://linked.open...bank/Refractivity
http://linked.open...atable-Bond-Count
http://linked.open.../affectedOrganism
  • Enteric bacteria and other eubacteria (en)
http://linked.open...casRegistryNumber
  • 16846-24-5 (en)
http://linked.open...drugbank/category
  • (en)
http://linked.open...k/Bioavailability
http://linked.open...bank/Ghose-Filter
http://linked.open...nk/MDDR-Like-Rule
http://linked.open...ank/Melting-Point
http://linked.open...k/Number-of-Rings
http://linked.open...siological-Charge
http://linked.open...bank/Rule-of-Five
http://linked.open...tional-IUPAC-Name
http://linked.open...strongest-acidic-
http://linked.open...-strongest-basic-
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