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Chemical Structure
Chemical Structure
Chemical Structure

Josamycin [16846-24-5]

Research Use Only
CDX-J0001
Chemodex
CAS Number16846-24-5
Product group Chemicals
Estimated Purity>90%
Molecular Weight827.99
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Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Josamycin [16846-24-5]
  • Delivery Days Customer
    10
  • CAS Number
    16846-24-5
  • Certification
    Research Use Only
  • Estimated Purity
    >90%
  • Molecular Formula
    C42H69NO15
  • Molecular Weight
    827.99
  • Scientific Description
    Chemical. CAS: 16846-24-5. Formula: C42H69NO15. MW: 827.99. Synthetic. A member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. May overcome anticancer drug resistance by inhibiting the binding of vinblastine or cyclosporin A to P-glycoprotein (Pgp). An antimicrobial against a wide variety of pathogens. - Josamycin is a member of the leucomycin family of macrolide antibiotics produced by Streptomyces kitasatoensis. It is an antimicrobial against a wide variety of pathogens. It has activity against Gram-positive an Gram-negative bacteria. The mechanism of action is via inhibition of bacterial protein biosynthesis by binding reversibly to the subunit 50S of the bacterial ribosome, inhibiting peptidyltransferase and ribosomal translocation, thereby inhibiting translocation of peptidyl tRNA. Josamycin may overcome anticancer drug resistance by inhibiting the binding of vinblastine or cyclosporin A to P-glycoprotein (Pgp). It is used to study the modification of phagocytosis and cytokine production by macrolide antibiotics and immunomodulatory effects.
  • SMILES
    CO[C@H]1[C@@H](CC(=O)O[C@H](C)C\C=C\C=C\[C@H](O)[C@H](C)CC(CC=O)[C@@H]1O[C@@H]1O[C@H](C)[C@@H](O[C@H]2C[C@@](C)(O)[C@@H](OC(=O)CC(C)C)[C@H](C)O2)C([C@H]1O)N(C)C)OC(C)=O
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200