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    Josamycin

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      Josamycin

      SKU
      J0001

      Category: Antibiotics

      16846-24-5
      CAS-Number
      C42H69NO15
      Molecular Formula
      827.99
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥90% (HPLC)
      Appearance
      White to off-white powder
      Identity
      1H-NMR

      Properties

      Solvents
      water

      Documentation

      Safety Data Sheet (SDS)
      CDX J0001 MSDS.pdf
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Transportation
      Not dangerous goods
      Description
      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.
      Smiles
      CO[C@H]1[C@@H](CC(=O)O[C@H](C)CC=CC=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
      InChi Key
      XJSFLOJWULLJQS-LAEWXYAOSA-N
      References
      (1) T. Osono et al.: J. Antibiot. 20:174-180 (1967) , (2) L. Wang et al.: Clin. Exp. Pharmacol. Physiol. 27: 587-593 (2000) , (3) M. Lovmar et al.: J. Biol. Chem. 279: 53506-53515 (2004)
      InChi
      InChI=1S/C42H69NO15/c1-23(2)19-32(47)56-40-27(6)53-34(22-42(40,8)50)57-37-26(5)54-41(36(49)35(37)43(9)10)58-38-29(17-18-44)20-24(3)30(46)16-14-12-13-15-25(4)52-33(48)21-31(39(38)51-11)55-28(7)45/h12-14,16,18,23-27,29-31,34-41,46,49-50H,15,17,19-22H2,1-11H3/b13-12+,16-14+/t24-,25-,26-,27+,29?,30+,31-,34+,35+,36-,37-,38+,39+,40+,41+,42-/m1/s1

      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.

      SKU: J0001 Category: Antibiotics
      • Additional information

      Additional information

      Purity

      ≥90% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      16846-24-5

      Molecular Formula

      C42H69NO15

      Molecular Weight

      827.99

      Identity

      1H-NMR

      Solvents

      water

      Smiles

      CO[C@H]1[C@@H](CC(=O)O[C@H](C)CC=CC=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

      InChi Key

      XJSFLOJWULLJQS-LAEWXYAOSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Transportation

      Not dangerous goods

      References

      (1) T. Osono et al.: J. Antibiot. 20:174-180 (1967), (2) L. Wang et al.: Clin. Exp. Pharmacol. Physiol. 27: 587-593 (2000), (3) M. Lovmar et al.: J. Biol. Chem. 279: 53506-53515 (2004)

      InChi

      InChI=1S/C42H69NO15/c1-23(2)19-32(47)56-40-27(6)53-34(22-42(40,8)50)57-37-26(5)54-41(36(49)35(37)43(9)10)58-38-29(17-18-44)20-24(3)30(46)16-14-12-13-15-25(4)52-33(48)21-31(39(38)51-11)55-28(7)45/h12-14,16,18,23-27,29-31,34-41,46,49-50H,15,17,19-22H2,1-11H3/b13-12+,16-14+/t24-,25-,26-,27+,29?,30+,31-,34+,35+,36-,37-,38+,39+,40+,41+,42-/m1/s1

      Quantity

      50 mg, 200 mg, 2.5 g, Bulk

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