Product overview

  • Name
    Boromycin
  • Short description
    Macrolide antibiotic with various biological actions
  • Biological description
    Boron-containing macrolide antibiotic. Antibacterial. Antiprotozoal (Plasmodium, Babesia). Anti-HIV compound. Ca2+ homeostasis modulator. Potentiator of bleomycin-induced anti-tumor activity. Used as a chiral selector in capillary electrophoresis.
  • Purity
    >99%
  • Our products in action

Properties

  • Chemical name
    [1-{(1R)-1-[(1R,2R,5S,6R,8R,12R,14S,17R,18R,22S,24Z,28S,30S,33R)-12,28-Dihydroxy-1,2,18,19-tetra(hydroxy-kO)-6,13,13,17,29,29,33-heptamethyl-3,20-dioxo-4,7,21,34,35-pentaoxatetracyclo[28.3.1.15,8.114,18]hexatriacont-24-en-22-yl]ethoxy}-3-methyl-1-oxo-2-butanaminiumato(4-)]boron
  • Molecular Weight
    879.9
  • Chemical structure
    Boromycin [34524-20-4]
  • Molecular Formula
    C45H74BNO15
  • CAS Number
    34524-20-4
  • PubChem identifier
    73656818
  • SMILES
    [B-]123OC4C(=O)OC(CC=CCCC(C(C5CCC(C(O1)(O5)C(O2)C(=O)OC6CC(CCCC(C(C7CCC(C4(O3)O7)C)(C)C)O)OC6C)C)(C)C)O)C(C)OC(=O)C(C(C)C)[NH3+]
  • Source
    Extracted from Streptomyces sp
  • InChi
    InChI=1S/C45H73BNO15/c1-24(2)36(47)39(50)54-27(5)30-16-12-11-13-17-32(48)42(7,8)34-21-19-26(4)45(57-34)38-41(52)56-31-23-29(53-28(31)6)15-14-18-33(49)43(9,10)35-22-20-25(3)44(58-35)37(40(51)55-30)59-46(60-38,61-44)62-45/h11-12,24-38,48-49H,13-23,47H2,1-10
  • InChiKey
    OOBFYEMEQCZLJL-UWTAGDQBSA-O
  • Appearance
    Off-white solid

Storing and Using Your Product

  • Storage instructions
    +4°C
  • Solubility overview
    Soluble in DMSO and in ethanol
  • Important
    This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

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