Lauryl sulfate propionyl erythromycin ester

Erythromycin Estolate A macrolide antibiotic, produced by Streptomyces erythreus. It is the lauryl sulfate salt of the propionic ester of erythromycin. This erythromycin salt acts primarily as a bacteriostatic agent. In sensitive organisms, it inhibits protein synthesis by binding to 50S ribosomal subunits. This binding process inhibits peptidyl transferase activity and interferes with translocation of amino acids during translation and assembly of proteins.

Molecular Formula: C₄₉H₉₃NO₁₇S

InChI: InChI=1/C37H67NO13.C12H26O4S/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26;1-2-3-4-5-6-7-8-9-10-11-12-16-17(13,14)15/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3;2-12H2,1H3,(H,13,14,15)/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-;/m1./s1/f/h;13H

InChIKey: InChIKey=SKDGGFHGLZBNBC-DKLAHUOIDD
SMILES: CCCCCCCCCCCCOS(O)(=O)=O.CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O

Names:
    CHEBI:4846
    ERYTHROMYCIN ESTOLATE
    Erythromycin estolate
    erythromycin estolate
    Erythromycin estorate
    Erythromycin 2'-propionate dodecyl sulfate (salt)
    Erythromycin 2'-propionate dodecyl sulfate (salt)
    Erythromycin, propionate (ester), compd. with monododecyl
    Ilosone (TN)
    Lauryl sulfate propionyl erythromycin ester
    (3R,4S,5R,6R,7R,9R,11R,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-dimethylamino-3-hydroxy-6-methyl-oxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyl-oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecane-2,10-dione; 1-sulfooxydodecane
    3521-62-8

Registries:
    PubChem CID 5702270
    ChEBI 4846
    Kegg C08031
    Kegg D00851
    PubChem ID 10231
    PubChem ID 11533961