Erythromycin C

Erythromycin A bacteriostatic antibiotic macrolide produced by Streptomyces erythreus. Erythromycin A is considered its major active component. 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: C₃₆H₆₅NO₁₃

InChI: InChI=1/C36H65NO13/c1-13-24-36(10,45)29(40)19(4)26(38)17(2)15-35(9,44)31(50-33-27(39)23(37(11)12)14-18(3)46-33)20(5)28(21(6)32(42)48-24)49-25-16-34(8,43)30(41)22(7)47-25/h17-25,27-31,33,39-41,43-45H,13-16H2,1-12H3/t17-,18u,19+,20+,21-,22u,23?,24-,25?,27?,28+,29-,30?,31-,33?,34?,35?,36?/m1/s1

InChIKey: InChIKey=MWFRKHPRXPSWNT-UPSHANLCBB
SMILES: CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)O)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O

Names:
    Erythromycin C
    (3R,4S,5R,6R,9R,11R,12R,14R)-4-(4,5-dihydroxy-4,6-dimethyl-oxan-2-yl)oxy-6-(4-dimethylamino-3-hydroxy-6-methyl-oxan-2-yl)oxy-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecane-2,10-dione

Registries:
    PubChem CID 6426643
    PubChem ID 10486427