Torlamicina

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: C₄₂H₇₃NO₁₆

InChI: InChI=1/C42H73NO16/c1-14-28-42(10,52)35(49)23(4)32(47)21(2)19-40(8,51)36(59-39-33(48)27(43(11)12)18-22(3)54-39)24(5)34(25(6)38(50)56-28)58-31-20-41(9,53-13)37(26(7)55-31)57-30(46)17-15-16-29(44)45/h21-28,31,33-37,39,48-49,51-52H,14-20H2,1-13H3,(H,44,45)/t21-,22u,23+,24+,25-,26u,27?,28-,31?,33?,34+,35-,36-,37?,39?,40-,41u,42-/m1/s1/f/h44H

InChIKey: InChIKey=DLXKPWOBAXEREQ-AUJPAIGRDO
SMILES: CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)OC(=O)CCCC(=O)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O

Names:
    Dowmycin hydrogen glutarate
    Erythrocin
    Erythromycin hydrogen glutarate
    E-Mycin
    Ilosone
    Ilotycin
    Retcin
    Robimycin
    RP-Mycin
    Torlamicina
    5-[6-[[(3R,4S,5R,6R,7R,9R,11R,12R,13S,14R)-6-(4-dimethylamino-3-hydroxy-6-methyl-oxan-2-yl)oxy-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-2,10-dioxo-1-oxacyclotetradec-4-yl]oxy]-4-methoxy-2,4-dimethyl-oxan-3-yl]oxy-5-oxo-pentanoic acid

Registries:
    PubChem CID 222619
    PubChem ID 74688