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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.
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pre_formula( "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", "jqp040/222619.html" ); ?>
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
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Registries:
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PubChem CID 222619
PubChem ID 74688
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