U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C37H65NO12
Molecular Weight 715.9115
Optical Activity UNSPECIFIED
Defined Stereocenters 17 / 17
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ERYTHROMYCIN A ENOL ETHER

SMILES

[H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]2[C@H](C)[C@@H](O[C@]3([H])O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@@]4(C)CC(C)=C(O4)[C@H](C)[C@@H](O)[C@](C)(O)[C@@H](CC)OC(=O)[C@@H]2C

InChI

InChIKey=JFVYXJKGJMUGRG-KJPZRSJGSA-N
InChI=1S/C37H65NO12/c1-14-25-37(10,43)30(40)20(4)28-18(2)16-36(9,50-28)32(49-34-27(39)24(38(11)12)15-19(3)45-34)21(5)29(22(6)33(42)47-25)48-26-17-35(8,44-13)31(41)23(7)46-26/h19-27,29-32,34,39-41,43H,14-17H2,1-13H3/t19-,20+,21+,22-,23+,24+,25-,26+,27-,29+,30-,31+,32-,34+,35-,36-,37-/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Desensitization of the human motilin receptor by motilides.
2005 Jun
Patents
Name Type Language
ERYTHROMYCIN A ENOL ETHER
Common Name English
ERYTHROMYCIN LACTOBIONATE IMPURITY E [EP IMPURITY]
Common Name English
ERYTHROMYCIN IMPURITY E [EP IMPURITY]
Common Name English
ERYTHROMYCIN ENOL ETHER
Common Name English
8,9-ANHYDROERYTHROMYCIN A 6,9-HEMIKETAL
Common Name English
ERYTHROMYCIN, 8,9-DIDEHYDRO-9-DEOXO-6-DEOXY-6,9-EPOXY-
Common Name English
EM-201
Code English
ERYTHROMYCIN ETHYLSUCCINATE IMPURITY E [EP IMPURITY]
Common Name English
ERYTHROMYCIN ESTOLATE IMPURITY E [EP IMPURITY]
Common Name English
(2R,3R,4S,5R,8R,9S,10S,11R,12R)-9-((2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-.ALPHA.-L-RIBO-HEXOPYRANOSYL)OXY)-5-ETHYL-3,4-DIHYDROXY-2,4,8,10,12,14-HEXAMETHYL-11-((3,4,6-TRIDEOXY-3-(DIMETHYLAMINO)-.BETA.-D-XYLO-HEXOPYRANOSYL)OXY)-6,15-DIOXABICYCLO(10.2.1)PENTAD
Systematic Name English
ERYTHROMYCIN STEARATE IMPURITY E [EP IMPURITY]
Common Name English
BRL-46357ER
Code English
ME-4
Code English
Code System Code Type Description
PUBCHEM
83954
Created by admin on Fri Dec 15 16:52:41 GMT 2023 , Edited by admin on Fri Dec 15 16:52:41 GMT 2023
PRIMARY
FDA UNII
32B40I7V7B
Created by admin on Fri Dec 15 16:52:41 GMT 2023 , Edited by admin on Fri Dec 15 16:52:41 GMT 2023
PRIMARY
CAS
33396-29-1
Created by admin on Fri Dec 15 16:52:41 GMT 2023 , Edited by admin on Fri Dec 15 16:52:41 GMT 2023
PRIMARY