ERYTHROMYCIN-G;[3R-(3R*,4S*,5S*,6R*,7R*,9R*,11R*,12R*,13S,14R*)]-4-[(2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBO-HEXOPYRANOSYL)-OXY]-14-E
Compound with spectra: 1 NMR
![ERYTHROMYCIN-G;[3R-(3R*,4S*,5S*,6R*,7R*,9R*,11R*,12R*,13S,14R*)]-4-[(2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBO-HEXOPYRANOSYL)-OXY]-14-E](/api/compound/2xHSJ5Cs8em.png?ph=true&h=300&w=458 "ERYTHROMYCIN-G;[3R-(3R*,4S*,5S*,6R*,7R*,9R*,11R*,12R*,13S,14R*)]-4-[(2,6-DIDEOXY-3-C-METHYL-3-O-METHYL-ALPHA-L-RIBO-HEXOPYRANOSYL)-OXY]-14-E")
| SpectraBase Compound ID | 2xHSJ5Cs8em |
|---|---|
| InChI | InChI=1S/C37H67NO13/c1-13-26-20(4)29(41)21(5)28(40)18(2)15-36(8,45)33(51-35-30(42)25(38(10)11)14-19(3)47-35)22(6)31(24(17-39)34(44)49-26)50-27-16-37(9,46-12)32(43)23(7)48-27/h18-27,29-33,35,39,41-43,45H,13-17H2,1-12H3/t18-,19+,20+,21+,22+,23+,24-,25-,26-,27+,29+,30+,31+,32+,33-,35-,36-,37-/m1/s1 |
| InChIKey | ZQLOQWOXRVAVOI-QGEOCIHXSA-N |
| Mol Weight | 733.9 g/mol |
| Molecular Formula | C37H67NO13 |
| Exact Mass | 733.461241 g/mol |
| Enantiomer InChIKey | ZQLOQWOXRVAVOI-NNLKHIISSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
EM-B;12-DEOXY-ERYTHROMYCIN-A;ERYTHROMYCIN-B
ERYTHROMYCIN-F
13-CYCLO-PENTYL-13-DESETHYL-ERYTHROMYCIN-B
De-N-methylamino-erythromycin B
(8S)-12-deoxy-8-fluoroerythromycin A
3'-DES-N-METHYL-9-DEOXO-9-HYDROXIMINO-ERYTHROMYCIN-A
Azithromycin dihydrate
LQRWEXBYGVYKQN-AVSNMUALSA-N
3'-Dedimethylamino-3',4'-dehydro-erythromycin A
OOJDTACNFHWCEU-OHXMYBKWSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Isolation and Structure of a New Macrolide Antibiotic, Erythromycin G, and a Related Biosynthetic Intermediate from a Culture of Saccharopolyspora erythraea. | The Journal of Antibiotics | 2003 |