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23893-13-2

23893-13-2 structure
23893-13-2 structure
  • Name: Anhydroerythromycin A
  • Chemical Name: Anhydro Erythromycin A
  • CAS Number: 23893-13-2
  • Molecular Formula: C37H65NO12
  • Molecular Weight: 715.911
  • Catalog: analytical chemistry Analytical reagent Ion chromatography reagent
  • Create Date: 2017-04-29 17:50:25
  • Modify Date: 2024-01-03 21:11:38
  • Anhydroerythromycin A is a degradation product of the macrolide antibiotic erythromycin. Anhydroerythromycin A is formed via degradation of erythromycin in acidic aqueous solutions in vitro as well as in vivo. Anhydroerythromycin A is active against S. aureus and B. cereus in vitro (MICs = 12.5 and 6.25 μg/ml, respectively). Anhydroerythromycin A also inhibits steroid 6β-hydroxylase activity associated with the cytochrome P450 (CYP) isoform CYP3A in human liver microsomes.

Name Anhydro Erythromycin A
Synonyms Erythromycin Anhydride,Impurity D
(1S,2R,3R,4S,5R,8R,9S,10S,11R,12R,14R)-11-{[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-5-ethyl-3-hydroxy-9-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahyd ;ro-2H-pyran-2-yl]oxy}-2,4,8,10,12,14-hexamethyl-6,15,16-trioxatricyclo[10.2.1.1]hexadecan-7-one (non-preferred name)
Erythromycin,9-deoxo-6,12-dideoxy-6,9:9,12-diepoxy
ANHYDROERYTHROMYCIN A
EM 202
9-Deoxo-6,12-dideoxy-6,9:9,12-diepoxy-erythromycin
Erythromycin anhydride
Anhydroerythromycin
(1S,2R,3R,4S,5R,8R,9S,10S,11R,12R,14R)-11-{[(2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-5-ethyl-3-hydroxy-9-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahyd ;ro-2H-pyran-2-yl]oxy}-2,4,8,10,12,14-hexamethyl-6,15,16-trioxatricyclo[10.2.1.1]hexadecan-7-one
6,9,12-Anhydroerythromycin A
6,9:9,12-Diepoxy-9-deoxo-6,12-dideoxyerythromycin
Description Anhydroerythromycin A is a degradation product of the macrolide antibiotic erythromycin. Anhydroerythromycin A is formed via degradation of erythromycin in acidic aqueous solutions in vitro as well as in vivo. Anhydroerythromycin A is active against S. aureus and B. cereus in vitro (MICs = 12.5 and 6.25 μg/ml, respectively). Anhydroerythromycin A also inhibits steroid 6β-hydroxylase activity associated with the cytochrome P450 (CYP) isoform CYP3A in human liver microsomes.
Density 1.2±0.1 g/cm3
Boiling Point 787.2±60.0 °C at 760 mmHg
Melting Point 125-127ºC
Molecular Formula C37H65NO12
Molecular Weight 715.911
Flash Point 429.9±32.9 °C
Exact Mass 715.450684
PSA 154.84000
LogP 3.93
Vapour Pressure 0.0±6.2 mmHg at 25°C
Index of Refraction 1.540
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
Precursor  3

DownStream  0