ChemicalBook--->CAS DataBase List--->59319-72-1

59319-72-1

59319-72-1 Structure

59319-72-1 Structure
IdentificationBack Directory
[Name]

ERYTHROMYCIN A DIHYDRATE
[CAS]

59319-72-1
[Synonyms]

ERYTHROMYCIN A, DIHYDRATE VETRANAL
[EINECS(EC#)]

204-040-1
[Molecular Formula]

C37H67NO13.H2O
[MDL Number]

MFCD00144254
[MOL File]

59319-72-1.mol
[Molecular Weight]

751.945
Chemical PropertiesBack Directory
[Melting point ]

197.6 °C
[form ]

neat
Safety DataBack Directory
[WGK Germany ]

2
[RTECS ]

KF4375000
Hazard InformationBack Directory
[Biological Activity]

Erythromycin dihyrate is a macrolide antibiotic produced by actinomycetes with broad antibacterial activity. It acts by binding to the bacterial 50S ribosomal subunit and inhibits RNA-dependent protein synthesis by blocking transpeptidation and/or translocation reactions without affecting nucleic acid synthesis .
[in vitro]

Erythromycin dihyrate inhibits growth of P. falciparum with IC 50 and IC 90 values of 58.2 μM and 104.0 μM, respectively .

[in vivo]

Mice of the ddY strain began to receive Erythromycin dihyrate 7 days after inoculation of EAC cells, and CDF mice begins to receive Erythromycin dihyrate immediately after inoculation of P388 cells. Erythromycin dihyrate (gastric intubation; 0.1-50 mg/ kg; 30-120 days) decreases tumor growth from the dose of 5 mg/kg, mice receiving 1-10 mg/kg of Erythromycin dihyrate survives much longer than control mice, Only 10% of mice treated with 5 mg/kg of Erythromycin dihyrate had no evidence of tumor formation on day 60, and the mice are alive even at 120 days after inoculation. However, treatment with 50 mg/kg of Erythromycin dihyrate shortens mean survival time in tumorbearing mice by 4-5 days when it compares to controls.

Animal Model: Female ddY mice at the age of 6 weeks with EAC cells or CDF mice at the age of 6 weeks with P388 ce lls
Dosage: 0.1 mg/kg; 0.5 mg/kg; 10 mg/kg; 30 mg/kg; 50 mg/kg
Administration: Gastric intubation; 30-120 days
Result: Decrease tumor growth and prolonged the mean survival time of mice from the dose of 5 mg/kg, however, the 50 mg/kg dosage shortens the MST in tumorbearing mice.
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