Dirithromycin
Title: Dirithromycin
CAS Registry Number: 62013-04-1
CAS Name: (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,15R,17S)-7-[(2,6-Dideoxy-3-C-methyl-3-O-methyl-a-L-ribo-hexopyranosyl)oxy]-3-ethyl-2,10-dihydroxy-15-[(2-methoxyethoxy)methyl]-2,6,8,10,12,17-hexamethyl-9-[[3,4,6-trideoxy-3-(dimethylamino)-b-D-xylo-hexopyranosyl]oxy]-4,16-dioxa-14-azabicyclo[11.3.1]heptadecan-5-one
Additional Names: [9S(R)]-9-deoxo-11-deoxy-9,11-[imino[2-(2-methoxyethoxy)ethylidene]oxy]erythromycin
Manufacturers' Codes: LY-237216; AS-E 136
Trademarks: Dynabac (Lilly); Noriclan (Lilly); Nortron (Lilly); Valodin (Ferrer)
Molecular Formula: C42H78N2O14
Molecular Weight: 835.07
Percent Composition: C 60.41%, H 9.41%, N 3.35%, O 26.82%
Literature References: Semi-synthetic derivative of erythromycin, q.v. Prepn: BE 840431 (1976 to Thomae); R. Maier et al., US 4048306 (1977 to Boehringer, Ing.). Synthesis, 1H- and 13C-NMR, and antimicrobial evaluation: F. T. Counter et al., Antimicrob. Agents Chemother. 35, 1116 (1991). X-ray structure determn: P. Luger, R. Maier, J. Cryst. Mol. Struct. 9, 329 (1979). HPLC determn in plasma: G. W. Whitaker, T. D. Lindstrom, J. Liq. Chromatogr. 11, 3011 (1988). Symposium on antibacterial activity, pharmacology, and clinical experience: J. Antimicrob. Chemother. 31, Suppl. C, 1-185 (1993).
Properties: Crystals from ethanol/water, mp 186-189° (dec) (Counter). pKa 9.0 in 66% aq dimethyl fluoride. LD50 in mice (g/kg): >1 s.c.; >1 orally (Maier).
Melting point: mp 186-189° (dec) (Counter)
pKa: pKa 9.0 in 66% aq dimethyl fluoride
Toxicity data: LD50 in mice (g/kg): >1 s.c.; >1 orally (Maier)
Therap-Cat: Antibacterial.
Keywords: Antibacterial (Antibiotics); Macrolides.

Others monographs:
Vinyl AcetateCatnepHasubanonineDigitoxin
5-Bromoanthranilic AcidNaphthaleneNitroscanate5-Hydroxytryptophan
Spirit of Ether CompoundLiothyronineAzobenzenePyridine 1-Oxide
Furaltadoneβ-Resorcylic AcidCefpimizoleDicapthon
©2016 DrugLead US FDA&EMEA