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Posaconazole (Noxafil, SCH 56592), a new azole antifungal drug, was a discovery based on the isolation and mass spectral characterization of a circulating metabolite of an earlier lead (SCH 51048)
Author(s) -
Nomeir Amin A.,
Pramanik Birendra N.,
Heimark Larry,
Bennett Frank,
Veals John,
Bartner Peter,
Hilbert Maryjane,
Saksena Anil,
McNamara Paul,
Girijavallabhan Viyyoor,
Ganguly Ashit K.,
Lovey Raymond,
Pike Russell,
Wang Haiyan,
Liu YiTsung,
Kumari Pramila,
Korfmacher Walter,
Lin ChinChung,
Cacciapuoti Anthony,
Loebenberg David,
Hare Roberta,
Miller George,
Pickett Cecil
Publication year - 2008
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/jms.1341
Subject(s) - metabolite , chemistry , posaconazole , active metabolite , high performance liquid chromatography , chromatography , in vivo , azole , diastereomer , pharmacokinetics , stereochemistry , pharmacology , antifungal , biochemistry , itraconazole , microbiology and biotechnology , biology
Abstract Posaconazole (SCH 56592) is a novel triazole antifungal drug that is marketed in Europe and the United States under the trade name ‘Noxafil’ for prophylaxis against invasive fungal infections. SCH 56592 was discovered as a possible active metabolite of SCH 51048, an earlier lead. Initial studies have shown that serum concentrations determined by a microbiological assay were higher than those determined by HPLC from animals dosed with SCH 51048. Subsequently, several animals species were dosed with 3 H‐SCH 51048 and the serum was analyzed for total radioactivity, SCH 51048 concentration and antifungal activity. The antifungal activity was higher than that expected based on SCH 51048 serum concentrations, confirming the presence of active metabolite(s). Metabolite profiling of serum samples at selected time intervals pinpointed the peak that was suspected to be the active metabolite. Consequently, 3 H‐SCH 51048 was administered to a large group of mice, the serum was harvested and the metabolite was isolated by extraction and semipreparative HPLC. LC‐MS/MS analysis suggested that the active metabolite is a secondary alcohol with the hydroxyl group in the aliphatic side chain of SCH 51048. All corresponding monohydroxylated diastereomeric mixtures were synthesized and characterized. The HPLC retention time and LC‐MS/MS spectra of the diastereomeric secondary alcohols of SCH 51048 were similar to those of the isolated active metabolite. Finally, all corresponding individual monohydroxylated diasteriomers were synthesized and evaluated for in vitro and in vivo antifungal potencies, as well as pharmacokinetics. SCH 56592 emerged as the candidate with the best overall profile. Copyright © 2007 John Wiley & Sons, Ltd.