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泊沙康唑(诺科飞,SCH 56592)是一种新型唑类抗真菌药物,它是基于对早期先导化合物(SCH 51048)的一种循环代谢物的分离和质谱表征而发现的。

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).

作者信息

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 Yi-Tsung, Kumari Pramila, Korfmacher Walter, Lin Chin-Chung, Cacciapuoti Anthony, Loebenberg David, Hare Roberta, Miller George, Pickett Cecil

机构信息

Department of Drug Metabolism and Pharmacokinetics, Schering-Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA.

出版信息

J Mass Spectrom. 2008 Apr;43(4):509-17. doi: 10.1002/jms.1341.

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.

摘要

泊沙康唑(SCH 56592)是一种新型三唑类抗真菌药物,在欧洲和美国以商品名“诺科飞”上市,用于预防侵袭性真菌感染。SCH 56592最初是作为早期先导化合物SCH 51048的一种可能的活性代谢产物被发现的。初步研究表明,通过微生物测定法测定的血清浓度高于用SCH 51048给药的动物通过高效液相色谱法测定的浓度。随后,给几种动物物种注射(3)H-SCH 51048,并分析血清中的总放射性、SCH 51048浓度和抗真菌活性。抗真菌活性高于根据SCH 51048血清浓度预期的活性,证实存在活性代谢产物。在选定的时间间隔对血清样品进行代谢产物谱分析,确定了疑似活性代谢产物的峰。因此,给一大群小鼠注射(3)H-SCH 51048,采集血清,通过萃取和半制备高效液相色谱法分离代谢产物。液相色谱-串联质谱分析表明,活性代谢产物是一种仲醇,其羟基位于SCH 51048的脂肪族侧链中。合成并表征了所有相应的单羟基化非对映异构体混合物。SCH 51048的非对映异构仲醇的高效液相色谱保留时间和液相色谱-串联质谱谱图与分离出的活性代谢产物相似。最后,合成了所有相应的单个单羟基化非对映异构体,并对其体外和体内抗真菌效力以及药代动力学进行了评估。SCH 56592成为总体特征最佳的候选药物。

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