Synthesis and Biochemical Evaluation of a Range of Non-Substituted Phenyl Alkyl Triazole-Based Compounds as Potential Inhibitors of the Enzyme Complex 17α -Hydroxylase/17,20-Lyase (P45017α)

Authors: Owen, Caroline P.; Patel, Chirag H.; Dhanani, Sachin; Ahmed, Sabbir

Source: Letters in Drug Design & Discovery, Volume 3, Number 10, December 2006 , pp. 761-765(5)

Publisher: Bentham Science Publishers

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Abstract:

We report the synthesis and evaluation of a range of triazole-based inhibitors of the two components of 17α-hydroxylase/17,20-lyase (P45017α). The results show that the compounds were poor inhibitors of 17α- OHase in comparison to lyase; they are therefore good lead compounds in the search for selective inhibitors of P45017α.

Keywords: 17α-Hydroxylase; 17; 20-Lyase; P45017α; Synthesis; Evaluation; Triazole

Document Type: Research article

DOI: http://dx.doi.org/10.2174/157018006778631857

Affiliations: 1: Department of Pharmacy,School of Pharmacy and Chemistry, Kingston University, Penrhyn Road,Kingston upon Thames, Surrey, KT1 2EE, UK.

Publication date: 2006-12-01

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  • Letters in Drug Design & Discovery publishes original letters on all areas of rational drug design and discovery including medicinal chemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, and structure-activity relationships. The emphasis will be on publishing quality papers very rapidly. Letters will be processed rapidly by taking full advantage of Internet technology for both the submission and review of manuscripts. The journal is essential reading to all pharmaceutical scientists involved in research in drug design and discovery.
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