Rational selection of structurally diverse natural product scaffolds with favorable ADME properties for drug discovery

Natural product analogs are significant sources for therapeutic agents. To capitalize efficiently on the effective features of naturally occurring substances, a natural product-based library production platform has been devised at Aurigene for drug lead discovery. This approach combines the attracti...

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Veröffentlicht in:Molecular diversity 2005, Vol.9 (1-3), p.131-139
Hauptverfasser: Samiulla, D S, Vaidyanathan, V V, Arun, P C, Balan, G, Blaze, M, Bondre, S, Chandrasekhar, G, Gadakh, A, Kumar, R, Kharvi, G, Kim, H O, Kumar, S, Malikayil, J A, Moger, M, Mone, M K, Nagarjuna, P, Ogbu, C, Pendhalkar, D, Rao, A V S Raja, Rao, G Venkateshwar, Sarma, V K, Shaik, S, Sharma, G V R, Singh, S, Sreedhar, C, Sonawane, R, Timmanna, U, Hardy, L W
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Sprache:eng
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Zusammenfassung:Natural product analogs are significant sources for therapeutic agents. To capitalize efficiently on the effective features of naturally occurring substances, a natural product-based library production platform has been devised at Aurigene for drug lead discovery. This approach combines the attractive biological and physicochemical properties of natural product scaffolds, provided by eons of natural selection, with the chemical diversity available from parallel synthetic methods. Virtual property analysis, using computational methods described here, guides the selection of a set of natural product scaffolds that are both structurally diverse and likely to have favorable pharmacokinetic properties. The experimental characterization of several in vitro ADME properties of twenty of these scaffolds, and of a small set of designed congeners based upon one scaffold, is also described. These data confirm that most of the scaffolds and the designed library members have properties favorable to their utilization for creating libraries of lead-like molecules.
ISSN:1381-1991
1573-501X
DOI:10.1007/s11030-005-1297-7