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Probing chemical space with alkaloid-inspired libraries.

ABSTRACT: Screening of small-molecule libraries is an important aspect of probe and drug discovery science. Numerous authors have suggested that bioactive natural products are attractive starting points for such libraries because of their structural complexity and sp(3)-rich character. Here, we describe the construction of a screening library based on representative members of four families of biologically active alkaloids (Stemonaceae, the structurally related cyclindricine and lepadiformine families, lupin and Amaryllidaceae). In each case, scaffolds were based on structures of the naturally occurring compounds or a close derivative. Scaffold preparation was pursued following the development of appropriate enabling chemical methods. Diversification provided 686 new compounds suitable for screening. The libraries thus prepared had structural characteristics, including sp(3) content, comparable to a basis set of representative natural products and were highly rule-of-five compliant.

SUBMITTER: McLeod MC

PROVIDER: S-EPMC4024831 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Probing chemical space with alkaloid-inspired libraries.

McLeod Michael C MC Singh Gurpreet G Plampin James N JN Rane Digamber D Wang Jenna L JL Day Victor W VW Aubé Jeffrey J

Nature chemistry 20140119 2

Screening of small-molecule libraries is an important aspect of probe and drug discovery science. Numerous authors have suggested that bioactive natural products are attractive starting points for such libraries because of their structural complexity and sp(3)-rich character. Here, we describe the construction of a screening library based on representative members of four families of biologically active alkaloids (Stemonaceae, the structurally related cyclindricine and lepadiformine families, lu ...[more]

PMID: 24451589

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