Literature DB >> 12133720

Modern methods to produce natural-product libraries.

Ulrich Abel1, Corinna Koch, Michael Speitling, Friedrich G Hansske.   

Abstract

Natural sources offer a wealth of chemically diverse compounds that have been evolutionary preselected to modulate biochemical pathways. Several industrial and academic groups are accessing this source using advanced technology platforms. Methods have been reported to generate large and diverse natural-product libraries optimised for high-throughput screening and for a fast discovery process. In addition to prefractionated and pure natural-product libraries, parallel synthesis gives access to synthetic, semi-synthetic and natural-product-like libraries. Natural-product chemistry and organic synthesis are powerful tools for optimising natural leads and for generating new diversity from natural scaffolds. The amalgamation of both may be expected to become an important strategy in future drug design.

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Year:  2002        PMID: 12133720     DOI: 10.1016/s1367-5931(02)00338-1

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  12 in total

Review 1.  Lessons from the past and charting the future of marine natural products drug discovery and chemical biology.

Authors:  William H Gerwick; Bradley S Moore
Journal:  Chem Biol       Date:  2012-01-27

2.  Synthesis of cyclic 1,3-diols as scaffolds for spatially directed libraries.

Authors:  Gurpreet Singh; Jeffrey Aubé
Journal:  Org Biomol Chem       Date:  2016-05-14       Impact factor: 3.876

Review 3.  Modern natural products drug discovery and its relevance to biodiversity conservation.

Authors:  David G I Kingston
Journal:  J Nat Prod       Date:  2010-12-07       Impact factor: 4.050

4.  Skeletal and Appendage Diversity as Design Elements in the Synthesis of a Discovery Library of Nonaromatic Polycyclic 5-Iminooxazolidin-2-ones, Hydantoins, and Acylureas.

Authors:  S Werner; D M Turner; P G Chambers; K M Brummond
Journal:  Tetrahedron       Date:  2008-07-14       Impact factor: 2.457

5.  Revisiting a classic approach to the Aspidosperma alkaloids: an intramolecular Schmidt reaction mediated synthesis of (+)-aspidospermidine.

Authors:  Rajesh Iyengar; Klaas Schildknegt; Martha Morton; Jeffrey Aubé
Journal:  J Org Chem       Date:  2005-12-23       Impact factor: 4.354

6.  Catalytic site-selective synthesis and evaluation of a series of erythromycin analogs.

Authors:  Chad A Lewis; Janie Merkel; Scott J Miller
Journal:  Bioorg Med Chem Lett       Date:  2008-09-09       Impact factor: 2.823

7.  An approach to the site-selective diversification of apoptolidin A with peptide-based catalysts.

Authors:  Chad A Lewis; Kate E Longcore; Scott J Miller; Paul A Wender
Journal:  J Nat Prod       Date:  2009-10       Impact factor: 4.050

Review 8.  Screening and identification of novel biologically active natural compounds.

Authors:  David Newman
Journal:  F1000Res       Date:  2017-06-05

9.  Identifying enriched drug fragments as possible candidates for metabolic engineering.

Authors:  Sunandini Sharma; Kritika Karri; Ishwor Thapa; Dhundy Bastola; Dario Ghersi
Journal:  BMC Med Genomics       Date:  2016-08-10       Impact factor: 3.063

10.  Characterization of the antibacterial activity of Bald's eyesalve against drug resistant Staphylococcus aureus and Pseudomonas aeruginosa.

Authors:  Amanda L Fuchs; Alan J Weaver; Brian P Tripet; Mary Cloud B Ammons; Martin Teintze; Valérie Copié
Journal:  PLoS One       Date:  2018-11-28       Impact factor: 3.240

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