Literature DB >> 21684804

Natural product-like synthetic libraries.

Gemma L Thomas1, Charles W Johannes.   

Abstract

There is a paucity of chemical matter suitably poised for effective drug development. Improving the quality and efficiency of research early on in the drug discovery process has been a long standing objective for the drug industry and improvements to the accessibility and quality of compound screening decks might have a significant and positive impact. In the absence of specific molecular information that can be modeled and used predicatively we are far from identifying which small molecules are most relevant to emerging biological targets such as protein-protein interactions. Natural products have been historically successful as an entry point for drug discovery and recently screening libraries are being synthesized to emulate natural product like features.
Copyright © 2011. Published by Elsevier Ltd.

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Year:  2011        PMID: 21684804     DOI: 10.1016/j.cbpa.2011.05.022

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


  9 in total

1.  Functional chromatographic technique for natural product isolation.

Authors:  Eric C Lau; Damian J Mason; Nicole Eichhorst; Pearce Engelder; Celestina Mesa; E M Kithsiri Wijeratne; G M Kamal B Gunaherath; A A Leslie Gunatilaka; James J La Clair; Eli Chapman
Journal:  Org Biomol Chem       Date:  2015-02-28       Impact factor: 3.876

Review 2.  Counting on natural products for drug design.

Authors:  Tiago Rodrigues; Daniel Reker; Petra Schneider; Gisbert Schneider
Journal:  Nat Chem       Date:  2016-04-25       Impact factor: 24.427

3.  Mechanism for phenanthridines synthesis by nitrogenation of 2-acetylbiphenyls in acidic solution: a DFT study.

Authors:  Lihui Guo; Fuqiang Zhang; Xiang Zhang
Journal:  J Mol Model       Date:  2016-10-28       Impact factor: 1.810

4.  Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases.

Authors:  Yuquan Xu; Tong Zhou; Shuwei Zhang; Patricia Espinosa-Artiles; Luoyi Wang; Wei Zhang; Min Lin; A A Leslie Gunatilaka; Jixun Zhan; István Molnár
Journal:  Proc Natl Acad Sci U S A       Date:  2014-07-21       Impact factor: 11.205

5.  Probing chemical space with alkaloid-inspired libraries.

Authors:  Michael C McLeod; Gurpreet Singh; James N Plampin; Digamber Rane; Jenna L Wang; Victor W Day; Jeffrey Aubé
Journal:  Nat Chem       Date:  2014-01-19       Impact factor: 24.427

6.  Direct comparison of linear and macrocyclic compound libraries as a source of protein ligands.

Authors:  Yu Gao; Thomas Kodadek
Journal:  ACS Comb Sci       Date:  2015-02-14       Impact factor: 3.784

7.  CFam: a chemical families database based on iterative selection of functional seeds and seed-directed compound clustering.

Authors:  Cheng Zhang; Lin Tao; Chu Qin; Peng Zhang; Shangying Chen; Xian Zeng; Feng Xu; Zhe Chen; Sheng Yong Yang; Yu Zong Chen
Journal:  Nucleic Acids Res       Date:  2014-11-20       Impact factor: 16.971

8.  Natural-like products as potential SARS-CoV-2 Mpro inhibitors: in-silico drug discovery.

Authors:  Mahmoud A A Ibrahim; Khlood A A Abdeljawaad; Alaa H M Abdelrahman; Mohamed-Elamir F Hegazy
Journal:  J Biomol Struct Dyn       Date:  2020-07-08

9.  Interaction of multimicrobial synthetic inhibitor 1,2-bis(2-benzimidazolyl)-1,2-ethanediol with serum albumin: spectroscopic and computational studies.

Authors:  Nayana Kamtekar; Anita Pandey; Neeraj Agrawal; Raghuvir R S Pissurlenkar; Mohanish Borana; Basir Ahmad
Journal:  PLoS One       Date:  2013-01-04       Impact factor: 3.240

  9 in total

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