Literature DB >> 15939325

Natural product-like chemical space: search for chemical dissectors of macromolecular interactions.

Ayub Reayi1, Prabhat Arya.   

Abstract

Macromolecular interactions (i.e. protein-protein or DNA/RNA-protein interactions) play important cellular roles, including cellular communication and programmed cell death. Small-molecule chemical probes are crucial for dissecting these highly organized interactions, for mapping their function at the molecular level and developing new therapeutics. The lack of ideal chemical probes required to understand macromolecular interactions is the missing link in the next step of dissecting such interactions. Unfortunately, the classical combinatorial-chemistry community has not successfully provided the required probes (i.e. natural product inspired chemical probes that are rich in stereochemical and three-dimensional structural diversity) to achieve these goals. The emerging area of diversity-oriented synthesis (DOS) is beginning to provide natural product-like chemical probes that may be useful in this arena.

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Year:  2005        PMID: 15939325     DOI: 10.1016/j.cbpa.2005.04.007

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


  13 in total

Review 1.  Natural products as sources of new drugs over the 30 years from 1981 to 2010.

Authors:  David J Newman; Gordon M Cragg
Journal:  J Nat Prod       Date:  2012-02-08       Impact factor: 4.050

Review 2.  Role of natural product diversity in chemical biology.

Authors:  Jiyong Hong
Journal:  Curr Opin Chem Biol       Date:  2011-04-12       Impact factor: 8.822

3.  Tetrahydroquinoline-derived macrocyclic toolbox: the discovery of antiangiogenesis agents in zebrafish assay.

Authors:  Shiva Krishna Reddy Guduru; Srinivas Chamakuri; Gayathri Chandrasekar; Satish Srinivas Kitambi; Prabhat Arya
Journal:  ACS Med Chem Lett       Date:  2013-05-24       Impact factor: 4.345

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.  Diversity-oriented synthesis of 13- to 18-membered macrolactams via ring-closing metathesis.

Authors:  Sivaraman Dandapani; Jason T Lowe; Eamon Comer; Lisa A Marcaurelle
Journal:  J Org Chem       Date:  2011-08-29       Impact factor: 4.354

6.  Skeletal diversity via cationic rearrangements of substituted dihydropyrans.

Authors:  Matthew R Medeiros; Radha S Narayan; Nolan T McDougal; Scott E Schaus; John A Porco
Journal:  Org Lett       Date:  2010-07-16       Impact factor: 6.005

7.  Ammosamides A and B target myosin.

Authors:  Chambers C Hughes; John B MacMillan; Susana P Gaudêncio; William Fenical; James J La Clair
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

Review 8.  Features of protein-protein interactions that translate into potent inhibitors: topology, surface area and affinity.

Authors:  Matthew C Smith; Jason E Gestwicki
Journal:  Expert Rev Mol Med       Date:  2012-07-26       Impact factor: 5.600

Review 9.  Towards the optimal screening collection: a synthesis strategy.

Authors:  Thomas E Nielsen; Stuart L Schreiber
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

10.  PAD4 mediated histone hypercitrullination induces heterochromatin decondensation and chromatin unfolding to form neutrophil extracellular trap-like structures.

Authors:  Marc Leshner; Shu Wang; Carrie Lewis; Han Zheng; Xiangyun Amy Chen; Lorraine Santy; Yanming Wang
Journal:  Front Immunol       Date:  2012-10-04       Impact factor: 7.561

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