Literature DB >> 19042133

Gamma-pyrone natural products--a privileged compound class provided by nature.

Wolfram Wilk1, Herbert Waldmann, Markus Kaiser.   

Abstract

In "Biology Oriented Synthesis" (BIOS), the inherent biological relevance of natural products is employed for the design and synthesis of compound libraries. Towards this end, library generation in BIOS is focused on compound classes from biologically relevant space such as the natural product space or also the drug space and only scaffolds of these areas of proven relevance are employed for synthesis of small focused libraries with limited diversity. We here present a short overview of gamma-pyrone natural products, highlighting their biological properties and their potential applicability in a BIOS of a compound library.

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Year:  2008        PMID: 19042133     DOI: 10.1016/j.bmc.2008.11.001

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  13 in total

1.  Synthesis and SAR of Lehualide B: a marine-derived natural product with potent anti-multiple myeloma activity.

Authors:  Valer Jeso; Chunying Yang; Michael D Cameron; John L Cleveland; Glenn C Micalizio
Journal:  ACS Chem Biol       Date:  2013-04-02       Impact factor: 5.100

2.  The cephalostatins. 22. synthesis of bis-steroidal pyrazine pyrones (1).

Authors:  George R Pettit; Bryan R Moser; Ricardo F Mendonça; John C Knight; Fiona Hogan
Journal:  J Nat Prod       Date:  2012-05-18       Impact factor: 4.050

3.  Development of an alkaloid-pyrone annulation: synthesis of pleiomaltinine.

Authors:  Robert E Ziegler; Shin-Jowl Tan; Toh-Seok Kam; John A Porco
Journal:  Angew Chem Int Ed Engl       Date:  2012-08-15       Impact factor: 15.336

4.  Exploiting enzymatic promiscuity to engineer a focused library of highly selective antifungal and antiproliferative aureothin analogues.

Authors:  Martina Werneburg; Benjamin Busch; Jing He; Martin E A Richter; Longkuan Xiang; Bradley S Moore; Martin Roth; Hans-Martin Dahse; Christian Hertweck
Journal:  J Am Chem Soc       Date:  2010-08-04       Impact factor: 15.419

5.  Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones.

Authors:  Roman N Vydzhak; Svitlana Ya Panchishin; Maryna V Kachaeva; Stepan G Pilyo; Viktoriia S Moskvina; Olga V Shablykina; Andriy V Kozytskiy; Volodymyr S Brovarets
Journal:  Mol Divers       Date:  2021-06-04       Impact factor: 3.364

6.  Structure and biosynthesis of sorangipyranone - a new γ-dihydropyrone from the myxobacterial strain MSr12020.

Authors:  Dorothy A Okoth; Joachim J Hug; Attila Mándi; Tibor Kurtán; Ronald Garcia; Rolf Müller
Journal:  J Ind Microbiol Biotechnol       Date:  2021-06-04       Impact factor: 4.258

7.  Synthesis of γ-pyrones via decarboxylative condensation of β-ketoacids.

Authors:  Jérémy Merad; Thomas Maier; Catarina A B Rodrigues; Nuno Maulide
Journal:  Monatsh Chem       Date:  2016-10-27       Impact factor: 1.451

8.  Isolation of Smenopyrone, a Bis-γ-Pyrone Polypropionate from the Caribbean Sponge Smenospongia aurea.

Authors:  Germana Esposito; Roberta Teta; Gerardo Della Sala; Joseph R Pawlik; Alfonso Mangoni; Valeria Costantino
Journal:  Mar Drugs       Date:  2018-08-17       Impact factor: 5.118

9.  Assessing medium constituents for optimal heterologous production of anhydromevalonolactone in recombinant Aspergillus oryzae.

Authors:  Songsak Wattanachaisaereekul; Anuwat Tachaleat; Juntira Punya; Rachada Haritakun; Chollaratt Boonlarppradab; Supapon Cheevadhanarak
Journal:  AMB Express       Date:  2014-06-27       Impact factor: 3.298

10.  Nocapyrones: α- and γ-pyrones from a marine-derived Nocardiopsis sp.

Authors:  Youngju Kim; Hiromu Ogura; Kazuaki Akasaka; Tsutomu Oikawa; Nobuyasu Matsuura; Chiaki Imada; Hisato Yasuda; Yasuhiro Igarashi
Journal:  Mar Drugs       Date:  2014-07-08       Impact factor: 5.118

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