Literature DB >> 18027097

Natural macrocyclic molecules have a possible limited structural diversity.

Aaron T Frank1, Nicola S Farina, Nahed Sawwan, Orrette R Wauchope, Mo Qi, Edyta M Brzostowska, Wang Chan, Frank W Grasso, Paul Haberfield, Alexander Greer.   

Abstract

This paper examines ring size patterns of natural product macrocycles. Evidence is presented that natural macrocycles containing 14-, 16-, and 18-membered rings are of frequent occurrence based on a data mining study. The results raise a question about the limited diversity of macrocycle ring sizes and the nature of the constraints that may cause them. The data suggest that the preference bears no relationship to the odd-even frequency in natural fatty acids. The trends reported here, along with those reported previously (Wessjohann et al. (2005) Mol Divers 9:171), may be generalized to better understand the possible structure preferences of natural macrocycles.

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Year:  2007        PMID: 18027097     DOI: 10.1007/s11030-007-9065-5

Source DB:  PubMed          Journal:  Mol Divers        ISSN: 1381-1991            Impact factor:   2.943


  7 in total

Review 1.  Do enzymes obey the Baldwin rules? A mechanistic imperative in enzymatic cyclization reactions.

Authors:  J A Piccirilli
Journal:  Chem Biol       Date:  1999-03

Review 2.  Polyketide and nonribosomal peptide antibiotics: modularity and versatility.

Authors:  Christopher T Walsh
Journal:  Science       Date:  2004-03-19       Impact factor: 47.728

Review 3.  What can a chemist learn from nature's macrocycles?--a brief, conceptual view.

Authors:  Ludger A Wessjohann; Eelco Ruijter; Daniel Garcia-Rivera; Wolfgang Brandt
Journal:  Mol Divers       Date:  2005       Impact factor: 2.943

4.  Enediynes in 11-membered rings. Synthesis, structure, and reactivity of highly strained but unusually stable macrocycles.

Authors:  Holger Wandel; Olaf Wiest
Journal:  J Org Chem       Date:  2002-01-25       Impact factor: 4.354

5.  Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.

Authors:  Bodo Scheiper; Frank Glorius; Andreas Leitner; Alois Fürstner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-12       Impact factor: 11.205

Review 6.  Macrocyclization strategies in polyketide and nonribosomal peptide biosynthesis.

Authors:  Florian Kopp; Mohamed A Marahiel
Journal:  Nat Prod Rep       Date:  2007-05-10       Impact factor: 13.423

Review 7.  Enediyne natural products: biosynthesis and prospect towards engineering novel antitumor agents.

Authors:  Ben Shen; Wen Liu; Koichi Nonaka
Journal:  Curr Med Chem       Date:  2003-11       Impact factor: 4.530

  7 in total
  4 in total

1.  Oxadiazole grafts in peptide macrocycles.

Authors:  John R Frost; Conor C G Scully; Andrei K Yudin
Journal:  Nat Chem       Date:  2016-10-24       Impact factor: 24.427

2.  Aza-Oxa-Triazole Based Macrocycles with Tunable Properties: Design, Synthesis, and Bioactivity.

Authors:  Subba Rao Cheekatla; Liya Thurakkal; Anna Jose; Debashis Barik; Mintu Porel
Journal:  Molecules       Date:  2022-05-25       Impact factor: 4.927

3.  Macrocycles: lessons from the distant past, recent developments, and future directions.

Authors:  Andrei K Yudin
Journal:  Chem Sci       Date:  2014-11-03       Impact factor: 9.825

4.  Benchmark of Generic Shapes for Macrocycles.

Authors:  Atilio Reyes Romero; Angel Jonathan Ruiz-Moreno; Matthew R Groves; Marco Velasco-Velázquez; Alexander Dömling
Journal:  J Chem Inf Model       Date:  2020-12-03       Impact factor: 6.162

  4 in total

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