Literature DB >> 22055715

Relevance of the C-5 position to schweinfurthin induced cytotoxicity.

Joseph J Topczewski1, Michael P Callahan, John G Kodet, Jery D Inbarasu, Nolan R Mente, John A Beutler, David F Wiemer.   

Abstract

The schweinfurthins are an intriguing group of anti-proliferative agents that display low nanomolar activities against several cell types, including the human-derived glioblastoma cell line SF-295, but have little impact on other cell lines even at micromolar concentrations. This activity has inspired the synthesis of seven of the natural schweinfurthins, all with the correct absolute stereochemistry, and a variety of analogues designed to probe different facets of the pharmacophore. Reported herein is the synthesis of several new schweinfurthin analogues varied at the C-5 position along with data on their biological activity in the NCI 60 cell-line assay.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22055715      PMCID: PMC3232010          DOI: 10.1016/j.bmc.2011.10.034

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


  21 in total

1.  Biologically active biotin derivatives of schweinfurthin F.

Authors:  Natalie C Ulrich; Craig H Kuder; Raymond J Hohl; David F Wiemer
Journal:  Bioorg Med Chem Lett       Date:  2010-09-06       Impact factor: 2.823

2.  Synthesis and structure-activity studies of schweinfurthin B analogs: Evidence for the importance of a D-ring hydrogen bond donor in expression of differential cytotoxicity.

Authors:  Jeffrey D Neighbors; Maya S Salnikova; John A Beutler; David F Wiemer
Journal:  Bioorg Med Chem       Date:  2005-11-14       Impact factor: 3.641

3.  Synthesis of nonracemic 3-deoxyschweinfurthin B.

Authors:  Jeffrey D Neighbors; John A Beutler; David F Wiemer
Journal:  J Org Chem       Date:  2005-02-04       Impact factor: 4.354

4.  Cytotoxic geranyl stilbenes from Macaranga schweinfurthii.

Authors:  J A Beutler; R H Shoemaker; T Johnson; M R Boyd
Journal:  J Nat Prod       Date:  1998-12       Impact factor: 4.050

5.  Natural products reveal cancer cell dependence on oxysterol-binding proteins.

Authors:  Anthony W G Burgett; Thomas B Poulsen; Kittikhun Wangkanont; D Ryan Anderson; Chikako Kikuchi; Kousei Shimada; Shuichi Okubo; Kevin C Fortner; Yoshihiro Mimaki; Minpei Kuroda; Jason P Murphy; David J Schwalb; Eugene C Petrella; Ivan Cornella-Taracido; Markus Schirle; John A Tallarico; Matthew D Shair
Journal:  Nat Chem Biol       Date:  2011-08-07       Impact factor: 15.040

Review 6.  The NCI60 human tumour cell line anticancer drug screen.

Authors:  Robert H Shoemaker
Journal:  Nat Rev Cancer       Date:  2006-10       Impact factor: 60.716

7.  Total synthesis of (R,R,R)- and (S,S,S)-schweinfurthin F: differences of bioactivity in the enantiomeric series.

Authors:  Nolan R Mente; Andrew J Wiemer; Jeffrey D Neighbors; John A Beutler; Raymond J Hohl; David F Wiemer
Journal:  Bioorg Med Chem Lett       Date:  2006-12-12       Impact factor: 2.823

8.  Organocatalytic asymmetric epoxidation of olefins by chiral ketones.

Authors:  Yian Shi
Journal:  Acc Chem Res       Date:  2004-08       Impact factor: 22.384

9.  Total synthesis of (+)-schweinfurthins B and E.

Authors:  Joseph J Topczewski; Jeffrey D Neighbors; David F Wiemer
Journal:  J Org Chem       Date:  2009-09-18       Impact factor: 4.354

10.  BF3 x Et2O-mediated cascade cyclizations: synthesis of schweinfurthins F and G.

Authors:  Nolan R Mente; Jeffrey D Neighbors; David F Wiemer
Journal:  J Org Chem       Date:  2008-09-17       Impact factor: 4.354

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  3 in total

1.  Synthesis and structure activity relationships of schweinfurthin indoles.

Authors:  John G Kodet; John A Beutler; David F Wiemer
Journal:  Bioorg Med Chem       Date:  2014-03-06       Impact factor: 3.641

2.  Synthesis of amide isosteres of schweinfurthin-based stilbenes.

Authors:  David P Stockdale; John A Beutler; David F Wiemer
Journal:  Bioorg Med Chem       Date:  2017-08-09       Impact factor: 3.641

3.  3-Deoxyschweinfurthin B Lowers Cholesterol Levels by Decreasing Synthesis and Increasing Export in Cultured Cancer Cell Lines.

Authors:  Craig H Kuder; Megan M Weivoda; Ying Zhang; Junjia Zhu; Jeffrey D Neighbors; David F Wiemer; Raymond J Hohl
Journal:  Lipids       Date:  2015-10-22       Impact factor: 1.880

  3 in total

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