Literature DB >> 24656801

Synthesis and structure activity relationships of schweinfurthin indoles.

John G Kodet1, John A Beutler2, David F Wiemer3.   

Abstract

As part of a program to explore the biological activity of analogues of the natural schweinfurthins, a set of compounds has been prepared where an indole system can be viewed as a substitution for the resorcinol substructure of the schweinfurthin's D-ring. Twelve of these schweinfurthin indoles have been prepared and evaluated in the 60 cell line screen of the National Cancer Institute. While a range of activity has been observed, it is now clear that schweinfurthin indoles can demonstrate the intriguing pattern of activity associated with the natural stilbenes. In the best cases, these indole analogues display both potency and differential activity across the various cell lines comparable to the best resorcinol analogues.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Indole; SAR; Schweinfurthin; Stilbene analogues

Mesh:

Substances:

Year:  2014        PMID: 24656801      PMCID: PMC4030441          DOI: 10.1016/j.bmc.2014.02.043

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


  20 in total

1.  Mappain, a new cytotoxic prenylated stilbene from Macaranga mappa.

Authors:  J E van Der Kaaden; T K Hemscheidt; S L Mooberry
Journal:  J Nat Prod       Date:  2001-01       Impact factor: 4.050

2.  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

Review 3.  Practical methodologies for the synthesis of indoles.

Authors:  Guy R Humphrey; Jeffrey T Kuethe
Journal:  Chem Rev       Date:  2006-07       Impact factor: 60.622

4.  Synthesis of indole analogues of the natural schweinfurthins.

Authors:  John G Kodet; David F Wiemer
Journal:  J Org Chem       Date:  2013-09-05       Impact factor: 4.354

5.  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

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

Authors:  Joseph J Topczewski; Michael P Callahan; John G Kodet; Jery D Inbarasu; Nolan R Mente; John A Beutler; David F Wiemer
Journal:  Bioorg Med Chem       Date:  2011-10-19       Impact factor: 3.641

7.  Regioselective synthesis of 3-alkylindoles mediated by zinc triflate.

Authors:  Xiuwen Zhu; A Ganesan
Journal:  J Org Chem       Date:  2002-04-19       Impact factor: 4.354

8.  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

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

View more
  5 in total

1.  Calcium and P-glycoprotein independent synergism between schweinfurthins and verapamil.

Authors:  Ryan M Sheehy; Craig H Kuder; Zoe Bachman; Raymond J Hohl
Journal:  Cancer Biol Ther       Date:  2015-06-05       Impact factor: 4.742

2.  Schweinfurthin natural products induce regression of murine melanoma and pair with anti-PD-1 therapy to facilitate durable tumor immunity.

Authors:  Kathleen M Kokolus; Jeremy S Haley; Emily J Koubek; Raghavendra Gowda; Saketh S Dinavahi; Arati Sharma; David F Claxton; Klaus F Helm; Joseph J Drabick; Gavin P Robertson; Jeffrey D Neighbors; Raymond J Hohl; Todd D Schell
Journal:  Oncoimmunology       Date:  2018-11-11       Impact factor: 8.110

3.  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

4.  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

5.  Schweinfurthin induces ICD without ER stress and caspase activation.

Authors:  Ruoheng Zhang; J D Neighbors; T D Schell; R J Hohl
Journal:  Oncoimmunology       Date:  2022-08-03       Impact factor: 7.723

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.