Literature DB >> 22329423

Synthesis and biological evaluation of neopeltolide and analogs.

Yubo Cui1, Raghavan Balachandran, Billy W Day, Paul E Floreancig.   

Abstract

The synthesis of neopeltolide analogues that contain variations in the oxazole-containing side chain and in the macrolide core are reported along with the GI(50) values for these compounds against MCF-7, HCT-116, and p53 knockout HCT-116 cell lines. Although biological activity is sensitive to changes in the macrocycle and the side chain, several analogues displayed GI(50) values of <25 nM. Neopeltolide and several of the more potent analogues were significantly less potent against p53 knockout cells, suggesting that p53 plays an auxiliary role in the activity of these compounds.

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Year:  2012        PMID: 22329423      PMCID: PMC3308185          DOI: 10.1021/jo2023685

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  34 in total

1.  Concise formal synthesis of (+)-neopeltolide.

Authors:  Zhen Yang; Bingbin Zhang; Gaoyuan Zhao; Juan Yang; Xingang Xie; Xuegong She
Journal:  Org Lett       Date:  2011-10-13       Impact factor: 6.005

2.  Mitsunobu and related reactions: advances and applications.

Authors:  K C Kumara Swamy; N N Bhuvan Kumar; E Balaraman; K V P Pavan Kumar
Journal:  Chem Rev       Date:  2009-06       Impact factor: 60.622

3.  Total synthesis of (+)-neopeltolide.

Authors:  Haruhiko Fuwa; Shinya Naito; Tomomi Goto; Makoto Sasaki
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

4.  Total synthesis and structure-activity investigation of the marine natural product neopeltolide.

Authors:  Daniel W Custar; Thomas P Zabawa; John Hines; Craig M Crews; Karl A Scheidt
Journal:  J Am Chem Soc       Date:  2009-09-02       Impact factor: 15.419

5.  Neopeltolide, a macrolide from a lithistid sponge of the family Neopeltidae.

Authors:  Amy E Wright; Julianne Cook Botelho; Esther Guzmán; Dedra Harmody; Patricia Linley; Peter J McCarthy; Tara P Pitts; Shirley A Pomponi; John K Reed
Journal:  J Nat Prod       Date:  2007-02-20       Impact factor: 4.050

6.  Concise enantioselective total synthesis of neopeltolide macrolactone highlighted by ether transfer.

Authors:  Rendy Kartika; Thomas R Gruffi; Richard E Taylor
Journal:  Org Lett       Date:  2008-10-15       Impact factor: 6.005

7.  Total synthesis and structural revision of the marine macrolide neopeltolide.

Authors:  Daniel W Custar; Thomas P Zabawa; Karl A Scheidt
Journal:  J Am Chem Soc       Date:  2008-01-23       Impact factor: 15.419

8.  Oxidative carbocation formation in macrocycles: synthesis of the neopeltolide macrocycle.

Authors:  Wangyang Tu; Paul E Floreancig
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

9.  Total synthesis and biological activity of neopeltolide and analogues.

Authors:  Viktor V Vintonyak; Brigitte Kunze; Florenz Sasse; Martin E Maier
Journal:  Chemistry       Date:  2008       Impact factor: 5.236

10.  Use of an aqueous soluble tetrazolium/formazan assay to measure viability and proliferation of lymphokine-dependent cell lines.

Authors:  T M Buttke; J A McCubrey; T C Owen
Journal:  J Immunol Methods       Date:  1993-01-04       Impact factor: 2.303

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  7 in total

1.  Enantioselective total synthesis of macrolide (+)-neopeltolide.

Authors:  Arun K Ghosh; Khriesto A Shurrush; Zachary L Dawson
Journal:  Org Biomol Chem       Date:  2013-10-11       Impact factor: 3.876

2.  Synthesis and biological properties of C-2 triazolylinosine derivatives.

Authors:  Mahesh K Lakshman; Amit Kumar; Raghavan Balachandran; Billy W Day; Graciela Andrei; Robert Snoeck; Jan Balzarini
Journal:  J Org Chem       Date:  2012-07-03       Impact factor: 4.354

3.  Strategies and Methods for the Synthesis of Anticancer Natural Product Neopeltolide and its Analogs.

Authors:  Yu Bai; Mingji Dai
Journal:  Curr Org Chem       Date:  2015       Impact factor: 2.180

4.  Synthesis of tetrahydropyran/tetrahydrofuran-containing macrolides by palladium-catalyzed alkoxycarbonylative macrolactonizations.

Authors:  Yu Bai; Dexter C Davis; Mingji Dai
Journal:  Angew Chem Int Ed Engl       Date:  2014-05-13       Impact factor: 15.336

5.  Programmed cell death induced by (-)-8,9-dehydroneopeltolide in human promyelocytic leukemia HL-60 cells under energy stress conditions.

Authors:  Haruhiko Fuwa; Mizuho Sato; Makoto Sasaki
Journal:  Mar Drugs       Date:  2014-11-20       Impact factor: 5.118

Review 6.  A look around the West Indies: The spices of life are secondary metabolites.

Authors:  Adrian Demeritte; William M Wuest
Journal:  Bioorg Med Chem       Date:  2020-10-01       Impact factor: 3.641

Review 7.  Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product.

Authors:  Haruhiko Fuwa
Journal:  Mar Drugs       Date:  2016-03-25       Impact factor: 5.118

  7 in total

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