Literature DB >> 16555343

Structure and total synthesis of aspernigerin: a novel cytotoxic endophyte metabolite.

Li Shen1, Yong-Hao Ye, Xiao-Ting Wang, Hai-Liang Zhu, Chen Xu, Yong-Cun Song, Hai Li, Ren-Xiang Tan.   

Abstract

Aspernigerin (1), a novel cytotoxic alkaloid consisting of an unprecedented structural framework has been isolated from the extract of a culture of Aspergillus niger IFB-E003, an endophyte in Cyndon dactylon. Its structure was elucidated on the basis of comprehensive NMR spectral analysis and confirmed by single-crystal X-ray analysis. Aspernigerin (1) has been shown to be cytotoxic to the tumor cell lines nasopharynyeal epidermoid KB, cervical carcinoma Hela, and colorectal carcinoma SW1116 with corresponding IC(50) values of 22, 46, and 35 microM, respectively. A feasible total synthetic route for aspernigerin (1) has been established for further pharmacological research.

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Year:  2006        PMID: 16555343     DOI: 10.1002/chem.200501423

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  New cytotoxic trichothecene macrolide epimers from endophytic Myrothecium roridum IFB-E012.

Authors:  Li Shen; Li Zhu; Qingwei Tan; Dan Wan; Ju Xie; Jiangnan Peng
Journal:  J Antibiot (Tokyo)       Date:  2016-07-13       Impact factor: 2.649

Review 2.  Safety of the fungal workhorses of industrial biotechnology: update on the mycotoxin and secondary metabolite potential of Aspergillus niger, Aspergillus oryzae, and Trichoderma reesei.

Authors:  Jens C Frisvad; Lars L H Møller; Thomas O Larsen; Ravi Kumar; José Arnau
Journal:  Appl Microbiol Biotechnol       Date:  2018-10-06       Impact factor: 4.813

3.  NMR-based investigations of acyl-functionalized piperazines concerning their conformational behavior in solution.

Authors:  Robert Wodtke; Janine Steinberg; Martin Köckerling; Reik Löser; Constantin Mamat
Journal:  RSC Adv       Date:  2018-12-06       Impact factor: 4.036

4.  Synthesis and fungicidal activity of pyrazole derivatives containing 1,2,3,4-tetrahydroquinoline.

Authors:  Peng Lei; Xuebo Zhang; Yan Xu; Gaofei Xu; Xili Liu; Xinling Yang; Xiaohe Zhang; Yun Ling
Journal:  Chem Cent J       Date:  2016-07-04       Impact factor: 4.215

  4 in total

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