Literature DB >> 22109836

Phytochemical investigation and in vitro cytotoxic evaluation of alkaloids from Abuta rufescens.

Diane S Swaffar1, Chad J Holley, Richard W Fitch, Kyle R Elkin, Clarice Zhang, Jennifer P Sturgill, Mary D Menachery.   

Abstract

A phytochemical investigation of Abuta rufescens was performed to authenticate plant material reported previously and to assess the cytotoxicity of the alkaloids obtained from the plant. Three alkaloids which have not previously been reported from this species, two phenolic (subsessiline, an oxoaporphine, and telitoxine, an azafluoranthene) and one non-phenolic (isoimerubrine, a tropoloisoquinoline), were isolated and identified. These alkaloids, along with others previously isolated from this and another Abuta species (grandirubrine, a tropoloisoquinoline), were evaluated for cytotoxic activity against several human cancer cell lines (HCT-116 colon adenocarcinoma, ACHN renal carcinoma, and A549 lung carcinoma). The tropoloisoquinoline alkaloids (grandirubrine, imerubrine, and isoimerubrine) exhibited the greatest cytotoxicity against the cell lines, especially ACHN and HCT-116 cells. The azafluoranthene alkaloid imeluteine exhibited lesser cytotoxicity, as did one of the oxoaporphine alkaloids. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2011        PMID: 22109836     DOI: 10.1055/s-0031-1280383

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  3 in total

1.  In Vitro and In Silico Evaluation of Cholinesterase Inhibition by Alkaloids Obtained from Branches of Abuta panurensis Eichler.

Authors:  Rochelly da Silva Mesquita; Andrii Kyrylchuk; Anton Cherednichenko; Ingrity Suelen Costa Sá; Lílian Macedo Bastos; Felipe Moura Araújo da Silva; Rita de Cássia Saraiva Nunomura; Andriy Grafov
Journal:  Molecules       Date:  2022-05-13       Impact factor: 4.927

2.  A New Route to Azafluoranthene Natural Products via Direct Arylation.

Authors:  Shashikanth Ponnala; Wayne W Harding
Journal:  European J Org Chem       Date:  2013-01-03

3.  Novel total syntheses of oxoaporphine alkaloids enabled by mild Cu-catalyzed tandem oxidation/aromatization of 1-Bn-DHIQs.

Authors:  Bo Zheng; Hui-Ya Qu; Tian-Zhuo Meng; Xia Lu; Jie Zheng; Yun-Gang He; Qi-Qi Fan; Xiao-Xin Shi
Journal:  RSC Adv       Date:  2018-08-14       Impact factor: 4.036

  3 in total

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