Literature DB >> 9140231

New aporphine alkaloids and cytotoxic constituents of Hernandia nymphaeifolia.

I S Chen1, J J Chen, C Y Duh, I L Tsai, C T Chang.   

Abstract

Two new aporphine alkaloids, (+)-N-hydroxyhernangerine (1) and N-formyldehydroovigerine (2) as minor bases, along with four known aporphines, (+)-magnoflorine, (+)-hernovine, (+)-N-methylhernovine, and (+)-laurotetanine, two known isoquinolones, thalifoline and northalifoline, and one benzylisoquinoline, (+)-reticuline, have been additionally isolated from the trunk bark of Hernandia nymphaeifolia. The structures of these compounds were elucidated by spectroscopic evidence. Six of the isolated compounds show significant cytotoxic activities (ED50 values < 1 microgram/ml) against P-388, KB16, A549, or HT-29 cell lines.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9140231     DOI: 10.1055/s-2006-957634

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


  3 in total

1.  Assessment of the cytotoxic effects of aporphine prototypes on head and neck cancer cells.

Authors:  Dorival Mendes Rodrigues-Junior; Nicolie Melanie de Almeida Pontes; Gabriela Estrela de Albuquerque; Viviane Carlin; Givago Prado Perecim; Cristiano Raminelli; André Luiz Vettore
Journal:  Invest New Drugs       Date:  2019-05-17       Impact factor: 3.850

Review 2.  Anti-Infective and Anti-Cancer Properties of the Annona Species: Their Ethnomedicinal Uses, Alkaloid Diversity, and Pharmacological Activities.

Authors:  Ari Satia Nugraha; Yuvita Dian Damayanti; Phurpa Wangchuk; Paul A Keller
Journal:  Molecules       Date:  2019-12-03       Impact factor: 4.411

3.  New Anti-Inflammatory Aporphine and Lignan Derivatives from the Root Wood of Hernandia nymphaeifolia.

Authors:  Chuan-Yen Wei; Shih-Wei Wang; Jin-Wang Ye; Tsong-Long Hwang; Ming-Jen Cheng; Ping-Jyun Sung; Tsung-Hsien Chang; Jih-Jung Chen
Journal:  Molecules       Date:  2018-09-07       Impact factor: 4.411

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.