Michellamines A6 and A7, and further mono- and dimeric naphthylisoquinoline alkaloids from a Congolese Ancistrocladus liana and their antiausterity activities against pancreatic cancer cells-Reference-Cited by-同舟云学术

Michellamines A6 and A7, and further mono- and dimeric naphthylisoquinoline alkaloids from a Congolese Ancistrocladus liana and their antiausterity activities against pancreatic cancer cells

Published:2018 Issue:10 Volume:8 Page:5243-5254
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Lombe Blaise Kimbadi¹²³⁴⁵^ORCID,Feineis Doris¹²³⁴,Mudogo Virima⁵⁶⁷⁸,Brun Reto⁹¹⁰¹¹¹²¹³,Awale Suresh¹⁴¹⁵¹⁶¹⁷¹⁸^ORCID,Bringmann Gerhard¹²³⁴^ORCID

Affiliation:

1. Institute of Organic Chemistry

2. University of Würzburg

3. D-97074 Würzburg

4. Germany

5. Faculté des Sciences

6. Université de Kinshasa

7. Kinshasa XI

8. Democratic Republic of the Congo

9. Swiss Tropical and Public Health Institute

10. CH-4002 Basel

11. Switzerland

12. University of Basel

13. CH-4003 Basel

14. Division of Natural Drug Discovery

15. Institute of Natural Medicine

16. University of Toyoma

17. Toyama 930-0194

18. Japan

Abstract

The first dimers of 5,8′-coupled naphthylisoquinolines with two 1,3-cis-configured tetrahydroisoquinoline portions and their cytotoxicities against cancer cells are described.

Funder

Deutscher Akademischer Austauschdienst

Deutsche Forschungsgemeinschaft

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA00363G

Reference33 articles.

1. G.Bringmann and F.Pokorny , in The Alkaloids , ed. G. A. Cordell , Academic Press Inc , New York , 1995 , vol. 46 , pp. 127–271