Abinukitrine A, a unique 17,18-cyclolanostane triterpenoid from Abies nukiangensis-Reference-Cited by-同舟云学术

Abinukitrine A, a unique 17,18-cyclolanostane triterpenoid from Abies nukiangensis

Published:2019 Issue:8 Volume:17 Page:2107-2109
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Yong-Li¹²³⁴⁵^ORCID,Xue Li-Jun⁶⁷⁸⁹⁵,Li Jie¹²³⁴⁵,Chen Li-Ming¹²³⁴⁵,Wu Jian-Jun¹²³⁴⁵,Xu Zhuo-Ni¹²³⁴⁵,Chen Ying¹²³⁴⁵,Tian Yu-Ping¹²³⁴⁵,Yang Xian-Wen¹⁰¹¹¹²¹³⁵^ORCID

Affiliation:

1. Physical and Chemical Analysis laboratory

2. Division of Material Science & Quality Test

3. Shanghai Institute of Measurement and Testing Technology

4. Shanghai 201203

5. China

6. Department of Medical Oncology

7. Jinling Hospital

8. Nanjing University Clinical School of Medicine

9. Nanjing

10. Key Laboratory of Marine Biogenetic Resources

11. Third Institute of Oceanography

12. Ministry of Natural Resources

13. Xiamen 361005

Abstract

Abinukitrine A was isolated from Abies nukiangensis as the first example of 17,18-cyclolanostane. It showed a potent anti-hepatitis C virus effect.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB03117G

Reference15 articles.

1. Phytochemical and Biological Studies ofAbies Species

2. Abibalsamins A and B, Two New Tetraterpenoids from Abies balsamea Oleoresin

3. Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis

4. Abiestetranes A and B, two unique tetraterpenes from Abies fabri

5. Abiesanol A, a novel biflavanol with unique six connective hexacyclic rings isolated from Abies georgei

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