Sporormielones A–E, bioactive novel C–C coupled orsellinic acid derivative dimers, and their biosynthetic origin-Reference-Cited by-同舟云学术

Sporormielones A–E, bioactive novel C–C coupled orsellinic acid derivative dimers, and their biosynthetic origin

Published:2020 Issue:33 Volume:56 Page:4607-4610
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Chen Guo-Dong¹²³⁴⁵,Hu Dan¹²³⁴⁵^ORCID,Huang Mei-Juan¹²³⁴⁵,Tang Jia¹²³⁴⁵,Wang Xiao-Xia¹²³⁴⁵,Zou Jian¹²³⁴⁵,Xie Jun¹²³⁴⁵,Zhang Wei-Guang⁶⁷⁸⁵,Guo Liang-Dong⁹¹⁰¹¹¹²⁵,Yao Xin-Sheng¹²³⁴⁵^ORCID,Abe Ikuro¹³¹⁴¹⁵¹⁶^ORCID,Gao Hao¹²³⁴⁵^ORCID

Affiliation:

1. Institute of Traditional Chinese Medicine & Natural Products

2. College of Pharmacy/Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research

3. Jinan University

4. Guangzhou 510632

5. China

6. School of Chemistry and Environment

7. South China Normal University

8. Guangzhou 510006

9. State Key Laboratory of Mycology

10. Institute of Microbiology

11. Chinese Academy of Sciences

12. Beijing 100190

13. Graduate School of Pharmaceutical Sciences

14. University of Tokyo

15. Tokyo113-003

16. Japan

Abstract

Sporormielones A–E, novel C–C coupled orsellinic acid derivative dimers containing tricyclic cores with a dimethylcyclopentenone unit, were isolated from Sporormiella sp., and their plausible biosynthetic mechanism was proposed.

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Ministry of Education of the People's Republic of China

Higher Education Discipline Innovation Project

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/D0CC00855A

Reference24 articles.

1. Chemistry and Biological Activity of Ramalina Lichenized Fungi

2. Biologically active fungal depsidones: Chemistry, biosynthesis, structural characterization, and bioactivities

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