Trichodermamides D–F, heterocyclic dipeptides with a highly functionalized 1,2-oxazadecaline core isolated from the endophytic fungus Penicillium janthinellum HDN13-309-Reference-Cited by-同舟云学术

Trichodermamides D–F, heterocyclic dipeptides with a highly functionalized 1,2-oxazadecaline core isolated from the endophytic fungus Penicillium janthinellum HDN13-309

Published:2017 Issue:76 Volume:7 Page:48019-48024
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Zhu Meilin¹²³⁴⁵,Yang Zhen⁶⁷⁸⁹¹⁰,Feng Huimin¹²³⁴⁵,Gan Qi¹²³⁴⁵,Che Qian¹²³⁴⁵,Zhu Tianjiao¹²³⁴⁵,Gu Qianqun¹²³⁴⁵,Han Bingnan⁶⁷⁸⁹¹⁰,Li Dehai¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Marine Drugs

2. Chinese Ministry of Education

3. School of Medicine and Pharmacy

4. Ocean University of China

5. Qingdao 266003

6. Department of Development Technology of Marine Resources

7. College of Life Sciences

8. Zhejiang Sci-Tech University

9. Hangzhou 310018

10. People's Republic of China

Abstract

Six trichodermamides, including three new ones, were isolated from an endophytic fungus, and two of them could function as antioxidants.

Funder

National Natural Science Foundation of China

Shandong Provincial Natural Science Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA10389A

Reference20 articles.

1. Trichodermamides A and B, Cytotoxic Modified Dipeptides from the Marine-Derived Fungus Trichoderma virens

2. Induced production of a new dipeptide with a disulfide bridge by long-term fermentation of marine-derived Trichoderma cf. brevicompactum

3. The isolation, structure determination and cytotoxicity of the new fungal metabolite, trichodermamide C

4. Aspergillazines A–E: novel heterocyclic dipeptides from an Australian strain of Aspergillus unilateralis

5. Cytotoxicity and Mechanism of Action of the Marine-Derived Fungal Metabolite Trichodermamide B and Synthetic Analogues

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