Isolation of Putative Biosynthetic Intermediates of Prenylated Indole Alkaloids from a Thermophilic Fungus Talaromyces thermophilus-Reference-Cited by-同舟云学术

Isolation of Putative Biosynthetic Intermediates of Prenylated Indole Alkaloids from a Thermophilic Fungus Talaromyces thermophilus

Published:2010-09-02 Issue:19 Volume:12 Page:4356-4359
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chu Yan-Sheng¹,Niu Xue-Mei¹,Wang Yan-Li¹,Guo Ji-Peng¹,Pan Wen-Zheng¹,Huang Xiao-Wei¹,Zhang Ke-Qin¹

Affiliation:

1. Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, Yunnan University, Kunming 650091, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol101817g

Reference20 articles.

1. Stephacidin A and B: Two Structurally Novel, Selective Inhibitors of the Testosterone-Dependent Prostate LNCaP Cells

2. Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp.

3. A Concise, Biomimetic Total Synthesis of Stephacidin A and Notoamide B

4. Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived Aspergillus sp.

5. Notoamide O, a Structurally Unprecedented Prenylated Indole Alkaloid, and Notoamides P−R from a Marine-Derived Fungus, Aspergillus sp.

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