Bioconversion of 6-epi-Notoamide T produces metabolites of unprecedented structures in a marine-derived Aspergillus sp.-Reference-Cited by-同舟云学术

Bioconversion of 6-epi-Notoamide T produces metabolites of unprecedented structures in a marine-derived Aspergillus sp.

Published:2015-01 Issue:1 Volume:56 Page:247-251
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kato Hikaru,Nakahara Takashi,Yamaguchi Michitaka,Kagiyama Ippei,Finefield Jennifer M.,Sunderhaus James D.,Sherman David H.,Williams Robert M.,Tsukamoto Sachiko

Funder

Grants-in-Aid for Scientific Research

Ministry of Education, Culture, Sports, Science and Technology of Japan

Nagase Science and Technology Foundation

National Institutes of Health

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

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

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

3. Isolation of Notoamide E, a Key Precursor in the Biosynthesis of Prenylated Indole Alkaloids in a Marine-Derived Fungus, Aspergillus sp.

4. Isolation of Antipodal (−)-Versicolamide B and Notoamides L−N 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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