Enzyme evolution in fungal indole alkaloid biosynthesis-Reference-Cited by-同舟云学术

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Enzyme evolution in fungal indole alkaloid biosynthesis

Published:2020-04 Issue:7 Volume:287 Page:1381-1402
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:FEBS J

Author:

Fraley Amy E.¹²^ORCID,Sherman David H.¹²³⁴^ORCID

Affiliation:

1. Department of Medicinal Chemistry University of Michigan Ann Arbor MI USA

2. Life Sciences Institute University of Michigan Ann Arbor MI USA

3. Department of Chemistry University of Michigan Ann Arbor MI USA

4. Department of Microbiology and Immunology University of Michigan Ann Arbor MI USA

Funder

Center for Selective C-H Functionalization, National Science Foundation

National Institutes of Health

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.15270

Reference82 articles.

1. Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(−)-notoamide, paraherquamide and malbrancheamide pathways

2. The structure of paraherquamide, a toxic metabolite from

3. Insecticidal Activity of Paraherquamides, Including Paraherquamide H and Paraherquamide I, Two New Alkaloids Isolated from Penicillium cluniae

4. Malbrancheamide, a new calmodulin inhibitor from the fungus Malbranchea aurantiaca

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

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1. Alkaloids of forest fungi: diversity and therapeutic applications;Forest Fungi;2025

2. Biomimetic and Concise Total Syntheses of Prenylated and Bicyclo[2.2.2]diazaoctane-Containing Indole Alkaloids Including Taichunamide A, Notoamide N and Versicolamide B;The Journal of Organic Chemistry;2024-08-23

3. Asymmetric Total Synthesis of (+)-Chuanxiongnolide L1 via a Stereoselective Oxidative Dearomatization/Diels–Alder Strategy;Organic Letters;2024-03-29

4. An efficient synthesis and anticancer evaluation of 1,2,3-triazolo-indole-2-carboxylate derivatives;Results in Chemistry;2024-01

5. Aspertaichamide a, a novel cytotoxic prenylated indole alkaloid possessing a bicyclo[2.2.2]diazaoctane framework from a marine algal-derived endophytic fungus aspergillus taichungensis 299;Fitoterapia;2024-01

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