Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp (Q35158442)

6 August 2017

title

Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp (English)

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6 August 2017

Sachiko Tsukamoto

9

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author name string

Hikaru Kato

1

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6 August 2017

Takashi Nakahara

2

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Michitaka Yamaguchi

3

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Ippei Kagiyama

4

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Jennifer M Finefield

5

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James D Sunderhaus

6

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David H Sherman

7

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Robert M Williams

8

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publication date

1 January 2015

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6 August 2017

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6 August 2017

volume

56

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6 August 2017

issue

1

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6 August 2017

page(s)

247-251

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Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B

6 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

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

13 July 2018

1 reference

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Titration-Based Screening for Evaluation of Natural Product Extracts: Identification of an Aspulvinone Family of Luciferase Inhibitors

13 July 2018

1 reference

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Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Notoamide O, a structurally unprecedented prenylated indole alkaloid, and notoamides P-R from a marine-derived fungus, Aspergillus sp.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Epigenome manipulation as a pathway to new natural product scaffolds and their congeners

13 July 2018

1 reference

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Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Isolation of notoamide E, a key precursor in the biosynthesis of prenylated indole alkaloids in a marine-derived fungus, Aspergillus sp

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Isolation of antipodal (-)-versicolamide B and notoamides L-N from a marine-derived Aspergillus sp.

13 July 2018

1 reference

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Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

Notoamides F-K, prenylated indole alkaloids isolated from a marine-derived Aspergillus sp.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4353397

A Concise Total Synthesis of the Notoamides C and D

27 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation and Photoinduced Conversion of 6-epi-Stephacidins from Aspergillus taichungensis

1 reference

12 December 2020

10.1016/J.TETLET.2014.11.083

Identifiers

DOI

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6 August 2017

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6 August 2017

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