(Q35141069)

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Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J.

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 August 2017

Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Sachiko Tsukamoto

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Sachiko Tsukamoto

3

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author name string

Jennifer M Finefield

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

David H Sherman

2

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Europe PubMed Central

PubMed publication ID

6 August 2017

Robert M Williams

4

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Europe PubMed Central

PubMed publication ID

6 August 2017

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publication date

28 June 2011

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Europe PubMed Central

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6 August 2017

Journal of Organic Chemistry

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Europe PubMed Central

PubMed publication ID

6 August 2017

76

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Europe PubMed Central

PubMed publication ID

6 August 2017

15

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

5954-5958

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Synthesis of notoamide J: a potentially pivotal intermediate in the biosynthesis of several prenylated indole alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Asymmetric total syntheses of (+)- and (-)-versicolamide B and biosynthetic implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Premalbrancheamide: synthesis, isotopic labeling, biosynthetic incorporation, and detection in cultures of Malbranchea aurantiaca

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Stephacidin A and B: two structurally novel, selective inhibitors of the testosterone-dependent prostate LNCaP cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Novel antinematodal and antiparasitic agents from Penicillium charlesii. II. Structure determination of paraherquamides B, C, D, E, F, and G.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Novel antinematodal and antiparasitic agents from Penicillium charlesii. I. Fermentation, isolation and biological activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

28 July 2018

Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148199

27 September 2018

Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Concise Total Synthesis of the Notoamides C and D

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on the Biosynthesis of Paraherquamide: Synthesis and Incorporation of a Hexacyclic Indole Derivative as an Advanced Metabolite This work was supported by the National Institutes of Health (Grant no. CA70375 to R.M.W.). We wish to acknowledge

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies in relation to biosynthesis. XLII. The structural elucidation and some aspects of the biosynthesis of the brevianamides-A and -E

1 reference

https://pubmed.ncbi.nlm.nih.gov/21504234

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JO200218A

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

ResearchGate publication ID

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