(Q34498887)

26489038

2 August 2017

title

1,3-Oxazin-6-one Derivatives and Bohemamine-Type Pyrrolizidine Alkaloids from a Marine-Derived Streptomyces spinoverrucosus (English)

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Streptomyces spinoverrucosus

2 August 2017

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[(1S)-1-carboxy-2-[2-[[(1S,2S,3S,8S)-1-hydroxy-3,8-dimethyl-5-(3-methylbut-2-enoylamino)-7-oxo-2,3-dihydro-1H-pyrrolizin-2-yl]sulfanyl]-1H-imidazol-5-yl]ethyl]-trimethylazanium

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[(1S)-1-carboxy-2-[2-[[(1S,2S,3S,8S)-1-hydroxy-3,8-dimethyl-5-(3-methylbut-2-enoylamino)-7-oxo-2,3-dihydro-1H-pyrrolizin-2-yl]sulfinyl]-1H-imidazol-5-yl]ethyl]-trimethylazanium

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pyrrolizidine alkaloid

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1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

John B. MacMillan

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

author name string

Scott La

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

publication date

21 October 2015

1 reference

26489038

Journal of Natural Products

2 August 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

volume

79

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

page(s)

455-462

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1021/acs.jnatprod.5b00604?email=unpaywall_01@example.com

access restriction status

open access

1 reference

inferred from online access status

cites work

Salinazinones A and B: Pyrrolidinyl-Oxazinones from Solar Saltern-Derived Streptomyces sp. KMF-004.

1 reference

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Spithioneines A and B, Two New Bohemamine Derivatives Possessing Ergothioneine Moiety from a Marine-Derived Streptomyces spinoverrucosus

7 July 2018

1 reference

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A carbonate-forming Baeyer-Villiger monooxygenase

7 July 2018

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Structure-activity relationship in the passage of different pyrrolizidine alkaloids through the gastrointestinal barrier: ABCB1 excretes heliotrine and echimidine

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Analysis of pyrrolizidine alkaloids and evaluation of some biological activities of Algerian Senecio delphinifolius (Asteraceae).

7 July 2018

1 reference

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Cyclopenicillone, a unique cyclopentenone from the cultures of Penicillium decumbens

7 July 2018

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Hepatotoxicity and tumorigenicity induced by metabolic activation of pyrrolizidine alkaloids in herbs

7 July 2018

1 reference

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Pyrrolizidine alkaloid biosynthesis, evolution of a pathway in plant secondary metabolism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Bohemamines from a marine-derived Streptomyces sp.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Jenamidines A to C: unusual alkaloids from Streptomyces sp. with specific antiproliferative properties obtained by chemical screening

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Antitumor agents from bohemic acid complex, III. The isolation of marcellomycin, musettamycin, rudolphomycin, mimimycin, collinemycin, alcindoromycin, and bohemamine

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Plant sources of hepatotoxic pyrrolizidine alkaloids

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Streptocarbazoles A and B, two novel indolocarbazoles from the marine-derived actinomycete strain Streptomyces sp. FMA.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Novel cyclic hexapeptides from marine-derived fungus, Aspergillus sclerotiorum PT06-1.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Determination of the absolute configurations of pharmacological natural products via density functional theory calculations of vibrational circular dichroism: the new cytotoxic iridoid prismatomerin

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Structure reassignment and synthesis of Jenamidines A1/A2, synthesis of (+)-NP25302, and formal synthesis of SB-311009 analogues

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Energy profiles for ketene cyclizations. Interconversion of 1,3-oxazin-6-ones, mesoionic 1,3-oxazinium olates and acylketenes, imidoylketenes, oxoketenimines, and cyclization products

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

Riddelliine N-oxide is a phytochemical and mammalian metabolite with genotoxic activity that is comparable to the parent pyrrolizidine alkaloid riddelliine

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

New cell-cell adhesion inhibitors from Streptomyces sp. UMA-044.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5435457

On the mechanism of conversion of N-acyl-4-acyloxy-beta-lactams into 2-substituted 1,3-oxazin-6-ones. Can a low-barrier transition state be antiaromatic?

27 October 2018

1 reference

12 December 2020

Absolute configuration of lippifoliane and africanane derivatives

1 reference

12 December 2020

Synthesis of jenamidines A1/A2

1 reference

12 December 2020

Bioactive sesquiterpenoids from the rhizomes of Acorus calamus

1 reference

12 December 2020

Conversion of N-acyl-4-acyloxy-beta-lactams into 1,3-oxazin-6-ones: two consecutive pseudopericyclic processes

1 reference

12 December 2020

Metabolic products of microorganisms, 256. Pyrrolams, new pyrrolizidinones produced byStreptomyces olivaceus

1 reference

COCI

https://opencitations.net/index/api/v1/citations/10.1002/JLAC.1990199001100

Jenamidines A to C: Unusual Alkaloids from Streptomyces sp. with Specific Antiproliferative Properties Obtained by Chemical Screening

9 March 2024

1 reference

COCI

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.56.747

10.1021/ACS.JNATPROD.5B00604

12 April 2024

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

26489038

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26489038%20AND%20SRC:MED&resulttype=core&format=json