(Q35954472)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

Reengineering an azaphilone biosynthesis pathway in Aspergillus nidulans to create lipoxygenase inhibitors (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

Putative salicylate hydroxylase

21 January 2020

main subject

0 references

Aspergillus nidulans

object named as

Aspergillus nidulans

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Berl R Oakley

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Amber D Somoza

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Kuan-Han Lee

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Clay C C Wang

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

language of work or name

English

0 references

publication date

1 February 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

page(s)

972-975

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

Synthesis of the azaphilones (+)-sclerotiorin and (+)-8-O-methylsclerotiorinamine utilizing (+)-sparteine surrogates in copper-mediated oxidative dearomatization

21 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

A gene cluster containing two fungal polyketide synthases encodes the biosynthetic pathway for a polyketide, asperfuranone, in Aspergillus nidulans

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Control of oxygenation in lipoxygenase and cyclooxygenase catalysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Sclerotiorin, a novel inhibitor of lipoxygenase from Penicillium frequentans

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Asymmetric syntheses of (-)-mitorubrin and related azaphilone natural products

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Total synthesis of (+/-)-mitorubrinic acid

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Synthesis of the azaphilones using copper-mediated enantioselective oxidative dearomatization

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Lipoxygenases: occurrence, functions, catalysis, and acquisition of substrate

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

IBX-I2 redox couple for facile generation of IOH and I+: expedient protocol for iodohydroxylation of olefins and iodination of aromatics

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3350772

Synthesis studies toward chloroazaphilone and vinylogous gamma-pyridones: two common natural product core structures

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22296232

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The chemistry of fungi. Part LXI. The synthesis of (±)-sclerotiorin, of (±)-4,6-dimethylocta-trans-2,trans-4-dienoic acid, and of an analogue of rotiorin

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22296232

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1021/OL203094K

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

PubMed publication ID

22296232

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22296232%20AND%20SRC:MED&resulttype=core&format=json