(Q41807968)

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Facile synthesis of substituted trans-2-arylcyclopropylamine inhibitors of the human histone demethylase LSD1 and monoamine oxidases A and B.

scientific article published on 8 January 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Facile synthesis of substituted trans-2-arylcyclopropylamine inhibitors of the human histone demethylase LSD1 and monoamine oxidases A and B. (English)

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Dewey G. McCafferty

5

object named as

Dewey G McCafferty

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

author name string

David M Gooden

1

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Dawn M Z Schmidt

2

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Julie A Pollock

3

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Ami M Kabadi

4

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Europe PubMed Central

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12 October 2017

language of work or name

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publication date

8 January 2008

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Europe PubMed Central

PMC publication ID

12 October 2017

Bioorganic & Medicinal Chemistry Letters

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Europe PubMed Central

PMC publication ID

12 October 2017

18

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Europe PubMed Central

PMC publication ID

12 October 2017

10

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

3047-3051

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Structural basis for the inhibition of the LSD1 histone demethylase by the antidepressant trans-2-phenylcyclopropylamine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

The putative oncogene GASC1 demethylates tri- and dimethylated lysine 9 on histone H3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

The transcriptional repressor JHDM3A demethylates trimethyl histone H3 lysine 9 and lysine 36.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Histone demethylation by a family of JmjC domain-containing proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Histone demethylation mediated by the nuclear amine oxidase homolog LSD1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Exploring distal regions of the A3 adenosine receptor binding site: sterically constrained N6-(2-phenylethyl)adenosine derivatives as potent ligands.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

trans-2-Aryl-N,N-dipropylcyclopropylamines: synthesis and interactions with 5-HT(1A) receptors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

N,N-Dialkylated monophenolic trans-2-phenylcyclopropylamines: novel central 5-hydroxytryptamine receptor agonists

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

6 June 2018

Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

18 August 2018

Fluorinated phenylcyclopropylamines. 2. Effects of aromatic ring substitution and of absolute configuration on inhibition of microbial tyramine oxidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2661354

18 August 2018

Identifiers

10.1016/J.BMCL.2008.01.003

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

ResearchGate publication ID

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