(Q34793685)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23824985%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

title

Lysine-specific demethylase 1-selective inactivators: protein-targeted drug delivery mechanism (English)

1 reference

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4 March 2020

1 reference

2

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4 March 2020

author name string

Daisuke Ogasawara

1

1 reference

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4 March 2020

Hiroki Tsumoto

3

1 reference

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4 March 2020

Taeko Kakizawa

4

1 reference

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4 March 2020

Koshiki Mino

5

1 reference

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4 March 2020

Kiyoshi Fukuhara

6

1 reference

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4 March 2020

Hidehiko Nakagawa

7

1 reference

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4 March 2020

Makoto Hasegawa

8

1 reference

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4 March 2020

Ryuzo Sasaki

9

1 reference

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4 March 2020

Tamio Mizukami

10

1 reference

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4 March 2020

Naoki Miyata

11

1 reference

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4 March 2020

Takayoshi Suzuki

12

1 reference

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4 March 2020

language of work or name

English

0 references

publication date

3 July 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23824985%20AND%20SRC:MED&resulttype=core&format=json

Angewandte Chemie International Edition

4 March 2020

published in

1 reference

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4 March 2020

volume

52

1 reference

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4 March 2020

issue

33

1 reference

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4 March 2020

page(s)

8620-8624

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23824985%20AND%20SRC:MED&resulttype=core&format=json

Histone lysine demethylases: emerging roles in development, physiology and disease

4 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Reversing histone methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

A crack in histone lysine methylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Histone demethylation mediated by the nuclear amine oxidase homolog LSD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

LSD1 and the chemistry of histone demethylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Inhibition of the histone demethylase LSD1 blocks alpha-herpesvirus lytic replication and reactivation from latency

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Lysine-specific demethylase 1 is strongly expressed in poorly differentiated neuroblastoma: implications for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Novel oligoamine analogues inhibit lysine-specific demethylase 1 and induce reexpression of epigenetically silenced genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Lysine-specific demethylase 1 (LSD1) is highly expressed in ER-negative breast cancers and a biomarker predicting aggressive biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Inhibition of the LSD1 (KDM1A) demethylase reactivates the all-trans-retinoic acid differentiation pathway in acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25 A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Identification of cell-active lysine specific demethylase 1-selective inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Synthesis and biological activity of optically active NCL-1, a lysine-specific demethylase 1 selective inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Biochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Lysine demethylases inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Human histone demethylase LSD1 reads the histone code

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

A mechanism-based inactivator for histone demethylase LSD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Comparative analysis of small molecules and histone substrate analogues as LSD1 lysine demethylase inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

Structural basis of histone demethylation by LSD1 revealed by suicide inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANIE.201303999

21 January 2018

Identifiers

DOI

10.1002/ANIE.201303999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23824985%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

1 reference