Identification of Cell-Active Lysine Specific Demethylase 1-Selective Inhibitors-Reference-Cited by-同舟云学术

Identification of Cell-Active Lysine Specific Demethylase 1-Selective Inhibitors

Published:2009-11-16 Issue:48 Volume:131 Page:17536-17537
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ueda Rie¹,Suzuki Takayoshi¹,Mino Koshiki¹,Tsumoto Hiroki¹,Nakagawa Hidehiko¹,Hasegawa Makoto¹,Sasaki Ryuzo¹,Mizukami Tamio¹,Miyata Naoki¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya, Aichi 467-8603, Japan, Graduate School of Bio-Science, Nagahama Institute of Bio-Science Technology, 1266 Tamura-cho, Nagahama, Shiga 526-0829, Japan, and Frontier Pharma Inc., 1281-8 Tamura-cho, Nagahama, Shiga 526-0829, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja907055q

Reference12 articles.

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

2. Histone Demethylation Mediated by the Nuclear Amine Oxidase Homolog LSD1

3. Epigenetic Control Using Natural Products and Synthetic Molecules

4. Structural Basis for the Inhibition of the LSD1 Histone Demethylase by the Antidepressant trans-2-Phenylcyclopropylamine,

5. LSD1 demethylates repressive histone marks to promote androgen-receptor-dependent transcription

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