Tranylcypromine Based Lysine-Specific Demethylase 1 Inhibitor: Summary and Perspective.
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
10 12 2020
10 12 2020
Historique:
pubmed:
16
9
2020
medline:
2
2
2021
entrez:
15
9
2020
Statut:
ppublish
Résumé
Histone lysine-specific demethylase 1 (LSD1/KDM1A) has become an important and promising anticancer target since it was first identified in 2004 and specially demethylates lysine residues of histone H3K4me1/2 and H3K9me1/2. LSD1 is ubiquitously overexpressed in diverse cancers, and abrogation of LSD1 results in inhibition of proliferation, invasion, and migration in cancer cells. Over the past decade, a number of biologically active small-molecule LSD1 inhibitors have been developed. To date, six
Identifiants
pubmed: 32931269
doi: 10.1021/acs.jmedchem.0c00919
doi:
Substances chimiques
Antineoplastic Agents
0
Enzyme Inhibitors
0
Tranylcypromine
3E3V44J4Z9
Histone Demethylases
EC 1.14.11.-
KDM1A protein, human
EC 1.5.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
14197-14215Commentaires et corrections
Type : ErratumIn