Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures
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LSD1 Histone Demethylase Assays and InhibitionSynthesis and Biological Evaluation of Amidinourea and Triazine Congeners as Inhibitors of MDA-MB-231 Human Breast Cancer Cell Proliferation.Inhibitors of Protein Methyltransferases and Demethylases.Functional interaction of histone deacetylase 5 (HDAC5) and lysine-specific demethylase 1 (LSD1) promotes breast cancer progression.Targeting polyamine metabolism for cancer therapy and prevention.Histone Lysine Demethylase Inhibitors.Structural insight into inhibitors of flavin adenine dinucleotide-dependent lysine demethylases.Cyclic by peptide inhibitors of lysine-specific demethylase 1 with improved potency identified by alanine scanning mutagenesis.Polyamines and Cancer.Antibacterial Diamines Targeting Bacterial Membranes.
P2860
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P2860
Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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name
Structure-activity study for ( ...... carbon backbone architectures
@en
type
label
Structure-activity study for ( ...... carbon backbone architectures
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prefLabel
Structure-activity study for ( ...... carbon backbone architectures
@en
P2093
P2860
P1476
Structure-activity study for ( ...... carbon backbone architectures
@en
P2093
Boobalan Pachaiyappan
Craig J Kutz
Robert A Casero
Shannon L Nowotarski
Shiv K Sharma
Steven L Holshouser
Youxuan Li
P2860
P304
P356
10.1016/J.BMC.2015.01.049
P407
P577
2015-02-07T00:00:00Z