Binding Database

The following articles (labelled with PubMed ID or TBD) are for your review

PMID

Data

Article Title

Organization

Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures.

John Hopkins University

Low molecular weight amidoximes that act as potent inhibitors of lysine-specific demethylase 1.

Wayne State University

(Bis)urea and (bis)thiourea inhibitors of lysine-specific demethylase 1 as epigenetic modulators.

Wayne State University

Terminally alkylated polyamine analogues as chemotherapeutic agents.

Wayne State University

Largazole Analogues Embodying Radical Changes in the Depsipeptide Ring: Development of a More Selective and Highly Potent Analogue.

The University of Toledo

Polyamine-based small molecule epigenetic modulators.

Wayne State University

Recent advances in the development of polyamine analogues as antitumor agents.

Johns Hopkins University

Polyaminohydroxamic acids and polyaminobenzamides as isoform selective histone deacetylase inhibitors.

Wayne State University

Alkyl-substituted polyaminohydroxamic acids: a novel class of targeted histone deacetylase inhibitors.

Wayne State University