Literature DB >> 14552787

A novel series of histone deacetylase inhibitors incorporating hetero aromatic ring systems as connection units.

Yujia Dai1, Yan Guo, Michael L Curtin, Junling Li, Lori J Pease, Jun Guo, Patrick A Marcotte, Keith B Glaser, Steven K Davidsen, Michael R Michaelides.   

Abstract

A series of structurally novel HDAC inhibitors, in which a hetero aromatic ring connects the spacer with the hydrophobic group, has been designed and synthesized. These new inhibitors are very potent in in vitro enzymatic assays and display antiproliferation activity against two human cancer cell lines.

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Year:  2003        PMID: 14552787     DOI: 10.1016/j.bmcl.2003.07.012

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  4 in total

1.  Pharmacophore-based virtual screening of ZINC database, molecular modeling and designing new derivatives as potential HDAC6 inhibitors.

Authors:  Priya Poonia; Monika Sharma; Prakash Jha; Madhu Chopra
Journal:  Mol Divers       Date:  2022-10-10       Impact factor: 3.364

2.  An E/Z conformational behaviour study on the trypanocidal action of lipophilic spiro carbocyclic 2,6-diketopiperazine-1-acetohydroxamic acids.

Authors:  Alexandra Tsatsaroni; Grigoris Zoidis; Panagiotis Zoumpoulakis; Andrew Tsotinis; Martin C Taylor; John M Kelly; George Fytas
Journal:  Tetrahedron Lett       Date:  2013-06-19       Impact factor: 2.415

3.  Search for the pharmacophore of histone deacetylase inhibitors using pharmacophore query and docking study.

Authors:  Atefeh Haji Agha Bozorgi; Afshin Zarghi
Journal:  Iran J Pharm Res       Date:  2014       Impact factor: 1.696

4.  Synthesis and antiproliferative assay of triazolyl-2,2-dimethyl-3-phenylpropanoates as potential HDAC inhibitors.

Authors:  Samir El-Rayes; Gomaa M S; Abouelmagd A; Walid Fathalla; Ibrahim A I Ali
Journal:  RSC Adv       Date:  2019-05-07       Impact factor: 4.036

  4 in total

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