Literature DB >> 25080080

Medicinal chemistry of catechol O-methyltransferase (COMT) inhibitors and their therapeutic utility.

László E Kiss1, Patrício Soares-da-Silva.   

Abstract

Catechol O-methyltransferase (COMT) is the enzyme responsible for the O-methylation of endogenous neurotransmitters and of xenobiotic substances and hormones incorporating catecholic structures. COMT is a druggable biological target for the treatment of various central and peripheral nervous system disorders, including Parkinson's disease, depression, schizophrenia, and other dopamine deficiency-related diseases. The purpose of this perspective is fourfold: (i) to summarize the physiological role of COMT inhibitors in central and peripheral nervous system disorders; (ii) to provide the history and perspective of the medicinal chemistry behind the discovery and development of COMT inhibitors; (iii) to discuss how the physicochemical properties of recognized COMT inhibitors are understood to exert influence over their pharmacological properties; and (iv) to evaluate the clinical benefits of the most relevant COMT inhibitors.

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Year:  2014        PMID: 25080080     DOI: 10.1021/jm500572b

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  23 in total

Review 1.  Targeting Metalloenzymes for Therapeutic Intervention.

Authors:  Allie Y Chen; Rebecca N Adamek; Benjamin L Dick; Cy V Credille; Christine N Morrison; Seth M Cohen
Journal:  Chem Rev       Date:  2018-09-07       Impact factor: 60.622

2.  Synthesis and Evaluation of Heterocyclic Catechol Mimics as Inhibitors of Catechol-O-methyltransferase (COMT).

Authors:  Scott T Harrison; Michael S Poslusney; James J Mulhearn; Zhijian Zhao; Nathan R Kett; Jeffrey W Schubert; Jeffrey Y Melamed; Timothy J Allison; Sangita B Patel; John M Sanders; Sujata Sharma; Robert F Smith; Dawn L Hall; Ronald G Robinson; Nancy A Sachs; Pete H Hutson; Scott E Wolkenberg; James C Barrow
Journal:  ACS Med Chem Lett       Date:  2015-01-26       Impact factor: 4.345

3.  Effectiveness and safety of opicapone in Parkinson's disease patients with motor fluctuations: the OPTIPARK open-label study.

Authors:  Heinz Reichmann; Andrew Lees; José-Francisco Rocha; Diogo Magalhães; Patrício Soares-da-Silva
Journal:  Transl Neurodegener       Date:  2020-03-04       Impact factor: 8.014

4.  Pharmacophore-based virtual screening of catechol-o-methyltransferase (COMT) inhibitors to combat Alzheimer's disease.

Authors:  Chirag N Patel; John J Georrge; Krunal M Modi; Moksha B Narechania; Daxesh P Patel; Frank J Gonzalez; Himanshu A Pandya
Journal:  J Biomol Struct Dyn       Date:  2017-12-27

5.  Effect of opicapone multiple-dose regimens on levodopa pharmacokinetics.

Authors:  José-Francisco Rocha; Éric Sicard; Nicolas Fauchoux; Amílcar Falcão; Ana Santos; Ana I Loureiro; Roberto Pinto; Maria João Bonifácio; Teresa Nunes; Luís Almeida; Patrício Soares-da-Silva
Journal:  Br J Clin Pharmacol       Date:  2016-12-02       Impact factor: 4.335

6.  1-Hydroxy-2(1H)-pyridinone-Based Chelators with Potential Catechol O-Methyl Transferase Inhibition and Neurorescue Dual Action against Parkinson's Disease.

Authors:  Joseph C J Bergin; Kean Kan Tan; Anya K Nelson; Cristina-Andreea Amarandei; Véronique Hubscher-Bruder; Jérémy Brandel; Varvara Voinarovska; Annick Dejaegere; Roland H Stote; David Tétard
Journal:  Molecules       Date:  2022-04-28       Impact factor: 4.927

7.  A Clinical Trial Simulation Evaluating Epinephrine Pharmacokinetics at various Dosing Frequencies during Cardiopulmonary Resuscitation.

Authors:  Andy R Eugene
Journal:  MEDtube Sci       Date:  2016-06-30

8.  Examining the Origin of Catalytic Power of Catechol O-Methyltransferase.

Authors:  Xi Chen; Steven D Schwartz
Journal:  ACS Catal       Date:  2019-09-17       Impact factor: 13.084

9.  1H, 15N, 13C backbone resonance assignments of human soluble catechol O-methyltransferase in complex with S-adenosyl-L-methionine and 3,5-dinitrocatechol.

Authors:  Sylwia Czarnota; Nicola J Baxter; Matthew J Cliff; Jonathan P Waltho; Nigel S Scrutton; Sam Hay
Journal:  Biomol NMR Assign       Date:  2016-12-15       Impact factor: 0.746

10.  The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells.

Authors:  Christopher L Cunningham; Zizhen Wu; Aria Jafari; Bo Zhao; Kat Schrode; Sarah Harkins-Perry; Amanda Lauer; Ulrich Müller
Journal:  Elife       Date:  2017-05-15       Impact factor: 8.140

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