4.7 Review

Unveiling the biopathway for the design of novel COMT inhibitors

期刊

DRUG DISCOVERY TODAY
卷 27, 期 10, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2022.07.013

关键词

Catechol-O-methyltransferase; COMT inhibitors; Computer-aided drug design; Up-/down-stream processing; Bioanalytical methods

资金

  1. FEDER [POCI-01-0145-FEDER-007491]
  2. National Funds [UID/Multi/00709/2013]
  3. CICS-UBI - Portuguese Foundation for Science and Technology/MCTES [UIDB/00709/2020, UIDP/00709/2020]
  4. FCT/MCTES [UIDB/04378/2020, UIDP/04378/2020, LA/P/0140/2020]
  5. Portuguese Foundation for Science and Technology (FCT) [SFRH/BD/147519/2019, SFRH/BD/130068/2017, SFRH/BSAB/150376/2019]
  6. European Social Fund
  7. MCTES

向作者/读者索取更多资源

This review summarizes the role of COMT in several neurological disorders, the development of COMT inhibitors, the application of computer-aided design in novel molecule design, and the current methods for assessing COMT enzymatic activity.
Catechol-O-methyltransferase (COMT) is an enzyme responsible for the O-methylation of biologically active catechol-based molecules. It has been associated with several neurological disorders, especially Parkinson's disease (PD), because of its involvement in catecholamine metabolism, and has been considered an important therapeutic target for central nervous system disorders. In this review, we summarize the biophysical, structural, and therapeutical relevance of COMT; the medicinal chemistry behind the development of COMT inhibitors and the application of computer-aided design to support the design of novel molecules; current methodologies for the biosynthesis, isolation, and purification of COMT; and revise existing bioanalytical approaches for the assessment of enzymatic activity in several biological matrices.

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