An Update on Arginase Inhibitors and Inhibitory Assays.
Arginase
assays
cell culture
colorimetric
evaluation
inhibitors
radiometric
Journal
Mini reviews in medicinal chemistry
ISSN: 1875-5607
Titre abrégé: Mini Rev Med Chem
Pays: Netherlands
ID NLM: 101094212
Informations de publication
Date de publication:
2022
2022
Historique:
received:
20
09
2021
revised:
18
10
2021
accepted:
22
10
2021
pubmed:
31
12
2021
medline:
17
9
2022
entrez:
30
12
2021
Statut:
ppublish
Résumé
Arginase, which converts arginine into ornithine and urea, is a promising therapeutic target. Arginase is involved in cardiovascular diseases, parasitic infections and through a critical role in immunity, in some cancers. There is a need to develop effective arginase inhibitors and therefore efforts to identify and optimize new inhibitors are increasing. Several methods of evaluating arginase activity are available, but few directly measure the product. Radiometric assays need to separate urea and dying reactions require acidic conditions and sometimes heating. Hence, there are a variety of different approaches available, and each approach has its own limits and benefits. In this review, we provide an update on arginase inhibitors, followed by a discussion on available arginase assays and alternative methods, focusing on the intrinsic biases and parameters that are likely to impact results.
Identifiants
pubmed: 34967285
pii: MRMC-EPUB-119750
doi: 10.2174/1389557522666211229105703
doi:
Substances chimiques
Urea
8W8T17847W
Arginine
94ZLA3W45F
Arginase
EC 3.5.3.1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1963-1976Informations de copyright
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