A perspective review on fatty acid amide hydrolase (FAAH) inhibitors as potential therapeutic agents
RKP Tripathi - European Journal of Medicinal Chemistry, 2020 - Elsevier
Fatty acid amide hydrolase (FAAH) is an important enzyme creditworthy of hydrolyzing
endocannabinoids and related-amidated signalling lipids, discovery of which has pioneered …
endocannabinoids and related-amidated signalling lipids, discovery of which has pioneered …
Strategies for tuning the selectivity of chemical probes that target serine hydrolases
Serine hydrolases comprise a large family of enzymes that have diverse roles in key cellular
processes, such as lipid metabolism, cell signaling, and regulation of post-translation …
processes, such as lipid metabolism, cell signaling, and regulation of post-translation …
Covalent docking in drug discovery: scope and limitations
A Scarpino, GG Ferenczy… - Current Pharmaceutical …, 2020 - ingentaconnect.com
Drug discovery efforts for new covalent inhibitors have drastically increased in the last few
years. The binding mechanism of covalent compounds entails the formation of a chemical …
years. The binding mechanism of covalent compounds entails the formation of a chemical …
Serine Hydrolase Activity‐Based Probes for Use in Chemical Proteomics
B Racioppo, N Qiu, A Adibekian - Israel Journal of Chemistry, 2023 - Wiley Online Library
Serine hydrolases (SHs) comprise a large superfamily of enzymes that play critical roles in
many biological processes. Despite their importance, many SHs remain uncharacterized …
many biological processes. Despite their importance, many SHs remain uncharacterized …
Advances in the discovery of fatty acid amide hydrolase inhibitors: what does the future hold?
D Fazio, E Criscuolo, A Piccoli, B Barboni… - Expert Opinion on …, 2020 - Taylor & Francis
Introduction Fatty acid amide hydrolase (FAAH) is a membrane-bound enzyme, that
inactivates endogenous signaling lipids of the fatty acid amide family, including the …
inactivates endogenous signaling lipids of the fatty acid amide family, including the …
A Review on Structurally Diversified Synthesized Molecules as Monoacylglycerol Lipase Inhibitors and their Therapeutic uses
Monoacylglycerol is a metabolic key serine hydrolase engaged in the regulation of the
signalling network system of endocannabinoids, which is associated with various …
signalling network system of endocannabinoids, which is associated with various …
[HTML][HTML] Computer-aided evaluation of targets and biological activity spectra for new piperidine derivatives
M Khaiitova - Journal of Clinical Medicine of Kazakhstan, 2023 - cyberleninka.ru
Background: The unique ability of piperidine to combine with various molecular fragments
makes it possible to use its chemical structure to create new drugs with potential …
makes it possible to use its chemical structure to create new drugs with potential …
Endocannabinoid Hydrolase Inhibitors: Potential Novel Anxiolytic Drugs
H Zhao, Y Liu, N Cai, X Liao, L Tang… - Drug Design …, 2024 - Taylor & Francis
Over the past decade, the idea of targeting the endocannabinoid system to treat anxiety
disorders has received increasing attention. Previous studies focused more on developing …
disorders has received increasing attention. Previous studies focused more on developing …
Synthesis and evaluation of carbamate derivatives as fatty acid amide hydrolase and monoacylglycerol lipase inhibitors
S Jaiswal, G Gupta, SR Ayyannan - Archiv der Pharmazie, 2022 - Wiley Online Library
Fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) are the primary
catabolic enzymes for endocannabinoids, anandamide (AEA), and 2‐arachidonoyl glycerol …
catabolic enzymes for endocannabinoids, anandamide (AEA), and 2‐arachidonoyl glycerol …
Interplay Between Endocannabinoid System and Neurodegeneration: Focus on Polypharmacology
F Seghetti, S Gobbi, F Belluti… - Current Medicinal …, 2022 - ingentaconnect.com
Pharmacological treatment of complex pathologies, such as neurodegenerative diseases
still represents a major challenge, due to the networked pathways involved in their onset …
still represents a major challenge, due to the networked pathways involved in their onset …