Detalhe da pesquisa
1.
1-, 2- and 3-AG as substrates of the endocannabinoid enzymes and endogenous ligands of the cannabinoid receptor 1.
Biochem Biophys Res Commun
; 591: 31-36, 2022 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34995983
2.
Design and synthesis of cyanamides as potent and selective N-acylethanolamine acid amidase inhibitors.
Bioorg Med Chem
; 28(1): 115195, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31761726
3.
Piperidine and piperazine inhibitors of fatty acid amide hydrolase targeting excitotoxic pathology.
Bioorg Med Chem
; 27(23): 115096, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31629610
4.
Design and Synthesis of Highly Potent and Specific ABHD6 Inhibitors.
ChemMedChem
; 18(21): e202100406, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34486233
5.
Design and Structure-Activity Relationships of Isothiocyanates as Potent and Selective N-Acylethanolamine-Hydrolyzing Acid Amidase Inhibitors.
J Med Chem
; 64(9): 5956-5972, 2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33900772
6.
Opportunities and Challenges for Natural Products as Novel Antituberculosis Agents.
Assay Drug Dev Technol
; 14(1): 29-38, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26565779