Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
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Inhibitors of Fatty Acid Amide Hydrolase and Monoacylglycerol Lipase: New Targets for Future AntidepressantsBiochemical and pharmacological characterization of the human lymphocyte antigen B-associated transcript 5 (BAT5/ABHD16A)Discovery of triterpenoids as reversible inhibitors of α/β-hydrolase domain containing 12 (ABHD12)Optimization of 1,2,5-thiadiazole carbamates as potent and selective ABHD6 inhibitors.Interaction of the N-(3-Methylpyridin-2-yl)amide Derivatives of Flurbiprofen and Ibuprofen with FAAH: Enantiomeric Selectivity and Binding ModeIdentification of selective covalent inhibitors of platelet activating factor acetylhydrolase 1B2 from the screening of an oxadiazolone-capped peptoid-azapeptoid hybrid library.4-Aryliden-2-methyloxazol-5(4H)-one as a new scaffold for selective reversible MAGL inhibitors.Cellular Activity of New Small Molecule Protein Arginine Deiminase 3 (PAD3) Inhibitors.Solid phase synthesis of 1,3,4-oxadiazin-5 (6R)-one and 1,3,4-oxadiazol-2-one scaffolds from acyl hydrazides.
P2860
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P2860
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@en
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@nl
type
label
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@en
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@nl
prefLabel
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@en
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@nl
P2093
P50
P356
P1476
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.
@en
P2093
Christopher J Fowler
Dina Navia-Paldanius
Juha R Savinainen
Jukka Leppänen
Mariateresa Cipriano
Susanna M Saario
Tapio Nevalainen
Teija Parkkari
Tuomo Laitinen
P304
P356
10.1021/JM400923S
P407
P577
2013-10-22T00:00:00Z