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New pyrazolyl and thienyl aminohydantoins as potent BACE1 inhibitors: Exploring the S2′ region
Online Contents | 2011| -
Highly Potent, Selective, and Orally Active Phosphodiesterase 10A Inhibitors
Online Contents | 2011| -
Novel pyrrolyl 2-aminopyridines as potent and selective human β-secretase (BACE1) inhibitors
Online Contents | 2010| -
Quinazolineacetic acids and related analogs as aldose reductase inhibitors
National licenceAmerican Chemical Society | 1991| -
Azole Phenoxy Hydroxyureas as Selective and Orally Active Inhibitors of 5-Lipoxygenase
Online Contents | 1996| -
Facile Synthesis of Novel Spiro(azetidine-2,4'(1'H)-isoquinoline)- 1',3',4(2'H)-triones
Online Contents | 1994| -
Jatrophone analogs: synthesis of cis- and trans-normethyljatropholactones
National licenceAmerican Chemical Society | 1982| -
N-Substituted Spirosuccinimide, Spiropyridazine, Spiroazetidine, and Acetic Acid Aldose Reductase Inhibitors Derived from Isoquinoline-1,3-diones. 2
National licenceAmerican Chemical Society | 1994| -
N-acylethanolamine hydrolyzing acid amidase (NAAA) inhibitors and use thereof
Free accessEuropean Patent Office | 2020| -
N-Acylethanolamine Hydrolyzing Acid Amidase (NAAA) Inhibitors And Use Thereof
Free accessEuropean Patent Office | 2019| -
Jatrophone, jatrophone derivatives, and analogs. Conformation and reactions with propanethiol
National licenceAmerican Chemical Society | 1983|
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