Compounds > zolpidem
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zolpidem and n-(indol-3-ylglyoxylyl)benzylamine

zolpidem has been researched along with n-(indol-3-ylglyoxylyl)benzylamine in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Besnard, F; Costa, B; Greco, G; Lavecchia, A; Marini, AM; Martini, C; Novellino, E; Primofiore, G; Settimo, FD; Taliani, S; Trincavelli, L1
Besnard, F; Calderone, V; Cosimelli, B; Da Settimo, F; Greco, G; La Motta, C; Marini, AM; Martini, C; Montali, M; Novellino, E; Patrizi, MP; Primofiore, G; Sergianni, V; Simorini, F; Taliani, S1
Cosconati, S; Cosimelli, B; Costa, B; Da Settimo, F; Greco, G; L'Abbate, G; La Motta, C; Marinelli, L; Marini, AM; Martini, C; Montali, M; Novellino, E; Salerno, S; Salvetti, F; Simorini, F; Taliani, S; Trasciatti, S1

Other Studies

3 other study(ies) available for zolpidem and n-(indol-3-ylglyoxylyl)benzylamine

ArticleYear
Novel N-(arylalkyl)indol-3-ylglyoxylylamides targeted as ligands of the benzodiazepine receptor: synthesis, biological evaluation, and molecular modeling analysis of the structure-activity relationships.
    Journal of medicinal chemistry, 2001, Jul-05, Volume: 44, Issue:14

    Topics: Amides; Animals; Brain; Cattle; Glyoxylates; In Vitro Techniques; Indoles; Ligands; Models, Molecular; Radioligand Assay; Receptors, GABA-A; Structure-Activity Relationship

2001
Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1/L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands.
    Journal of medicinal chemistry, 2007, Apr-05, Volume: 50, Issue:7

    Topics: Amides; Animals; Cattle; Cell Line; Cerebral Cortex; GABA-A Receptor Agonists; Glyoxylates; Hypnotics and Sedatives; In Vitro Techniques; Indoles; Ligands; Male; Mice; Mice, Inbred BALB C; Molecular Conformation; Motor Activity; Radioligand Assay; Rats; Structure-Activity Relationship

2007
Identification of anxiolytic/nonsedative agents among indol-3-ylglyoxylamides acting as functionally selective agonists at the gamma-aminobutyric acid-A (GABAA) alpha2 benzodiazepine receptor.
    Journal of medicinal chemistry, 2009, Jun-25, Volume: 52, Issue:12

    Topics: Anti-Anxiety Agents; Binding Sites; Computer Simulation; GABA-A Receptor Agonists; Models, Chemical; Models, Molecular; Molecular Structure; Stereoisomerism; Structure-Activity Relationship

2009