Page last updated: 2024-08-26

sr141716 and cp 945598

sr141716 has been researched along with cp 945598 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Black, SC; Carpino, PA; DaSilva-Jardine, P; Day, R; DiBrino, J; Dow, RL; Griffith, DA; Hadcock, JR; Iredale, PA; Landis, MS; O'Connor, RE; Scott, DO1
Erdélyi, P; Fischer, J; Gyertyán, I; Hegyi, E; Kiss, B; Laszy, J; Páyer-Lengyel, D; Szabó, G; Szemzo, A; Szikra, J; Varga, B; Vastag, M; Vukics, K1
Bortoff, K; Fennell, T; Fulp, A; Maitra, R; Mathews, J; Seltzman, H; Snyder, R; Zhang, Y1
Azzara, AV; Baska, RA; Behnia, K; Carlson, KE; Cullen, MJ; Devenny, JJ; Ellsworth, BA; Everlof, GG; Ewing, WR; Godonis, HE; Gu, Z; Gudmundsson, O; Harvey, SJ; Johnghar, S; Kang, L; Keim, WJ; Lee, N; Murphy, BJ; Murugesan, N; Pelleymounter, MA; Ranasinghe, A; Rohrbach, KW; Sher, PM; Sitkoff, DF; Stetsko, PI; Sulsky, RB; Thomas, MA; Wu, G; Wu, X; Yang, Y; Yu, G; Zhu, Y; Zuvich, E1
Amato, GS; Cortes, R; Harris, DL; Lefever, TW; Maitra, R; Manke, A; Runyon, SP; Snyder, RW; Vasukuttan, V; Wang, S; Wiethe, RW; Zhang, Y1

Other Studies

5 other study(ies) available for sr141716 and cp 945598

ArticleYear
Discovery of 1-[9-(4-chlorophenyl)-8-(2-chlorophenyl)-9H-purin-6-yl]-4-ethylaminopiperidine-4-carboxylic acid amide hydrochloride (CP-945,598), a novel, potent, and selective cannabinoid type 1 receptor antagonist.
    Journal of medicinal chemistry, 2009, Jan-22, Volume: 52, Issue:2

    Topics: Animals; Dogs; Drug Discovery; Energy Metabolism; Fats; Oxidation-Reduction; Piperidines; Purines; Receptor, Cannabinoid, CB1; Structure-Activity Relationship

2009
Chemical and biological investigation of cyclopropyl containing diaryl-pyrazole-3-carboxamides as novel and potent cannabinoid type 1 receptor antagonists.
    Journal of medicinal chemistry, 2009, Jul-23, Volume: 52, Issue:14

    Topics: Animals; Anti-Obesity Agents; Body Weight; Cattle; Drug Design; Eating; Humans; Lipids; Pyrazoles; Rats; Receptor, Cannabinoid, CB1; Structure-Activity Relationship

2009
Design and synthesis of cannabinoid receptor 1 antagonists for peripheral selectivity.
    Journal of medicinal chemistry, 2012, Mar-22, Volume: 55, Issue:6

    Topics: Animals; Blood-Brain Barrier; Calcium; Cell Line; Cell Membrane Permeability; Dogs; Drug Design; Humans; Ligands; Male; Piperidines; Pyrazoles; Radioligand Assay; Rats; Rats, Sprague-Dawley; Receptor, Cannabinoid, CB1; Stereoisomerism; Structure-Activity Relationship; Urea

2012
Reductions in log P improved protein binding and clearance predictions enabling the prospective design of cannabinoid receptor (CB1) antagonists with desired pharmacokinetic properties.
    Journal of medicinal chemistry, 2013, Dec-12, Volume: 56, Issue:23

    Topics: Animals; Cytochrome P-450 Enzyme System; Drug Discovery; Half-Life; Protein Binding; Pyridazines; Rats; Receptor, Cannabinoid, CB1; Structure-Activity Relationship; Triazoles

2013
Blocking Alcoholic Steatosis in Mice with a Peripherally Restricted Purine Antagonist of the Type 1 Cannabinoid Receptor.
    Journal of medicinal chemistry, 2018, 05-24, Volume: 61, Issue:10

    Topics: Alcohols; Animals; Cannabinoid Receptor Antagonists; Fatty Liver; Female; Humans; Mice; Mice, Inbred C57BL; Models, Molecular; Molecular Structure; Protein Conformation; Receptor, Cannabinoid, CB1; Structure-Activity Relationship; Tissue Distribution

2018