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Otenabant
Known as:
1-(8-(2-Chlorophenyl)-9-(4-Chlorophenyl)-9H-Purin-6-yl)-4-(Ethylamino)Piperidine-4-Carboxamide
, 4-Piperidinecarboxamide, 1-(8-(2-Chlorophenyl)-9-(4-Chlorophenyl)-9H-Purin-6-yl)-4- (Ethylamino)-
National Institutes of Health
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CP-945,598
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Advances in the Understanding of the Cannabinoid Receptor 1 - Focusing on the Inverse Agonists Interactions
Silvana Russo
,
W. F. de Azevedo
Current Medicinal Chemistry
2019
Corpus ID: 4974659
BACKGROUND Cannabinoid Receptor 1 (CB1) is a membrane protein prevalent in the central nervous system, whose crystallographic…
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2019
2019
Functionalized 6-(Piperidin-1-yl)-8,9-Diphenyl Purines as Peripherally Restricted Inverse Agonists of the CB1 Receptor.
G. Amato
,
Amruta Manke
,
+6 authors
Rangan Maitra
Journal of Medicinal Chemistry
2019
Corpus ID: 186204373
Antagonists of peripheral type 1 cannabinoid receptors (CB1) have potential utility in the treatment of various diseases…
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2017
2017
Pharmacological comparison of traditional and non-traditional cannabinoid receptor 1 blockers in rodent models in vivo
B. Varga
,
F. Kassai
,
G. Szabó
,
P. Kovacs
,
J. Fischer
,
I. Gyertyán
Pharmacology, Biochemistry and Behavior
2017
Corpus ID: 19202820
2015
2015
(4-(Bis(4-Fluorophenyl)Methyl)Piperazin-1-yl)(Cyclohexyl)Methanone Hydrochloride (LDK1229): A New Cannabinoid CB1 Receptor Inverse Agonist from the Class of Benzhydryl Piperazine Analogs
M. Mahmoud
,
T. Olszewska
,
+5 authors
D. Kendall
Molecular Pharmacology
2015
Corpus ID: 168371
Some inverse agonists of cannabinoid receptor type 1 (CB1) have been demonstrated to be anorectic antiobesity drug candidates…
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2014
2014
Relative Contributions of Cytochrome CYP 3 A 4 Versus CYP 3 A 5 for CYP 3 A-Cleared Drugs Assessed In Vitro Using a CYP 3 A 4-Selective Inactivator ( CYP 3 cide ) s
E. Tseng
,
R. Walsky
,
+5 authors
R. Obach
2014
Corpus ID: 486548
Metabolism by cytochrome P4503A (CYP3A) is the most prevalent clearance pathway for drugs. Designation of metabolism by CYP3A…
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