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N-Methyl-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamides as a novel class of cannabinoid receptors agonists with low CNS penetration
- Source :
- Bioorganicmedicinal chemistry letters. 22(12)
- Publication Year :
- 2012
-
Abstract
- Cannabinoid CB1 receptor agonists exhibit potent analgesic effects in rodents and humans, but their clinical utility as analgesic drugs is often limited by centrally mediated side effects. We report herein the preparation of N-methyl-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamides as a novel class of hCB1/hCB2 dual agonists with attractive physicochemical properties. More specifically, (R)-N,9-dimethyl-N-(4-(methylamino)-4-oxobutyl)-3-(tetrahydro-2H-pyran-4-yl)-2,3,4,9-tetrahydro-1H-carbazole-6-carboxamide, displayed an extremely low level of CNS penetration (Rat Cbr/Cplasma = 0.005 or 0.5%) and was devoid of CNS side effects during pharmaco-dynamic testing.
- Subjects :
- Central Nervous System
Cannabinoid receptor
Stereochemistry
medicine.medical_treatment
Clinical Biochemistry
Analgesic
Carbazoles
Pharmaceutical Science
Biological Availability
Pain
Pharmacology
Biochemistry
Permeability
Cns penetration
Rats, Sprague-Dawley
chemistry.chemical_compound
Structure-Activity Relationship
Receptor, Cannabinoid, CB1
Drug Discovery
medicine
Animals
Humans
Molecular Biology
Analgesics
Carbazole
Organic Chemistry
Stereoisomerism
Rats
chemistry
Solubility
Pyran
Molecular Medicine
Cannabinoid
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 22
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....8398b5e47f84620dc49296ccdf8d606e