Results 81 to 90 of about 312 (115)
Some of the next articles are maybe not open access.
Journal of Medicinal Chemistry, 2009
A novel class of CB1 inverse agonists was discovered. To efficiently establish structure-activity relationships (SARs), new synthetic methodologies amenable for parallel synthesis were developed. The compounds were evaluated in a mammalian cell-based functional assay and in radioligand binding assays expressing recombinant human cannabinoid receptors ...
Fredrik Ek +2 more
exaly +3 more sources
A novel class of CB1 inverse agonists was discovered. To efficiently establish structure-activity relationships (SARs), new synthetic methodologies amenable for parallel synthesis were developed. The compounds were evaluated in a mammalian cell-based functional assay and in radioligand binding assays expressing recombinant human cannabinoid receptors ...
Fredrik Ek +2 more
exaly +3 more sources
Phosphorous and Sulfur and the Related Elements, 1978
Abstract Owing to increasing demand for phenothiazine compounds both in medicine and industry, novel rings in these series have been prepared and evaluated. The benzene rings have been replaced with pyrrole, pyrazole, pyridine, pyridazine, pyrimidine, pyrazine, thiazine and triazine rings or their combinations leading to twelve new polyaza- and thia ...
Charles O Okafor
exaly +2 more sources
Abstract Owing to increasing demand for phenothiazine compounds both in medicine and industry, novel rings in these series have been prepared and evaluated. The benzene rings have been replaced with pyrrole, pyrazole, pyridine, pyridazine, pyrimidine, pyrazine, thiazine and triazine rings or their combinations leading to twelve new polyaza- and thia ...
Charles O Okafor
exaly +2 more sources
The pharmacological properties of a potent neurotropic compound from the dibenzothiazepine group
International Journal of Neuropharmacology, 1965Abstract The new compound HF-2159 (2-chloro-ll-(4'-methyl)piperazino-dibenzo-[b,f] [1,4]-thiazepine) studied in this paper in comparison with chlorpromazine shows the following properties: 1. Inhibition of motor drive, as manifested in the locomotor activity of mice and in the ‘open field’ test with rats. Its effectiveness here is respectively six
G, Stille +3 more
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ChemInform Abstract: Synthesis and Antibacterial Activities of New Dibenzothiazepine Derivatives.
ChemInform, 2011AbstractThe newly synthesized dibenzothiazepines (III) are evaluated for their activity against both Gram‐positive and Gram‐negative bacteria.
Ganesh D. Mahale +5 more
openaire +1 more source
ChemInform Abstract: Dibenzothiazepine a Break Through Heterocyclic Nucleus in Medicinal Chemistry
ChemInform, 2015AbstractReview: 23 refs.
openaire +1 more source
Synthesis of Dibenzothiazepine Dioxides by Reductive Heck Cyclization
Synfacts, 2015openaire +1 more source
Pharmacology of ‘Seroquel’ (ICI 204,636): An atypical dibenzothiazepine antipsychotic
European Neuropsychopharmacology, 1996openaire +1 more source
COMPARATIVE ACTIVITIES OF A SUBSTITUTED DIBENZOTHIAZEPINE, OF IMIPRAMINE AND OF DESIPRAMINE.
Archives internationales de pharmacodynamie et de therapie, 1996Z P, HOROVITZ +3 more
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