Results 31 to 40 of about 82 (78)
Local buccal mucosal effects of aspirin, indomethacin and isoxepac: their relationship to gastrointestinal damage. [PDF]
Huston GJ.
europepmc +1 more source
Haemodynamic effects of BM 10.188, a new orally active inotropic agent, in healthy volunteers. [PDF]
Whiting B +4 more
europepmc +1 more source
KW-4679-induced inhibition of tachykininergic contraction in the guinea-pig bronchi by prejunctional inhibition of peripheral sensory nerves. [PDF]
Ikemura T +4 more
europepmc +1 more source
P-5227: an active dibenzoxepine antipsychotic.
A A, Sugerman, F J, Lichtigfeld
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Some of the next articles are maybe not open access.
Recent Advances on the Development of Synthetic Strategies to Access Dibenzoxepine Derivatives
Synthesis, 2022AbstractDibenzoxepines have gained privileged status in medicinal chemistry and drug discovery due to their appearance in various natural products and life-saving drug molecules. Dibenzoxepine-based molecules, such as artocarpols, asenapine, and pacharin, possess a wide range of biological activities including anti-inflammatory, antidepressant ...
Surisetti Suresh +2 more
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Synthesis of antimicrotubule dibenzoxepines
Tetrahedron Letters, 2010Abstract New dibenzoxepines 5a–i bearing various substituents on B- and C-rings were synthesized in a straightforward manner using a Suzuki–Miyaura coupling, a Grignard addition, and a cyclodehydration as key steps. The antimicrotubule activity of all analogues was evaluated and compared to reference compounds.
Colombel, V. +6 more
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Dibenzoxepines as treatments for neurodegenerative diseases
Pure and Applied Chemistry, 1999Abstract
Kaspar Zimmermann +2 more
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Organic & Biomolecular Chemistry, 2021
DAST-mediated intramolecular Friedel–Crafts cyclization is developed for the synthesis of novel spirooxindoles fused with dibenzoxepine moieties.
Ramesh Samikannu +10 more
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DAST-mediated intramolecular Friedel–Crafts cyclization is developed for the synthesis of novel spirooxindoles fused with dibenzoxepine moieties.
Ramesh Samikannu +10 more
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A Synthetic Route to (±)-Clavizepine through a Dibenzoxepine Intermediate
The Journal of Organic Chemistry, 1996A new synthesis of (±)-clavizepine (1a), based on the dibenzoxepinediol 10 as main intermediate is described. The key step is the contraction of the oxepine ring to give the xanthene-9-carboxyaldehyde 11, on which the nitrogenated ring can be readily assembled.
M. C. de la Fuente +2 more
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