Design, synthesis, and BK channel-opening activity of hexahydrodibenzazepinone derivatives

scientific article published on 10 August 2006

Design, synthesis, and BK channel-opening activity of hexahydrodibenzazepinone derivatives is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.BMC.2006.07.042
P698PubMed publication ID16904328

P2093author name stringTomohiko Ohwada
Toshihiko Tashima
Hiromichi Tsuru
Satomi Adachi-Akahane
Yumi Mochizuki
Yoshimi Toriumi
Taro Nonomura
Katsuo Furukawa
Satoru Nagaoka
P2860cites workThe large-conductance Ca2+-activated K+ channel is essential for innate immunityQ34301370
P433issue23
P407language of work or nameEnglishQ1860
P304page(s)8014-8031
P577publication date2006-08-10
P1433published inBioorganic & Medicinal ChemistryQ2904200
P1476titleDesign, synthesis, and BK channel-opening activity of hexahydrodibenzazepinone derivatives
P478volume14

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cites work (P2860)
Q34201175Central role of the BK channel in urinary bladder smooth muscle physiology and pathophysiology
Q37000100Deficit of Kcnma1 mRNA expression in the dentate gyrus of epileptic rats.
Q42822550Design, synthesis, and characterization of BK channel openers based on oximation of abietane diterpene derivatives
Q30989304Resin-acid derivatives as potent electrostatic openers of voltage-gated K channels and suppressors of neuronal excitability
Q89885966Synthesis, antitumor and DNA cleavage activities of a novel class of dehydroabietylamine derivatives