Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Masaaki Ban"'
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 105:106827
Publikováno v:
British Journal of Pharmacology. 156:1167-1177
Background and purpose: The purine compounds, adenosine 5′-triphosphate (ATP) and adenosine, are known to accumulate in the extracellular space and to elicit various cellular responses during hypoxia/ischemia, whereas the roles of purines during hy
Publikováno v:
The Journal of Physiology. 574:835-847
Adenosine is one of the most important neuromodulators in the CNS, both under physiological and pathological conditions. In the isolated spinal cord of the neonatal rat in vitro, acute hypercapnic acidosis (20% CO2, pH 6.7) reversibly depressed elect
Publikováno v:
Chemical and Pharmaceutical Bulletin. 45:765-768
The Friedel-Crafts acylation of 1-acetylindoline with (S)-2- or (R)-2-(methanesulfonyloxy)propionyl chloride, and aluminum chloride in dichloromethane at room temperature did not afford the expected (S)- or (R)-1-acetyl-5-[2-(methanesulfonyloxy)propi
Autor:
Nakano Yasushi, Yukiyoshi Ajisawa, Makio Kitazawa, Kosuke Okazaki, Michihiro Kobayashi, Atsushi Tsubaki, Masaaki Ban, Sato Kazuaki
Publikováno v:
YAKUGAKU ZASSHI. 116:396-410
A number of sulfur-containing amide-carboxylic acid derivatives were synthesized and tested for cholecystokinin A (CCK-A) receptor inhibitory activity in order to study structure-activity relationships. Significant CCK-A receptor inhibitory activitie
Autor:
A. Tsubaki, Makio Kitazawa, Masaaki Ban, Kosuke Okazaki, Y. Ajisawa, Y. Nakano, M. Uchida, K. Sato, Michihiro Kobayashi
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
The Friedel-Crafts acylation of 1-acetylindoline with (S)-2- or (R)-2-(methanesulfonyloxy)propionyl chloride, and aluminum chloride in dichloromethane at room temperature did not afford the expected (S)- or (R)-1-acetyl-5-[2-(methanesulfonyloxy)propi
Publikováno v:
Tetrahedron Letters. 32:4027-4030
A stereocontrolled synthesis of the hitherto unknown (±)-6,7-dideoxyforskolin has been accomplished, incorporating controlled C-ring annulation with simultaneous creation of the stereogenic center at C-13 via oxymercuration. An alternative attempt a
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 35(3)
Pilocarpine is a cholinergic agonist that is metabolized to pilocarpic acid by serum esterase. In this study, we discovered a novel metabolite in human urine after the oral administration of pilocarpine hydrochloride, and we investigated the metaboli
Adenosine is one of the most important neuromodulators in the CNS, both under physiological and pathological conditions. In the isolated spinal cord of the neonatal rat in vitro, acute hypercapnic acidosis (20% CO2, pH 6.7) reversibly depressed elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::941767111dc51842781d092365be8823
https://europepmc.org/articles/PMC1817731/
https://europepmc.org/articles/PMC1817731/