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1, 4 : 3, 6-Dianhydrohexitol Nitrate Derivatives. I. Synthesis and Antianginal Activity of Alkylpiperazine Derivatives
1, 4 : 3, 6-Dianhydrohexitol Nitrate Derivatives. I. Synthesis and Antianginal Activity of Alkylpiperazine Derivatives
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1, 4 : 3, 6-Dianhydrohexitol Nitrate Derivatives. I. Synthesis and Antianginal Activity of Alkylpiperazine Derivatives

HAYASHI, Hiroaki ; IKEDA, Junichi ; KURODA, Takeshi ; KUBO, Kazuhiro ; SANO, Tomoyuki ; SUZUKI, Fumio

Chemical and Pharmaceutical Bulletin, 1993/06/15, Vol.41(6), pp.1091-1099 [Periódico revisado por pares]

Tokyo: The Pharmaceutical Society of Japan

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2
1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial .beta.-stimulants/.beta.-blockers
1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial .beta.-stimulants/.beta.-blockers
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1-Alkylamino-3-(2-thiazolyloxy)-2-propanols. Novel class of mixed myocardial .beta.-stimulants/.beta.-blockers

Edwards, J. A ; Berkoz, B ; Lewis, G. S ; Halpern, O ; Fried, J. H ; Strosberg, A. M ; Miller, L. M ; Urich, S ; Liu, F ; Roszkowski, A. P

Journal of medicinal chemistry, 1974-02, Vol.17 (2), p.200-203 [Periódico revisado por pares]

United States: American Chemical Society

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3
1-Aminoacyl-2,3-dihydro-4(1H)-quinazolinone derivatives with choleretic and antifibrillatory activity
1-Aminoacyl-2,3-dihydro-4(1H)-quinazolinone derivatives with choleretic and antifibrillatory activity
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1-Aminoacyl-2,3-dihydro-4(1H)-quinazolinone derivatives with choleretic and antifibrillatory activity

Bonola, G ; Da Re, P ; Magistretti, M. J ; Massarani, E ; Setnikar, I

Journal of medicinal chemistry, 1968-11, Vol.11 (6), p.1136-1139 [Periódico revisado por pares]

United States: American Chemical Society

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4
17(R),18(S)-Epoxyeicosatetraenoic Acid, a Potent Eicosapentaenoic Acid (EPA) Derived Regulator of Cardiomyocyte Contraction: Structure–Activity Relationships and Stable Analogues
17(R),18(S)-Epoxyeicosatetraenoic Acid, a Potent Eicosapentaenoic Acid (EPA) Derived Regulator of Cardiomyocyte Contraction: Structure–Activity Relationships and Stable Analogues
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17(R),18(S)-Epoxyeicosatetraenoic Acid, a Potent Eicosapentaenoic Acid (EPA) Derived Regulator of Cardiomyocyte Contraction: Structure–Activity Relationships and Stable Analogues

Falck, John R ; Wallukat, Gerd ; Puli, Narender ; Goli, Mohan ; Arnold, Cosima ; Konkel, Anne ; Rothe, Michael ; Fischer, Robert ; Müller, Dominik N ; Schunck, Wolf-Hagen

Journal of medicinal chemistry, 2011-06, Vol.54 (12), p.4109-4118 [Periódico revisado por pares]

United States: American Chemical Society

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5
18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels
18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels
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18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels

Du, Yi-mei ; Xia, Cheng-kun ; Zhao, Ning ; Dong, Qian ; Lei, Ming ; Xia, Jia-hong

Acta pharmacologica Sinica, 2012-06, Vol.33 (6), p.752-760 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
3-(Dialkylamino)methyladamantane-1-carboxylic acids
3-(Dialkylamino)methyladamantane-1-carboxylic acids
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3-(Dialkylamino)methyladamantane-1-carboxylic acids

Kontonassios, Demetrios ; Sandris, Constantine ; Tsatsas, Georges ; Casadio, Silvano ; Lumachi, Bruno ; Turba, Carla

Journal of medicinal chemistry, 1969-01, Vol.12 (1), p.170-172 [Periódico revisado por pares]

United States: American Chemical Society

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7
3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent
3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent
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3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent

Villa, Stefania ; Barlocco, Daniela ; Cignarella, Giorgio ; Papp, Gyula Julius ; Baláti, Beáta ; Takács, János ; Varró, András ; Borosy, András ; Keserû, Katalin ; Mátyus, Péter

European journal of medicinal chemistry, 2001-06, Vol.36 (6), p.495-506 [Periódico revisado por pares]

Oxford: Elsevier Masson SAS

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8
4'-[(4-Piperidyl)carbonyl]methanesulfonanilides as potent, selective, bioavailable class III antiarrhythmic agents
4'-[(4-Piperidyl)carbonyl]methanesulfonanilides as potent, selective, bioavailable class III antiarrhythmic agents
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4'-[(4-Piperidyl)carbonyl]methanesulfonanilides as potent, selective, bioavailable class III antiarrhythmic agents

Oinuma, Hitoshi ; Miyake, Kazutoshi ; Yamanaka, Motosuke ; Nomoto, Kenichi ; Katoh, Hiroshi ; Sawada, Kohei ; Shino, Mitsumasa ; Hamano, Sachiyuki

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.903-905 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
4-Oxospiro[benzopyran-2,4'-piperidines] as class III antiarrhythmic agents. Pharmacological studies on 3,4-dihydro-1'-[2-(benzofurazan-5-yl)- ethyl]-6-methanesulfonamidospiro[(2H)-1-benzopyran-2,4'-piperidin]-4-on e (L-691,121)
4-Oxospiro[benzopyran-2,4'-piperidines] as class III antiarrhythmic agents. Pharmacological studies on 3,4-dihydro-1'-[2-(benzofurazan-5-yl)- ethyl]-6-methanesulfonamidospiro[(2H)-1-benzopyran-2,4'-piperidin]-4-on e (L-691,121)
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4-Oxospiro[benzopyran-2,4'-piperidines] as class III antiarrhythmic agents. Pharmacological studies on 3,4-dihydro-1'-[2-(benzofurazan-5-yl)- ethyl]-6-methanesulfonamidospiro[(2H)-1-benzopyran-2,4'-piperidin]-4-on e (L-691,121)

Elliott, J M ; Selnick, H G ; Claremon, D A ; Baldwin, J J ; Buhrow, S A ; Butcher, J W ; Habecker, C N ; King, S W ; Lynch, Jr, J J ; Phillips, B T

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3973-3976 [Periódico revisado por pares]

United States

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10
4,5-Dihydro-1-phenyl-1H-2,4-benzodiazepines: Novel antiarrhythmic agents
4,5-Dihydro-1-phenyl-1H-2,4-benzodiazepines: Novel antiarrhythmic agents
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4,5-Dihydro-1-phenyl-1H-2,4-benzodiazepines: Novel antiarrhythmic agents

Johnson, Robert E ; Baizman, Eugene R ; Becker, Carolyn ; Bohnet, Eric A ; Bell, Rebecca H ; Birsner, Nancy C ; Busacca, Carl A ; Carabateas, Philip M ; Chadwick, Christopher C

Journal of medicinal chemistry, 1993-10, Vol.36 (22), p.3361-3370 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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