Synthesis and Pharmacological Evaluation of N-(6-Functionalized-amino-3-pyridyl)-N'-bicycloalkyl-N"-cyanoguanidines as Antihypertensive Agents
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概要
- 論文の詳細を見る
A series of amino acid conjugates of N-(6-amino-3-pyridyl)-N'-[exo-bicyclo[2.2.1]hept-2-yl]-N"-cyanoguanidine (4) were prepared and evaluated as antihypertensive agents. The parent compound 4 showed potent potassium channel-opening and antihypertensive activities, but with undesirable changes of the urinary balance of electrolytes. Howere, alanine and histidine congeners (9,19) reduced this undesirable side effect of 4 through improved pharmacokinetics without loss of antihypertensive activity. They also provided additional information on the structural requirements for pinacidil-type potassium channel openers.
- 公益社団法人日本薬学会の論文
- 1996-02-15
著者
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Fukaya Chikara
Research Division The Green Cross Corporation
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Hayashi Kazutaka
Research Division The Green Cross Corporation
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Eda M
Research Division The Green Cross Corporation
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Nakamura Norifumi
Research Division The Green Cross Corporation
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Nakamura Norifumi
Research Division The Green Cross Corp.
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Matzno Sumio
Research Division The Green Cross Corporation
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EDA Masahiro
Research Division, The Green Cross Corporation
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TAKEMOTO Tadahiro
Research Division, The Green Cross Corporation
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OKADA Takehiro
Research Division, The Green Cross Corporation
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SAKASHITA Hiroshi
Research Division, The Green Cross Corporation
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GOHDA Maki
Research Division, The Green Cross Corporation
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Gohda Maki
Research Division The Green Cross Corporation
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Okada Takehiro
Research Division The Green Cross Corporation
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Sakashita Hiroshi
Research Division The Green Cross Corporation
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Tanaka T
Research Division The Green Cross Corporation
関連論文
- Platelet Aggregation Activity of Thrombin Receptor-Tethered Peptide Ligand Containing Free Thiol or Activated SH Group
- Synthesis and Pharmacological Evaluation of N-(6-Functionalized-amino-3-pyridyl)-N'-bicycloalkyl-N"-cyanoguanidines as Antihypertensive Agents
- Novel Histamine H_3 Receptor Antagonists : Synthesis and Evaluation of Formamidine and S-Methylisothiourea Derivatives