首页> 外文OA文献 >Nonpeptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 4'-(5-(Substituted Methylidene)-2,3,4,5-tetrahydro-1H-1-benzoazepine-1-carbonyl)benzanilide and 4'-(5-(Substituted Methyl)-2,3-dihydro-1H-1-benzoazepine-1-carbonyl)benzanilide Derivatives.

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Nonpeptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 4'-(5-(Substituted Methylidene)-2,3,4,5-tetrahydro-1H-1-benzoazepine-1-carbonyl)benzanilide and 4'-(5-(Substituted Methyl)-2,3-dihydro-1H-1-benzoazepine-1-carbonyl)benzanilide Derivatives.

机译：v1a和v2受体的非肽精氨酸血管加压素拮抗剂：合成和药理学特性为4' - （5-（取代的亚甲基）-2,3,4,5-四氢-1h-1-苯并嗪-1-羰基）苯并偶联和4 ' - （5-（取代的甲基）-2,3-二氢-1H-1-苯并嗪-1-羰基）苯硅氧烷衍生物。

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Akira MATSUHISA; Kazumi KIKUCHI; Kenichiro SAKAMOTO; Takeyuki YATSU; Akihiro TANAKA;
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年度 1999
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1. Nonpeptide arginine vasopressin antagonists for both V1A and V2 receptors: synthesis and pharmacological properties of 4'-(5-(substituted methylidene)-2,3,4,5-tetrahydro-1H-1-ben zoazepine-1-carbonyl)benzanilide and 4'-(5-(substituted methyl)-2,3-dih [J] . Matsuhisa A, Kikuchi K, Sakamoto K, Chemical and Pharmaceutical Bulletin . 1999,第3期

机译：V1A和V2受体的非肽精氨酸加压素拮抗剂：4'-（5-（取代的亚甲基）-2,3,4,5-四氢-1H-1-苯唑氮平-1-羰基）苯甲腈和4'-（5-（取代甲基）-2,3-dih
2. Nonpeptide arginine vasopressin antagonists for both V1A and V2 receptors: synthesis and pharmacological properties of 2-phenyl-4'-(2,3,4,5-tetrahydro-1H-1,5-benzodiazepine-1-carbonyl) benzanilide derivatives. [J] . Matsuhisa A, Koshio H, Sakamoto K, Chemical and Pharmaceutical Bulletin . 1998,第10期

机译：V1A和V2受体的非肽精氨酸加压素拮抗剂：2-苯基-4'-（2,3,4,5-四氢-1H-1,5-苯并二氮杂-1-羰基）苯甲酰苯胺衍生物的合成和药理特性。
3. Nonpeptide arginine vasopressin antagonists for both V1A and V2 receptors: synthesis and pharmacological properties of 4-(1,4,5,6-tetrahydroimidazo(4,5-d)(1)benzoazepine-6-carbonyl)benzanili de derivatives and 4'-(5,6-dihydro-4H-thiazolo(5,4-d)(1)ben [J] . Matsuhisa A, Taniguchi N, Koshio H, Chemical and Pharmaceutical Bulletin . 2000,第1期

机译：V1A和V2受体的非肽精氨酸加压素拮抗剂：4-（1,4,5,6-四氢咪唑并（4,5-d）（1）苯并ze庚因-6-羰基）苯并尼利衍生物和4'的合成和药理特性-（5,6-二氢-4H-噻唑洛（5,4-d）（1）苯
4. Biochemical and pharmacological properties of SR 49059 a new potent nonpeptide antagonist of rat and human vasopressin V1a receptors. [O] . C Serradeil-Le Gal, J Wagnon, C Garcia, 1993

机译：SR 49059（一种新的有效的大鼠和人血管加压素V1a受体非肽拮抗剂）的生物化学和药理特性。
5. Nonpeptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 2-Phenyl-4'-(2,3,4,5-tetrahydro-1H-1,5-benzodiazepine-1-carbonyl)benzanilide Derivatives. [O] . Akira MATSUHISA, Hiroyuki KOSHIO, Kenichiro SAKAMOTO, 1998

机译：对于V1A和V2受体的非肽精氨酸加压素拮抗剂：2-苯基-4' - （2,3,4,5-四氢-1H-1,5-苯并二氮杂甲基-1-羰基）的合成和药理学性质。苯硅氧烷衍生物。

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