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Preparation of Highly Potent and Selective Non-Peptide Antagonists of the Arginine Vasopressin V1A Receptor by Introduction of a 2-Ethyl-1H-1-imidazolyl Group

机译：通过引入2-乙基-1H-1-Imidazolyl基金制备精氨酸加压素V1A受体的高效和选择性非肽拮抗剂

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Yoshiaki Shimada; Hiroaki Akane; Nobuaki Taniguchi; Akira Matsuhisa; Noriyuki Kawano; Kazumi Kikuchi; Takeyuki Yatsu; Atsuo Tahara; Yuichi Tomura; Toshiyuki Kusayama; Koh-ichi Wada; Junko Tsukada; Takashi Tsunoda; Akihiro Tanaka;
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1. Preparation of highly potent and selective non-peptide antagonists of the arginine vasopressin V1A receptor by introduction of a 2-ethyl-1H-1-imidazolyl group. [J] . Shimada Y, Akane H, Taniguchi N, Chemical and Pharmaceutical Bulletin . 2005,第7期

机译：通过引入2-乙基-1H-1-咪唑基，制备精氨酸加压素V1A受体的高效选择性非肽拮抗剂。
2. Preparation of non-peptide, highly potent and selective antagonists of arginine vasopressin V1A receptor by introduction of alkoxy groups. [J] . Shimada Y, Taniguchi N, Matsuhisa A, Chemical and Pharmaceutical Bulletin . 2003,第9期

机译：通过引入烷氧基来制备精氨酸加压素V1A受体的非肽，高效和选择性拮抗剂。
3. The Non-Peptide Arginine-Vasopressin v1a Selective Receptor Antagonist, SR49059, Blocks the Rewarding, Prosocial, and Anxiolytic Effects of 3,4-Methylenedioxymethamphetamine and Its Derivatives in Zebra Fish [J] . Ponzoni, Luisa Frontiers in Psychiatry . 2017,第2期

机译：非肽精氨酸-加压素v1a选择性受体拮抗剂SR49059阻止斑马鱼中3,4-亚甲二氧基甲基苯丙胺及其衍生物的报酬，亲社会和抗焦虑作用
4. Synthesis and in vitro Pharmacological Profile of Potent and Selective Peptidic V1a Receptor Agonists. [C] . Kazinlierz Wisniewski, Robert Galyean, Hiroe Taki American Peptide Symposium . 2009

机译：效力和选择性肽V1A受体激动剂的合成与体外药理学谱。
5. Potent derivatives of the bradykinin B2 receptor antagonist Hoe 140 containing analogues of arginine and lysine with increased hydrophobicity. [D] . Kennedy, Kevin Joseph. 1999

机译：缓激肽B2受体拮抗剂Hoe 140的强效衍生物含有精氨酸和赖氨酸的类似物，疏水性增强。
6. The Non-Peptide Arginine-Vasopressin v1a Selective Receptor Antagonist SR49059 Blocks the Rewarding Prosocial and Anxiolytic Effects of 34-Methylenedioxymethamphetamine and Its Derivatives in Zebra Fish [O] . Luisa Ponzoni, Daniela Braida, Gianpietro Bondiolotti, 2017

机译：非肽精氨酸-加压素v1a选择性受体拮抗剂SR49059阻止斑马鱼中34-亚甲二氧基甲基苯丙胺及其衍生物的报酬亲社会和抗焦虑作用
7. Preparation of Non-peptide, Highly Potent and Selective Antagonists of Arginine Vasopressin V1A Receptor by Introduction of Alkoxy Groups [O] . Yoshiaki Shimada, Nobuaki Taniguchi, Akira Matsuhisa, 2003

机译：通过引入烷氧基制备精氨酸加压素V1A受体的非肽，高效和选择性拮抗剂

Preparation of Highly Potent and Selective Non-Peptide Antagonists of the Arginine Vasopressin V1A Receptor by Introduction of a 2-Ethyl-1H-1-imidazolyl Group

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