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Studies on the Synthesis of Cholecystokinin A Receptor Antagonists. II. Synthesis and Cholecystokinin A Receptor Inhibitory Activities of Sulfur-Containing Amide-Carboxylic Acid Derivatives

机译：Cholecystokinina受体拮抗剂的合成研究。 II。合成和胆囊酮蛋白的含硫酰胺 - 羧酸衍生物的受体抑制活性

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Yukiyoshi AJISAWA; Makio KITAZAWA; Yasushi NAKANO; Atsushi TSUBAKI; Masaaki BAN; Kazuaki SATO; Kosuke OKAZAKI; Michihiro KOBAYASHI;
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年度 1996
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1. Synthesis of phenoxyacetic acid derivatives as highly potent antagonists of gastrin/cholecystokinin-B receptors. II. [J] . Takeda Y, Kawagoe K, Yokomizo A, Chemical and Pharmaceutical Bulletin . 1998,第6期

机译：苯氧乙酸衍生物的合成作为胃泌素/胆囊收缩素-B受体的高效拮抗剂。二。
2. Synthesis and structure-activity relationship of new 1,5-dialkyl-1,5-benzodiazepines as cholecystokinin-2 receptor antagonists. [J] . Roberts K, Ursini A, Barnaby R, Bioorganic and medicinal chemistry . 2011,第14期

机译：新型1,5-二烷基-1,5-苯并二氮杂作为胆囊收缩素2受体拮抗剂的合成及其构效关系。
3. Synthesis and structure-activity relationship of new 1,5-dialkyl-1,5-benzodiazepines as cholecystokinin-2 receptor antagonists. [J] . Roberts K, Ursini A, Barnaby R, Bioorganic and medicinal chemistry . 2011,第14期

机译：新型1,5-二烷基-1,5-苯并二氮杂作为胆囊收缩素2受体拮抗剂的合成及其构效关系。
4. Characterizing the interactions between cholecystokinin and the G-protein coupled receptors CCK_1 and CCK_2:an NMR-based study [C] . Craig Giragossian, Maria Pellegrini, Dale F.Mierke the International Peptide Symposium . 2001

机译：表征胆囊蛋白和G蛋白偶联受体CCK_1和CCK2的相互作用：基于NMR的研究
5. Part One. Synthesis of optically active tryptophan derivatives with potential activity as indoleamine 2,3-dioxygenase inhibitors: An approach via asymmetric catalytic hydrogenation. Part Two. Design, synthesis and pharmacology of selective ligands for alpha1-containing GABA(A)/benzodiazepine receptor subtypes: SAR studies of beta-carbolines at positions -3 and -6 and their corresponding bivalent ligands. Part Three. First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A. [D] . Yin, Wenyuan. 2007

机译：第一部分。具有吲哚胺2,3-二加氧酶抑制剂潜在活性的旋光色氨酸衍生物的合成：一种通过不对称催化氢化的方法。第二部分。含α1的GABA（A）/苯并二氮杂receptor受体亚型的选择性配体的设计，合成和药理作用：位于-3和-6位的β-咔啉及其相应的二价配体的SAR研究。第三部分。重要生物遗传中间体，（+）-聚神经氨酸和（+）-聚神经氨酸醛，以及16-表-维西辛和Macusine A的首次对映体全合成。
6. Convenient and Efficient Synthesis of a Lanthanide3+-Coordinated Diethylene Triamine Pentaacetic Acid Labeled Biopolymer as an Assay for the Cholecystokinin B Receptor [O] . F. Gao, H. Handl, J. Vagner, -1

机译：方便高效合成镧系元素配位的二亚乙基三胺五乙酸标记的生物聚合物作为胆囊收缩素B受体的测定方法
7. Studies on the Synthesis of Cholecystokinin A Receptor Antagonists. I. Synthesis and Cholecystokinin A Receptor Inhibitory Activities of Malonamide Derivatives [O] . Yukiyoshi AJISAWA, Makio KITAZAWA, Masahiko UCHIDA, 1996

机译：Cholecystokinina受体拮抗剂的合成研究。 I.合成和胆囊酮蛋白的丙酰胺衍生物的受体抑制活性
8. Cholecystokinin Type A and Type B Receptor Antagonists Produce Opposing Effectson Cholecystokinin-Stimulated Beta-Endorphin Secretion from the Rat Pituitary [R] . Millington, W. R., Mueller, G. P., Lavigne, G. J. 1992

机译：胆囊收缩素a型和B型受体拮抗剂对大鼠垂体中胆囊收缩素刺激的β-内啡肽分泌产生反作用

Studies on the Synthesis of Cholecystokinin A Receptor Antagonists. II. Synthesis and Cholecystokinin A Receptor Inhibitory Activities of Sulfur-Containing Amide-Carboxylic Acid Derivatives

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