首页> 外文OA文献 >Biological Activity of Analogues of YM022. Novel (3-Amino Substituted Phenyl)urea Derivatives of 1,4-Benzodiazepin-2-one as Gastrin/Cholecystokinin-B Receptor Antagonists.

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Biological Activity of Analogues of YM022. Novel (3-Amino Substituted Phenyl)urea Derivatives of 1,4-Benzodiazepin-2-one as Gastrin/Cholecystokinin-B Receptor Antagonists.

机译：YM022类似物的生物活性。 1,4-苯并二嗪-2-1的新型（3-氨基取代的苯基）尿素衍生物作为胃泌素/胆囊蛋白-B受体拮抗剂。

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Masato SATOH; Yoshinori OKAMOTO; Hiroyuki KOSHIO; Mitsuaki OHTA; Akito NISHIDA; Shinobu AKUZAWA; Keiji MIYATA; Toshiyasu MASE; Graeme SEMPLE;
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1. Biological Activity of Analogues of YM022. Novel (3-Amino Substituted Phenyl)urea Derivatives of l,4-Benzodiazepin-2-one as Gastrin/Cholecystokinin-B Receptor Antagonists [J] . Masato Satoh, Yoshinori Okamoto, Hiroyuki Koshio, Chemical and Pharmaceutical Bulletin . 1996,第7期

机译：YM022类似物的生物活性。 1,4-苄二氮杂-2--2-酮的新型（3-氨基取代的苯基）脲衍生物作为胃泌素/胆囊收缩素-B受体拮抗剂
2. New l,4-Benzodiazepin-2-one Derivatives as Gastrin/Cholecystokinin-B Antagonists [J] . Masato Satoh, Yutaka Kondoh, Yoshinori Okamoto, Chemical and Pharmaceutical Bulletin . 1995,第12期

机译：新的l，4-Benzodiazepin-2-one衍生物作为胃泌素/胆囊收缩素-B拮抗剂
3. Synthesis and biological effect of halogen substituted phenyl acetic acid derivatives of progesterone as potent progesterone receptor antagonists. [J] . Cabeza M, Bratoeff E, Gomez G, The Journal of Steroid Biochemistry and Molecular Biology . 2008,第3a5期

机译：孕酮的卤代苯基乙酸衍生物作为强效孕酮受体拮抗剂的合成及其生物学作用。
4. Design, Synthesis and Biological Activities of Novel Substituted Phenyl Oxazol-based Neonicotinoid Analogues [C] . Shaohua Liu, Yongqiang Li, Yun Ling, Proceedings of 4th international symposium on pesticides and environmental safety amp; 5th pan Pacific confernce on pesticide science amp; 8th international workshop on crop protection chemistry and regulatory harmonization . 2012

机译：新型取代的苯基恶唑基新烟碱类似物的设计，合成及生物活性
5. Synthesis of new glutamate receptor probes: I. Total synthesis of dysiherbaine, a potent glutamate receptor excitotoxin; II. Design and synthesis of dysiherbaine analogues; III. Synthesis and structure-activity relationships of substituted benzothiadiazides and their role as AMPA receptor modulators. [D] . Phillips, Dean Paul. 2001

机译：新型谷氨酸受体探针的合成：I. dysiherbaine的全合成，一种有效的谷氨酸受体兴奋性毒素；二。 dysiherbaine类似物的设计和合成；三，取代的苯并噻二叠氮化物的合成及其构效关系及其作为AMPA受体调节剂的作用。
6. Molecular docking studies of 1-(substituted phenyl)-3-(naphtha 1 2-d thiazol-2-yl) urea/thiourea derivatives with human adenosine A2A receptor [O] . Faizul Azam, Medapati Vijaya Vara Prasad, Neelaveni Thangavel, 2011

机译：1-（取代的苯基）-3-（石脑油12-d噻唑-2-基）脲/硫脲衍生物与人腺苷A2A受体的分子对接研究
7. New 1,4-Benzodiazepin-2-one Derivatives as Gastrin/Cholecystokinin-B Antagonists. [O] . Masato SATOH, Yutaka KONDOH, Yoshinori OKAMOTO, 1995

机译：新的1,4-苯并二氮素-2-一种衍生物作为胃泌素/胆囊蛋白-B拮抗剂。
8. Synthesis and Biological Activity of Substituted Urea and Thiourea Derivatives Containing 1,2,4-Triazole Moieties. [R] . Kocyigit-Kaymakcioglu, B., Celen, A. O., Tabanca, N., 2013

机译：含1,2,4-三唑部分的取代脲和硫脲衍生物的合成及生物活性。

Biological Activity of Analogues of YM022. Novel (3-Amino Substituted Phenyl)urea Derivatives of 1,4-Benzodiazepin-2-one as Gastrin/Cholecystokinin-B Receptor Antagonists.

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