Synthesis of New Phenoxypropylamines and Evaluation of Their Antiuicer Activity as H_2-Receptor Antagonist

机译：新苯氧基丙胺的合成及其抗血糖活性评价为H_2-受体拮抗剂

获取原文

页面导航

摘要
著录项
相似文献
相关主题

摘要

More new phenoxypropylamines have been synthesized. All the products have been characterized by elemental analysis, ~1H-NMR, ~1C-NMR and MS. The biological activity effects of the title compounds were examined. From the biological activity results, we found that some of them showed significant gastric acid antisecretory activity.

机译：更新的苯氧基丙胺已经合成。所有产品都以元素分析为特征，〜1H-NMR，〜1C-NMR和MS。检查标题化合物的生物活性效应。从生物活性结果中发现，他们中的一些人表现出显着的胃酸防盗活动。

著录项

来源
《International Conference on Chemical Engineering and Advanced Materials》|2012年||共4页
会议地点
作者
Hui Zhang; Min-fan Wu; Yu Tian;
展开▼
作者单位

展开▼
会议组织
原文格式 PDF
正文语种
中图分类 TB3-532;
关键词
roxatidine; phenoxypropylamines; synthesis; antiuicer agents; biological activity;

机译：Roxatidine;苯氧基丙胺;合成;抗组织剂;生物活性;

相似文献

外文文献
中文文献
专利

1. Synthesis and evaluation of 4- and 5-pyridazin-3-one phenoxypropylamine analogues as histamine-3 receptor antagonists [J] . BecknellN.C., LyonsJ.A., AimoneL.D., Bioorganic and medicinal chemistry . 2012,第12期

机译：作为组胺3受体拮抗剂的4-和5-哒嗪-3-酮苯氧基丙胺类似物的合成和评价
2. Synthesis and evaluation of 4- and 5-pyridazin-3-one phenoxypropylamine analogues as histamine-3 receptor antagonists [J] . BecknellN.C., LyonsJ.A., AimoneL.D., Bioorganic and medicinal chemistry . 2012,第12期

机译：4-吡啶基-3-一苯氧基丙胺类似物作为组胺-3受体拮抗剂的合成与评价
3. Optimization of 5-pyridazin-3-one phenoxypropylamines as potent, selective histamine H _3 receptor antagonists with potent cognition enhancing activity [J] . Tao M., Aimone L.D., Huang Z., Journal of Medicinal Chemistry . 2012,第1期

机译：作为有效的选择性增强组胺H _3受体拮抗剂的5-哒嗪-3-酮苯氧丙胺的优化
4. Synthesis of New Phenoxypropylamines and Evaluation of Their Antiuicer Activity as H_2-Receptor Antagonist [C] . Hui Zhang, Min-fan Wu, Yu Tian International Conference on Chemical Engineering and Advanced Materials . 2012

机译：新苯氧基丙胺的合成及其抗血糖活性评价为H_2-受体拮抗剂
5. Synthesis and pharmacological activity of 1,3,6-trisubstituted-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid derivatives as selective ET(A) antagonists. [D] . Patel, Hardik J. 2009

机译：1,3,6-三取代-4-氧代-1,4-二氢喹啉-2-羧酸衍生物作为选择性ET（A）拮抗剂的合成及药理活性。
6. Phenoxypropylamines: Synthesis and Antiulcer Evaluation [O] . Hui Zhang, Bao-Yan Zhang, Qian-Yun Zhang, 2009

机译：苯氧丙胺：合成和抗溃疡评估
7. Phenoxypropylamines: Synthesis and Antiulcer Evaluation [O] . Dong-Mei Zhao, Jia-Mei Wang, Qian-Yun Zhang, 2009

机译：苯氧丙胺：合成和抗溃疡评估

Synthesis of New Phenoxypropylamines and Evaluation of Their Antiuicer Activity as H_2-Receptor Antagonist

摘要

著录项

相似文献

相关主题

期刊订阅