• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Diastereomeric separation of 1,5-benzodiazepines due to the presence of a chiral centre on the N-5 alkylic chain.

作者信息

Araldi G L, Donati D, Tranquillini M E, Ursini A

机构信息

Glaxo Wellcome S.p.A., Medicines Research Centre, Verona, Italy.

出版信息

Farmaco. 1998 Jan;53(1):49-54. doi: 10.1016/s0014-827x(97)00004-9.

DOI:10.1016/s0014-827x(97)00004-9
PMID:9543726
Abstract

The presence of a chain bearing a stereogenic centre at the N-5 position of 1-(1-adamantylmethyl)-3-arylureido-2,4-dioxo-1,5-benzodiazep ines induces optical resolution. The synthesis of these compounds and their potency as potential CCK-B receptor antagonists is discussed briefly here.

摘要

相似文献

1
Diastereomeric separation of 1,5-benzodiazepines due to the presence of a chiral centre on the N-5 alkylic chain.
Farmaco. 1998 Jan;53(1):49-54. doi: 10.1016/s0014-827x(97)00004-9.
2
Synthesis and SAR of new 5-phenyl-3-ureido-1,5-benzodiazepines as cholecystokinin-B receptor antagonists.新型5-苯基-3-脲基-1,5-苯并二氮杂䓬类作为胆囊收缩素-B受体拮抗剂的合成与构效关系
J Med Chem. 2000 Oct 5;43(20):3596-613. doi: 10.1021/jm990967h.
3
Synthesis and evaluation of 1,5-benzodiazepines with bridged cycloalkyl substituents at the N-1 position as potent and selective CCK-B Ligands.
Arch Pharm (Weinheim). 1998 Jan;331(1):41-4. doi: 10.1002/(sici)1521-4184(199801)331:1<41::aid-ardp41>3.0.co;2-s.
4
Potent and subtype-selective CCK-B/gastrin receptor antagonists: 2,4-dioxo-1,5-benzodiazepines with a plane of symmetry.
Bioorg Med Chem. 1997 Jul;5(7):1433-46. doi: 10.1016/s0968-0896(97)00083-7.
5
Development of 1,4-benzodiazepine cholecystokinin type B antagonists.1,4-苯二氮䓬类胆囊收缩素B型拮抗剂的研发
J Med Chem. 1993 Dec 24;36(26):4276-92. doi: 10.1021/jm00078a018.
6
Selective non-peptide ligands for an accommodating peptide receptor. Imidazobenzodiazepines as potent cholecystokinin type B receptor antagonists.用于适应性肽受体的选择性非肽配体。咪唑并苯二氮䓬类作为强效的胆囊收缩素B型受体拮抗剂。
Bioorg Med Chem. 1994 Sep;2(9):987-98. doi: 10.1016/s0968-0896(00)82047-7.
7
Quantitative structure-activity relationship study on some nonpeptidal cholecystokinin antagonists.一些非肽类胆囊收缩素拮抗剂的定量构效关系研究
Bioorg Med Chem. 1999 Jun;7(6):1127-30. doi: 10.1016/s0968-0896(99)00013-9.
8
Novel 1,5-benzodiazepines as CCK-B ligands. Effect of aryl-carbamic substituents at the C-3 position together with halogen substitution on the benzo-fused ring.新型1,5-苯二氮䓬类作为胆囊收缩素B受体配体。C-3位芳基氨基甲酰基取代基以及苯并稠环上的卤素取代的影响。
Arch Pharm (Weinheim). 1997 Nov;330(11):353-7. doi: 10.1002/ardp.19973301107.
9
Relationship between dihedral angles of N1 and C9 substituents in 1,4-benzodiazepines and dual cholecystokinin-A and -B antagonistic activities.
Bioorg Med Chem Lett. 1998 Jun 16;8(12):1449-54. doi: 10.1016/s0960-894x(98)00237-6.
10
5-(Piperidin-2-yl)- and 5-(homopiperidin-2-yl)-1,4-benzodiazepines: high-affinity, basic ligands for the cholecystokinin-B receptor.5-(哌啶-2-基)-和5-(高哌啶-2-基)-1,4-苯并二氮杂卓类:胆囊收缩素-B受体的高亲和力碱性配体。
J Med Chem. 1997 Aug 1;40(16):2491-501. doi: 10.1021/jm9608523.