• 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

(S)-(+)-4-[7-(2,2-dimethyl-1-oxopropoxy)-4-methyl-2-[4-[2-(1-piperidinyl)-ethoxy]phenyl]-2H-1-benzopyran-3-yl]-phenyl 2,2-dimethylpropanoate (EM-800): a highly potent, specific, and orally active nonsteroidal antiestrogen.

作者信息

Gauthier S, Caron B, Cloutier J, Dory Y L, Favre A, Larouche D, Mailhot J, Ouellet C, Schwerdtfeger A, Leblanc G, Martel C, Simard J, Mérand Y, Bélanger A, Labrie C, Labrie F

机构信息

Laboratory of Molecular Endocrinology, CHUL Research Centre, Le Centre Hospitalier Universitaire de Québec, Canada.

出版信息

J Med Chem. 1997 Jul 4;40(14):2117-22. doi: 10.1021/jm970095o.

DOI:10.1021/jm970095o
PMID:9216828
Abstract
摘要

相似文献

1
(S)-(+)-4-[7-(2,2-dimethyl-1-oxopropoxy)-4-methyl-2-[4-[2-(1-piperidinyl)-ethoxy]phenyl]-2H-1-benzopyran-3-yl]-phenyl 2,2-dimethylpropanoate (EM-800): a highly potent, specific, and orally active nonsteroidal antiestrogen.(S)-(+)-4-[7-(2,2-二甲基-1-氧代丙氧基)-4-甲基-2-[4-[2-(1-哌啶基)乙氧基]苯基]-2H-1-苯并吡喃-3-基]-苯基 2,2-二甲基丙酸酯(EM-800):一种高效、特异且口服有效的非甾体类抗雌激素药物。
J Med Chem. 1997 Jul 4;40(14):2117-22. doi: 10.1021/jm970095o.
2
Structure-activity relationship of antiestrogens. Phenolic analogues of 2,3-diaryl-2H-1-benzopyrans.抗雌激素的构效关系。2,3-二芳基-2H-1-苯并吡喃的酚类类似物。
J Med Chem. 1990 Dec;33(12):3222-9. doi: 10.1021/jm00174a020.
3
Structure-activity relationship of antiestrogens. Effect of the side chain and its position on the activity of 2,3-diaryl-2H-1-benzopyrans.抗雌激素的构效关系。侧链及其位置对2,3-二芳基-2H-1-苯并吡喃活性的影响。
J Med Chem. 1990 Dec;33(12):3216-22. doi: 10.1021/jm00174a019.
4
Structure-activity relationship of antiestrogens. Studies on 2,3-diaryl-1-benzopyrans.抗雌激素的构效关系。关于2,3-二芳基-1-苯并吡喃的研究。
J Med Chem. 1990 Dec;33(12):3210-6. doi: 10.1021/jm00174a018.
5
Effects of 3-phenyl-4-[[4-[2-(1-piperidinyl)ethoxy]phenyl]methyl]- 2H-1-benzopyran-7-ol (CHF 4056), a novel nonsteroidal estrogen agonist/antagonist, on reproductive and nonreproductive tissue.新型非甾体雌激素激动剂/拮抗剂3-苯基-4-[[4-[2-(1-哌啶基)乙氧基]苯基]甲基]-2H-1-苯并吡喃-7-醇(CHF 4056)对生殖和非生殖组织的影响。
J Pharmacol Exp Ther. 2002 Mar;300(3):802-9. doi: 10.1124/jpet.300.3.802.
6
Resolution, molecular structure and biological activities of the D- and L-enantiomers of potent anti-implantation agent, DL-2-[4-(2-piperidinoethoxy)phenyl]-3-phenyl-2H-1-benzopyran.强效抗着床剂DL-2-[4-(2-哌啶基乙氧基)苯基]-3-苯基-2H-1-苯并吡喃的D-和L-对映体的拆分、分子结构及生物活性
Bioorg Med Chem. 1999 Sep;7(9):2083-90. doi: 10.1016/s0968-0896(99)00131-5.
7
Pharmacological actions of a novel, potent, tissue-selective benzopyran estrogen.一种新型、强效、组织选择性苯并吡喃雌激素的药理作用
J Pharmacol Exp Ther. 2002 Oct;303(1):196-203. doi: 10.1124/jpet.102.038034.
8
Duration of antiestrogenecity of compound CDRI-85/287: a new orally active nonsteroidal antiimplantation agent.化合物CDRI-85/287的抗雌激素活性持续时间:一种新型口服活性非甾体抗着床剂。
Indian J Exp Biol. 1992 Nov;30(11):968-71.
9
CDRI-85/287: studies on competition to estrogen binding sites in the immature rat uterus.
Indian J Exp Biol. 1992 Dec;30(12):1115-7.
10
Comparison of the effects of the new orally active antiestrogen EM-800 with ICI 182 780 and toremifene on estrogen-sensitive parameters in the ovariectomized mouse.
Endocrinology. 1998 May;139(5):2486-92. doi: 10.1210/endo.139.5.5968.

引用本文的文献

1
Structure‒tissue exposure/selectivity relationship (STR) correlates with clinical efficacy/safety.结构-组织暴露/选择性关系(STR)与临床疗效/安全性相关。
Acta Pharm Sin B. 2022 May;12(5):2462-2478. doi: 10.1016/j.apsb.2022.02.015. Epub 2022 Feb 23.
2
Recent progress in selective estrogen receptor downregulators (SERDs) for the treatment of breast cancer.用于治疗乳腺癌的选择性雌激素受体下调剂(SERDs)的最新进展。
RSC Med Chem. 2020 Mar 6;11(4):438-454. doi: 10.1039/c9md00570f. eCollection 2020 Apr 1.
3
Antiestrogenic Activity and Possible Mode of Action of Certain New Nonsteroidal Coumarin-4-acetamides.
某些新型非甾体香豆素-4-乙酰胺的抗雌激素活性及可能作用模式。
Molecules. 2020 Mar 28;25(7):1553. doi: 10.3390/molecules25071553.
4
Copper-catalyzed oxidative cross-dehydrogenative coupling of 2H-chromenes and terminal alkynes.铜催化的 2H-色烯和末端炔烃的氧化交叉脱氢偶联反应。
Org Biomol Chem. 2018 Jul 18;16(28):5144-5149. doi: 10.1039/c8ob00949j.
5
Flexible small molecular anti-estrogens with N,N-dialkylated-2,5-diethoxy-4-morpholinoaniline scaffold targets multiple estrogen receptor conformations.具有 N,N-二烷基-2,5-二乙氧基-4-吗啉苯胺骨架的柔性小分子抗雌激素靶向多种雌激素受体构象。
Cell Cycle. 2017 Aug 3;16(15):1465-1477. doi: 10.1080/15384101.2017.1339848. Epub 2017 Jul 19.
6
Enantioselective copper-catalyzed alkynylation of benzopyranyl oxocarbenium ions.苯并吡喃基氧鎓离子的对映选择性铜催化炔基化反应
J Org Chem. 2015 Apr 17;80(8):4003-16. doi: 10.1021/acs.joc.5b00364. Epub 2015 Apr 7.
7
Bioactive chemical constituents from the brown alga Homoeostrichus formosana.来自褐藻台湾同形藻的生物活性化学成分。
Int J Mol Sci. 2014 Dec 30;16(1):736-46. doi: 10.3390/ijms16010736.
8
Potential activity of fevicordin-A from Phaleria macrocarpa (Scheff) Boerl. seeds as estrogen receptor antagonist based on cytotoxicity and molecular modelling studies.基于细胞毒性和分子建模研究的大麦克魔芋种子中的 fevicordin-A 作为雌激素受体拮抗剂的潜在活性。
Int J Mol Sci. 2014 Apr 25;15(5):7225-49. doi: 10.3390/ijms15057225.
9
Metalloradical approach to 2H-chromenes.2H-色烯的金属自由基合成方法。
J Am Chem Soc. 2014 Jan 22;136(3):1090-6. doi: 10.1021/ja4111336. Epub 2014 Jan 8.
10
Construction of a database for the evaluation and the clinical management of patients with breast cancer treated with antiestrogens and/or aromatase inhibitors.构建用于评估和临床管理接受抗雌激素和/或芳香化酶抑制剂治疗的乳腺癌患者的数据库。
Clin Cases Miner Bone Metab. 2011 Jan;8(1):37-50.