• 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

DOV 216,303, a "triple" reuptake inhibitor: safety, tolerability, and pharmacokinetic profile.

作者信息

Beer Bernard, Stark Jill, Krieter Philip, Czobor Pal, Beer Gary, Lippa Arnold, Skolnick Phil

机构信息

DOV Pharmaceutical, Inc, Continental Plaza, 433 Hackensack Avenue, Hackensack, NJ 07601, USA.

出版信息

J Clin Pharmacol. 2004 Dec;44(12):1360-7. doi: 10.1177/0091270004269560.

DOI:10.1177/0091270004269560
PMID:15545306
Abstract

This report describes the first evaluation in humans of DOV 216,303, a putative antidepressive that inhibits the reuptake of norepinephrine, serotonin, and dopamine. Subjects received single oral doses of 5 to 150 mg of DOV 216,303 or placebo. At 150 mg, 4 of 7 subjects reported gastrointestinal disturbances. In the multiple-dose phase of the evaluation, subjects received total daily doses of 50, 75, or 100 mg of DOV 216,303 or placebo for 10 days. At a total daily dose of 100 mg, gastrointestinal disturbances were reported in 4 of 6 volunteers. In both the single- and multiple-dose evaluations, no significant changes were noted in vital signs, electrocardiogram, hematology, or clinical chemistry. DOV 216,303 was rapidly absorbed (plasma t(max) of 0.7-1.2 hours and t(1/2) of 3.3-4.4 hours), with dose-proportional C(max) and AUC values. Furthermore, no remarkable difference was apparent in either the C(max) or AUC(tau) of DOV 216,303 following 1 and 10 days of dosing. The present results demonstrate that DOV 216,303 is safe and well tolerated both at single doses of up to 100 mg and multiple doses of up to 100 mg/day for 10 days. Plasma concentrations of DOV 216,303 after doses > 10 mg exceed its reported IC(50) values for inhibition of biogenic amine reuptake.

摘要

相似文献

1
DOV 216,303, a "triple" reuptake inhibitor: safety, tolerability, and pharmacokinetic profile.
J Clin Pharmacol. 2004 Dec;44(12):1360-7. doi: 10.1177/0091270004269560.
2
Preclinical and clinical pharmacology of DOV 216,303, a "triple" reuptake inhibitor.DOV 216,303(一种“三重”再摄取抑制剂)的临床前和临床药理学
CNS Drug Rev. 2006 Summer;12(2):123-34. doi: 10.1111/j.1527-3458.2006.00123.x.
3
The potential and limitations of DOV 216,303 as a triple reuptake inhibitor for the treatment of major depression: a microdialysis study in olfactory bulbectomized rats.多韦替尼(DOV)216,303 作为治疗重度抑郁症的三重再摄取抑制剂的潜力和局限性:嗅球切除术大鼠的微透析研究。
Pharmacol Biochem Behav. 2011 Jan;97(3):444-52. doi: 10.1016/j.pbb.2010.10.001. Epub 2010 Oct 8.
4
The putative antidepressant DOV 216,303, a triple reuptake inhibitor, increases monoamine release in the prefrontal cortex of olfactory bulbectomized rats.拟用于抗抑郁的 DOV 216,303,一种三重再摄取抑制剂,增加嗅球切除术大鼠前额皮质中单胺的释放。
Eur J Pharmacol. 2010 May 10;633(1-3):55-61. doi: 10.1016/j.ejphar.2010.02.009. Epub 2010 Feb 12.
5
The novel triple reuptake inhibitor JZAD-IV-22 exhibits an antidepressant pharmacological profile without locomotor stimulant or sensitization properties.新型三重再摄取抑制剂 JZAD-IV-22 具有抗抑郁药理学特性,无运动兴奋剂或敏化特性。
J Pharmacol Exp Ther. 2010 Dec;335(3):762-70. doi: 10.1124/jpet.110.174011. Epub 2010 Sep 23.
6
Pharmacokinetics, safety and tolerability of Bencycloquidium bromide, a novel selective muscarinic M1/M3 receptor antagonist, after single and multiple intranasal doses in healthy chinese subjects: an open-label, single-center, first-in-human study.Bencycloquidium bromide 是一种新型选择性毒蕈碱 M1/M3 受体拮抗剂,在健康中国受试者中单次和多次经鼻给药的药代动力学、安全性和耐受性:一项开放标签、单中心、首次人体研究。
Drugs R D. 2012 Mar 1;12(1):17-28. doi: 10.2165/11599330-000000000-00000.
7
Antidepressant-like actions of DOV 21,947: a "triple" reuptake inhibitor.DOV 21,947的抗抑郁样作用:一种“三重”再摄取抑制剂。
Eur J Pharmacol. 2003 Feb 14;461(2-3):99-104. doi: 10.1016/s0014-2999(03)01310-4.
8
"Broad spectrum" antidepressants: is more better for the treatment of depression?“广谱”抗抑郁药:治疗抑郁症效果更佳?
Life Sci. 2003 Nov 7;73(25):3175-9. doi: 10.1016/j.lfs.2003.06.007.
9
Linagliptin, a dipeptidyl peptidase-4 inhibitor in development for the treatment of type 2 diabetes mellitus: a Phase I, randomized, double-blind, placebo-controlled trial of single and multiple escalating doses in healthy adult male Japanese subjects.利拉利汀,一种开发用于治疗 2 型糖尿病的二肽基肽酶-4 抑制剂:在健康成年日本男性受试者中进行的单次和多次递增剂量、随机、双盲、安慰剂对照的 I 期临床试验。
Clin Ther. 2010 Jun;32(6):1188-204. doi: 10.1016/j.clinthera.2010.06.004.
10
The triple uptake inhibitor (1R,5S)-(+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0] hexane hydrochloride (DOV 21947) reduces body weight and plasma triglycerides in rodent models of diet-induced obesity.三联摄取抑制剂(1R,5S)-(+)-1-(3,4-二氯苯基)-3-氮杂双环[3.1.0]己烷盐酸盐(DOV 21947)可降低饮食诱导肥胖啮齿动物模型的体重和血浆甘油三酯水平。
J Pharmacol Exp Ther. 2008 Mar;324(3):1111-26. doi: 10.1124/jpet.107.133132. Epub 2007 Dec 18.

引用本文的文献

1
Therapeutic Potential of Ursolic Acid to Manage Neurodegenerative and Psychiatric Diseases.熊果酸的治疗潜力可用于治疗神经退行性和精神疾病。
CNS Drugs. 2017 Dec;31(12):1029-1041. doi: 10.1007/s40263-017-0474-4.
2
Palladium-catalysed transannular C-H functionalization of alicyclic amines.钯催化脂环族胺的跨环C-H官能团化反应
Nature. 2016 Mar 10;531(7593):220-224. doi: 10.1038/nature16957. Epub 2016 Feb 17.
3
Triple reuptake inhibitors as potential next-generation antidepressants: a new hope?三重再摄取抑制剂作为潜在的下一代抗抑郁药:新希望?
Future Med Chem. 2015;7(17):2385-406. doi: 10.4155/fmc.15.134. Epub 2015 Nov 30.
4
Structural exploration of (3S,6S)-6-benzhydryl-N-benzyltetrahydro-2H-pyran-3-amine analogues: identification of potent triple monoamine reuptake inhibitors as potential antidepressants.(3S,6S)-6-苄基-N-苄基四氢-2H-吡喃-3-胺类似物的结构探索:作为潜在抗抑郁药的强效三单胺再摄取抑制剂的鉴定。
ChemMedChem. 2012 Dec;7(12):2093-100. doi: 10.1002/cmdc.201200352. Epub 2012 Oct 11.
5
Triple reuptake inhibitors: a premise and promise.三重再摄取抑制剂:前提与希望。
Psychiatry Investig. 2008 Sep;5(3):142-7. doi: 10.4306/pi.2008.5.3.142. Epub 2008 Sep 30.
6
Triple reuptake inhibitors: the next generation of antidepressants.三重再摄取抑制剂:新一代抗抑郁药。
Curr Neuropharmacol. 2008 Dec;6(4):338-43. doi: 10.2174/157015908787386078.
7
Emerging targets for antidepressant therapies.抗抑郁治疗的新兴靶点。
Curr Opin Chem Biol. 2009 Jun;13(3):291-302. doi: 10.1016/j.cbpa.2009.04.617. Epub 2009 Jun 6.
8
Novel targets for antidepressant therapies.抗抑郁疗法的新靶点。
Curr Psychiatry Rep. 2008 Dec;10(6):465-73. doi: 10.1007/s11920-008-0075-5.
9
Narcolepsy: current treatment options and future approaches.发作性睡病:当前的治疗选择和未来的方法。
Neuropsychiatr Dis Treat. 2008 Jun;4(3):557-66.
10
Preclinical and clinical pharmacology of DOV 216,303, a "triple" reuptake inhibitor.DOV 216,303(一种“三重”再摄取抑制剂)的临床前和临床药理学
CNS Drug Rev. 2006 Summer;12(2):123-34. doi: 10.1111/j.1527-3458.2006.00123.x.