• 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

二氢吡啶类药物:评估其当前和未来的药理学应用。

Dihydropyridines: evaluation of their current and future pharmacological applications.

机构信息

Medicinal & Natural Product Chemistry Research Centre, Shiraz University of Medical Sciences, P.O. Box 71345-3288, Shiraz, Iran.

出版信息

Drug Discov Today. 2009 Nov;14(21-22):1058-66. doi: 10.1016/j.drudis.2009.08.004. Epub 2009 Sep 1.

DOI:10.1016/j.drudis.2009.08.004
PMID:19729074
Abstract

The 1,4-dihydropyridines (DHPs), a class of drugs, possess a wide variety of biological and pharmacological actions, have represented one of the most important groups of calcium-channel-modulating agents and have experienced widespread use in the treatment of cardiovascular disease. Moreover, it has been demonstrated that DHPs could prove to be highly important as multidrug-resistance-reversing agents in cancer chemotherapy. Recent reports suggest that this class also has other notable activities, particularly as antimycobacterial and anticonvulsant agents. Finally, it might be possible for the DHP motif to serve as a scaffold for other pharmacological applications.

摘要

1,4-二氢吡啶(DHPs)类药物具有广泛的生物学和药理学作用,是一类重要的钙通道调节剂,已广泛用于心血管疾病的治疗。此外,DHPs 已被证明在癌症化疗中作为多药耐药逆转剂可能具有重要意义。最近的报告表明,该类药物还具有其他显著的活性,特别是作为抗分枝杆菌和抗惊厥药物。最后,DHPs 可能成为其他药理学应用的支架。

相似文献

1
Dihydropyridines: evaluation of their current and future pharmacological applications.二氢吡啶类药物:评估其当前和未来的药理学应用。
Drug Discov Today. 2009 Nov;14(21-22):1058-66. doi: 10.1016/j.drudis.2009.08.004. Epub 2009 Sep 1.
2
Dihydropyridines and atypical MDR: a novel perspective of designing general reversal agents for both typical and atypical MDR.二氢吡啶类与非典型多药耐药:设计针对典型和非典型多药耐药的通用逆转剂的新视角。
Bioorg Med Chem. 2008 Sep 15;16(18):8329-34. doi: 10.1016/j.bmc.2008.07.025. Epub 2008 Jul 18.
3
Design and synthesis of new symmetrical derivatives of dihydropyridine containing a pyridyl group on the 3, 5-positions and evaluation of their cytotoxic and multidrug resistance reversal activity.3,5-位含吡啶基的新型对称二氢吡啶衍生物的设计、合成及其细胞毒性和多药耐药逆转活性评价
J Pharm Pharmacol. 2008 Nov;60(11):1481-9. doi: 10.1211/jpp/60.11.0009.
4
Dihydropyridine derivatives to overcome atypical multidrug resistance: design, synthesis, QSAR studies, and evaluation of their cytotoxic and pharmacological activities.克服非典型多药耐药性的二氢吡啶衍生物:设计、合成、定量构效关系研究及其细胞毒性和药理活性评估
Chem Biol Drug Des. 2007 Oct;70(4):337-46. doi: 10.1111/j.1747-0285.2007.00569.x.
5
1, 4-Dihydropyridines: a class of pharmacologically important molecules.1,4 - 二氢吡啶类:一类具有重要药理学意义的分子。
Mini Rev Med Chem. 2014;14(3):282-90.
6
Synthesis, evaluation of pharmacological activities and quantitative structure-activity relationship studies of a novel group of bis(4-nitroaryl-1,4-dihyropyridine).新型双(4-硝基芳基-1,4-二氢吡啶)类化合物的合成、药理活性评价及定量构效关系研究
Chem Biol Drug Des. 2009 Feb;73(2):225-35. doi: 10.1111/j.1747-0285.2008.00770.x.
7
Dihydropyridines and multidrug resistance: previous attempts, present state, and future trends.二氢吡啶类药物与多药耐药性:既往尝试、当前状况与未来趋势。
Chem Biol Drug Des. 2010 Nov;76(5):369-81. doi: 10.1111/j.1747-0285.2010.01025.x.
8
Five different profiles of dihydropyridines in blocking T-type Ca(2+) channel subtypes (Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I))) expressed in Xenopus oocytes.在非洲爪蟾卵母细胞中表达的二氢吡啶对T型钙通道亚型(Ca(v)3.1(α(1G))、Ca(v)3.2(α(1H))和Ca(v)3.3(α(1I)))的五种不同阻断情况。
Eur J Pharmacol. 2009 Jun 24;613(1-3):100-7. doi: 10.1016/j.ejphar.2009.04.036. Epub 2009 May 3.
9
Selectivities of dihydropyridine derivatives in blocking Ca(2+) channel subtypes expressed in Xenopus oocytes.二氢吡啶衍生物对非洲爪蟾卵母细胞中表达的钙通道亚型的阻断选择性。
J Pharmacol Exp Ther. 1999 Nov;291(2):464-73.
10
Synthesis, study of 3D structures, and pharmacological activities of lipophilic nitroimidazolyl-1,4-dihydropyridines as calcium channel antagonist.亲脂性硝基咪唑基-1,4-二氢吡啶作为钙通道拮抗剂的合成、三维结构研究及药理活性
Bioorg Med Chem. 2006 Jul 15;14(14):4842-9. doi: 10.1016/j.bmc.2006.03.016. Epub 2006 Apr 5.

引用本文的文献

1
Effect of Nifedipine in Preventing Ovarian Hyperstimulation Syndrome through TRPC1 Ion Channel Inhibition.硝苯地平通过抑制TRPC1离子通道预防卵巢过度刺激综合征的作用。
Reprod Sci. 2025 Jun 18. doi: 10.1007/s43032-025-01913-8.
2
Lercanidipine Enhances Cisplatin Activity: Dual Anticancer and Anti-Inflammatory Effects via Caspase Activation and MAPK Inhibition.乐卡地平增强顺铂活性:通过半胱天冬酶激活和丝裂原活化蛋白激酶抑制发挥双重抗癌和抗炎作用。
Pharmaceuticals (Basel). 2025 Apr 29;18(5):651. doi: 10.3390/ph18050651.
3
Mechanism of nimodipine in treating neurodegenerative diseases: in silico target identification and molecular dynamic simulation.
尼莫地平治疗神经退行性疾病的机制:计算机靶点识别与分子动力学模拟
Front Pharmacol. 2025 Mar 13;16:1549953. doi: 10.3389/fphar.2025.1549953. eCollection 2025.
4
Biginelli dihydropyrimidines and their acetylated derivatives as L-/T-type calcium channel blockers: Synthesis, enantioseparation, and molecular modeling studies.作为L型/T型钙通道阻滞剂的Biginelli二氢嘧啶及其乙酰化衍生物:合成、对映体拆分及分子模拟研究
Arch Pharm (Weinheim). 2025 Mar;358(3):e2400584. doi: 10.1002/ardp.202400584.
5
- Simplifying the Complex: Building, Simulating, and Analyzing Protein-Ligand Systems in .简化复杂问题:构建、模拟和分析蛋白质-配体系统
J Chem Inf Model. 2025 Feb 24;65(4):1967-1978. doi: 10.1021/acs.jcim.4c02158. Epub 2025 Feb 11.
6
One-pot reaction of 3-vinylchromones, aromatic aldehydes, and ammonium acetate: an efficient approach to highly functionalized 1,6-dihydropyridine derivatives.3-乙烯基色酮、芳香醛和醋酸铵的一锅反应:一种高效合成高度官能化1,6-二氢吡啶衍生物的方法。
RSC Adv. 2025 Jan 27;15(4):2602-2607. doi: 10.1039/d4ra07863b. eCollection 2025 Jan 23.
7
Updates on Intrinsic Medicinal Chemistry of 1,4-dihydropyridines, Perspectives on Synthesis and Pharmacokinetics of Novel 1,4-dihydropyrimidines as Calcium Channel Blockers: Clinical Pharmacology.1,4 - 二氢吡啶的内在药物化学进展,新型1,4 - 二氢嘧啶作为钙通道阻滞剂的合成与药代动力学展望:临床药理学
Curr Top Med Chem. 2025 Jan 1. doi: 10.2174/0115680266323908241114064318.
8
Microwave-assisted synthesis of base-modified fluorescent 1,4-dihydropyridine nucleosides: photophysical characterization and insights.微波辅助合成碱基修饰的荧光1,4-二氢吡啶核苷:光物理表征及见解
RSC Adv. 2024 Dec 18;14(54):39833-39843. doi: 10.1039/d4ra07295b. eCollection 2024 Dec 17.
9
Acyl-1,4-Dihydropyridines: Universal Acylation Reagents for Organic Synthesis.酰基-1,4-二氢吡啶:有机合成中的通用酰化试剂。
Molecules. 2024 Aug 13;29(16):3844. doi: 10.3390/molecules29163844.
10
Acridinedione-phthalimide conjugates: Intramolecular electron transfer and singlet oxygen generation studies for optical and photodynamic therapy applications.吖啶二酮-邻苯二甲酰亚胺轭合物:用于光动力治疗的分子内电子转移和单线态氧生成研究。
Photochem Photobiol Sci. 2024 Aug;23(8):1445-1455. doi: 10.1007/s43630-024-00603-9. Epub 2024 Jun 27.