• 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

2-溴-5-氯噻吩的一锅法选择性芳基化;通过密度泛函理论(DFT)、X射线分析对分子结构的研究及其生物活性

One Pot Selective Arylation of 2-Bromo-5-Chloro Thiophene; Molecular Structure Investigation via Density Functional Theory (DFT), X-ray Analysis, and Their Biological Activities.

作者信息

Rasool Nasir, Kanwal Aqsa, Rasheed Tehmina, Ain Quratulain, Mahmood Tariq, Ayub Khurshid, Zubair Muhammad, Khan Khalid Mohammed, Arshad Muhammad Nadeem, M Asiri Abdullah, Zia-Ul-Haq Muhammad, Jaafar Hawa Z E

机构信息

Department of Chemistry, Government College University Faisalabad, Faisalabad 38000, Pakistan.

Department of Chemistry, COMSATS Institute of Information Technology, University Road, Tobe Camp, Abbottabad 22060, Pakistan.

出版信息

Int J Mol Sci. 2016 Jun 28;17(7):912. doi: 10.3390/ijms17070912.

DOI:10.3390/ijms17070912
PMID:27367666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4964363/
Abstract

Synthesis of 2,5-bisarylthiophenes was accomplished by sequential Suzuki cross coupling reaction of 2-bromo-5-chloro thiophenes. Density functional theory (DFT) studies were carried out at the B3LYP/6-31G(d, p) level of theory to compare the geometric parameters of 2,5-bisarylthiophenes with those from X-ray diffraction results. The synthesized compounds are screened for in vitro bacteria scavenging abilities. At the concentration of 50 and 100 μg/mL, compounds 2b, 2c, 2d, 3c, and 3f with IC50-values of 51.4, 52.10, 58.0, 56.2, and 56.5 μg/mL respectively, were found most potent against E. coli. Among all the synthesized compounds 2a, 2d, 3c, and 3e with the least values of IC50 77, 76.26, 79.13 μg/mL respectively showed significant antioxidant activities. Almost all of the compounds showed good antibacterial activity against Escherichia coli, whereas 2-chloro-5-(4-methoxyphenyl) thiophene (2b) was found most active among all synthesized compound with an IC50 value of 51.4 μg/mL. All of the synthesized compounds were screened for nitric oxide scavenging activity as well. Frontier molecular orbitals (FMOs) and molecular electrostatic potentials of the target compounds were also studied theoretically to account for their relative reactivity.

摘要

通过2-溴-5-氯噻吩的连续铃木交叉偶联反应完成了2,5-二芳基噻吩的合成。在B3LYP/6-31G(d, p)理论水平上进行了密度泛函理论(DFT)研究,以比较2,5-二芳基噻吩的几何参数与X射线衍射结果的几何参数。对合成的化合物进行体外细菌清除能力筛选。在50和100μg/mL的浓度下,发现化合物2b、2c、2d、3c和3f对大肠杆菌最有效,其IC50值分别为51.4、52.10、58.0、56.2和56.5μg/mL。在所有合成化合物中,IC50值最低的2a、2d、3c和3e分别为77、76.26、79.13μg/mL,显示出显著的抗氧化活性。几乎所有化合物对大肠杆菌都表现出良好的抗菌活性,而2-氯-5-(4-甲氧基苯基)噻吩(2b)在所有合成化合物中活性最高,IC50值为51.4μg/mL。还对所有合成化合物进行了一氧化氮清除活性筛选。还从理论上研究了目标化合物的前沿分子轨道(FMOs)和分子静电势,以解释它们的相对反应活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/fd60c0c58004/ijms-17-00912-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/b9f2a228b631/ijms-17-00912-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/431482d2b088/ijms-17-00912-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/3f8647836822/ijms-17-00912-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/dbc23efad8a1/ijms-17-00912-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/6752c5f2f228/ijms-17-00912-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/7ada01d2ff5f/ijms-17-00912-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/bde786c44904/ijms-17-00912-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/3430ff962810/ijms-17-00912-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/91787c3fab0c/ijms-17-00912-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/fa0208bf9770/ijms-17-00912-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/fd60c0c58004/ijms-17-00912-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/b9f2a228b631/ijms-17-00912-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/431482d2b088/ijms-17-00912-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/3f8647836822/ijms-17-00912-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/dbc23efad8a1/ijms-17-00912-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/6752c5f2f228/ijms-17-00912-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/7ada01d2ff5f/ijms-17-00912-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/bde786c44904/ijms-17-00912-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/3430ff962810/ijms-17-00912-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/91787c3fab0c/ijms-17-00912-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/fa0208bf9770/ijms-17-00912-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d394/4964363/fd60c0c58004/ijms-17-00912-g009.jpg

相似文献

1
One Pot Selective Arylation of 2-Bromo-5-Chloro Thiophene; Molecular Structure Investigation via Density Functional Theory (DFT), X-ray Analysis, and Their Biological Activities.2-溴-5-氯噻吩的一锅法选择性芳基化;通过密度泛函理论(DFT)、X射线分析对分子结构的研究及其生物活性
Int J Mol Sci. 2016 Jun 28;17(7):912. doi: 10.3390/ijms17070912.
2
Synthesis, Density Functional Theory (DFT), Urease Inhibition and Antimicrobial Activities of 5-Aryl Thiophenes Bearing Sulphonylacetamide Moieties.含磺酰基乙酰胺基团的5-芳基噻吩的合成、密度泛函理论(DFT)、脲酶抑制及抗菌活性
Molecules. 2015 Nov 5;20(11):19914-28. doi: 10.3390/molecules201119661.
3
Design, synthesis, antimicrobial evaluation and molecular docking studies of some new thiophene, pyrazole and pyridone derivatives bearing sulfisoxazole moiety.含磺胺甲噁唑部分的新型噻吩、吡唑和吡啶酮衍生物的设计、合成、抗菌评价及分子对接研究。
Eur J Med Chem. 2014 Sep 12;84:491-504. doi: 10.1016/j.ejmech.2014.07.052. Epub 2014 Jul 16.
4
Benzothiazole Clubbed Imidazolone Derivatives: Synthesis, Molecular Docking, DFT Studies, and Antimicrobial Studies.苯并噻唑稠合咪唑酮衍生物的合成、分子对接、DFT 研究及抗菌研究。
Curr Comput Aided Drug Des. 2023;19(2):123-136. doi: 10.2174/1573409919666221121115556.
5
Efficient Synthesis of Novel Pyridine-Based Derivatives via Suzuki Cross-Coupling Reaction of Commercially Available 5-Bromo-2-methylpyridin-3-amine: Quantum Mechanical Investigations and Biological Activities.通过市售的5-溴-2-甲基吡啶-3-胺的铃木交叉偶联反应高效合成新型吡啶基衍生物:量子力学研究及生物活性
Molecules. 2017 Jan 27;22(2):190. doi: 10.3390/molecules22020190.
6
Discovery of diethyl 2,5-diaminothiophene-3,4-dicarboxylate derivatives as potent anticancer and antimicrobial agents and screening of anti-diabetic activity: synthesis and in vitro biological evaluation. Part 1.二乙 2,5-二氨基噻吩-3,4-二羧酸酯衍生物的发现作为有效的抗癌和抗菌剂和抗糖尿病活性的筛选:合成和体外生物学评价。第 1 部分。
Eur J Med Chem. 2014 Sep 12;84:739-45. doi: 10.1016/j.ejmech.2014.07.065. Epub 2014 Jul 21.
7
Synthesis and antibacterial activity of some new thiazole and thiophene derivatives.一些新的噻唑和噻吩衍生物的合成及抗菌活性。
Eur J Med Chem. 2009 Nov;44(11):4434-40. doi: 10.1016/j.ejmech.2009.06.002. Epub 2009 Jun 13.
8
Design and synthesis of arylthiophene-2-carbaldehydes via Suzuki-Miyaura reactions and their biological evaluation.通过 Suzuki-Miyaura 反应设计和合成芳基噻吩-2-醛及其生物评价。
Molecules. 2013 Nov 27;18(12):14711-25. doi: 10.3390/molecules181214711.
9
Anti-tyrosinase, antioxidant, and antibacterial activities of novel 5-hydroxy-4-acetyl-2,3-dihydronaphtho[1,2-b]furans.新型5-羟基-4-乙酰基-2,3-二氢萘并[1,2-b]呋喃的抗酪氨酸酶、抗氧化和抗菌活性
Eur J Med Chem. 2014 Oct 30;86:605-12. doi: 10.1016/j.ejmech.2014.09.025. Epub 2014 Sep 9.
10
Synthesis and structure-activity relationship of amidine derivatives of 3,4-ethylenedioxythiophene as novel antibacterial agents.3,4-亚乙基二氧噻吩脒衍生物的合成及结构-活性关系研究作为新型抗菌剂。
Eur J Med Chem. 2015 Jan 27;90:68-81. doi: 10.1016/j.ejmech.2014.11.003. Epub 2014 Nov 4.

引用本文的文献

1
Sulfonamide drugs: structure, antibacterial property, toxicity, and biophysical interactions.磺胺类药物:结构、抗菌特性、毒性及生物物理相互作用。
Biophys Rev. 2021 Mar 29;13(2):259-272. doi: 10.1007/s12551-021-00795-9. eCollection 2021 Apr.
2
The BH3 mimetic (±) gossypol induces ROS-independent apoptosis and mitochondrial dysfunction in human A375 melanoma cells in vitro.BH3模拟物(±)棉酚在体外可诱导人A375黑色素瘤细胞发生不依赖活性氧的凋亡和线粒体功能障碍。
Arch Toxicol. 2021 Apr;95(4):1349-1365. doi: 10.1007/s00204-021-02987-4. Epub 2021 Feb 1.
3
Sensor applications of polypyrrole for oxynitrogen analytes: a DFT study.

本文引用的文献

1
Synthesis, Density Functional Theory (DFT), Urease Inhibition and Antimicrobial Activities of 5-Aryl Thiophenes Bearing Sulphonylacetamide Moieties.含磺酰基乙酰胺基团的5-芳基噻吩的合成、密度泛函理论(DFT)、脲酶抑制及抗菌活性
Molecules. 2015 Nov 5;20(11):19914-28. doi: 10.3390/molecules201119661.
2
Isolation, spectroscopic and density functional theory studies of 7-(4-methoxyphenyl)-9H-furo[2,3-f]chromen-9-one: a new flavonoid from the bark of Millettia ovalifolia.7-(4-甲氧基苯基)-9H-呋喃并[2,3-f]色烯-9-酮的分离、光谱及密度泛函理论研究:一种来自椭圆叶崖豆藤树皮的新型黄酮类化合物
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Jul 5;146:24-32. doi: 10.1016/j.saa.2015.03.061. Epub 2015 Mar 9.
3
聚吡咯用于氧氮分析物的传感器应用:一项密度泛函理论研究。
J Mol Model. 2018 Oct 5;24(11):308. doi: 10.1007/s00894-018-3843-0.
Synthesis, crystal structure, spectroscopic and density functional theory (DFT) study of N-[3-anthracen-9-yl-1-(4-bromo-phenyl)-allylidene]-N-benzenesulfonohydrazine.
N-[3-蒽-9-基-1-(4-溴苯基)-亚烯丙基]-N-苯磺酰肼的合成、晶体结构、光谱及密度泛函理论(DFT)研究
Spectrochim Acta A Mol Biomol Spectrosc. 2015 May 5;142:364-74. doi: 10.1016/j.saa.2015.01.101. Epub 2015 Feb 11.
4
Regioselective synthesis of 2-(bromomethyl)-5-aryl-thiophene derivatives via palladium (0) catalyzed suzuki cross-coupling reactions: as antithrombotic and haemolytically active molecules.通过钯(0)催化的铃木交叉偶联反应区域选择性合成2-(溴甲基)-5-芳基噻吩衍生物:作为抗血栓和具有溶血活性的分子。
Chem Cent J. 2014 Dec 17;8:74. doi: 10.1186/s13065-014-0074-z. eCollection 2014.
5
Continuous flow magnesiation of functionalized heterocycles and acrylates with TMPMgCl⋅LiCl.TMPMgCl·LiCl 引发的功能化杂环和丙烯酸酯的连续流动镁化反应。
Angew Chem Int Ed Engl. 2014 Jul 21;53(30):7933-7. doi: 10.1002/anie.201404221. Epub 2014 Jun 24.
6
Design and synthesis of arylthiophene-2-carbaldehydes via Suzuki-Miyaura reactions and their biological evaluation.通过 Suzuki-Miyaura 反应设计和合成芳基噻吩-2-醛及其生物评价。
Molecules. 2013 Nov 27;18(12):14711-25. doi: 10.3390/molecules181214711.
7
Synthesis and antimicrobial activity of some novel hydrazide, benzochromenone, dihydropyridine, pyrrole, thiazole and thiophene derivatives.合成及某些新型酰肼、苯并色酮、二氢吡啶、吡咯、噻唑和噻吩衍生物的抗菌活性。
Eur J Med Chem. 2013;70:419-26. doi: 10.1016/j.ejmech.2013.09.003. Epub 2013 Oct 12.
8
Efficient synthesis of 2-amino-6-arylbenzothiazoles via Pd(0) Suzuki cross coupling reactions: potent urease enzyme inhibition and nitric oxide scavenging activities of the products.通过 Pd(0)Suzuki 交叉偶联反应高效合成 2-氨基-6-芳基苯并噻唑:产物对脲酶的强烈抑制作用和对一氧化氮的清除活性。
Molecules. 2013 Jul 25;18(8):8845-57. doi: 10.3390/molecules18088845.
9
Synthesis, spectral characterization and antioxidant activity studies of a bidentate Schiff base, 5-methyl thiophene-2-carboxaldehyde-carbohydrazone and its Cd(II), Cu(II), Ni(II) and Zn(II) complexes.合成、光谱表征及双齿席夫碱 5-甲基噻吩-2-甲醛缩氨基硫脲及其 Cd(II)、Cu(II)、Ni(II)和 Zn(II)配合物的抗氧化活性研究。
Spectrochim Acta A Mol Biomol Spectrosc. 2013 Jan 15;101:264-72. doi: 10.1016/j.saa.2012.09.085. Epub 2012 Oct 5.
10
A C-H borylation approach to Suzuki-Miyaura coupling of typically unstable 2-heteroaryl and polyfluorophenyl boronates.一种 C-H 硼化方法,用于通常不稳定的 2-杂芳基和多氟代苯基硼酸酯的铃木-宫浦偶联反应。
Org Lett. 2012 Aug 17;14(16):4266-9. doi: 10.1021/ol301570t. Epub 2012 Aug 2.