Suppr超能文献

杂环苯基磺酰基和4-氨基苯基磺酰基甲脒的合成、结构及抗菌活性

Synthesis, structure, and antimicrobial activity of heterocyclic phenylsulfonyl- and 4-aminophenylsulfonyl-carboximidamides.

作者信息

Gobis Katarzyna, Foks Henryk, Wiśniewska Katarzyna, Dąbrowska-Szponar Maria, Augustynowicz-Kopeć Ewa, Napiórkowska Agnieszka, Sikorski Artur

机构信息

Department of Organic Chemistry, Medical University of Gdańsk, Gdańsk, Poland.

Department of Medicinal Microbiology, Chair of Microbiology, Medical University of Gdańsk, Gdańsk, Poland.

出版信息

Monatsh Chem. 2012;143(8):1161-1169. doi: 10.1007/s00706-012-0769-6. Epub 2012 May 15.

Abstract

ABSTRACT

A series of novel phenylsulfonyl- and 4-aminophenylsulfonyl-carboximidamides were synthesized by condensation of sulfonamides with heterocyclic methyl carbimidates obtained from heterocyclic carbonitriles and used 'at its inception.' The molecular structure of the obtained compounds is discussed. Compounds possessing heterocyclic systems with a nitrogen atom in the α position to the functional group showed a different single-crystal structure than expected. The synthesized derivatives were evaluated for antimicrobial activities: tuberculostatic, antibacterial, and antifungal.

摘要

摘要

通过磺酰胺与由杂环腈获得的杂环甲基氨基甲酰亚胺缩合,合成了一系列新型苯基磺酰基和4-氨基苯基磺酰基-羧基亚胺酰胺,并在其初始阶段使用。讨论了所得化合物的分子结构。在官能团α位具有含氮原子杂环体系的化合物显示出与预期不同的单晶结构。对合成的衍生物进行了抗菌活性评估:抗结核、抗菌和抗真菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c8/4494770/760f1c442867/706_2012_769_Sch1_HTML.jpg

相似文献

1
Synthesis, structure, and antimicrobial activity of heterocyclic phenylsulfonyl- and 4-aminophenylsulfonyl-carboximidamides.
Monatsh Chem. 2012;143(8):1161-1169. doi: 10.1007/s00706-012-0769-6. Epub 2012 May 15.
2
Synthesis, structure, and biological activity of novel heterocyclic sulfonyl-carboximidamides.
Monatsh Chem. 2013;144(5):647-658. doi: 10.1007/s00706-012-0888-0. Epub 2013 Jan 25.
3
Synthesis and antimicrobial activity of novel heterocyclic sulfamoyl-phenyl-carboximidamides derived from clinically applied sulfonamides.
Arch Pharm (Weinheim). 2012 Nov;345(11):911-7. doi: 10.1002/ardp.201200160. Epub 2012 Aug 7.
6
Synthesis of hydrazides of heterocyclic amines and their antimicrobial and spasmolytic activity.
Saudi Pharm J. 2022 Jul;30(7):1036-1043. doi: 10.1016/j.jsps.2022.04.009. Epub 2022 Apr 26.
9
Synthesis, molecular docking and biological evaluation of novel 6-(4-(4-aminophenylsulfonyl)phenylamino)-5H-benzo[a]phenothiazin-5-one derivatives.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Mar 15;139:477-87. doi: 10.1016/j.saa.2014.12.036. Epub 2014 Dec 19.
10
Synthesis and antimicrobial evaluation of some fused heterocyclic [1,2,4]triazolo[3,4-b][1,3,4]thiadiazole derivatives.
Eur J Med Chem. 2010 Dec;45(12):6139-46. doi: 10.1016/j.ejmech.2010.10.007. Epub 2010 Oct 15.

引用本文的文献

2
4
Synthesis, structure, and biological activity of novel heterocyclic sulfonyl-carboximidamides.
Monatsh Chem. 2013;144(5):647-658. doi: 10.1007/s00706-012-0888-0. Epub 2013 Jan 25.
5
Synthesis, anticancer and antibacterial activity of salinomycin N-benzyl amides.
Molecules. 2014 Nov 25;19(12):19435-59. doi: 10.3390/molecules191219435.

本文引用的文献

2
Multidrug-resistant and extensively drug-resistant tuberculosis: a threat to global control of tuberculosis.
Lancet. 2010 May 22;375(9728):1830-43. doi: 10.1016/S0140-6736(10)60410-2.
4
Test tube evaluation of tuberculostatic agents.
Am Rev Tuberc. 1947 Nov;56(5):376. doi: 10.1164/art.1947.56.5.376.
5
Synthesis and antiviral evaluation of acyclic azanucleosides developed from sulfanilamide as a lead structure.
Bioorg Med Chem. 2008 Sep 15;16(18):8379-89. doi: 10.1016/j.bmc.2008.08.041. Epub 2008 Aug 26.
6
Carbonic anhydrases: novel therapeutic applications for inhibitors and activators.
Nat Rev Drug Discov. 2008 Feb;7(2):168-81. doi: 10.1038/nrd2467.
7
Microbiology of antibiotic resistance in Staphylococcus aureus.
Clin Infect Dis. 2007 Sep 15;45 Suppl 3:S165-70. doi: 10.1086/519474.
8
HIV infection and multidrug-resistant tuberculosis: the perfect storm.
J Infect Dis. 2007 Aug 15;196 Suppl 1:S86-107. doi: 10.1086/518665.
9
A METHOD FOR THE DETERMINATION OF THE RATE OF GROWTH OF TUBERCLE BACILLI BY THE USE OF SMALL INOCULA.
J Bacteriol. 1949 Aug;58(2):247-55. doi: 10.1128/jb.58.2.247-255.1949.
10
Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors.
Bioorg Med Chem. 2006 Feb 15;14(4):1078-88. doi: 10.1016/j.bmc.2005.09.037. Epub 2005 Nov 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验