SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES

Synthesis, electronic, infrared, elemental micro analytical studies were carried on N-(benzothiazol-2-yl)trichloroethanamide [4] and N-(benzothiazol-2-yl)chloroethanamide [5]. They were also screened in vitro and in vivo for antibacterial activity. The results indicate that the compounds are very st...

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Main Authors: L.N. Obasi, P. O. Ukoha, K. F. Chah, A. O. Anaga
Format: Article
Language:English
Published: Universidade Estadual Paulista 2018-04-01
Series:Eclética Química
Online Access:https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/127
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spelling doaj-22b853fb635b40c897e9ff614b424dcd2020-11-24T21:59:56ZengUniversidade Estadual PaulistaEclética Química1678-46182018-04-01361071710.26850/1678-4618eqj.v36.1.2011.p07-17127SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDESL.N. Obasi0P. O. Ukoha1K. F. Chah2A. O. Anaga3Department of Pure & Industrial Chemistry, University of Nigeria, Nsukka.Department of Pure & Industrial Chemistry, University of Nigeria, Nsukka.Department of Veterinary Pathology and Microbiology, University of Nigeria, Nsukka.3Department of Physiology and Pharmacology, University of Nigeria, NsukkaSynthesis, electronic, infrared, elemental micro analytical studies were carried on N-(benzothiazol-2-yl)trichloroethanamide [4] and N-(benzothiazol-2-yl)chloroethanamide [5]. They were also screened in vitro and in vivo for antibacterial activity. The results indicate that the compounds are very stable and that they show high antibacterial activities against both grampositive and gram-negative bacteria tested. Both derivatives of 2-aminobenzothiazole were active against the multiresistant bacteria with IZD ranging from 9 -18 mm [5] and 9 – 20mm [4]. From the MIC results it is observed that the [5] derivative produced a better antibacterial activity than the [4] derivative. The lethal concentrations (LC50) of the compounds were also determined. Their solubilities and melting points were also determined.https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/127
collection DOAJ
language English
format Article
sources DOAJ
author L.N. Obasi
P. O. Ukoha
K. F. Chah
A. O. Anaga
spellingShingle L.N. Obasi
P. O. Ukoha
K. F. Chah
A. O. Anaga
SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
Eclética Química
author_facet L.N. Obasi
P. O. Ukoha
K. F. Chah
A. O. Anaga
author_sort L.N. Obasi
title SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
title_short SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
title_full SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
title_fullStr SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
title_full_unstemmed SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND ANTIBACTERIAL SCREENING OF NOVEL N-(BENZOTHIAZOL-2-YL)ETHANAMIDES
title_sort synthesis, spectroscopic characterization and antibacterial screening of novel n-(benzothiazol-2-yl)ethanamides
publisher Universidade Estadual Paulista
series Eclética Química
issn 1678-4618
publishDate 2018-04-01
description Synthesis, electronic, infrared, elemental micro analytical studies were carried on N-(benzothiazol-2-yl)trichloroethanamide [4] and N-(benzothiazol-2-yl)chloroethanamide [5]. They were also screened in vitro and in vivo for antibacterial activity. The results indicate that the compounds are very stable and that they show high antibacterial activities against both grampositive and gram-negative bacteria tested. Both derivatives of 2-aminobenzothiazole were active against the multiresistant bacteria with IZD ranging from 9 -18 mm [5] and 9 – 20mm [4]. From the MIC results it is observed that the [5] derivative produced a better antibacterial activity than the [4] derivative. The lethal concentrations (LC50) of the compounds were also determined. Their solubilities and melting points were also determined.
url https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/127
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AT kfchah synthesisspectroscopiccharacterizationandantibacterialscreeningofnovelnbenzothiazol2ylethanamides
AT aoanaga synthesisspectroscopiccharacterizationandantibacterialscreeningofnovelnbenzothiazol2ylethanamides
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