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Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase

We have synthesized twelve 2-substituted benzimidazole, benzothiazole and indole derivatives using on both microwave irradiation and conventional heating methods. The microwave method was observed to be more beneficial as it provides an increase of yield from 3% to 113% and a 95 to 98 % reduction in...

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Detalles Bibliográficos
Autores principales: Algul, Oztekin, Kaessler, Andre, Apcin, Yagmur, Yilmaz, Akin, Jose, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245189/
https://www.ncbi.nlm.nih.gov/pubmed/18463575
http://dx.doi.org/10.3390/molecules13040736
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author Algul, Oztekin
Kaessler, Andre
Apcin, Yagmur
Yilmaz, Akin
Jose, Joachim
author_facet Algul, Oztekin
Kaessler, Andre
Apcin, Yagmur
Yilmaz, Akin
Jose, Joachim
author_sort Algul, Oztekin
collection PubMed
description We have synthesized twelve 2-substituted benzimidazole, benzothiazole and indole derivatives using on both microwave irradiation and conventional heating methods. The microwave method was observed to be more beneficial as it provides an increase of yield from 3% to 113% and a 95 to 98 % reduction in time. All compounds were tested by a stains-all assay at pH 7 and by a Morgan-Elson assay at pH 3.5 for hyaluronidase inhibitory activity at a concentration of 100 µM. The most potent compound was 2-(4-hydroxyphenyl)-3-phenylindole (12) with an IC(50) value of 107 µM at both pH 7 and 3.5.
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spelling pubmed-62451892018-11-26 Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase Algul, Oztekin Kaessler, Andre Apcin, Yagmur Yilmaz, Akin Jose, Joachim Molecules Full Paper We have synthesized twelve 2-substituted benzimidazole, benzothiazole and indole derivatives using on both microwave irradiation and conventional heating methods. The microwave method was observed to be more beneficial as it provides an increase of yield from 3% to 113% and a 95 to 98 % reduction in time. All compounds were tested by a stains-all assay at pH 7 and by a Morgan-Elson assay at pH 3.5 for hyaluronidase inhibitory activity at a concentration of 100 µM. The most potent compound was 2-(4-hydroxyphenyl)-3-phenylindole (12) with an IC(50) value of 107 µM at both pH 7 and 3.5. MDPI 2008-03-27 /pmc/articles/PMC6245189/ /pubmed/18463575 http://dx.doi.org/10.3390/molecules13040736 Text en © 2008 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes.
spellingShingle Full Paper
Algul, Oztekin
Kaessler, Andre
Apcin, Yagmur
Yilmaz, Akin
Jose, Joachim
Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title_full Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title_fullStr Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title_full_unstemmed Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title_short Comparative Studies on Conventional and Microwave Synthesis of Some Benzimidazole, Benzothiazole and Indole Derivatives and Testing on Inhibition of Hyaluronidase
title_sort comparative studies on conventional and microwave synthesis of some benzimidazole, benzothiazole and indole derivatives and testing on inhibition of hyaluronidase
topic Full Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245189/
https://www.ncbi.nlm.nih.gov/pubmed/18463575
http://dx.doi.org/10.3390/molecules13040736
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