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Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids
Certain 2-(1'-iminothioimido substituted)-1'-substituted phenybenzoic acids (P(1-9)) were synthesized by reaction of phthalic anhydride with benzotriazole, 2-mercapto benzothiazole and 2-p-amino phenyl benzimidazole, respectively (A(1-3)) followed by imine formation with Schiff bases of th...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792522/ https://www.ncbi.nlm.nih.gov/pubmed/20046753 http://dx.doi.org/10.4103/0250-474X.43009 |
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author | Subudhi, B. B. Bhatta, D. Panda, P. K. Mishra, P. Pradhan, D. |
author_facet | Subudhi, B. B. Bhatta, D. Panda, P. K. Mishra, P. Pradhan, D. |
author_sort | Subudhi, B. B. |
collection | PubMed |
description | Certain 2-(1'-iminothioimido substituted)-1'-substituted phenybenzoic acids (P(1-9)) were synthesized by reaction of phthalic anhydride with benzotriazole, 2-mercapto benzothiazole and 2-p-amino phenyl benzimidazole, respectively (A(1-3)) followed by imine formation with Schiff bases of thiourea with salicylaldehyde, furfuraldehyde and 1-phenyl-3-methyl-5-pyrazolone. Antiulcer activity was evaluated using reduction in total acidity, free acidity and ulcer index as parameters. Compounds P(3), P(6), P(7) and P(9)(100 mg/kg) showed significant (P< 0.001) antiulcer action compared to control and omeprazole (40 mg/kg). |
format | Text |
id | pubmed-2792522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-27925222009-12-14 Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids Subudhi, B. B. Bhatta, D. Panda, P. K. Mishra, P. Pradhan, D. Indian J Pharm Sci Short Communications Certain 2-(1'-iminothioimido substituted)-1'-substituted phenybenzoic acids (P(1-9)) were synthesized by reaction of phthalic anhydride with benzotriazole, 2-mercapto benzothiazole and 2-p-amino phenyl benzimidazole, respectively (A(1-3)) followed by imine formation with Schiff bases of thiourea with salicylaldehyde, furfuraldehyde and 1-phenyl-3-methyl-5-pyrazolone. Antiulcer activity was evaluated using reduction in total acidity, free acidity and ulcer index as parameters. Compounds P(3), P(6), P(7) and P(9)(100 mg/kg) showed significant (P< 0.001) antiulcer action compared to control and omeprazole (40 mg/kg). Medknow Publications 2008 /pmc/articles/PMC2792522/ /pubmed/20046753 http://dx.doi.org/10.4103/0250-474X.43009 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Subudhi, B. B. Bhatta, D. Panda, P. K. Mishra, P. Pradhan, D. Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title | Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title_full | Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title_fullStr | Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title_full_unstemmed | Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title_short | Synthesis and Antiulcer Activity Studies of 2-(1′-Iminothioimido Substituted)-1′-Substituted Phenylbenzoic acids |
title_sort | synthesis and antiulcer activity studies of 2-(1′-iminothioimido substituted)-1′-substituted phenylbenzoic acids |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792522/ https://www.ncbi.nlm.nih.gov/pubmed/20046753 http://dx.doi.org/10.4103/0250-474X.43009 |
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