Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60823
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dc.contributor.authorKantar, Cihan-
dc.contributor.authorBaltaş, Nimet-
dc.contributor.authorDereci, Oğuz Kağan-
dc.contributor.authorŞaşmaz, Selami-
dc.date.accessioned2022-11-11T09:42:13Z-
dc.date.available2022-11-11T09:42:13Z-
dc.date.issued2022-11-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60823-
dc.description1188-1193en_US
dc.description.abstractBased on the relationship between Helicobacter pylori and Alzehimer’s disease, new azo phthalonitrile compounds containing different amino pyridines have been synthesized. These compounds can inhibit both Urease and Acetylcholinesterase, which are the most important enzymes in the treatment of Helicobacter pylori and Alzehimer’s disease, respectively. All compounds have shown better inhibition than standards in the presence of both enzymes. Especialy, azo phthalonitrile compound 4 is more active than other compounds and standards, showed a significant inhibition performance and efficient IC50 values to Urease (20.47±0.14 μM) and Acetylcholinesterase (4.73±0.07 μM) enzymes. Interestingly, the inhibitory effect of the newly synthesized compounds against to Urease and Acetylcholinesterase is same ranking.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(11) [Nov 2022]en_US
dc.subjectPhthalonitrileen_US
dc.subjectAzo dyesen_US
dc.subjectUreaseen_US
dc.subjectAcetylcholinesteraseen_US
dc.subjectEnzyme inhibitionen_US
dc.titleUrease and acetylcholinesterase enzyme inhibitor novel phthalonitrile azo compoundsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i11.68270en_US
Appears in Collections:IJC Vol.61(11) [Nov 2022]

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