Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1613
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dc.contributor.authorKalavadiya, Prakash L.-
dc.contributor.authorKapupara, Vimal H.-
dc.contributor.authorGojiya, Dinesh G.-
dc.contributor.authorBhatta, Tejal D.-
dc.contributor.authorHadiyala, Sanjay D.-
dc.contributor.authorJoshi, Hitendra S.-
dc.date.accessioned2024-11-18T05:59:02Z-
dc.date.available2024-11-18T05:59:02Z-
dc.date.issued2020-
dc.identifier.citationKalavadiya, P. L., Kapupara, V. H., Gojiya, D. G., Bhatt, T. D., Hadiyal, S. D., & Joshi, D. H. S. (2020). Ultrasonic-assisted synthesis of pyrazolo [3, 4-d] pyrimidin-4-ol tethered with 1, 2, 3-triazoles and their anticancer activity. Russian Journal of Bioorganic Chemistry, 46, 803-813.en_US
dc.identifier.issn1068-1620-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/1613-
dc.description.abstractIn the presents work synthesis and characterization of new heterocyclic derivatives containing pyr-azolo[3,4-d]pyrimidine linkage with 1,4-disubstituted-1,2,3-triazoles via methylene-oxy group. The selected synthesized compounds were tested for their in-vitro anticancer activity against various cancer cell lines. Synthesis of compounds was done under ultrasonic-assisted Huisgen 1,3-dipolar cycloaddition reaction with good yields. Some of the newly synthesized compounds demonstrated good to moderate anticancer activity, most of compounds shows activity against renal cancer cell lines.en_US
dc.language.isoenen_US
dc.publisherPleiades Publishing, Ltd. /Russian Journal of Bioorganic Chemistryen_US
dc.relation.ispartofseries;46, 803-813-
dc.subjectpyrazolo[3,4-d]pyrimidin-4-olen_US
dc.subject1,4-disubstituted-1,2,3-triazole derivativesen_US
dc.subjectin-vitro anticancer screeningen_US
dc.subjectultrasonic-assisted mild reaction conditionsen_US
dc.titleUltrasonic-assisted synthesis of pyrazolo [3, 4-d] pyrimidin-4-ol tethered with 1, 2, 3-triazoles and their anticancer activityen_US
dc.typeArticleen_US
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