{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,29]],"date-time":"2026-07-29T13:05:42Z","timestamp":1785330342529,"version":"3.55.0"},"reference-count":22,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T00:00:00Z","timestamp":1785196800000},"content-version":"vor","delay-in-days":27,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T00:00:00Z","timestamp":1782864000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chemistry &amp; Biodiversity"],"published-print":{"date-parts":[[2026,7]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    A new library of aryl(benzofuran\u20105\u2010yl)\u2010[1,2,4]triazolo[4,3\u2010a]pyridines (\n                    <jats:bold>12a\u2010j<\/jats:bold>\n                    ) has been synthesized, and their chemical structures were confirmed by\n                    <jats:sup>1<\/jats:sup>\n                    H NMR,\n                    <jats:sup>13<\/jats:sup>\n                    C NMR, and mass spectral data. Further, these derivatives were assessed against four human cancer cell lines, including human prostate cancer (PC3), human lung cancer (A549), human breast cancer (MCF\u20107), and human ovarian cancer (A2780) by using the MTT method. Among the tested compounds, five compounds,\n                    <jats:bold>12a\u2010<\/jats:bold>\n                    <jats:bold>12e<\/jats:bold>\n                    , showed the most potent activity. Particularly, one compound,\n                    <jats:bold>12a,<\/jats:bold>\n                    possessed the most promising activity.\n                  <\/jats:p>","DOI":"10.1002\/cbdv.71541","type":"journal-article","created":{"date-parts":[[2026,7,28]],"date-time":"2026-07-28T17:56:48Z","timestamp":1785261408000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Synthesis and Biological Evaluation of Aryl(Benzofuran\u20105\u2010yl)\u2010[1,2,4]Triazolo[4,3\u2010a]Pyridine Derivatives as Anticancer Agents"],"prefix":"10.1002","volume":"23","author":[{"given":"Raju","family":"Veeramalla","sequence":"first","affiliation":[{"name":"Department of Chemistry Anurag University  Hyderabad India"},{"name":"Department of Research and Development Granules India Limited  Hyderabad India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7387-0929","authenticated-orcid":false,"given":"Savita","family":"Belwal","sequence":"additional","affiliation":[{"name":"Department of Chemistry Anurag University  Hyderabad India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4465-042X","authenticated-orcid":false,"given":"Laxminarayana","family":"Eppakayala","sequence":"additional","affiliation":[{"name":"Department of Chemistry Anurag University  Hyderabad India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,7,28]]},"reference":[{"key":"e_1_2_11_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/352760183X"},{"key":"e_1_2_11_3_1","doi-asserted-by":"publisher","DOI":"10.1517\/13543776.2013.801455"},{"key":"e_1_2_11_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bmcl.2010.08.129"},{"key":"e_1_2_11_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0960-894X(02)00380-3"},{"issue":"5","key":"e_1_2_11_6_1","first-page":"417","article-title":"2\u2010Phenylbenzo [b] Furans: Relationship Between Structure, Estrogen Receptor Affinity and Cytostatic Activity Against Mammary Tumor Cells","volume":"6","author":"Erber S.","year":"1991","journal-title":"Anti\u2010Cancer Drug Design"},{"key":"e_1_2_11_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bmc.2013.07.002"},{"key":"e_1_2_11_8_1","doi-asserted-by":"publisher","DOI":"10.1248\/cpb.60.110"},{"key":"e_1_2_11_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmech.2005.07.004"},{"key":"e_1_2_11_10_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-2006-961473"},{"key":"e_1_2_11_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmech.2014.10.044"},{"key":"e_1_2_11_12_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.tetlet.2014.02.116"},{"key":"e_1_2_11_13_1","doi-asserted-by":"publisher","DOI":"10.1021\/np9904861"},{"key":"e_1_2_11_14_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11154-007-9039-z"},{"key":"e_1_2_11_15_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bmcl.2005.02.052"},{"key":"e_1_2_11_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0040-4039(00)02163-8"},{"key":"e_1_2_11_17_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ceb.2004.09.014"},{"key":"e_1_2_11_18_1","doi-asserted-by":"publisher","DOI":"10.1002\/jhet.966"},{"key":"e_1_2_11_19_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bmcl.2009.04.024"},{"key":"e_1_2_11_20_1","doi-asserted-by":"publisher","DOI":"10.1002\/jhet.5570320155"},{"key":"e_1_2_11_21_1","doi-asserted-by":"publisher","DOI":"10.1186\/s13588-014-0014-x"},{"key":"e_1_2_11_22_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.rechem.2023.101248"},{"key":"e_1_2_11_23_1","doi-asserted-by":"publisher","DOI":"10.1002\/cmdc.202100446"}],"container-title":["Chemistry &amp; 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