{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T21:25:27Z","timestamp":1768425927360,"version":"3.49.0"},"reference-count":21,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2021,2,1]],"date-time":"2021-02-01T00:00:00Z","timestamp":1612137600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,2,1]],"date-time":"2021-02-01T00:00:00Z","timestamp":1612137600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100009007","name":"Guangxi Normal University","doi-asserted-by":"publisher","award":["CMEMR2018-B13"],"award-info":[{"award-number":["CMEMR2018-B13"]}],"id":[{"id":"10.13039\/501100009007","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100012246","name":"Priority Academic Program Development of Jiangsu Higher Education Institutions","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100012246","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100010023","name":"Natural Science Research of Jiangsu Higher Education Institutions of China","doi-asserted-by":"publisher","award":["18KJA150006"],"award-info":[{"award-number":["18KJA150006"]}],"id":[{"id":"10.13039\/501100010023","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy"],"published-print":{"date-parts":[[2021,2]]},"DOI":"10.1016\/j.saa.2020.118944","type":"journal-article","created":{"date-parts":[[2020,9,15]],"date-time":"2020-09-15T02:46:35Z","timestamp":1600137995000},"page":"118944","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":15,"special_numbering":"C","title":["Discovery of novel dehydroabietic acid derivatives as DNA\/BSA binding and anticancer agents"],"prefix":"10.1016","volume":"246","author":[{"given":"Lin-Ying","family":"Li","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bao-Li","family":"Fei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pingping","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ling-Yan","family":"Kong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jian-Ying","family":"Long","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.saa.2020.118944_bb0005","doi-asserted-by":"crossref","first-page":"15646","DOI":"10.1039\/C9DT01942A","article-title":"Biological evaluation of optically pure chiral binuclear copper(II) complexes based on a rosin derivative as highly potential anticancer agents","volume":"48","author":"Fei","year":"2019","journal-title":"Dalton Trans."},{"key":"10.1016\/j.saa.2020.118944_bb0010","doi-asserted-by":"crossref","first-page":"2004","DOI":"10.1021\/acs.jafc.8b06985","article-title":"Rheological behavior of environmentally friendly viscoelastic solutions formed by a rosin-based anionic surfactant","volume":"67","author":"Chen","year":"2019","journal-title":"J. Agric. Food Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0015","doi-asserted-by":"crossref","first-page":"4144","DOI":"10.1021\/acs.jafc.0c00562","article-title":"Antifungal application of rosin derivatives from renewable pine resin in crop protection","volume":"68","author":"Tao","year":"2020","journal-title":"J. Agric. Food Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0020","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/j.ejmech.2019.05.030","article-title":"Optically pure chiral copper(II) complexes of rosin derivative as attractive anticancer agents with potential anti-metastatic and anti-angiogenic activities","volume":"176","author":"Fei","year":"2019","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0025","doi-asserted-by":"crossref","first-page":"2263","DOI":"10.4155\/fmc-2016-0153","article-title":"A survey of the mechanisms of action of anticancer transition metal complexes","volume":"8","author":"Marloye","year":"2016","journal-title":"Future Med. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0030","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/j.ejmech.2016.09.023","article-title":"Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities","volume":"125","author":"Akhtar","year":"2017","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0035","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1039\/C4MB00548A","article-title":"Elucidating the interaction of lLimonene with bovine serum albumin: a multi-technique approach","volume":"11","author":"Chaturvedi","year":"2015","journal-title":"Mol. BioSyst."},{"key":"10.1016\/j.saa.2020.118944_bb0040","doi-asserted-by":"crossref","first-page":"109030","DOI":"10.1016\/j.cbi.2020.109030","article-title":"DNA-binding and DNA-protecting activities of small natural organic molecules and food extracts","volume":"323","author":"Sjakste","year":"2020","journal-title":"Chem. Biol. Interact."},{"key":"10.1016\/j.saa.2020.118944_bb0045","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1016\/j.jorganchem.2019.02.021","article-title":"Synthesis, characterization and antitumor activity of (E)-2-methyl-3-ferrocenyl-N-acrylamide derivatives","volume":"887","author":"Liu","year":"2019","journal-title":"J. Organomet. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0050","doi-asserted-by":"crossref","first-page":"5919","DOI":"10.1002\/ejic.201300685","article-title":"Synthesis, crystal structure, DNA binding, antibacterial, and cytotoxic activities of two chiral cCopper(II) complexes","volume":"34","author":"Fei","year":"2013","journal-title":"Eur. J. Inorg. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0055","doi-asserted-by":"crossref","first-page":"3370","DOI":"10.1016\/j.bmcl.2017.06.004","article-title":"Synthesis and biological evaluation of 5-fatty-acylamido-1,3, 4-thiadiazole-2-thioglycosides","volume":"27","author":"Vudhgiri","year":"2017","journal-title":"Bioorg. Med. Chem. Lett."},{"key":"10.1016\/j.saa.2020.118944_bb0060","doi-asserted-by":"crossref","first-page":"907","DOI":"10.1172\/JCI103873","article-title":"Studies of the uricogenic effect of 2-substituted thiadiazoles in man","volume":"38","author":"Krakoff","year":"1959","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.saa.2020.118944_bb0065","doi-asserted-by":"crossref","first-page":"4189","DOI":"10.1021\/jm2015809","article-title":"Analogues of fenarimol are potent inhibitors of trypanosoma cruzi and are efficacious in a murine model of chagas disease","volume":"55","author":"Keenan","year":"2012","journal-title":"J. Med. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0070","doi-asserted-by":"crossref","first-page":"6691","DOI":"10.1021\/jo901236d","article-title":"Mechanistic insights on the magnesium(II) ion-activated reduction of methyl benzoylformate with chelated NADH peptide beta-lactam models","volume":"74","author":"Aizpurua","year":"2009","journal-title":"J. Org. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0075","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1016\/j.jphotobiol.2014.01.018","article-title":"Effects of copper ions on DNA binding and cytotoxic activity of a chiral salicylidene Schiff base","volume":"132","author":"Fei","year":"2014","journal-title":"J. Photochem. Photobiol. B"},{"key":"10.1016\/j.saa.2020.118944_bb0080","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1007\/s00775-017-1505-9","article-title":"DNA and HSA interaction of vanadium (IV), copper (II), and zinc (II) complexes derived from an asymmetric bidentate Schiff-base ligand: multi spectroscopic, viscosity measurements, molecular docking, and ONIOM studies","volume":"23","author":"Dehkhodaei","year":"2018","journal-title":"J. Biol. Inorg. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0085","doi-asserted-by":"crossref","first-page":"9452","DOI":"10.1021\/acs.inorgchem.9b01298","article-title":"Diastereomeric crowding effects in the competitive DNA intercalation of Ru(phenanthroline)2dipyridophenazine2+ enantiomers","volume":"58","author":"Martensson","year":"2019","journal-title":"Inorg. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0090","doi-asserted-by":"crossref","first-page":"117525","DOI":"10.1016\/j.saa.2019.117525","article-title":"Study on the interactions between B-norcholesteryl benzimidazole compounds with ct-DNA","volume":"227","author":"Gan","year":"2020","journal-title":"Spectrochim. Acta A"},{"key":"10.1016\/j.saa.2020.118944_bb0095","doi-asserted-by":"crossref","first-page":"111592","DOI":"10.1016\/j.ejmech.2019.111592","article-title":"Novel 4-quinoline-thiosemicarbazone derivatives: synthesis, antiproliferative activity, in vitro and in silico biomacromolecule interaction studies and topoisomerase inhibition","volume":"182","author":"Ribeiro","year":"2019","journal-title":"Eur. J. Med. Chem."},{"key":"10.1016\/j.saa.2020.118944_bb0100","doi-asserted-by":"crossref","DOI":"10.1016\/j.jinorgbio.2019.110823","article-title":"New sulfonamide complexes with essential metal ions [Cu(II), Co(II), Ni(II) and Zn(II)]. Effect of the geometry and the metal ion on DNA binding and nuclease activity. BSA protein interaction","volume":"202","author":"Topala","year":"2020","journal-title":"J. Inorg. Biochem."},{"key":"10.1016\/j.saa.2020.118944_bb0105","doi-asserted-by":"crossref","first-page":"795","DOI":"10.1080\/07391102.2017.1298470","article-title":"Multi-spectroscopic and molecular modelling approach to investigate the interaction of riboflavin with human serum albumin","volume":"36","author":"Alam","year":"2018","journal-title":"J. Biomol. Struct. Dyn."}],"container-title":["Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1386142520309239?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1386142520309239?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,25]],"date-time":"2025-10-25T01:29:58Z","timestamp":1761355798000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1386142520309239"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,2]]},"references-count":21,"alternative-id":["S1386142520309239"],"URL":"https:\/\/doi.org\/10.1016\/j.saa.2020.118944","relation":{},"ISSN":["1386-1425"],"issn-type":[{"value":"1386-1425","type":"print"}],"subject":[],"published":{"date-parts":[[2021,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Discovery of novel dehydroabietic acid derivatives as DNA\/BSA binding and anticancer agents","name":"articletitle","label":"Article Title"},{"value":"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.saa.2020.118944","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Published by Elsevier B.V.","name":"copyright","label":"Copyright"}],"article-number":"118944"}}