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Senkuytu, Elif; Davarci, Derya; Olcer, Zehra; Ciftci, Gonul Yenilmez
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/109994</identifier> <creators> <creator> <creatorName>Senkuytu, Elif</creatorName> <givenName>Elif</givenName> <familyName>Senkuytu</familyName> </creator> <creator> <creatorName>Davarci, Derya</creatorName> <givenName>Derya</givenName> <familyName>Davarci</familyName> <affiliation>Gebze Tech Univ, Dept Chem, TR-41400 Kocaeli, Turkey</affiliation> </creator> <creator> <creatorName>Olcer, Zehra</creatorName> <givenName>Zehra</givenName> <familyName>Olcer</familyName> <affiliation>Gebze Tech Univ, Dept Chem, TR-41400 Kocaeli, Turkey</affiliation> </creator> <creator> <creatorName>Ciftci, Gonul Yenilmez</creatorName> <givenName>Gonul Yenilmez</givenName> <familyName>Ciftci</familyName> <affiliation>Gebze Tech Univ, Dept Chem, TR-41400 Kocaeli, Turkey</affiliation> </creator> </creators> <titles> <title>Dna Interaction Analysis With Automated Biosensor Of Paraben Derivative S-Triazines</title> </titles> <publisher>Aperta</publisher> <publicationYear>2020</publicationYear> <dates> <date dateType="Issued">2020-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/109994</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.molstruc.2020.128925</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract">Among all heterocyclic compounds, the triazine scaffold has an important place due to its wide range of biological activities. Triazine has been preferred by many researchers as the target structure for the design and development of new drugs, as it is found in many biologically active molecules with promising biological potential such as anti-inflammatory, anti-mycobacterial, anti-viral, anti-cancer properties. In this study, a series of paraben substituted s-triazine compounds 1-5 were synthesized and their structures were determined by H-1 and C-13 NMR spectroscopies as well as mass spectrometry. Also, structure of compound 5 was adjusted by X-ray crystallographic technique and crystallographic analysis revealed that 5 was crystallized in the trigonal space group R-3. According to X-ray analysis, compound 5 has very important intermolecular interaction such as nonclassical H-bond and pi-pi interaction. These interactions lead formation of supramolecular network. The thermal stabilities were investigated by thermogravimetric analysis. According to thermogravimetric analysis results, all of the synthesized compounds have high thermal stability. DNA interaction studies of the compounds 1-5 were performed with an automatic biosensor device that can measure the efficiency of DNA hybridization on the biochip surface. The biosensor results show that benzyl paraben substituted s-triazine compound 5, the most reactive compound at low concentration, was showed 61% and 75% activity reduction at concentrations 12.5 and 25 mu M. (C) 2020 Elsevier B.V. All rights reserved.</description> </descriptions> </resource>
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