1 Ocak 2017 Dergi makalesi Açık Erişim

Yilmaz, Hasibe; Carikci, Sema; Kilic, Turgut; Dirmenci, Tuncay; Arabaci, Turan; Goren, Ahmet C.

DataCite XML

<?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/90191</identifier>
  <creators>
    <creator>
      <creatorName>Yilmaz, Hasibe</creatorName>
      <givenName>Hasibe</givenName>
      <familyName>Yilmaz</familyName>
      <affiliation>TUBITAK Natl Metrol Inst UME, Dept Chem, Gebze, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Carikci, Sema</creatorName>
      <givenName>Sema</givenName>
      <familyName>Carikci</familyName>
      <affiliation>Balikesir Univ, Fac Sci &amp; Arts, Dept Chem, Campus Cagis, Balikesir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Kilic, Turgut</creatorName>
      <givenName>Turgut</givenName>
      <familyName>Kilic</familyName>
      <affiliation>Balikesir Univ, Necatibey Educ Fac, Dept Sci Educ, Balikesir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Dirmenci, Tuncay</creatorName>
      <givenName>Tuncay</givenName>
      <familyName>Dirmenci</familyName>
      <affiliation>Balikesir Univ, Necatibey Educ Fac, Dept Biol Educ, Balikesir, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Arabaci, Turan</creatorName>
      <givenName>Turan</givenName>
      <familyName>Arabaci</familyName>
      <affiliation>Inonu Univ, Dept Pharmaceut Bot, Fac Pharm, Malatya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Goren, Ahmet C.</creatorName>
      <givenName>Ahmet C.</givenName>
      <familyName>Goren</familyName>
      <affiliation>TUBITAK Natl Metrol Inst UME, Dept Chem, Gebze, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Screening Of Chemical Composition, Antioxidant And Anticholinesterase Activity Of Section Brevifilamentum Of Origanum (L.) Species</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2017</publicationYear>
  <dates>
    <date dateType="Issued">2017-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/90191</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.25135/acg.rnp.56.17.04.029</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">Six Origanum species, Origanum acutidens (Hand. -Mazz.) Ietsw. (OA), Origanum brevidens (Bornm.) Dinsm. (OB), Origanum haussknechtii Boiss. (OC), Origanum husnucan-baseri H. Duman, Aytac &amp;amp; A. Duran (OHB), Origanum leptocladum Boiss. (OL), Origanum rotundifolium Boiss. (OR), belonging to sect. Brevifilamentum were analyzed for their essential oil and phenolic components. For the essential oil analyses, GC-MS and GC-FID were used. Phenolic contents of the aerial parts of the chloroform, acetone, and methanol extracts were analyzed using LC-MS/MS. Antioxidant activity of the species was investigated by three methods; DPPH free radical scavenging activity, beta-carotene linoleic acid assays and CUPRAC assays. Also, acetyl and butyrylcholinesterase inhibition of the extracts were investigated. While the essential oil contents of the section Brevifilamentum showed difference in chemotype, the phenolic contents were found to be coumaric acids and derivatives. These groups were the most abundant components of the extracts. Especially rosmarinic acid was detected in high amounts in acetone and methanol extracts. OA had the best activity both in antioxidant and anticholinesterase assays.</description>
  </descriptions>
</resource>