View Item 
      •   UMY Repository
      • 03. DISSERTATIONS AND THESIS
      • Students
      • Undergraduate Thesis
      • Faculty of Medicine and Health Science
      • Department of Pharmacy
      • View Item
      •   UMY Repository
      • 03. DISSERTATIONS AND THESIS
      • Students
      • Undergraduate Thesis
      • Faculty of Medicine and Health Science
      • Department of Pharmacy
      • View Item
      JavaScript is disabled for your browser. Some features of this site may not work without it.

      UJI AKTIVITAS ANTAGONISME ETIL P-METOKSISINAMAT SENYAWAAKTIF KENCUR (Kaempferia galanga L) TERHADAP RESEPTOR ASETILKOLIN MUSKARINIK 3 PADA ORGAN ILEUM Cavia porcellus TERISOLASI: STUDI IN VITRO DAN IN SILICO

      Thumbnail
      View/Open
      COVER (109.9Kb)
      HALAMAN JUDUL (404.9Kb)
      HALAMAN PENGESAHAN (460.4Kb)
      ABSTRAK (103.2Kb)
      BAB I (257.9Kb)
      BAB II (258.4Kb)
      BAB III (320.6Kb)
      BAB IV (693.9Kb)
      BAB V (91.39Kb)
      DAFTAR PUSTAKA (237.2Kb)
      LAMPIRAN (993.9Kb)
      NASKAH PUBLIKASI (573.7Kb)
      Date
      2019-12-10
      Author
      PAMBUDI, CATUR AGENG
      Metadata
      Show full item record
      Abstract
      Etil p-metoxycynamate (EPMC) is the second largest compound in Kaempferia galanga L. It contains about 31,36% of the EPMC. EPMC has been reported to have anti-diarrhea and anti-inflammatory effects. The purpose of this research is the use of EPMC as an antagonism by inhibiting a muscarinic acetylcholine 3 receptor (Ach M3) which causes smooth muscle contraction at ileum. Maceration is used to obtain an EPMC extract from Kaempferia galanga L. EPMC are identified using Thin Layer Chromatography with the motion phase toluene ethyl : acetate (19:1). The activity of ileum antagonism against acetylcholine test using ileum of hamster isolated in vitro with a dose of EPMC 100 μM and 200 μM. The results obtained will be processed into the value of pD2 and analyzed statistically using One Way ANOVA and carried out to LSD test using trusted level 95%. The AutoDock device is used as a test In Silico against the Ach M3 receptor. Final results showed that EPMC 100 μM and 200 μM were able to inject the Ach M3 indicated by shifting barriers of hamster ileum contraction curves against the acetylcholine agonist. The pD2 value displayed EPMC 100 μM is 7,1 and 200 μM is 6,98 shifted significantly (p<0,5) against pD2 acetylcholine agonists is 8,16. The value of affinity shows the number -5,2.
      URI
      http://repository.umy.ac.id/handle/123456789/32618
      Collections
      • Department of Pharmacy

      DSpace software copyright © 2002-2015  DuraSpace
      Contact Us | Send Feedback
      Theme by 
      @mire NV
       

       

      Browse

      All of UMY RepositoryCollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

      My Account

      Login

      DSpace software copyright © 2002-2015  DuraSpace
      Contact Us | Send Feedback
      Theme by 
      @mire NV