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Mematine HCI and amino-alkyl-cyclohexanes (621,625) inhibit HSV-1 in SK-N-SH neuronal cells /

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dc.contributor.author Caplinger, John N. en_US
dc.contributor.author Youngstown State University. Dept. of Chemistry. en_US
dc.date.accessioned 2011-01-31T14:17:33Z
dc.date.accessioned 2019-09-08T02:29:17Z
dc.date.available 2011-01-31T14:17:33Z
dc.date.available 2019-09-08T02:29:17Z
dc.date.created 2001 en_US
dc.date.issued 2001 en_US
dc.identifier 47280342 en_US
dc.identifier.other b18796874 en_US
dc.identifier.uri http://jupiter.ysu.edu/record=b1879687 en_US
dc.identifier.uri http://hdl.handle.net/1989/6156
dc.description viii, 66 leaves : ill. ; 29 cm. en_US
dc.description Thesis (M.S.)--Youngstown State University, 2001. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract Memantine HCI and a series of amino-alkyl-cyclohexanes (AAC) are NMDA receptor antagonists in neuronal cells. Memantine is structurally similar to amantadine and tromantadine, both of which show anti-HSV properties. The activity of memantine and several other AAC's was evaluated by plaque reduction assay of HSV-l KOS in SKN- SH transformed neuronal cells. Memantine and two of the AAC's (621,625) inhibited the formation of plaques in SK-N-SH. Memantine showed a 85 % decrease in plaque formation at 0.03 mM and an ill 50 of 0.023 mM (Figure 2.1a), compound 621 showed a 100% decrease in plaque formation at 0.05 mM and an ill 50 of 0.008 mM (Figure 2.1b), and compound 625 showed a 70% decrease in plaque formation at 0.55 mM and an ill 50 of 0.120 mM (Figure 2.1c). en_US
dc.description.statementofresponsibility by John N. Caplinger. en_US
dc.language.iso en_US en_US
dc.relation.ispartofseries Master's Theses no. 0708 en_US
dc.subject.classification Master's Theses no. 0708 en_US
dc.subject.lcsh Herpes simplex virus. en_US
dc.subject.lcsh Neurons. en_US
dc.title Mematine HCI and amino-alkyl-cyclohexanes (621,625) inhibit HSV-1 in SK-N-SH neuronal cells / en_US
dc.type Thesis en_US


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