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Synthesis of C3, C5, and C7 pregnane derivatives and their effect on NMDA receptor responses in cultured rat hippocampal neurons
E. Šťastná, H. Chodounská, V. Pouzar, V. Kapras, J. Borovská, O. Cais, L. Vyklický, jr.
Jazyk angličtina Země Spojené státy americké
- MeSH
- elektrická vodivost MeSH
- financování organizované MeSH
- hipokampus cytologie MeSH
- inhibiční koncentrace 50 MeSH
- krysa rodu rattus MeSH
- kultivované buňky MeSH
- metoda terčíkového zámku MeSH
- neurony metabolismus účinky léků MeSH
- pregnany farmakologie chemická syntéza chemie MeSH
- receptory N-methyl-D-aspartátu antagonisté a inhibitory MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
The synthesis of several novel 5alpha- and 5beta-20-oxo-pregnane derivatives substituted in the position 3 and 7 of the steroid skeleton is described. Activity of synthesized compounds was studied in voltage-clamped cultured rat hippocampal neurons. Substituted derivatives inhibited NMDA-elicited neuronal activity. The relationship between biological activity and structure is discussed.
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- $a Šťastná, Eva $7 xx0068402
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- $a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, v.v.i.,166 10 Prague 6, Czech Republic.
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- $a The synthesis of several novel 5alpha- and 5beta-20-oxo-pregnane derivatives substituted in the position 3 and 7 of the steroid skeleton is described. Activity of synthesized compounds was studied in voltage-clamped cultured rat hippocampal neurons. Substituted derivatives inhibited NMDA-elicited neuronal activity. The relationship between biological activity and structure is discussed.
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- $a 2011-2B09/jvme