Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Christine N. Hinko"'
Autor:
Jonathan R. Dimmock, Christine N. Hinko, Puthucode Ramanan Narayan, James P. Stables, Glen B. Baker, John M. Tuchek, Caren L. Steinmiller
Publikováno v:
Drug Development Research. 46:112-125
A series of aryloxyaryl semicarbazones had been shown previously to possess significant anticonvulsant activity in the maximal electroshock screen in both rats and mice as well as in the subcutaneous pentylenetetrazol test in mice. One member of this
Autor:
David S. Roane, Bin Ho, Prabha Venkatarangan, A. M. Crider, Ahmad A. Adloo, Sharon F. Cruse, Christine N. Hinko, James P. Stables, Peter H. Andersen
Publikováno v:
European Journal of Medicinal Chemistry. 33:23-31
A variety of 2-piperidinecarboxamides were synthesized and evaluated for anticonvulsant activity using the MES and sc PTZ tests in mice and rats. Neurotoxicity was determined by the rotorod test. Several N-(benzyl)-2-piperidinecarboxamides exhibited
Autor:
M. Ciechanowicz-Rutkowska, P. Serda, Afif A. El-Assadi, Vida A. Farrar, J. Grochowski, G. Filippini, Jacqueline A. Moore, T. Pilati, Christine N. Hinko
Publikováno v:
Journal of Medicinal Chemistry. 36:3517-3525
Continuing structure-activity studies on the anticonvulsant activity of analogs of N-(benzyloxy)-2-azaspiro[4.4]nonane-1,3-dione (2a), which displayed anti-electroshock seizure (MES) activity and a protective index (TD50/ED50) of > 4.5 are reported.
Autor:
K. R. Scott, Vida A. Farrar, Christine N. Hinko, Hyejung Chang, Jacqueline A. Moore, Elizabeth I. Tietz, Jesse M. Nicholson, Ivan O. Edafiogho, Erica L. Richardson, Afif A. El-Assadi
Publikováno v:
Journal of Medicinal Chemistry. 36:1947-1955
This report continues the in-depth evaluation of methyl 4-[(p-chlorophenyl)amino]-6-methyl-2-oxocyclohex-3-en-1-oate , 1 (ADD 196022), and methyl 4-(benzylamino)-6-methyl-2-oxocyclohex-3-en-1-oate, 2, two potent anticonvulsant enaminones. These compo
Autor:
K. R. Scott, Hyejung Chang, Ivan O. Edafiogho, Dianna Mulzac, Jesse M. Nicholson, Christine N. Hinko, Jacqueline A. Moore
Publikováno v:
ChemInform. 23
A new series of novel enaminones has been synthesized from cyclic beta-dicarbonyl precursors which were condensed with morpholine, pyrrolidine, phenethylamine, hydrazines, substituted benzyl amines, and substituted anilines. These compounds were subs
Autor:
Sharon F. Cruse, Ahmad A. Adloo, James P. Stables, Christine N. Hinko, David S. Roane, Peter H. Andersen, Prabha Venkatarangan, Bin Ho, A. M. Crider
Publikováno v:
ChemInform. 29
A variety of 2-piperidinecarboxamides were synthesized and evaluated for anticonvulsant activity using the MES and sc PTZ tests in mice and rats. Neurotoxicity was determined by the rotorod test. Several N-(benzyl)-2-piperidinecarboxamides exhibited
Autor:
M.A. Kliem, Bin Ho, H. Klitgaard, Christine N. Hinko, C.M. Burns, C.L. Steinmiller, Afif A. El-Assadi, A. M. Crider, P. Venkatarangan, Peter H. Andersen, T.H. Seo, Hyejung Chang, Elizabeth I. Tietz
Publikováno v:
Neuropharmacology. 35(12)
The relative ability of derivatives of 2-piperidinecarboxylic acid (2-PC; pipecolic acid) and 3-piperidinecarboxylic acid (3-PC; nipecotic acid) to block maximal electroshock (MES)-induced seizures, elevate the threshold for electroshock-induced seiz
Autor:
Jesse M. Nicholson, Christine N. Hinko, Hyejung Chang, K. R. Scott, Dianna Mulzac, Jacqueline A. Moore, Ivan O. Edafiogho
Publikováno v:
Journal of medicinal chemistry. 35(15)
A new series of novel enaminones has been synthesized from cyclic beta-dicarbonyl precursors which were condensed with morpholine, pyrrolidine, phenethylamine, hydrazines, substituted benzyl amines, and substituted anilines. These compounds were subs
Autor:
Charmaine Rozanov, Christine N. Hinko
Publikováno v:
European journal of pharmacology. 182(2)
Ethanol's intoxicating effects may result from ethanol-induced changes in central gamma-aminobutyric acid (GABA) mechanisms. To further test this hypothesis, mice were pretreated with bicuculline (1 mg/kg s.c.), aminooxyacetic acid (15, 20, 25 or 30
Publikováno v:
Neuropharmacology. 23:1009-1014
The nipecotic acid ester, (±)-m-nitrophenyl-3-piperidinecarboxylate hydrochloride (MNPC) is a potent inhibitor of uptake of GABA in vitro and should be able to penetrate into the brain much more readily than the parent compound nipecotic acid. A stu