N L Papp
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Explore the profile of N L Papp including associated specialties, affiliations and a list of published articles.
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8
Citations
31
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Recent Articles
1.
Martin G, Papp N
Pharmacol Biochem Behav
. 1984 Jun;
20(6):893-7.
PMID: 6146989
Previously the ipsiversive turning response elicited by MK-801 in rats with unilateral 6-hydroxydopamine lesions of the substantia nigra has been shown to be reduced by the alpha 1-receptor antagonist, prazosin....
2.
Martin G, Bacino C, Papp N
Peptides
. 1981 Jan;
2(2):213-7.
PMID: 6270636
Methergoline, an antagonist of cerebral serotonin receptors, has been shown to significantly reduce the rise in rectal temperature (Tre) produced by the intracerebral microinjection of beta-endorphin. In this study the...
3.
4.
Martin G, Bacino C, Papp N
Peptides
. 1980 Jan;
1(4):333-9.
PMID: 7301636
Changes in rectal temperature were measured after the intracerebral microinjection of neurotensin (2.5 micrograms/0.5 microliters) at 135 sites in the rat. At 63 of the 135 microinjection sites, the tridecapeptide...
5.
Clineschmidt B, McKENDRY M, Papp N, Pflueger A, Stone C, TOTARO J, et al.
J Pharmacol Exp Ther
. 1979 Mar;
208(3):460-7.
PMID: 34710
(+/-)-CTC, a cyproheptadine derivative, possesses both antidopaminergic and anticholinergic activities which can be resolved, respectively, into its component (-)- and (+)-enantiomers. Both in vivo (antagonism of apomorphine-induced stereotypy, elevation of...
6.
Martin G, Papp N
Pharmacol Biochem Behav
. 1979 Feb;
10(2):313-5.
PMID: 450944
The changes in core temperature (Tc) evoked by morphine in the Sprague-Dawley rate were altered by restraining the rat. The Tc of the free-moving rat rose after the IP (5,...
7.
Martin G, Papp N, Bacino C
Brain Res
. 1978 Oct;
155(2):297-312.
PMID: 567515
Contraversive turning was evoked by the microinjection of GABAergic agents into the substantia nigra (SN) of the rat. Muscimol, the most potent GABA agonist, evoked contralateral turning when injected into...
8.
REMY D, Rittle K, Hunt C, Anderson P, ARISON B, Engelhardt E, et al.
J Med Chem
. 1977 Aug;
20(8):1013-9.
PMID: 19627
The synthesis and resolution of 3-iodocyproheptadine [(+/-)-5a] and 1-cyclopropylmethyl-4-(3-iodo-5H-dibenzo-[a,d]cyclohepten-5-ylidene)piperidine [(+/-)-5b] are described. The resulting atropisomers undergo reaction with trifluoromethylthiocopper to give optically active products without extensive racemization. In this manner,...