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TL 99

Known as: TL-99 
 
National Institutes of Health

Papers overview

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Highly Cited
1987
Highly Cited
1987
Abstract: Synaptosomes prepared from rat cerebral cortex and labeled with [3H]noradrenaline (NA) were superfused with calcium… Expand
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1984
1984
Dopaminergic agonists, apomorphine (APO) (0.025-0.25 mg/kg, s.c.), TL-99 (0.5-3 mg/kg, s.c.) and 3-PPP (0.15-10 mg/kg, s.c… Expand
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Highly Cited
1984
Highly Cited
1984
: A significant advance in the field of neurotransmission was made with the discovery of presynaptic release-modulating alpha… Expand
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Highly Cited
1984
Highly Cited
1984
The efficacy of several drugs to elicit yawning and penile erections were determined in rats. The dopamine agonists, N… Expand
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Highly Cited
1983
Highly Cited
1983
The specific D2 receptor agonist, LY 141865, but not the specific D1-receptor agonist, SK&F 38393, potently inhibited… Expand
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1982
1982
The claim that the 2-aminotetralin analogue TL-99 is a selective presynaptic dopamine (DA) receptor agonist has been investigated… Expand
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1982
1982
The putative dopamine autoreceptor agonists, 3-PPP and TL-99 were examined for their ability to stimulate postsynaptic dopamine… Expand
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Highly Cited
1981
Highly Cited
1981
The putative dopamine (DA) autoreceptor agonists, N-n-propyl-3-(3-hydroxyphenyl)-piperidine (3-PPP) and 6, 7-dihydroxy-2… Expand
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Highly Cited
1980
Highly Cited
1980
A new dopamine analog, 6,7-dihydroxy-2-dimethylaminotetralin (TL-99), was compared to apomorphine in three tests of dopaminergic… Expand
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1978
1978
6,7-Dihydroxy-2-dimethylaminotetralin (TL-99), the 5,6-dihydroxy isomer (M-7) and dopamine were studied for cardiovascular… Expand
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