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MDL 72145

Known as: MDL-72145 
 
National Institutes of Health

Papers overview

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2004
2004
Summary1.The pharmacological properties of two selective inhibitors of monoamine oxidase (MAO) type B,l-deprenyl and MDL 72145… Expand
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Highly Cited
1999
Highly Cited
1999
The endogenous substrate(s) and physiological function(s) of semicarbazide-sensitive amine oxidase (SSAO), a group of enzymes… Expand
1996
1996
Tianeptine is a substance enhancing the serotonir uptake while sertraline and clomipramine inhibit it. By means of 5-hydroxyin… Expand
1989
1989
Abstract— One hour after MDL 72145 ((E)‐2‐(3′,4′‐dimethoxyphenyl)‐3‐fluoroallylamine) (2·5 mg kg−1) was given by intraperitoneal… Expand
1989
1989
1 The pressor response to the infusion of tyramine (Tyr) into the isolated perfused mesenteric arterial bed of the rat has been… Expand
1988
1988
1. Selective inhibitors of the monoamine oxidase (MAO) isoenzymes, types A and B, are of potential therapeutic utility. Brain… Expand
Highly Cited
1987
Highly Cited
1987
1-Methyl-4-(2'-methylphenyl)-1,2,3,6-tetrahydropyridine (2'CH3-MPTP) was shown previously to be a more potent neurotoxicant than… Expand
1986
1986
Pretreatment of mice with the potent and selective monoamine oxidase B (MAO-B) inhibitor MDL 72145 ((E)-2-(3',4'-dimethoxyphenyl… Expand
1986
1986
Albino mice and pigmented mice were treated for 6 days with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) at the maximum… Expand
1985
1985
(E)‐2‐(3, 4‐dimethoxyphenyl)‐3‐fluoroallylamine (MDL 72145) was found to be an extremely potent inhibitor of the semicarbazide… Expand