نتایج جستجو برای: N-Methyl-3,4-methylenedioxyamphetamine
تعداد نتایج: 1151220 فیلتر نتایج به سال:
Determining the structural elements that define substrates and inhibitors at the monoamine transporters is critical to elucidating the mechanisms underlying these disparate functions. In this study, we addressed this question directly by generating a series of N-substituted 3,4-methylenedioxyamphetamine analogs that differ only in the number of methyl substituents on the terminal amine group. S...
تعدادی از کمپلکس های باز شیف محلول در آب n,n?-bis{5[(triphenylphosphoniumchloride)-methyl]salicylidine}-4-methyl-o-phenylenediamine]copper(??) ([cu(5-ch2pph3-4-methyl-1,2-salophen)](clo4)2), n,n?-bis{5-[(triphenylphosphoniumchloride)-methyl]salicylidine}-4-methyl-o-phenylenediamine]nickel(??) ([ni(5-ch2pph3-4-methyl-1,2-salophen)](clo4)2), و کمپلکس های نانو باز شیف محلول در آب n,n?-bis{5...
The human cytochrome P450 (CYP) isozymes catalyzing the oxidative metabolism of the widely abused amphetamine derivatives MDMA (N-methyl-3,4-methylenedioxyamphetamine, "Ecstasy"), MDE (N-ethyl-3, 4-methylenedioxyamphetamine, "Eve"), and MDA (3, 4-methylenedioxyamphetamine) were identified. Using a simplified non-extractive reversed-phase HPLC assay with fluorescence detection, biphasic Michaeli...
چکیده: خواص مولکولی 5کمپلکسni(ii) شیف باز که شامل کره کئوردیناسیون nnos: methyl-2-{n-[2-(acetone)triflourolidynenitrilo]ethyl}amino-1-yclopentenedithi-ocarboxylate l1= methyl-2-{n-[2-(acetone)ethylidyneni-trilo]ethyl}amino-1-lopentenedithi-ocarboxylate l2= methyl-2-{n-[2-(acetone)phenylidy-nenitrilo]ethyl}amino-1-cyclopentenedithi-ocarboxylate l3= methyl-2-{[1-methyl-2-(ace-tone)ethylid...
The selective serotonergic neurotoxicity of 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) depends on their systemic metabolism. We have recently shown that inhibition of brain endothelial cell gamma-glutamyl transpeptidase (gamma-GT) potentiates the neurotoxicity of both MDMA and MDA, indicating that metabolites that are substrates for this enzyme con...
Drug interaction with P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) may influence its tissue disposition including blood-brain barrier transport and result in potent drug-drug interactions. The limited data obtained using in-vitro models indicate that methadone, buprenorphine, and cannabinoids may interact with human P-gp; but almost nothing is known about drugs of abuse and...
Driving under the influence of drugs is an issue of growing concern in the industrialized countries as a risk and a cause for road accidents. In forensic toxicology, the increasing number of samples for determination of drugs in blood is mainly due to zero-tolerance laws in several countries and well-trained police officers who can better recognize drivers under the influence of drugs of abuse....
Biochemical, pharmacological, and toxic effects of n-metil 3,4-methylenedioxyamphetamine - "ecstasy"
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