54 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Discovery of 1,3-diethyl-7-methyl-8-(phenoxymethyl)-xanthine derivatives as novel adenosine A
North-West University
2-Benzylidene-1-indanone derivatives as inhibitors of monoamine oxidase.
North-West University
Triazolylthioacetamide: A Valid Scaffold for the Development of New Delhi Metallo-ß-Lactmase-1 (NDM-1) Inhibitors.
North-West University
Carbamate substituted 2-amino-4,6-diphenylpyrimidines as adenosine receptor antagonists.
North-West University
Monoamine oxidase inhibitory activities of heterocyclic chalcones.
North-West University
1,3,7-Triethyl-substituted xanthines--possess nanomolar affinity for the adenosine A1 receptor.
North-West University
Amino Acid Thioester Derivatives: A Highly Promising Scaffold for the Development of Metallo-ß-lactamase L1 Inhibitors.
North-West University
Azolylthioacetamide: A Highly Promising Scaffold for the Development of Metallo-ß-lactamase Inhibitors.
North-West University
The synthesis and evaluation of sesamol and benzodioxane derivatives as inhibitors of monoamine oxidase.
North-West University
Synthesis and evaluation of several oleanolic acid glycoconjugates as protein tyrosine phosphatase 1B inhibitors.
North-West University
Synthesis and biological evaluation of oleanolic acid derivatives as PTP1B inhibitors.
North-West University
Inhibition of monoamine oxidase by 8-phenoxymethylcaffeine derivatives.
North-West University
Inhibition of monoamine oxidase by 8-[(phenylethyl)sulfanyl]caffeine analogues.
North-West University
Sulfanylphthalonitrile analogues as selective and potent inhibitors of monoamine oxidase B.
North-West University
Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B.
North-West University
Inhibition of monoamine oxidase by selected C6-substituted chromone derivatives.
North-West University
Synthesis, characterization and activity of new phosphonate dipeptides as potential inhibitors of VanX.
North-West University
Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase.
North-West University
Inhibition of monoamine oxidase by C5-substituted phthalimide analogues.
North-West University
8-Aryl- and alkyloxycaffeine analogues as inhibitors of monoamine oxidase.
North-West University
Synthesis and evaluation of fluorescent heterocyclic aminoadamantanes as multifunctional neuroprotective agents.
North-West University
Inhibition of monoamine oxidase by selected C5- and C6-substituted isatin analogues.
North-West University
Inhibition of monoamine oxidase by indole and benzofuran derivatives.
North-West University
Synthesis and in vitro evaluation of pteridine analogues as monoamine oxidase B and nitric oxide synthase inhibitors.
North-West University
Dual inhibition of monoamine oxidase B and antagonism of the adenosine A(2A) receptor by (E,E)-8-(4-phenylbutadien-1-yl)caffeine analogues.
North-West University
The inhibition of monoamine oxidase by 2H-1,4-benzothiazin-3(4H)-ones.
North-West University
The evaluation of N-propargylamine-2-aminotetralin as an inhibitor of monoamine oxidase.
North-West University
Phenothiazine, anthraquinone and related tricyclic derivatives as inhibitors of monoamine oxidase.
North-West University
Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective.
North-West University
Evaluation of nitrocatechol chalcone and pyrazoline derivatives as inhibitors of catechol-O-methyltransferase and monoamine oxidase.
North-West University
Synthesis and evaluation of 7-azaindole derivatives bearing benzocycloalkanone motifs as protein kinase inhibitors.
North-West University
Inhibition of monoamine oxidase by 3,4-dihydro-2(1H)-quinolinone derivatives.
North-West University
Synthesis and evaluation of 2-substituted 4(3H)-quinazolinone thioether derivatives as monoamine oxidase inhibitors.
North-West University
The evaluation of 1,4-benzoquinones as inhibitors of human monoamine oxidase.
North-West University
Benzyloxynitrostyrene analogues - A novel class of selective and highly potent inhibitors of monoamine oxidase B.
North-West University
Antipsychotic drugs: importance of dopamine receptors for mechanisms of therapeutic actions and side effects.
University of Reading
Synthesis and biological evaluation of 4-imidazolylflavans as nonsteroidal aromatase inhibitors.
BiomolÉCules Et Cibles Cellulaires Tumorales