<p>Inhibition potencies of 1,2-diarylethylamines as monoamine transporter reuptake inhibitors.</p
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>Compounds that shows inhibition of PTP1B at 1.25 μM concentration in <i>in vitro</i> assays.</p
In humans and other organisms, monoaminergic systems are crucial in neuronal function and behavior. ...
<p>The metabolism enzymes of a drug are characterized with major, partial, or not. The inhibition po...
A series of benzothienyloxy propylamines have been prepared and are demonstrated to be inhibitors of...
<p>Inhibitory activity (IC<sub>50</sub>, μM) against MAO-A and -B and selectivity index for LSD1.</p
<div><p>1,2-Diarylethylamines including lanicemine, lefetamine, and remacemide have clinical relevan...
<p>The Inhibition of ligand binding to neurotransmitter receptors by <i>l</i>-THBr.</p
<p>The number of compounds found to demonstrate inhibition at 10μM overall and with respect to the t...
<p>The Inhibition parameters of compounds Y<sub>1</sub>-Y<sub>3</sub> on tyrosianse.</p
Fourteen substances from the class of drugs sometimes known as legal highs were screened against a b...
<p>Biochemical and cellular potencies and physicochemical properties of SMYD2 and SMYD3 inhibitors u...
This article has not been copyedited and formatted. The final version may differ from this version
Amphetamine and its derivatives exhibit a wide range of pharmacological activities, including psycho...
<p>Amino acid sequences and minimal inhibitory concentrations of CATH-2 analogs.</p
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>Compounds that shows inhibition of PTP1B at 1.25 μM concentration in <i>in vitro</i> assays.</p
In humans and other organisms, monoaminergic systems are crucial in neuronal function and behavior. ...
<p>The metabolism enzymes of a drug are characterized with major, partial, or not. The inhibition po...
A series of benzothienyloxy propylamines have been prepared and are demonstrated to be inhibitors of...
<p>Inhibitory activity (IC<sub>50</sub>, μM) against MAO-A and -B and selectivity index for LSD1.</p
<div><p>1,2-Diarylethylamines including lanicemine, lefetamine, and remacemide have clinical relevan...
<p>The Inhibition of ligand binding to neurotransmitter receptors by <i>l</i>-THBr.</p
<p>The number of compounds found to demonstrate inhibition at 10μM overall and with respect to the t...
<p>The Inhibition parameters of compounds Y<sub>1</sub>-Y<sub>3</sub> on tyrosianse.</p
Fourteen substances from the class of drugs sometimes known as legal highs were screened against a b...
<p>Biochemical and cellular potencies and physicochemical properties of SMYD2 and SMYD3 inhibitors u...
This article has not been copyedited and formatted. The final version may differ from this version
Amphetamine and its derivatives exhibit a wide range of pharmacological activities, including psycho...
<p>Amino acid sequences and minimal inhibitory concentrations of CATH-2 analogs.</p
<p>Inhibition of PARP activity by selected seven compounds whose tested concentrations were 0.1 µM, ...
<p>Compounds that shows inhibition of PTP1B at 1.25 μM concentration in <i>in vitro</i> assays.</p
In humans and other organisms, monoaminergic systems are crucial in neuronal function and behavior. ...
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