A novel series of 2-pyrazoline and hydrazone derivatives were synthesized and investigated
for their human monoamine oxidase (hMAO) inhibitory activity. All compounds inhibited the …

A group of 3, 5‐diaryl‐2‐pyrazoline and hydrazone derivatives was prepared via the
reaction of various chalcones with hydrazide compounds in ethanol. Twenty original …

Thirty compounds having 1-[2-(5-substituted-2-benzoxazolinone-3-yl) acetyl]-3, 5-
disubstitutedphenyl-2-pyrazoline structure and nine compounds having N′-(1, 3 …

A new series of N-pyridyl-hydrazone derivatives was synthesized by using a simple and
efficient method. The final compounds obtained were screened for their inhibitory potency …

A novel series of hydrazone derivatives were designed and synthesized. Their structures
were characterized by IR, 1 H NMR, 13 C NMR and HR-MS spectroscopic methods. The …

Ten novel 3, 5-diaryl pyrazolines were synthesized and investigated for their monoamine
oxidase (MAO) inhibitory property. All the molecules were found to be reversible and …

In an effort to develop potent monoamine oxidase (MAO) inhibitors, new pyrrole derivatives
were obtained via the selective reduction of the C C bonds of 1‐(1‐methyl‐1H‐pyrrol‐2‐yl) …

A series of 2-thiazolylhydrazone derivatives have been investigated for the ability to inhibit
the activity of the A and B isoforms of monoamine oxidase (MAO) selectively. All of the …

Abstract Several (thiazol-2-yl) hydrazone derivatives from 2-, 3-and 4-acetylpyridine were
synthesized and tested against human monoamine oxidase (hMAO) A and B enzymes. Most …

A series of new 2-methoxy-4-(5-phenyl-4, 5-dihydro-1 H-pyrazol-3-yl) phenolderivatives, 4–
13, were synthesized and tested for their human MAO inhibitory activity. All the compounds …