Two new pyrazole derivatives, namely compound 1 and compound 2, have been synthesized, and their biological activity has been evaluated. Monocrystals of the obtained compounds were thoroughly investigated using single-crystal X-ray diffraction analysis, FTIR spectroscopy, and NMR spectroscopy. The results gathered from all three techniques are in good agreement, provide complete information about the structures of 1 and 2, and confirm their high purity. Thermal properties were studied using thermogravimetric analysis; both 1 and 2 are stable at room temperature. In order to better characterize 1 and 2, some physicochemical and biological properties have been evaluated using ADMET analysis. The cytotoxic activity of both compounds was determ...
In present study, a series of new synthesized condensed pyrazole derivatives 1a-f have evaluated in ...
A new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique under utili...
International audienceA concise and versatile synthetic strategy for the synthesis of original subst...
With the aim of developing novel antitumor scaffolds, a novel series of polysubstituted pyrazole der...
A series of highly functionalized pyrazole derivatives has been prepared by a one-pot, versatile and...
Defined with a dual-mode of action, the hybrid molecule synthesis is an attractive strategy to endur...
In search of synthetic chemotherapeutic substances capable of inhibiting, retarding, or reversing th...
New pyrazole derivatives were designed and synthesized as potential protein kinase inhibitors in the...
Pyrazole moiety is one of the main scaffold for many anticancer drug candidates.Many pyrazole deriva...
The synthesis of twenty seven novel pyrazole derivatives bearing aryl substituted groups at position...
Pyrazole moiety represents an important category of heterocyclic compound in pharmaceutical and medi...
A series of forty different pyrazole containing benzimidazole hybrids (6e45) have been designed, syn...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
Twenty five 4-aminomethylidene derivatives obtained from 3-phenyl-2-pyrazolin-5-one and 1,3-diphenyl...
The current study presents the synthesis of functionalized pyrazoles (18–29) through 3 + 2 annulatio...
In present study, a series of new synthesized condensed pyrazole derivatives 1a-f have evaluated in ...
A new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique under utili...
International audienceA concise and versatile synthetic strategy for the synthesis of original subst...
With the aim of developing novel antitumor scaffolds, a novel series of polysubstituted pyrazole der...
A series of highly functionalized pyrazole derivatives has been prepared by a one-pot, versatile and...
Defined with a dual-mode of action, the hybrid molecule synthesis is an attractive strategy to endur...
In search of synthetic chemotherapeutic substances capable of inhibiting, retarding, or reversing th...
New pyrazole derivatives were designed and synthesized as potential protein kinase inhibitors in the...
Pyrazole moiety is one of the main scaffold for many anticancer drug candidates.Many pyrazole deriva...
The synthesis of twenty seven novel pyrazole derivatives bearing aryl substituted groups at position...
Pyrazole moiety represents an important category of heterocyclic compound in pharmaceutical and medi...
A series of forty different pyrazole containing benzimidazole hybrids (6e45) have been designed, syn...
New pyrazoline derivatives were synthesized and evaluated for their cytotoxic effects on AsPC-1 huma...
Twenty five 4-aminomethylidene derivatives obtained from 3-phenyl-2-pyrazolin-5-one and 1,3-diphenyl...
The current study presents the synthesis of functionalized pyrazoles (18–29) through 3 + 2 annulatio...
In present study, a series of new synthesized condensed pyrazole derivatives 1a-f have evaluated in ...
A new sequence of pyrazole derivatives (1–6) was synthesized from condensation technique under utili...
International audienceA concise and versatile synthetic strategy for the synthesis of original subst...