Angiogenesis is a mulit-step process by which new blood vessels are formed from preexisting vasculature. It is a key rate limiting factor in tumor growth since new blood vessels are necessary to increase tumor size. In this context it has been shown that anti-angiogenic factors can be used in cancer therapy. Among the plethora of heterocyclic compounds administered as anti-angiogenesis agents, ...

Background: Pyrazole is a simple aromatic ring an organic compound of the heterocyclic series that characterized five-membered ring structure which comprises located adjacent two nitrogen atoms and three carbon atoms. In recent years interest in the pyrazole chemistry excessively has increased due to many a wide range of properties. Because they have a wide range of specific properties such as ...

A copper(II)-mediated regioselective N-arylation of azoles has been developed using 8-aminoquinoline amide as a directing group. This reaction shows a broad substrate scope with different azoles such as pyrroles, indoles, pyrazoles and carbazole with good yields.

Decomposition of donor-acceptor diazo compounds leads to the formation reactive carbene intermediates. These can undergo a wide variety transfer reactions yield synthetically useful products. Herein, we report selective borane catalyzed cyclization reaction from combination two different afford N-substituted pyrazoles. The decomposition more α-aryl α-diazoester and subsequent with vinyl diazoac...

The development of a mild, general, and green method for the C-H arylation pyrazoles with relatively unreactive aryl halides is an ongoing challenge in organic synthesis. We describe herein novel sonophotoreactor based on ultrasonic cleaning bath blue LED light (visible light) that induce copper-catalyzed monoarylation pharmacologically relevant pyrazoles. hybrid effect irradiation discussed to...

a series of curcumin derivatives containing heterocyclic moiety have been synthesized and evaluated for their antibacterial activities. the chemical structures of the synthesized compounds were verified on the basis of spectral data and elemental analyses. investigation of antimicrobial activity of the derivatives demonstrated the ability to inhibit gram-positive microorganisms with zone of inh...

3(5)-Phenyl-1H-pyrazoles are employed in this study to develop highly efficient organic crystalline solids with deep-blue ESIPT fluorescence as well as provide novel experimental insight into the mechanism of ESIPT fluorescence and generate an intriguing fluorescence "ON/OFF" switching.

In the title compound, [Co(II)Cl(2)(C(6)H(10)N(2))(2)], a pair of 3,4,5-trimethyl-pyrazoles act as monodentate ligands. Two Cl(-) anions are also bonded directly to the Co(II) atom, which has a CoN(2)Cl(2) chromophore in a slightly distorted tetra-hedral geometry. The two mol-ecules in the asymmetric unit are related by an approximate twofold rotation roughly parallel to the a axis. The amino H...

Synthesis of di-pyrrolyl-substituted pyrazoles (dpp) and anion binding studies in protonated form are reported. Dpp show [2 + 2] binding of trifluoroacetate in the solid state to afford nanometer- and micrometer-scale architectures.

A series of 1-phenyl-3-aryl-5-(4-(3-propanoloxy) phenyl)-1H-pyrazoles were synthesized from chalcones and studied for their in vitro antibacterial activity. Chalcones i.e.,1-aryl-3-(4hydroxyphenyl) prop-2-en-1-ones (1) on reaction with phenyl hydrazine in presence of acetic acid and few drops of HCl yielded the corresponding 1-phenyl-3-aryl-5-(4-hydroxyphenyl)-1H-pyrazoles (2) which on further ...