Synthesis, investigation of the crystal structure, DFT and in silico medicinal potential of nicotinonitrile substituted quinazolindione as potential anticancer scaffold
Cancer is now regarded as one of the leading causes of death for people worldwide. Here, we have reported the synthesis of a new dihydroquinazoline derivative namely, 5-acetyl-4-(4-methoxyphenyl)-6-methyl-2-(((4-oxo-3,4-dihydro-quinazolin-2-yl)methyl)thio)nicotinonitrile (4). Its structure was characterised by IR and NMR and confirmed by XRD analysis. In the molecule (4), the dihydroquinazoline moiety is planar. The acetyl and phenyl substituents on the pyridine ring are rotated out of its plane to minimise steric interactions. In the crystal, a layered structure is formed by N—H···O, C—H···O, and C—H···N hydrogen bonds and π-stacking interactions. The large gap between the highest and lowest molecular orbitals indicates high stability. Moreover, the synthesised nicotinonitrile-substituted quinazolinone was screened for medicinal characteristics and drug-likeness estimates. The synthetic ligand was docked …
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Sabir Ali Siddique, Shaaban K Mohamed, Muhammad Sarfraz, Etify A Bakhite, Islam S Marae, Abdelhamid AE Soliman, Esraa Khamies, Ahmed F Selim, Maha QM Qahtan, Hatem A Abuelizz, Rashad Al-Salahi, Joel T Mague, Youness El Bakri
Theoretical and experimental investigation on newly synthesized pyrazolopyridine derivatives: Insight into the compound activity, NLO response, and molecular dynamics
Pyrazolopyridine derivatives exhibiting biological activity are widely present in drug molecules. The title compound, ethyl 3-amino-6-methyl-4-(thiophen-2-yl)-1H-pyrazolo[3,4-b]pyridine-5-carboxylate (II), was designed and synthesized and the structure characterized by spectroscopic techniques and confirmed by single-crystal X-ray diffraction. The pyrazolopyridine moiety is not quite planar and the thiophene and ester groups are rotated well out of the mean plane of the pyridine ring. N—H···N and C—H···O hydrogen bonds plus π-stacking interactions form thick layers of molecules parallel to (001). Based on structural activity relationship studies, II exhibits potent activity against fibroblast collagenase-1 complexed to a diphenyl-ether sulphone-based hydroxamic acid or Matrix Metalloproteinase (MMP-1). Theoretical simulations were performed to probe the reactivity and electronic properties of II where the quantum …
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Youness El Bakri, Shaaban K Mohamed, Subramani Karthikeyan, Etify A Bakhite, Atazaz Ahsin, Suzan Abuelhassan, Islam S Marae, Abdelhamid AE Soliman, Esraa Khamies, Maha QM Qahtan, Hatem A Abuelizz, Rashad Al-Salahi, Joel T Mague