نتایج جستجو برای: quinazoline

تعداد نتایج: 941  

Journal: :Molecules 2017
Hatem A Abuelizz Rabab El Dib Mohamed Marzouk El-Hassane Anouar Yousreya A Maklad Hanan N Attia Rashad Al-Salahi

A new series of quinazoline-4(3H)-ones are evaluated for anticonvulsant activity. After intraperitoneal (ip) injection to albino mice at a dose of 100 mg/kg body weight, synthesized quinazolin-4(3H)-ones (1-24) were examined in the maximal electroshock (MES) induced seizures and subcutaneous pentylenetetrazole (scPTZ) induced seizure models in mice. The Rotarod method was applied to determine t...

Journal: :Molecules 2005
Muborak Tulyasheva Bakhtiyor F Rasulev Akmal G Tojiboev Kambarali K Turgunov Bakhodir Tashkhodjaev Nasrulla D Abdullaev Khusnutdin M Shakhidoyatov

The new compounds (Z)-ethyl 2-cyano-2-(3H- and 2-methyl-3H-quinazoline-4-ylidene) acetate (1 and 2, respectively) were synthesized by multi-step reactions. The structures in a solution have been determined by (1)H-NMR spectroscopy and in the crystal form by X-ray analysis. Molecule 1 crystallized in a primitive monoclinic cell, space group capital ER, P2(1/c). The cell dimensions are a=7.970(6)...

2017
Bikui Tang Meili Wei Qun Niu Yinjiu Huang Shuo Ru Xiaofen Liu Lin Shen Qiang Fang

Mycobacterium tuberculosis (M. tuberculosis) is one of the leading causes of morbidity and mortality. Currently, the emergence of drug resistance has an urgent need for new drugs. In previous study, we found that 1,2-di(quinazolin-4-yl)diselane (DQYD), a quinazoline derivative, has anticancer activities against many cancers. However, whether DQYD has the activity of antimycobacterium is still l...

2016
Alan M. Jones Isaac M. Westwood James D. Osborne Thomas P. Matthews Matthew D. Cheeseman Martin G. Rowlands Fiona Jeganathan Rosemary Burke Diane Lee Nadia Kadi Manjuan Liu Meirion Richards Craig McAndrew Norhakim Yahya Sarah E. Dobson Keith Jones Paul Workman Ian Collins Rob L. M. van Montfort

The heat shock protein 70s (HSP70s) are molecular chaperones implicated in many cancers and of significant interest as targets for novel cancer therapies. Several HSP70 inhibitors have been reported, but because the majority have poor physicochemical properties and for many the exact mode of action is poorly understood, more detailed mechanistic and structural insight into ligand-binding to HSP...

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