نتایج جستجو برای: n 2 chloroquinolin 3 yl methylene 4 methylbenzenamine

تعداد نتایج: 4273066  

Kiran Gadekar, Vikas Gopalrao Rajurkar Vinayak K Deshmukh

Pathogenic infections and inflammation are very common ailments humans suffer. Upsurge of resistant pathogens has impeded the antimicrobial drug development process in recent years and the search of new antimicrobial agents is clearly evident from the literature. In line with these developments the synthesis of N-substituted aryl-2-({4-[(substituted aryl carbamoyl) methyl]-5-(pyridin-4-yl)-4H-1...

Journal: :Dalton transactions 2016
Lei-Lei Liu Cai-Xia Yu Ji-Min Du Shi-Min Liu Jing-Shuai Cao Lu-Fang Ma

Solvothermal reactions of Cd(OAc)2/Zn(OAc)2 with a new ligand, (pyridin-3-yl)methyl 4-(2-(4-((pyridin-3-yl)methoxy)phenyl)diazenyl)benzoate (L1), under different templates via an in situ ligand transformation reaction produced five coordination polymers, [CdL2(H2O)]n (1), [Cd1.5L3]n (2), [Cd2L4]n (3), [(ZnL2)·H2O]n (4) and {[Zn(1,3-BDC)(L1)]·MeCN·0.5H2O}n (5), where HL = 4-(2-(4-((pyridin-3-yl)...

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

Journal: :European Journal of Chemistry 2021

The Schiff base compound, N-((2-ethoxynaphthalen-1-yl)methylene)-4-fluoroaniline, has been synthesized and characterized by X-ray diffraction method. title C19H16FNO, crystallizes in triclinic, space group P-1 (no. 2), a = 10.6343(9) Å, b 11.4720(10) c 13.8297(13) α 102.466(7)°, β 104.763(7)°, γ 98.972(7)°, V 1552.7(2) Å3, Z 4, T 293(2) K, μ(MoKα) 0.086 mm-1, Dcalc 1.255 g/cm3, 24355 reflection...

Journal: :Acta Crystallographica Section E Structure Reports Online 2011

2013
Tim J. Blackburn Shafiq Ahmed Christopher R. Coxon Junfeng Liu Xiaohong Lu Bernard T. Golding Roger J. Griffin Claire Hutton David R. Newell Stephen Ojo Anna F. Watson Andrey Zaytzev Yan Zhao John Lunec Ian R. Hardcastle

Screening identified 2-(3-((4,6-dioxo-2-thioxotetrahydropyrimidin-5(2H)-ylidene)methyl)-2,5-dimethyl-1H-pyrrol-1-yl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carbonitrile as an MDM2-p53 inhibitor (IC50 = 12.3 μM). MDM2-p53 and MDMX-p53 activity was seen for 5-((1-(4-chlorophenyl)-2,5-diphenyl-1H-pyrrol-3-yl)methylene)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione (MDM2 IC50 = 0.11 μM; MDMX IC50 = 4.2...

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