16434-76-7Relevant academic research and scientific papers
Novel copper(II) and zinc(II) complexes of halogenated bidentate N,O-donor Schiff base ligands: Synthesis, characterization, crystal structures, DNA binding, molecular docking, DFT and TD-DFT computational studies
Ashfaq, Muhammad,Behjatmanesh-Ardakani, Reza,Chavoshpour-Natanzi, Zahra,Kargar, Hadi,Kazemi, Zahra,Mirkhani, Valiollah,Nawaz Tahir, Muhammad,Sahraei, Atefeh,Sarvian, Asiyehalsadat,Torabi, Vajiheh
, (2020/10/08)
Eight novel complexes, including: [Cu(L1)2]: C1, [Cu(L2)2]: C2, [Cu(L3)2]: C3, [Cu(L4)2]: C4, [Zn(L1)2]: Z1, [Zn (L2)2]: Z2
A quick route for the synthesis of 3-Aryl-3,4-dihydro-2H-benz[e]-1,3- oxazin-2-ones
Shukla, Davender Kumar,Rani, Manju,Khan, Arif Ali
, p. 4537 - 4540 (2013/06/27)
N-(2-Hydroxy)-benzyl-arylamines (1) gave substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazin-2-one 2 on cyclization with carbonyldiimidazole in DMSO in 20-30 min at 20-25 °C in excellent yields.
Vanadyl binary schiff base complexes containing N2O2 coordination sphere: Synthesis, ab initio calculations and thermodynamic properties
Asadi, Mozaffar,Ghatee, Mohammad Hadi,Torabi, Susan,Mohammadi, Khosro,Moosavi, Fatemeh
, p. 63 - 72 (2013/07/25)
Some vanadyl complexes were synthesized by treating a methanolic solution of the appropriate Schiff base ligand and one equivalent of VO(SO 4)2 to yield [(VOL2 1-14)](L= Salicylaldehyde's derivatives, Schemes 1,
Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors
Li, Zi-Lin,Li, Qing-Shan,Zhang, Hong-Jia,Hu, Yang,Zhu, Di-Di,Zhu, Hai-Liang
experimental part, p. 4413 - 4420 (2011/09/19)
FabH, β-ketoacyl-acyl carrier protein (ACP) synthase III, is a particularly attractive target, since it is central to the initiation of fatty acid biosynthesis and is highly conserved among Gram-positive and Gram-negative bacteria. A series of o-hydroxybe
Antihyperglycemic, α-glucosidase inhibitory and DPPH free radical scavenging activity of 5-bromosalicylaldehyde and schiff bases
Misra, Sristicheta,Pandeya, Krishna Bihari,Tiwari, Ashok Kumar,Ali, Amtul Zehra,Saradamani, Thimmapatruni,Agawane, Sachin Bharat,Madhusudana, Kuncha
experimental part, p. 1431 - 1437 (2012/05/20)
α-Glucosidase inhibition and DPPH free radical scavenging by 5-bromosalicylaldehyde and some Schiff bases have been measured. 5-Bromosalicylaldehyde shows lowest IC50 value (8.80 μM) for α-glucosidase inhibition and also shows good results in in vivo experiments for antihyperglycemic potential. Springer Science+Business Media, LLC 2010.
Stability Constants of Some Bivalent Metal Ion Chelates of Schiff Bases Derived from 2-Hydroxy-5-bromobenzaldehyde
Mayadeo, M. S.,Nalgirkar, Jyoti V.
, p. 456 - 457 (2007/10/02)
Potentiometric studies have been carried out on metal chelates of Mg(2+), Cd(2+), Zn(2+), Co(2+), Ni(2+) and Cu(2+) with N-(2-hydroxy-5-bromobenzylidene)-aniline, N-(2-hydroxy-5-bromobenzylidene)-4-methylaniline, and N-(2-hydroxy-5-bromobenzylidene)-4-chl
