1761-38-2Relevant academic research and scientific papers
Vanadium complex: an appropriate candidate for killing hepatocellular carcinoma cancerous cells
Bakhshi Aliabad, Hamid,Khanamani Falahati-pour, Soudeh,Ahmadirad, Hadis,Mohamadi, Maryam,Hajizadeh, Mohammad Reza,Mahmoodi, Mehdi
, p. 981 - 990 (2018)
Hepatocellular carcinoma (HCC) is a prevalent human malignancy which its drug resistance is increasing world-wide. This project was designed to assess the anti-cancer effects of 4-bromo-2-(((5-chloro-2-hydroxyphenyl) imino) methyl) phenol ([IV(L)] complex
Synthesis, structural, and thermal analyses of copper(II) and oxido-vanadium(IV) complexes of 4-bromo-2-(((5-chloro-2-hydroxyphenyl)imino) methyl)phenol
Takjoo, Reza,Mague, Joel T.,Akbari, Alireza,Ebrahimipour, S. Yousef
, p. 2852 - 2862 (2013)
Reaction of 4-bromo-2-(((5-chloro-2-hydroxyphenyl)imino)methyl)phenol (H2L) with Cu(OAc)2·4H2O or VOSO4·3H2O and 2,2′-bipyridine (bipy) or 1,10-phenanthroline (phen) in a 1: 1: 1 mol ratio led to [CuL(phen)] and [VOL(bipy)] which have distorted square pyr
Spectral characterization and antimicrobial activity of some schiff bases derived from 4-chloro-2-aminophenol and various salicylaldehyde derivatives
Cinarli, Adem,Guerbuez, Demet,Tavman, Aydin,Birteksoez, A. Seher
experimental part, p. 449 - 459 (2012/05/04)
A series of N-(5-chloro-2-hydroxyphenyl)-(3/4/5-substituted)- salicylaldimines (I-XI) were synthesized using appropriate synthetic route. Their structures were characterized by FT-IR, UV-Visible, ESI-MS, 1H and 13C NMR spectroscopic techniques and analytical methods. The crystal structure of N-(5-chloro-2-hydroxyphenyl)-5-bromosalicylaldimine (V) was determined by X-ray diffraction at room temperature. Relationship between the melting points and the structures of the compounds was examined. Antimicrobial activity of the compounds was evaluated against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Proteus mirabilis. Antifungal activities were reported for Candida albicans. Schiff bases showed considerable antimicrobial activity against S. aureus, S. epidermidis and C. albicans. N-(5-Chloro-2-hydroxyphenyl)-3-hydroxy- salicylaldimine (II) has the broadest and highest antimicrobial activity according to the others. A series of N-(5-chloro-2-hydroxyphenyl)-(3/4/5- substituted)-salicylaldimines (I-XI) were synthesized using appropriate synthetic route. Relationship between the melting points and the structures of the compounds was examined. Antifungal activities were reported for Candida albicans. Schiff bases showed considerable antimicrobial activity against S. aureus, S. epidermidis and C. albicans. N-(5-Chloro-2-hydroxyphenyl)-3-hydroxy- salicylaldimine (II) has the broadest and highest antimicrobial activity. Copyright
