32061-14-6Relevant academic research and scientific papers
Efficient interrupting skills of amino acid metallointercalators with DNA at physiological pH: Evaluation of biological assays
Raman, Natarajan,Selvaganapathy, Muthusamy,Radhakrishnan, Srinivasan
, p. 185 - 195 (2014)
The 4-aminoantipyrine derivatives (NO2, OCH3) and their mixed-ligand complexes with amino acids have been synthesized and investigated for their binding with CT DNA using UV-visible spectroscopy, cyclic voltammetry, and viscosity mea
UV-vis, IR and 1H NMR spectroscopic studies of some Schiff bases derivatives of 4-aminoantipyrine
Issa, Raafat M.,Khedr, Abdalla M.,Rizk, Helen F.
, p. 621 - 629 (2005)
Five Schiff bases derived from 4-aminoantipyrine and benzaldehyde derivatives (I) are prepared and their UV-vis, IR, 1H NMR and fluorescence spectra are investigated and discussed. The electronic absorption spectra of the hydroxy 4-aminoantipyr
Characterization of antimicrobial, antioxidant, and leishmanicidal activities of Schiff base derivatives of 4-aminoantipyrine
Teran, Rommy,Guevara, Rommel,Mora, Jessica,Dobronski, Lizeth,Barreiro-Costa, Olalla,Beske, Timo,Pérez-Barrera, Jorge,Araya-Maturana, Ramiro,Rojas-Silva, Patricio,Poveda, Ana,Heredia-Moya, Jorge
, (2019/08/07)
Our main interest is the characterization of compounds to support the development of alternatives to currently marketed drugs that are losing effectiveness due to the development of resistance. Schiff bases are promising biologically interesting compounds
Synthesis of 4-amino-1,5-dimethyl-2-phenylpyrazolone derivatives and their antioxidant activity
Khan, Khalid Mohammed,Khan, Akbar,Taha, Muhammad,Salar, Uzma,Hameed, Abdul,Ismail, Nor Hadiani,Jamil, Waqas,Saad, Syed Muhammad,Perveen, Shahnaz,Kashif, Syed Muhammad
, p. 802 - 810 (2016/01/12)
Schiff bases of 4-amino-1,5-dimethyl-2-phenylpyrazolone (2-18) were synthesized by treating with different benzaldehyde derivatives and tested for in vitro antioxidant activity. Synthesized Schiff base derivatives (2-18) were characterized by various spec
Tribological studies of some SAPS-free Schiff bases derived from 4-aminoantipyrine and aromatic aldehydes and their synergistic interaction with borate ester
Jaiswal, Vinay,Kalyani,Rastogi, Rashmi B.,Kumar, Rajesh
supporting information, p. 10424 - 10434 (2014/07/07)
Tribological performance of sulfur, phosphorous and metal-free Schiff bases of 4-aminoantipyrine with benzaldehyde (AAPB), salicylaldehyde (AAPS), p-chlorobenzaldehyde (AAPC) and p-methoxybenzaldehyde (AAPM) and their synergistic formulations with borate
Activated fly ash catalyzing the synthesis of novel potent 4-thiazolidinones of 4-amino antipyrine anils using CEM discover microwave methodology and their virtual screening
Shanti, Manoj Dilip,Shanti, Kaveri,Meshram, Jyotsana
, p. 1351 - 1360 (2013/10/08)
Fly ash, an industrial waste, has been used as an efficient and cost-effective activating catalyst for the synthesis of new potent thiazolidinones (4a-n), starting from imine (3a-n) and thioacetic acid. The reactions were performed under CEM Discover micr
Supramolecular coordination and antimicrobial activities of constructed mixed ligand complexes
El-Sonbati,Diab,El-Bindary,Abou-Dobara,Seyam
, p. 213 - 221 (2013/04/10)
A novel series of copper(II) and palladium(II) with 4-derivatives benzaldehyde pyrazolone (Ln) were synthesized. The mixed ligand complexes were prepared by using 1,10-phenanthroline (Phen) as second ligand. The structure of these complexes was
Predictions and correlations of structure activity relationship of some aminoantipyrine derivatives on the basis of theoretical and experimental ground
Ali, Parvez,Meshram, Jyotsna,Sheikh, Javed,Tiwari, Vandana,Dongre, Rajendra,Hadda, Taibi B.
experimental part, p. 157 - 164 (2012/07/28)
A series of 4-aminoantipyrine derivatives were produced by condensing aromatic primary amine, namely, 4-aminoantipyrine with different aryl carbonyls which occurred cleanly and efficiently without using any catalyst at room temperature. Their structures w
Design, synthesis, antimicrobial, anticancer evaluation, and QSAR studies of 4-(substituted benzylidene-Amino)-1,5-dimethyl-2-phenyl-1,2-dihydropyrazol-3- ones
Sigroha, Sumit,Narasimhan, Balasubramanian,Kumar, Pradeep,Khatkar, Anurag,Ramasamy, Kalavathy,Mani, Vasudevan,Mishra, Rakesh Kumar,Majeed, Abu Bakar Abdul
, p. 3863 - 3875 (2013/02/25)
A series of 4-(substituted benzylidene-Amino)-1,5-dimethyl-2-phenyl-1,2- dihydropyrazol-3-ones (1-17) was synthesized and tested in vitro for its antimicrobial and anticancer potentials. The biological screening results indicated that compounds having m-c
Synthesis of novel Schiff base analogues of 4-amino-1,5-dimethyl-2- phenylpyrazol-3-one and their evaluation for antioxidant and anti-inflammatory activity
Alam, Mohammad Sayed,Choi, Jung-Hyun,Lee, Dong-Ung
experimental part, p. 4103 - 4108 (2012/09/21)
4-Aminoantipyrine (4-amino-1,5-dimethyl-2-phenylpyrazole-3-one) and its analogues have been found to be compounds of interest for their anti-inflammatory, analgesic, antiviral, antipyretic, antirheumatic and antimicrobial activities. In the present study,
