Combined experimental and computational approach toward biological, physicochemical and quantum chemical aspects of substituted 1-[5-phenyl-3-(2-trifluoromethyl-phenyl)-4,5-dihydro-pyrazol-1-yl]-ethanone
Tài liệu tham khảo
Qin, 2015, Molecular docking studies and biological evaluation of chalcone based pyrazolines as tyrosinase inhibitors and potential anticancer agents, RSC Advances, 5, 46330, 10.1039/C5RA02995C
Farooq, 2022, In vitro Cytotoxic Activities, Molecular Docking and Density Functional Theory (DFT) Evaluation of Chalcone Derived Pyrazolines, Chemistry Africa, 1
Insuasty, 2010, Synthesis of novel pyrazolic analogues of chalcones and their 3-aryl-4-(3-aryl-4, 5-dihydro-1H-pyrazol-5-yl)-1-phenyl-1H-pyrazole derivatives as potential antitumor agents, Bioorganic & medicinal chemistry, 18, 4965, 10.1016/j.bmc.2010.06.013
Sivakumar, 2010, Novel chalcones and 1, 3, 5-triphenyl-2-pyrazoline derivatives as antibacterial agents, Chemical biology & drug design, 76, 407, 10.1111/j.1747-0285.2010.01020.x
Bukhari, 2015, Synthesis, molecular modeling, and biological evaluation of novel 1, 3-diphenyl-2-propen-1-one based pyrazolines as anti-inflammatory agents, Chemical biology & drug design, 85, 729, 10.1111/cbdd.12457
Chovatia, 2006, Synthesis and selective antitubercular and antimicrobial inhibitory activity of 1-acetyl-3, 5-diphenyl-4, 5-dihydro-(1H)-pyrazole derivatives, Journal of the Serbian Chemical Society, 71, 713, 10.2298/JSC0607713C
Badavath, 2021, MAO Inhibitory Activity Of 4, 5-Dihydro-1 H-Pyrazole Derivatives: A Platform To Design Novel Antidepressants, Frontiers in Drug Design & Discovery:, 10, 47, 10.2174/9789811421563121100005
Beyhan, 2017, Synthesis and anticonvulsant activity of some 2-pyrazolines derived from chalcones, Arabian Journal of Chemistry, 10, S2073, 10.1016/j.arabjc.2013.07.037
Abu-Melha, 2020, Clean grinding technique: A facile synthesis and in silico antiviral activity of hydrazones, pyrazoles, and pyrazines bearing thiazole moiety against SARS-CoV-2 main protease (Mpro), Molecules, 25, 4565, 10.3390/molecules25194565
Taj, 2011, One-pot synthesis of pyrazoline derivatised carbazoles as antitubercular, anticancer agents, their DNA cleavage and antioxidant activities, European journal of medicinal chemistry, 46, 4366, 10.1016/j.ejmech.2011.07.007
Sarkar, 2011, Antimicrobial activity of some novel pyrazoline derivatives, Journal of Advanced Pharmacy Education & Research, 1, 243
Hitge, 2020, Evaluation of nitrocatechol chalcone and pyrazoline derivatives as inhibitors of catechol-O-methyltransferase and monoamine oxidase, Bioorganic & Medicinal Chemistry Letters, 30, 10.1016/j.bmcl.2020.127188
Kumar, 2018, Pyrazole-pyrazoline as promising novel antimalarial agents: a mechanistic study, European journal of medicinal chemistry, 149, 139, 10.1016/j.ejmech.2018.01.082
Jin, 2004, Synthesis and properties of photoluminescence and electroluminescence of pyrazoline derivatives, Synthetic metals, 140, 37, 10.1016/S0379-6779(02)01320-6
Al Sabahi, 2019, Synthesis, photophysical and theoretical studies of substituted ethyl 4-(3-(naphthalen-1-yl)-1-phenyl-4, 5-dihydro-1H-pyrazol-5-yl) benzoate, Journal of Luminescence, 205, 572, 10.1016/j.jlumin.2018.10.013
Wagner, 1966, Aryl-Δ2-pyrazolines as optical brighteners, Angewandte Chemie International Edition in English, 5, 699, 10.1002/anie.196606991
Rawat, 2016, Assessment of Antimicrobial Activity, Reactivity and Non-Linear Optical Properties of New Pyrazoline Derivatives having Pyrrole moiety, ChemistrySelect, 1, 4008, 10.1002/slct.201600826
Nayak, 2021, Synthesis, Crystal Structure, Biological Evaluation, DFT Calculations and Third Order Nonlinear Optical Studies of Pyrazolines, Journal of Molecular Structure, 1243, 10.1016/j.molstruc.2021.130780
Asad, 2020, Cyclization of chalcones into N-propionyl pyrazolines for their single crystal X-ray, computational and antibacterial studies, Journal of Molecular Structure, 1201, 10.1016/j.molstruc.2019.127186
Rasool, 2021, Facile synthesis, DNA binding, Urease inhibition, anti-oxidant, molecular docking and DFT studies of 3-(3-Bromo-phenyl)-1-(2-trifluoromethyl-phenyl)-propenone and 3-(3-Bromo-5 chloro-phenyl)-1-(2-trifluoromethyl-phenyl)-propenone, Journal of Molecular Liquids, 336, 10.1016/j.molliq.2021.116302
Rasool, F., Hussain, A., Ayub, K., Tariq, M., Mahmood, K., Yousuf, S., Yar, Muhammad., Khalid, M., Samreen, H, S., Lateef, M., & Malik, A. (2022). Experimental and Theoretical investigations on (E)-3-(4-ethoxyphenyl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one and (E)-3-(naphthalen-2-yl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one: DNA binding, Urease inhibition and Promising NLO response.Journal of Molecular Structure,1253, 132194.
Pages, 2015, Metal complex interactions with DNA, Dalton transactions, 44, 3505, 10.1039/C4DT02700K
Sirajuddin, 2013, Drug–DNA interactions and their study by UV–Visible, fluorescence spectroscopies and cyclic voltametry, Journal of Photochemistry and Photobiology B: Biology, 124, 1, 10.1016/j.jphotobiol.2013.03.013
Raziq, 2017, A new glycosidic antioxidant from Ranunculus muricatus L. (Ranunculaceae) exhibited lipoxygenasae and xanthine oxidase inhibition properties, Nat Prod Res., 31, 1251, 10.1080/14786419.2016.1236098
Weatherburn, 1967, Phenol-hypochlorite reaction for determination of ammonia, Analytical chemistry, 39, 971, 10.1021/ac60252a045
Lee, 1988, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density, Physical review B, 37, 785, 10.1103/PhysRevB.37.785
Chemcraft-Citation.” [Online]. Available: https://www.chemcraftprog.com/citation.html. [Accessed: 31-Mar-2019].
Hanwell, 2012, Avogadro: an advanced semantic chemical editor, visualization, and analysis platform, Journal of cheminformatics, 4, 17, 10.1186/1758-2946-4-17
O’Boyle, 2008, cclib: a library for package-independent computational chemistry algorithms, J. Comput. Chem., 29, 839, 10.1002/jcc.20823
GaussView Version 5 Dennington R Keith T Millam J Semichem Inc Shawnee.” [Online]. Available: https://www.coursehero.com/file/p6dg8n/2-GaussView-Version-5-Dennington-R-Keith-T-Millam-J-Semichem-Inc-Shawnee/. [Accessed: 07-Apr-2019].
Truhlar, 1981
Basri, 2022, Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies, Scientific reports, 12, 1, 10.1038/s41598-022-08860-3
Liu, 2005, Study on the prediction of visible absorption maxima of azobenzene compounds, J. Zhejiang Univ. Sci. B, 6, 584, 10.1631/jzus.2005.B0584
Adeel, 2017, Synthesis, X-ray crystallographic, spectroscopic and computational studies of aminothiazole derivatives, Journal of Molecular Structure, 1131, 136, 10.1016/j.molstruc.2016.11.046
Ali, 2020, Efficient synthesis, SC-XRD, and theoretical studies of O-Benzenesulfonylated pyrimidines: Role of noncovalent interaction influence in their supramolecular network, ACS omega, 5, 15115, 10.1021/acsomega.0c00975
Rasool, 2022, Experimental and Theoretical investigations on (E)-3-(4-ethoxyphenyl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one and (E)-3-(naphthalen-2-yl)-1-(2-(trifluoromethyl) phenyl) prop–2-en-1-one: DNA binding, Urease inhibition and Promising NLO response, Journal of Molecular Structure, 1253, 10.1016/j.molstruc.2021.132194
Slonimskaya, 1986, Interpretation of the IR spectra of celadonites and glauconites in the region of OH-stretching frequencies, Clay Minerals, 21, 377, 10.1180/claymin.1986.021.3.09
Alaşalvar, 2014, Crystal structure and DFT calculations of 5-(4-Chlorophenyl)-1-(6-methoxypyridazin-3-yl)-1H-pyrazole-3-carboxylic acid, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 132, 555, 10.1016/j.saa.2014.05.014
Powell, 1972, Infrared and Raman spectra and the vC=C stretching frequencies of some silver-olefin and platinum-olefin complexes, Spectrochimica Acta Part A: Molecular Spectroscopy, 28, 327, 10.1016/0584-8539(72)80256-3
Kovacic, 1967, The C=N stretching frequency in the infrared spectra of Schiff's base complexes—I. Copper complexes of salicylidene anilines, Spectrochimica Acta Part A: Molecular Spectroscopy, 23, 183, 10.1016/0584-8539(67)80219-8
Cassidy, 1979, Nonlinear optical properties of urea, Optics Communications, 29, 243, 10.1016/0030-4018(79)90027-0
