Biological Effects and Crystal X-Ray Study of Novel Schiff Base Containing Pentafluorophenyl Hydrazine: In Vitro and in Silico Studies.
Schiff base
antibacterial activity molecular docking
anticancer
enzyme inhibition
hydrazone
Journal
Chemistry & biodiversity
ISSN: 1612-1880
Titre abrégé: Chem Biodivers
Pays: Switzerland
ID NLM: 101197449
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
received:
29
07
2023
accepted:
24
09
2023
medline:
29
11
2023
pubmed:
25
9
2023
entrez:
24
9
2023
Statut:
ppublish
Résumé
A novel Schiff base namely 3,5-di-tert-butyl-6-((2-(perfluorophenyl)hydrazono)methyl)phenol was successfully synthesized and characterized using FT-IR and
Identifiants
pubmed: 37743325
doi: 10.1002/cbdv.202301132
doi:
Substances chimiques
Schiff Bases
0
(pentafluorophenyl)hydrazine
828-73-9
Hydrazines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202301132Subventions
Organisme : Bartin University, Scientific Research Coordination Unit
ID : 2019-FEN-A-004
Informations de copyright
© 2023 Wiley-VHCA AG, Zurich, Switzerland.
Références
S. Patai, ′Carbon-Nitrogen Double Bonds′, John Wiley & Sons NY, USA, 1970.
O. S. Şentürk, Ü. Özdemir, S. Sert, N. Karacan, F. Uğur, J. Coord. Chem. 2007, 60, 229.
Ü. Özdemir, N. Karacan, O. S. Şentürk, S. Sert, F. Uğur, Synth. React. Inorg. Met.-Org. Chem. 2004, 34, 1057.
A. L. Berhanu, Gaurav, I. Mohiuddin, A. K. Malik, J. S. Aulakh, V. Kumar, K. H. Kim, TrAC Trends Anal. Chem. 2019, 116, 74-91.
C. M. da Silva, D. L. da Silva, L. V. Modolo, R. B. Alves, M. A. de Resende, C. V. B. Martins, Â. de Fátima, J. Adv. Res. 2011, 2, 1.
I. M. Müller, S. Spillmann, H. Franck, R. Pietschnig, Chem. Eur. J. 2004, 10, 2207.
M. S. More, P. G. Joshi, Y. K. Mishra, P. K. Khanna, Mater. Today Chem. 2019, 14, 100195.
Ü. Özdemir, O. S. Şentürk, S. Sert, N. Karacan, F. Uğur, J. Coord. Chem. 2006, 59, 1905.
C. M. Sharaby, M. F. Amine, A. A. Hamed, J. Mol. Struct. 2017, 1134, 208.
C. Redshaw, Catalysts. 2017, 7, 165.
M. Mitani, R. Furuyama, J. Mohri, J. Saito, S. Ishii, H. Terao, T. Nakano, H. Tanaka, T. Fujita, J. Am. Chem. Soc. 2003, 125, 4293.
D. Raj Meena, Deepa, M. Jubair Aalam, P. Chaudhary, G. Devi Yadav, S. Singh, Polyhedron. 2022, 222, 115931.
D. W. Roberts, T. W. Schultz, A. M. Api, Chem. Res. Toxicol. 2017, 30, 1309.
R. J. DiRisio, J. E. Armstrong, M. A. Frank, W. R. Lake, W. R. McNamara, Dalton Trans. 2017, 46, 10418.
A. Prakash, D. Adhikari, Int. J. Chemtech Res. 2003, 3, 1891.
H. P. Koeffler, F. McCormick, C. Denny, West. J. Med. 1991, 155, 505.
C. Pereira, M. Leão, J. Soares, C. Bessa, L. Saraiva, Curr. Pharm. Des. 2012, 18, 4223.
H. W. Boucher, G. H. Talbot, J. S. Bradley, J. E. Edwards, D. Gilbert, L. B. Rice, M. Scheld, B. Spellberg, J. Bartlett, Clin. Infect. Dis. 2009, 48, 1.
F. Li, J. G. Collins, F. R. Keene, Chem. Soc. Rev. 2015, 44, 2529.
J. Davies, Ups J Med Sci 2014, 119, 65.
H. Genc Bilgicli, A. Kestane, P. Taslimi, O. Karabay, A. Bytyqi-Damoni, M. Zengin, I. Gulcin, Bioorg. Chem. 2019, 88, 102931.
U. M. Kocyigit, Y. Budak, M. B. Gürdere, N. Dürü, P. Taslimi, İ. Gülçin, M. Ceylan, Monatsh. Chem. 2019, 150, 721.
O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard, H. Puschmann, J. Appl. Crystallogr. 2009, 42, 339.
L. J. Bourhis, O. V. Dolomanov, R. J. Gildea, J. A. Howard, H. Puschmann, Acta Crystallogr. A: Found. Adv. 2015, 71, 59.
S. Tekin, Y. Erden, S. Sandal, B. Yilmaz, Medi Sci. 2015, 4, 2172.
A. L. Brandt, A. Castillo, K. B. Harris, J. T. Keeton, M. D. Hardin, T. M. Taylor, J. Food Sci. 2010, 75, M557.
S. Alyar, Ü. Ö. Özmen, Ş. Adem, H. Alyar, E. Bilen, K. Kaya, J. Mol. Struct. 2021, 1223, 128911.
M. Pietsch, M. Gütschow, J. Biol. Chem. 2002, 277, 24006.
Ö. Şahin, Ü. Özmen Özdemir, N. Seferoğlu, Ş. Adem, Z. Seferoğlu, J. Biomol. Struct. Dyn. 2022, 40(10), 4460-4474.
S. Terzyan, C. S. Wang, D. Downs, B. Hunter, X. C. Zhang, Protein Sci. 2000, 9, 1783.
J. Ivanova, J. Leitans, M. Tanc, A. Kazaks, R. Zalubovskis, C. T. Supuran, K. Tars, Chem. Commun. 2015, 51, 7108.
A. Zubrienė, J. Smirnovienė, A. Smirnov, V. Morkūnaitė, V. Michailovienė, J. Jachno, V. Juozapaitienė, P. Norvaišas, E. Manakova, S. Gražulis, Biophys. Chem. 2015, 205, 51.
E. F. Pettersen, T. D. Goddard, C. C. Huang, G. S. Couch, D. M. Greenblatt, E. C. Meng, T. E. Ferrin, J. Comput. Chem. 2004, 25, 1605.
A. Molegro, DK-8000 Aarhus C, Denmark 2019.
F. Hamurcu, S. Mamaş, U. O. Ozdemir, A. B. Gündüzalp, O. S. Senturk, J. Mol. Struct. 2016, 1118, 18.
K. Kaya, Master Thesis, Istanbul Technical University, Istanbul, 2011.
E. H. Avdović, D. L. J. Stojković, V. V. Jevtić, M. Kosić, B. Ristić, L. Harhaji-Trajković, M. Vukić, N. Vuković, Z. S. Marković, I. Potočňák, S. R. Trifunović, Inorg. Chim. Acta 2017, 466, 188.
M. Lewis, C. L. Barnes, B. A. Hathaway, R. Glaser, Acta Crystallogr. C Struct. Chem. 1999, 55, 975.
A. R. Chowdhury, P. Ghosh, B. G. Roy, S. K. Mukhopadhyay, N. C. Murmu, P. Banerjee, Sens. Actuators B 2015, 220, 347.
A. Roy Chowdhury, A. Mondal, B. G. Roy, J. C. B. K, S. Mukhopadhyay, P. Banerjee, Photochem. Photobiol. Sci. 2017, 16, 1654.
V. V. Padma, Biomedicine (Taipei). 2015, 5, 19.
N. Terzioglu, A. Gürsoy, Eur. J. Med. Chem. 2003, 38, 781.
S. H. Alotabi, Arab. J. Chem. 2020, 13, 4771.
P. Kumar, B. Narasimhan, Mini-Rev. Med. Chem. 2013, 13, 971.
M. B. Muluk, A. S. Ubale, S. T. Dhumal, N. N. M. A. Rehman, P. P. Dixit, K. K. Kharat, P. B. Choudhari, K. P. Haval, Synth. Commun. 2020, 50, 243.
P. Shah, L. F. Abadi, S. Gaikwad, D. Chaudhari, V. Kushwah, S. Jain, K. K. Bhutani, S. Kulkarni, I. P. Singh, ChemistrySelect. 2018, 3, 10727.
Y. Özkay, Y. Tunalı, H. Karaca, İ. Işıkdağ, Eur. J. Med. Chem. 2010, 45, 3293.
S. K. Sridhar, M. Saravanan, A. Ramesh, Eur. J. Med. Chem. 2001, 36, 615.
R. M. Zaki, Y. A. Elossaily, A. M. El-Dean, Bioorg. Khim. 2012, 38, 721.
M. Rudrapal, R. S. Satyanandam, T. S. Swaroopini, T. N. Lakshmi, S. K. Jaha, S. Zaheera, Med. Chem. Res. 2013, 22, 2840.
A. Lapasam, L. Dkhar, N. Joshi, K. M. Poluri, M. R. Kollipara, Inorg. Chim. Acta 2019, 484, 255.
C. T. Supuran, Nat. Rev. Drug Discovery 2008, 7, 168.