Synthetic 4,4′-{(Arylmethylene)}bis(1H-pyrazol-5-ols): Efficient Radical Scavenger

被引:0
|
作者
Qurat-ul-ain [1 ]
Perveen, Shahida [1 ]
Muhammad, Munira Taj [1 ]
Yousuf, Sahar [1 ]
Khan, Khalid Mohammed [1 ,3 ,4 ]
Choudhary, M. Iqbal [1 ,2 ]
机构
[1] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan
[2] Univ Karachi, Dr Panjwani Ctr Mol Med & Drug Res, Int Ctr Chem & Biol sci, Karachi 75270, Pakistan
[3] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat, Dept Clin Pharm, POB 31441, Dammam, Saudi Arabia
[4] King Abdulaziz Univ, Fac Sci, Dept Biochem, Jeddah 21412, Saudi Arabia
来源
关键词
Antioxidants; Radical Scavengers; DPPH; Bis-pyrazolone; ANTIOXIDANT ACTIVITY; DERIVATIVES; CATALYST;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Functionalized 4,4'-{(arylmethylene)}bis(1H-pyrazol-5-ols) 1-22 were screened for their antioxidant activity. Antioxidant activity was performed by measuring their radical scavenging activity. These compounds demonstrated diverse in vitro DPPH radical scavenging activities with IC(50 )values ranging between 55.2 +/- 1.2-149.6 +/- 1.7 mu M, as compared to standard BHT (butylated hydroxytoluene) (IC50 = 128.8 +/- 2.1 mu M). Compounds 4,4'-((4-bromo-2,6-dimethoxyphenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol 18) IC50 = 5 5. 2 +/- 1.2 mu M, 4,4'-(naphthalen-1-ylmethylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol 20) (IC50 = 58.3 +/- 0.9 mu M), 4,4'-((3-bromo-4-methoxyphenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol 19) (IC50 = 59.6 +/- 0.1 mu M), 4, 4'-((4-methoxyphenyl)methylene)bis(3-methyl-1-phenyl-1H-pyraz ol-5-ol 6) (IC50 = 60 .0 1 +/- 0.7 mu M), 4,4'-((4-(methylthio)phenyOmethylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol 10) (IC50 = 6 1. 5 +/- 0.6 mu M), 4, 4'-((2,4-dimethylphenyOm ethylene)bis(3-methyl-1-phenyl- 1H-pyraz ol-5-ol) (1) (IC50 = 68.3 +/- 0.2 mu M), 4,4'-((2-ethoxyphenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) (8) (IC50 = 80.5 +/- 1.5 mu M), 4,4'-((3-nitrophenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) (12) (IC50 = 70.8 +/- 1.4 mu M), 4, 4'-((3 -bromophenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) (17) (IC50 = 77.9 +/- 2.06 mu M), and 4,4'--((2-fluorophenyl)methylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) (22) (IC50 80.0 +/- 2.3 mu M) showed better antioxidant activity than the standard BHT. Varying substituents at aryl part (aldehydic part) have been responsible for diversified activity.
引用
收藏
页码:563 / 567
页数:5
相关论文
共 50 条
  • [41] Synthesis, characterization and application of a magnetically separable nanocatalyst for the preparation of 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) derivatives
    Jazinizadeh, Elham
    Zare, Abdolkarim
    Sajadikhah, Seyed Sajad
    Barzegar, Marziyeh
    Kohzadian, Alireza
    RESEARCH ON CHEMICAL INTERMEDIATES, 2022, 48 (12) : 5059 - 5075
  • [42] Greener and facile synthesis of 4,4′-(arylmethylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ol)s through a conventional heating procedure
    Khaligh, Nader Ghaffari
    Mihankhah, Taraneh
    Gorjian, Hayedeh
    Johan, Mohd Rafie
    SYNTHETIC COMMUNICATIONS, 2020, 50 (21) : 3276 - 3286
  • [43] Synthesis, characterization and application of a magnetically separable nanocatalyst for the preparation of 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) derivatives
    Elham Jazinizadeh
    Abdolkarim Zare
    Seyed Sajad Sajadikhah
    Marziyeh Barzegar
    Alireza Kohzadian
    Research on Chemical Intermediates, 2022, 48 : 5059 - 5075
  • [44] Rapid cesium fluoride-catalyzed Knoevenagel condensation for the synthesis of highly functionalized 4,4′-(arylmethylene)bis(1H-pyrazol-5-ol) derivatives
    Khalid Mohammed Khan
    Munira Taj Muhammad
    Imran Khan
    Shahnaz Perveen
    Wolfgang Voelter
    Monatshefte für Chemie - Chemical Monthly, 2015, 146 : 1587 - 1590
  • [45] Rapid cesium fluoride-catalyzed Knoevenagel condensation for the synthesis of highly functionalized 4,4'-(arylmethylene)bis(1H-pyrazol-5-ol) derivatives
    Khan, Khalid Mohammed
    Muhammad, Munira Taj
    Khan, Imran
    Perveen, Shahnaz
    Voelter, Wolfgang
    MONATSHEFTE FUR CHEMIE, 2015, 146 (09): : 1587 - 1590
  • [46] One-pot synthesis of 4,4′-(arylmethylene)-bis-(3-methyl-1-phenyl-1H-pyrazol-5-ols) catalyzed by Bronsted acidic ionic liquid supported on nanoporous Na+-montmorillonite
    Shirini, Farhad
    Seddighi, Mohadeseh
    Mazloumi, Masoumeh
    Makhsous, Masoumeh
    Abedini, Masoumeh
    JOURNAL OF MOLECULAR LIQUIDS, 2015, 208 : 291 - 297
  • [47] Efficient pseudo five-component synthesis of 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1H-pyrazol-5-ol) derivatives promoted by a novel ionic liquid catalyst
    Abshirini, Zahra
    Zare, Abdolkarim
    ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 2018, 73 (3-4): : 191 - 195
  • [48] Poly(4-vinylpyridine)-supported dual acidic ionic liquid: an environmentally friendly heterogeneous catalyst for the one-pot synthesis of 4,4′-(arylmethylene)bis(3-methyl-1phenyl-1H-pyrazol-5-ols)
    Parvanak Boroujen, Kaveh
    Shojaei, Pegah
    TURKISH JOURNAL OF CHEMISTRY, 2013, 37 (05) : 756 - 764
  • [49] REACTIONS AND TAUTOMERIC BEHAVIOR OF 1-(2-PYRIDINYL)-1H-PYRAZOL-5-OLS
    Pfaffenhuemer, Peter
    Laggner, Christian
    Deibl, Stefan
    Datterl, Barbara
    Holzer, Wolfgang
    HETEROCYCLES, 2011, 83 (07) : 1567 - 1585
  • [50] Ni-guanidine@MCM-41 NPs: a new catalyst for the synthesis of 4,4ʹ-(arylmethylene)-bis-(3-methyl-1-phenyl-1H-pyrazol-5-ols) and symmetric di-aryl sulfides
    Hossein Filian
    Arash Ghorbani-Choghamarani
    Elham Tahanpesar
    Journal of the Iranian Chemical Society, 2019, 16 : 2673 - 2681