TY - JOUR
T1 - In-vitro cytotoxicity, antioxidant, bleomycin-dependent DNA damage and immunomodulatory evaluation of 1-(4-acetylphenyl)-3-aryloxypyrrolidine-2,5-dione based derivatives
AU - Patel, Jigarkumar R.
AU - Dhorajiya, Bhaveshkumar D.
AU - Dholakiya, Bharatkumar Z.
AU - Badria, Farid A.
AU - Ibrahim, Ahmed S.
N1 - Funding Information:
Acknowledgments The authors thank the S.V.National Institute of Technology, Surat, for the financial support, and the members of the analytical group of the Central Salt & Marine Chemicals Research Institute, Bhavnagar, and Oxygen Healthcare Private Ltd. Ahmeda-bad, Gujarat, India, for spectral measurements. The biological part of this work was supported by the Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt. We thank Dr. Farid A Badria and his research team for excellent technical assistance.
PY - 2014/8
Y1 - 2014/8
N2 - A one pot, economical, and efficient synthesis of 1-(4-acetylphenyl)-3- aryloxypyrrolidine-2,5-diones-based derivatives 5a-l have been accomplished in single steps and in satisfactory yields from 1-(4-acetylphenyl)-pyrrole-2,5- diones 3 and phenols 4a-l. All the compounds were characterized by physical, spectroscopic, and elemental analysis. The selection of the bioassays was based on proving the drug receptor binding concept. Compounds 5g, 5k, 5h, 5i, 5a, and 5f showed the highest inhibitory antioxidant activity using ABTS methods. Compounds 5k, 5g, 5c, 5h, 5b, 5d, 5f, and 5j manifested the best protective effect against DNA damage induced by bleomycin. Moreover, an in-vitro cytotoxic activity evaluation of all synthesized compounds was against four cancer cell lines using 5-Fluorouracil as a standard anticancer drug.
AB - A one pot, economical, and efficient synthesis of 1-(4-acetylphenyl)-3- aryloxypyrrolidine-2,5-diones-based derivatives 5a-l have been accomplished in single steps and in satisfactory yields from 1-(4-acetylphenyl)-pyrrole-2,5- diones 3 and phenols 4a-l. All the compounds were characterized by physical, spectroscopic, and elemental analysis. The selection of the bioassays was based on proving the drug receptor binding concept. Compounds 5g, 5k, 5h, 5i, 5a, and 5f showed the highest inhibitory antioxidant activity using ABTS methods. Compounds 5k, 5g, 5c, 5h, 5b, 5d, 5f, and 5j manifested the best protective effect against DNA damage induced by bleomycin. Moreover, an in-vitro cytotoxic activity evaluation of all synthesized compounds was against four cancer cell lines using 5-Fluorouracil as a standard anticancer drug.
KW - Antioxidant
KW - Bleomycin-dependent DNA damage
KW - Cytotoxicity
KW - Lymphocyte transformation
KW - Oxa-michael adducts
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U2 - 10.1007/s00044-014-0965-5
DO - 10.1007/s00044-014-0965-5
M3 - Article
AN - SCOPUS:84904445304
SN - 1054-2523
VL - 23
SP - 3907
EP - 3915
JO - Medicinal Chemistry Research
JF - Medicinal Chemistry Research
IS - 8
ER -
