New ferrocenyl guanidines as potent antioxidants, protein kinase inhibitors and cytotoxic agents against human leukemia THP-1 cell line

التفاصيل البيبلوغرافية
العنوان: New ferrocenyl guanidines as potent antioxidants, protein kinase inhibitors and cytotoxic agents against human leukemia THP-1 cell line
المؤلفون: A. Ali Altaf, Saira Tabassum, Muhammad Zia, Rukhsana Gul, Amin Badshah
المصدر: Russian Journal of General Chemistry. 87:2684-2689
بيانات النشر: Pleiades Publishing Ltd, 2017.
سنة النشر: 2017
مصطلحات موضوعية: Antioxidant, biology, 010405 organic chemistry, DPPH, medicine.medical_treatment, Brine shrimp, General Chemistry, 010402 general chemistry, biology.organism_classification, 01 natural sciences, 0104 chemical sciences, chemistry.chemical_compound, Biochemistry, chemistry, Cell culture, medicine, THP1 cell line, Cytotoxicity, Protein kinase A, IC50
الوصف: Six new ferrocenyl guanidines were synthesized and characterized by elemental analysis, FT-IR and 1H and 13C NMR. Compounds 1–6 were screened for antioxidant, protein kinase inhibition, lethality of brine shrimp, and cytotoxicity against the human leukemia THP-1 cell line. The compounds demonstrated moderate to significant activities. Antioxidant activity of the synthesized compounds was evaluated by DPPH % inhibition with IC50 values. All compounds 1–6 showed notable antioxidant activity with DPPH having IC50 values between 23.2–15.1 and noteworthy brine shrimp lethality. Compound 6 demonstrated the highest cytotoxicity against brine shrimps with LC50 of 9.09 μg/mL. Protein kinase inhibition activity showed significant hyphea formation inhibition at 100 μg/disc with 10 to 13 mm clear zone of inhibition for the compounds 2–6. The compounds were screened for in vitro cytotoxicity using human leukemia cell line (THP-1 ATCC#TIB-202). Among all compounds, the most significant activity was demonstrated by compounds 6 and 5 with IC50 of 3.88 and 5.59 μg/mL which was comparable with the standard 5-flourouracil and vincristine drugs.
تدمد: 1608-3350
1070-3632
DOI: 10.1134/s1070363217110251
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::81a20311a7a7cc0ee6b583706325368c
https://doi.org/10.1134/s1070363217110251
Rights: CLOSED
رقم الانضمام: edsair.doi...........81a20311a7a7cc0ee6b583706325368c
قاعدة البيانات: OpenAIRE
الوصف
تدمد:16083350
10703632
DOI:10.1134/s1070363217110251