Chrysin-piperazine conjugates as antioxidant and anticancer agents
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26924226
DOI
10.1016/j.ejps.2016.02.011
PII: S0928-0987(16)30041-0
Knihovny.cz E-zdroje
- Klíčová slova
- Anticancer, Antioxidant, Chrysin, Flavones, Piperazines,
- MeSH
- antioxidancia chemie farmakologie MeSH
- buněčné linie MeSH
- farmaceutická chemie MeSH
- flavonoidy chemie farmakologie MeSH
- lidé MeSH
- molekulární struktura MeSH
- piperazin MeSH
- piperaziny chemie farmakologie MeSH
- protinádorové látky chemie farmakologie MeSH
- psi MeSH
- vztahy mezi strukturou a aktivitou MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- psi MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antioxidancia MeSH
- chrysin MeSH Prohlížeč
- flavonoidy MeSH
- piperazin MeSH
- piperaziny MeSH
- protinádorové látky MeSH
Synthesis of 7-(4-bromobutoxy)-5-hydroxy-2-phenyl-4H-chromen-4-one intermediate treating chrysin with 1,4-dibromobutane facilitated combination of chrysin with a wide range of piperazine moieties which were equipped via reacting the corresponding amines with bis(2-chloroethyl)amine hydrochloride in diethylene glycol monomethyl ether solvent. Free radical scavenging potential of prepared products was analyzed in vitro adopting DPPH and ABTS bioassay in addition to the evaluation of in vitro anticancer efficacies against cervical cancer cell lines (HeLa and CaSki) and an ovarian cancer cell line SK-OV-3 using SRB assay. Bearable toxicity of 7a-w was examined employing Madin-Darby canine kidney (MDCK) cell line. In addition, cytotoxic nature of the presented compounds was inspected utilizing Human bone marrow derived mesenchymal stem cells (hBM-MSCs). Overall, 7a-w indicated remarkable antioxidant power in scavenging DPPH(·) and ABTS(·+), particularly analogs 7f, 7j, 7k, 7l, 7n, 7q, 7v, 7w have shown promising free radical scavenging activity. Analogs 7j and 7o are identified to be highly active candidates against HeLa and CaSki cell lines, whereas 7h and 7l along with 7j proved to be very sensitive towards ovarian cancer cell line SKOV-3. None of the newly prepared scaffolds showed cytotoxic nature toward hBM-MSCs cells. From the structure-activity point of view, nature and position of the electron withdrawing and electron donating functional groups on the piperazine core may contribute to the anticipated antioxidant and anticancer action. Different spectroscopic techniques (FT-IR, (1)H NMR, (13)C NMR, Mass) and elemental analysis (CHN) were utilized to confirm the desired structure of final compounds.
Department of Chemistry J N T University Kukatpally Hyderabad 500 085 India
Department of Life Science Dongguk University Goyang Gyeonggi do 10326 Republic of Korea
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