Cytotoxic and apoptotic potential of some coumarin and 2-amino-3-carbonitrile selenophene derivatives in prostate cancer

3-acetyl coumarin derivatives (1a-d) are formed as a result of condensation of salicylaldehyde derivatives and ethyl acetoacetate and were converted into coumarin-selenophene hybrid compounds (2a-d) in the basic medium by modified Gewald reaction in the presence of malononitrile and selenium. Products are characterized by nuclear magnetic resonance (NMR). The prepared compounds are screened for their anticancer activity against DU-145 cell line. In addition, selected target compounds are evaluated for apoptosis and oxidative stress on DU-145 (prostate carcinoma) cell lines.

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  • Akkol EK, 2020, CANCERS, V12, DOI 10.3390/cancers12071959
  • Amin KM, 2008, BIOORGAN MED CHEM, V16, P5377, DOI 10.1016/j.bmc.2008.04.021
  • Anand P, 2013, ARCH PHARM RES, V36, P375, DOI 10.1007/s12272-013-0036-3
  • BEUTLER E, 1963, EXPERIENTIA, V19, P96, DOI 10.1007/BF02148042
  • Bui CT, 2006, J COMB CHEM, V8, P163, DOI 10.1021/cc050066w
  • Catto M, 2013, BIOORGAN MED CHEM, V21, P146, DOI 10.1016/j.bmc.2012.10.045
  • Circu ML, 2008, FREE RADICAL RES, V42, P689, DOI 10.1080/10715760802317663
  • Curini M, 2003, AUST J CHEM, V56, P59, DOI 10.1071/CH02177
  • de Souza LG, 2016, CHEM-BIOL INTERACT, V254, P11, DOI 10.1016/j.cbi.2016.05.001
  • Dominguez-Alvarez E, 2016, BIOORG MED CHEM LETT, V26, P2821, DOI 10.1016/j.bmcl.2016.04.064
  • Domracheva I, 2017, LIFE SCI, V186, P92, DOI 10.1016/j.lfs.2017.08.011
  • Ebrahimi SES, 2016, MED CHEM RES, V25, P1831, DOI 10.1007/s00044-016-1626-7
  • Emami S, 2015, EUR J MED CHEM, V102, P611, DOI 10.1016/j.ejmech.2015.08.033
  • Ersatir M, 2021, SYNTHETIC COMMUN, V51, P290, DOI 10.1080/00397911.2020.1825744
  • Ersatir M, 2020, MONATSH CHEM, V151, P625, DOI 10.1007/s00706-020-02573-x
  • Ersatir M, 2017, SYNTHETIC COMMUN, V47, P68, DOI 10.1080/00397911.2016.1252047
  • Fallarero A, 2008, PHARMACOL RES, V58, P215, DOI 10.1016/j.phrs.2008.08.001
  • Gandin V, 2018, FREE RADICAL BIO MED, V127, P80, DOI 10.1016/j.freeradbiomed.2018.05.001
  • Hacioglu C, 2020, BIOL TRACE ELEM RES, V195, P436, DOI 10.1007/s12011-019-01879-0
  • Hamulakova S, 2014, J MED CHEM, V57, P7073, DOI 10.1021/jm5008648
  • Hassan MZ, 2016, EUR J MED CHEM, V123, P236, DOI 10.1016/j.ejmech.2016.07.056
  • Hejchman E, 2015, PHARMACOL REP, V67, P236, DOI 10.1016/j.pharep.2014.09.008
  • Jain P. K., 2012, Journal of Applied Pharmaceutical Science, V2, P236
  • Kar F, 2019, CELL STRESS CHAPERON, V24, P871, DOI 10.1007/s12192-019-01022-x
  • Kim DH, 2016, MOL CARCINOGEN, V55, P1096, DOI 10.1002/mc.22353
  • Mirunalini S., 2014, BIOMED AGING PATHOL, V4, P131, DOI [10.1016/j.biomag.2014.01.006, DOI 10.1016/J.BIOMAG.2014.01.006]
  • Muller-Schiffmann A, 2012, BIODRUGS, V26, P21, DOI 10.2165/11597630-000000000-00000
  • MYERS RB, 1994, J CANCER RES CLIN, V120, pS11, DOI 10.1007/BF01377115
  • OHKAWA H, 1979, ANAL BIOCHEM, V95, P351, DOI 10.1016/0003-2697(79)90738-3
  • Reddy NS, 2004, BIOORG MED CHEM LETT, V14, P4093, DOI 10.1016/j.bmcl.2004.05.016
  • Shiah HS, 2007, BIOCHEM PHARMACOL, V73, P610, DOI 10.1016/j.bcp.2006.10.019
  • Siddiqui N, 2009, ACTA POL PHARM, V66, P161
  • Tung DT, 2008, ADV SYNTH CATAL, V350, P2109, DOI 10.1002/adsc.200800316
  • Umar S, 2020, J BIOCHEM MOL TOXIC, V34, DOI 10.1002/jbt.22553
  • Waterborg JH, 2019, LOWRY METHOD PROTEIN
  • Wiles JA, 2011, J MED CHEM, V54, P3418, DOI 10.1021/jm2002124
  • Zhang LF, 2019, EUR J MED CHEM, V181, DOI 10.1016/j.ejmech.2019.111587