Production of new dietetic milk products for risk populations based on qualitative and quantitative analysis of health risk markers in milk consumption

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Production of new dietetic milk products for risk populations based on qualitative and quantitative analysis of health risk markers in milk consumption (en)
Производња нових дијететских млечних производа за ризичне популације заснована на квалитативној и квантитативној анализи биохемијских маркера здравственог ризика конзумирања млека (sr)
Proizvodnja novih dijetetskih mlečnih proizvoda za rizične populacije zasnovana na kvalitativnoj i kvantitativnoj analizi biohemijskih markera zdravstvenog rizika konzumiranja mleka (sr_RS)
Authors

Publications

Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study

Veselinović, Jovana; Kocić, Gordana M.; Pavić, Aleksandar; Nikodinović-Runić, Jasmina; Šenerović, Lidija; Nikolić, Goran M.; Veselinović, Aleksandar

(Elsevier Ireland Ltd, Clare, 2015)

TY  - JOUR
AU  - Veselinović, Jovana
AU  - Kocić, Gordana M.
AU  - Pavić, Aleksandar
AU  - Nikodinović-Runić, Jasmina
AU  - Šenerović, Lidija
AU  - Nikolić, Goran M.
AU  - Veselinović, Aleksandar
PY  - 2015
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1699
AB  - A study of structure cytotoxic-activity relationship of three hydroxy 4-phenyl-coumarins and basic coumarin molecule against two human cell lines (MRC5 fibroblasts and A375 melanoma cells) is presented. Of all investigated compounds the highest cytotoxic activity in both cell lines was determined for 7,8-dihydroxy-4-phenyl coumarin. SAR studies revealed the influence of phenyl group and hydroxyl group's number and position on cytotoxic activity. In addition, to get an insight about their binding preferences at the active site of the receptor (catalytic subunit of cAMP-dependent protein kinase) molecular docking studies were performed. Docking studies suggest that 4-phenyl hydroxycoumarins are potent cAMP-dependent protein kinase inhibitors, better than their analogs without phenyl group. The teratogenic potential was assessed in zebrafish embryo toxicity test and results showed that 4-phenyl dihydroxycoumarins were more while 7-hydroxy-4-phenyl coumarin was less embryo toxic in comparison to coumarin. In order to examine selected 4-phenyl hydroxycoumarins as a new lead compounds the druglikeness of selected 4-phenyl hydroxycoumarins was estimated by using Lipinski's "rule of five". All selected 4-phenyl hydroxycoumarins proved to have satisfying pharmacokinetic profile.
PB  - Elsevier Ireland Ltd, Clare
T2  - Chemico-biological Interactions
T1  - Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study
VL  - 231
SP  - 10
EP  - 17
DO  - 10.1016/j.cbi.2015.02.011
ER  - 
@article{
author = "Veselinović, Jovana and Kocić, Gordana M. and Pavić, Aleksandar and Nikodinović-Runić, Jasmina and Šenerović, Lidija and Nikolić, Goran M. and Veselinović, Aleksandar",
year = "2015",
abstract = "A study of structure cytotoxic-activity relationship of three hydroxy 4-phenyl-coumarins and basic coumarin molecule against two human cell lines (MRC5 fibroblasts and A375 melanoma cells) is presented. Of all investigated compounds the highest cytotoxic activity in both cell lines was determined for 7,8-dihydroxy-4-phenyl coumarin. SAR studies revealed the influence of phenyl group and hydroxyl group's number and position on cytotoxic activity. In addition, to get an insight about their binding preferences at the active site of the receptor (catalytic subunit of cAMP-dependent protein kinase) molecular docking studies were performed. Docking studies suggest that 4-phenyl hydroxycoumarins are potent cAMP-dependent protein kinase inhibitors, better than their analogs without phenyl group. The teratogenic potential was assessed in zebrafish embryo toxicity test and results showed that 4-phenyl dihydroxycoumarins were more while 7-hydroxy-4-phenyl coumarin was less embryo toxic in comparison to coumarin. In order to examine selected 4-phenyl hydroxycoumarins as a new lead compounds the druglikeness of selected 4-phenyl hydroxycoumarins was estimated by using Lipinski's "rule of five". All selected 4-phenyl hydroxycoumarins proved to have satisfying pharmacokinetic profile.",
publisher = "Elsevier Ireland Ltd, Clare",
journal = "Chemico-biological Interactions",
title = "Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study",
volume = "231",
pages = "10-17",
doi = "10.1016/j.cbi.2015.02.011"
}
Veselinović, J., Kocić, G. M., Pavić, A., Nikodinović-Runić, J., Šenerović, L., Nikolić, G. M.,& Veselinović, A.. (2015). Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study. in Chemico-biological Interactions
Elsevier Ireland Ltd, Clare., 231, 10-17.
https://doi.org/10.1016/j.cbi.2015.02.011
Veselinović J, Kocić GM, Pavić A, Nikodinović-Runić J, Šenerović L, Nikolić GM, Veselinović A. Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study. in Chemico-biological Interactions. 2015;231:10-17.
doi:10.1016/j.cbi.2015.02.011 .
Veselinović, Jovana, Kocić, Gordana M., Pavić, Aleksandar, Nikodinović-Runić, Jasmina, Šenerović, Lidija, Nikolić, Goran M., Veselinović, Aleksandar, "Selected 4-phenyl hydroxycoumarins: In vitro cytotoxicity, teratogenic effect on zebrafish (Danio rerio) embryos and molecular docking study" in Chemico-biological Interactions, 231 (2015):10-17,
https://doi.org/10.1016/j.cbi.2015.02.011 . .
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