TY  - JOUR
AU  - Jelača, Sanja
AU  - Dajić-Stevanović, Zora
AU  - Vuković, Nenad
AU  - Kolašinac, Stefan
AU  - Trendafilova, Antoaneta
AU  - Nedialkov, Paraskev
AU  - Stanković, Miroslava
AU  - Tanić, Nasta
AU  - Tanić, Nikola
AU  - Acović, Aleksandar
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela
PY  - 2022
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5300
AB  - Alchemilla vulgaris L. (lady’s mantle) was used for centuries in Europe and Balkan countries for treatments of numerous conditions and diseases of the reproductive system, yet some of the biological activities of lady’s mantle have been poorly studied and neglected. The present study aimed to estimate the potential of A. vulgaris ethanolic extract from Southeast Serbia to prevent and suppress tumor development in vitro, validated by antioxidant, genoprotective, and cytotoxic properties. A total of 45 compounds were detected by UHPLC–HRMS analysis in A. vulgaris ethanolic extract. Measurement of antioxidant activity revealed the significant potential of the tested extract to scavenge free radicals. In addition, the analysis of micronuclei showed an in vitro protective effect on chromosome aberrations in peripheral human lymphocytes. A. vulgaris extract strongly suppressed the growth of human cell lines derived from different types of tumors (MCF-7, A375, A549, and HCT116). The observed antitumor effect is realized through the blockade of cell division, caspase-dependent apoptosis, and autophagic cell death. Our study has shown that Alchemilla vulgaris L. is a valuable source of bioactive compounds able to protect the subcellular structure from damage, thus preventing tumorigenesis as well as suppressing tumor cell growth.
PB  - Basel: MDPI
T2  - Molecules
T1  - Beyond Traditional Use of Alchemilla vulgaris: Genoprotective and Antitumor Activity In Vitro
IS  - 23
VL  - 27
DO  - 10.3390/molecules27238113
SP  - 8113
ER  - 

@article{
author = "Jelača, Sanja and Dajić-Stevanović, Zora and Vuković, Nenad and Kolašinac, Stefan and Trendafilova, Antoaneta and Nedialkov, Paraskev and Stanković, Miroslava and Tanić, Nasta and Tanić, Nikola and Acović, Aleksandar and Mijatović, Sanja and Maksimović-Ivanić, Danijela",
year = "2022",
abstract = "Alchemilla vulgaris L. (lady’s mantle) was used for centuries in Europe and Balkan countries for treatments of numerous conditions and diseases of the reproductive system, yet some of the biological activities of lady’s mantle have been poorly studied and neglected. The present study aimed to estimate the potential of A. vulgaris ethanolic extract from Southeast Serbia to prevent and suppress tumor development in vitro, validated by antioxidant, genoprotective, and cytotoxic properties. A total of 45 compounds were detected by UHPLC–HRMS analysis in A. vulgaris ethanolic extract. Measurement of antioxidant activity revealed the significant potential of the tested extract to scavenge free radicals. In addition, the analysis of micronuclei showed an in vitro protective effect on chromosome aberrations in peripheral human lymphocytes. A. vulgaris extract strongly suppressed the growth of human cell lines derived from different types of tumors (MCF-7, A375, A549, and HCT116). The observed antitumor effect is realized through the blockade of cell division, caspase-dependent apoptosis, and autophagic cell death. Our study has shown that Alchemilla vulgaris L. is a valuable source of bioactive compounds able to protect the subcellular structure from damage, thus preventing tumorigenesis as well as suppressing tumor cell growth.",
publisher = "Basel: MDPI",
journal = "Molecules",
title = "Beyond Traditional Use of Alchemilla vulgaris: Genoprotective and Antitumor Activity In Vitro",
number = "23",
volume = "27",
doi = "10.3390/molecules27238113",
pages = "8113"
}

Jelača, S., Dajić-Stevanović, Z., Vuković, N., Kolašinac, S., Trendafilova, A., Nedialkov, P., Stanković, M., Tanić, N., Tanić, N., Acović, A., Mijatović, S.,& Maksimović-Ivanić, D.. (2022). Beyond Traditional Use of Alchemilla vulgaris: Genoprotective and Antitumor Activity In Vitro. in Molecules
Basel: MDPI., 27(23), 8113.
https://doi.org/10.3390/molecules27238113

Jelača S, Dajić-Stevanović Z, Vuković N, Kolašinac S, Trendafilova A, Nedialkov P, Stanković M, Tanić N, Tanić N, Acović A, Mijatović S, Maksimović-Ivanić D. Beyond Traditional Use of Alchemilla vulgaris: Genoprotective and Antitumor Activity In Vitro. in Molecules. 2022;27(23):8113.
doi:10.3390/molecules27238113 .

Jelača, Sanja, Dajić-Stevanović, Zora, Vuković, Nenad, Kolašinac, Stefan, Trendafilova, Antoaneta, Nedialkov, Paraskev, Stanković, Miroslava, Tanić, Nasta, Tanić, Nikola, Acović, Aleksandar, Mijatović, Sanja, Maksimović-Ivanić, Danijela, "Beyond Traditional Use of Alchemilla vulgaris: Genoprotective and Antitumor Activity In Vitro" in Molecules, 27, no. 23 (2022):8113,
https://doi.org/10.3390/molecules27238113 . .

TY  - JOUR
AU  - Grbović, Filip
AU  - Gajić, Gordana
AU  - Branković, Snezana
AU  - Simić, Zoran
AU  - Vuković, Nenad
AU  - Pavlović, Pavle
AU  - Topuzović, Marina
PY  - 2020
UR  - http://www.doiserbia.nb.rs/Article.aspx?ID=0352-51391900062G
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3721
AB  - Asbestos is widely mined and used around the globe posing a great risk to environment and human health. The main objective of this study was to determine allelopathic potential of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on the asbestos deposits at abandoned mine “Stragari” in central Serbia. The pH, content of carbon, nitrogen, calcium car­bonate, available phosphorous and potassium, content of Fe, Ni, Cu, Zn, Pb, Mn, and phenolics were analyzed in the control asbestos (zones without vege­tation cover) and plant rhizospheric asbestos. Allelopathic activity of plant species was assessed by “rhizosphere soil method”, and Trifolium pratense L. and Medicago sativa L. were used as the indicator species. A. altissima showed higher allelopathic potential compared to R. pseudoacacia for T. pratense and M. sativa due to greater content of phenolics. Alleopathic activity of phenolics in rhizospheric asbestos was highly correlated with pH, content of carbon and nitrogen, available phosphate and potassium, and content of Ni, Cu, Zn, Pb and Mn. A. altissima increased phenolics content in rhizospheric asbestos inhi­biting the plant growth. This woody plant in spite of high allelopathic potential is suitable for revegetation of distrurbed ecosystems because it initiates pedo­gen­esis and affects the asbestos chemistry.
T2  - Journal of the Serbian Chemical Society
T1  - Complex effect of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on asbestos deposits: Allelopathy and biogeochemistry
IS  - 1
VL  - 85
DO  - 10.2298/JSC190416062G
SP  - 141
EP  - 153
ER  - 

@article{
author = "Grbović, Filip and Gajić, Gordana and Branković, Snezana and Simić, Zoran and Vuković, Nenad and Pavlović, Pavle and Topuzović, Marina",
year = "2020",
abstract = "Asbestos is widely mined and used around the globe posing a great risk to environment and human health. The main objective of this study was to determine allelopathic potential of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on the asbestos deposits at abandoned mine “Stragari” in central Serbia. The pH, content of carbon, nitrogen, calcium car­bonate, available phosphorous and potassium, content of Fe, Ni, Cu, Zn, Pb, Mn, and phenolics were analyzed in the control asbestos (zones without vege­tation cover) and plant rhizospheric asbestos. Allelopathic activity of plant species was assessed by “rhizosphere soil method”, and Trifolium pratense L. and Medicago sativa L. were used as the indicator species. A. altissima showed higher allelopathic potential compared to R. pseudoacacia for T. pratense and M. sativa due to greater content of phenolics. Alleopathic activity of phenolics in rhizospheric asbestos was highly correlated with pH, content of carbon and nitrogen, available phosphate and potassium, and content of Ni, Cu, Zn, Pb and Mn. A. altissima increased phenolics content in rhizospheric asbestos inhi­biting the plant growth. This woody plant in spite of high allelopathic potential is suitable for revegetation of distrurbed ecosystems because it initiates pedo­gen­esis and affects the asbestos chemistry.",
journal = "Journal of the Serbian Chemical Society",
title = "Complex effect of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on asbestos deposits: Allelopathy and biogeochemistry",
number = "1",
volume = "85",
doi = "10.2298/JSC190416062G",
pages = "141-153"
}

Grbović, F., Gajić, G., Branković, S., Simić, Z., Vuković, N., Pavlović, P.,& Topuzović, M.. (2020). Complex effect of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on asbestos deposits: Allelopathy and biogeochemistry. in Journal of the Serbian Chemical Society, 85(1), 141-153.
https://doi.org/10.2298/JSC190416062G

Grbović F, Gajić G, Branković S, Simić Z, Vuković N, Pavlović P, Topuzović M. Complex effect of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on asbestos deposits: Allelopathy and biogeochemistry. in Journal of the Serbian Chemical Society. 2020;85(1):141-153.
doi:10.2298/JSC190416062G .

Grbović, Filip, Gajić, Gordana, Branković, Snezana, Simić, Zoran, Vuković, Nenad, Pavlović, Pavle, Topuzović, Marina, "Complex effect of Robinia pseudoacacia L. and Ailanthus altissima (Mill.) Swingle growing on asbestos deposits: Allelopathy and biogeochemistry" in Journal of the Serbian Chemical Society, 85, no. 1 (2020):141-153,
https://doi.org/10.2298/JSC190416062G . .

TY  - CONF
AU  - Jelača, Sanja
AU  - Dajić-Stevanović, Zora
AU  - Vuković, Nenad
AU  - Trifunović, Srećko
AU  - Drača, Dijana
AU  - Tanić, Nikola
AU  - Arsenijević, Nebojša
AU  - Tanić, Nasta
AU  - Mijatović, Sanja
AU  - Maksimović-Ivanić, Danijela
PY  - 2019
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5591
AB  - U okviru projekta bilateralne saradnje Republike Srbije i Narodne Republike Kine testirana su antitumorska svojstva ukupnih ekstrakata izolovanih iz biljaka: rtanjski čaj (Satureja montana subsp. kitaibelii), trava iva (Teucrium montanum), virak (Alchemilla vulgaris agg.), bela imela (Viscum album subsp. album), zečiji trn (Ononis spinosa), detelina kamenjarka (Anthyllis vulneraria), čestoslavica (Veronica chamaedrys), različak (Centaurea cyanis), svećica (Gentiana asclepiadea), vilino sito (Carlina acaulis), mirisni zdravac (Geranium macrorrhyzum), kotrljan (Eryngium amethystinum), izop (Hyssopus officinalis) i slatinski pelin (Artemisia santonicum). Efekat ekstrakata ispitivan je na humanim ćelijskim linijama tumora dojke MCF-7, melanoma A375, karcinoma pluća A549 i kolona HCT116, kao i ćelijama peritonealnog eksudata miša. Uticaj na vijabilnost tumorskih ćelija praćen je sulforodamin (SRB) i testom mitohondrijalne dehidrogenaze (MTT). Ekstrakti biljaka svećice, različka, vilinog sita i izopa nisu redukovali vijabilitet tumorskih ćelija. Sa druge strane ekstrakti ive, virka, mirisnog zdravca i kotrljana su pokazali značajan potencijal da ograniče rast ćelijske linije karcinoma pluća inhibirajući deobu ćelija i indukujući kaspazama posredovanu apoptozu. Tumoricidna aktivnost ekstrakata deteline kamenjarke i rtanjskog čaja je bila najsnažnija na liniji kancera dojke dok je pad vijabilnosti najverovatnije posledica intenzivirane autofagije i smanjenog proliferativnog kapaciteta ćelija. Tretmani ćelija ispitivanim ekstraktima bili su praćeni smanjenjem produkcije slobodnih radikala kiseonika/ azota ukazujući na to da ekstrakti poseduju izvestan antioksidativni potencijal ali da ove reaktivne vrste nisu medijatori njihove tumoricidne aktivnosti. Testirani ekstrakti koji su ispoljili antitumorsku aktivnost, sa izuzetkom ekstrakta kotrljana, su bili u istom opsegu doza netoksični za ćelije peritonealnog eksudata zdravih miševa ukazujući na selektivnost prema malignom fenotipu.
PB  - Kragujevac: Fakultet medicinskih nauka Univerziteta
C3  - Knjiga sažetaka: Simpozijum Efekti aktivnih supstanci u eksperimentalnim in vitro i in vivo modelima; 2019 Dec 26; Kragujevac, Serbia
T1  - Antitumorska svojstva ekstrakata biljaka sa teritorije Balkana
T1  - Антитуморска својства eкстраката биљака са територије Балкана
SP  - 16
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5591
ER  - 

@conference{
author = "Jelača, Sanja and Dajić-Stevanović, Zora and Vuković, Nenad and Trifunović, Srećko and Drača, Dijana and Tanić, Nikola and Arsenijević, Nebojša and Tanić, Nasta and Mijatović, Sanja and Maksimović-Ivanić, Danijela",
year = "2019",
abstract = "U okviru projekta bilateralne saradnje Republike Srbije i Narodne Republike Kine testirana su antitumorska svojstva ukupnih ekstrakata izolovanih iz biljaka: rtanjski čaj (Satureja montana subsp. kitaibelii), trava iva (Teucrium montanum), virak (Alchemilla vulgaris agg.), bela imela (Viscum album subsp. album), zečiji trn (Ononis spinosa), detelina kamenjarka (Anthyllis vulneraria), čestoslavica (Veronica chamaedrys), različak (Centaurea cyanis), svećica (Gentiana asclepiadea), vilino sito (Carlina acaulis), mirisni zdravac (Geranium macrorrhyzum), kotrljan (Eryngium amethystinum), izop (Hyssopus officinalis) i slatinski pelin (Artemisia santonicum). Efekat ekstrakata ispitivan je na humanim ćelijskim linijama tumora dojke MCF-7, melanoma A375, karcinoma pluća A549 i kolona HCT116, kao i ćelijama peritonealnog eksudata miša. Uticaj na vijabilnost tumorskih ćelija praćen je sulforodamin (SRB) i testom mitohondrijalne dehidrogenaze (MTT). Ekstrakti biljaka svećice, različka, vilinog sita i izopa nisu redukovali vijabilitet tumorskih ćelija. Sa druge strane ekstrakti ive, virka, mirisnog zdravca i kotrljana su pokazali značajan potencijal da ograniče rast ćelijske linije karcinoma pluća inhibirajući deobu ćelija i indukujući kaspazama posredovanu apoptozu. Tumoricidna aktivnost ekstrakata deteline kamenjarke i rtanjskog čaja je bila najsnažnija na liniji kancera dojke dok je pad vijabilnosti najverovatnije posledica intenzivirane autofagije i smanjenog proliferativnog kapaciteta ćelija. Tretmani ćelija ispitivanim ekstraktima bili su praćeni smanjenjem produkcije slobodnih radikala kiseonika/ azota ukazujući na to da ekstrakti poseduju izvestan antioksidativni potencijal ali da ove reaktivne vrste nisu medijatori njihove tumoricidne aktivnosti. Testirani ekstrakti koji su ispoljili antitumorsku aktivnost, sa izuzetkom ekstrakta kotrljana, su bili u istom opsegu doza netoksični za ćelije peritonealnog eksudata zdravih miševa ukazujući na selektivnost prema malignom fenotipu.",
publisher = "Kragujevac: Fakultet medicinskih nauka Univerziteta",
journal = "Knjiga sažetaka: Simpozijum Efekti aktivnih supstanci u eksperimentalnim in vitro i in vivo modelima; 2019 Dec 26; Kragujevac, Serbia",
title = "Antitumorska svojstva ekstrakata biljaka sa teritorije Balkana, Антитуморска својства eкстраката биљака са територије Балкана",
pages = "16",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5591"
}

Jelača, S., Dajić-Stevanović, Z., Vuković, N., Trifunović, S., Drača, D., Tanić, N., Arsenijević, N., Tanić, N., Mijatović, S.,& Maksimović-Ivanić, D.. (2019). Antitumorska svojstva ekstrakata biljaka sa teritorije Balkana. in Knjiga sažetaka: Simpozijum Efekti aktivnih supstanci u eksperimentalnim in vitro i in vivo modelima; 2019 Dec 26; Kragujevac, Serbia
Kragujevac: Fakultet medicinskih nauka Univerziteta., 16.
https://hdl.handle.net/21.15107/rcub_ibiss_5591

Jelača S, Dajić-Stevanović Z, Vuković N, Trifunović S, Drača D, Tanić N, Arsenijević N, Tanić N, Mijatović S, Maksimović-Ivanić D. Antitumorska svojstva ekstrakata biljaka sa teritorije Balkana. in Knjiga sažetaka: Simpozijum Efekti aktivnih supstanci u eksperimentalnim in vitro i in vivo modelima; 2019 Dec 26; Kragujevac, Serbia. 2019;:16.
https://hdl.handle.net/21.15107/rcub_ibiss_5591 .

Jelača, Sanja, Dajić-Stevanović, Zora, Vuković, Nenad, Trifunović, Srećko, Drača, Dijana, Tanić, Nikola, Arsenijević, Nebojša, Tanić, Nasta, Mijatović, Sanja, Maksimović-Ivanić, Danijela, "Antitumorska svojstva ekstrakata biljaka sa teritorije Balkana" in Knjiga sažetaka: Simpozijum Efekti aktivnih supstanci u eksperimentalnim in vitro i in vivo modelima; 2019 Dec 26; Kragujevac, Serbia (2019):16,
https://hdl.handle.net/21.15107/rcub_ibiss_5591 .

TY  - JOUR
AU  - Avdović, Edina H.
AU  - Stojković, Danijela L.J.
AU  - Jevtić, Verica V.
AU  - Kosić, Milica
AU  - Ristić, Biljana
AU  - Harhaji-Trajković, Ljubica
AU  - Vukić, Milena
AU  - Vuković, Nenad
AU  - Marković, Zoran S.
AU  - Potočňák, Ivan
AU  - Trifunović, Srećko R.
PY  - 2017
UR  - http://linkinghub.elsevier.com/retrieve/pii/S0020169317301597
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/2792
AB  - The new coumarine derivative, 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione, and corresponding palladium(II) complex have been synthesized and characterized by microanalysis, infrared, 1H and 13C NMR spectroscopy. The structure of the ligand, solved using a monocrystal X-ray structural analysis, consists of two crystallographic different pseudocentrosymmetrically related molecules of 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione, while the structure of the square-planar palladium(II) complex was proposed on the basis of DFT calculations. The palladium(II) complex decreased viability of U251 human glioma and B16 mouse melanoma cells in a dose and time dependent manner, while its ligand exhibited only moderate cytotoxicity.
T2  - Inorganica Chimica Acta
T1  - Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione. Crystal structure of the 3-(1-(3-hydroxypropylamino)ethylidene)-chroman-2,4-dione
VL  - 466
DO  - 10.1016/j.ica.2017.06.015
SP  - 188
EP  - 196
ER  - 

@article{
author = "Avdović, Edina H. and Stojković, Danijela L.J. and Jevtić, Verica V. and Kosić, Milica and Ristić, Biljana and Harhaji-Trajković, Ljubica and Vukić, Milena and Vuković, Nenad and Marković, Zoran S. and Potočňák, Ivan and Trifunović, Srećko R.",
year = "2017",
abstract = "The new coumarine derivative, 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione, and corresponding palladium(II) complex have been synthesized and characterized by microanalysis, infrared, 1H and 13C NMR spectroscopy. The structure of the ligand, solved using a monocrystal X-ray structural analysis, consists of two crystallographic different pseudocentrosymmetrically related molecules of 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione, while the structure of the square-planar palladium(II) complex was proposed on the basis of DFT calculations. The palladium(II) complex decreased viability of U251 human glioma and B16 mouse melanoma cells in a dose and time dependent manner, while its ligand exhibited only moderate cytotoxicity.",
journal = "Inorganica Chimica Acta",
title = "Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione. Crystal structure of the 3-(1-(3-hydroxypropylamino)ethylidene)-chroman-2,4-dione",
volume = "466",
doi = "10.1016/j.ica.2017.06.015",
pages = "188-196"
}

Avdović, E. H., Stojković, D. L.J., Jevtić, V. V., Kosić, M., Ristić, B., Harhaji-Trajković, L., Vukić, M., Vuković, N., Marković, Z. S., Potočňák, I.,& Trifunović, S. R.. (2017). Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione. Crystal structure of the 3-(1-(3-hydroxypropylamino)ethylidene)-chroman-2,4-dione. in Inorganica Chimica Acta, 466, 188-196.
https://doi.org/10.1016/j.ica.2017.06.015

Avdović EH, Stojković DL, Jevtić VV, Kosić M, Ristić B, Harhaji-Trajković L, Vukić M, Vuković N, Marković ZS, Potočňák I, Trifunović SR. Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione. Crystal structure of the 3-(1-(3-hydroxypropylamino)ethylidene)-chroman-2,4-dione. in Inorganica Chimica Acta. 2017;466:188-196.
doi:10.1016/j.ica.2017.06.015 .

Avdović, Edina H., Stojković, Danijela L.J., Jevtić, Verica V., Kosić, Milica, Ristić, Biljana, Harhaji-Trajković, Ljubica, Vukić, Milena, Vuković, Nenad, Marković, Zoran S., Potočňák, Ivan, Trifunović, Srećko R., "Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand 3-(1-(3-hydroxypropylamino)ethylidene)chroman-2,4-dione. Crystal structure of the 3-(1-(3-hydroxypropylamino)ethylidene)-chroman-2,4-dione" in Inorganica Chimica Acta, 466 (2017):188-196,
https://doi.org/10.1016/j.ica.2017.06.015 . .

TY  - JOUR
AU  - Mladenović, Milan
AU  - Stanković, Nevena
AU  - Matić, Sanja
AU  - Stanić, Snežana
AU  - Mihailović, Mirjana
AU  - Mihailović, Vladimir
AU  - Katanić, Jelena
AU  - Boroja, Tatjana
AU  - Vuković, Nenad
PY  - 2015
UR  - http://www.scopus.com/inward/record.url?eid=2-s2.0-84943457635&partnerID=tZOtx3y1
UR  - http://linkinghub.elsevier.com/retrieve/pii/S0006295215005511
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3175
AB  - Eight chroman-2,4-diones, namely 2a-h, previously investigated as anticoagulants, of which 2a and 2f as the most active, were evaluated as in vivo genotoxic agents in Wistar rat livers and kidneys using the comet assay. Compounds 2a, 2b, and 2f without genotoxic activity were applied prior to ethyl methanesulfonate (EMS) and diminished EMS-induced DNA damage according to the total score and percentage of reduction. EMS produce harmful O(6)-ethylguanine lesion which is incorporated in aberrant genotoxic GT and TG pairing after ATP-dependent DNA strand breaks have been catalyzed by rat Topoisomerase IIα (rTopIIα, EC 5.99.1.3). Therefore, the mechanism of 2a, 2b, and 2f antigenotoxic activity was investigated on the enzyme level using molecular docking and molecular dynamics simulations insamuch as it had been determined that compounds do not intercalate DNA but instead inhibit the ATPase activity. Calculations predicted that compounds inhibit ATP hydrolysis before the DNA-EMS cleavage is being catalyzed by rTopIIα, prevent EMS mutagenic and carcinogenic effects, and beside anticoagulant activity can even be applied in the cancer treatment to control the rate of anticancer alkylation drugs.
PB  - Elsevier
T2  - Biochemical Pharmacology
T1  - Newly discovered chroman-2,4-diones neutralize the in vivo DNA damage induced by alkylation through the inhibition of Topoisomerase IIα: A story behind the molecular modeling approach
IS  - 1
VL  - 98
DO  - 10.1016/j.bcp.2015.08.106
SP  - 243
EP  - 266
ER  - 

@article{
author = "Mladenović, Milan and Stanković, Nevena and Matić, Sanja and Stanić, Snežana and Mihailović, Mirjana and Mihailović, Vladimir and Katanić, Jelena and Boroja, Tatjana and Vuković, Nenad",
year = "2015",
abstract = "Eight chroman-2,4-diones, namely 2a-h, previously investigated as anticoagulants, of which 2a and 2f as the most active, were evaluated as in vivo genotoxic agents in Wistar rat livers and kidneys using the comet assay. Compounds 2a, 2b, and 2f without genotoxic activity were applied prior to ethyl methanesulfonate (EMS) and diminished EMS-induced DNA damage according to the total score and percentage of reduction. EMS produce harmful O(6)-ethylguanine lesion which is incorporated in aberrant genotoxic GT and TG pairing after ATP-dependent DNA strand breaks have been catalyzed by rat Topoisomerase IIα (rTopIIα, EC 5.99.1.3). Therefore, the mechanism of 2a, 2b, and 2f antigenotoxic activity was investigated on the enzyme level using molecular docking and molecular dynamics simulations insamuch as it had been determined that compounds do not intercalate DNA but instead inhibit the ATPase activity. Calculations predicted that compounds inhibit ATP hydrolysis before the DNA-EMS cleavage is being catalyzed by rTopIIα, prevent EMS mutagenic and carcinogenic effects, and beside anticoagulant activity can even be applied in the cancer treatment to control the rate of anticancer alkylation drugs.",
publisher = "Elsevier",
journal = "Biochemical Pharmacology",
title = "Newly discovered chroman-2,4-diones neutralize the in vivo DNA damage induced by alkylation through the inhibition of Topoisomerase IIα: A story behind the molecular modeling approach",
number = "1",
volume = "98",
doi = "10.1016/j.bcp.2015.08.106",
pages = "243-266"
}

Mladenović, M., Stanković, N., Matić, S., Stanić, S., Mihailović, M., Mihailović, V., Katanić, J., Boroja, T.,& Vuković, N.. (2015). Newly discovered chroman-2,4-diones neutralize the in vivo DNA damage induced by alkylation through the inhibition of Topoisomerase IIα: A story behind the molecular modeling approach. in Biochemical Pharmacology
Elsevier., 98(1), 243-266.
https://doi.org/10.1016/j.bcp.2015.08.106

Mladenović M, Stanković N, Matić S, Stanić S, Mihailović M, Mihailović V, Katanić J, Boroja T, Vuković N. Newly discovered chroman-2,4-diones neutralize the in vivo DNA damage induced by alkylation through the inhibition of Topoisomerase IIα: A story behind the molecular modeling approach. in Biochemical Pharmacology. 2015;98(1):243-266.
doi:10.1016/j.bcp.2015.08.106 .

Mladenović, Milan, Stanković, Nevena, Matić, Sanja, Stanić, Snežana, Mihailović, Mirjana, Mihailović, Vladimir, Katanić, Jelena, Boroja, Tatjana, Vuković, Nenad, "Newly discovered chroman-2,4-diones neutralize the in vivo DNA damage induced by alkylation through the inhibition of Topoisomerase IIα: A story behind the molecular modeling approach" in Biochemical Pharmacology, 98, no. 1 (2015):243-266,
https://doi.org/10.1016/j.bcp.2015.08.106 . .

TY  - JOUR
AU  - Stanković, Nevena
AU  - Mladenović, Milan
AU  - Mihailović, Mirjana
AU  - Arambašić Jovanović, Jelena
AU  - Uskoković, Aleksandra
AU  - Stanković, Vesna
AU  - Mihailović, Vladimir
AU  - Katanić, Jelena
AU  - Matić, Sanja
AU  - Solujić, Slavica
AU  - Vuković, Nenad
AU  - Sukdolak, Slobodan
PY  - 2014
UR  - http://www.ncbi.nlm.nih.gov/pubmed/24468630
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3185
AB  - Eight synthesized 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones were evaluated as in vivo anticoagulants by intraperitoneal application to adult male Wistar rats in order to examine their pharmacological potential, evaluate ther toxicity and propose the mechanism of action. Two of them, 2f and 2a, in concentration of 2mg/kg of body weight, presented remarkable activity (PT=130s; PT=90s) upon seven days of continuous application. The results of rat serum and liver biochemical screening, as well those of histopathological studies, proved the compounds to be non-toxic. Activity of the compounds was further examined on the molecular level. Here, molecular docking studies were performed to position the compounds in relation to the active site of VKORC1 and determine the bioactive conformations. Docking results suggested a non-covalent mode of action during which the proton transfer occurs from Cys135 SH towards 4-carbonyl group of anticoagulant. All crucial interactions for anticoagulant activity were confirmed in generated structure-based 3-D pharmacophore model, consisted of hydrogen bond acceptor and hydrophobic aromatic features, and quantified by a best correlation coefficient of 0.97.
PB  - Elsevier
T2  - European Journal of Pharmaceutical Sciences
T1  - Synthesis and toxicological studies of in vivo anticoagulant activity of novel 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones combined with a structure-based 3-D pharmacophore model.
IS  - 1
VL  - 55
DO  - 10.1016/j.ejps.2014.01.004
SP  - 20
EP  - 35
ER  - 

@article{
author = "Stanković, Nevena and Mladenović, Milan and Mihailović, Mirjana and Arambašić Jovanović, Jelena and Uskoković, Aleksandra and Stanković, Vesna and Mihailović, Vladimir and Katanić, Jelena and Matić, Sanja and Solujić, Slavica and Vuković, Nenad and Sukdolak, Slobodan",
year = "2014",
abstract = "Eight synthesized 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones were evaluated as in vivo anticoagulants by intraperitoneal application to adult male Wistar rats in order to examine their pharmacological potential, evaluate ther toxicity and propose the mechanism of action. Two of them, 2f and 2a, in concentration of 2mg/kg of body weight, presented remarkable activity (PT=130s; PT=90s) upon seven days of continuous application. The results of rat serum and liver biochemical screening, as well those of histopathological studies, proved the compounds to be non-toxic. Activity of the compounds was further examined on the molecular level. Here, molecular docking studies were performed to position the compounds in relation to the active site of VKORC1 and determine the bioactive conformations. Docking results suggested a non-covalent mode of action during which the proton transfer occurs from Cys135 SH towards 4-carbonyl group of anticoagulant. All crucial interactions for anticoagulant activity were confirmed in generated structure-based 3-D pharmacophore model, consisted of hydrogen bond acceptor and hydrophobic aromatic features, and quantified by a best correlation coefficient of 0.97.",
publisher = "Elsevier",
journal = "European Journal of Pharmaceutical Sciences",
title = "Synthesis and toxicological studies of in vivo anticoagulant activity of novel 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones combined with a structure-based 3-D pharmacophore model.",
number = "1",
volume = "55",
doi = "10.1016/j.ejps.2014.01.004",
pages = "20-35"
}

Stanković, N., Mladenović, M., Mihailović, M., Arambašić Jovanović, J., Uskoković, A., Stanković, V., Mihailović, V., Katanić, J., Matić, S., Solujić, S., Vuković, N.,& Sukdolak, S.. (2014). Synthesis and toxicological studies of in vivo anticoagulant activity of novel 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones combined with a structure-based 3-D pharmacophore model.. in European Journal of Pharmaceutical Sciences
Elsevier., 55(1), 20-35.
https://doi.org/10.1016/j.ejps.2014.01.004

Stanković N, Mladenović M, Mihailović M, Arambašić Jovanović J, Uskoković A, Stanković V, Mihailović V, Katanić J, Matić S, Solujić S, Vuković N, Sukdolak S. Synthesis and toxicological studies of in vivo anticoagulant activity of novel 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones combined with a structure-based 3-D pharmacophore model.. in European Journal of Pharmaceutical Sciences. 2014;55(1):20-35.
doi:10.1016/j.ejps.2014.01.004 .

Stanković, Nevena, Mladenović, Milan, Mihailović, Mirjana, Arambašić Jovanović, Jelena, Uskoković, Aleksandra, Stanković, Vesna, Mihailović, Vladimir, Katanić, Jelena, Matić, Sanja, Solujić, Slavica, Vuković, Nenad, Sukdolak, Slobodan, "Synthesis and toxicological studies of in vivo anticoagulant activity of novel 3-(1-aminoethylidene)chroman-2,4-diones and 4-hydroxy-3-(1-iminoethyl)-2H-chromen-2-ones combined with a structure-based 3-D pharmacophore model." in European Journal of Pharmaceutical Sciences, 55, no. 1 (2014):20-35,
https://doi.org/10.1016/j.ejps.2014.01.004 . .

TY  - JOUR
AU  - Jevtić, Verica V
AU  - Pešić, Milica
AU  - Radić, Gordana P
AU  - Vuković, Nenad
AU  - Sukdolak, Slobodan B
AU  - Klisurić, Olivera R
AU  - Podolski-Renić, Ana
AU  - Tanić, Nikola T
AU  - Trifunović, Srecko R
PY  - 2013
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/1010
AB  - The new coumarine derivative, 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one, and corresponding palladium(II) complex have been synthesized and characterized by microanalysis, infrared, H-1 and C-13 NMR spectroscopy. The proposed structure of the complex was confirmed on the basis of an X-ray structural study. In vitro antitumor activity for the ligand and complex was investigated. (C) 2013 Elsevier B.V. All rights reserved.
T2  - Journal of Molecular Structure
T1  - Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand. Crystal structure of 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one-palladium(II) complex
IS  - null
VL  - 1040
SP  - 5
EP  - 220
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_1010
ER  - 

@article{
author = "Jevtić, Verica V and Pešić, Milica and Radić, Gordana P and Vuković, Nenad and Sukdolak, Slobodan B and Klisurić, Olivera R and Podolski-Renić, Ana and Tanić, Nikola T and Trifunović, Srecko R",
year = "2013",
abstract = "The new coumarine derivative, 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one, and corresponding palladium(II) complex have been synthesized and characterized by microanalysis, infrared, H-1 and C-13 NMR spectroscopy. The proposed structure of the complex was confirmed on the basis of an X-ray structural study. In vitro antitumor activity for the ligand and complex was investigated. (C) 2013 Elsevier B.V. All rights reserved.",
journal = "Journal of Molecular Structure",
title = "Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand. Crystal structure of 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one-palladium(II) complex",
number = "null",
volume = "1040",
pages = "5-220",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_1010"
}

Jevtić, V. V., Pešić, M., Radić, G. P., Vuković, N., Sukdolak, S. B., Klisurić, O. R., Podolski-Renić, A., Tanić, N. T.,& Trifunović, S. R.. (2013). Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand. Crystal structure of 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one-palladium(II) complex. in Journal of Molecular Structure, 1040(null), 5-220.
https://hdl.handle.net/21.15107/rcub_ibiss_1010

Jevtić VV, Pešić M, Radić GP, Vuković N, Sukdolak SB, Klisurić OR, Podolski-Renić A, Tanić NT, Trifunović SR. Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand. Crystal structure of 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one-palladium(II) complex. in Journal of Molecular Structure. 2013;1040(null):5-220.
https://hdl.handle.net/21.15107/rcub_ibiss_1010 .

Jevtić, Verica V, Pešić, Milica, Radić, Gordana P, Vuković, Nenad, Sukdolak, Slobodan B, Klisurić, Olivera R, Podolski-Renić, Ana, Tanić, Nikola T, Trifunović, Srecko R, "Synthesis, characterization and cytotoxicity of a new palladium(II) complex with a coumarin-derived ligand. Crystal structure of 4-hydroxy-3-(1-(p-tolylimino)ethyl)-2H-chromen-2-one-palladium(II) complex" in Journal of Molecular Structure, 1040, no. null (2013):5-220,
https://hdl.handle.net/21.15107/rcub_ibiss_1010 .

TY  - JOUR
AU  - Mladenović, Milan
AU  - Mihailović, Mirjana
AU  - Bogojević, Desanka
AU  - Vuković, Nenad
AU  - Sukdolak, Slobodan
AU  - Matić, Sanja
AU  - Nićiforović, Neda
AU  - Mihailović, Vladimir
AU  - Mašković, Pavle
AU  - Vrvić, Miroslav M.
AU  - Solujić, Slavica
PY  - 2012
UR  - https://www.sciencedirect.com/science/article/pii/S0223523412002887?via%3Dihub
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3201
AB  - The objective of this study was to investigate in vitro and in vivo anticoagulant activity of sixteen 4-hydroxycoumarin derivatives bearing polar C-3 scaffolds. The activity was evaluated by measuring prothrombin time. Enhanced anticoagulant activity in vitro was observed for all tested compounds. Upon successive administration of 0.5 mg/kg of body weight to adult Wistar rats, over a period of five days, four derivatives (2b, 4c, 5c and 9c) presented anticoagulant activity in vivo. The most active compound was 2b, with PT = 30.0 s. Low or non-toxic effects in vivo were determined based on the catalytic activity of liver enzymes and the concentration of bilirubin, iron and proteins. Metabolic pathways of the most active compounds in vivo were determined after GC/MS analysis of collected rat urine samples. The excretion occurs by glucuronidation of 7-hydroxy forms of tested derivatives. In vivo results were described using PLS-based CoMFA and CoMSIA 3D-QSAR studies, which showed CoMFA-SE (q2 = 0.738) and CoMSIA-SEA (q2 = 0.763) to be the statistically most relevant models. Furthermore, molecular docking and DFT mechanistic studies performed on the rat VKORC1 homology model revealed interactions between the 4-OH coumarin group in the form of phenolic anion and the Cys135 catalytic site in the transition state.
T2  - European Journal of Medicinal Chemistry
T1  - Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants
VL  - 54
DO  - 10.1016/J.EJMECH.2012.04.036
SP  - 144
EP  - 158
ER  - 

@article{
author = "Mladenović, Milan and Mihailović, Mirjana and Bogojević, Desanka and Vuković, Nenad and Sukdolak, Slobodan and Matić, Sanja and Nićiforović, Neda and Mihailović, Vladimir and Mašković, Pavle and Vrvić, Miroslav M. and Solujić, Slavica",
year = "2012",
abstract = "The objective of this study was to investigate in vitro and in vivo anticoagulant activity of sixteen 4-hydroxycoumarin derivatives bearing polar C-3 scaffolds. The activity was evaluated by measuring prothrombin time. Enhanced anticoagulant activity in vitro was observed for all tested compounds. Upon successive administration of 0.5 mg/kg of body weight to adult Wistar rats, over a period of five days, four derivatives (2b, 4c, 5c and 9c) presented anticoagulant activity in vivo. The most active compound was 2b, with PT = 30.0 s. Low or non-toxic effects in vivo were determined based on the catalytic activity of liver enzymes and the concentration of bilirubin, iron and proteins. Metabolic pathways of the most active compounds in vivo were determined after GC/MS analysis of collected rat urine samples. The excretion occurs by glucuronidation of 7-hydroxy forms of tested derivatives. In vivo results were described using PLS-based CoMFA and CoMSIA 3D-QSAR studies, which showed CoMFA-SE (q2 = 0.738) and CoMSIA-SEA (q2 = 0.763) to be the statistically most relevant models. Furthermore, molecular docking and DFT mechanistic studies performed on the rat VKORC1 homology model revealed interactions between the 4-OH coumarin group in the form of phenolic anion and the Cys135 catalytic site in the transition state.",
journal = "European Journal of Medicinal Chemistry",
title = "Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants",
volume = "54",
doi = "10.1016/J.EJMECH.2012.04.036",
pages = "144-158"
}

Mladenović, M., Mihailović, M., Bogojević, D., Vuković, N., Sukdolak, S., Matić, S., Nićiforović, N., Mihailović, V., Mašković, P., Vrvić, M. M.,& Solujić, S.. (2012). Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants. in European Journal of Medicinal Chemistry, 54, 144-158.
https://doi.org/10.1016/J.EJMECH.2012.04.036

Mladenović M, Mihailović M, Bogojević D, Vuković N, Sukdolak S, Matić S, Nićiforović N, Mihailović V, Mašković P, Vrvić MM, Solujić S. Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants. in European Journal of Medicinal Chemistry. 2012;54:144-158.
doi:10.1016/J.EJMECH.2012.04.036 .

Mladenović, Milan, Mihailović, Mirjana, Bogojević, Desanka, Vuković, Nenad, Sukdolak, Slobodan, Matić, Sanja, Nićiforović, Neda, Mihailović, Vladimir, Mašković, Pavle, Vrvić, Miroslav M., Solujić, Slavica, "Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants" in European Journal of Medicinal Chemistry, 54 (2012):144-158,
https://doi.org/10.1016/J.EJMECH.2012.04.036 . .

TY  - JOUR
AU  - Mladenović, Milan
AU  - Mihailović, Mirjana
AU  - Bogojević, Desanka
AU  - Matić, Sanja
AU  - Nićiforović, Neda
AU  - Mihailović, Vladimir
AU  - Vuković, Nenad
AU  - Sukdolak, Slobodan
AU  - Solujić, Slavica
PY  - 2011
UR  - http://www.scopus.com/inward/record.url?eid=2-s2.0-79957795403&partnerID=tZOtx3y1
UR  - https://radar.ibiss.bg.ac.rs/handle/123456789/3207
AB  - The series of fifteen synthesized 4-hydroxycoumarin derivatives was subjected to antioxidant activity evaluation in vitro, through total antioxidant capacity, 1,1-diphenyl-2-picryl-hydrazyl (DPPH), hydroxyl radical, lipid peroxide scavenging and chelating activity. The highest activity was detected during the radicals scavenging, with 2b, 6b, 2c, and 4c noticed as the most active. The antioxidant activity was further quantified by the quantitative structure-activity relationships (QSAR) studies. For this purpose, the structures were optimized using Paramethric Method 6 (PM6) semi-empirical and Density Functional Theory (DFT) B3LYP methods. Bond dissociation enthalpies of coumarin 4-OH, Natural Bond Orbital (NBO) gained hybridization of the oxygen, acidity of the hydrogen atom and various molecular descriptors obtained, were correlated with biological activity, after which we designed 20 new antioxidant structures, using the most favorable structural motifs, with much improved predicted activity in vitro.
T2  - International Journal of Molecular Sciences
T1  - In vitro antioxidant activity of selected 4-hydroxy-chromene-2-one derivatives-SAR, QSAR and DFT studies.
IS  - 5
VL  - 12
DO  - 10.3390/ijms12052822
SP  - 2822
EP  - 2841
ER  - 

@article{
author = "Mladenović, Milan and Mihailović, Mirjana and Bogojević, Desanka and Matić, Sanja and Nićiforović, Neda and Mihailović, Vladimir and Vuković, Nenad and Sukdolak, Slobodan and Solujić, Slavica",
year = "2011",
abstract = "The series of fifteen synthesized 4-hydroxycoumarin derivatives was subjected to antioxidant activity evaluation in vitro, through total antioxidant capacity, 1,1-diphenyl-2-picryl-hydrazyl (DPPH), hydroxyl radical, lipid peroxide scavenging and chelating activity. The highest activity was detected during the radicals scavenging, with 2b, 6b, 2c, and 4c noticed as the most active. The antioxidant activity was further quantified by the quantitative structure-activity relationships (QSAR) studies. For this purpose, the structures were optimized using Paramethric Method 6 (PM6) semi-empirical and Density Functional Theory (DFT) B3LYP methods. Bond dissociation enthalpies of coumarin 4-OH, Natural Bond Orbital (NBO) gained hybridization of the oxygen, acidity of the hydrogen atom and various molecular descriptors obtained, were correlated with biological activity, after which we designed 20 new antioxidant structures, using the most favorable structural motifs, with much improved predicted activity in vitro.",
journal = "International Journal of Molecular Sciences",
title = "In vitro antioxidant activity of selected 4-hydroxy-chromene-2-one derivatives-SAR, QSAR and DFT studies.",
number = "5",
volume = "12",
doi = "10.3390/ijms12052822",
pages = "2822-2841"
}

Mladenović, M., Mihailović, M., Bogojević, D., Matić, S., Nićiforović, N., Mihailović, V., Vuković, N., Sukdolak, S.,& Solujić, S.. (2011). In vitro antioxidant activity of selected 4-hydroxy-chromene-2-one derivatives-SAR, QSAR and DFT studies.. in International Journal of Molecular Sciences, 12(5), 2822-2841.
https://doi.org/10.3390/ijms12052822

Mladenović M, Mihailović M, Bogojević D, Matić S, Nićiforović N, Mihailović V, Vuković N, Sukdolak S, Solujić S. In vitro antioxidant activity of selected 4-hydroxy-chromene-2-one derivatives-SAR, QSAR and DFT studies.. in International Journal of Molecular Sciences. 2011;12(5):2822-2841.
doi:10.3390/ijms12052822 .

Mladenović, Milan, Mihailović, Mirjana, Bogojević, Desanka, Matić, Sanja, Nićiforović, Neda, Mihailović, Vladimir, Vuković, Nenad, Sukdolak, Slobodan, Solujić, Slavica, "In vitro antioxidant activity of selected 4-hydroxy-chromene-2-one derivatives-SAR, QSAR and DFT studies." in International Journal of Molecular Sciences, 12, no. 5 (2011):2822-2841,
https://doi.org/10.3390/ijms12052822 . .