TY  - JOUR
AU  - Popović-Djordjević, Jelena
AU  - Došen-Mićović, Ljiljana I.
AU  - Juranić, Ivan O.
AU  - Drakulić, Branko J.
PY  - 2010
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2335
AB  - Alignment-free, three dimensional structure-activity relationships (3D QSAR) of the antiproliferative potency of twenty-two glutarimide-containing compounds, taken from National Cancer Institute Developmental therapeutics Program database, toward eight representative human tumour cell lines are reported. The descriptors used in the QSAR study were derived from GRID molecular interaction fields. The obtained models readily detect structural motifs positively or negatively correlated with the potency of the studied compounds toward each cell line. In this way, the pharmacophoric pattern required for high potency of compounds is reported. This pattern can serve as guidance for the design and syntheses of novel congeners, planned to be tested toward human tumour cell lines.
AB  - U tekstu je opisan odnos strukture i antiproliferativne aktivnosti 22 glutarimidna derivata prema osam reprezentativnih linija humanih tumora. Podaci o strukturi jedinjenja i njihovoj aktivnosti su preuzeti iz baze podataka Nacionalnog Instituta za rak, SAD. Deskriptori, nezavisni od poravnavanja molekula (GRIND-2), korišćeni u proučavanju odnosa strukture i aktivnosti su dobijeni upotrebom programa GRID. Modeli jasno prikazuju strukturne elemente jedinjenja koji se pozitivno ili negativno korelišu sa biološkom aktivnošću. Farmakoforna slika dobijena iz modela će biti korišćena za planiranje novih analoga koji sadrže glutarimidni prsten i za koje se očekuje da će pokazati značajnu antiproliferativnu aktivnost.
PB  - Srpsko hemijsko društvo, Beograd
T2  - JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
T1  - Antiproliferative activity of NCI-DTP glutarimide derivatives: An alignment independent 3D QSAR study
T1  - Antiproliferativna aktivnost glutarimidnih derivata iz baze podataka Nacionalnog instituta za rak, SAD - 3D odnos strukture i aktivnosti nezavisan od poravnavanja molekula
EP  - 1179
IS  - 9
SP  - 1167
VL  - 75
DO  - 10.2298/JSC091202076P
ER  - 

@article{
author = "Popović-Djordjević, Jelena and Došen-Mićović, Ljiljana I. and Juranić, Ivan O. and Drakulić, Branko J.",
year = "2010",
abstract = "Alignment-free, three dimensional structure-activity relationships (3D QSAR) of the antiproliferative potency of twenty-two glutarimide-containing compounds, taken from National Cancer Institute Developmental therapeutics Program database, toward eight representative human tumour cell lines are reported. The descriptors used in the QSAR study were derived from GRID molecular interaction fields. The obtained models readily detect structural motifs positively or negatively correlated with the potency of the studied compounds toward each cell line. In this way, the pharmacophoric pattern required for high potency of compounds is reported. This pattern can serve as guidance for the design and syntheses of novel congeners, planned to be tested toward human tumour cell lines., U tekstu je opisan odnos strukture i antiproliferativne aktivnosti 22 glutarimidna derivata prema osam reprezentativnih linija humanih tumora. Podaci o strukturi jedinjenja i njihovoj aktivnosti su preuzeti iz baze podataka Nacionalnog Instituta za rak, SAD. Deskriptori, nezavisni od poravnavanja molekula (GRIND-2), korišćeni u proučavanju odnosa strukture i aktivnosti su dobijeni upotrebom programa GRID. Modeli jasno prikazuju strukturne elemente jedinjenja koji se pozitivno ili negativno korelišu sa biološkom aktivnošću. Farmakoforna slika dobijena iz modela će biti korišćena za planiranje novih analoga koji sadrže glutarimidni prsten i za koje se očekuje da će pokazati značajnu antiproliferativnu aktivnost.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "JOURNAL OF THE SERBIAN CHEMICAL SOCIETY",
title = "Antiproliferative activity of NCI-DTP glutarimide derivatives: An alignment independent 3D QSAR study, Antiproliferativna aktivnost glutarimidnih derivata iz baze podataka Nacionalnog instituta za rak, SAD - 3D odnos strukture i aktivnosti nezavisan od poravnavanja molekula",
pages = "1179-1167",
number = "9",
volume = "75",
doi = "10.2298/JSC091202076P"
}

Popović-Djordjević, J., Došen-Mićović, L. I., Juranić, I. O.,& Drakulić, B. J.. (2010). Antiproliferative activity of NCI-DTP glutarimide derivatives: An alignment independent 3D QSAR study. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
Srpsko hemijsko društvo, Beograd., 75(9), 1167-1179.
https://doi.org/10.2298/JSC091202076P

Popović-Djordjević J, Došen-Mićović LI, Juranić IO, Drakulić BJ. Antiproliferative activity of NCI-DTP glutarimide derivatives: An alignment independent 3D QSAR study. in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY. 2010;75(9):1167-1179.
doi:10.2298/JSC091202076P .

Popović-Djordjević, Jelena, Došen-Mićović, Ljiljana I., Juranić, Ivan O., Drakulić, Branko J., "Antiproliferative activity of NCI-DTP glutarimide derivatives: An alignment independent 3D QSAR study" in JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, 75, no. 9 (2010):1167-1179,
https://doi.org/10.2298/JSC091202076P . .

TY  - JOUR
AU  - Vitnik, Vesna
AU  - Ivanović, M.D.
AU  - Vitnik, Željko J.
AU  - Popović-Djordjević, Jelena
AU  - Zizak, Z.S.
AU  - Juranić, Zorica
AU  - Juranić, Ivan O.
PY  - 2009
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/2112
AB  - Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of alpha,beta-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conjugated acids were obtained from cyclic or aromatic ketones, whereas bromo acids were obtained from 4-oxo-piperidine-1-carboxylic acid ethyl ester (13) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14).
PB  - Taylor & Francis Inc, Philadelphia
T2  - Synthetic Communications
T1  - One-Step Conversion of Ketones to Conjugated Acids Using Bromoform
EP  - 1471
IS  - 8
SP  - 1457
VL  - 39
DO  - 10.1080/00397910802531955
ER  - 

@article{
author = "Vitnik, Vesna and Ivanović, M.D. and Vitnik, Željko J. and Popović-Djordjević, Jelena and Zizak, Z.S. and Juranić, Zorica and Juranić, Ivan O.",
year = "2009",
abstract = "Phase-transfer-catalyzed (PTC) reactions of ketones with bromoform and aqueous lithium hydroxide in alcoholic solvent result in the formation of alpha,beta-unsaturated carboxylic acids. The reaction was performed at room temperature for 24h. The corresponding conjugated acids were obtained from cyclic or aromatic ketones, whereas bromo acids were obtained from 4-oxo-piperidine-1-carboxylic acid ethyl ester (13) and 4-oxo-piperidine-1-carboxylic acid tert-butyl ester (14).",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Synthetic Communications",
title = "One-Step Conversion of Ketones to Conjugated Acids Using Bromoform",
pages = "1471-1457",
number = "8",
volume = "39",
doi = "10.1080/00397910802531955"
}

Vitnik, V., Ivanović, M.D., Vitnik, Ž. J., Popović-Djordjević, J., Zizak, Z.S., Juranić, Z.,& Juranić, I. O.. (2009). One-Step Conversion of Ketones to Conjugated Acids Using Bromoform. in Synthetic Communications
Taylor & Francis Inc, Philadelphia., 39(8), 1457-1471.
https://doi.org/10.1080/00397910802531955

Vitnik V, Ivanović M, Vitnik ŽJ, Popović-Djordjević J, Zizak Z, Juranić Z, Juranić IO. One-Step Conversion of Ketones to Conjugated Acids Using Bromoform. in Synthetic Communications. 2009;39(8):1457-1471.
doi:10.1080/00397910802531955 .

Vitnik, Vesna, Ivanović, M.D., Vitnik, Željko J., Popović-Djordjević, Jelena, Zizak, Z.S., Juranić, Zorica, Juranić, Ivan O., "One-Step Conversion of Ketones to Conjugated Acids Using Bromoform" in Synthetic Communications, 39, no. 8 (2009):1457-1471,
https://doi.org/10.1080/00397910802531955 . .

TY  - CONF
AU  - Marinković, Katarina
AU  - Mančić, Lidija
AU  - Pavlović, Vladimir B.
AU  - Dramićanin, Miroslav
AU  - Milošević, Olivera
PY  - 2008
UR  - http://dais.sanu.ac.rs/123456789/292
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/5664
AB  - Poster presented at the 10th Conference of the Materials Research Society of Serbia - YUCOMAT 2008, Herceg Novi, Crna Gora, 8-12. septembar 2008
T1  - Urea-Assisted Self-Combustion Aerosol Synthesis of Y3Al5O12:Ce3+
UR  - https://hdl.handle.net/21.15107/rcub_dais_292
ER  - 

@conference{
author = "Marinković, Katarina and Mančić, Lidija and Pavlović, Vladimir B. and Dramićanin, Miroslav and Milošević, Olivera",
year = "2008",
abstract = "Poster presented at the 10th Conference of the Materials Research Society of Serbia - YUCOMAT 2008, Herceg Novi, Crna Gora, 8-12. septembar 2008",
title = "Urea-Assisted Self-Combustion Aerosol Synthesis of Y3Al5O12:Ce3+",
url = "https://hdl.handle.net/21.15107/rcub_dais_292"
}

Marinković, K., Mančić, L., Pavlović, V. B., Dramićanin, M.,& Milošević, O.. (2008). Urea-Assisted Self-Combustion Aerosol Synthesis of Y3Al5O12:Ce3+. .
https://hdl.handle.net/21.15107/rcub_dais_292

Marinković K, Mančić L, Pavlović VB, Dramićanin M, Milošević O. Urea-Assisted Self-Combustion Aerosol Synthesis of Y3Al5O12:Ce3+. 2008;.
https://hdl.handle.net/21.15107/rcub_dais_292 .

Marinković, Katarina, Mančić, Lidija, Pavlović, Vladimir B., Dramićanin, Miroslav, Milošević, Olivera, "Urea-Assisted Self-Combustion Aerosol Synthesis of Y3Al5O12:Ce3+" (2008),
https://hdl.handle.net/21.15107/rcub_dais_292 .