TY  - CONF
AU  - Trifunović, Jelena
AU  - Jadranin, Milka
AU  - Damjanović, Ana
AU  - Rašković, Sanvila S.
AU  - Djurovic, M. N.
AU  - Draskovic, D.
AU  - Pudar, G.
AU  - Tešević, Vele
AU  - Juranić, Ivan O.
AU  - Juranić, Z.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1535
PB  - Wiley-Blackwell, Hoboken
C3  - Immunology
T1  - LC/DAD analysis of serum biogenic amines in patients with diabetes mellitus, chronic urticaria and Hashimoto's thyroiditis
VL  - 137
SP  - 673
EP  - 673
UR  - https://hdl.handle.net/21.15107/rcub_cherry_1535
ER  - 

@conference{
author = "Trifunović, Jelena and Jadranin, Milka and Damjanović, Ana and Rašković, Sanvila S. and Djurovic, M. N. and Draskovic, D. and Pudar, G. and Tešević, Vele and Juranić, Ivan O. and Juranić, Z.",
year = "2012",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Immunology",
title = "LC/DAD analysis of serum biogenic amines in patients with diabetes mellitus, chronic urticaria and Hashimoto's thyroiditis",
volume = "137",
pages = "673-673",
url = "https://hdl.handle.net/21.15107/rcub_cherry_1535"
}

Trifunović, J., Jadranin, M., Damjanović, A., Rašković, S. S., Djurovic, M. N., Draskovic, D., Pudar, G., Tešević, V., Juranić, I. O.,& Juranić, Z.. (2012). LC/DAD analysis of serum biogenic amines in patients with diabetes mellitus, chronic urticaria and Hashimoto's thyroiditis. in Immunology
Wiley-Blackwell, Hoboken., 137, 673-673.
https://hdl.handle.net/21.15107/rcub_cherry_1535

Trifunović J, Jadranin M, Damjanović A, Rašković SS, Djurovic MN, Draskovic D, Pudar G, Tešević V, Juranić IO, Juranić Z. LC/DAD analysis of serum biogenic amines in patients with diabetes mellitus, chronic urticaria and Hashimoto's thyroiditis. in Immunology. 2012;137:673-673.
https://hdl.handle.net/21.15107/rcub_cherry_1535 .

Trifunović, Jelena, Jadranin, Milka, Damjanović, Ana, Rašković, Sanvila S., Djurovic, M. N., Draskovic, D., Pudar, G., Tešević, Vele, Juranić, Ivan O., Juranić, Z., "LC/DAD analysis of serum biogenic amines in patients with diabetes mellitus, chronic urticaria and Hashimoto's thyroiditis" in Immunology, 137 (2012):673-673,
https://hdl.handle.net/21.15107/rcub_cherry_1535 .

TY  - CONF
AU  - Trifunović, Jelena
AU  - Jadranin, Milka
AU  - Damjanović, Ana
AU  - Ristic, D.
AU  - Milanovic, N.
AU  - Tešević, Vele
AU  - Juranić, Ivan O.
AU  - Ristić, S.
AU  - Juranić, Z.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1571
PB  - Elsevier Sci Ltd, Oxford
C3  - European Journal of Cancer / EJC
T1  - Serum Polyamines in Patients With Non-Hodgkin's Lymphoma
VL  - 48
DO  - 10.1016/S0959-8049(12)71111-5
ER  - 

@conference{
author = "Trifunović, Jelena and Jadranin, Milka and Damjanović, Ana and Ristic, D. and Milanovic, N. and Tešević, Vele and Juranić, Ivan O. and Ristić, S. and Juranić, Z.",
year = "2012",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "European Journal of Cancer / EJC",
title = "Serum Polyamines in Patients With Non-Hodgkin's Lymphoma",
volume = "48",
doi = "10.1016/S0959-8049(12)71111-5"
}

Trifunović, J., Jadranin, M., Damjanović, A., Ristic, D., Milanovic, N., Tešević, V., Juranić, I. O., Ristić, S.,& Juranić, Z.. (2012). Serum Polyamines in Patients With Non-Hodgkin's Lymphoma. in European Journal of Cancer / EJC
Elsevier Sci Ltd, Oxford., 48.
https://doi.org/10.1016/S0959-8049(12)71111-5

Trifunović J, Jadranin M, Damjanović A, Ristic D, Milanovic N, Tešević V, Juranić IO, Ristić S, Juranić Z. Serum Polyamines in Patients With Non-Hodgkin's Lymphoma. in European Journal of Cancer / EJC. 2012;48.
doi:10.1016/S0959-8049(12)71111-5 .

Trifunović, Jelena, Jadranin, Milka, Damjanović, Ana, Ristic, D., Milanovic, N., Tešević, Vele, Juranić, Ivan O., Ristić, S., Juranić, Z., "Serum Polyamines in Patients With Non-Hodgkin's Lymphoma" in European Journal of Cancer / EJC, 48 (2012),
https://doi.org/10.1016/S0959-8049(12)71111-5 . .

TY  - CONF
AU  - Žižak, Željko S.
AU  - Opsenica, Dejan M.
AU  - Šolaja, Bogdan A.
AU  - Juranić, Z.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1572
PB  - Elsevier Sci Ltd, Oxford
C3  - European Journal of Cancer / EJC
T1  - Investigation of Some Small Heterocyclic Compounds as Potential Antitumor Agents
VL  - 48
DO  - 10.1016/S0959-8049(12)71674-X
ER  - 

@conference{
author = "Žižak, Željko S. and Opsenica, Dejan M. and Šolaja, Bogdan A. and Juranić, Z.",
year = "2012",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "European Journal of Cancer / EJC",
title = "Investigation of Some Small Heterocyclic Compounds as Potential Antitumor Agents",
volume = "48",
doi = "10.1016/S0959-8049(12)71674-X"
}

Žižak, Ž. S., Opsenica, D. M., Šolaja, B. A.,& Juranić, Z.. (2012). Investigation of Some Small Heterocyclic Compounds as Potential Antitumor Agents. in European Journal of Cancer / EJC
Elsevier Sci Ltd, Oxford., 48.
https://doi.org/10.1016/S0959-8049(12)71674-X

Žižak ŽS, Opsenica DM, Šolaja BA, Juranić Z. Investigation of Some Small Heterocyclic Compounds as Potential Antitumor Agents. in European Journal of Cancer / EJC. 2012;48.
doi:10.1016/S0959-8049(12)71674-X .

Žižak, Željko S., Opsenica, Dejan M., Šolaja, Bogdan A., Juranić, Z., "Investigation of Some Small Heterocyclic Compounds as Potential Antitumor Agents" in European Journal of Cancer / EJC, 48 (2012),
https://doi.org/10.1016/S0959-8049(12)71674-X . .

TY  - CONF
AU  - Matic, I.
AU  - Juranić, Z.
AU  - Žižak, Željko S.
AU  - Vajs, Vlatka
AU  - Aljančić, Ivana
AU  - Milosavljević, Slobodan M.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1164
PB  - Pergamon-Elsevier Science Ltd, Oxford
C3  - European Journal of Cancer Supplements / EJC Supplements
T1  - Extracts from endemic plant Helichrysum zivojini suppress survival of malignant cells
VL  - 8
IS  - 5
SP  - 150
EP  - 150
DO  - 10.1016/S1359-6349(10)71390-2
ER  - 

@conference{
author = "Matic, I. and Juranić, Z. and Žižak, Željko S. and Vajs, Vlatka and Aljančić, Ivana and Milosavljević, Slobodan M.",
year = "2010",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "European Journal of Cancer Supplements / EJC Supplements",
title = "Extracts from endemic plant Helichrysum zivojini suppress survival of malignant cells",
volume = "8",
number = "5",
pages = "150-150",
doi = "10.1016/S1359-6349(10)71390-2"
}

Matic, I., Juranić, Z., Žižak, Ž. S., Vajs, V., Aljančić, I.,& Milosavljević, S. M.. (2010). Extracts from endemic plant Helichrysum zivojini suppress survival of malignant cells. in European Journal of Cancer Supplements / EJC Supplements
Pergamon-Elsevier Science Ltd, Oxford., 8(5), 150-150.
https://doi.org/10.1016/S1359-6349(10)71390-2

Matic I, Juranić Z, Žižak ŽS, Vajs V, Aljančić I, Milosavljević SM. Extracts from endemic plant Helichrysum zivojini suppress survival of malignant cells. in European Journal of Cancer Supplements / EJC Supplements. 2010;8(5):150-150.
doi:10.1016/S1359-6349(10)71390-2 .

Matic, I., Juranić, Z., Žižak, Željko S., Vajs, Vlatka, Aljančić, Ivana, Milosavljević, Slobodan M., "Extracts from endemic plant Helichrysum zivojini suppress survival of malignant cells" in European Journal of Cancer Supplements / EJC Supplements, 8, no. 5 (2010):150-150,
https://doi.org/10.1016/S1359-6349(10)71390-2 . .

TY  - CONF
AU  - Žižak, Željko S.
AU  - Juranić, Z.
AU  - Opsenica, Dejan M.
AU  - Šolaja, Bogdan A.
AU  - Besu, I.
PY  - 2010
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1163
PB  - Pergamon-Elsevier Science Ltd, Oxford
C3  - European Journal of Cancer Supplements / EJC Supplements
T1  - Tetraoxanes induced ROS production and activation of caspase 3 in HeLa cells
VL  - 8
IS  - 5
SP  - 131
EP  - 131
DO  - 10.1016/S1359-6349(10)71313-6
ER  - 

@conference{
author = "Žižak, Željko S. and Juranić, Z. and Opsenica, Dejan M. and Šolaja, Bogdan A. and Besu, I.",
year = "2010",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "European Journal of Cancer Supplements / EJC Supplements",
title = "Tetraoxanes induced ROS production and activation of caspase 3 in HeLa cells",
volume = "8",
number = "5",
pages = "131-131",
doi = "10.1016/S1359-6349(10)71313-6"
}

Žižak, Ž. S., Juranić, Z., Opsenica, D. M., Šolaja, B. A.,& Besu, I.. (2010). Tetraoxanes induced ROS production and activation of caspase 3 in HeLa cells. in European Journal of Cancer Supplements / EJC Supplements
Pergamon-Elsevier Science Ltd, Oxford., 8(5), 131-131.
https://doi.org/10.1016/S1359-6349(10)71313-6

Žižak ŽS, Juranić Z, Opsenica DM, Šolaja BA, Besu I. Tetraoxanes induced ROS production and activation of caspase 3 in HeLa cells. in European Journal of Cancer Supplements / EJC Supplements. 2010;8(5):131-131.
doi:10.1016/S1359-6349(10)71313-6 .

Žižak, Željko S., Juranić, Z., Opsenica, Dejan M., Šolaja, Bogdan A., Besu, I., "Tetraoxanes induced ROS production and activation of caspase 3 in HeLa cells" in European Journal of Cancer Supplements / EJC Supplements, 8, no. 5 (2010):131-131,
https://doi.org/10.1016/S1359-6349(10)71313-6 . .

TY  - CONF
AU  - Žižak, Željko S.
AU  - Opsenica, Dejan M.
AU  - Šolaja, Bogdan A.
AU  - Juranić, Z.
PY  - 2007
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/884
PB  - Pergamon-Elsevier Science Ltd, Oxford
C3  - European Journal of Cancer Supplements / EJC Supplements
T1  - Investigation of some tetraoxanes as potential antitumour agents
VL  - 5
IS  - 4
SP  - 89
EP  - 89
DO  - 10.1016/S1359-6349(07)70436-6
ER  - 

@conference{
author = "Žižak, Željko S. and Opsenica, Dejan M. and Šolaja, Bogdan A. and Juranić, Z.",
year = "2007",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "European Journal of Cancer Supplements / EJC Supplements",
title = "Investigation of some tetraoxanes as potential antitumour agents",
volume = "5",
number = "4",
pages = "89-89",
doi = "10.1016/S1359-6349(07)70436-6"
}

Žižak, Ž. S., Opsenica, D. M., Šolaja, B. A.,& Juranić, Z.. (2007). Investigation of some tetraoxanes as potential antitumour agents. in European Journal of Cancer Supplements / EJC Supplements
Pergamon-Elsevier Science Ltd, Oxford., 5(4), 89-89.
https://doi.org/10.1016/S1359-6349(07)70436-6

Žižak ŽS, Opsenica DM, Šolaja BA, Juranić Z. Investigation of some tetraoxanes as potential antitumour agents. in European Journal of Cancer Supplements / EJC Supplements. 2007;5(4):89-89.
doi:10.1016/S1359-6349(07)70436-6 .

Žižak, Željko S., Opsenica, Dejan M., Šolaja, Bogdan A., Juranić, Z., "Investigation of some tetraoxanes as potential antitumour agents" in European Journal of Cancer Supplements / EJC Supplements, 5, no. 4 (2007):89-89,
https://doi.org/10.1016/S1359-6349(07)70436-6 . .

TY  - JOUR
AU  - Milić, Dragana
AU  - Kop, Tatjana
AU  - Juranić, Z.
AU  - Gasic, MJ
AU  - Tinant, B
AU  - Pocsfalvi, G
AU  - Šolaja, Bogdan A.
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/748
AB  - A simple approach to aromatization of steroidal quinols and epoxyquinols using a catalytic amount of TMSOTf is reported. Beside acetylation of the angular OH, the acid-catalyzed (TfOH) dienone-phenol rearrangement occurred affording "para" products, or in the case of blocked position 4, the acetoxy group 1,2-migration leads to the formation of "meta" products. Using epoxyquinol derivative as a substrate, the acetoxy group elimination was observed, followed by acid-catalyzed epoxy-ring opening and subsequent double bond migration, giving as a final product Delta(9,11) A-ring aromatized compounds. Synthesis of conduritol-like compounds and structure confirmation by X-ray crystallography of the precursor of steroidal conduritol is also described. In addition, the results of extensive antiproliferative screening against a panel of 60 cancer cell lines are presented. (c) 2005 Elsevier Inc. All rights reserved.
PB  - Elsevier Science Inc, New York
T2  - Steroids
T1  - Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds
VL  - 70
IS  - 14
SP  - 922
EP  - 932
DO  - 10.1016/j.steroids.2005.07.001
ER  - 

@article{
author = "Milić, Dragana and Kop, Tatjana and Juranić, Z. and Gasic, MJ and Tinant, B and Pocsfalvi, G and Šolaja, Bogdan A.",
year = "2005",
abstract = "A simple approach to aromatization of steroidal quinols and epoxyquinols using a catalytic amount of TMSOTf is reported. Beside acetylation of the angular OH, the acid-catalyzed (TfOH) dienone-phenol rearrangement occurred affording "para" products, or in the case of blocked position 4, the acetoxy group 1,2-migration leads to the formation of "meta" products. Using epoxyquinol derivative as a substrate, the acetoxy group elimination was observed, followed by acid-catalyzed epoxy-ring opening and subsequent double bond migration, giving as a final product Delta(9,11) A-ring aromatized compounds. Synthesis of conduritol-like compounds and structure confirmation by X-ray crystallography of the precursor of steroidal conduritol is also described. In addition, the results of extensive antiproliferative screening against a panel of 60 cancer cell lines are presented. (c) 2005 Elsevier Inc. All rights reserved.",
publisher = "Elsevier Science Inc, New York",
journal = "Steroids",
title = "Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds",
volume = "70",
number = "14",
pages = "922-932",
doi = "10.1016/j.steroids.2005.07.001"
}

Milić, D., Kop, T., Juranić, Z., Gasic, M., Tinant, B., Pocsfalvi, G.,& Šolaja, B. A.. (2005). Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds. in Steroids
Elsevier Science Inc, New York., 70(14), 922-932.
https://doi.org/10.1016/j.steroids.2005.07.001

Milić D, Kop T, Juranić Z, Gasic M, Tinant B, Pocsfalvi G, Šolaja BA. Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds. in Steroids. 2005;70(14):922-932.
doi:10.1016/j.steroids.2005.07.001 .

Milić, Dragana, Kop, Tatjana, Juranić, Z., Gasic, MJ, Tinant, B, Pocsfalvi, G, Šolaja, Bogdan A., "Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds" in Steroids, 70, no. 14 (2005):922-932,
https://doi.org/10.1016/j.steroids.2005.07.001 . .

TY  - CONF
AU  - Žižak, Željko S.
AU  - Kop, Tatjana
AU  - Šolaja, Bogdan A.
AU  - Stanojković, Tatjana
AU  - Juranić, Z.
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/844
PB  - Pergamon-Elsevier Science Ltd, Oxford
C3  - European Journal of Cancer Supplements / EJC Supplements
T1  - Investigation of some quinols and epoxyquinols as potential antitumor agents
VL  - 3
IS  - 2
SP  - 63
EP  - 63
UR  - https://hdl.handle.net/21.15107/rcub_cherry_844
ER  - 

@conference{
author = "Žižak, Željko S. and Kop, Tatjana and Šolaja, Bogdan A. and Stanojković, Tatjana and Juranić, Z.",
year = "2005",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "European Journal of Cancer Supplements / EJC Supplements",
title = "Investigation of some quinols and epoxyquinols as potential antitumor agents",
volume = "3",
number = "2",
pages = "63-63",
url = "https://hdl.handle.net/21.15107/rcub_cherry_844"
}

Žižak, Ž. S., Kop, T., Šolaja, B. A., Stanojković, T.,& Juranić, Z.. (2005). Investigation of some quinols and epoxyquinols as potential antitumor agents. in European Journal of Cancer Supplements / EJC Supplements
Pergamon-Elsevier Science Ltd, Oxford., 3(2), 63-63.
https://hdl.handle.net/21.15107/rcub_cherry_844

Žižak ŽS, Kop T, Šolaja BA, Stanojković T, Juranić Z. Investigation of some quinols and epoxyquinols as potential antitumor agents. in European Journal of Cancer Supplements / EJC Supplements. 2005;3(2):63-63.
https://hdl.handle.net/21.15107/rcub_cherry_844 .

Žižak, Željko S., Kop, Tatjana, Šolaja, Bogdan A., Stanojković, Tatjana, Juranić, Z., "Investigation of some quinols and epoxyquinols as potential antitumor agents" in European Journal of Cancer Supplements / EJC Supplements, 3, no. 2 (2005):63-63,
https://hdl.handle.net/21.15107/rcub_cherry_844 .

TY  - JOUR
AU  - Opsenica, Dejan M.
AU  - Angelovski, G
AU  - Pocsfalvi, G
AU  - Juranić, Z.
AU  - Žižak, Željko S.
AU  - Kyle, D
AU  - Milhous, WK
AU  - Šolaja, Bogdan A.
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/559
AB  - Several cis and trans bis-steroidal 1,2,4,5-tetraoxanes possessing amide terminus were synthesised and evaluated as antimalarials and antiproliferatives. The compounds exhibited submicromolar antimalarial activity against Plasmodium falciparum D6 and W2 strains. The existence of HN-C(O) moiety was found necessary for pronounced antimalarial and antiproliferative activity. In antiproliferative screen, the trans tetraoxane 6 was found to exhibit a pronounced cytotoxicity on 14 cancer cell lines. In addition, tetraoxanes 11 and 12 exhibited significant cytotoxic activity too; microscopic examination of treated HeLa cells showed morphological appearance reminiscent for apoptosis (condensed and/or fragmented nuclei). (C) 2003 Elsevier Science Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Bioorganic and Medicinal Chemistry
T1  - Antimalarial and antiproliferative evaluation of bis-steroidal tetraoxanes
VL  - 11
IS  - 13
SP  - 2761
EP  - 2768
DO  - 10.1016/S0968-0896(03)00224-4
ER  - 

@article{
author = "Opsenica, Dejan M. and Angelovski, G and Pocsfalvi, G and Juranić, Z. and Žižak, Željko S. and Kyle, D and Milhous, WK and Šolaja, Bogdan A.",
year = "2003",
abstract = "Several cis and trans bis-steroidal 1,2,4,5-tetraoxanes possessing amide terminus were synthesised and evaluated as antimalarials and antiproliferatives. The compounds exhibited submicromolar antimalarial activity against Plasmodium falciparum D6 and W2 strains. The existence of HN-C(O) moiety was found necessary for pronounced antimalarial and antiproliferative activity. In antiproliferative screen, the trans tetraoxane 6 was found to exhibit a pronounced cytotoxicity on 14 cancer cell lines. In addition, tetraoxanes 11 and 12 exhibited significant cytotoxic activity too; microscopic examination of treated HeLa cells showed morphological appearance reminiscent for apoptosis (condensed and/or fragmented nuclei). (C) 2003 Elsevier Science Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Bioorganic and Medicinal Chemistry",
title = "Antimalarial and antiproliferative evaluation of bis-steroidal tetraoxanes",
volume = "11",
number = "13",
pages = "2761-2768",
doi = "10.1016/S0968-0896(03)00224-4"
}

Opsenica, D. M., Angelovski, G., Pocsfalvi, G., Juranić, Z., Žižak, Ž. S., Kyle, D., Milhous, W.,& Šolaja, B. A.. (2003). Antimalarial and antiproliferative evaluation of bis-steroidal tetraoxanes. in Bioorganic and Medicinal Chemistry
Pergamon-Elsevier Science Ltd, Oxford., 11(13), 2761-2768.
https://doi.org/10.1016/S0968-0896(03)00224-4

Opsenica DM, Angelovski G, Pocsfalvi G, Juranić Z, Žižak ŽS, Kyle D, Milhous W, Šolaja BA. Antimalarial and antiproliferative evaluation of bis-steroidal tetraoxanes. in Bioorganic and Medicinal Chemistry. 2003;11(13):2761-2768.
doi:10.1016/S0968-0896(03)00224-4 .

Opsenica, Dejan M., Angelovski, G, Pocsfalvi, G, Juranić, Z., Žižak, Željko S., Kyle, D, Milhous, WK, Šolaja, Bogdan A., "Antimalarial and antiproliferative evaluation of bis-steroidal tetraoxanes" in Bioorganic and Medicinal Chemistry, 11, no. 13 (2003):2761-2768,
https://doi.org/10.1016/S0968-0896(03)00224-4 . .

TY  - JOUR
AU  - Pajic, I
AU  - Kljajic, Z
AU  - Dogovic, N
AU  - Sladić, Dušan
AU  - Juranić, Z.
AU  - Gasic, MJ
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/501
AB  - A lectin from the Adriatic sponge Haliclona cratera was purified by ion-exchange and gel chromatography The molecular mass of the lectin is approximately 29 kDa. Purified lectin is rich in hydrophobic and basic amino acids and has an isoelectric point at pH 8.6. H. cratera lectin is relatively heat- and pH-stable. It agglutinates native and trypsinized, papainized and neuraminidase-treated human A, B, O, AB and sheep erythrocytes, and the hemagglutinating activity is independent of Ca2+, Mn2+ and Mg2+ ions; D-galactose and N-acetyl-D-galactosamine are found to be moderate inhibitors of the activity. H. cratera lectin displays cytotoxic effect on HeLa and FemX cells and weak mitogenic effect on human T-lymphocytes pretreated with phytohemagglutinin (PHA). (C) 2002 Elsevier Science Inc. All rights reserved.
PB  - Elsevier Science Inc, New York
T2  - Comparative Biochemistry and Physiology. C: Toxicology and Pharmacology
T1  - A novel lectin from the sponge Haliclona cratera: isolation, characterization and biological activity
VL  - 132
IS  - 2
SP  - 213
EP  - 221
DO  - 10.1016/S1532-0456(02)00068-6
ER  - 

@article{
author = "Pajic, I and Kljajic, Z and Dogovic, N and Sladić, Dušan and Juranić, Z. and Gasic, MJ",
year = "2002",
abstract = "A lectin from the Adriatic sponge Haliclona cratera was purified by ion-exchange and gel chromatography The molecular mass of the lectin is approximately 29 kDa. Purified lectin is rich in hydrophobic and basic amino acids and has an isoelectric point at pH 8.6. H. cratera lectin is relatively heat- and pH-stable. It agglutinates native and trypsinized, papainized and neuraminidase-treated human A, B, O, AB and sheep erythrocytes, and the hemagglutinating activity is independent of Ca2+, Mn2+ and Mg2+ ions; D-galactose and N-acetyl-D-galactosamine are found to be moderate inhibitors of the activity. H. cratera lectin displays cytotoxic effect on HeLa and FemX cells and weak mitogenic effect on human T-lymphocytes pretreated with phytohemagglutinin (PHA). (C) 2002 Elsevier Science Inc. All rights reserved.",
publisher = "Elsevier Science Inc, New York",
journal = "Comparative Biochemistry and Physiology. C: Toxicology and Pharmacology",
title = "A novel lectin from the sponge Haliclona cratera: isolation, characterization and biological activity",
volume = "132",
number = "2",
pages = "213-221",
doi = "10.1016/S1532-0456(02)00068-6"
}

Pajic, I., Kljajic, Z., Dogovic, N., Sladić, D., Juranić, Z.,& Gasic, M.. (2002). A novel lectin from the sponge Haliclona cratera: isolation, characterization and biological activity. in Comparative Biochemistry and Physiology. C: Toxicology and Pharmacology
Elsevier Science Inc, New York., 132(2), 213-221.
https://doi.org/10.1016/S1532-0456(02)00068-6

Pajic I, Kljajic Z, Dogovic N, Sladić D, Juranić Z, Gasic M. A novel lectin from the sponge Haliclona cratera: isolation, characterization and biological activity. in Comparative Biochemistry and Physiology. C: Toxicology and Pharmacology. 2002;132(2):213-221.
doi:10.1016/S1532-0456(02)00068-6 .

Pajic, I, Kljajic, Z, Dogovic, N, Sladić, Dušan, Juranić, Z., Gasic, MJ, "A novel lectin from the sponge Haliclona cratera: isolation, characterization and biological activity" in Comparative Biochemistry and Physiology. C: Toxicology and Pharmacology, 132, no. 2 (2002):213-221,
https://doi.org/10.1016/S1532-0456(02)00068-6 . .

TY  - JOUR
AU  - Aranđelović, Sandra
AU  - Tešić, Živoslav Lj.
AU  - Juranić, Z.
AU  - Radulović, Siniša
AU  - Vrvić, Miroslav M.
AU  - Potkonjak, B
AU  - Ilic, Z
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/540
AB  - Purpose of this work was to synthesize several cis-/trans- isomer pairs of the platinum(II) complexes, and study the extent and the mode of their antiproliferative activity on HeLa cells. Six platinum(II) isomer pairs have a general formula cis-/trans-[PtA(2) X-2] where A is ligand: ammonia (NH3), pyridine (Py); and X is ligand: chloride ion (Cl-), bromide ion (Br-), iodide ion (I-), thiocyanato, ion (SCN-); four compounds have different structural formulas, and these are cis-/trans-[Pt(NH2OH)(2) (NH3)(2)]Cl-2, and cis-/trans- Pt(Gly)(2), where Gly is bidentate glycinato ligand. Results of the MTT assay, showed that six cis- and one trans-platinum(II) complexes exhibited cytotoxicity (IC50) ranging between 5 and 33 muM. Most of the cis-platinum(II) isomers caused significant alteration of cell cycle phases progression, and induced apoptosis in degree that varied among different compounds, as evaluated using flowcytometry and morphological study. Spectrophotometric analysis (AAS) indicated that there is no correlation between intracellular platinum(II) accumulation and cytotoxicity of tested complexes.
PB  - Bmc, London
T2  - Journal of Experimental and Clinical Cancer Research
T1  - Antiproliferative activity of some cis-/trans-platinum(II) complexes on HeLa cells
VL  - 21
IS  - 4
SP  - 519
EP  - 526
UR  - https://hdl.handle.net/21.15107/rcub_cherry_540
ER  - 

@article{
author = "Aranđelović, Sandra and Tešić, Živoslav Lj. and Juranić, Z. and Radulović, Siniša and Vrvić, Miroslav M. and Potkonjak, B and Ilic, Z",
year = "2002",
abstract = "Purpose of this work was to synthesize several cis-/trans- isomer pairs of the platinum(II) complexes, and study the extent and the mode of their antiproliferative activity on HeLa cells. Six platinum(II) isomer pairs have a general formula cis-/trans-[PtA(2) X-2] where A is ligand: ammonia (NH3), pyridine (Py); and X is ligand: chloride ion (Cl-), bromide ion (Br-), iodide ion (I-), thiocyanato, ion (SCN-); four compounds have different structural formulas, and these are cis-/trans-[Pt(NH2OH)(2) (NH3)(2)]Cl-2, and cis-/trans- Pt(Gly)(2), where Gly is bidentate glycinato ligand. Results of the MTT assay, showed that six cis- and one trans-platinum(II) complexes exhibited cytotoxicity (IC50) ranging between 5 and 33 muM. Most of the cis-platinum(II) isomers caused significant alteration of cell cycle phases progression, and induced apoptosis in degree that varied among different compounds, as evaluated using flowcytometry and morphological study. Spectrophotometric analysis (AAS) indicated that there is no correlation between intracellular platinum(II) accumulation and cytotoxicity of tested complexes.",
publisher = "Bmc, London",
journal = "Journal of Experimental and Clinical Cancer Research",
title = "Antiproliferative activity of some cis-/trans-platinum(II) complexes on HeLa cells",
volume = "21",
number = "4",
pages = "519-526",
url = "https://hdl.handle.net/21.15107/rcub_cherry_540"
}

Aranđelović, S., Tešić, Ž. Lj., Juranić, Z., Radulović, S., Vrvić, M. M., Potkonjak, B.,& Ilic, Z.. (2002). Antiproliferative activity of some cis-/trans-platinum(II) complexes on HeLa cells. in Journal of Experimental and Clinical Cancer Research
Bmc, London., 21(4), 519-526.
https://hdl.handle.net/21.15107/rcub_cherry_540

Aranđelović S, Tešić ŽL, Juranić Z, Radulović S, Vrvić MM, Potkonjak B, Ilic Z. Antiproliferative activity of some cis-/trans-platinum(II) complexes on HeLa cells. in Journal of Experimental and Clinical Cancer Research. 2002;21(4):519-526.
https://hdl.handle.net/21.15107/rcub_cherry_540 .

Aranđelović, Sandra, Tešić, Živoslav Lj., Juranić, Z., Radulović, Siniša, Vrvić, Miroslav M., Potkonjak, B, Ilic, Z, "Antiproliferative activity of some cis-/trans-platinum(II) complexes on HeLa cells" in Journal of Experimental and Clinical Cancer Research, 21, no. 4 (2002):519-526,
https://hdl.handle.net/21.15107/rcub_cherry_540 .

TY  - JOUR
AU  - Milić, Dragana
AU  - Kop, Tatjana
AU  - Juranić, Z.
AU  - Gasic, MJ
AU  - Šolaja, Bogdan A.
PY  - 2001
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/468
AB  - Based on biological properties of epoxyquinols from natural sources, bromo and epoxyquinols derived from estrone were synthesized and screened against Fem-X. HeLa and K-562 cell lines. Evidence was found that the bromine atom and the epoxy moiety significantly increase the antiproliferative activity within the series. (C) 2001 Elsevier Science Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Bioorganic and Medicinal Chemistry Letters
T1  - Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone
VL  - 11
IS  - 16
SP  - 2197
EP  - 2200
DO  - 10.1016/S0960-894X(01)00402-4
ER  - 

@article{
author = "Milić, Dragana and Kop, Tatjana and Juranić, Z. and Gasic, MJ and Šolaja, Bogdan A.",
year = "2001",
abstract = "Based on biological properties of epoxyquinols from natural sources, bromo and epoxyquinols derived from estrone were synthesized and screened against Fem-X. HeLa and K-562 cell lines. Evidence was found that the bromine atom and the epoxy moiety significantly increase the antiproliferative activity within the series. (C) 2001 Elsevier Science Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Bioorganic and Medicinal Chemistry Letters",
title = "Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone",
volume = "11",
number = "16",
pages = "2197-2200",
doi = "10.1016/S0960-894X(01)00402-4"
}

Milić, D., Kop, T., Juranić, Z., Gasic, M.,& Šolaja, B. A.. (2001). Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone. in Bioorganic and Medicinal Chemistry Letters
Pergamon-Elsevier Science Ltd, Oxford., 11(16), 2197-2200.
https://doi.org/10.1016/S0960-894X(01)00402-4

Milić D, Kop T, Juranić Z, Gasic M, Šolaja BA. Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone. in Bioorganic and Medicinal Chemistry Letters. 2001;11(16):2197-2200.
doi:10.1016/S0960-894X(01)00402-4 .

Milić, Dragana, Kop, Tatjana, Juranić, Z., Gasic, MJ, Šolaja, Bogdan A., "Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone" in Bioorganic and Medicinal Chemistry Letters, 11, no. 16 (2001):2197-2200,
https://doi.org/10.1016/S0960-894X(01)00402-4 . .

TY  - JOUR
AU  - Opsenica, Dejan M.
AU  - Pocsfalvi, G
AU  - Juranić, Z.
AU  - Tinant, B
AU  - Declercq, JP
AU  - Kyle, DE
AU  - Milhous, WK
AU  - Šolaja, Bogdan A.
PY  - 2000
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/441
AB  - Cholic acid-derived 1,2,4,5-tetraoxanes were synthesized in order to explore the influence of steroid carrier on its antimalarial and antiproliferative activity in vitro. Starting with chiral ketones, cis and trans series of diastereomeric tetraoxanes were obtained, and the cis series was found to be similar to 2 times as active as the trans against Plasmodium falciparum DG and W2 clones. The same tendency was observed against human melanoma (Fem-X) and human cervix carcinoma (HeLa) cell lines. The amide C(24) termini, for the first time introduced into the carrier molecule of a tetraoxane pharmacophore, significantly enhanced both antimalarial and antiproliferative activity, as compared to the corresponding methyl esters, with cis-bis(N-propylamide) being most efficient against the chloroquine-susceptible D6 clone (IC50 = 9.29 nM). cis- and trans-bis(N-propylamides) were also screened against PBMC, and PRA-stimulated PBMC, showing a cytotoxicity/antimalarial potency ratio of 1/10 000.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Medicinal Chemistry
T1  - Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity
VL  - 43
IS  - 17
SP  - 3274
EP  - 3282
DO  - 10.1021/jm000952f
ER  - 

@article{
author = "Opsenica, Dejan M. and Pocsfalvi, G and Juranić, Z. and Tinant, B and Declercq, JP and Kyle, DE and Milhous, WK and Šolaja, Bogdan A.",
year = "2000",
abstract = "Cholic acid-derived 1,2,4,5-tetraoxanes were synthesized in order to explore the influence of steroid carrier on its antimalarial and antiproliferative activity in vitro. Starting with chiral ketones, cis and trans series of diastereomeric tetraoxanes were obtained, and the cis series was found to be similar to 2 times as active as the trans against Plasmodium falciparum DG and W2 clones. The same tendency was observed against human melanoma (Fem-X) and human cervix carcinoma (HeLa) cell lines. The amide C(24) termini, for the first time introduced into the carrier molecule of a tetraoxane pharmacophore, significantly enhanced both antimalarial and antiproliferative activity, as compared to the corresponding methyl esters, with cis-bis(N-propylamide) being most efficient against the chloroquine-susceptible D6 clone (IC50 = 9.29 nM). cis- and trans-bis(N-propylamides) were also screened against PBMC, and PRA-stimulated PBMC, showing a cytotoxicity/antimalarial potency ratio of 1/10 000.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Medicinal Chemistry",
title = "Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity",
volume = "43",
number = "17",
pages = "3274-3282",
doi = "10.1021/jm000952f"
}

Opsenica, D. M., Pocsfalvi, G., Juranić, Z., Tinant, B., Declercq, J., Kyle, D., Milhous, W.,& Šolaja, B. A.. (2000). Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity. in Journal of Medicinal Chemistry
Amer Chemical Soc, Washington., 43(17), 3274-3282.
https://doi.org/10.1021/jm000952f

Opsenica DM, Pocsfalvi G, Juranić Z, Tinant B, Declercq J, Kyle D, Milhous W, Šolaja BA. Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity. in Journal of Medicinal Chemistry. 2000;43(17):3274-3282.
doi:10.1021/jm000952f .

Opsenica, Dejan M., Pocsfalvi, G, Juranić, Z., Tinant, B, Declercq, JP, Kyle, DE, Milhous, WK, Šolaja, Bogdan A., "Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity" in Journal of Medicinal Chemistry, 43, no. 17 (2000):3274-3282,
https://doi.org/10.1021/jm000952f . .

TY  - JOUR
AU  - Milić, Dragana
AU  - Kapor, A
AU  - Markov, B
AU  - Ribar, B
AU  - Strumpel, M
AU  - Juranić, Z.
AU  - Gasic, MJ
AU  - Šolaja, Bogdan A.
PY  - 1999
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/426
AB  - Based on the biological properties of epoxyquinols from natural sources, the title compound was synthesised as a potential antitumor agent. Its molecular structure was partially confirmed by NMR studies. The detailed structure was established by X-ray analysis revealing two symmetry independent molecules in the asymmetric unit each consisting of four fused rings with the C(10) beta-oriented hydroxy group and beta-oriented O atom bridging C(4) and C(5). The conformation of A ring in both conformers A and B is boat (B-3,B-6), while rings B and C are chairs (C-1(4)) and the five-membered D ring is in an envelope (E-2) conformation. The in vitro antitumor activity of title compound and its 17 beta-acetoxy analogue against HeLa and Fem-x cells revealed IC50 values of 5.7 and 7.1 mu M, and 2.25 and 1.58 mu M, respectively. Corresponding quinols were tested on 47 cell lines with 10 beta-hydroxy-17 beta-acetoxyestra-1,4-dien-3-one being most active against leukemia SR cells (GI(50) = 0.17 mu M).
PB  - Mdpi Ag, Basel
T2  - Molecules
T1  - X-ray crystal structure of 10 beta-hydroxy-4 beta,5 beta P-epoxyestr-1-en-3,17-dione and antitumor activity of its congeners
VL  - 4
IS  - 12
SP  - 338
EP  - 352
DO  - 10.3390/41200338
ER  - 

@article{
author = "Milić, Dragana and Kapor, A and Markov, B and Ribar, B and Strumpel, M and Juranić, Z. and Gasic, MJ and Šolaja, Bogdan A.",
year = "1999",
abstract = "Based on the biological properties of epoxyquinols from natural sources, the title compound was synthesised as a potential antitumor agent. Its molecular structure was partially confirmed by NMR studies. The detailed structure was established by X-ray analysis revealing two symmetry independent molecules in the asymmetric unit each consisting of four fused rings with the C(10) beta-oriented hydroxy group and beta-oriented O atom bridging C(4) and C(5). The conformation of A ring in both conformers A and B is boat (B-3,B-6), while rings B and C are chairs (C-1(4)) and the five-membered D ring is in an envelope (E-2) conformation. The in vitro antitumor activity of title compound and its 17 beta-acetoxy analogue against HeLa and Fem-x cells revealed IC50 values of 5.7 and 7.1 mu M, and 2.25 and 1.58 mu M, respectively. Corresponding quinols were tested on 47 cell lines with 10 beta-hydroxy-17 beta-acetoxyestra-1,4-dien-3-one being most active against leukemia SR cells (GI(50) = 0.17 mu M).",
publisher = "Mdpi Ag, Basel",
journal = "Molecules",
title = "X-ray crystal structure of 10 beta-hydroxy-4 beta,5 beta P-epoxyestr-1-en-3,17-dione and antitumor activity of its congeners",
volume = "4",
number = "12",
pages = "338-352",
doi = "10.3390/41200338"
}

Milić, D., Kapor, A., Markov, B., Ribar, B., Strumpel, M., Juranić, Z., Gasic, M.,& Šolaja, B. A.. (1999). X-ray crystal structure of 10 beta-hydroxy-4 beta,5 beta P-epoxyestr-1-en-3,17-dione and antitumor activity of its congeners. in Molecules
Mdpi Ag, Basel., 4(12), 338-352.
https://doi.org/10.3390/41200338

Milić D, Kapor A, Markov B, Ribar B, Strumpel M, Juranić Z, Gasic M, Šolaja BA. X-ray crystal structure of 10 beta-hydroxy-4 beta,5 beta P-epoxyestr-1-en-3,17-dione and antitumor activity of its congeners. in Molecules. 1999;4(12):338-352.
doi:10.3390/41200338 .

Milić, Dragana, Kapor, A, Markov, B, Ribar, B, Strumpel, M, Juranić, Z., Gasic, MJ, Šolaja, Bogdan A., "X-ray crystal structure of 10 beta-hydroxy-4 beta,5 beta P-epoxyestr-1-en-3,17-dione and antitumor activity of its congeners" in Molecules, 4, no. 12 (1999):338-352,
https://doi.org/10.3390/41200338 . .