{"personrec":{"StatusID":1,"PersStatus":null,"Status":"Valid","PersID":34845,"PersName":"Kiss, Robert","PublicFlag":1,"CheckedFlag":0,"Surname":"Kiss","Firstname":"Robert","Initials":"R.","AddressedAs":null,"Function":null,"DateLastModified":{"date":"2023-05-02 10:08:18.393000","timezone_type":1,"timezone":"+00:00"},"PersTitle":null,"PersStatusID":null,"AbstractEnglish":null,"AbstractOtherLang":null,"AbstractLangCode":null,"AbstractLangID":null,"AutID":178188,"ND":"2017-06-14","UD":"2017-06-14"},"loaninfo":null,"pictures":[],"institutes":[{"instituterec":{"OrderNr":1,"Acronym":"LCTE","ENFunction":null,"InsIDtmp":13950,"OrigNameLangCode":null,"OrigNameLangID":null,"FullOrigName":null,"InsID":13950,"Function":null,"BeginDay":null,"BeginMonth":null,"BeginYear":null,"Begindate":"","Enddate":"","PIAdrID":null,"AdrID":160126,"Line1":"Campus de la Plaine","Line2":"ULB CP205/01, boulevard du Triomphe","Line3":"1050 Bruxelles","Line4":null,"Phone":null,"GSM":null,"Email":null,"EnvName":"Belgium","EncAddress":"Campus de la Plaine, ULB CP205/01, boulevard du Triomphe, 1050 Bruxelles, Belgium","FullStandardName":"Université Libre de Bruxelles; Laboratoire de Cancérologie et Toxicologie Expérimentale","DirectorFlag":null,"MarineSciFlag":null,"SpecializedFlag":null},"parent":null,"institutes":null,"references":null,"conferences":null,"datasets":null,"persons":null,"pastpers":null,"subpers":null,"projects":null,"urls":null,"pictures":null,"published":null,"affrefs":null,"collections":null,"thesterms":null,"taxterms":null,"geoterms":null,"thestermsFRIS":null,"nXtins":null,"previns":null,"spcols":null,"resmessage":"no id specified","complete":0,"participantrec":null,"peerrevs":null,"urlmaps":null}],"pastins":[],"projects":[],"datasets":null,"references":{"A1":[{"BRefID":324955,"RR":"<b>Ciavatta, M.L.; Lefranc, F.; Vieira, L.M.; Kiss, R.; Carbone, M.; van Otterlo, W.A.L.; Lopanik, N.B.; Waeschenbach, A.</b> (2020). The phylum Bryozoa: from biology to biomedical potential. <i>Mar. Drugs 18(4)</i>: 200. <a href=\"https://dx.doi.org/10.3390/md18040200\" target=\"_blank\">https://dx.doi.org/10.3390/md18040200</a>","AutID":241593,"MonDate":null,"AnaDate":2020,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":322783,"RR":"<b>Smyrniotopoulos, V.; de Andrade Tomaz, A.C.; de Souza, M.F.V.; da Cunha, E.L.; Kiss, R.; Mathieu, V.; Ioannou, E.; Roussis, V.</b> (2020). Halogenated diterpenes with in vitro antitumor activity from the red alga <i>Sphaerococcus coronopifolius</i>. <i>Mar. Drugs 18(1)</i>: 29. <a href=\"https://dx.doi.org/10.3390/md18010029\" target=\"_blank\">https://dx.doi.org/10.3390/md18010029</a>","AutID":241593,"MonDate":null,"AnaDate":2020,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":304598,"RR":"<b>Lefranc, F.; Koutsaviti, A.; Ioannou, E.; Kornienko, A.; Roussis, V.; Kiss, R.; Newman, D.</b> (2019). Algae metabolites: from in vitro growth inhibitory effects to promising anticancer activity. <i>Nat. Prod. Rep. 36(5)</i>: 810-841. <a href=\"https://dx.doi.org/10.1039/c8np00057c\" target=\"_blank\">https://dx.doi.org/10.1039/c8np00057c</a>","AutID":241593,"MonDate":null,"AnaDate":2019,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":293734,"RR":"<b>Carbone, M.; Ciavatta, M.L.; Mathieu, V.; Ingels, A.; Kiss, R.; Pascale, P.; Mono, E.; Ungur, N.; Guo, Y.-W.; Gavagnin, M.</b> (2017). Marine terpenoid diacylguanidines: structure, synthesis, and biological evaluation of naturally occurring actinofide and synthetic analogues. <i>J. Nat. Prod. 80(5)</i>: 1339-1346. <a href=\"https://dx.doi.org/10.1021/acs.jnatprod.6b00941\" target=\"_blank\">https://dx.doi.org/10.1021/acs.jnatprod.6b00941</a>","AutID":259702,"MonDate":null,"AnaDate":2017,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":287080,"RR":"<b>Ciavatta, M.L.; Lefranc, F.; Carbone, M.; Mollo, E.; Gavagnin, M.; Betancourt, T.; Dasari, R.; Kornienko, A.; Kiss, R.</b> (2017). Marine mollusk-derived agents with antiproliferative activity as promising anticancer agents to overcome chemotherapy resistance. <i>Medicinal Research Reviews 37(4)</i>: 702-801. <a href=\"https://dx.doi.org/10.1002/med.21423\" target=\"_blank\">https://dx.doi.org/10.1002/med.21423</a>","AutID":259702,"MonDate":null,"AnaDate":2017,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":256698,"RR":"<b>Ciavatta, M.; Devi, P.; Carbone, M.; Mathieu, V.; Kiss, R.; Casapullo, A.; Gavagnin, M.</b> (2016). Kahalalide F analogues from the mucous secretion of Indian sacoglossan mollusc <i>Elysia ornata</i>. <i>Tetrahedron 72(5)</i>: 625-631. <a href=\"https://dx.doi.org/10.1016/j.tet.2015.12.003\" target=\"_blank\">https://dx.doi.org/10.1016/j.tet.2015.12.003</a>","AutID":259699,"MonDate":null,"AnaDate":2016,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":285610,"RR":"<b>Gomes, N.G.M.; Dasari, R.; Chandra, S.; Kiss, R.; Kornienko, A.</b> (2016). Marine invertebrate metabolites with anticancer activities: solutions to the \"supply problem\". <i>Mar. Drugs 14(5)</i>: 98. <a href=\"https://dx.doi.org/10.3390/md14050098\" target=\"_blank\">https://dx.doi.org/10.3390/md14050098</a>","AutID":259699,"MonDate":null,"AnaDate":2016,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":285707,"RR":"<b>Kiss, R.</b> (2016). How can we improve in vitro and in vivo preclinical screening of promising marine-derived anticancer compounds? <i>International Journal of Molecular Medicine 38</i>: S9-S9","AutID":241593,"MonDate":null,"AnaDate":2016,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":285711,"RR":"<b>Romdhane, Y.B.; Elbour, M.; Carbone, M.; Ciavatta, M.L.; Gavagnin, M.; Mathieu, V.; Lefranc, F.; Ktari, L.; Ben Mustapha, K.; Boudabous, A.; Kiss, R.; Mollo, E.</b> (2016). In vitro growth inhibitory activities of natural products from irciniid sponges against cancer cells: a comparative study. <i>Biomed. Res. Int. 2016</i>: 6 pp. <a href=\"https://dx.doi.org/10.1155/2016/5318176\" target=\"_blank\">https://dx.doi.org/10.1155/2016/5318176</a>","AutID":259702,"MonDate":null,"AnaDate":2016,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":287093,"RR":"<b>Evidente, A.; Kornienko, A.; Lefranc, F.; Cimmino, A.; Dasari, R.; Evidente, M.; Mathieu, V.; Kiss, R.</b> (2015). Sesterterpenoids with anticancer activity. <i>Curr. Med. Chem. 22(30)</i>: 3502-3522. <a href=\"https://dx.doi.org/10.2174/0929867322666150821101047\" target=\"_blank\">https://dx.doi.org/10.2174/0929867322666150821101047</a>","AutID":329927,"MonDate":null,"AnaDate":2015,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":256978,"RR":"<b>Gomes, N.; Lefranc, F.; Kijjoa, A.; Kiss, R.</b> (2015). Can some marine-derived fungal metabolites become actual anticancer agents? <i>Mar. Drugs 13(6)</i>: 3950-3991. <a href=\"https://dx.doi.org/10.3390/md13063950\" target=\"_blank\">https://dx.doi.org/10.3390/md13063950</a>","AutID":259699,"MonDate":null,"AnaDate":2015,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":246721,"RR":"<b>Lavrard, H; Salvetti, B; Mathieu, V.; Rodriguez, F; Kiss, R.; Delfourne, E</b> (2015). Synthesis and in vitro antiproliferative activity of amido and amino analogues of the marine alkaloid isogranulatimide. <i>ChemMedChem 10(4)</i>: 607-609. <a href=\"https://dx.doi.org/10.1002/cmdc.201500025\" target=\"_blank\">https://dx.doi.org/10.1002/cmdc.201500025</a>","AutID":259699,"MonDate":null,"AnaDate":2015,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":280662,"RR":"<b>Smyrniotopoulos, V.; Kiss, R.; Mathieu, V.; Vagias, C.; Roussis, V.</b> (2015). Diterpenes with unprecedented skeletons from the red alga <i>Sphaerococcus coronopifolius</i>. <i>European Journal of Organic Chemistry 2015(13)</i>: 2848-2853. <a href=\"https://dx.doi.org/10.1002/ejoc.201500133\" target=\"_blank\">https://dx.doi.org/10.1002/ejoc.201500133</a>","AutID":259699,"MonDate":null,"AnaDate":2015,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":301297,"RR":"<b>Evidente, A.; Kornienko, A.; Cimmino, A.; Andolfi, A.; Lefranc, F.; Mathieu, V.; Kiss, R.</b> (2014). Fungal metabolites with anticancer activity. <i>Nat. Prod. Rep. 31(5)</i>: 617-627. <a href=\"https://dx.doi.org/10.1039/c3np70078j\" target=\"_blank\">https://dx.doi.org/10.1039/c3np70078j</a>","AutID":259702,"MonDate":null,"AnaDate":2014,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":238140,"RR":"<b>Carbone, M.; Ciavatta, M.L.; Wang, J.R.; Cirillo, I.; Mathieu, V.; Kiss, R.; Mollo, E.; Guo, Y.W.; Gavagnin, M.</b> (2013). Extending the record of bis-gamma-pyrone polypropionates from marine pulmonate mollusks. <i>J. Nat. Prod. 76(11)</i>: 2065-2073. <a href=\"https://dx.doi.org/10.1021/np400483c\" target=\"_blank\">https://dx.doi.org/10.1021/np400483c</a>","AutID":178188,"MonDate":null,"AnaDate":2013,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":257327,"RR":"<b>Frolova, L.; Magedov, I.; Romero, A.; Karki, M.; Otero, I.; Hayden, K.; Evdokimov, N.; Banuls, L.M.Y.; Rastogi, S.; Smith, W.; Lu, S.; Kiss, R.; Shuster, C.; Hamel, E.; Betancourt, T.; Rogelj, S.; Kornienko, A.</b> (2013). Exploring natural product chemistry and biology with multicomponent reactions. 5. Discovery of a novel tubulin-targeting scaffold derived from the rigidin family of marine alkaloids. <i>J. Med. Chem. 56(17)</i>: 6886-6900. <a href=\"https://dx.doi.org/10.1021/jm400711t\" target=\"_blank\">https://dx.doi.org/10.1021/jm400711t</a>","AutID":223803,"MonDate":null,"AnaDate":2013,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":247129,"RR":"<b>Lefranc, F.; Nuzzo, G; Hamdy, A; Fakhr, I; Banuls, L.M.Y.; Van Goietsenoven, G.; Villani, G; Mathieu, V.; van Soest, R; Kiss, R.; Ciavatta, L</b> (2013). <i>In vitro</i> pharmacological and toxicological effects of Norterpene Peroxides isolated from the Red Sea sponge <i>Diacarnus erythraeanus</i> on normal and cancer cells. <i>J. Nat. Prod. 76(9)</i>: 1541-1547. <a href=\"http://dx.doi.org/10.1021/np400107t\" target=\"_blank\">http://dx.doi.org/10.1021/np400107t</a>","AutID":197008,"MonDate":null,"AnaDate":2013,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":257358,"RR":"<b>Mathieu, V.; Wauthoz, N.; Lefranc, F.; Niemann, H.; Amighi, K.; Kiss, R.; Proksch, P.</b> (2013). Cyclic versus hemi-bastadins. Pleiotropic anti-cancer effects: from apoptosis to anti-angiogenic and anti-migratory effects. <i>Molecules 18(3)</i>: 3543-3561. <a href=\"http://dx.doi.org/10.3390/molecules18033543\" target=\"_blank\">http://dx.doi.org/10.3390/molecules18033543</a>","AutID":224046,"MonDate":null,"AnaDate":2013,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":257460,"RR":"<b>Deslandes, S.; Lamoral-Theys, D.; Frongia, C.; Chassaing, S.; Bruyère, C.; Lozach, O.; Meijer, L.; Ducommun, B.; Kiss, R.; Delfourne, E.</b> (2012). Synthesis and biological evaluation of analogs of the marine alkaloids granulatimide and isogranulatimide. <i>Eur. J. Med. Chem. 54</i>: 626-636. <a href=\"https://dx.doi.org/10.1016/j.ejmech.2012.06.012\" target=\"_blank\">https://dx.doi.org/10.1016/j.ejmech.2012.06.012</a>","AutID":197008,"MonDate":null,"AnaDate":2012,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":280700,"RR":"<b>Genta-Jouve, G.; Ioannou, E.; Mathieu, V.; Bruyère, C.; Lefranc, F.; Thomas, O.P.; Kiss, R.; Roussis, V.</b> (2012). Determination of the absolute configuration and evaluation of the in vitro antitumor activity of dilospirane B. <i>Phytochemistry Letters 5(4)</i>: 747-751. <a href=\"https://dx.doi.org/10.1016/j.phytol.2012.08.005\" target=\"_blank\">https://dx.doi.org/10.1016/j.phytol.2012.08.005</a>","AutID":240629,"MonDate":null,"AnaDate":2012,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":238478,"RR":"<b>Nuzzo, G.; Ciavatta, M.L.; Kiss, R.; Mathieu, V.; Leclercqz, H.; Manzo, E.; Villani, G.; Mollo, E.; Lefranc, F.; D'Souza, L.; Gavagnin, M.; Cimino, G.</b> (2012). Chemistry of the nudibranch <i>Aldisa andersoni</i>: structure and biological activity of phorbazole metabolites. <i>Mar. Drugs 10(8)</i>: 1799-1811. <a href=\"http://dx.doi.org/10.3390/md10081799\" target=\"_blank\">http://dx.doi.org/10.3390/md10081799</a>","AutID":180772,"MonDate":null,"AnaDate":2012,"PeerRev":1,"outputType":"1_A1","OpenAcc":1},{"BRefID":257585,"RR":"<b>Lamoral-Theys, D.; Fattorusso, E.; Mangoni, A.; Perinu, C.; Kiss, R.; Costantino, V.</b> (2011). Evaluation of the antiproliferative activity of diterpene isonitriles from the sponge <i>Pseudoaxinella flava</i> in apoptosis-sensitive and apoptosis-resistant cancer cell lines. <i>J. Nat. Prod. 74(10)</i>: 2299-2303. <a href=\"https://dx.doi.org/10.1021/np2005055\" target=\"_blank\">https://dx.doi.org/10.1021/np2005055</a>","AutID":197008,"MonDate":null,"AnaDate":2011,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":257838,"RR":"<b>Rives, A.; Le Calvé, B.; Delaine, T.; Legentil, L.; Kiss, R.; Delfourne, E.</b> (2010). Synthesis and antitumor evaluation of analogues of the marine pyrroloiminoquinone tsitsikammamines. <i>Eur. J. Med. Chem. 45(1)</i>: 343-351. <a href=\"http://dx.doi.org/10.1016/j.ejmech.2009.10.019\" target=\"_blank\">http://dx.doi.org/10.1016/j.ejmech.2009.10.019</a>","AutID":227260,"MonDate":null,"AnaDate":2010,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":257818,"RR":"<b>Smyrniotopoulos, V.; Vagias, C.; Bruyère, C.; Lamoral-Theys, D.; Kiss, R.; Roussis, V.</b> (2010). Structure and in vitro antitumor activity evaluation of brominated diterpenes from the red alga <i>Sphaerococcus coronopifolius</i>. <i>Bioorg. Med. Chem. 18(3)</i>: 1321-1330. <a href=\"http://dx.doi.org/10.1016/j.bmc.2009.12.025\" target=\"_blank\">http://dx.doi.org/10.1016/j.bmc.2009.12.025</a>","AutID":227260,"MonDate":null,"AnaDate":2010,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":280858,"RR":"<b>Salmoun, M.; Braekman, J.C.; Dewelle, J.; Darro, F.; Kiss, R.; De Voogd, N.J.; Van Soest, R.W.M.</b> (2007). New terpenoids from two Indonesian marine sponges. <i>Nat. Prod. Res. 21(2)</i>: 149-155. <a href=\"http://dx.doi.org/10.1080/14786410600899233\" target=\"_blank\">http://dx.doi.org/10.1080/14786410600899233</a>","AutID":243128,"MonDate":null,"AnaDate":2007,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":281031,"RR":"<b>Agami, C.; Couty, F.; Evano, G.; Darro, F.; Kiss, R.</b> (2003). Enantioselective synthesis of clavepictine analogues and evaluation of their cytotoxic activity. <i>European Journal of Organic Chemistry 2003(11)</i>: 2062-2070. <a href=\"https://dx.doi.org/10.1002/ejoc.200300057\" target=\"_blank\">https://dx.doi.org/10.1002/ejoc.200300057</a>","AutID":241593,"MonDate":null,"AnaDate":2003,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":338233,"RR":"<b>Brahic, C.; Darro, F.; Belloir, M.; Bastide, J.; Kiss, R.; Delfourne, E.</b> (2002). Synthesis and cytotoxic evaluation of analogues of the marine pyridoacridine amphimedine. <i>Bioorg. Med. Chem. 10(9)</i>: 2845-2853. <a href=\"https://hdl.handle.net/10.1016/S0968-0896(02)00148-7\" target=\"_blank\">https://hdl.handle.net/10.1016/S0968-0896(02)00148-7</a>","AutID":455623,"MonDate":null,"AnaDate":2002,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":338234,"RR":"<b>Delfourne, E.; Darro, F.; Portefaix, P.; Galaup, C.; Bayssade, S.; Bouteillé, A.; Le Corre, L.; Bastide, J.; Collignon, F.; Lesur, B.; Frydman, A.; Kiss, R.</b> (2002). Synthesis and in vitro antitumor activity of novel ring D analogues of the marine pyridoacridine asicididemin: structure-activity relationship. <i>J. Med. Chem. 45(17)</i>: 3765-3771. <a href=\"https://hdl.handle.net/10.1021/jm0208774\" target=\"_blank\">https://hdl.handle.net/10.1021/jm0208774</a>","AutID":455623,"MonDate":null,"AnaDate":2002,"PeerRev":1,"outputType":"1_A1","OpenAcc":0},{"BRefID":338236,"RR":"<b>Delfourne, E.; Darro, F.; Bontemps-Subielos, N.; Decaestecker, C.; Bastide, J.; Frydman, A.; Kiss, R.</b> (2001). Synthesis and characterization of the antitumor activities of analogues of meridine, a marine pyridoacridine alkaloid. <i>J. Med. Chem. 44(20)</i>: 3275-3282. <a href=\"https://hdl.handle.net/10.1021/jm0108496\" target=\"_blank\">https://hdl.handle.net/10.1021/jm0108496</a>","AutID":455623,"MonDate":null,"AnaDate":2001,"PeerRev":1,"outputType":"1_A1","OpenAcc":0}]},"urls":null,"spcols":null,"thesterms":null,"taxterms":null,"pub":1,"newses":{"SesID":85279,"LoginName":"VLIZ2000\\zohrab","LoginID":435,"DD":"2017-06-14"},"updses":{"SesID":85279,"LoginName":"VLIZ2000\\zohrab","LoginID":435,"DD":"2017-06-14"},"urlmaps":[],"resmessage":"no id specified","complete":1}