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Email:
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jana.raschmanova@upjs.sk | |
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Homepage:
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https://www.upjs.sk/PF/zamestnanec/jana.raschmanova | |
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Faculty:
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PF UPJŠ
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Pavol Jozef Šafárik University in Košice, Faculty of Science
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Department:
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ÚCHV
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Institute of Chemistry
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Office:
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RB2L07 | |
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Phone:
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+421 55 234 1195, 1256,2349 | |
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ORCID ID:
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https://orcid.org/ 0000-0003-0859-6892 |
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Profile courses
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ÚCHV/PRCH1/10 Chemistry seminar I - Chemistry - Chb, Single degree study, bachelor I. deg., Full-Time form degree
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ÚCHV/POC1/03 Organic chemistry - Lab - Chemistry - Chb, Single degree study, bachelor I. deg., Full-Time form degree
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Selected publications
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V3: Divergent access to a novel 3,4-diaminophytosphingosine-like ceramide via sequential Overman rearrangement, Martin Fábian, Michaela Novotná, Jana Špaková Raschmanová, Kristína Vargová, Miroslava Martinková, Martina Bago Pilátová, Alexandra Kešeľáková, Carbohydrate Research ISSN 00086215, Vol. 530 (2023), article number 108874, DOI 10.1016/j.carres.2023.108874 IF:3.1 Q:2 Citations: 0 |
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V3: Synthesis and in vitro antiproliferative profile of novel isomeric aza-analogues of natural jaspine B, Michaela Novotná, Jana Špaková Raschmanová, Miroslava Martinková, Martina Bago Pilátová, Juraj Kuchár, Miroslava Litecká, Dávid Jáger, Tetrahedron ISSN 00404020, Vol. 103 (2022), article number 132570, DOI 10.1016/j.tet.2021.132570 IF:2.1 Q:2 Citations: 1 |
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ADC: Synthesis and in vitro anticancer activity of penaresidin-related stereoisomeric analogues, Jana Špaková Raschmanová, Miroslava Martinková, Martina Bago Pilátová, Natália Nosálová, Juraj Kuchár, Gergo Bodnár, Carbohydrate Research ISSN 00086215, Vol. 508 (2021), pp. 108419-108428, DOI 10.1016/j.carres.2021.108419 Q:2 Citations: 1 |
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ADC: Synthesis and in vitro biological evaluation of 3-amino-3-deoxydihydrosphingosines and their analogues, Jana Špaková Raschmanová, Miroslava Martinková, Jozef Gonda, Martina Bago Pilátová, Juraj Kuchár, Dávid Jáger, Tetrahedron ISSN 00404020, Vol. 76, Iss. 2 (2020), pp. 130803-130819, DOI 10.1016/j.tet.2019.130803 IF: 2,289 Q:2 Citations: 1 |
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ADC: Synthesis of the cytotoxic phytosphingosines and their isomeric analogues, Jana Špaková Raschmanová, Miroslava Martinková, Jozef Gonda, Martina Bago Pilátová, Dávid Kupka, Dávid Jáger, Carbohydrate Research ISSN 00086215, Vol. 468 (2018), pp. 1–12, DOI 10.1016/j.carres.2018.08.001 IF: 1,944 Q:2 Citations: 3 |
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Selected projects
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Open scientific community for modern interdisciplinary research in medicine (OPENMED), ITMS2014+: 313011V455 supported by the Operational Programme Integrated Infrastructure, funded by the ERDF. 09/2020 – 06/2023, participation in conducting - H3 activity. "Development of intelligent photosensitive drugs and nanoporous drug delivery systems" |
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APVV-14-0883: Stereoselective synthesis and in vitro structural modulation of biological activity of functionalized sphingosines, participation in conducting |
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VEGA 1/0047/18: Stereoconvergent synthesis of isomeric sphingoid bases and related long-chain amino alcohols as potential anticancer agents, participation in conducting |
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International mobilities and visits
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Syngenta Crop Protection, Basel (Switzerland), 01.03.2008–30.11.2008
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Politechnika Krakowska, Krakow (Poland), 19.11.2007–14.12.2007, COST, section D-32
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Université Louis Pasteur, ECPM, Laboratoire de Stéreochimie Organometallique, Strasbourg (Francúzsko), 01.02.2005–30.06.2005, Socrates-Erasmus
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Awards
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2009 - Dean's award for the scientific and research activities of PhD. students in 2008 2006 - Prize of rector awarded for excellent study results
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Projects
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1. Open scientific community for modern interdisciplinary research in medicine (OPENMED), ITMS2014+: 313011V455 supported by the Operational Programme Integrated Infrastructure, funded by the ERDF. 09/2020 – 06/2023, participation in conducting - H3 activity. "Development of intelligent photosensitive drugs and nanoporous drug delivery systems" 2. APVV-14-0883: Stereoselective synthesis and in vitro structural modulation of biological activity of functionalized sphingosines, participation in conducting 3. VEGA 1/0047/18: Stereoconvergent synthesis of isomeric sphingoid bases and related long-chain amino alcohols as potential anticancer agents, participation in conducting
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