Design, synthesis and cytotoxicity of BODIPY FL labelled triterpenoids

Authors: Brandes, Benjamin, Hoenke, Sophie, Fischer, Lucie, Csuk, René

Source: In European Journal of Medicinal Chemistry 1 January 2020 185

The cytotoxicity of oleanane derived aminocarboxamides depends on their aminoalkyl substituents

Authors: Kahnt, Michael, Loesche, Anne, Serbian, Immo, Hoenke, Sophie, Fischer, Lucie, Al-Harrasi, Ahmed, Csuk, René

Source: In Steroids September 2019 149

Synthesis of new boswellic acid derivatives as potential antiproliferative agents

Authors: Shamraiz, Umair, Hussain, Hidayat, Ur Rehman, Najeeb, Al-Shidhani, Sulaiman, Saeed, Aasim, Khan, Husain Yar, Khan, Ajmal, Fischer, Lucie, Csuk, René, Badshah, Amin, Al-Rawahi, Ahmed, Hussain, Javid, Al-Harrasi, Ahmed

Source: Natural product research. 34(13):1845-1852

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100110644847.0x000001&indx=1&recIds=ETOCvdc_100110644847.0x000001

Transformation of asiatic acid into a mitocanic, bimodal-acting rhodamine B conjugate of nanomolar cytotoxicity

Authors: Kahnt, Michael, Wiemann, Jana, Fischer, Lucie, Sommerwerk, Sven, Csuk, René

Source: In European Journal of Medicinal Chemistry 5 November 2018 159:143-148

Syntheses of C-ring modified dehydroabietylamides and their cytotoxic activity

Authors: Wiemann, Jana, Fischer, Lucie, Rohmer, Matthias, Csuk, René

Source: In European Journal of Medicinal Chemistry 5 August 2018 156:861-870

Homopiperazine-rhodamine B adducts of triterpenoic acids are strong mitocans

Authors: Wolfram, Ratna Kancana, Fischer, Lucie, Kluge, Ralph, Ströhl, Dieter, Al-Harrasi, Ahmed, Csuk, René

Source: In European Journal of Medicinal Chemistry 15 July 2018 155:869-879

2, 4-Disubstituted Quinazoline Derivatives Act as Inducers of Tubulin Polymerization: Synthesis and Cytotoxicity

Authors: Moghadam, Ebrahim S., Tehrani, Maryam H., Csuk, René, Fischer, Lucie, Faramarzi, Mohammad Ali, Rashidi, Arezoo, Javadi, Iraj, Amini, Mohsen

Source: Anti-cancer agents in medicinal chemistry. 19(8):1048-1057

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100088617503.0x000001&indx=1&recIds=ETOCvdc_100088617503.0x000001

2,4-Disubstituted Quinazoline Derivatives Act as Inducers of Tubulin Polymerization: Synthesis and Cytotoxicity

Authors: Moghadam, Ebrahim S., Tehrani, Maryam H., Csuk, René, Fischer, Lucie, Faramarzi, Mohammad A., Rashidi, Arezoo, Javadi, Iraj, Amini, Mohsen

Source: Anti-Cancer Agents in Medicinal Chemistry; May 2019, Vol. 19 Issue: 8 p1048-1057, 10p

Cytotoxic Potential of a-Azepano- and 3-Amino-3,4-SeCo-Triterpenoids.

Authors: Kazakova, Oxana, Smirnova, Irina, Tret'yakova, Elena, Csuk, René, Hoenke, Sophie, Fischer, Lucie, Santi, Claudio

Source: International Journal of Molecular Sciences; Feb2021, Vol. 22 Issue 4, p1714-1714, 1p

Subject Terms: BECKMANN rearrangement, CELL lines, COLON cancer, CARBOXYL group, AMIDE derivatives, ANTINEOPLASTIC antibiotics, GLUCOSIDASES

4-Benzyloxylonchocarpin and Muracatanes A-C from Ranunculus muricatus L. and Their Biological Effects.

Authors: Hussain, Hidayat, Ali, Iftikhar, Wang, Daijie, Mamadalieva, Nilufar Z., Hussain, Wahid, Csuk, René, Loesche, Anne, Fischer, Lucie, Staerk, Dan, Anam, Syariful, AlZain, Mashail N., Mushtaq, Maria, Ul-Haq, Zaheer, Ullah, Riaz, Noman, Omar M., Abbas, Ghulam, Green, Ivan R.

Source: Biomolecules (2218-273X); Nov2020, Vol. 10 Issue 11, p1562-1562, 1p

Subject Terms: RANUNCULUS, NUCLEAR magnetic resonance spectroscopy, THYROID cancer, CHALCONE, BUTYRYLCHOLINESTERASE, TACRINE

Synthesis and Cytotoxicity Evaluation of DOTA-Conjugates of Ursolic Acid.

Authors: Kahnt, Michael, Hoenke, Sophie, Fischer, Lucie, Al-Harrasi, Ahmed, Csuk, René, Nakagawa-Goto, Kyoko

Source: Molecules; Jun2019, Vol. 24 Issue 12, p2254-2254, 1p, 2 Color Photographs, 1 Illustration, 5 Diagrams, 2 Charts

Subject Terms: URSOLIC acid, FLUORESCENCE microscopy, CELL cycle, CELL analysis, CELL lines

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