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Lucie Heller

Showing results (1-10 of 27) with videos related to

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Bioorganic & Medicinal Chemistry|May 27, 2015
Simple structural modifications confer cytotoxicity to allobetulinLucie Heller, Anja Obernauer, René Csuk
European Journal of Medicinal Chemistry|March 13, 2018
An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactionsJana Wiemann, Lucie Heller, René Csuk
Archiv Der Pharmazie|January 13, 2015
Synthesis and cytotoxic activity of pentacyclic triterpenoid sulfamatesSven Sommerwerk, Lucie Heller, René Csuk
Bioorganic & Medicinal Chemistry Letters|January 12, 2016
Targeting cancer cells with oleanolic and ursolic acid derived hydroxamatesJana Wiemann, Lucie Heller, René Csuk
European Journal of Medicinal Chemistry|April 24, 2018
Targeting mitochondria: Esters of rhodamine B with triterpenoids are mitocanic triggers of apoptosisRatna Kancana Wolfram, Lucie Heller, René Csuk
Bioorganic & Medicinal Chemistry|July 28, 2015
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analoguesSven Sommerwerk, Lucie Heller, Bianka Siewert, et al.
European Journal of Medicinal Chemistry|May 6, 2016
Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell linesSven Sommerwerk, Lucie Heller, Julia Kuhfs, et al.
European Journal of Medicinal Chemistry|July 15, 2016
Selective killing of cancer cells with triterpenoic acid amides - The substantial role of an aromatic moiety alignmentSven Sommerwerk, Lucie Heller, Julia Kuhfs, et al.
Bioorganic & Medicinal Chemistry Letters|May 19, 2015
Allobetulin derived seco-oleananedicarboxylates act as inhibitors of acetylcholinesteraseLucie Heller, Stefan Schwarz, Anja Obernauer, et al.
Archiv Der Pharmazie|July 22, 2014
Gypsogenin derivatives: an unexpected class of inhibitors of cholinesterasesLucie Heller, Stefan Schwarz, Björn A Weber, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Bioorganic & Medicinal Chemistry|May 27, 2015
Simple structural modifications confer cytotoxicity to allobetulinLucie Heller, Anja Obernauer, René Csuk
European Journal of Medicinal Chemistry|March 13, 2018
An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactionsJana Wiemann, Lucie Heller, René Csuk
Archiv Der Pharmazie|January 13, 2015
Synthesis and cytotoxic activity of pentacyclic triterpenoid sulfamatesSven Sommerwerk, Lucie Heller, René Csuk
Bioorganic & Medicinal Chemistry Letters|January 12, 2016
Targeting cancer cells with oleanolic and ursolic acid derived hydroxamatesJana Wiemann, Lucie Heller, René Csuk
European Journal of Medicinal Chemistry|April 24, 2018
Targeting mitochondria: Esters of rhodamine B with triterpenoids are mitocanic triggers of apoptosisRatna Kancana Wolfram, Lucie Heller, René Csuk
Bioorganic & Medicinal Chemistry|July 28, 2015
Chemoenzymatic synthesis and cytotoxicity of oenanthotoxin and analoguesSven Sommerwerk, Lucie Heller, Bianka Siewert, et al.
European Journal of Medicinal Chemistry|May 6, 2016
Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell linesSven Sommerwerk, Lucie Heller, Julia Kuhfs, et al.
European Journal of Medicinal Chemistry|July 15, 2016
Selective killing of cancer cells with triterpenoic acid amides - The substantial role of an aromatic moiety alignmentSven Sommerwerk, Lucie Heller, Julia Kuhfs, et al.
Bioorganic & Medicinal Chemistry Letters|May 19, 2015
Allobetulin derived seco-oleananedicarboxylates act as inhibitors of acetylcholinesteraseLucie Heller, Stefan Schwarz, Anja Obernauer, et al.
Archiv Der Pharmazie|July 22, 2014
Gypsogenin derivatives: an unexpected class of inhibitors of cholinesterasesLucie Heller, Stefan Schwarz, Björn A Weber, et al.
Pageof 3