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Novel trisubstituted harmine derivatives with original in v..:
Frédérick, Raphaël
;
Bruyére, Céline
;
Vancraeynest, Christelle
...
boreal:162942. , 2012
Link:
http://hdl.handle.net/2078.1/162942
RT Journal T1
Novel trisubstituted harmine derivatives with original in vitro anticancer activity
UL https://suche.suub.uni-bremen.de/peid=base-ftunivlouvain:oai:dial.uclouvain.be:boreal:162942&Exemplar=1&LAN=DE A1 Frédérick, Raphaël A1 Bruyére, Céline A1 Vancraeynest, Christelle A1 Reniers, Jérémy A1 Meinguet, Céline A1 Pochet, Lionel A1 Backlund, Anders A1 Masereel, Bernard A1 Kiss, Robert A1 Wouters, Johan PB American Chemical Society YR 2012 K1 1 methyl 2 (4 fluorobenzyl) 7 (3 fluorobenzyl)oxy 9 (3 fluorobenzyl) beta carboline 2 ium bromide K1 Nsc 24030 K1 Nsc 267709 K1 Nsc 342443 K1 Nsc 58924 K1 Nsc 634791 K1 Nsc 644614 K1 Nsc 747162 K1 Phyllantoside K1 Protein dyrk1a K1 Protein kinase K1 1 methyl 2 benzyl 7 benzyloxy 9 benzyl beta carbolin 2 ium bromide K1 Protein synthesis inhibitor K1 Tubulin K1 Unclassified drug K1 Undulatone K1 Algorithm K1 Antineoplastic activity K1 Apoptosis K1 Article K1 Cancer cell culture K1 Cancer inhibition K1 1 methyl 2 benzyl 7 cyclohexylmethyloxy 9 cyclohexylmethyl beta carbolin 2 ium bromide K1 Cancer resistance K1 Controlled study K1 Cytostasis K1 Drug cytotoxicity K1 Drug design K1 Drug potency K1 Drug screening K1 Drug synthesis K1 Enzyme inhibition K1 Human K1 Antineoplastic agent K1 Human cell K1 IC 50 K1 In vitro study K1 Lipophilicity K1 Structure activity relation K1 Antineoplastic Agents K1 Cell Line K1 Tumor K1 Cell Proliferation K1 Harmine K1 Beta carboline derivative K1 Humans K1 Inhibitory Concentration 50 K1 Protein-Serine-Threonine Kinases K1 Protein-Tyrosine Kinases JF boreal:162942 LK http://hdl.handle.net/2078.1/162942 DO http://hdl.handle.net/2078.1/162942 SF ELIB - SuUB Bremen
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