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Design, synthesis, biological evaluation and X-ray structur..:
SAINAS, STEFANO
;
PIPPIONE, Agnese Chiara
;
GIORGIS, Marta
...
info:eu-repo/semantics/altIdentifier/pmid/28235702. , 2017
Link:
http://hdl.handle.net/2318/1634271
RT Journal T1
Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds
UL https://suche.suub.uni-bremen.de/peid=base-ftunivtorino:oai:iris.unito.it:2318_1634271&Exemplar=1&LAN=DE A1 SAINAS, STEFANO A1 PIPPIONE, Agnese Chiara A1 GIORGIS, Marta A1 LUPINO, Elisa A1 RAMONDETTI, Cristina A1 BUCCINNA', Barbara A1 PICCININI, Marco A1 BOSCHI, Donatella A1 LOLLI, Marco Lucio A1 Goyal, Parveen A1 Braga, Rodolpho C A1 Andrade, Carolina H A1 Andersson, Mikael A1 Moritzer, Ann Christin A1 Friemann, Rosmarie A1 Mensa, Stefano A1 Al Kadaraghi, Salam YR 2017 K1 Autoimmune disease K1 Bioisosterism K1 Brequinar K1 Dihydroorotate dehydrogenase (DHODH) inhibitor K1 Leflunomide K1 X-ray-crystallography K1 Azole K1 Binding Site K1 Cell Proliferation K1 Cell Survival K1 Cells K1 Cultured K1 Drug Design K1 Enzyme Inhibitor K1 Human K1 Hydroxylation K1 Immunosuppression K1 Jurkat Cell K1 Models K1 Molecular K1 Molecular Structure K1 Oxidoreductases Acting on CH-CH Group Donor K1 Structure-Activity Relationship K1 X-Ray Diffraction K1 Pharmacology K1 Drug Discovery3003 Pharmaceutical Science K1 Organic Chemistry JF info:eu-repo/semantics/altIdentifier/pmid/28235702 LK http://hdl.handle.net/2318/1634271 DO http://hdl.handle.net/2318/1634271 SF ELIB - SuUB Bremen
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