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TITLE:
Fluorinated triazole-containing sphingosine analogues. Syntheses and in vitro evaluation as SPHK inhibitors - imarina:5133170

URV's Author/s:Beltrán Debón, Raúl Alejandro / Castillón Miranda, Sergio / Díaz Giménez, María Yolanda / Matheu Malpartida, María Isabel
Author, as appears in the article.:Escudero-Casao M, Cardona A, Beltrán-Debón R, Díaz Y, Matheu MI, Castillón S.
Author's mail:yolanda.diaz@urv.cat
maribel.matheu@urv.cat
raul.beltran@urv.cat
sergio.castillon@urv.cat
Author identifier:0000-0001-5567-8108
0000-0001-5216-9260
0000-0001-9691-1906
0000-0002-0690-7549
Journal publication year:2018
Publication Type:Journal Publications
ISSN:14770520
APA:Escudero-Casao M, Cardona A, Beltrán-Debón R, Díaz Y, Matheu MI, Castillón S. (2018). Fluorinated triazole-containing sphingosine analogues. Syntheses and in vitro evaluation as SPHK inhibitors. Organic & Biomolecular Chemistry, 16(39), 7230-7235. DOI: 10.1039/c8ob01867g
Papper original source:Organic & Biomolecular Chemistry. 16 (39): 7230-7235
Abstract:Sphingosine analogues with a rigid triazole moiety in the aliphatic chain and systematic modifications in the polar head and different degrees of fluorination at the terminus of the alkylic chain were synthesized from a common alkynyl aziridine key synthon. This key synthon was obtained by enantioselective organocatalyzed aziridination and it was subsequently ring opened in a regioselective manner in acidic medium. Up to 16 sphingosine analogues were prepared in a straightforward manner. The in vitro activity of the obtained products as SPHK1 and SPHK2 inhibitors was evaluated, displaying comparable activity to that of DMS.
Article's DOI:10.1039/c8ob01867g
Link to the original source:https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01867g#!divAbstract
Papper version:info:eu-repo/semantics/publishedVersion
licence for use:https://creativecommons.org/licenses/by/3.0/es/
Department:Química Analítica i Química Orgànica
Bioquímica i Biotecnologia
Licence document URL:https://repositori.urv.cat/ca/proteccio-de-dades/
Thematic Areas:Química
Physical and theoretical chemistry
Organic chemistry
Odontología
Medicina ii
Medicina i
Materiais
Interdisciplinar
General medicine
Farmacia
Ciências biológicas iii
Ciências biológicas ii
Ciências biológicas i
Ciências agrárias i
Chemistry, organic
Biotecnología
Biodiversidade
Biochemistry
Keywords:Flúor
Esfingolipidos
Entity:Universitat Rovira i Virgili
Record's date:2024-09-07
First page:7230
Last page:7235
Journal volume:16
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