159139-35-2Relevant academic research and scientific papers
COMPOUNDS FORTREATMENT OF CARDIOVASCULAR DISEASES
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, (2008/06/13)
Pharmaceutical compositions containing sodium-hydrogen exchanger type 1 (NHE-1) inhibitors in combination with Ca 2+ overload inhibitors, and the use of such combination inhibitors to treat, for example, cardiovascular disease, such as ischemia, particularly, perioperative myocardial ischemic injury in mammals, including humans, are disclosed.
Tetrahydronaphthyridinyl-carboxamides having anti-convulsant activity
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, (2008/06/13)
Compounds of formula (I) and pharmaceutically acceptable salts and solvates: where R1is hydrogen, C1-6alkyl (optionally substituted by hydroxy or C1-4alkoxy), phenyl-C1-4alkyl-, C1-6alkenyl, C1-6
Substituted isoquinoline derivatives and their use as anticonvulsivants
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, (2008/06/13)
This invention relates to novel substituted isoquinoline derivatives and their use as anticonvulsants.
Benzoylguanidines, pharmaceutical composition containing them and treatment of arrthythmias therewith
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, (2008/06/13)
Benzoylguanidines, process for their preparation, their use as a medicament and medicament containing them. The invention relates to benzoylguanidines of the formula I STR1 where R(1) or R(2) is R(3)-S(O)n -- or R(4)R(5)N--O2 S-- and
Synthesis of the highly selective Na+/H+ exchange inhibitors cariporide mesilate and (3-methanesulfonyl-4-piperidino-benzoyl) guanidine methanesulfonate
Weichert, Andreas,Faber, Sabine,Jansen, Hans W.,Scholz, Wolfgang,Lang, Hans J.
, p. 1204 - 1207 (2007/10/03)
The syntheses of cariporide mesilate ((4-isopropyl-3-methanesulfonyl-benzoyl) guanidine methanesulfonate, HOE 642, CAS 159138-81-5), currently being clinically investigated as a protective drug in cardiac ischemia and reperfusion states, and of HOE 694 ((3-methanesulfonyl-4-piperidino-benzoyl)guanidine methanesulfonate, CAS 149725-40-6), widely used as a physiological and pharmacological research tool in studies comprising Na+/H+ exchange (NHE) inhibition, are described. Additionally, their selectivity on the different subtypes is disclosed.
