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Application filed by Uniwersytet Medyczny W Lublinie, Instytut Medycyny Wsi Im. Witolda ChodźkifiledCriticalUniwersytet Medyczny W Lublinie
Priority to PL397269ApriorityCriticalpatent/PL220232B1/en
Publication of PL397269A1publicationCriticalpatent/PL397269A1/en
Publication of PL220232B1publicationCriticalpatent/PL220232B1/en
Pharmaceuticals Containing Other Organic And Inorganic Compounds
(AREA)
Abstract
Przedmiotem wynalazku jest zastosowanie 5-(3-chlorofenylo)-4-(4-chlorofenylo)-2,4-dihydro-3H-1,2,4-triazolo-3-tionu o wzorze 1 o dzialaniu przeciwdrgawkowym, do wytwarzania leku do leczenia napadów toniczno-klonicznych oraz napadów czesciowych z wtórnym lub bez wtórnego uogólnienia.The subject of the invention is the use of 5- (3-chlorophenyl) -4- (4-chlorophenyl) -2,4-dihydro-3H-1,2,4-triazol-3-thione of formula 1 with anticonvulsant activity in the manufacture of a medicament for treatment of tonic-clonic seizures and partial seizures with or without secondary generalization.
PL397269A2011-12-072011-12-07Medical use of the substance of 5-(3-chlorophenyl)-4-(4-chlorophenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione
PL220232B1
(en)
1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea as raf kinase modulator in the treatment of cancer diseases
combination therapy comprising a tor kinase inhibitor and n- (3- (5-fluoro-2- (4- (2-methoxyethoxy) phenylamino) pyrimidin-4-ylamino) phenyl) acrylamide for cancer treatment
Inhibitor of human myeloid leukemia based on N-(4-(5-(pyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-2-(pyridin-2-ylmethylen)-hydrazinecarbothioamide
Compounds derived from spiro-conjugated pyrazoles, inhibitors of ksp kinesin activity; pharmaceutical composition comprising said compound; and use of the compound for the treatment of proliferative diseases.
Inhibitors of human myeloid leukemia based on 2-[2-(pyridine-2-ilmethylidene)hydrazine]-1,3-benzothiazole and 2-[2-(1-pyridine-2-ilethylidene)hydrazine]-1,3-benzothiazole dihydrate