Abstract:
This invention relates to 1-amino-3-phenoxy-propane-derivatives of formula (1) (in which A, B, R, R , X and Z are defined as in the specification described) and methods for their preparation. These compounds may be used as modulators of multi-drug resistance in cancer chemotherapy and for circumvention of resistance in the treatment of malaria.
Abstract:
Described are triazolopyrimidones of the formula (I) in which A, B and X are as defined in the description, plus their preparation and use. Such compounds are suitable for use in the treatment of disorders of the central nervous system, in particular conditions caused by acute or chronic disorders of the circulation and/or of cell metabolism, such as ischaemic cerebral insults, vascular encephalopathy and resulting demential illnesses, epilepsy, Parkinsons's disease, depression, migraine, as well as traumatic lesions of the brain and spinal cord.
Abstract:
Described is the use of triazoloquinazolines in the preparation of drugs for use in the treatment of diseases of the central nervous system. The triazoloquinazolines have formula (I) in which R , R and X are as defined in the description.
Abstract:
Disclosed are new triazoloquinazolines having the formula (I), in which A, X, R?1 and R2¿ have the meaning given in the description, as well as their production. These compounds (I) are suitable as active substances for human and veterinary medicaments and may be used for producing drugs for treating neurodegenerative diseases and neurotoxic disorders of the central nervous system, as well as for preparing spasmolytic, anti-epileptic, anxiolytic and anti-depressive drugs.
Abstract:
Medicament for oral administration which contains as active substance per individual dose, besides the customary galenic auxiliaries, 10 to 1000 mg of a compound of general formula (I) or (II) in which W is a carbonyl group or a single bond, R1 is a hydrogen atom or a group of the general formula R3CO in which R3 is a lower alkyl, lower alkoxy, mono lower alkylamino or di lower alkylamino group, R2 is an alkyl residue with 3 to 20 carbon atoms which may be branched or unbranched and contain 1 to 3 double bonds, a saturated cycle of 3 to 7 carbon atoms integrated into the chain or as substituent, or may be substituted by one or more aromatic rings or contain an oxygen or sulphur atom, as a racemate and as isolated enantiomers; or the addition salt thereof with a physiologically acceptable acid, and the active substances themselves insofar as they are novel.
Abstract:
Described are triazolopyrimidones of the formula (I) in which A, B and X are as defined in the description, plus their preparation and use. Such compounds are suitable for use in the treatment of disorders of the central nervous system, in particular conditions caused by acute or chronic disorders of the circulation and/or of cell metabolism, such as ischaemic cerebral insults, vascular encephalopathy and resulting demential illnesses, epilepsy, Parkinsons's disease, depression, migraine, as well as traumatic lesions of the brain and spinal cord.
Abstract:
This invention relates to 1-amino-3-phenoxy-propane-derivatives of formula (1) (in which A, B, R, Rx, X and Z are defined as in the specification described) and methods for their preparation. These compounds may be used as modulators of multi-drug resistance in cancer chemotherapy and for circumvention of resistance in the treatment of malaria.
Abstract:
Disclosed are new triazoloquinazolines having the formula (I), in which A, X, R?1 and R2¿ have the meaning given in the description, as well as their production. These compounds (I) are suitable as active substances for human and veterinary medicaments and may be used for producing drugs for treating neurodegenerative diseases and neurotoxic disorders of the central nervous system, as well as for preparing spasmolytic, anti-epileptic, anxiolytic and anti-depressive drugs.
Abstract:
Described is the use of triazoloquinazolines in the preparation of drugs for use in the treatment of diseases of the central nervous system. The triazoloquinazolines have formula (I) in which R1, R2 and X are as defined in the description.