Abstract:
Use for the vasculopathy treatment of compounds or salts thereof, having the following general formula: A-(B)b0-(C)c0-NO2 wherein A is the radical of the precursor drug selected between the salicylic or acetylsalicylic acid, B and C are bivalent linking groups as defined in the invention.
Abstract:
The present invention relates to β-adrenergic blockers nitrooxyderivatives of general formula (I): A-(Y-ONO2)s, wherein s is an integer equal to 1 or 2; A is selected from the following β-adrenergic blockers residues of formula (II), wherein R1 is selected from the group consisting of: formula (IIa), formula (IIb), formula (IIc) or other residues defined in claim 1; R2 is selected from the group consisting of: -CH(CH3)2, -C(CH3)3 or formula (IIIa), formula (IIIb), Z is H or is a group capable of binding Y as defined in claim 1, Z1 is H or a -C(O)- capable of binding Y; the other substituents are defined in claim 1; and enantiomers and diastereoisomers and pharmaceutically acceptable salts thereof, pharmaceutical compositions containing them and their use for the treatment of hypertension, cardiovascular diseases, glaucoma, migraine headache and vascular diseases.
Abstract:
The present invention relates to new pharmaceutical compositions for the administration of liquid drugs in solid oral forms, said compositions comprising one or more active ingredients, one or more surface-active agents and optionally a co-surfactant and/or an absorption enhancer absorbed on a solid inert carrier.
Abstract:
Nitrooxyderivatives of fluvastatin, cerivastatin, atorvastatin and rosuvastatin having improved pharmacological activity and enhanced tolerability are described. They can be employed for treating and/or preventing several diseases, in particular coronary syndromes, neurodegenerative disorders as well as for reducing cholesterol levels.
Abstract:
Nitrate salts of antimicrobial agents for the preparation of antimicrobial medicaments, specifically antiviral, antifungal and antibacterial medicaments.
Abstract:
Compounds or their salts of general formula (I): A B N(O)s wherein: s is an integer equal to 1 or 2; A = R T1-, wherein R is the drug radical and T1 = (CO)t or (X)t', wherein X = O, S, NR1c, R1c is H or a linear or branched alkyl or a free valence, t and t' are integers and equal to zero or 1, with the proviso that t = 1 when t' = 0; t = 0 when t' = 1; B = -TB X2 O- wherein TB = (CO) when t = 0, TB = X when t' = 0, X being as above defined; X2, bivalent radical, is such that the precursor drug of A and the precursor of B meet respectively the pharmacological tests described in the description.
Abstract translation:通式(I)的化合物或其盐:A B N(O)s其中:s是等于1或2的整数; A = R T1-,其中R是药物基团并且T 1 =(CO)t或(X)t',其中X = O,S,NR 1c,R 1c是H或直链或支链烷基或自由价,t 和t'是整数并且等于零或1,条件是当t'= 0时t = 1; 当t'= 1时t = 0; B = -TB X2 O-其中当t = 0时TB =(CO),当t'= 0时TB = X,X如上所定义; X2是二价基团,使得A的前体药物和B的前体分别满足说明书中描述的药理学试验。
Abstract:
Compounds or their salts of general formula (I): A-(B) wherein A = R-T1-, wherein R is the drug radical and T1 = (CO)t or (X)t', wherein X = O, S, NR1C, R1C is H or an alkyl having from 1 to 5 carbon atoms, or a free valence, t and t' are integers and equal to zero or 1, with the proviso that t = 1 when t' = 0; t = 0 when t' = 1; B = -TB-X2 wherein TB = (CO) when t = 0, TB = X when t' = -, X being as above defined; X2, monovalent radical, is such that the precursor drug of A and the precursor of B respectively meet the pharmacological tests described in the application.