Combinations

Abstract

The present invention relates to a pharmaceutical composition, comprising (a) a phosphodiesterase 5 inhibitor or a pharmaceutically acceptable salt thereof and (b) at least one of the active ingredients selected from the group consisting of (i) an anti-diabetic agent; (ii) HMG-Co-A reductase inhibitors; (iii) an anti-hypertensive agent; and (iv) a serotonin reuptake inhibitor (SSRI) or, in each case, or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. The pharmaceutical composition may be employed for the treatment of sexual dysfunction, hyperglycemia, hyperinsulinaemia, hyperlipidaemia, hypertriglyceridemia, diabetes, insulin resistance, impaired glucose metabolism, conditions of impaired glucose tolerance (IGT), conditions of impaired fasting plasma glucose, obesity, diabetic retinopathy, diabetic nephropathy, glomerulosclerosis, diabetic neuropathy, syndrome X, erectile dysfunction, coronary heart disease, hypertension, especially ISH, angina pectoris, myocardial infarction, stroke, vascular restenosis, endothelial dysfunction, impaired vascular compliance, congestive heart failure.

1 - 10 . (canceled)  
   
   
       11 . A pharmaceutical composition comprising a PDE 5 inhibitor of formula  
     
       
         
         
             
             
         
       
     
     in free or salt form, where 
 R 1  is hydrogen or alkyl optionally substituted by hydroxy, alkoxy, or alkylthio,  
 R 2  is hydrogen, alkyl, hydroxyalkyl, alkylcarbonyloxyalkyl, alkoxyalkyl, alkylthioalkyl, alkenyl, cycloalkylalkyl, heterocyclylalkyl, aralkyl in which the aryl ring thereof is optionally fused to a 5-membered heterocyclic group or is optionally substituted by one or more substituents selected from alkoxy, amino, alkylamino, dialkylamino, acylamino, halogen, hydroxy, aminosulfonyl, alkylaminosulfonyl, dialkylaminosulfonyl, alkylsulfonylamino or dialkylaminosulfonylamino,  
 R 3  is hydrogen or alkyl optionally substituted by hydroxy, alkoxy, or alkylthio,  
 R 4  is hydrogen or alkyl,  
 R 5  is a quinolinyl, isoquinolinyl or oxodihydroisoquinolinyl group optionally fused to a 5-membered heterocyclic group and optionally substituted by one or more substituents selected from halogen, cyano, hydroxy, alkyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, alkoxy, alkylthio, alkenyl, alkoxycarbonyl, alkynyl, carboxyl, acyl, a group of formula —N(R 6 )R 7 , aryl optionally substituted by one or more substituents selected from halogen or alkoxy, or heteroaryl having 5 or 6 ring atoms attached through a ring carbon atom to the indicated carbon atom, and  
 R 6  and R 7  are each independently hydrogen or alkyl optionally substituted by hydroxy or alkoxy or one of R 6  and R 7  is hydrogen and the other is acyl, or R 6  and R 7  together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclyl group;  
 and a serotonin reuptake inhibitor (SSRI) and a pharmaceutically acceptable carrier.  
 
   
   
       12 . The pharmaceutical composition of  claim 11  wherein the PDE 5 inhibitor is 3-isobutyl-8-(6-methoxy-isoquinolin-4-ylmethyl)-1-methyl-3,7-dihydro-purine-2,6-dione.  
   
   
       13 . The pharmaceutical composition of  claim 11  wherein the serotonin reuptake inhibitor is selected from the group consisting of fluvoxamine, fluoxetine, paroxetine and sertraline, citalopram, venlafaxine, cericlamine, duloxetine, milnacipran, nefazodone and cyanodothiepin.  
   
   
       14 . The pharmaceutical composition of  claim 11  in which R 5  is a quinolinyl group of formula  
     
       
         
         
             
             
         
       
     
     or an isoquinolinyl group of formula  
     
       
         
         
             
             
         
       
     
     or an oxodihydroisoquinolinyl group of formula  
     
       
         
         
             
             
         
       
     
     where R 8 , R 9 , R 10 , R 11 , R 12  and R 13  are each independently hydrogen or a substituent selected from halogen, cyano, hydroxy, alkyl, hydroxyalkyl, alkoxyalkyl, alkylthioalkyl, alkoxy, alkylthio, alkenyl, alkoxycarbonyl, alkynyl, carboxyl, acyl, a group of formula —N(R 6 )R 7 , aryl optionally substituted by one or more substituents selected from halogen or alkoxy, or heteroaryl having 5 or 6 ring atoms, and R 6  and R 7  are each independently hydrogen or alkyl optionally substituted by hydroxy or alkoxy or one of R 6  and R 7  is hydrogen and the other is acyl, or R 6  and R 7  together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclyl group, or R 11  and R 12  together with the carbon atoms to which they are attached denote a 5-membered heterocyclic group having two oxygen or nitrogen atoms in the ring, and R a  is hydrogen or C 1 -C 4 -alkyl.  
   
   
       15 . The pharmaceutical composition of  claim 14  in which R 1  is hydrogen or C 1 -C 4 -alkyl, R 2  is hydrogen, C 1 -C 8 -alkyl, hydroxy-C 1 -C 8 -alkyl, or C 1 -C 4 -alkylcarbonyloxy-C 1 -C 8 -alkyl, C 2 -C 4 -alkenyl, C 3 -C 6 -cycloalkyl-C 1 -C 4 -alkyl, heterocyclyl-C 1 -C 4 -alkyl where the heterocyclyl group is a 5-membered heterocyclyl group having one nitrogen or oxygen atom in the ring, phenyl-C 1 -C 4 -alkyl in which the phenyl ring is optionally substituted by one or two substituents selected from C 1 -C 4 -alkoxy, amino, C 1 -C 4 -alkylcarbonylamino, chlorine, bromine, C 1 -C 4 -alkylsulfonylamino, or di(C 1 -C 4 -alkyl)aminosulfonylamino and is optionally fused to a 5-membered heterocyclic ring having two oxygen atoms in the ring, 
 R 3  is hydrogen or C 1 -C 4 -alkyl,    R 4  is hydrogen or C 1 -C 4 -alkyl,    R 5  is a quinolinyl group of formula II, an isoquinolinyl group of formula III or an oxodihydroisoquinolinyl group of formula IIIA, where R 8 , R 9 , R 10 , R 11 , R 12  and R 13  are each independently selected from hydrogen, halogen, cyano, carboxy, hydroxy, C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthioC 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -alkylcarbonyl, a group —N(R 6 )R 7  or phenyl optionally substituted by one or two substituents selected from halogen or C 1 -C 4 -alkoxy, or R 11  and R 12  together with the carbon atoms to which they are attached denote a 5-membered heterocyclic group having two oxygen atoms in the ring, and    R 6  and R 7  are each independently hydrogen or C 1 -C 4 -alkyl optionally substituted by hydroxy or alkoxy or one of R 6  and R 7  is hydrogen and the other is C 1 -C 4 -alkylcarbonyl, or R 6  and R 7  together with the nitrogen atom to which they are attached denote a 6-membered heterocyclyl group having one or two nitrogen atoms, or one nitrogen atom and one oxygen atom, in the ring.    
   
   
       16 . The pharmaceutical composition of  claim 15  in which R 5  is an isoquinolinyl group of formula III in which R 8  is hydrogen, C 1 -C 4 -alkyl, halogen, cyano, —N(R 6 )R 7  where R 6  and R 7  are independently C 1 -C 4 -alkyl or R 6  and R 7  together with the nitrogen atom to which they are attached denote a 6-membered heterocyclyl group having one or two nitrogen atoms, or one nitrogen atom and one oxygen atom, in the ring, or phenyl substituted by one or two C 1 -C 4 -alkoxy groups; R 9  and R 10  are each independently hydrogen, C 1 -C 4 -alkyl or halogen; R 11  and R 12  are each independently hydrogen, halogen, cyano, carboxy, hydroxy, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy or C 2 -C 4 -alkynyl, or R 11  and R 12  together with the carbon atoms to which they are attached denote a 5-membered heterocycle having two oxygen atoms in the ring; and R 13  is hydrogen or halogen.  
   
   
       17 . The pharmaceutical composition of  claim 11  in which R 1  is hydrogen or C 1 -C 4 -alkyl optionally substituted by hydroxy, C 1 -C 4 -alkoxy or C 1 -C 4 -alkylthio, 
 R 2  is hydrogen, C 1 -C 8 -alkyl, hydroxy-C 1 -C 8 -alkyl, C 1 -C 4 -alkylcarbonyloxy-C 1 -C 8 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 8 -alkyl, C 1 -C 4 -alkylthio-C 1 -C 8 -alkyl, C 2 -C 4 -alkenyl, C 3 -C 8 -Cycloalkyl-C 1 -C 4 -alkyl, heterocyclyl-C 1 -C 4 -alkyl where the heterocyclyl group is a 5- or 6-membered heterocyclyl group having one or two hetero atoms selected from nitrogen and oxygen atoms in the ring, phenyl-C 1 -C 4 -alkyl in which the phenyl ring is optionally substituted by one or more substituents selected from C 1 -C 4 -alkoxy, amino, C 1 -C 4 -alkylamino, di(C 1 -C 4 -alkyl)amino, C 1 -C 4 -alkylcarbonylamino, halogen, C 1 -C 4 -alkylsulfonylamino, or di(C 1 -C 4 -alkyl)aminosulfonylamino, and is optionally fused to a 5-membered heterocyclic ring having two oxygen or two nitrogen atoms in the ring,    R 3  is hydrogen or C 1 -C 4 -alkyl optionally substituted by hydroxy, C 1 -C 4 -alkoxy or C 1 -C 4 -alkylthio,    R 4  is hydrogen or C 1 -C 4 -alkyl,    R 5  is a quinolinyl, isoquinolinyl or oxodihydroisoquinolinyl group optionally fused to a 5-membered heterocyclic group having two oxygen or two nitrogen atoms in the ring and optionally substituted by one or more substituents selected from halogen, cyano, carboxy hydroxy, C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkylthio-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -alkylcarbonyl, a group —N(R 6 )R 7  or phenyl optionally substituted by one or more substituents selected from halogen or C 1 -C 4 -alkoxy and    R 6  and R 7  are each independently hydrogen or C 1 -C 4 -alkyl optionally substituted by hydroxy or alkoxy, or one of R 6  and R 7  is hydrogen and the other is C 1 -C 4 -alkylcarbonyl, or R 6  and R 7  together with the nitrogen atom to which they are attached denote a 5- or 6-membered heterocyclyl group having one or two nitrogen atoms and, optionally, an oxygen atom in the ring.    
   
   
       18 . A pharmaceutical composition comprising a compound of formula V  
     
       
         
         
             
             
         
       
     
     in free or salt form, wherein 
 (i) R 1  is CH 3 , R 2  is (CH 3 ) 2 CHCH 2 , R 3  and R 4  are each H, R 8  is CH 3 , R 9  and R 10  are each H, and R 11  and R 12  are each OCH 3 ; or  
 (ii) R 1  is CH 3 , R 2  is (CH 3 ) 2 CHCH 2 , R 3 , R 4 , R 8 , R 9  and R 10  are each H, and R 11  and R 12  are each OCH 3 ; or  
 (iii) R 1  is CH 3 , R 2  is (CH 3 ) 3 CCH 2 , R 3 , R 4 , R 8 , R 9  and R 10  are each H, and R 11  and R 12  are each OCH 3 ; or  
 (iv) R 1  is CH 3 , R 2  is (CH 3 ) 2 CHCH 2 , R 3 , R 4 , R 9  and R 10  are each H, R 8  is Cl and R 11  and R 12  are each OCH 3 ; or  
 (v) R 1  is CH 3 , R 2  is (CH 3 ) 2 CHCH 2 , R 3 , R 4 , R 8 , R 9  and R 10  are each H, R 11  is OCH 3  and R 12  is H; or  
 (vi) R 1  is CH 3 , R 2  is cyclopropylmethyl, R 3 , R 4 , R 8 , R 9 , R 10  and R 12  are each H and R 11  is OCH 3 ; or  
 (vii) R 1  is CH 3 , R 2  is (CH 3 ) 2 CHCH 2 , R 3 , R 4 , R 8 , R 9 , R 10  and R 12  are each H and R 11  is CH≡C; or  
 (viii) R 1  is CH 3 , R 2  is 4-N-dimethylaminosulfonylamino)benzyl, R 3 , R 4 , R 8 , R 9  and R 10  are each H and R 11  and R 12  are each OCH 3 ; or  
 (ix) R 1  is CH 3 , R 2  is HOCH2CH(CH3)CH2, R 3 , R 4 , R 8 , R 9  and R 10  are each H and R 11  and R 12  are each OCH 3 ; or  
 (x) R 1  is CH3, R 2  is I-methylcyclopropylmethyl, R 3 , R 4 , R 8 , R 9  and R 10  are each H and R 11  and R 12  are each OCH 3 , and  
 a serotonin reuptake inhibitor (SSRI).  
 
   
   
       19 . The pharmaceutical composition of  claim 18  wherein the serotonin reuptake inhibitor is selected from the group consisting of fluvoxamine, fluoxetine, paroxetine and sertraline, citalopram, venlafaxine, cericlamine, duloxetine, milnacipran, nefazodone and cyanodothiepin.  
   
   
       20 . A pharmaceutical composition comprising 3-isobutyl-8-(6-methoxy-isoquinolin-4-ylmethyl)-1-methyl-3,7-dihydro-purine-2,6-dione and a serotonin reuptake inhibitor selected from the group consisting of fluvoxamine, fluoxetine, paroxetine and sertraline, citalopram, venlafaxine, cericlamine, duloxetine, milnacipran, nefazodone and cyanodothiepin.