Heterocyclic inhibitors of an Hh-signal cascade, medicinal compositions based thereon and methods for treating diseases caused by the aberrant activity of an Hh-signal system
The invention relates to novel heterocyclic compounds and to the use thereof, to pharmaceutical compositions containing said chemical compounds as an active ingredient and to the use thereof for producing medicinal preparations for the human being and warm-blood animals for treating diseases caused by the aberrant activity of an Hedgehog (Hh)-signal system, in particular oncological diseases. The invention also relates to the use of the above-mentioned compounds in the form of ‘molecular pharmacological tools’ for examining (in vitro and in vivo) the biochemical features of the Hh-signal system, in particular, the interaction of Hh protein and transmembrane proteins, namely, suppressor Patched (Ptc) and protooncogenic proteins. The eight groups of the claimed compounds comprise the derivatives of 2,6-dihydro-7H-pyrazolo[3,4-d]pyridazine-7-one and 1,4-dihydropyrazolo[3,4-b][1,4]thiazine-5-one; N-acidylated 4-imidazo[1,2-a]pyrimidine-2-il-anilines; ([4H-thino[3,2-b]pyrrol-5-il) carbonyl]piperidine-4-carbonic acid amides; 2-(4carbomoilpyperidine-1-il)-isonicotinic acid amides; N-sylphonyl-1,2,3,4-tetrahydroquinoline-6-carbonic acid amides; and pyridine 2-amino-4,5,6,7-tetrahydrothieno[2,3-c]N-acidylated 3-azole derivatives.
1. A compound of a 2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one of general formula I or a pharmaceutically acceptable salt thereof,
wherein:
n is integer number 0, 1, 2 or 3;
R1 represents H, inert substituent, NH-protective or electrophilic substituent;
R2, R5 represent H or lower alkyl;
R3 represents H or inert substituent;
R4 represents H or inert substituents or R4a and R4b together with the nitrogen atom they are attached to via R4a and R4b may form a substituted azaheterocycle.
2. The compound of claim 1 , which is a substituted 2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one of general formula I-1 or pharmaceutically acceptable salts thereof,
wherein:
R4 is as defined above;
i is integer number 0, 1 or 2;
R26 represents H, halogen, CF 3 , CF 3 O, CN, nitro group or inert substituent;
R27 represents H, optionally substituted benzyl, optionally substituted aryl or optionally substituted lower alkyl.
3. A compound selected from the group consisting of
2-Phenyl-3,4-dimethyl-6-{2-[4-(3-methoxyphenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-(3-chlorophenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-phenylpiperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-(2,3-dimethylphenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-(2,5-dimethylphenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-(4-fluorophenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{2-[4-(2-fluorophenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-phenylpiperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-(3-chlorophenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-cyclohexylpiperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-(2,3-dimethylphenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-benzylpiperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-{1-methyl-2-[4-(2-fluorophenyl)piperazin-1-yl]-2-oxoethyl}-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-[2-(2,4-dimethylphenyl)-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl]-N-(2-fluorophenyl)acetamide;
2-Phenyl-3,4-dimethyl-6-[1-(morpholin-4-ylcarbonyl)propyl]-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-[2-(4-Methylphenyl)-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl]-N-[(5-methylfuran-2-yl)methyl]acetamide;
2-[2-(4-Methylphenyl)-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl)-N-(2-thien-2-ylethyl)propanamide;
2-[2-(4-Methylphenyl)-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-c]pyridazin-6-yl]-N-(cyclopropyl)butanamide;
3-(2-Phenyl-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl)-N-(pyridin-3-ylmethyl)propanamide;
3-(2-Phenyl-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl)-N-(furan-2-ylmethyl)propanamide;
2-Phenyl-3,4-dimethyl-6-(3-morpholin-4-yl-3-oxopropyl)-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
3-(2-Phenyl-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl)-N-(thien-2-ylmethyl)propanamide;
4-[2-(4-Methylphenyl)-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl]-N-(2-furan-2-ylethyl)butanamide;
2-(4-Methylphenyl)-3,4-dimethyl-6-[4-(4-ethylpiperazin-1-yl)-4-oxobutyl]-2,6-dihydro-7H-pyrazolo[3,4-d]pyridazin-7-one;
2-Phenyl-3,4-dimethyl-6-(4-morpholino-4-yl-4-oxobutyl)-2,6-dihydro-2H-pyrazolo[3,4-d]pyridazin-7-one;
4-(2-Phenyl-3,4-dimethyl-7-oxo-2,7-dihydro-6H-pyrazolo[3,4-d]pyridazin-6-yl)-N-[(1-methylethyl)phenyl]butanamide;
2-(2-Phenyl-3,4-dimethyl-7-oxo-2H-pyrazolo[4,3-d]pyridazin-6-yl)-N-[2-(4-benzylpiperidin-1-yl)ethyl]acetamide;
2-Phenyl-3,4-dimethyl-2H-pyrazolo[4,3-d]pyridazin-6-[2-(4-benzylpiperazin-1-yl)-4-oxoethyl]-7-one;
4-(2-p-Tolyl-3,4-dimethyl-7-oxo-2H-pyrazolo[3,4-d]pyridazin-6-yl)-N-(benzo[d][1,3]-dioxol-5-ylmethyl)butanamide;
2-p-Tolyl-3,4-dimethyl-6-[4-oxo-4-(4-(pyridin-2-yl)piperazin-1-yl)butyl]-2H-pyrazolo[3,4-d]pyridazin-7-one;
and pharmaceutical acceptable salts thereof.
4. A pharmaceutical composition, comprising an effective amount of at least one compound of claim 1 or a pharmaceutically acceptable salt thereof, and an excipient.
5. The pharmaceutical composition of claim 4 in the form of a tablet, a sheath, or an injection placed in pharmaceutically acceptable packing.