HRP20170484T1 - Novi kondenzirani spojevi piridina kao inhibitori kazeinske kinaze - Google Patents
Novi kondenzirani spojevi piridina kao inhibitori kazeinske kinaze Download PDFInfo
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- HRP20170484T1 HRP20170484T1 HRP20170484TT HRP20170484T HRP20170484T1 HR P20170484 T1 HRP20170484 T1 HR P20170484T1 HR P20170484T T HRP20170484T T HR P20170484TT HR P20170484 T HRP20170484 T HR P20170484T HR P20170484 T1 HRP20170484 T1 HR P20170484T1
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- Croatia
- Prior art keywords
- methyl
- pyrazol
- fluorophenyl
- pyrrolo
- dihydro
- Prior art date
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- 102000005403 Casein Kinases Human genes 0.000 title 1
- 108010031425 Casein Kinases Proteins 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 150000003222 pyridines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 14
- 150000003839 salts Chemical class 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 208000035475 disorder Diseases 0.000 claims 4
- XISSYJGQGSMWHO-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-furo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)OCC=3N=CC=2)C=1C1=CC=C(F)C=C1 XISSYJGQGSMWHO-UHFFFAOYSA-N 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 208000019022 Mood disease Diseases 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 208000019116 sleep disease Diseases 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 claims 1
- YKLKIDCWMLBXQV-UHFFFAOYSA-N 1-[4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-5,7-dihydropyrrolo[3,4-b]pyridin-6-yl]propan-1-one Chemical compound C=12CN(C(=O)CC)CC2=NC=CC=1C1=CN(C)N=C1C1=CC=C(F)C=C1 YKLKIDCWMLBXQV-UHFFFAOYSA-N 0.000 claims 1
- MPHOHULBRJTEQS-UHFFFAOYSA-N 3-[4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-5-oxo-7h-pyrrolo[3,4-b]pyridin-6-yl]propanenitrile Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CCC#N)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 MPHOHULBRJTEQS-UHFFFAOYSA-N 0.000 claims 1
- BSYXDCSTPIHJLY-UHFFFAOYSA-N 3-[[4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-5-oxo-7h-pyrrolo[3,4-b]pyridin-6-yl]methyl]benzonitrile Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CC=4C=C(C=CC=4)C#N)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 BSYXDCSTPIHJLY-UHFFFAOYSA-N 0.000 claims 1
- MKTSLGTZIKIVQO-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6,7-dihydropyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)NCC=3N=CC=2)C=1C1=CC=C(F)C=C1 MKTSLGTZIKIVQO-UHFFFAOYSA-N 0.000 claims 1
- SFGFXQRSJQFYRR-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-(oxolan-3-ylmethyl)-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CC4COCC4)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 SFGFXQRSJQFYRR-UHFFFAOYSA-N 0.000 claims 1
- QMYMODQJZUCBDM-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-(pyridin-3-ylmethyl)-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CC=4C=NC=CC=4)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 QMYMODQJZUCBDM-UHFFFAOYSA-N 0.000 claims 1
- QTZWQUWFGJPEBB-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-[(1-methylpyrazol-4-yl)methyl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound C1=NN(C)C=C1CN1C(=O)C2=C(C=3C(=NN(C)C=3)C=3C=CC(F)=CC=3)C=CN=C2C1 QTZWQUWFGJPEBB-UHFFFAOYSA-N 0.000 claims 1
- UENLCEMZMZCOPR-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-[(6-methylpyridin-3-yl)methyl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound C1=NC(C)=CC=C1CN1C(=O)C2=C(C=3C(=NN(C)C=3)C=3C=CC(F)=CC=3)C=CN=C2C1 UENLCEMZMZCOPR-UHFFFAOYSA-N 0.000 claims 1
- GNUDHCJLTHZJDF-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-[2-(3-methyl-1,2,4-oxadiazol-5-yl)ethyl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound CC1=NOC(CCN2C(C3=C(C=4C(=NN(C)C=4)C=4C=CC(F)=CC=4)C=CN=C3C2)=O)=N1 GNUDHCJLTHZJDF-UHFFFAOYSA-N 0.000 claims 1
- NGDXEOHYWJHBTJ-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-methyl-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound C=12C(=O)N(C)CC2=NC=CC=1C1=CN(C)N=C1C1=CC=C(F)C=C1 NGDXEOHYWJHBTJ-UHFFFAOYSA-N 0.000 claims 1
- UFCMFJLZOSWNDV-UHFFFAOYSA-N 4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-6-methylsulfonyl-5,7-dihydropyrrolo[3,4-b]pyridine Chemical compound N=1N(C)C=C(C=2C=3CN(CC=3N=CC=2)S(C)(=O)=O)C=1C1=CC=C(F)C=C1 UFCMFJLZOSWNDV-UHFFFAOYSA-N 0.000 claims 1
- YHYANTPTKIBUGR-UHFFFAOYSA-N 6-(3-bicyclo[1.1.1]pentanyl)-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CC=3N=CC=2)C23CC(C2)C3)C=1C1=CC=C(F)C=C1 YHYANTPTKIBUGR-UHFFFAOYSA-N 0.000 claims 1
- BZOIBBGFFYYFJR-UHFFFAOYSA-N 6-[(1,5-dimethylpyrazol-3-yl)methyl]-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound CN1C(C)=CC(CN2C(C3=C(C=4C(=NN(C)C=4)C=4C=CC(F)=CC=4)C=CN=C3C2)=O)=N1 BZOIBBGFFYYFJR-UHFFFAOYSA-N 0.000 claims 1
- QOTQMRDUISRNTF-UHFFFAOYSA-N 6-[(1,5-dimethylpyrazol-4-yl)methyl]-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound C1=NN(C)C(C)=C1CN1C(=O)C2=C(C=3C(=NN(C)C=3)C=3C=CC(F)=CC=3)C=CN=C2C1 QOTQMRDUISRNTF-UHFFFAOYSA-N 0.000 claims 1
- FLOCRZOELBFREL-UHFFFAOYSA-N 6-benzyl-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(CC=4C=CC=CC=4)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 FLOCRZOELBFREL-UHFFFAOYSA-N 0.000 claims 1
- XDZASHKAJTZMIT-UHFFFAOYSA-N 6-cyclopentyl-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound N=1N(C)C=C(C=2C=3C(=O)N(C4CCCC4)CC=3N=CC=2)C=1C1=CC=C(F)C=C1 XDZASHKAJTZMIT-UHFFFAOYSA-N 0.000 claims 1
- IJWJTLLIGDSXET-UHFFFAOYSA-N 6-ethyl-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-7h-pyrrolo[3,4-b]pyridin-5-one Chemical compound C=12C(=O)N(CC)CC2=NC=CC=1C1=CN(C)N=C1C1=CC=C(F)C=C1 IJWJTLLIGDSXET-UHFFFAOYSA-N 0.000 claims 1
- BYVHQGZXFKZAHT-UHFFFAOYSA-N 6-ethylsulfonyl-4-[3-(4-fluorophenyl)-1-methylpyrazol-4-yl]-5,7-dihydropyrrolo[3,4-b]pyridine Chemical compound C=12CN(S(=O)(=O)CC)CC2=NC=CC=1C1=CN(C)N=C1C1=CC=C(F)C=C1 BYVHQGZXFKZAHT-UHFFFAOYSA-N 0.000 claims 1
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 1
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- 208000020401 Depressive disease Diseases 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 208000012902 Nervous system disease Diseases 0.000 claims 1
- 208000025966 Neurological disease Diseases 0.000 claims 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 1
- 230000000926 neurological effect Effects 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 208000020016 psychiatric disease Diseases 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 208000020685 sleep-wake disease Diseases 0.000 claims 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- Bioinformatics & Cheminformatics (AREA)
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- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Biomedical Technology (AREA)
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- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Anesthesiology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
Claims (13)
1. Spoj Formule I:
[image]
,
naznačen time što:
X je NR1, a navedeni R1 na N je C1-4 alkil ili C3-4cikloalkil;
Y je CR1, a navedeni R1 na C je H ili CH3;
prsten A je
[image]
,
[image]
ili
[image]
gdje je svaki R2 neovisno H, C1-6alkil, C4-10-bicikloalkil, -(CH2)t-CN, -SO2C1-6alkil, -SO2(CH2)t-C3-6cikloalkil, -C1-6alkil-O-C1-6alkil, -C1-6alkil-C(O)O-C1-6alkil, -C3-6cikloalkil-C(O)O-C1-6alkil, -C(O)-(O)u-C1-6alkil, -C(O)-C1-6alkil-O-C1-6alkil, -C(O)-(O)u-(CH2)t-(C6-10aril), -(CH2)t-(C6-10aril), -C(O)-(O)u-(CH2)t-(5- do 10-eročlani heteroaril), -(CH2)t-C(O)-NR5R6, -(CH2)t-(5- do 10-eročlani heteroaril), -C(O)-(O)u-(CH2)t-(3- do 10-eročlani heterocikloalkil), -(CH2)t-(4- do 10-eročlani heterocikloalkil), -C(O)-(O)u-(CH2)t-(3- do 10-eročlani cikloalkil) ili -(CH2)t-(3- do 10-eročlani cikloalkil),
gdje navedeni aril, heteroaril, cikloalkil i heterocikloalkil u R2 može biti supstituiran s do dva supstituenta, koje se neovisno bira između halogena, OH, cijano, C1-6alkila, -C(O)-O-C1-3alkila ili C1-6alkil-O-C1-6alkila,
i gdje bilo koji alkil, cikloalkil i heterocikloalkil u R2 može biti dodatno supstituiran s okso, gdje to valencija dopušta;
svaki R4 je F;
svaki R5 je neovisno H ili C1-6alkil;
svaki R6 je neovisno H ili C1-6alkil;
R7 je H;
n je 0, 1 ili 2;
svaki t je neovisno 0, 1 ili 2; i
svaki u je neovisno 0 ili 1;
ili njegova farmaceutski prihvatljiva sol.
2. Spoj u skladu s patentnim zahtjevom 1, ili njegova farmaceutski prihvatljiva sol,
naznačen time što
X je NR1, a navedeni R1 na N je C1-4alkil;
svaki R2 je neovisno H, C1-6alkil, -SO2C1-6alkil, -SO2(CH2)t-C3-6cikloalkil, -C1-6alkil-O-C1-6alkil, -C(O)-(O)u-C1-6alkil, -(CH2)t-(C6-10aril), -C(O)-(O)u-(CH2)t-(5- do 10-eročlani heteroaril), -(CH2)t-C(O)-NR5R6, -(CH2)t-(5- do 10-eročlani heteroaril), -(CH2)t-(4- do 10-eročlani heterocikloalkil) ili -(CH2)t-(3- do 10-eročlani cikloalkil),
gdje navedeni aril, heteroaril, cikloalkil i heterocikloalkil u R2 može biti supstituiran s do dva supstituenta, koje se neovisno bira između halogena, OH, cijano, C1-6alkila, -C(O)-O-C1-3alkila ili C1-6alkil-O-C1-6alkila,
i gdje bilo koji alkil, cikloalkil i heterocikloalkil u R2 može biti dodatno supstituiran s okso, gdje to valencija dopušta;
svaki R5 je H;
n je 1; i
Y, R4, R6, R7, t, u i A su definirani kao u patentnom zahtjevu 1.
3. Spoj u skladu s patentnim zahtjevom 1 ili 2, ili njegova farmaceutski prihvatljiva sol, naznačen time što je R2 neovisno H, -CH3 ili SO2CH3.
4. Spoj u skladu s patentnim zahtjevom 1, ili njegova farmaceutski prihvatljiva sol, naznačen time što je spoj:
4-(3-(4-fluorfenil)-1-metil-1H-pirazol-4-il)furo[3,4-b]piridin-5(7H)-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-metil-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-benzil-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-(metilsulfonil)-6,7-dihidro-5H-pirolo[3,4-b]piridin;
6-(etilsulfonil)-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-propionil-6,7-dihidro-5H-pirolo[3,4-b]piridin;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-[(1-metil-1H-pirazol-4-il)metil]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-(tetrahidrofuran-3-ilmetil)-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-[(1,5-dimetil-1H-pirazol-3-il)metil]-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-ciklopentil-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-etil-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-[(1,5-dimetil-1H-pirazol-4-il)metil]-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-(ciklopropilmetil)-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-[2-(3-metil-1,2,4-oksadiazol-5-il)etil]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
3-{4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-5-okso-5,7-dihidro-6H-pirolo[3,4-b]piridin-6-il}propanonitril;
3-({4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-5-okso-5,7-dihidro-6H-pirolo[3,4-b]piridin-6-il}metil)benzonitril;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-[(1R,5S,6R)-3-oksabiciklo[3.1.0]heks-6-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-biciklo[1.1.1]pent-1-il-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-(piridin-3-ilmetil)-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on;
6-(3-etoksipropil)-4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on; ili
4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]-6-[(6-metilpiridin-3-il)metil]-6,7-dihidro-5H-pirolo[3,4-b]piridin-5-on.
5. Spoj u skladu s patentnim zahtjevom 1, naznačen time što je 4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]furo[3,4-b]piridin-5(7H)-on ili njegova farmaceutski prihvatljiva sol.
6. Spoj u skladu s patentnim zahtjevom 5, naznačen time što je 4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]furo[3,4-b]piridin-5(7H)-on.
7. Spoj u skladu s patentnim zahtjevom 5, naznačen time što je farmaceutski prihvatljiva sol of 4-[3-(4-fluorfenil)-1-metil-1H-pirazol-4-il]furo[3,4-b]piridin-5(7H)-on.
8. Spoj u skladu s bilo kojim od patentnih zahtjeva 1 do 7, ili njegova farmaceutski prihvatljiva sol, naznačen time što je namijenjen upotrebi u liječenju poremećaja spavanja, te neurološke ili psihijatrijske bolesti ili poremećaja kod sisavca.
9. Spoj namijenjen upotrebi u skladu s patentnim zahtjevom 8, naznačen time što je bolest ili poremećaj poremećaj raspoloženja ili poremećaj spavanja.
10. Spoj namijenjen upotrebi u skladu s patentnim zahtjevom 9, naznačen time što se poremećaj raspoloženja bira iz skupine koju čine depresivni poremećaj i bipolarni poremećaj.
11. Spoj namijenjen upotrebi u skladu s patentnim zahtjevom 8, naznačen time što je bolest ili poremećaj poremećaj nedostatka pažnje s hiperaktivnošću, shizofrenija ili Alzheimerova bolest.
12. Spoj namijenjen upotrebi u skladu s patentnim zahtjevom 11, naznačen time što je bolest ili poremećaj Alzheimerova bolest.
13. Farmaceutski pripravak, naznačen time što sadrži spoj u skladu s bilo kojim od patentnih zahtjeva 1 do 7, ili njegovu farmaceutski prihvatljivu sol, kao i farmaceutski prihvatljivu podlogu.
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US201061425213P | 2010-12-20 | 2010-12-20 | |
EP11805210.9A EP2654750B1 (en) | 2010-12-20 | 2011-12-06 | Novel fused pyridine compounds as casein kinase inhibitors |
PCT/IB2011/055489 WO2012085721A1 (en) | 2010-12-20 | 2011-12-06 | Novel fused pyridine compounds as casein kinase inhibitors |
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HRP20170484TT HRP20170484T1 (hr) | 2010-12-20 | 2017-03-22 | Novi kondenzirani spojevi piridina kao inhibitori kazeinske kinaze |
HRP20191469 HRP20191469T1 (hr) | 2010-12-20 | 2019-08-14 | Novi kondenzirani spojevi piridina kao inhibitori kazeinske kinase |
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US (1) | US8536164B2 (hr) |
EP (2) | EP3181133B1 (hr) |
JP (2) | JP5684923B2 (hr) |
KR (1) | KR101590236B1 (hr) |
CN (1) | CN103260622B (hr) |
AR (1) | AR084412A1 (hr) |
AU (1) | AU2011346733C1 (hr) |
CA (1) | CA2819961C (hr) |
CY (2) | CY1118772T1 (hr) |
DK (2) | DK2654750T3 (hr) |
ES (2) | ES2623387T3 (hr) |
HK (1) | HK1188145A1 (hr) |
HR (2) | HRP20170484T1 (hr) |
HU (2) | HUE032405T2 (hr) |
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LT (2) | LT2654750T (hr) |
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PL (2) | PL2654750T3 (hr) |
PT (2) | PT3181133T (hr) |
RS (2) | RS59098B1 (hr) |
SG (1) | SG190802A1 (hr) |
SI (2) | SI3181133T1 (hr) |
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SI2493876T1 (sl) * | 2009-10-28 | 2014-04-30 | Pfizer Inc. | Derivati imidazola kot inhibitorji kazein-kinaze |
US9938269B2 (en) * | 2011-06-30 | 2018-04-10 | Abbvie Inc. | Inhibitor compounds of phosphodiesterase type 10A |
EP2935272B1 (en) * | 2012-12-21 | 2017-02-22 | Bristol-Myers Squibb Company | Pyrazole substituted imidazopyrazines as casein kinase 1 d/e inhibitors |
WO2015163446A1 (ja) * | 2014-04-25 | 2015-10-29 | 協和発酵キリン株式会社 | イミダゾール化合物の製造方法 |
JP2017222576A (ja) * | 2014-10-31 | 2017-12-21 | 石原産業株式会社 | 有害生物防除剤 |
CN107365315B (zh) * | 2016-05-11 | 2024-08-09 | 国药集团国瑞药业有限公司 | 一种吡唑类化合物、其晶型及其制备方法 |
US10973820B2 (en) * | 2017-12-13 | 2021-04-13 | Facio Intellectual Property B.V. | Compounds for treatment of diseases related to DUX4 expression |
TW202112368A (zh) | 2019-06-13 | 2021-04-01 | 荷蘭商法西歐知識產權股份有限公司 | 用於治療有關dux4表現之疾病的抑制劑組合 |
EP4126878A4 (en) * | 2020-03-27 | 2024-07-10 | Gritscience Biopharmaceuticals Co Ltd | COMPOUNDS USED AS CASEIN KINASE INHIBITORS |
CN115335057A (zh) * | 2020-03-27 | 2022-11-11 | 北京原基华毅生物科技有限公司 | 抑制酪蛋白激酶的方法 |
CN111808102B (zh) * | 2020-08-03 | 2021-12-31 | 南通大学 | 一种3-甲氧基-6,7-二氢-5H-吡咯并[3,4-b]吡啶盐酸盐及其合成方法 |
AU2021342792A1 (en) * | 2020-09-17 | 2023-06-01 | Janssen Pharmaceutica Nv | Casein kinase 1 delta modulators |
KR20230069169A (ko) * | 2020-09-17 | 2023-05-18 | 얀센 파마슈티카 엔.브이. | 카제인 키나제 1 델타 조절제 |
WO2022115301A1 (en) * | 2020-11-24 | 2022-06-02 | Merck Sharp & Dohme Corp. | Modified isoindolinones as glucosylceramide synthase inhibitors |
WO2022127755A1 (en) * | 2020-12-15 | 2022-06-23 | Gritscience Biopharmaceuticals Co., Ltd. | Compounds as casein kinase inhibitors |
US20230053307A1 (en) * | 2021-07-19 | 2023-02-16 | Buddhist Tzu Chi Medical Foundation | Method for preventing or treating skin disorders and conditions |
WO2023241552A1 (en) * | 2022-06-14 | 2023-12-21 | Gritscience Biopharmaceuticals Co., Ltd | Salt and/or crystal form for compounds as casein kinase inhibitors |
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EP0151962A3 (en) | 1984-01-25 | 1985-10-02 | Beecham Group Plc | Pyrazolopyridine derivatives |
AU754830C (en) * | 1997-05-22 | 2004-02-12 | G.D. Searle Llc | Substituted pyrazoles as p38 kinase inhibitors |
AU2728201A (en) * | 1999-12-21 | 2001-07-03 | Sugen, Inc. | 4-substituted 7-aza-indolin-2-ones and their use as protein kinase inhibitors |
KR20140026644A (ko) | 2005-06-22 | 2014-03-05 | 케모센트릭스, 인크. | 아자인다졸 화합물 및 사용방법 |
US7897595B2 (en) | 2006-05-26 | 2011-03-01 | Forest Laboratories Holdings Limited | Pyridoazepine derivatives |
EP2308866A1 (de) * | 2009-10-09 | 2011-04-13 | Bayer CropScience AG | Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide |
SI2493876T1 (sl) * | 2009-10-28 | 2014-04-30 | Pfizer Inc. | Derivati imidazola kot inhibitorji kazein-kinaze |
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