HRP20100408T1 - DERIVATI 2-ARIL-6-FENILIMIDAZO[1,2-a]PIRIDINA, NJIHOVO DOBIVANJE I UPOTREBA U TERAPIJI - Google Patents
DERIVATI 2-ARIL-6-FENILIMIDAZO[1,2-a]PIRIDINA, NJIHOVO DOBIVANJE I UPOTREBA U TERAPIJI Download PDFInfo
- Publication number
- HRP20100408T1 HRP20100408T1 HR20100408T HRP20100408T HRP20100408T1 HR P20100408 T1 HRP20100408 T1 HR P20100408T1 HR 20100408 T HR20100408 T HR 20100408T HR P20100408 T HRP20100408 T HR P20100408T HR P20100408 T1 HRP20100408 T1 HR P20100408T1
- Authority
- HR
- Croatia
- Prior art keywords
- cycloalkyl
- alkyl
- phenyl
- pyridin
- imidazo
- Prior art date
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- 238000002360 preparation method Methods 0.000 title claims 9
- 230000001225 therapeutic effect Effects 0.000 title 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims abstract 85
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 72
- 229910052736 halogen Inorganic materials 0.000 claims abstract 55
- 125000003118 aryl group Chemical group 0.000 claims abstract 47
- 150000002367 halogens Chemical class 0.000 claims abstract 44
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims abstract 42
- 150000001875 compounds Chemical class 0.000 claims abstract 35
- 125000002947 alkylene group Chemical group 0.000 claims abstract 33
- 229910003827 NRaRb Inorganic materials 0.000 claims abstract 25
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 23
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 20
- 125000001424 substituent group Chemical group 0.000 claims abstract 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 16
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 14
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims abstract 12
- 125000004429 atom Chemical group 0.000 claims abstract 10
- 125000005529 alkyleneoxy group Chemical group 0.000 claims abstract 8
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 6
- 125000001624 naphthyl group Chemical group 0.000 claims abstract 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims abstract 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims abstract 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 4
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical group C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims abstract 2
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 claims abstract 2
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 claims abstract 2
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000005843 halogen group Chemical group 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 11
- 239000002253 acid Substances 0.000 claims 10
- 229940079593 drug Drugs 0.000 claims 8
- 239000003814 drug Substances 0.000 claims 8
- 230000002265 prevention Effects 0.000 claims 7
- -1 (C3-C7)CycloAlkoxy Chemical group 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 125000006557 (C2-C5) alkylene group Chemical group 0.000 claims 2
- MYONEJYVJVQVAF-UHFFFAOYSA-N 1-[3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=C1 MYONEJYVJVQVAF-UHFFFAOYSA-N 0.000 claims 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 2
- 238000006482 condensation reaction Methods 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- PDCSZSDAIIGGJS-UHFFFAOYSA-N 1-[3-[2-(2,4-difluorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C(=CC(F)=CC=2)F)=C1 PDCSZSDAIIGGJS-UHFFFAOYSA-N 0.000 claims 1
- YSCIMARAKJTOQO-UHFFFAOYSA-N 1-[3-[2-(2-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C(=CC=CC=2)Cl)=C1 YSCIMARAKJTOQO-UHFFFAOYSA-N 0.000 claims 1
- VAQRCUNRDMEKOK-UHFFFAOYSA-N 1-[3-[2-(3,4-difluorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=C(F)C(F)=CC=2)=C1 VAQRCUNRDMEKOK-UHFFFAOYSA-N 0.000 claims 1
- ZSUXFNRFDYZPEB-UHFFFAOYSA-N 1-[3-[2-(3-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol 4-[6-[3-(hydroxymethyl)phenyl]imidazo[1,2-a]pyridin-2-yl]phenol Chemical compound OCC=1C=C(C=CC1)C=1C=CC=2N(C1)C=C(N2)C2=CC=C(C=C2)O.ClC=2C=C(C=CC2)C=2N=C1N(C=C(C=C1)C=1C=C(C=CC1)C(C)O)C2 ZSUXFNRFDYZPEB-UHFFFAOYSA-N 0.000 claims 1
- SOLQRLFTNWMKLR-UHFFFAOYSA-N 1-[3-[2-(3-fluorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=C(F)C=CC=2)=C1 SOLQRLFTNWMKLR-UHFFFAOYSA-N 0.000 claims 1
- UBTSBKDDTUQXRU-UHFFFAOYSA-N 1-[3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]-3-methylbutan-1-ol Chemical compound CC(C)CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=C1 UBTSBKDDTUQXRU-UHFFFAOYSA-N 0.000 claims 1
- JZTXDXUREYZCFA-UHFFFAOYSA-N 1-[3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]heptan-1-ol Chemical compound CCCCCCC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=C1 JZTXDXUREYZCFA-UHFFFAOYSA-N 0.000 claims 1
- LGZVZMDOBADMFD-UHFFFAOYSA-N 1-[3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]pentan-1-ol Chemical compound CCCCC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=C1 LGZVZMDOBADMFD-UHFFFAOYSA-N 0.000 claims 1
- PCLPUMSFIGAPDD-UHFFFAOYSA-N 1-[3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]propan-1-ol Chemical compound CCC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=C1 PCLPUMSFIGAPDD-UHFFFAOYSA-N 0.000 claims 1
- JTTPDWXPTGRTJI-UHFFFAOYSA-N 1-[3-[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound CC(O)C1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(F)=CC=2)=C1 JTTPDWXPTGRTJI-UHFFFAOYSA-N 0.000 claims 1
- NFXJURRZLLYBPN-UHFFFAOYSA-N 1-[4-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]ethanol Chemical compound C1=CC(C(O)C)=CC=C1C1=CN2C=C(C=3C=CC(Cl)=CC=3)N=C2C=C1 NFXJURRZLLYBPN-UHFFFAOYSA-N 0.000 claims 1
- ZYANTTOKFDWNGJ-UHFFFAOYSA-N 1-[4-[[3-[2-(4-methylphenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]methoxy]phenyl]ethanone 2-(4-methylphenyl)-6-[3-[[4-(trifluoromethyl)phenoxy]methyl]phenyl]imidazo[1,2-a]pyridine Chemical compound FC(C1=CC=C(OCC=2C=C(C=CC2)C=2C=CC=3N(C2)C=C(N3)C3=CC=C(C=C3)C)C=C1)(F)F.C1(=CC=C(C=C1)C=1N=C3N(C=C(C=C3)C=3C=C(COC2=CC=C(C=C2)C(C)=O)C=CC3)C1)C ZYANTTOKFDWNGJ-UHFFFAOYSA-N 0.000 claims 1
- HYURVCUMJWEFMW-UHFFFAOYSA-N 2-(4-chlorophenyl)-6-[2-(methoxymethyl)phenyl]imidazo[1,2-a]pyridine;hydrochloride Chemical compound Cl.COCC1=CC=CC=C1C1=CN2C=C(C=3C=CC(Cl)=CC=3)N=C2C=C1 HYURVCUMJWEFMW-UHFFFAOYSA-N 0.000 claims 1
- OBWVJVVNWMBROP-UHFFFAOYSA-N 2-(4-chlorophenyl)-6-[4-(methoxymethyl)phenyl]imidazo[1,2-a]pyridine Chemical compound C1=CC(COC)=CC=C1C1=CN2C=C(C=3C=CC(Cl)=CC=3)N=C2C=C1 OBWVJVVNWMBROP-UHFFFAOYSA-N 0.000 claims 1
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- QUXHWCXYIKKQDS-UHFFFAOYSA-N COC1=C(C=CC=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.COC=1C=C(C=CC1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.COC1=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1 Chemical compound COC1=C(C=CC=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.COC=1C=C(C=CC1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.COC1=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1 QUXHWCXYIKKQDS-UHFFFAOYSA-N 0.000 claims 1
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- OKOGJTHOFMPIHZ-UHFFFAOYSA-N OCC=1C=C(C=CC1)C=1C=CC=2N(C1)C=C(N2)C=2C=C(C#N)C=CC2.OCC2=CC=C(C=C2)C=2C=CC=1N(C2)C=C(N1)C=1C=C(C#N)C=CC1.C1(=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C2=CC=C(C=C2)CO)C1)C1=CC=CC=C1 Chemical compound OCC=1C=C(C=CC1)C=1C=CC=2N(C1)C=C(N2)C=2C=C(C#N)C=CC2.OCC2=CC=C(C=C2)C=2C=CC=1N(C2)C=C(N1)C=1C=C(C#N)C=CC1.C1(=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C2=CC=C(C=C2)CO)C1)C1=CC=CC=C1 OKOGJTHOFMPIHZ-UHFFFAOYSA-N 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000034799 Tauopathies Diseases 0.000 claims 1
- HOTODYIWLPMBRK-UHFFFAOYSA-N [3-[2-(2-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]methanol [3-[2-[4-(trifluoromethyl)phenyl]imidazo[1,2-a]pyridin-6-yl]phenyl]methanol Chemical compound FC(C1=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1)(F)F.ClC1=C(C=CC=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1 HOTODYIWLPMBRK-UHFFFAOYSA-N 0.000 claims 1
- XVDHAJOPZBKJTP-UHFFFAOYSA-N [3-[2-(3,4-difluorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]methanol;hydrochloride Chemical compound Cl.OCC1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=C(F)C(F)=CC=2)=C1 XVDHAJOPZBKJTP-UHFFFAOYSA-N 0.000 claims 1
- LJPGFWXYBPREBX-UHFFFAOYSA-N [3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]-cyclopentylmethanol Chemical compound C=1C=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=CC=1C(O)C1CCCC1 LJPGFWXYBPREBX-UHFFFAOYSA-N 0.000 claims 1
- FLRVREFLPLXHCL-UHFFFAOYSA-N [3-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]phenyl]-phenylmethanol Chemical compound C=1C=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(Cl)=CC=2)=CC=1C(O)C1=CC=CC=C1 FLRVREFLPLXHCL-UHFFFAOYSA-N 0.000 claims 1
- FMDRXVFYGAJKFK-UHFFFAOYSA-N [3-[2-[4-(difluoromethyl)phenyl]imidazo[1,2-a]pyridin-6-yl]phenyl]methanol Chemical compound OCC1=CC=CC(C2=CN3C=C(N=C3C=C2)C=2C=CC(=CC=2)C(F)F)=C1 FMDRXVFYGAJKFK-UHFFFAOYSA-N 0.000 claims 1
- DKKXSGSGLOGHSR-UHFFFAOYSA-N [N+](=O)([O-])C1=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.FC(OC=1C=C(C=CC1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1)(F)F Chemical compound [N+](=O)([O-])C1=CC=C(C=C1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1.FC(OC=1C=C(C=CC1)C=1N=C2N(C=C(C=C2)C=2C=C(C=CC2)CO)C1)(F)F DKKXSGSGLOGHSR-UHFFFAOYSA-N 0.000 claims 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 1
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- 229940126601 medicinal product Drugs 0.000 claims 1
- 229910052987 metal hydride Inorganic materials 0.000 claims 1
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- 201000006417 multiple sclerosis Diseases 0.000 claims 1
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Classifications
-
- 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
-
- 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
- A61K31/437—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 nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- 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
- A61P25/08—Antiepileptics; Anticonvulsants
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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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0608350A FR2906250B1 (fr) | 2006-09-22 | 2006-09-22 | Derives de 2-aryl-6phenyl-imidazo(1,2-a) pyridines, leur preparation et leur application en therapeutique |
| PCT/FR2007/001517 WO2008034974A1 (fr) | 2006-09-22 | 2007-09-19 | DERIVES DE 2-ARYL-6-PHENYL-IMIDAZO[1,2-α]PYRIDINES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20100408T1 true HRP20100408T1 (hr) | 2010-09-30 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20100408T HRP20100408T1 (hr) | 2006-09-22 | 2010-07-23 | DERIVATI 2-ARIL-6-FENILIMIDAZO[1,2-a]PIRIDINA, NJIHOVO DOBIVANJE I UPOTREBA U TERAPIJI |
Country Status (44)
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
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| FR2928921B1 (fr) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines, leur preparation et leur application en therapeutique |
| FR2928923B1 (fr) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 2-heteroaryl-6-phenyl-imidazo °1,2-a!pyridines, leur preparation et leur application en therapeutiques |
| FR2928924B1 (fr) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique |
| FR2928922B1 (fr) * | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines polysubstitues, leur preparation et leur application en therapeutique |
| FR2933609B1 (fr) * | 2008-07-10 | 2010-08-27 | Fournier Lab Sa | Utilisation de derives d'indole comme activateurs de nurr-1, pour le traitement de la maladie de parkinson. |
| FR2950344B1 (fr) * | 2009-09-18 | 2011-11-25 | Sanofi Aventis | Derives de 5-phenyl-pyrazolopyridine, leur preparation et leur aplication en therapeutique. |
| FR2950345B1 (fr) * | 2009-09-18 | 2011-09-23 | Sanofi Aventis | Derives acetyleniques de 5-phenyl-pyrazolopyridine, leur preparation et leur application en therapeutique |
| FR2953520B1 (fr) * | 2009-12-04 | 2011-11-25 | Sanofi Aventis | Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique |
| WO2014082979A1 (en) * | 2012-11-29 | 2014-06-05 | F. Hoffmann-La Roche Ag | Imidazopyridine derivatives |
| TWI644899B (zh) | 2013-02-04 | 2018-12-21 | 健生藥品公司 | Ｆｌａｐ調節劑 |
| US9745328B2 (en) | 2013-02-04 | 2017-08-29 | Janssen Pharmaceutica Nv | Flap modulators |
| KR102292293B1 (ko) * | 2013-08-02 | 2021-08-23 | 재단법인 한국파스퇴르연구소 | 항감염성 화합물 |
| CN107531693B (zh) | 2015-04-10 | 2021-07-06 | 百济神州有限公司 | 作为吲哚胺、色氨酸二加氧酶抑制剂的5或8-取代的咪唑并[1，5-a]吡啶 |
| MA52119A (fr) | 2015-10-19 | 2018-08-29 | Ncyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
| SG10202004618TA (en) | 2015-11-19 | 2020-06-29 | Incyte Corp | Heterocyclic compounds as immunomodulators |
| MD3394033T2 (ro) | 2015-12-22 | 2021-04-30 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
| US20170320875A1 (en) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| LT3472167T (lt) | 2016-06-20 | 2022-11-10 | Incyte Corporation | Heterocikliniai junginiai kaip imunomoduliatoriai |
| US20180016260A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| US20180057486A1 (en) | 2016-08-29 | 2018-03-01 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| WO2018054365A1 (en) * | 2016-09-24 | 2018-03-29 | Beigene, Ltd. | NOVEL 5 or 8-SUBSTITUTED IMIDAZO [1, 5-a] PYRIDINES AS SELECTIVE INHIBITORS OF INDOLEAMINE AND/OR TRYPTOPHANE 2, 3-DIOXYGENASES |
| WO2018119236A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
| MA47120A (fr) | 2016-12-22 | 2021-04-28 | Incyte Corp | Dérivés pyridine utilisés en tant qu'immunomodulateurs |
| KR102641030B1 (ko) | 2016-12-22 | 2024-02-29 | 인사이트 코포레이션 | Pd-l1 내재화 유도제로서의 테트라하이드로 이미다조[4,5-c]피리딘 유도체 |
| BR112019012993A2 (pt) | 2016-12-22 | 2019-12-03 | Incyte Corp | derivados de benzo-oxazol como imunomoduladores |
| CN111386114A (zh) | 2017-11-25 | 2020-07-07 | 百济神州有限公司 | 作为吲哚胺2,3-双加氧酶的选择性抑制剂的新颖苯并咪唑 |
| LT3774791T (lt) | 2018-03-30 | 2023-04-11 | Incyte Corporation | Hererocikliniai junginiai kaip imunomoduliatoriai |
| HRP20230306T1 (hr) | 2018-05-11 | 2023-05-12 | Incyte Corporation | Derivati tetrahidro-imidazo[4,5-c]piridina kao pd-l1 imunomodulatori |
| WO2021030162A1 (en) | 2019-08-09 | 2021-02-18 | Incyte Corporation | Salts of a pd-1/pd-l1 inhibitor |
| KR20220075382A (ko) | 2019-09-30 | 2022-06-08 | 인사이트 코포레이션 | 면역조절제로서의 피리도[3,2-d]피리미딘 화합물 |
| MX2022005651A (es) | 2019-11-11 | 2022-07-27 | Incyte Corp | Sales y formas cristalinas de un inhibidor de la proteina de muerte celular programada 1 (pd-1)/ligando de muerte celular programada 1 (pd-l1). |
| WO2022099075A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Crystalline form of a pd-1/pd-l1 inhibitor |
| AU2021373044A1 (en) | 2020-11-06 | 2023-06-08 | Incyte Corporation | Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof |
| WO2022099018A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process of preparing a pd-1/pd-l1 inhibitor |
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| JP4041624B2 (ja) * | 1999-07-21 | 2008-01-30 | 三井化学株式会社 | 有機電界発光素子 |
| US6489337B1 (en) * | 2000-03-31 | 2002-12-03 | Ortho-Mcneil Pharmaceutical, Inc. | Method for treating histamine H3 receptor-mediated disorders with 2- or 3-aryl substituted imidazo[1,2-a] pyridines |
| GB0119911D0 (en) * | 2001-08-15 | 2001-10-10 | Novartis Ag | Organic Compounds |
| AR041291A1 (es) * | 2002-09-19 | 2005-05-11 | Schering Corp | Imidazopiridinas como inhibidores de quinasa dependientes de ciclina |
| GB0303503D0 (en) * | 2003-02-14 | 2003-03-19 | Novartis Ag | Organic compounds |
| AU2005220882A1 (en) * | 2004-03-08 | 2005-09-22 | Georgia State University Research Foundation, Inc | Novel dicationic imidazo(1,2-a)pyridines and 5,6,7,8-tetrahydro-imidazo(1,2a)pyridines as antiprotozoal agents |
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2006
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2007
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- 2007-09-19 AR ARP070104136A patent/AR062897A1/es not_active Application Discontinuation
- 2007-09-20 PE PE2007001266A patent/PE20080671A1/es not_active Application Discontinuation
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