HRP20100258T1 - Heksahidro ciklooktil pirazol kanabinoidni modulatori - Google Patents
Heksahidro ciklooktil pirazol kanabinoidni modulatori Download PDFInfo
- Publication number
- HRP20100258T1 HRP20100258T1 HR20100258T HRP20100258T HRP20100258T1 HR P20100258 T1 HRP20100258 T1 HR P20100258T1 HR 20100258 T HR20100258 T HR 20100258T HR P20100258 T HRP20100258 T HR P20100258T HR P20100258 T1 HRP20100258 T1 HR P20100258T1
- Authority
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- Croatia
- Prior art keywords
- halogen
- optionally substituted
- hydroxy
- absent
- alkyl
- Prior art date
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- NNRSEKSIYNJCLU-UHFFFAOYSA-N 5-cyclooctyl-1h-pyrazole Chemical compound C1CCCCCCC1C1=NNC=C1 NNRSEKSIYNJCLU-UHFFFAOYSA-N 0.000 title 1
- 229930003827 cannabinoid Natural products 0.000 title 1
- 239000003557 cannabinoid Substances 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 claims abstract 66
- 150000002367 halogens Chemical class 0.000 claims abstract 66
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 60
- 125000000217 alkyl group Chemical group 0.000 claims abstract 54
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 48
- 125000003118 aryl group Chemical group 0.000 claims abstract 44
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 38
- 150000001875 compounds Chemical class 0.000 claims abstract 37
- 150000003839 salts Chemical class 0.000 claims abstract 20
- 125000002947 alkylene group Chemical group 0.000 claims abstract 17
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 12
- 239000001257 hydrogen Substances 0.000 claims abstract 12
- 125000004103 aminoalkyl group Chemical group 0.000 claims abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 10
- 150000002431 hydrogen Chemical class 0.000 claims abstract 7
- 125000001118 alkylidene group Chemical group 0.000 claims abstract 6
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims abstract 5
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 10
- 125000005102 carbonylalkoxy group Chemical group 0.000 claims 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 7
- 238000000034 method Methods 0.000 claims 7
- -1 carboxy, carbonyl Chemical group 0.000 claims 6
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims 5
- 125000004104 aryloxy group Chemical group 0.000 claims 5
- 125000005242 carbamoyl alkyl group Chemical group 0.000 claims 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 5
- 239000003433 contraceptive agent Substances 0.000 claims 5
- 208000035475 disorder Diseases 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 230000002254 contraceptive effect Effects 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 229940125425 inverse agonist Drugs 0.000 claims 4
- 208000011580 syndromic disease Diseases 0.000 claims 4
- 102000009132 CB1 Cannabinoid Receptor Human genes 0.000 claims 3
- 108010073366 CB1 Cannabinoid Receptor Proteins 0.000 claims 3
- 102000018208 Cannabinoid Receptor Human genes 0.000 claims 3
- 108050007331 Cannabinoid receptor Proteins 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 230000006872 improvement Effects 0.000 claims 3
- 230000001404 mediated effect Effects 0.000 claims 3
- 230000002265 prevention Effects 0.000 claims 3
- UGJMXCAKCUNAIE-UHFFFAOYSA-N Gabapentin Chemical compound OC(=O)CC1(CN)CCCCC1 UGJMXCAKCUNAIE-UHFFFAOYSA-N 0.000 claims 2
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical class C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims 2
- KJADKKWYZYXHBB-XBWDGYHZSA-N Topiramic acid Chemical group C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 KJADKKWYZYXHBB-XBWDGYHZSA-N 0.000 claims 2
- 239000005557 antagonist Substances 0.000 claims 2
- 230000001773 anti-convulsant effect Effects 0.000 claims 2
- 239000001961 anticonvulsive agent Substances 0.000 claims 2
- 230000036528 appetite Effects 0.000 claims 2
- 235000019789 appetite Nutrition 0.000 claims 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000004615 ingredient Substances 0.000 claims 2
- 230000004060 metabolic process Effects 0.000 claims 2
- 239000000583 progesterone congener Substances 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- MNHBMBLQTYNCLS-SXKRPYPPSA-N (9e)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-n-[(1r)-1-phenylethyl]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound N([C@H](C)C=1C=CC=CC=1)C(=O)C1=NN(C=2C(=CC(Cl)=CC=2)Cl)C2=C1CCCCC\C2=C/C1=CC=C(F)C=C1 MNHBMBLQTYNCLS-SXKRPYPPSA-N 0.000 claims 1
- JXIBYNYOXLGQRZ-OXMAITBSSA-N (9e)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-n-[(1r)-1-pyridin-2-ylethyl]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound N([C@H](C)C=1N=CC=CC=1)C(=O)C1=NN(C=2C(=CC(Cl)=CC=2)Cl)C2=C1CCCCC\C2=C/C1=CC=C(F)C=C1 JXIBYNYOXLGQRZ-OXMAITBSSA-N 0.000 claims 1
- MNHBMBLQTYNCLS-KNOQIOAQSA-N (9e)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-n-[(1s)-1-phenylethyl]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound N([C@@H](C)C=1C=CC=CC=1)C(=O)C1=NN(C=2C(=CC(Cl)=CC=2)Cl)C2=C1CCCCC\C2=C/C1=CC=C(F)C=C1 MNHBMBLQTYNCLS-KNOQIOAQSA-N 0.000 claims 1
- NIHUXQKCSPXBKR-LVZFUZTISA-N (9e)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-n-piperidin-1-yl-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound C1=CC(F)=CC=C1\C=C/1C(N(N=C2C(=O)NN3CCCCC3)C=3C(=CC(Cl)=CC=3)Cl)=C2CCCCC\1 NIHUXQKCSPXBKR-LVZFUZTISA-N 0.000 claims 1
- YPDNHQRYJSSZOF-NBVRZTHBSA-N (9e)-n',1-bis(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carbohydrazide Chemical compound C1=CC(F)=CC=C1\C=C/1C(N(N=C2C(=O)NNC=3C(=CC(Cl)=CC=3)Cl)C=3C(=CC(Cl)=CC=3)Cl)=C2CCCCC\1 YPDNHQRYJSSZOF-NBVRZTHBSA-N 0.000 claims 1
- OWGJZOMZWAGXRN-HMMYKYKNSA-N (9e)-n-(3,3a,4,5,6,6a-hexahydro-1h-cyclopenta[c]pyrrol-2-yl)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound C1=CC(F)=CC=C1\C=C/1C(N(N=C2C(=O)NN3CC4CCCC4C3)C=3C(=CC(Cl)=CC=3)Cl)=C2CCCCC\1 OWGJZOMZWAGXRN-HMMYKYKNSA-N 0.000 claims 1
- ITQYXNBKWNXDRL-SXKRPYPPSA-N (9e)-n-[(1r)-1-cyclohexylethyl]-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound N([C@H](C)C1CCCCC1)C(=O)C1=NN(C=2C(=CC(Cl)=CC=2)Cl)C2=C1CCCCC\C2=C/C1=CC=C(F)C=C1 ITQYXNBKWNXDRL-SXKRPYPPSA-N 0.000 claims 1
- ITQYXNBKWNXDRL-KNOQIOAQSA-N (9e)-n-[(1s)-1-cyclohexylethyl]-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazole-3-carboxamide Chemical compound N([C@@H](C)C1CCCCC1)C(=O)C1=NN(C=2C(=CC(Cl)=CC=2)Cl)C2=C1CCCCC\C2=C/C1=CC=C(F)C=C1 ITQYXNBKWNXDRL-KNOQIOAQSA-N 0.000 claims 1
- JXJUOZBHERCWDJ-UHFFFAOYSA-N 1-cyclohexyl-n-(2,2,4-trimethyl-3-bicyclo[2.2.1]heptanyl)-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carboxamide Chemical compound C1C2(C)CCC1C(C)(C)C2NC(=O)C(C=1CCCCCCC=11)=NN1C1CCCCC1 JXJUOZBHERCWDJ-UHFFFAOYSA-N 0.000 claims 1
- 102000009135 CB2 Cannabinoid Receptor Human genes 0.000 claims 1
- 108010073376 CB2 Cannabinoid Receptor Proteins 0.000 claims 1
- 102100033868 Cannabinoid receptor 1 Human genes 0.000 claims 1
- 208000010412 Glaucoma Diseases 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- 208000016285 Movement disease Diseases 0.000 claims 1
- 208000007101 Muscle Cramp Diseases 0.000 claims 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 claims 1
- 208000008589 Obesity Diseases 0.000 claims 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 claims 1
- 208000005392 Spasm Diseases 0.000 claims 1
- SPKANWAMBRARSP-LVZFUZTISA-N [(9e)-1-(2,4-dichlorophenyl)-9-[(4-fluorophenyl)methylidene]-5,6,7,8-tetrahydro-4h-cycloocta[c]pyrazol-3-yl]-piperidin-1-ylmethanone Chemical compound C1=CC(F)=CC=C1\C=C/1C(N(N=C2C(=O)N3CCCCC3)C=3C(=CC(Cl)=CC=3)Cl)=C2CCCCC\1 SPKANWAMBRARSP-LVZFUZTISA-N 0.000 claims 1
- 239000000556 agonist Substances 0.000 claims 1
- 229940125681 anticonvulsant agent Drugs 0.000 claims 1
- 229960003965 antiepileptics Drugs 0.000 claims 1
- 229960000623 carbamazepine Drugs 0.000 claims 1
- FFGPTBGBLSHEPO-UHFFFAOYSA-N carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 claims 1
- 230000010261 cell growth Effects 0.000 claims 1
- 230000019771 cognition Effects 0.000 claims 1
- 229940124558 contraceptive agent Drugs 0.000 claims 1
- 230000008602 contraction Effects 0.000 claims 1
- NIJJYAXOARWZEE-UHFFFAOYSA-N di-n-propyl-acetic acid Natural products CCCC(C(O)=O)CCC NIJJYAXOARWZEE-UHFFFAOYSA-N 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000000262 estrogen Substances 0.000 claims 1
- 229940011871 estrogen Drugs 0.000 claims 1
- VPYISQPGRNSXRT-UHFFFAOYSA-N ethyl 3-[(1-cyclohexyl-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carbonyl)amino]bicyclo[2.2.1]heptane-3-carboxylate Chemical compound C1C(C2)CCC2C1(C(=O)OCC)NC(=O)C(C=1CCCCCCC=11)=NN1C1CCCCC1 VPYISQPGRNSXRT-UHFFFAOYSA-N 0.000 claims 1
- 229960000304 folic acid Drugs 0.000 claims 1
- 235000019152 folic acid Nutrition 0.000 claims 1
- 239000011724 folic acid Substances 0.000 claims 1
- 229960002870 gabapentin Drugs 0.000 claims 1
- 208000026278 immune system disease Diseases 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 208000028774 intestinal disease Diseases 0.000 claims 1
- 230000004410 intraocular pressure Effects 0.000 claims 1
- 229960001848 lamotrigine Drugs 0.000 claims 1
- PYZRQGJRPPTADH-UHFFFAOYSA-N lamotrigine Chemical compound NC1=NC(N)=NN=C1C1=CC=CC(Cl)=C1Cl PYZRQGJRPPTADH-UHFFFAOYSA-N 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 230000006742 locomotor activity Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- JUAASCSVJGFOKG-UHFFFAOYSA-N n-(1-adamantylmethyl)-1-cyclohexyl-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carboxamide Chemical compound C1C(C2)CC(C3)CC2CC13CNC(=O)C(C=1CCCCCCC=11)=NN1C1CCCCC1 JUAASCSVJGFOKG-UHFFFAOYSA-N 0.000 claims 1
- JCPDFDIHQOALNH-UHFFFAOYSA-N n-(1-adamantylmethyl)-1-cyclopentyl-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carboxamide Chemical compound C1C(C2)CC(C3)CC2CC13CNC(=O)C(C=1CCCCCCC=11)=NN1C1CCCC1 JCPDFDIHQOALNH-UHFFFAOYSA-N 0.000 claims 1
- TUKOQUXZXVOJHW-UHFFFAOYSA-N n-[1-(1-adamantyl)ethyl]-1-cyclohexyl-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carboxamide Chemical compound C1C(C2)CC(C3)CC2CC13C(C)NC(=O)C(C=1CCCCCCC=11)=NN1C1CCCCC1 TUKOQUXZXVOJHW-UHFFFAOYSA-N 0.000 claims 1
- NYAGJMVAYPPWBV-UHFFFAOYSA-N n-[1-(1-adamantyl)ethyl]-1-cyclopentyl-4,5,6,7,8,9-hexahydrocycloocta[c]pyrazole-3-carboxamide Chemical compound C1C(C2)CC(C3)CC2CC13C(C)NC(=O)C(C=1CCCCCCC=11)=NN1C1CCCC1 NYAGJMVAYPPWBV-UHFFFAOYSA-N 0.000 claims 1
- 230000004112 neuroprotection Effects 0.000 claims 1
- 235000020824 obesity Nutrition 0.000 claims 1
- 229940127234 oral contraceptive Drugs 0.000 claims 1
- 239000003539 oral contraceptive agent Substances 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- 229960002036 phenytoin Drugs 0.000 claims 1
- 102000005962 receptors Human genes 0.000 claims 1
- 108020003175 receptors Proteins 0.000 claims 1
- 208000023504 respiratory system disease Diseases 0.000 claims 1
- 239000000779 smoke Substances 0.000 claims 1
- 201000009032 substance abuse Diseases 0.000 claims 1
- 231100000736 substance abuse Toxicity 0.000 claims 1
- 208000011117 substance-related disease Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 229960004394 topiramate Drugs 0.000 claims 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 claims 1
- 229960000604 valproic acid Drugs 0.000 claims 1
- 230000004580 weight loss Effects 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
-
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
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- 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
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
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- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Addiction (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Physical Education & Sports Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US71988405P | 2005-09-23 | 2005-09-23 | |
PCT/US2006/037350 WO2007044215A1 (en) | 2005-09-23 | 2006-09-22 | Hexahydro cyclooctyl pyrazole cannabinoid modulators |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20100258T1 true HRP20100258T1 (hr) | 2010-06-30 |
Family
ID=37651059
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20100258T HRP20100258T1 (hr) | 2005-09-23 | 2010-05-10 | Heksahidro ciklooktil pirazol kanabinoidni modulatori |
Country Status (27)
Country | Link |
---|---|
US (2) | US7851498B2 (zh) |
EP (1) | EP1931335B1 (zh) |
JP (1) | JP5162461B2 (zh) |
KR (1) | KR20080066924A (zh) |
CN (1) | CN101312725B (zh) |
AT (1) | ATE458480T1 (zh) |
AU (1) | AU2006302659A1 (zh) |
BR (1) | BRPI0616401A2 (zh) |
CA (1) | CA2623535A1 (zh) |
CY (1) | CY1110020T1 (zh) |
DE (1) | DE602006012514D1 (zh) |
DK (1) | DK1931335T3 (zh) |
EA (1) | EA200800889A1 (zh) |
EC (1) | ECSP088315A (zh) |
ES (1) | ES2340201T3 (zh) |
HR (1) | HRP20100258T1 (zh) |
IL (1) | IL190348A0 (zh) |
MY (1) | MY148863A (zh) |
NO (1) | NO20081950L (zh) |
NZ (1) | NZ567006A (zh) |
PL (1) | PL1931335T3 (zh) |
PT (1) | PT1931335E (zh) |
RS (1) | RS51298B (zh) |
SI (1) | SI1931335T1 (zh) |
UA (1) | UA93389C2 (zh) |
WO (1) | WO2007044215A1 (zh) |
ZA (1) | ZA200803533B (zh) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7825151B2 (en) * | 2005-09-23 | 2010-11-02 | Janssen Pharmaceutica Nv | Hexahydro-cyclooctyl pyrazole cannabinoid modulators |
US8378117B2 (en) * | 2005-09-23 | 2013-02-19 | Janssen Pharmaceutica N.V. | Hexahydro-cycloheptapyrazole cannabinoid modulators |
KR20090047458A (ko) | 2006-08-08 | 2009-05-12 | 사노피-아벤티스 | 아릴아미노아릴-알킬-치환된 이미다졸리딘-2,4-디온, 이의 제조방법, 이들 화합물을 포함하는 약제 및 이의 용도 |
CA2681384A1 (en) * | 2007-03-21 | 2008-09-25 | Janssen Pharmaceutica N.V. | Method for treating cb2 receptor mediated pain |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
PT2963031T (pt) | 2007-11-30 | 2019-03-20 | Zynerba Pharmaceuticals Inc | Pró-fármacos de tetrahidrocanabinol, composições compreendendo pró-fármacos de tetrahidrocanabinol e métodos de utilização dos mesmos |
WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
ES2443016T3 (es) | 2009-08-26 | 2014-02-17 | Sanofi | Nuevos hidratos cristalinos de fluoroglicósidos heteroaromáticos, productos farmacéuticos que comprenden estos compuestos, y su empleo |
US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
EP2683705B1 (de) | 2011-03-08 | 2015-04-22 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2683700B1 (de) | 2011-03-08 | 2015-02-18 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2948718A (en) | 1960-08-09 | New n-heterocyclic compounds | ||
US4087544A (en) | 1974-12-21 | 1978-05-02 | Warner-Lambert Company | Treatment of cranial dysfunctions using novel cyclic amino acids |
DE2460891C2 (de) | 1974-12-21 | 1982-09-23 | Gödecke AG, 1000 Berlin | 1-Aminomethyl-1-cycloalkanessigsäuren und deren Ester, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
PL124029B1 (en) | 1979-06-01 | 1982-12-31 | Wellcome Found | Process for preparing novel derivatives of 1,2,4-triazine |
LU83729A1 (fr) | 1981-11-04 | 1983-09-01 | Galephar | Sels d'acide valproique,leur preparation et leur utilisation |
US4513006A (en) | 1983-09-26 | 1985-04-23 | Mcneil Lab., Inc. | Anticonvulsant sulfamate derivatives |
US5242942A (en) | 1992-04-28 | 1993-09-07 | Mcneilab, Inc. | Anticonvulsant fructopyranose cyclic sulfites and sulfates |
US5384327A (en) | 1992-12-22 | 1995-01-24 | Mcneilab, Inc. | Anticonvulsant sorbopyranose sulfamates |
FR2800375B1 (fr) * | 1999-11-03 | 2004-07-23 | Sanofi Synthelabo | Derives tricycliques d'acide pyrazolecarboxylique, leur preparation, les compositions pharmaceutiques en contenant |
FR2800372B1 (fr) * | 1999-11-03 | 2001-12-07 | Sanofi Synthelabo | Derives tricycliques d'acide 1-benzylpyrazole-3- carboxylique, leur preparation, les medicaments en contenant |
JPWO2005063241A1 (ja) * | 2003-12-26 | 2007-07-19 | 小野薬品工業株式会社 | ミトコンドリアベンゾジアゼピン受容体介在性疾患の予防および/または治療剤 |
CN1956964B (zh) | 2004-03-24 | 2011-06-15 | 詹森药业有限公司 | 四氢-吲唑大麻素调节剂 |
FR2875230A1 (fr) * | 2004-09-13 | 2006-03-17 | Sanofi Aventis Sa | Derives de pyrazole condense, leur preparation et leur application en therapeutique |
BRPI0517378A (pt) | 2004-10-27 | 2008-10-07 | Janssen Pharmaceutica Nv | moduladores de tetraidro piridinil pirazol canabinóide |
-
2006
- 2006-09-22 UA UAA200803833A patent/UA93389C2/ru unknown
- 2006-09-22 US US11/525,573 patent/US7851498B2/en not_active Expired - Fee Related
- 2006-09-22 NZ NZ567006A patent/NZ567006A/en not_active IP Right Cessation
- 2006-09-22 CN CN200680043512XA patent/CN101312725B/zh not_active Expired - Fee Related
- 2006-09-22 ES ES06804133T patent/ES2340201T3/es active Active
- 2006-09-22 DK DK06804133.4T patent/DK1931335T3/da active
- 2006-09-22 JP JP2008532489A patent/JP5162461B2/ja not_active Expired - Fee Related
- 2006-09-22 AT AT06804133T patent/ATE458480T1/de active
- 2006-09-22 WO PCT/US2006/037350 patent/WO2007044215A1/en active Application Filing
- 2006-09-22 KR KR1020087009596A patent/KR20080066924A/ko not_active Application Discontinuation
- 2006-09-22 EP EP06804133A patent/EP1931335B1/en active Active
- 2006-09-22 MY MYPI20080784A patent/MY148863A/en unknown
- 2006-09-22 SI SI200630638T patent/SI1931335T1/sl unknown
- 2006-09-22 AU AU2006302659A patent/AU2006302659A1/en not_active Abandoned
- 2006-09-22 RS RSP-2010/0185A patent/RS51298B/sr unknown
- 2006-09-22 BR BRPI0616401-3A patent/BRPI0616401A2/pt not_active IP Right Cessation
- 2006-09-22 PL PL06804133T patent/PL1931335T3/pl unknown
- 2006-09-22 CA CA002623535A patent/CA2623535A1/en not_active Abandoned
- 2006-09-22 PT PT06804133T patent/PT1931335E/pt unknown
- 2006-09-22 EA EA200800889A patent/EA200800889A1/ru unknown
- 2006-09-22 DE DE602006012514T patent/DE602006012514D1/de active Active
-
2008
- 2008-03-20 IL IL190348A patent/IL190348A0/en unknown
- 2008-03-26 EC EC2008008315A patent/ECSP088315A/es unknown
- 2008-04-22 ZA ZA200803533A patent/ZA200803533B/xx unknown
- 2008-04-23 NO NO20081950A patent/NO20081950L/no not_active Application Discontinuation
-
2010
- 2010-05-07 CY CY20101100396T patent/CY1110020T1/el unknown
- 2010-05-10 HR HR20100258T patent/HRP20100258T1/hr unknown
- 2010-05-24 US US12/785,625 patent/US8101592B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
WO2007044215A1 (en) | 2007-04-19 |
SI1931335T1 (sl) | 2010-06-30 |
RS51298B (sr) | 2010-12-31 |
CN101312725B (zh) | 2012-01-11 |
DK1931335T3 (da) | 2010-06-07 |
UA93389C2 (en) | 2011-02-10 |
ES2340201T3 (es) | 2010-05-31 |
CN101312725A (zh) | 2008-11-26 |
EP1931335B1 (en) | 2010-02-24 |
JP5162461B2 (ja) | 2013-03-13 |
MY148863A (en) | 2013-06-14 |
EA200800889A1 (ru) | 2008-12-30 |
CA2623535A1 (en) | 2007-04-19 |
US20100234331A1 (en) | 2010-09-16 |
NZ567006A (en) | 2010-11-26 |
AU2006302659A1 (en) | 2007-04-19 |
ATE458480T1 (de) | 2010-03-15 |
NO20081950L (no) | 2008-05-16 |
US20070129417A1 (en) | 2007-06-07 |
KR20080066924A (ko) | 2008-07-17 |
CY1110020T1 (el) | 2015-01-14 |
IL190348A0 (en) | 2009-09-22 |
US7851498B2 (en) | 2010-12-14 |
ZA200803533B (en) | 2009-10-28 |
DE602006012514D1 (de) | 2010-04-08 |
US8101592B2 (en) | 2012-01-24 |
EP1931335A1 (en) | 2008-06-18 |
BRPI0616401A2 (pt) | 2011-06-21 |
JP2009509973A (ja) | 2009-03-12 |
ECSP088315A (es) | 2008-04-28 |
PL1931335T3 (pl) | 2010-07-30 |
PT1931335E (pt) | 2010-03-23 |
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