AR044010A1 - Uso de derivados de 4-fenil-4- [1h-imidazol-2-il]- piperidina sustituidos como agonistas delta opioideos no peptidos selectivos, con actividad antidepresiva y ansiolitica - Google Patents
Uso de derivados de 4-fenil-4- [1h-imidazol-2-il]- piperidina sustituidos como agonistas delta opioideos no peptidos selectivos, con actividad antidepresiva y ansioliticaInfo
- Publication number
- AR044010A1 AR044010A1 ARP040101193A ARP040101193A AR044010A1 AR 044010 A1 AR044010 A1 AR 044010A1 AR P040101193 A ARP040101193 A AR P040101193A AR P040101193 A ARP040101193 A AR P040101193A AR 044010 A1 AR044010 A1 AR 044010A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- het
- group
- alkyloxy
- thio
- Prior art date
Links
- 229940127450 Opioid Agonists Drugs 0.000 title 1
- 230000001430 anti-depressive effect Effects 0.000 title 1
- 230000000694 effects Effects 0.000 title 1
- 102000004196 processed proteins & peptides Human genes 0.000 title 1
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 1
- -1 phenyloxy, phenylcarbonyloxy Chemical group 0.000 abstract 11
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 150000001875 compounds Chemical class 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 4
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 208000035475 disorder Diseases 0.000 abstract 3
- 229930195733 hydrocarbon Natural products 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 208000019901 Anxiety disease Diseases 0.000 abstract 2
- 125000000815 N-oxide group Chemical group 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 210000003169 central nervous system Anatomy 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 208000020401 Depressive disease Diseases 0.000 abstract 1
- 208000030814 Eating disease Diseases 0.000 abstract 1
- 208000019454 Feeding and Eating disease Diseases 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 208000019022 Mood disease Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 230000036506 anxiety Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 235000014632 disordered eating Nutrition 0.000 abstract 1
- 125000005883 dithianyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000005067 haloformyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000002632 imidazolidinyl group Chemical group 0.000 abstract 1
- 125000002636 imidazolinyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 239000011630 iodine Substances 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 abstract 1
- 125000002755 pyrazolinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 125000001422 pyrrolinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 abstract 1
- 125000004306 triazinyl group Chemical group 0.000 abstract 1
Classifications
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- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
-
- 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
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Epidemiology (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Anesthesiology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Uso de un compuesto conforme a la fórmula (1), las sales de adición de base o ácido farmacéuticamente aceptables de dicho compuesto, las formas estereoquímicamente isómeras de dicho compuesto, sus formas tautómeras y las formas de N-óxido de dicho compuesto, para la elaboración de un medicamento para utilización en la prevención y/o tratamiento de trastornos del sistema nervioso central, en donde: A=B es C=O, C=N-R6, en donde R6 es hidrógeno o ciano, C=S, S=O, SO2 y C=CR7R8, en donde R7 y R8 son, cada uno de manera independiente, hidrógeno, nitro o alquilo; X es un enlace covalente, -CH2- o CH2CH2-; R1 es hidrógeno, hidroxi, alquiloxi, alquilcarboniloxi, Ar-oxi, Het-oxi, -Ar-carboniloxi, Het-carboniloxi, Ar-alquiloxi, Het-alquiloxi, alquilo, polihaloalquilo, alquiloxialquilo, Ar-alquilo, Het-alquilo, Ar, Het, tio, alquiltio, Ar-tio, Het-tio, o NR9R10, en donde R9 y R10 son, cada uno de manera independiente, hidrógeno, alquilo, Ar, Ar-alquilo, Het, Het-alquilo, Ar- carbonilo, alquilcarbonilo, Het-carbonilo o alquiloxicarbonilalquilo; o A=B y R1 juntos forman un radical Het2 o Het3 carbocíclico o heterocíclico, aromático o semiaromático, opcionalmente sustituido; R2 es hidroxi, alquiloxi, alquilcarboniloxi, feniloxi, fenilcarboniloxi, halo, ciano, alquilo, polihaloalquilo, alquiloxialquilo, formilo, carboxi, alquilcarbonilo, alquiloxicarbonilo, aminocarbonilo, mono o dialquilaminocarbonilo, fenilo, nitro, amino, mono o dialquil-amino, tio o alquiltio; R3 es alquilo, Ar, Ar-alquilo, Ar-alquenilo, Ar-carbonilo, Het, Het-alquilo, Het-alquenilo o Het-carbonilo; R4, R5 cada uno en forma independiente, es hidrógeno, alquilo, carboxi, aminocarbonilo, alquiloxicarbonilo, halo o hidroxialquilo; p es un entero igual a cero, 1, 2 ó 3; alquilo es un radical hidrocarburo saturado, recto o ramificado que tiene C1-6; o es un radical hidrocarburo saturado cíclico (cicloalquilo) que tiene C3-7; o es un radical hidrocarburo saturado cíclico que tiene C3-7, unido a un radical hidrocarburo saturado, recto o ramificado que tiene C1-6; en donde cada átomo de carbono puede estar opcionalmente sustituido con amino, nitro, tio, hidroxi, oxo, ciano, formilo o carboxi; alquenilo es un radical alquilo que tiene uno o más enlaces dobles; Ar es un homociclo seleccionado entre el grupo que consiste en fenilo y naftilo, cada uno opcionalmente sustituido con uno o más sustituyentes, en donde cada sustituyente se selecciona de manera independiente entre el grupo que comprende hidroxi, alquiloxi, alquilcarboniloxi, feniloxi, fenilcarboniloxi, polihaloalquiloxi, halo, ciano, alquilo, polihaloalquilo, alquiloxialquilo, formilo, haloformilo, carboxi, alquilcarbonilo, alquiloxicarbonilo, aminocarbonilo, mono o dialquilaminocarbonilo, fenilalquilo, fenilo, nitro, amino, mono o dialquil-amino, tio, alquiltio o SO2-CH3; halo es un sustituyente que se selecciona entre el grupo que comprende flúor, cloro, bromo y yodo; polihaloalquilo es un radical hidrocarburo saturado, recto o ramificado que tiene C1-6, o un radical hidrocarburo saturado cíclico que tiene C3-7, en donde uno o más átomos están sustituidos con uno o más átomos de halo; Het es un radical heterocíclico seleccionado entre el grupo que comprende Het1, Het2 y Het3; en donde cada radical heterocíclico Het1, Het2 y Het3 puede estar opcionalmente sustituido en un carbono y/o un heteroátomo con halo, hidroxi, alquiloxi, alquilo, Ar, Ar-alquilo o piridinilo. Het1 es un radical heterocíclico monocíclico alifático seleccionado entre el grupo que comprende pirrolidinilo, dioxolilo, imidazolidinilo, pirazolidinilo, piperidinilo, dioxilo, morfolinilo, ditianilo, tiomorfolinilo, piperazinilo y tetrahidrofuranilo; Het2 es un radical heterocíclico monocíclico semiaromático seleccionado entre el grupo de 2H-pirrolillo, pirrolinilo, imidazolinilo y pirazolinilo; Het3 es un radical heterocíclico monocíclico aromático seleccionado entre el grupo de pirrolilo, pirazolilo, imidazolilo, furanilo, tienilo, oxazolilo, isoxazolilo, tiazolilo, isotiazolilo, piridinilo, pirimidinilo, pirazinilo, piridazinilo y triazinilo; o un radical heterocíclico bicíclico aromático seleccionado entre el grupo que consiste en quinolinilo, quinoxalinilo, indolilo, bencimidazolilo, benzoxazolilo, benzisoxazolilo, benzotiazolilo, benzisotiazolilo, benzofuranilo y benzotienilo. Reivindicación 14: Un método de tratamiento de un ser humano que sufre de un trastorno del sistema nervioso central, en particular, un trastorno del estado de ánimo, trastornos depresivos, trastornos de ansiedad, trastornos relacionados con el estrés asociados con depresión y/o ansiedad y desórdenes de la alimentación o cualquier combinación de ellos, que comprende administrar al ser humano que necesita dicho tratamiento, una cantidad terapéuticamente eficaz de un compuesto conforme a la fórmula (1), las sales de adición de ácido o base farmacéuticamente aceptables de dicho compuesto, sus formas estereoquímicamente isómeras, sus formas tautómeras y las formas de N-óxido de dicho compuesto.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP0303879 | 2003-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR044010A1 true AR044010A1 (es) | 2005-08-24 |
Family
ID=33154992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040101193A AR044010A1 (es) | 2003-04-11 | 2004-04-07 | Uso de derivados de 4-fenil-4- [1h-imidazol-2-il]- piperidina sustituidos como agonistas delta opioideos no peptidos selectivos, con actividad antidepresiva y ansiolitica |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20060287345A1 (es) |
| EP (1) | EP1615644B1 (es) |
| JP (1) | JP2006522775A (es) |
| AR (1) | AR044010A1 (es) |
| AT (1) | ATE353649T1 (es) |
| AU (1) | AU2004228960A1 (es) |
| CA (1) | CA2521186A1 (es) |
| CL (1) | CL2004000754A1 (es) |
| DE (1) | DE602004004771T2 (es) |
| ES (1) | ES2282858T3 (es) |
| TW (1) | TW200509913A (es) |
| WO (1) | WO2004089372A1 (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2149370A1 (en) | 2008-07-31 | 2010-02-03 | Neuroscienze Pharmaness S.C. A R.L. | Diazabicyclic compounds and microemulsions thereof |
| IT1390848B1 (it) | 2008-07-31 | 2011-10-19 | Neuroscienze Pharmaness S C A R L | Composti farmaceutici |
| JP2011030565A (ja) * | 2009-07-06 | 2011-02-17 | Yokohama City Univ | 社会的隔離モデル動物 |
| IT1396951B1 (it) | 2009-12-18 | 2012-12-20 | Neuroscienze Pharmaness S C A R L | Composti farmaceutici |
| JP2016519161A (ja) * | 2013-05-24 | 2016-06-30 | アルカームス ファーマ アイルランド リミテッド | モルファン及びモルフィナン類似物及び使用の方法 |
| ES2904511T3 (es) | 2015-03-17 | 2022-04-05 | Nippon Chemiphar Co | Derivado de morfinano |
| WO2018030382A1 (ja) | 2016-08-09 | 2018-02-15 | 国立大学法人 筑波大学 | モルヒナン誘導体 |
| KR102605763B1 (ko) | 2016-09-16 | 2023-11-23 | 닛뽕 케미파 가부시키가이샤 | 모르피난 유도체의 오피오이드 δ 수용체 아고니스트 관련 질환의 치료를 위한 사용 |
| CN112119076B (zh) * | 2018-05-01 | 2025-01-10 | 默沙东有限责任公司 | 烟碱乙酰胆碱受体的螺哌啶变构调节剂 |
| EP4062972A4 (en) | 2019-11-22 | 2023-11-22 | The Kitasato Institute | PYRAZOLOMORPHINAND DERIVATIVES |
| EP4299074A4 (en) | 2021-02-26 | 2024-12-18 | Tokyo University Of Science Foundation | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OR PREVENTION OF STRESS-RELATED DISEASES |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5354863A (en) * | 1992-01-21 | 1994-10-11 | G. D. Searle & Co. | Opioid agonist compounds |
| DE19805370A1 (de) * | 1997-03-14 | 1998-09-17 | Gruenenthal Gmbh | Substituierte Aminoverbindungen und ihre Verwendung als analgetisch wirksame Substanzen |
| HN1999000149A (es) * | 1998-09-09 | 2000-01-12 | Pfizer Prod Inc | Derivados de 4,4-biarilpiperidina |
| EP1038872A1 (en) * | 1999-02-22 | 2000-09-27 | Pfizer Products Inc. | 4-Phenyl-4-heteroarylpiperdine derivatives as opioid receptor ligands |
| DE19939044A1 (de) * | 1999-08-18 | 2001-03-15 | Gruenenthal Gmbh | Verwendung von Morphinanderivaten als Arzneimittel |
| SE0101767D0 (sv) * | 2001-05-18 | 2001-05-18 | Astrazeneca Ab | Novel compounds |
| ATE347549T1 (de) * | 2001-10-15 | 2006-12-15 | Janssen Pharmaceutica Nv | Neue substituierte 4-phenyl-4-(1h-imidazo-2-yl)- piperidin-derivate und ihre anwendung als selective delta-opioid-agonisten |
| HUP0402332A3 (en) * | 2001-10-15 | 2009-07-28 | Janssen Pharmaceutica Nv | Substituted 4-phenyl-4-(1h-imidazol-2-yl)-piperidine derivatives for reducing ischaemic damage and pharmaceutical compositions containing them |
-
2004
- 2004-04-07 AR ARP040101193A patent/AR044010A1/es not_active Application Discontinuation
- 2004-04-07 CL CL200400754A patent/CL2004000754A1/es unknown
- 2004-04-08 JP JP2006505540A patent/JP2006522775A/ja not_active Withdrawn
- 2004-04-08 AU AU2004228960A patent/AU2004228960A1/en not_active Abandoned
- 2004-04-08 ES ES04726520T patent/ES2282858T3/es not_active Expired - Lifetime
- 2004-04-08 WO PCT/EP2004/050492 patent/WO2004089372A1/en not_active Ceased
- 2004-04-08 US US10/552,527 patent/US20060287345A1/en not_active Abandoned
- 2004-04-08 CA CA002521186A patent/CA2521186A1/en not_active Abandoned
- 2004-04-08 EP EP04726520A patent/EP1615644B1/en not_active Expired - Lifetime
- 2004-04-08 DE DE602004004771T patent/DE602004004771T2/de not_active Expired - Fee Related
- 2004-04-08 AT AT04726520T patent/ATE353649T1/de not_active IP Right Cessation
- 2004-04-09 TW TW093109827A patent/TW200509913A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2004000754A1 (es) | 2005-02-25 |
| EP1615644B1 (en) | 2007-02-14 |
| ES2282858T3 (es) | 2007-10-16 |
| US20060287345A1 (en) | 2006-12-21 |
| AU2004228960A1 (en) | 2004-10-21 |
| CA2521186A1 (en) | 2004-10-21 |
| DE602004004771T2 (de) | 2007-12-06 |
| ATE353649T1 (de) | 2007-03-15 |
| WO2004089372A1 (en) | 2004-10-21 |
| TW200509913A (en) | 2005-03-16 |
| EP1615644A1 (en) | 2006-01-18 |
| DE602004004771D1 (de) | 2007-03-29 |
| JP2006522775A (ja) | 2006-10-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |