AR057374A1 - Moduladres opioides triciclicos y composiciones farmaceuticas y veterinarias - Google Patents
Moduladres opioides triciclicos y composiciones farmaceuticas y veterinariasInfo
- Publication number
- AR057374A1 AR057374A1 ARP060102540A ARP060102540A AR057374A1 AR 057374 A1 AR057374 A1 AR 057374A1 AR P060102540 A ARP060102540 A AR P060102540A AR P060102540 A ARP060102540 A AR P060102540A AR 057374 A1 AR057374 A1 AR 057374A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkanyl
- phenyl
- amino
- group
- aminocarbonyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 2
- -1 (phenylmethyl) aminocarbonyl Chemical group 0.000 abstract 10
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 1
- 102000003840 Opioid Receptors Human genes 0.000 abstract 1
- 108090000137 Opioid Receptors Proteins 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 abstract 1
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005047 dihydroimidazolyl group Chemical group N1(CNC=C1)* 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 abstract 1
- 125000001786 isothiazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000003373 pyrazinyl 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
- 125000004076 pyridyl 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
- 150000003839 salts Chemical class 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical group [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000003831 tetrazolyl 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
- 125000004001 thioalkyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- A—HUMAN NECESSITIES
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/14—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Addiction (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Otolaryngology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Gynecology & Obstetrics (AREA)
- Reproductive Health (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychology (AREA)
- Vascular Medicine (AREA)
- Immunology (AREA)
Abstract
La presente se refiere un los compuestos de formula (1) utiles como moduladores de los receptores opioides delta y (mu). También se describen composiciones farmacéuticas y veterinarias y Kits. Estos compuestos son utiles para tratar el dolor leve un severo y diversas enfermedades utilizando los compuestos de la presente. Reivindicacion 1: Un compuesto de la formula (1), donde: R1 es hidroxi; mercapto; aminocarbonilo; alcanilC1-4-aminocarbonilo; di(alcanilC1-4)aminocarbonilo; (fenilmetílico)aminocarbonilo; (4-metoxi-fenilmetílico)aminocarbonilo; alcanilC1-4-oxicarbonilo; aminotiocarbonilo; amidino; hidroxiamidino; fenilcarbonilo; -C(=NOH)fenilo; amino; alcanilC1-4-amino; di(alcanilC1-4)amino; aminometilo; hidroximetilo; metansulfonilamino; arilC6-10-amino, donde arilo está opcionalmente sustituido con uno un tres sustituyentes seleccionados independientemente del grupo formado por alcanilo C1-6, alcoxi C1-6, halogeno, hidroxi; dihidroimidazolilo; formilamino; tioformilamino; o piridinilamino; u, opcionalmente, R1 es -S-C(NH2)=N- para formar una porcion fusionada en la cual el segundo punto de union es un átomo de carbono no puente adyacente; R2 es un sustituyente seleccionado del grupo formado por hidrogeno, alcanilo C1-8, halo1-3-alcanilo C1-8, alquenilo C2-8, alquinilo C2-8, cicloalcanilo C3-8, cicloalcanilalcanilo C1-8, alcanilC1-8-oxialcaniloC1-8, alcanilC1-8-tioalcaniloC1-8, hidroxialcanilo C1-8, alcanilC1-8-oxicarbonilo, halo1-3- alcanilC1-8-carbonilo, formilo, tioformilo, carbamimidoilo, feniliminoalcanilo C1-8, fenilalcanilo C1-8, fenilalquenilo C1-8, fenilalquinilo C1-8 naftilalcanilo C1-8 y heteroarilalcanilo C1-8, donde el heteroarilo se selecciona del grupo formado por benzo[1,3]dioxolilo, imidazolilo, furanilo, piridinilo, tienilo, indazolilo, indolilo, indolinilo, isoindolinilo, isoquinolinilo, isotiazolilo, isoxazolilo, oxazolilo, pirazinilo, pirazolilo, piridazinilo, pimidinilo, pirrolilo, quinolinilo, isoquinolinilo, tetrazolilo, tiazolilo; donde fenilo, naftilo y heteroarilo son opcionalmente sustituidos con fenilo, y de uno a tres sustituyentes seleccionados independientemente del grupo formado por alcanilo C1-6, alquenilo C2-6, alcanilC1-6oxi, amino, alcanilC1-6-amino, di(alcanilC1-6)amino, alcanilC1-6-carbonilo, alcanilC1-6-carboniloxi, alcanilC1-6-carboniloamino, alcanilC1-6-tio, alcanilC1-6-sulfonilo, halogeno, hidroxi, ciano, fluoralcanilo C1-6, tioureido, y fluoralcanilC1-6-oxi; alternativamente, cuando fenilo y heteroarilo son opcionalmente sustituidos con sustituyentes alcanilo o alcaniloxi unidos a átomos de carbono adyacentes, los dos sustituyentes pueden formar en conjunto un alcanilo o cicloheteroalcanilo cíclico fusionado seleccionado del grupo formado por -(CH2)3-5-, -O(CH2)2-4-, - (CH2)2-4O-, y -O(CH2)1-3O-; A es ausente o -(CH2)2-3-; Y es O o S; y enantiomeros, diastereomeros, tautomeros, o las sales farmacéuticamente aceptables de los mismos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69110105P | 2005-06-16 | 2005-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057374A1 true AR057374A1 (es) | 2007-11-28 |
Family
ID=37334600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060102540A AR057374A1 (es) | 2005-06-16 | 2006-06-15 | Moduladres opioides triciclicos y composiciones farmaceuticas y veterinarias |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US7582650B2 (es) |
| EP (1) | EP1896467B1 (es) |
| JP (1) | JP2008543866A (es) |
| CN (1) | CN101243079A (es) |
| AR (1) | AR057374A1 (es) |
| AT (1) | ATE490251T1 (es) |
| AU (1) | AU2006259273A1 (es) |
| BR (1) | BRPI0611885A2 (es) |
| CA (1) | CA2612491A1 (es) |
| DE (1) | DE602006018604D1 (es) |
| RU (1) | RU2008101667A (es) |
| TW (1) | TW200716134A (es) |
| WO (1) | WO2006138528A2 (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1644373A1 (en) | 2003-06-27 | 2006-04-12 | Janssen Pharmaceutica N.V. | Tricyclic delta opioid modulators |
| BRPI0513075A (pt) * | 2004-08-05 | 2008-04-22 | Janssen Pharmaceutica Nv | moduladores gama-opióides tricìclicos |
| AU2005319059A1 (en) * | 2004-12-22 | 2006-06-29 | Janssen Pharmaceutica N.V. | Tricyclic delta-opioid modulators |
| MX2007007626A (es) * | 2004-12-22 | 2008-01-28 | Johnson & Johnson | Moduladores delta-opioides triciclicos. |
| CA2592464A1 (en) * | 2004-12-22 | 2006-06-29 | Janssen Pharmaceutica N.V. | Tricyclic .delta.-opioid modulators |
| CA2594347A1 (en) * | 2005-01-06 | 2006-07-13 | Janssen Pharmaceutica N.V. | Tricyclic d-opioid modulators |
| JP2008543866A (ja) | 2005-06-16 | 2008-12-04 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 三環式オピオイドモジュレーター |
| ES2480390T3 (es) | 2005-07-21 | 2014-07-28 | Rensselaer Polytechnic Institute | 2,6-metano-3-benzazocinas 8-carboxamido sustituidas y morfanos 3-carboxamido sustituidos como ligandos de los receptores opioides |
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-
2006
- 2006-06-15 JP JP2008517127A patent/JP2008543866A/ja not_active Withdrawn
- 2006-06-15 TW TW095121331A patent/TW200716134A/zh unknown
- 2006-06-15 AT AT06773315T patent/ATE490251T1/de not_active IP Right Cessation
- 2006-06-15 BR BRPI0611885-2A patent/BRPI0611885A2/pt not_active Application Discontinuation
- 2006-06-15 RU RU2008101667/04A patent/RU2008101667A/ru not_active Application Discontinuation
- 2006-06-15 CA CA002612491A patent/CA2612491A1/en not_active Abandoned
- 2006-06-15 AR ARP060102540A patent/AR057374A1/es unknown
- 2006-06-15 AU AU2006259273A patent/AU2006259273A1/en not_active Abandoned
- 2006-06-15 US US11/424,311 patent/US7582650B2/en not_active Expired - Fee Related
- 2006-06-15 EP EP06773315A patent/EP1896467B1/en not_active Not-in-force
- 2006-06-15 WO PCT/US2006/023429 patent/WO2006138528A2/en not_active Ceased
- 2006-06-15 DE DE602006018604T patent/DE602006018604D1/de active Active
- 2006-06-15 CN CNA2006800295853A patent/CN101243079A/zh active Pending
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2009
- 2009-07-10 US US12/500,706 patent/US20090275610A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW200716134A (en) | 2007-05-01 |
| AU2006259273A1 (en) | 2006-12-28 |
| DE602006018604D1 (de) | 2011-01-13 |
| BRPI0611885A2 (pt) | 2010-10-05 |
| US7582650B2 (en) | 2009-09-01 |
| WO2006138528A3 (en) | 2007-03-15 |
| EP1896467B1 (en) | 2010-12-01 |
| WO2006138528A2 (en) | 2006-12-28 |
| US20060287297A1 (en) | 2006-12-21 |
| JP2008543866A (ja) | 2008-12-04 |
| ATE490251T1 (de) | 2010-12-15 |
| EP1896467A2 (en) | 2008-03-12 |
| CA2612491A1 (en) | 2006-12-28 |
| RU2008101667A (ru) | 2009-07-27 |
| US20090275610A1 (en) | 2009-11-05 |
| CN101243079A (zh) | 2008-08-13 |
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