AR058406A1 - Antagonistas del receptor de proquineticina 1 - Google Patents
Antagonistas del receptor de proquineticina 1Info
- Publication number
- AR058406A1 AR058406A1 ARP060105853A ARP060105853A AR058406A1 AR 058406 A1 AR058406 A1 AR 058406A1 AR P060105853 A ARP060105853 A AR P060105853A AR P060105853 A ARP060105853 A AR P060105853A AR 058406 A1 AR058406 A1 AR 058406A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- phenyl
- amino
- pyridin
- alkoxy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/42—One nitrogen atom
- C07D251/46—One nitrogen atom with oxygen or sulfur atoms attached to the two other ring carbon atoms
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D405/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D405/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Antagonistas del receptor de proquineticina 1, y métodos para preparar estos compuestos, composiciones, intermediarios y derivados de los mismos y para el tratamiento de trastornos producidos por los receptores de proquineticina 1 o de proquinetina 1. Reivindicacion 1: Un compuesto de formula (1), donde, A1 es CF3, alcoxi C1-4, arilo, ariloxi, heterociclilo benzofusionado, o heteroarilo; donde arilo, ariloxi, y heteroarilo están opcionalmente sustituidos con pirazol-1-ilo [1,2,3]tiadiazol-4- ilo; o arilo, ariloxi, la porcion benzo del heterociclilo benzofusionado, y heteroarilo están opcionalmente sustituidos con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-6, hidroxialquilo C1-6, alcoxi C1- 6, halogeno, nitro, alquilo C1-6 halogenado, alcoxi C1-6 halogenado, alquiltio C1-6, alcoxi C1-6carbonilo, amino, alquil C1-6amino, di(alquil C1-6)amino, ciano, hidroxi, aminocarbonilo, alquil C1-6aminocarbonilo, di(alquil C1-6)aminocarbonilo, alcoxi C1-6carbonilamino, alquil C1-6carbonilo, alquiltio C1-6carbonilo, formilo, alquil C1-6sulfonilo, alquil C1-6sulfonilamino, aminosulfonilo, alquil C1-6aminosulfonilo, y di(alquil C1-6)aminosulfonilo; siempre y cuando A1 no sea 3,5-di-t-butil- fenilo; L1 es -(CH2)r-, -CH2-alquenil C2-4-, o -CH2CH2X(CH2)s-, donde L1 está opcionalmente sustituido con uno a dos sustituyentes independientemente seleccionados del grupo formado por alquilo C1-6, alquenilo C2-6, alquinilo C2-6, y halogeno; y, r es un numero entero de 1 a 5; de tal modo que r es mayor que o igual a 4 cuando A1 es alcoxi C1-4; s es un numero entero de 1 a 3; X es O o S; D es -P-A2; donde P es -(CH2)1-2- o -CH2CH=CH- cuando A2 es fenilo, heterociclilo benzofusionado, heteroarilo, o cicloalquilo C3-8; alternativamente, P es -(CH2)3-6- cuando A2 es hidrogeno, alcoxi C1-4, o alcoxi C1-4carbonilo; y donde P está opcionalmente sustituido con uno a dos sustituyentes independientemente seleccionados del grupo formado por alquilo C1-6, alquenilo C2-6, alquinilo C2-6, y halogeno; A2 es hidrogeno, alcoxi C1-4, alcoxi(C1-4)carbonilo, fenilo, heterociclilo benzofusionado, heteroarilo, tetrahidro-piranilo, piperidinilo, o cicloalquilo C3-8; donde fenilo, heteroarilo, la porcion benzo del heterociclilo benzofusionado, y cicloalquilo C3-8 están opcionalmente sustituidos con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-6, alcoxi C1-6, halogeno, alquilo C1-6 halogenado, alcoxi C1-6 halogenado, arilalcoxi C1-6, fenilo, N-isoindol-1,3-diona, alquiltio C1-6, alquil C1-6sulfonilo, alcoxi C1-6carbonilo, amino, alquil C1-6amino, di(alquil C1-6)amino, ciano, hidroxi, nitro, alquil C1-6carbonilo, alquiltio C1-6carbonilo, aminocarbonilo, alquil C1-6aminocarbonilo, di(alquil C1-6)aminocarbonilo, alquil C1-6carbonilamino, y un cicloalquiloxi C3-6 no fusionado; de tal modo que no más de dos sustituyentes en A2 son arilalcoxi C1-6, fenilo, N-isoindol-1,3-diona, o un cicloalquiloxi C3-6 no fusionado; siempre y cuando A2 no sea 3,5-di-t-butil-fenilo; W es N o C(Rw); donde Rw es H o alquilo C1-2; Q se selecciona del grupo formado por (a) a (g), donde (a) es -NH(CH2)Ar1 donde Ar1 es piridinilo opcionalmente sustituido con uno a tres sustituyentes alquilo C1-4 o un sustituyente seleccionado del grupo formado por alcoxi C1-4 y amino; siempre que cuando Ar1 es piridin-3-ilo no sustituido o piridin-4-ilo no sustituido, y A2 es 4-metoxi-fenilo, A1 no sea fenilo no sustituido o 3,4-dicloro-fenilo; (b) es -NHCH(Rz)-Ar2 donde Rz es H o alquilo C1-3; Ar2 es piridinilo, pirimidinilo, pirazinilo, la estructura de formula (2), 1,2,3,4-tetrahidro-[1,8]naftiridinilo, imidazo[1,2-a]piridinilo, o quinolinilo; de tal modo que el punto de union al 1,2,3,4-tetrahidro-[1,8]naftiridinilo está en la posicion 6 o 7, y el punto de union al quinolinilo está en la posicion 2, 3 o 4; y donde Ar2 está opcionalmente sustituido con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4, trifluorometilo, hidroxil-alquilo C1-4, aminoalquilo C1-4, (alquil C1-4)amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alcoxi C1-4, cicloalquil C3-8amino, amino, (alquil C1- 6)amino, y di(alquil C1-4)amino; o Ar2 está opcionalmente sustituido con un grupo amino y tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4 y alcoxi C1-4, donde el grupo alquilo C1-6 de alquil C1-6amino y di(alquil C1-6)amino está opcionalmente sustituido con amino, alquil C1-4amino, di(alquil C1-4)amino, cicloalquil C3-8amino, alcoxi C1-4, alquiltio C1-4, hidroxi, un heteroarilo de 5 a 6 miembros, o un heterociclilo de 5 a 6 miembros; donde un átomo de nitrogeno del heterociclilo de 5 a 6 miembros está opcionalmente sustituido con un sustituyente alquilo C1-4; y donde piridin-2-ilo y piridin-3-ilo están además opcionalmente sustituidos con N-pirrolidinilo, N-piperazinilo, N-piperidinilo, N- morfolinilo, N-tiomorfolinilo, -CH2-O-CH2-PH, y fenilo; donde el sustituyente fenilo de piridin-2-ilo y piridin-3-ilo está opcionalmente sustituido con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4, alcoxi C1-4, y halogeno; siempre que cuando Q es -NHCH2(2-amino-piridin-3-il), y A1 es piridin-4-ilo, 4-alquil C1-6-fenilo, 3,4-dicloro-fenilo, o 4-metansulfonil-fenilo, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(2-amino-piridin-3- il), L1 es -(CH2)2- o .(CH2)5-, y A1 es metoxi, A2 no sea 4-difluorometoxi-fenilo o 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(2-amino-piridin-3-il), y A1 es benzotriazol1-ilo, A2 no sea 4-difluorometoxi-fenilo; siempre que cuando Q es -NHCH2(2- amino-piridin-3-il), L1 es -(CH2)3-, y A1 es pirrol-1-ilo, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(2-amino-piridin-3-il), L1 es -(CH2)2-, y A1 es 4-nitro-fenilo o etoxi, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(2- amino-piridin-3-il), y A1 es 4-fluoro-fenilo, A2 no sea 4fluoro-fenilo; siempre que cuando Q es -NHCH2(6-amino-piridin-2-il), y A1 es 4-fluoro-fenilo, A2 no sea 4-trifluorometoxi-fenilo; siempre que cuando Q es .NHCH2(6-metil-piridin-2-il), y A1 es 4-metoxi-fenilo, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(imidazo[1,2-a]piridinil), y A1 es 4-fluoro-fenilo, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(piridin-4-il), y A1 es fenilo no sustituido o 3,4-dicloro-fenilo, A2 no sea 4-metoxi-fenilo; siempre que cuando Q es -NHCH2(4,6-dimetil-piridin-3-il), y A1 es 4-metoxi- fenilo, -P-A2 no sea -(CH2)5-metoxi; siempre que cuando Q es -NHCH2(4,6-dimetil-piridin-3-il), L1 es -(CH2)2-, y A1 es pirazol-1-ilo, A2 no sea 4- difluorometoxi-fenilo; siempre que cuando Q es -NHCH2(4,6-dimetil-piridin-3-il) y A1 es 4-metoxi-fenilo, A2 no sea 2-etil-fenilo, 4-etil-fenilo, 3-metoxi-fenilo, 3-ciano-fenilo, 3-nitro-fenilo, y 3-trifluorometil-4-nitro-fenilo; siempre que cuando Q es -NHCH2(4,6-dimetil-piridin-3-il) y A1 es quinolin-8-ilo, benzotriazol-1-ilo, 3,5-dimetil-pirazolilo, 2-fluoro-fenilo, 2-cloro-fenilo, 2-nitro-fenilo, 2-trifluorometil-fenilo, 2-difluorometoxi-fenilo, 3-difluorometoxi-fenilo, 2-trifluorometoxi- fenilo, 2,4-difluoro-fenilo, 2,6-difluoro-fenilo, 2,6-dicloro-fenilo, 2-cloro-4-fluoro-fenilo, 2,6-difluoro-4-metoxi-fenilo, o 4-trifluorometoxi-fenilo, A2 no sea 4-difluorometoxi-fenilo; y, siempre que cuando Q es -NHCH2(4,6-dimetil-piridin-3-il) y A1 es 3-nitro-4-metoxi-fenilo, 2,6-difluoro-4-metoxi-fenilo, o 3,4-dicloro-fenilo, A2 no sea 4-metoxi-fenilo; (c) es -CH2NHCH2-Ar3, donde W es N o CH, y Ar3 es piridinilo, pirimidinilo, 1,2,3,4-tetrahidro[1,8]naftiridinilo, imidazo[1,2-a]piridinilo, o quinolinilo; de tal modo que el punto de union al 1,2,3,4-tetrahidro-[1,8]naftiridinilo está en la posicion 6 o 7, y que el punto de union al quinolinilo está en la posicion 2, 3 o 4; donde Ar3 está opcionalmente sustituido con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4, aminoalquilo C1-4, (alquil C1-4amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alcoxi C1-4, amino, (alquil C1-6)amino, y di(alquil C1-6)amino; y donde el grupo alquilo C1-6 de (alquil C1-6)amino y di(alquil C1-6)amino está opcionalmente sustituido con amino, (alquil C1-4)amino, di(alquil C1-4)amino, cicloalquil C3-8amino, alcoxi C1-4, o hidroxi; (d) es -(CH2)2-Ar4, donde Ar4 es piridinilo, pirimidinilo, 1,2,3,4-tetrahidro-[1,8]naftiridinilo, imidazo[1,2-a]piridinilo, o quinolinilo; de tal modo que el punto de union a 1,2,3,4-tetrahidro-[1,8]naftiridinilo está en la posicion 6 o 7, y el punto de union al quinolinilo está en la posicion 2, 3 o 4; donde Ar4 está opcionalmente sustituido con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4, aminoalquilo C1-4, (alquil C1-4)amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alcoxi C1-4, amino, (alquil C1-6)amino, di(alquil C1-6)amino, halogeno, y aminocarbonilo; y donde el grupo alquilo C1-6 de (alquil C1-6)amino y di(alquil C1-6)amino está opcionalmente sustituido con amino, (alquil C1-4)amino, di(alquil C1-4)amino, cicloalquil C3- 8amino, alcoxi C1-4, o hidroxi; (e) es -CH=CH-Ar5 donde Ar5 es piridinilo, pirimidinilo, 1,2,3,4-tetrahidro-[1,8]naftiridinilo, imidazo[1,2-a]piridinilo, o quinolinilo; de tal modo que el punto de union al 1,2,3,4-tetrahidro-[1,8]naftiridinilo está en la posicion 6 o 7, y el punto de union al quinolinilo está en la posicion 2, 3 o 4; donde Ar5 está opcionalmente sustituido con uno a tres sustituyentes independientemente seleccionados del grupo formado por alquilo C1-4, aminoalquilo C1-4, (alquil C1-4)amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, alcoxi C1-4, amino, (alquil C1-6)amino, di(alquil C1-6)amino, halogeno, y aminocarbonilo; y donde el grupo alquilo C1-6 de (alquil C1-6)amino y di(alquil C1-6)amino está opcionalmente sustituido con amino, (alquil C1-4)amino, di(alquil C1-4)amino, cicloalquil C3-8amino, alcoxi C1-4, o hidroxi
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75493905P | 2005-12-29 | 2005-12-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR058406A1 true AR058406A1 (es) | 2008-01-30 |
Family
ID=38158058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060105853A AR058406A1 (es) | 2005-12-29 | 2006-12-28 | Antagonistas del receptor de proquineticina 1 |
Country Status (10)
Country | Link |
---|---|
US (2) | US7902358B2 (es) |
EP (2) | EP1973886B1 (es) |
JP (1) | JP5452934B2 (es) |
CN (2) | CN101495464B (es) |
AR (1) | AR058406A1 (es) |
CA (1) | CA2635842C (es) |
CL (1) | CL2006003736A1 (es) |
DK (1) | DK1973886T3 (es) |
IL (1) | IL192424A0 (es) |
WO (1) | WO2007079163A2 (es) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006104715A1 (en) * | 2005-03-24 | 2006-10-05 | Janssen Pharmaceutica, N.V. | Prokineticin 1 receptor antagonists |
CN101495464B (zh) * | 2005-12-29 | 2014-03-05 | 詹森药业有限公司 | 激肽原1受体拮抗剂 |
SG174016A1 (en) * | 2006-07-24 | 2011-09-29 | Korea Res Inst Chem Tech | Hiv reverse transcriptase inhibitors |
JP2011502154A (ja) * | 2007-10-30 | 2011-01-20 | 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 | アミノヘテロアリールを含むプロキネチシン1受容体拮抗物質連邦政府支援研究又は開発に関する陳述下に記述される本発明の研究及び開発は、連邦政府の支援によるものではない。 |
MX2011008362A (es) | 2009-02-13 | 2011-08-24 | Shionogi & Co | Derivado novedoso de triazina y composicion farmaceutica que comprende el mismo. |
WO2012006004A1 (en) * | 2010-06-28 | 2012-01-12 | Janssen Pharmaceutica Nv | Prokineticin 1 receptor antagonists for the treatment of pain |
CA2807947C (en) | 2010-08-10 | 2018-06-19 | Shionogi & Co., Ltd. | Triazine derivative and pharmaceutical compound that contains same and exhibits analgesic activity |
JP6075621B2 (ja) | 2010-08-10 | 2017-02-08 | 塩野義製薬株式会社 | 新規複素環誘導体およびそれらを含有する医薬組成物 |
US9351972B2 (en) * | 2010-11-29 | 2016-05-31 | Galleon Pharmaceuticals, Inc. | Compounds as respiratory stimulants for treatment of breathing control disorders or diseases |
US9550763B2 (en) | 2012-02-09 | 2017-01-24 | Shionogi & Co., Ltd. | Heterocyclic ring and carbocyclic derivative |
GB201209587D0 (en) | 2012-05-30 | 2012-07-11 | Takeda Pharmaceutical | Therapeutic compounds |
TWI637949B (zh) | 2013-06-14 | 2018-10-11 | 塩野義製藥股份有限公司 | 胺基三衍生物及含有其等之醫藥組合物 |
GB201314286D0 (en) | 2013-08-08 | 2013-09-25 | Takeda Pharmaceutical | Therapeutic Compounds |
GB201320905D0 (en) * | 2013-11-27 | 2014-01-08 | Takeda Pharmaceutical | Therapeutic compounds |
US9988373B2 (en) | 2013-12-26 | 2018-06-05 | Shionogi & Co., Ltd. | Nitrogen-containing six-membered cyclic derivatives and pharmaceutical composition comprising the same |
EP3957627B1 (en) | 2015-04-24 | 2024-06-19 | Shionogi & Co., Ltd | 6-membered heterocyclic derivative and pharmaceutical composition comprising same |
WO2018074390A1 (ja) | 2016-10-17 | 2018-04-26 | 塩野義製薬株式会社 | 二環性含窒素複素環誘導体およびそれらを含有する医薬組成物 |
CN110606827B (zh) * | 2019-09-26 | 2023-03-14 | 西安凯立新材料股份有限公司 | 一步法合成甲氨基吡啶类化合物的方法 |
WO2022138988A1 (ja) * | 2021-04-14 | 2022-06-30 | 塩野義製薬株式会社 | ウイルス増殖阻害作用を有するトリアジン誘導体およびそれらを含有する医薬組成物 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61205261A (ja) * | 1985-03-08 | 1986-09-11 | Sagami Chem Res Center | 6―置換―5―フルオロウラシル誘導体 |
SE9704272D0 (sv) * | 1997-11-21 | 1997-11-21 | Astra Pharma Prod | Novel Compounds |
US6485938B1 (en) | 1999-11-16 | 2002-11-26 | Zymogenetics, Inc. | Nucleic acid molecules that encodes human Zven1 |
EP1332157A2 (en) | 2000-11-03 | 2003-08-06 | The Regents of the University of California | Prokineticin polypeptides, related compositions and methods |
BR0313385A (pt) | 2002-08-13 | 2005-06-14 | Warner Lambert Co | Derivados de pirimidina-2,4-diona como inibidores de metaloproteinase da matriz |
WO2004014354A1 (en) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | 1,6-fused uracil derivatives as matrix metalloproteinase inhibitors |
WO2004032850A2 (en) | 2002-10-07 | 2004-04-22 | Zymogenetics, Inc. | Uses of human zven antagonists |
US7115560B2 (en) | 2003-03-25 | 2006-10-03 | The Regents Of The University Of California | Methods for modulating gastric secretion using prokineticin receptor antagonists |
CN102134229B (zh) * | 2004-03-15 | 2020-08-04 | 武田药品工业株式会社 | 二肽基肽酶抑制剂 |
AU2006229791A1 (en) | 2005-03-24 | 2006-10-05 | Janssen Pharmaceutica, N.V. | Pyrimidindione derivatives as prokineticin 2 receptor antagonists |
WO2006104715A1 (en) * | 2005-03-24 | 2006-10-05 | Janssen Pharmaceutica, N.V. | Prokineticin 1 receptor antagonists |
EP1868609A2 (en) * | 2005-03-24 | 2007-12-26 | Janssen Pharmaceutica N.V. | Prokineticin 1 receptor |
CN101495464B (zh) * | 2005-12-29 | 2014-03-05 | 詹森药业有限公司 | 激肽原1受体拮抗剂 |
-
2006
- 2006-12-28 CN CN200680053507.7A patent/CN101495464B/zh not_active Expired - Fee Related
- 2006-12-28 DK DK06849064.8T patent/DK1973886T3/da active
- 2006-12-28 CN CN2012103335116A patent/CN103396398A/zh active Pending
- 2006-12-28 CL CL200603736A patent/CL2006003736A1/es unknown
- 2006-12-28 AR ARP060105853A patent/AR058406A1/es not_active Application Discontinuation
- 2006-12-28 EP EP06849064A patent/EP1973886B1/en not_active Not-in-force
- 2006-12-28 EP EP11157226.9A patent/EP2385042B1/en not_active Not-in-force
- 2006-12-28 US US11/647,091 patent/US7902358B2/en not_active Expired - Fee Related
- 2006-12-28 WO PCT/US2006/049460 patent/WO2007079163A2/en active Application Filing
- 2006-12-28 JP JP2008548735A patent/JP5452934B2/ja not_active Expired - Fee Related
- 2006-12-28 CA CA2635842A patent/CA2635842C/en not_active Expired - Fee Related
-
2008
- 2008-06-24 IL IL192424A patent/IL192424A0/en unknown
-
2010
- 2010-12-16 US US12/970,461 patent/US8372973B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
US20080269225A1 (en) | 2008-10-30 |
IL192424A0 (en) | 2009-02-11 |
DK1973886T3 (da) | 2013-03-18 |
US20120028997A1 (en) | 2012-02-02 |
CN101495464A (zh) | 2009-07-29 |
EP2385042B1 (en) | 2015-11-25 |
US7902358B2 (en) | 2011-03-08 |
EP2385042A1 (en) | 2011-11-09 |
JP2009522283A (ja) | 2009-06-11 |
CA2635842C (en) | 2015-02-17 |
WO2007079163A2 (en) | 2007-07-12 |
CL2006003736A1 (es) | 2008-05-16 |
EP1973886A2 (en) | 2008-10-01 |
CN103396398A (zh) | 2013-11-20 |
CN101495464B (zh) | 2014-03-05 |
EP1973886B1 (en) | 2013-02-27 |
WO2007079163A3 (en) | 2007-08-30 |
CA2635842A1 (en) | 2007-07-12 |
US8372973B2 (en) | 2013-02-12 |
JP5452934B2 (ja) | 2014-03-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR058406A1 (es) | Antagonistas del receptor de proquineticina 1 | |
AR058407A1 (es) | Antagonistas del receptor de proquineticina 2 | |
TN2018000295A1 (en) | Pyrazolo[1,5-a]pyrazin-4-yl derivatives as jak-inhibitors | |
EP1243582A4 (en) | CHINOLINE AND CHINAZOLINE DERIVATIVES AND MEDICATIONS CONTAINING THEM | |
DE60219672D1 (de) | Imidazopyridine, -pyrimidine und -triazine als gaba-a alpha 5 rezeptor subtyp liganden zur verbesserung kognitiver eigenschaften | |
WO2002051410A3 (en) | Phenylthiazole and thiazoline derivatives and their use as antiparasitics | |
ATE294796T1 (de) | Chinazolin derivate | |
DK0622361T3 (da) | Heterocykliske forbindelser som bradykininantagonister | |
AR053700A1 (es) | Antagonistas del receptor de proquineticina 2 | |
DK7280A (da) | Fremgangsmaade til fremstilling af (piperidinylalkyl) quinazolin-derivater | |
MX9804108A (es) | Derivados de quinolina-4-carboxamida, su preparacion y uso como antagonistas receptores de neuroquinina 3 (nk-3)- y neuroquinina 2 (kn-2). | |
MX9700883A (es) | Derivados sustituidos de la quinazolina. | |
MY118109A (en) | Novel aralkyl amines of spirofuropyridines useful in therapy | |
AR047537A1 (es) | Piridazinonaureas como antagonistas de integrinas | |
EA200400466A1 (ru) | Производные пиперазина с антагонистической активностью к рецептору ccr1 | |
AR069127A1 (es) | Antagonistas del receptor de procineticina 1 que contienen amino-heteroarilo | |
RS51550B (en) | KAO DERIVATIVES KAO MODULATORS CCR5 | |
AR053451A1 (es) | Antagonistas del receptor de proquineticina 1 | |
HUP0400246A2 (hu) | 1,2,4-Trioxolánt tartalmazó maláriaellenes gyógyszerkészítmények és eljárás az előállításukra és az alkalmazásukra | |
HRP20110344T1 (hr) | Derivati dihidropiridina | |
AP9901695A0 (en) | Quinoline-4-carbaoxamide derivatives as NK-2 and NK-3 receptor antagonists. | |
CA2371712A1 (en) | Cyclothiocarbamate derivatives as progesterone receptor modulators | |
ATE274518T1 (de) | 6-(2-chlor-6-fluor-phenyl)-triazolpyrimidine | |
RU2149000C1 (ru) | Применение карбоциклически и гетероциклически анеллированных дигидропиридинов и их фармацевтически приемлемых солей в качестве блокатора неселективных каналов катионов при защите головного мозга и лечении хронической бронхиальной астмы | |
BRPI0212215B8 (pt) | compostos de ciclopenta[g]quinazolina anticâncer, uso dos mesmos para o tratamento de câncer e composição farmacêutica compreendendo dito composto |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |