NO20052995L - 1,5-diaryl-pyrrol-3-karboksamid-derivater, og deres anvendelse som kannabinoid reseptormodulatorer. - Google Patents
1,5-diaryl-pyrrol-3-karboksamid-derivater, og deres anvendelse som kannabinoid reseptormodulatorer.Info
- Publication number
- NO20052995L NO20052995L NO20052995A NO20052995A NO20052995L NO 20052995 L NO20052995 L NO 20052995L NO 20052995 A NO20052995 A NO 20052995A NO 20052995 A NO20052995 A NO 20052995A NO 20052995 L NO20052995 L NO 20052995L
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- group
- alkyl group
- optionally substituted
- alkyl
- heterocyclic group
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- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- A61K31/402—1-aryl substituted, e.g. piretanide
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- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- 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
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- 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
Abstract
Foreliggende oppfinnelse angår en forbindelse med formel I hvor R1 og R2 uavhengig representerer fenyl, tienyl eller pyridyl som hver eventuelt er substituert med én, to eller tre grupper representert ved Z; og R3er H, en C1-3alkylgruppe, en C1-3alkoksymetylgruppe, trifluormetyl, en hydroksyC1-3alkylgruppe, en aminoC1-3alkylgruppe, C1-3alkoksykarbonyl, karboksy, cyano, karbamoyl, mono- eller di- C1-3alkylkarbamoyl, acetyl eller hydrazinokarbonyl med formelen CONHNRaRb hvor Ra og Rb er som definert for henholdsvis R4 og R5; X er CO eller SO2; Y er fraværende eller representerer NH eventuelt substituert med en C1-3alkylgruppe; R4 og R5 representerer uavhengig: en C1-6alkylgruppe; en (amino)C1-4alkylgruppe hvor amino eventuelt er substituert med én eller flere C1-3alkylgrupper; en eventuelt substituert ikke-aromatisk C3-15karbocyklisk gruppe; en (C3-12cykloalkyl)C1-3a1kylgruppe; en gruppe -(CH2)r(fenyl )5; naftyl; antracenyl; en mettet 5- til 8-leddet heterocyklisk gruppe inneholdende ett nitrogen og eventuelt ett av de følgende: oksygen, svovel eller et ytterligere nitrogen hvor den heterocykliske gruppen eventuelt er substituert; 1-adamantylmetyl; en gruppe -(CH2)Het, hvor Het representerer en aromatisk heterocyklisk gruppe eventuelt substituert; eller R4 representerer H og R5 er som definert ovenfor; eller R og R sammen med nitrogenatomet som de er bundet til representerer en mettet 5- til 8-leddet heterocyklisk gruppe; R6 er H, en C1-3alkylgruppe, en C1-3alkoksymetylgruppe, trifluormetyl, en hydroksyC1-3alkylgruppe, C1-3alkoksykarbonyl, karboksy, cyano, karbamoyl, mono- eller di- C1-3alkylkarbamoyl, acetyl eller hydrazinokarbonyl med formelen -CONHNRaRb; med forbehold; fremgangsmåter for fremstilling av slike forbindelser, anvendelse av dem ved behandling av fedme, psykiatriske og nevrologiske lidelser, spesielt fedme, metoder for deres terapeutiske anvendelse og farmasøytiske preparater inneholdende dem.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0230088.7A GB0230088D0 (en) | 2002-12-24 | 2002-12-24 | Therapeutic agents |
PCT/GB2003/005569 WO2004058249A1 (en) | 2002-12-24 | 2003-12-18 | 1,5-diaryl-pyrrole-3-carboxamide derivatives and their use as cannabinoid receptor modulators |
Publications (2)
Publication Number | Publication Date |
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NO20052995D0 NO20052995D0 (no) | 2005-06-17 |
NO20052995L true NO20052995L (no) | 2005-07-22 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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NO20052995A NO20052995L (no) | 2002-12-24 | 2005-06-17 | 1,5-diaryl-pyrrol-3-karboksamid-derivater, og deres anvendelse som kannabinoid reseptormodulatorer. |
Country Status (20)
Country | Link |
---|---|
US (1) | US20060122230A1 (no) |
EP (1) | EP1578417A1 (no) |
JP (1) | JP2006513201A (no) |
KR (1) | KR20050086931A (no) |
CN (1) | CN1753668A (no) |
AR (1) | AR042658A1 (no) |
AU (1) | AU2003290292A1 (no) |
BR (1) | BR0317705A (no) |
CA (1) | CA2511601A1 (no) |
CL (1) | CL2003002720A1 (no) |
GB (1) | GB0230088D0 (no) |
IS (1) | IS7944A (no) |
MX (1) | MXPA05006919A (no) |
NO (1) | NO20052995L (no) |
PL (1) | PL377296A1 (no) |
RU (1) | RU2005117783A (no) |
TW (1) | TW200503692A (no) |
UY (1) | UY28144A1 (no) |
WO (1) | WO2004058249A1 (no) |
ZA (1) | ZA200504822B (no) |
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GB0403780D0 (en) * | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Therapeutic agents |
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CN101006052B (zh) * | 2004-07-30 | 2013-11-06 | 埃克塞利希斯股份有限公司 | 作为药用制剂的吡咯衍生物 |
FR2874012B1 (fr) * | 2004-08-09 | 2008-08-22 | Sanofi Synthelabo | Derives de pyrrole, leur preparation et leur utlisation en therapeutique |
FR2882054B1 (fr) | 2005-02-17 | 2007-04-13 | Sanofi Aventis Sa | Derives de 1,5-diarylpyrrole, leur preparation et leur application en therapeutique |
FR2887548B1 (fr) * | 2005-06-27 | 2007-09-21 | Sanofi Aventis Sa | Derives de 4,5-diarylpyrrole, leur preparation et leur application en therapeutique |
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WO2007020502A2 (en) * | 2005-08-16 | 2007-02-22 | Pharmacia & Upjohn Company Llc | Cannabinoid receptor ligands and uses thereof |
JP2009510090A (ja) | 2005-09-27 | 2009-03-12 | ミリアド ジェネティックス インコーポレーティッド | 治療化合物としてのピロール誘導体 |
CN101384549B (zh) * | 2006-02-20 | 2011-04-13 | 安斯泰来制药株式会社 | 吡咯衍生物或其盐 |
AU2007283113A1 (en) | 2006-08-08 | 2008-02-14 | Sanofi-Aventis | Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, processes for preparing them, medicaments comprising these compounds, and their use |
CA2662870A1 (en) * | 2006-09-07 | 2008-03-13 | Myriad Genetics, Inc. | Therapeutic compounds for diseases and disorders |
TW200831080A (en) * | 2006-12-15 | 2008-08-01 | Irm Llc | Compounds and compositions as inhibitors of cannabinoid receptor 1 activity |
TW200848019A (en) | 2007-03-06 | 2008-12-16 | Wyeth Corp | Aryl sulfonamides useful for modulation of the progesterone receptor |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
LT2963031T (lt) | 2007-11-30 | 2019-04-10 | Zynerba Pharmaceuticals, Inc. | Tetrahidrokanabinolio provaistai, provaistus apimančios tetrahidrokanabinolio kompozicijos ir jų panaudojimo būdai |
CN102119029B (zh) * | 2008-04-22 | 2013-03-13 | 伊莱利利公司 | 作为cb-1配体的1,5-二苯基-吡咯烷-2-酮化合物 |
FR2930939B1 (fr) | 2008-05-09 | 2010-07-30 | Sanofi Aventis | Derives de pyrrole, leur preparation et leur application en therapeutique |
UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
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 |
CA2771278A1 (en) | 2009-08-26 | 2011-03-03 | Sanofi | Novel crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use |
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EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120057A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
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DE4440337A1 (de) * | 1994-11-11 | 1996-05-15 | Dds Drug Delivery Services Ges | Pharmazeutische Nanosuspensionen zur Arzneistoffapplikation als Systeme mit erhöhter Sättigungslöslichkeit und Lösungsgeschwindigkeit |
US5665331A (en) * | 1995-01-10 | 1997-09-09 | Nanosystems L.L.C. | Co-microprecipitation of nanoparticulate pharmaceutical agents with crystal growth modifiers |
US6074966A (en) * | 1996-09-09 | 2000-06-13 | Zlatkus; Frank P. | Nonwoven fabric composite having multi-directional stretch properties utilizing a cellular or foam layer |
US6048550A (en) * | 1996-10-03 | 2000-04-11 | Chan; Daniel C. F. | Hydrophilic microparticles and methods to prepare same |
FR2758723B1 (fr) * | 1997-01-28 | 1999-04-23 | Sanofi Sa | Utilisation des antagonistes des recepteurs aux cannabinoides centraux pour la preparation de medicaments |
US6127520A (en) * | 1997-04-15 | 2000-10-03 | Regents Of The University Of Michigan | Compositions and methods for the inhibition of neurotransmitter uptake of synaptic vesicles |
FR2766368B1 (fr) * | 1997-07-24 | 2000-03-31 | Univ Claude Bernard Lyon | Procede de preparation de nanocapsules de type vesiculaire, utilisables notamment comme vecteurs colloidaux de principes actifs pharmaceutiques ou autres |
US6375986B1 (en) * | 2000-09-21 | 2002-04-23 | Elan Pharma International Ltd. | Solid dose nanoparticulate compositions comprising a synergistic combination of a polymeric surface stabilizer and dioctyl sodium sulfosuccinate |
FR2789079B3 (fr) * | 1999-02-01 | 2001-03-02 | Sanofi Synthelabo | Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant |
US6383471B1 (en) * | 1999-04-06 | 2002-05-07 | Lipocine, Inc. | Compositions and methods for improved delivery of ionizable hydrophobic therapeutic agents |
US6372777B1 (en) * | 1999-12-23 | 2002-04-16 | Icos Corporation | Cyclic AMP-specific phosphodiesterase inhibitors |
CA2399791A1 (en) * | 2000-02-11 | 2001-08-16 | Bristol-Myers Squibb Company | Cannabinoid receptor modulators, their processes of preparation, and use of cannabinoid receptor modulators in treating respiratory and non-respiratory diseases |
CN1254233C (zh) * | 2001-08-06 | 2006-05-03 | 阿斯特拉曾尼卡有限公司 | 含有水不溶性的稳定纳米颗粒和赋形剂如中链甘油三酯(mct)的水性分散体 |
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US20060003012A9 (en) * | 2001-09-26 | 2006-01-05 | Sean Brynjelsen | Preparation of submicron solid particle suspensions by sonication of multiphase systems |
SE0104330D0 (sv) * | 2001-12-19 | 2001-12-19 | Astrazeneca Ab | Therapeutic agents |
GB0216700D0 (en) * | 2002-07-18 | 2002-08-28 | Astrazeneca Ab | Process |
GB0302671D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
GB0302672D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
GB0302673D0 (en) * | 2003-02-06 | 2003-03-12 | Astrazeneca Ab | Pharmaceutical formulations |
GB0314057D0 (en) * | 2003-06-18 | 2003-07-23 | Astrazeneca Ab | Therapeutic agents |
US20060135523A1 (en) * | 2003-06-18 | 2006-06-22 | Astrazeneca Ab | 2-substituted 5,6-diaryl-pyrazine derivatives as cb1 modulator |
-
2002
- 2002-12-24 GB GBGB0230088.7A patent/GB0230088D0/en not_active Ceased
-
2003
- 2003-12-18 EP EP03782654A patent/EP1578417A1/en not_active Withdrawn
- 2003-12-18 MX MXPA05006919A patent/MXPA05006919A/es not_active Application Discontinuation
- 2003-12-18 JP JP2004563346A patent/JP2006513201A/ja not_active Withdrawn
- 2003-12-18 CN CNA2003801099724A patent/CN1753668A/zh active Pending
- 2003-12-18 BR BR0317705-0A patent/BR0317705A/pt not_active Application Discontinuation
- 2003-12-18 US US10/540,276 patent/US20060122230A1/en not_active Abandoned
- 2003-12-18 WO PCT/GB2003/005569 patent/WO2004058249A1/en active Application Filing
- 2003-12-18 TW TW092135979A patent/TW200503692A/zh unknown
- 2003-12-18 KR KR1020057011696A patent/KR20050086931A/ko not_active Application Discontinuation
- 2003-12-18 AU AU2003290292A patent/AU2003290292A1/en not_active Abandoned
- 2003-12-18 PL PL377296A patent/PL377296A1/pl not_active Application Discontinuation
- 2003-12-18 CA CA002511601A patent/CA2511601A1/en not_active Abandoned
- 2003-12-18 RU RU2005117783/04A patent/RU2005117783A/ru not_active Application Discontinuation
- 2003-12-22 CL CL200302720A patent/CL2003002720A1/es unknown
- 2003-12-22 AR ARP030104797A patent/AR042658A1/es unknown
- 2003-12-22 UY UY28144A patent/UY28144A1/es unknown
-
2005
- 2005-06-17 NO NO20052995A patent/NO20052995L/no not_active Application Discontinuation
- 2005-07-18 IS IS7944A patent/IS7944A/is unknown
-
2006
- 2006-01-19 ZA ZA200504822A patent/ZA200504822B/en unknown
Also Published As
Publication number | Publication date |
---|---|
CL2003002720A1 (es) | 2005-01-07 |
UY28144A1 (es) | 2004-07-30 |
MXPA05006919A (es) | 2005-08-18 |
BR0317705A (pt) | 2005-11-22 |
EP1578417A1 (en) | 2005-09-28 |
AU2003290292A1 (en) | 2004-07-22 |
RU2005117783A (ru) | 2006-02-10 |
JP2006513201A (ja) | 2006-04-20 |
KR20050086931A (ko) | 2005-08-30 |
WO2004058249A1 (en) | 2004-07-15 |
NO20052995D0 (no) | 2005-06-17 |
ZA200504822B (en) | 2006-03-29 |
TW200503692A (en) | 2005-02-01 |
GB0230088D0 (en) | 2003-01-29 |
AR042658A1 (es) | 2005-06-29 |
CN1753668A (zh) | 2006-03-29 |
IS7944A (is) | 2005-07-18 |
PL377296A1 (pl) | 2006-01-23 |
CA2511601A1 (en) | 2004-07-15 |
US20060122230A1 (en) | 2006-06-08 |
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