NO20030471L - Carboxamide compounds and their use as antagonists for an 11CBY receptor - Google Patents
Carboxamide compounds and their use as antagonists for an 11CBY receptorInfo
- Publication number
- NO20030471L NO20030471L NO20030471A NO20030471A NO20030471L NO 20030471 L NO20030471 L NO 20030471L NO 20030471 A NO20030471 A NO 20030471A NO 20030471 A NO20030471 A NO 20030471A NO 20030471 L NO20030471 L NO 20030471L
- Authority
- NO
- Norway
- Prior art keywords
- optionally substituted
- antagonists
- heterocyclic ring
- carboxamide compounds
- hydroxyl
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title abstract 2
- -1 Carboxamide compounds Chemical class 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
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- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/08—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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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Abstract
Forbindelser med formel (1) hvor: hver A uavhengig er hydrogen, Ci-6 alkyl eventuelt substituert med hydroksyl, Ci-6 alkoksy, Ci.6 alkenyl eller Ci.6 acyl eller et halogenatom eller hydroksyl, CN eller CF; R3 er hydrogen, metyl eller etyl, R4 er en eventuelt substituert aromatisk karbocyklisk eller heterocyklisk ring, Z er et O- eller S-atom, eller en NH- eller CH-gruppe eller en enkeltbinding, i 3- eller 4-stilling av R4 i forhold til karbonylgruppen, R5 er en eventuelt substituert aromatisk karbocyklisk eller heterocyklisk ring eller en i eventuelt substituert, mettet eller umettet, karbocyklisk eller heterocyklisk ring; og Q er (a) hvor X, Y, RI og R2 er som definert i krav 1, er antagonister av en human 1 lCBy-reseptor.Compounds of formula (1) wherein: each A is independently hydrogen, C 1-6 alkyl optionally substituted with hydroxyl, C 1-6 alkoxy, C 1-6 alkenyl or C 1-6 acyl or a halogen atom or hydroxyl, CN or CF; R 3 is hydrogen, methyl or ethyl, R 4 is an optionally substituted aromatic carbocyclic or heterocyclic ring, Z is an O or S atom, or an NH or CH group or a single bond, in the 3- or 4-position of R 4 relative to the carbonyl group, R 5 is an optionally substituted aromatic carbocyclic or heterocyclic ring or an optionally substituted, saturated or unsaturated, carbocyclic or heterocyclic ring; and Q is (a) wherein X, Y, R 1 and R 2 are as defined in claim 1, are antagonists of a human 11CBy receptor.
Applications Claiming Priority (3)
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| GBGB0018758.3A GB0018758D0 (en) | 2000-07-31 | 2000-07-31 | Novel use and compunds |
| GB0112544A GB0112544D0 (en) | 2001-05-23 | 2001-05-23 | Novel use and compounds |
| PCT/EP2001/008637 WO2002010146A1 (en) | 2000-07-31 | 2001-07-26 | Carboxamide compounds and their use as antagonists of a human 11cby receptor |
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| NO20030471D0 NO20030471D0 (en) | 2003-01-30 |
| NO20030471L true NO20030471L (en) | 2003-03-28 |
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| US7141561B2 (en) | 2002-07-25 | 2006-11-28 | Sanofi-Aventis Deutschland Gmbh | Substituted diaryl heterocycles, process for their preparation and their use as medicaments |
| DE10233817A1 (en) * | 2002-07-25 | 2004-02-12 | Aventis Pharma Deutschland Gmbh | Substituted diaryl heterocycles, process for their preparation and their use as medicaments |
| DE10306250A1 (en) * | 2003-02-14 | 2004-09-09 | Aventis Pharma Deutschland Gmbh | Substituted N-aryl heterocycles, processes for their preparation and their use as pharmaceuticals |
| US7223788B2 (en) | 2003-02-14 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Substituted N-aryl heterocycles, process for their preparation and their use as medicaments |
| EP2385041B1 (en) * | 2003-05-01 | 2013-09-18 | Bristol-Myers Squibb Company | Pyrazole-amine compounds useful as kinase inhibitors |
| CA2532965C (en) | 2003-07-22 | 2013-05-14 | Astex Therapeutics Limited | 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
| US7037927B2 (en) * | 2003-10-16 | 2006-05-02 | Abbott Laboratories | Amides that inhibit vanilloid receptor subtype 1 (VR1) receptor |
| US7319108B2 (en) | 2004-01-25 | 2008-01-15 | Sanofi-Aventis Deutschland Gmbh | Aryl-substituted heterocycles, process for their preparation and their use as medicaments |
| US7241787B2 (en) | 2004-01-25 | 2007-07-10 | Sanofi-Aventis Deutschland Gmbh | Substituted N-cycloexylimidazolinones, process for their preparation and their use as medicaments |
| JP2007526332A (en) * | 2004-03-02 | 2007-09-13 | ニューロジェン・コーポレーション | Heteroalkyl-substituted biphenyl-4-carboxylic acid arylamide analogs |
| DE102004010893A1 (en) * | 2004-03-06 | 2005-09-22 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New β-ketoamide compounds having MCH antagonist activity and medicaments containing these compounds |
| US7605176B2 (en) | 2004-03-06 | 2009-10-20 | Boehringer Ingelheim International Gmbh | β-ketoamide compounds with MCH antagonistic activity |
| TW200613272A (en) | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
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| US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
| AR054425A1 (en) | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO. |
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| AR056155A1 (en) | 2005-10-26 | 2007-09-19 | Bristol Myers Squibb Co | ANTAGONISTS OF NON-BASIC MELANINE CONCENTRATION HORMONE RECEIVER 1 |
| US7553836B2 (en) | 2006-02-06 | 2009-06-30 | Bristol-Myers Squibb Company | Melanin concentrating hormone receptor-1 antagonists |
| KR20080094699A (en) | 2006-02-15 | 2008-10-23 | 사노피-아벤티스 | Novel aminoalcohol-substituted aryldihydroisoquinolinones, methods for their preparation and use as drugs |
| GB0625523D0 (en) * | 2006-12-21 | 2007-01-31 | Ge Healthcare Ltd | In vivo imaging agents |
| TWI417100B (en) | 2007-06-07 | 2013-12-01 | Astrazeneca Ab | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators-842 |
| EP2025674A1 (en) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituted tetra hydro naphthalines, method for their manufacture and their use as drugs |
| PE20091928A1 (en) | 2008-05-29 | 2009-12-31 | Bristol Myers Squibb Co | HAVE HYDROXYSUSTITUTED PYRIMIDINES AS NON-BASIC MELANIN-CONCENTRATING HORMONE RECEPTOR-1 ANTAGONISTS |
| US7790760B2 (en) | 2008-06-06 | 2010-09-07 | Astrazeneca Ab | Metabotropic glutamate receptor isoxazole ligands and their use as potentiators 286 |
| AR072297A1 (en) | 2008-06-27 | 2010-08-18 | Novartis Ag | DERIVATIVES OF INDOL-2-IL-PIRIDIN-3-ILO, PHARMACEUTICAL COMPOSITION THAT INCLUDES THEM AND ITS USE IN MEDICINES FOR THE TREATMENT OF DISEASES MEDIATED BY THE SYNTHESIS ALDOSTERONE. |
| CA2739488A1 (en) | 2008-10-15 | 2010-04-22 | Boehringer Ingelheim International Gmbh | Fused heteroaryl diamide compounds useful as mmp-13 inhibitors |
| CA2738929A1 (en) | 2008-10-17 | 2010-04-22 | Boehringer Ingelheim International Gmbh | Heteroaryl substituted indole compounds useful as mmp-13 inhibitors |
| AR075401A1 (en) | 2009-02-13 | 2011-03-30 | Sanofi Aventis | SUBSTITUTED INDANS, PROCESSES FOR THEIR PREPARATION AND USE OF THE SAME AS A MEDICINAL PRODUCT |
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| WO2013130968A1 (en) * | 2012-03-01 | 2013-09-06 | University Of Cincinnati | Ros-activated compounds as selective anti-cancer therapeutics |
| WO2020140054A1 (en) | 2018-12-28 | 2020-07-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| FI4225753T3 (en) * | 2020-10-08 | 2024-08-29 | Leukos Biotech S L | Potent and selective compounds as serotonin 1b receptor modulators |
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| JP2002521436A (en) * | 1998-07-28 | 2002-07-16 | スミスクライン・ビーチャム・コーポレイション | Substituted anilide compounds and methods |
| MXPA01008142A (en) * | 1999-02-10 | 2003-07-21 | Welfide Corp | Amide compounds and medicinal use thereof. |
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| IL153645A0 (en) | 2003-07-06 |
| PL365183A1 (en) | 2004-12-27 |
| MA25829A1 (en) | 2003-07-01 |
| BR0112856A (en) | 2003-07-01 |
| HUP0302966A2 (en) | 2003-12-29 |
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| BG107510A (en) | 2003-09-30 |
| EA200300064A1 (en) | 2003-06-26 |
| AP2003002720A0 (en) | 2003-06-30 |
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| SK1142003A3 (en) | 2003-06-03 |
| CZ2003297A3 (en) | 2003-05-14 |
| MXPA03000923A (en) | 2003-06-09 |
| CA2417638A1 (en) | 2002-02-07 |
| CN1444573A (en) | 2003-09-24 |
| JP2004505070A (en) | 2004-02-19 |
| KR20030059084A (en) | 2003-07-07 |
| AU2001278508A1 (en) | 2002-02-13 |
| EP1305304A1 (en) | 2003-05-02 |
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