JP2006509781A - インドール−3−カルボキサミドの誘導体、それらの製造方法および治療用途 - Google Patents
インドール−3−カルボキサミドの誘導体、それらの製造方法および治療用途 Download PDFInfo
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- JP2006509781A JP2006509781A JP2004556430A JP2004556430A JP2006509781A JP 2006509781 A JP2006509781 A JP 2006509781A JP 2004556430 A JP2004556430 A JP 2004556430A JP 2004556430 A JP2004556430 A JP 2004556430A JP 2006509781 A JP2006509781 A JP 2006509781A
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- indole
- methyl
- formula
- carboxamide
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- 230000001225 therapeutic effect Effects 0.000 title abstract description 3
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 125000005843 halogen group Chemical group 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
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- 125000002837 carbocyclic group Chemical group 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 62
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 36
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 20
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- QKBDQOSMXRXTGL-UHFFFAOYSA-N 7-chloro-2-methyl-1-(3-methylsulfanylpropyl)-n-(2,2,4-trimethyl-3-bicyclo[2.2.1]heptanyl)indole-3-carboxamide Chemical compound C12=CC=CC(Cl)=C2N(CCCSC)C(C)=C1C(=O)NC1C(C2)(C)CCC2C1(C)C QKBDQOSMXRXTGL-UHFFFAOYSA-N 0.000 claims description 5
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| FR0215086A FR2847899B1 (fr) | 2002-11-29 | 2002-11-29 | Derives d'indole-3-carboxamide, leur preparation et leur application en therapeutique |
| PCT/FR2003/003499 WO2004050086A1 (fr) | 2002-11-29 | 2003-11-27 | Derives d'indole-3-carboxamide, leur preparation et leur application en therapeutique |
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| WO2008032764A1 (en) * | 2006-09-13 | 2008-03-20 | Kyowa Hakko Kirin Co., Ltd. | Fused heterocyclic derivative |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1833824B1 (en) * | 2004-12-21 | 2016-08-03 | AbbVie Inc. | 3-cycloalkylcarbonyl indoles as cannabinoid receptor ligands |
| FR2893615B1 (fr) * | 2005-11-18 | 2008-03-07 | Sanofi Aventis Sa | Derives de 3-acylindole, leur preparation et leur application en therapeutique |
| US8841334B2 (en) | 2006-05-31 | 2014-09-23 | Abbvie Inc. | Compounds as cannabinoid receptor ligands and uses thereof |
| CN101448800A (zh) | 2006-05-31 | 2009-06-03 | 艾博特公司 | 作为大麻素受体配体的新型化合物及其用途 |
| MX2009010363A (es) | 2007-03-28 | 2009-12-04 | Abbott Lab | Compuestos de 1,3-tiazol-2(3h)-ilideno como ligandos del receptor canabinoide. |
| US7872033B2 (en) | 2007-04-17 | 2011-01-18 | Abbott Laboratories | Compounds as cannabinoid receptor ligands |
| US8735434B2 (en) | 2007-05-18 | 2014-05-27 | Abbvie Inc. | Compounds as cannabinoid receptor ligands |
| US9193713B2 (en) | 2007-10-12 | 2015-11-24 | Abbvie Inc. | Compounds as cannabinoid receptor ligands |
| US8846730B2 (en) | 2008-09-08 | 2014-09-30 | Abbvie Inc. | Compounds as cannabinoid receptor ligands |
| TW201016692A (en) | 2008-09-16 | 2010-05-01 | Abbott Lab | Novel compounds as cannabinoid receptor ligands |
| WO2010077839A1 (en) * | 2008-12-15 | 2010-07-08 | Wyeth Llc (Formerly Known As Wyeth) | Substituted oxindol cb2 agonists for pain treatment |
| PA8854001A1 (es) | 2008-12-16 | 2010-07-27 | Abbott Lab | Compuestos novedosos como ligandos de receptores de canabinoides |
| CN108794379A (zh) * | 2017-04-26 | 2018-11-13 | 华东师范大学 | 1h-吲哚-2-甲酰胺衍生物及其制备方法和应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2001058869A2 (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 |
| WO2002042269A1 (fr) * | 2000-11-22 | 2002-05-30 | Sanofi-Synthelabo | Derives de 3-aroylindole et leur utilisation en tant qu'agonistes des recepteurs cb2 |
| WO2002060447A1 (en) * | 2001-01-29 | 2002-08-08 | University Of Connecticut | Receptor selective cannabimimetic aminoalkylindoles |
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| US4973587A (en) * | 1990-03-08 | 1990-11-27 | Sterling Drug Inc. | 3-arylcarbonyl-1-aminoalkyl-1H-indole-containing antiglaucoma method |
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001058869A2 (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 |
| WO2002042269A1 (fr) * | 2000-11-22 | 2002-05-30 | Sanofi-Synthelabo | Derives de 3-aroylindole et leur utilisation en tant qu'agonistes des recepteurs cb2 |
| WO2002060447A1 (en) * | 2001-01-29 | 2002-08-08 | University Of Connecticut | Receptor selective cannabimimetic aminoalkylindoles |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032764A1 (en) * | 2006-09-13 | 2008-03-20 | Kyowa Hakko Kirin Co., Ltd. | Fused heterocyclic derivative |
| US8236841B2 (en) | 2006-09-13 | 2012-08-07 | Kyowa Hakko Kirin Co., Ltd. | Fused heterocycle derivative |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003294092A1 (en) | 2004-06-23 |
| FR2847899B1 (fr) | 2006-04-28 |
| EP1567150A1 (fr) | 2005-08-31 |
| US20050288356A1 (en) | 2005-12-29 |
| DE60328819D1 (de) | 2009-09-24 |
| US7202268B2 (en) | 2007-04-10 |
| FR2847899A1 (fr) | 2004-06-04 |
| WO2004050086A1 (fr) | 2004-06-17 |
| ATE439128T1 (de) | 2009-08-15 |
| WO2004050086A8 (fr) | 2004-07-29 |
| EP1567150B1 (fr) | 2009-08-12 |
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