ES2292488T3 - Derivados de la urea, como agentes antiinflamatorios. - Google Patents
Derivados de la urea, como agentes antiinflamatorios. Download PDFInfo
- Publication number
- ES2292488T3 ES2292488T3 ES00978751T ES00978751T ES2292488T3 ES 2292488 T3 ES2292488 T3 ES 2292488T3 ES 00978751 T ES00978751 T ES 00978751T ES 00978751 T ES00978751 T ES 00978751T ES 2292488 T3 ES2292488 T3 ES 2292488T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- branched
- tert
- butyl
- naphthalen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical class NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title claims description 6
- 229940121363 anti-inflammatory agent Drugs 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 70
- -1 pridinyl Chemical group 0.000 claims abstract description 55
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 34
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 8
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims abstract description 7
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 7
- 150000002367 halogens Chemical class 0.000 claims abstract description 7
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims abstract description 7
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 5
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 5
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 4
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- 125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 4
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
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- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims abstract description 3
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- 125000002883 imidazolyl group Chemical group 0.000 claims abstract description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims abstract description 3
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- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 claims description 2
- 230000009885 systemic effect Effects 0.000 claims description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims 1
- ZGXFVYOWURGVSM-UHFFFAOYSA-N 4-[4-(2-morpholin-4-yl-2-thiomorpholin-4-ylthiomorpholin-4-yl)sulfinyl-2-thiomorpholin-4-ylthiomorpholin-2-yl]morpholine Chemical compound C1CSC(N2CCSCC2)(N2CCOCC2)CN1S(=O)N(C1)CCSC1(N1CCSCC1)N1CCOCC1 ZGXFVYOWURGVSM-UHFFFAOYSA-N 0.000 abstract description 2
- NNLBRYQGMOYARS-UHFFFAOYSA-N thiane 1-oxide Chemical compound O=S1CCCCC1 NNLBRYQGMOYARS-UHFFFAOYSA-N 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
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- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 54
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 40
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 23
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- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16590399P | 1999-11-16 | 1999-11-16 | |
| US165903P | 1999-11-16 |
Publications (1)
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| US (2) | US6492393B1 (enExample) |
| EP (1) | EP1232150B1 (enExample) |
| JP (1) | JP4955171B2 (enExample) |
| AT (1) | ATE375334T1 (enExample) |
| AU (1) | AU1617901A (enExample) |
| CA (1) | CA2389360C (enExample) |
| DE (1) | DE60036726T2 (enExample) |
| ES (1) | ES2292488T3 (enExample) |
| MX (2) | MXPA02004594A (enExample) |
| WO (1) | WO2001036403A1 (enExample) |
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| ES2224462T3 (es) * | 1997-12-11 | 2005-03-01 | Janssen Pharmaceutica N.V. | Anilidas mimeticas del acido retinoico. |
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| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US20020065296A1 (en) * | 1999-01-13 | 2002-05-30 | Bayer Corporation | Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors |
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| RU2319693C9 (ru) | 1999-01-13 | 2008-08-20 | Байер Копэрейшн | Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты) |
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-
2000
- 2000-11-16 CA CA002389360A patent/CA2389360C/en not_active Expired - Lifetime
- 2000-11-16 DE DE60036726T patent/DE60036726T2/de not_active Expired - Lifetime
- 2000-11-16 ES ES00978751T patent/ES2292488T3/es not_active Expired - Lifetime
- 2000-11-16 AU AU16179/01A patent/AU1617901A/en not_active Abandoned
- 2000-11-16 MX MXPA02004594A patent/MXPA02004594A/es active IP Right Grant
- 2000-11-16 MX MXPA02004879A patent/MXPA02004879A/es unknown
- 2000-11-16 JP JP2001538892A patent/JP4955171B2/ja not_active Expired - Lifetime
- 2000-11-16 AT AT00978751T patent/ATE375334T1/de active
- 2000-11-16 EP EP00978751A patent/EP1232150B1/en not_active Expired - Lifetime
- 2000-11-16 WO PCT/US2000/031582 patent/WO2001036403A1/en not_active Ceased
- 2000-11-16 US US09/714,539 patent/US6492393B1/en not_active Expired - Lifetime
-
2002
- 2002-10-15 US US10/271,301 patent/US7241758B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ATE375334T1 (de) | 2007-10-15 |
| AU1617901A (en) | 2001-05-30 |
| JP4955171B2 (ja) | 2012-06-20 |
| EP1232150B1 (en) | 2007-10-10 |
| DE60036726T2 (de) | 2008-02-07 |
| CA2389360C (en) | 2008-06-03 |
| MXPA02004594A (es) | 2002-10-23 |
| DE60036726D1 (de) | 2007-11-22 |
| WO2001036403A1 (en) | 2001-05-25 |
| US7241758B2 (en) | 2007-07-10 |
| US20030125354A1 (en) | 2003-07-03 |
| US6492393B1 (en) | 2002-12-10 |
| EP1232150A1 (en) | 2002-08-21 |
| MXPA02004879A (es) | 2002-08-30 |
| CA2389360A1 (en) | 2001-05-25 |
| JP2003514808A (ja) | 2003-04-22 |
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