CN101273034B - 抑制由vla-4介导的白细胞粘附的嘧啶基酰胺化合物 - Google Patents
抑制由vla-4介导的白细胞粘附的嘧啶基酰胺化合物 Download PDFInfo
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- CN101273034B CN101273034B CN2006800356541A CN200680035654A CN101273034B CN 101273034 B CN101273034 B CN 101273034B CN 2006800356541 A CN2006800356541 A CN 2006800356541A CN 200680035654 A CN200680035654 A CN 200680035654A CN 101273034 B CN101273034 B CN 101273034B
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- nitrogen
- ring
- heterocycle
- alkyl
- ethyl
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- LDHRGPOHUJCJBV-GHXQVECXSA-N CCN(C(N1CSCC1)O)C1=CN(C)C(N(CC)C=C)N=C1N[C@@H](Cc(cc1)ccc1OC(N1CCCC1)=O)C(O)=O Chemical compound CCN(C(N1CSCC1)O)C1=CN(C)C(N(CC)C=C)N=C1N[C@@H](Cc(cc1)ccc1OC(N1CCCC1)=O)C(O)=O LDHRGPOHUJCJBV-GHXQVECXSA-N 0.000 description 1
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen 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
- C07D401/12—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
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- 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
- C07D405/12—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 chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
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- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72235805P | 2005-09-29 | 2005-09-29 | |
| US60/722,358 | 2005-09-29 | ||
| PCT/US2006/038009 WO2007041270A1 (en) | 2005-09-29 | 2006-09-28 | Pyrimidinyl amide compounds which inhibit leukocyte adhesion mediated by vla-4 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101273034A CN101273034A (zh) | 2008-09-24 |
| CN101273034B true CN101273034B (zh) | 2011-07-27 |
Family
ID=37592431
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2006800356541A Expired - Fee Related CN101273034B (zh) | 2005-09-29 | 2006-09-28 | 抑制由vla-4介导的白细胞粘附的嘧啶基酰胺化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7511052B2 (enExample) |
| EP (1) | EP1940826B1 (enExample) |
| JP (1) | JP5101512B2 (enExample) |
| KR (1) | KR20080059268A (enExample) |
| CN (1) | CN101273034B (enExample) |
| AT (1) | ATE493405T1 (enExample) |
| AU (1) | AU2006297220B8 (enExample) |
| BR (1) | BRPI0616687A2 (enExample) |
| CA (1) | CA2624450C (enExample) |
| DE (1) | DE602006019296D1 (enExample) |
| DK (1) | DK1940826T3 (enExample) |
| EA (1) | EA015388B1 (enExample) |
| IL (1) | IL190084A (enExample) |
| NO (1) | NO20082002L (enExample) |
| NZ (1) | NZ567270A (enExample) |
| WO (1) | WO2007041270A1 (enExample) |
| ZA (2) | ZA200803280B (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE455106T1 (de) * | 1999-01-22 | 2010-01-15 | Elan Pharm Inc | Acyl derivate zur behandlung von krankheiten die in zusammenhang mit vla-4 stehen |
| AU2006297180A1 (en) * | 2005-09-29 | 2007-04-12 | Elan Pharmaceuticals, Inc. | Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| WO2007041270A1 (en) * | 2005-09-29 | 2007-04-12 | Elan Pharmaceuticals, Inc. | Pyrimidinyl amide compounds which inhibit leukocyte adhesion mediated by vla-4 |
| EP1996559A1 (en) | 2006-02-27 | 2008-12-03 | Elan Pharmaceuticals Inc. | Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4 |
| WO2007100763A2 (en) * | 2006-02-28 | 2007-09-07 | Elan Pharmaceuticals, Inc. | Methods of treating inflammatory and autoimmune diseases with alpha-4 inhibitory compounds |
| HUE047230T2 (hu) * | 2006-02-28 | 2020-04-28 | Biogen Ma Inc | Gyulladásos és autoimmun betegségek natalizumabbal való kezelésének módszerei |
| EP4582099A3 (en) * | 2006-03-03 | 2025-10-01 | Biogen MA Inc. | Methods of treating inflammatory and autoimmune diseases with natalizumab |
| CA2708262A1 (en) | 2007-12-07 | 2009-06-18 | Elan Pharmaceuticals, Inc. | Methods and compositions for treating liquid tumors |
| CA2760151A1 (en) * | 2009-04-27 | 2010-11-04 | Elan Pharmaceuticals, Inc. | Pyridinone antagonists of alpha-4 integrins |
| WO2011020874A1 (en) | 2009-08-20 | 2011-02-24 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Vla-4 as a biomarker for prognosis and target for therapy in duchenne muscular dystrophy |
| US11287423B2 (en) | 2010-01-11 | 2022-03-29 | Biogen Ma Inc. | Assay for JC virus antibodies |
| EP4152004B9 (en) | 2010-01-11 | 2025-04-09 | Biogen MA Inc. | Assay for jc virus antibodies |
| EP3243526B1 (en) | 2010-07-06 | 2019-11-27 | GlaxoSmithKline Biologicals S.A. | Delivery of rna to trigger multiple immune pathways |
| PT2591114T (pt) | 2010-07-06 | 2016-08-02 | Glaxosmithkline Biologicals Sa | Imunização de mamíferos de grande porte com doses baixas de arn |
| EP2590626B1 (en) | 2010-07-06 | 2015-10-28 | GlaxoSmithKline Biologicals SA | Liposomes with lipids having an advantageous pka-value for rna delivery |
| PL4066857T3 (pl) | 2010-08-31 | 2023-03-20 | Glaxosmithkline Biologicals Sa | Pegylowane liposomy do dostarczania rna kodującego immunogen |
| CA2814386C (en) | 2010-10-11 | 2019-08-20 | Novartis Ag | Antigen delivery platforms |
| LT3575792T (lt) | 2011-05-31 | 2023-03-10 | Biogen Ma Inc. | Pdl rizikos vertinimo būdas |
| CA2840989A1 (en) | 2011-07-06 | 2013-01-10 | Novartis Ag | Immunogenic combination compositions and uses thereof |
| WO2014193804A1 (en) | 2013-05-28 | 2014-12-04 | Biogen Idec Ma Inc. | Method of assessing risk of pml |
| US20240301512A1 (en) | 2021-01-29 | 2024-09-12 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods of assessing the risk of developing progressive multifocal leukoencephalopathy in patients treated with vla-4 antagonists |
| CN118871130A (zh) * | 2022-03-11 | 2024-10-29 | 国立大学法人大阪大学 | 包含vla-4阻断物质的用于预防或治疗心肌炎的组合物 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000043372A1 (en) * | 1999-01-22 | 2000-07-27 | Elan Pharmaceuticals, Inc. | Acyl derivatives which treat vla-4 related disorders |
| WO2003099809A1 (en) * | 2002-05-24 | 2003-12-04 | Elan Pharmaceuticals, Inc. | HETEROCYCLIC COMPOUNDS WHICH INHIBIT LEUKOCYTE ADHESION MEDIATED BY α4 INTEGRINS |
| WO2005000246A2 (en) * | 2003-06-25 | 2005-01-06 | Elan Pharmaceuticals, Inc. | Methods and compositions for treating rheumatoid arthritis |
| CN1652789A (zh) * | 2002-05-24 | 2005-08-10 | 伊兰制药公司 | 抑制由α4整合素介导的白细胞粘附的杂芳基化合物 |
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| DE2525656A1 (de) | 1974-06-19 | 1976-01-15 | Sandoz Ag | Verfahren zur herstellung neuer heterocyclischer verbindungen |
| US4096255A (en) | 1974-11-08 | 1978-06-20 | Mitsubishi Chemical Industries Limited | N2 -naphthalenesulfonyl-L-argininamides, and pharmaceutical salts, compositions and methods |
| US4055651A (en) | 1974-11-08 | 1977-10-25 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4055636A (en) | 1974-11-08 | 1977-10-25 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
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| US4046876A (en) | 1974-11-08 | 1977-09-06 | Mitsubishi Chemical Industries Limited | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4018915A (en) | 1976-01-05 | 1977-04-19 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4041156A (en) | 1974-11-08 | 1977-08-09 | Mitsubishi Chemical Industries Limited | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4073914A (en) | 1974-11-08 | 1978-02-14 | Mitsubishi Chemical Industries Limited | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4104392A (en) | 1974-11-08 | 1978-08-01 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof, and antithrombotic compositions and methods employing them |
| JPS5727454B2 (enExample) | 1975-02-21 | 1982-06-10 | ||
| CA1102316A (en) | 1975-12-09 | 1981-06-02 | Shosuke Okamoto | N su2 xx-arylsulfonyl-l-argininamides and the pharmaceutically acceptable salts thereof |
| US4018913A (en) | 1976-01-14 | 1977-04-19 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4036955A (en) | 1976-07-22 | 1977-07-19 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4070914A (en) * | 1976-09-17 | 1978-01-31 | Jack Reinhardt | Hydraulic clutch-controlled transmission gear detent system |
| DE2742173A1 (de) | 1977-09-20 | 1979-03-29 | Bayer Ag | Phenoxy-pyridinyl(pyrimidinyl)-alkanole, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
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- 2006-09-28 DK DK06804253.0T patent/DK1940826T3/da active
- 2006-09-28 EP EP06804253A patent/EP1940826B1/en active Active
- 2006-09-28 JP JP2008533649A patent/JP5101512B2/ja not_active Expired - Fee Related
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- 2006-09-28 AU AU2006297220A patent/AU2006297220B8/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| EA200800975A1 (ru) | 2008-08-29 |
| ZA200906610B (en) | 2011-05-25 |
| BRPI0616687A2 (pt) | 2011-06-28 |
| US7763632B2 (en) | 2010-07-27 |
| US20090192181A1 (en) | 2009-07-30 |
| DE602006019296D1 (de) | 2011-02-10 |
| AU2006297220A1 (en) | 2007-04-12 |
| US20070142416A1 (en) | 2007-06-21 |
| JP5101512B2 (ja) | 2012-12-19 |
| AU2006297220B8 (en) | 2013-01-31 |
| NO20082002L (no) | 2008-06-03 |
| DK1940826T3 (da) | 2011-04-18 |
| ATE493405T1 (de) | 2011-01-15 |
| KR20080059268A (ko) | 2008-06-26 |
| IL190084A (en) | 2013-05-30 |
| NZ567270A (en) | 2011-06-30 |
| IL190084A0 (en) | 2008-08-07 |
| US7511052B2 (en) | 2009-03-31 |
| AU2006297220B2 (en) | 2012-04-26 |
| JP2009510097A (ja) | 2009-03-12 |
| EP1940826B1 (en) | 2010-12-29 |
| CN101273034A (zh) | 2008-09-24 |
| WO2007041270A1 (en) | 2007-04-12 |
| CA2624450A1 (en) | 2007-04-12 |
| EA015388B1 (ru) | 2011-08-30 |
| ZA200803280B (en) | 2009-11-25 |
| CA2624450C (en) | 2014-02-04 |
| AU2006297220C1 (en) | 2012-11-29 |
| EP1940826A1 (en) | 2008-07-09 |
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