ZA200803016B - Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4 - Google Patents
Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4Info
- Publication number
- ZA200803016B ZA200803016B ZA200803016A ZA200803016A ZA200803016B ZA 200803016 B ZA200803016 B ZA 200803016B ZA 200803016 A ZA200803016 A ZA 200803016A ZA 200803016 A ZA200803016 A ZA 200803016A ZA 200803016 B ZA200803016 B ZA 200803016B
- Authority
- ZA
- South Africa
- Prior art keywords
- compounds
- vla
- leukocyte adhesion
- adhesion mediated
- inhibit leukocyte
- Prior art date
Links
Classifications
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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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- 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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- C—CHEMISTRY; METALLURGY
- 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
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- 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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- C—CHEMISTRY; METALLURGY
- 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
-
- 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
- C07D409/02—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
- 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
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72235505P | 2005-09-29 | 2005-09-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200803016B true ZA200803016B (en) | 2009-10-28 |
Family
ID=37591849
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200803016A ZA200803016B (en) | 2005-09-29 | 2006-09-28 | Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4 |
Country Status (11)
Country | Link |
---|---|
US (3) | US7727996B2 (xx) |
EP (1) | EP1940827B1 (xx) |
JP (2) | JP5081828B2 (xx) |
CN (1) | CN101273035A (xx) |
AT (1) | ATE502031T1 (xx) |
AU (1) | AU2006297180A1 (xx) |
BR (1) | BRPI0616643A2 (xx) |
CA (2) | CA2851103A1 (xx) |
DE (1) | DE602006020754D1 (xx) |
WO (1) | WO2007041324A1 (xx) |
ZA (1) | ZA200803016B (xx) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002535314A (ja) * | 1999-01-22 | 2002-10-22 | エラン ファーマシューティカルズ,インコーポレイテッド | Vla−4により媒介される白血球接着を阻害する化合物 |
CN101273035A (zh) * | 2005-09-29 | 2008-09-24 | 伊兰制药公司 | 抑制由vla-4介导的白细胞粘附的氨基甲酸酯化合物 |
NZ567270A (en) * | 2005-09-29 | 2011-06-30 | Elan Pharm Inc | Pyrimidinyl amide compounds which inhibit leukocyte adhesion mediated by VLA-4 |
EA017110B1 (ru) * | 2006-02-27 | 2012-09-28 | Элан Фамэсьютикэлс, Инк. | ПИРИМИДИНИЛСУЛЬФОНАМИДНЫЕ СОЕДИНЕНИЯ (ВАРИАНТЫ), СПОСОБ ПОЛУЧЕНИЯ ПИРИМИДИНИЛСУЛЬФОНАМИДНЫХ СОЕДИНЕНИЙ (ВАРИАНТЫ), ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЯ, ОПОСРЕДОВАННОГО ИНТЕГРИНОМ α4, СПОСОБ СНИЖЕНИЯ И/ИЛИ ПРЕДУПРЕЖДЕНИЯ ВОСПАЛИТЕЛЬНОГО КОМПОНЕНТА ЗАБОЛЕВАНИЯ ИЛИ АУТОИММУННОГО ОТВЕТА |
MX2011011326A (es) * | 2009-04-27 | 2012-02-13 | Elan Pharm Inc | Antagonistas de piridinona de las integrinas alfa-4. |
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 |
US20190077868A1 (en) * | 2016-03-14 | 2019-03-14 | Millennium Pharmaceuticals, Inc. | Methods of treating or preventing graft versus host disease |
CN111417634A (zh) * | 2017-10-04 | 2020-07-14 | 细胞基因公司 | 用于制备顺式-4-[2-{[(3s,4r)-3-氟噁烷-4-基]氨基}-8-(2,4,6-三氯苯胺基)-9h-嘌呤-9-基]-1-甲基环己烷-1-甲酰胺的方法 |
AU2020334194A1 (en) * | 2019-08-16 | 2022-02-24 | Volker Adams | Compounds suitable for the treatment and prophylaxis of muscle wasting and other conditions |
EP4284947A1 (en) | 2021-01-29 | 2023-12-06 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods of assessing the risk of developing progressive multifocal leukoencephalopathy in patients treated with vla-4 antagonists |
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US408A (en) * | 1837-09-25 | Machine for | ||
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US4041156A (en) | 1974-11-08 | 1977-08-09 | Mitsubishi Chemical Industries Limited | 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 |
US4070457A (en) | 1974-11-08 | 1978-01-24 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
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 |
US4096255A (en) | 1974-11-08 | 1978-06-20 | Mitsubishi Chemical Industries Limited | N2 -naphthalenesulfonyl-L-argininamides, and pharmaceutical salts, compositions and methods |
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-
2006
- 2006-09-28 CN CNA200680035707XA patent/CN101273035A/zh active Pending
- 2006-09-28 AU AU2006297180A patent/AU2006297180A1/en not_active Abandoned
- 2006-09-28 CA CA2851103A patent/CA2851103A1/en not_active Abandoned
- 2006-09-28 ZA ZA200803016A patent/ZA200803016B/xx unknown
- 2006-09-28 DE DE602006020754T patent/DE602006020754D1/de active Active
- 2006-09-28 AT AT06804266T patent/ATE502031T1/de not_active IP Right Cessation
- 2006-09-28 US US11/541,205 patent/US7727996B2/en not_active Expired - Fee Related
- 2006-09-28 EP EP06804266A patent/EP1940827B1/en active Active
- 2006-09-28 WO PCT/US2006/038113 patent/WO2007041324A1/en active Application Filing
- 2006-09-28 BR BRPI0616643-1A patent/BRPI0616643A2/pt not_active IP Right Cessation
- 2006-09-28 CA CA2624524A patent/CA2624524C/en not_active Expired - Fee Related
- 2006-09-28 JP JP2008533682A patent/JP5081828B2/ja not_active Expired - Fee Related
-
2009
- 2009-10-15 US US12/579,828 patent/US8158642B2/en not_active Expired - Fee Related
-
2010
- 2010-04-13 US US12/759,419 patent/US8367688B2/en not_active Expired - Fee Related
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2012
- 2012-07-19 JP JP2012160870A patent/JP2012197319A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
CA2624524A1 (en) | 2007-04-12 |
JP2012197319A (ja) | 2012-10-18 |
US7727996B2 (en) | 2010-06-01 |
JP2009510103A (ja) | 2009-03-12 |
CA2851103A1 (en) | 2007-04-12 |
BRPI0616643A2 (pt) | 2011-06-28 |
CN101273035A (zh) | 2008-09-24 |
AU2006297180A1 (en) | 2007-04-12 |
WO2007041324A1 (en) | 2007-04-12 |
EP1940827A1 (en) | 2008-07-09 |
DE602006020754D1 (de) | 2011-04-28 |
US20100261715A1 (en) | 2010-10-14 |
US20100113434A1 (en) | 2010-05-06 |
CA2624524C (en) | 2014-07-08 |
US20070129390A1 (en) | 2007-06-07 |
EP1940827B1 (en) | 2011-03-16 |
ATE502031T1 (de) | 2011-04-15 |
US8158642B2 (en) | 2012-04-17 |
JP5081828B2 (ja) | 2012-11-28 |
US8367688B2 (en) | 2013-02-05 |
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