BR9811594A - Sulphonylated dipeptide compounds that inhibit vla-4 mediated leukocyte adhesion - Google Patents
Sulphonylated dipeptide compounds that inhibit vla-4 mediated leukocyte adhesionInfo
- Publication number
- BR9811594A BR9811594A BR9811594-4A BR9811594A BR9811594A BR 9811594 A BR9811594 A BR 9811594A BR 9811594 A BR9811594 A BR 9811594A BR 9811594 A BR9811594 A BR 9811594A
- Authority
- BR
- Brazil
- Prior art keywords
- compounds
- leukocyte adhesion
- vla
- sulphonylated
- mediated leukocyte
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06165—Dipeptides with the first amino acid being heterocyclic and Pro-amino acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
Patente de Invenção:<B>"COMPOSTOS DE DIPEPTìDEO SULFONILADOS QUE INIBEM ADESãO DE LEUCóCITOS MEDIADA POR VLA-4"<D>. Descritos são os compostos que ligam VLA-4. Certos desses compostos também inibem adesão de leucócito e, em particular, adesão de leucócito mediada por VLA-4. Tais compostos são úteis no tratamento de doenças inflamatórias em um paciente mamífero, por exemplo, ser humano, tais como asma, doença de Alzheimer, aterosclerose, demência da AIDS, diabetes, doença de intestino inflamatório, artrite reumatóide, transplante de tecido, metástase de tumor e isquemia miocardial. Os compostos podem também ser administrados para o tratamento de doenças de cérebro inflamatórias tal como esclerose múltipla.Invention Patent: <B> "SULPHONYLATED DIPEPTIDE COMPOUNDS INHIBIT VLA-4 MEDIATED LEUKOCYTE ADHESION" <D>. Described are the compounds that bind VLA-4. Certain of these compounds also inhibit leukocyte adhesion and, in particular, VLA-4 mediated leukocyte adhesion. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, for example, a human being, such as asthma, Alzheimer's disease, atherosclerosis, AIDS dementia, diabetes, inflammatory bowel disease, rheumatoid arthritis, tissue transplantation, metastasis of tumor and myocardial ischemia. The compounds can also be administered for the treatment of inflammatory brain diseases such as multiple sclerosis.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90442397A | 1997-07-31 | 1997-07-31 | |
PCT/US1998/016070 WO1999006437A1 (en) | 1997-07-31 | 1998-07-31 | Sulfonylated dipeptide compounds which inhibit leukocyte adhesion mediated by vla-4 |
Publications (1)
Publication Number | Publication Date |
---|---|
BR9811594A true BR9811594A (en) | 2000-09-05 |
Family
ID=25419137
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR9811594-4A BR9811594A (en) | 1997-07-31 | 1998-07-31 | Sulphonylated dipeptide compounds that inhibit vla-4 mediated leukocyte adhesion |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP0994896A1 (en) |
JP (1) | JP2001512139A (en) |
KR (1) | KR20010022405A (en) |
CN (1) | CN1265672A (en) |
AU (1) | AU8823498A (en) |
BR (1) | BR9811594A (en) |
CA (1) | CA2290748A1 (en) |
HU (1) | HUP0003921A3 (en) |
IL (1) | IL133637A0 (en) |
NO (1) | NO20000452L (en) |
PL (1) | PL338457A1 (en) |
WO (1) | WO1999006437A1 (en) |
Families Citing this family (59)
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US6903075B1 (en) | 1997-05-29 | 2005-06-07 | Merck & Co., Inc. | Heterocyclic amide compounds as cell adhesion inhibitors |
WO1998054207A1 (en) * | 1997-05-30 | 1998-12-03 | Celltech Therapeutics Limited | Anti-inflammatory tyrosine derivatives |
DK0991619T3 (en) | 1997-06-23 | 2003-12-29 | Tanabe Seiyaku Co | Inhibitors of alpha 4-beta 1-mediated cell adhesion |
US6645939B1 (en) | 1997-11-24 | 2003-11-11 | Merck & Co., Inc. | Substituted β-alanine derivatives as cell adhesion inhibitors |
ATE267168T1 (en) * | 1997-11-24 | 2004-06-15 | Merck & Co Inc | BETA-ALANINE DERIVATIVES AS CELL ADHESION INHIBITORS |
US6197794B1 (en) * | 1998-01-08 | 2001-03-06 | Celltech Therapeutics Limited | Phenylalanine derivatives |
MY153569A (en) | 1998-01-20 | 2015-02-27 | Mitsubishi Tanabe Pharma Corp | Inhibitors of ?4 mediated cell adhesion |
US6329372B1 (en) | 1998-01-27 | 2001-12-11 | Celltech Therapeutics Limited | Phenylalanine derivatives |
EP1056714B1 (en) | 1998-02-26 | 2004-08-11 | Celltech Therapeutics Limited | Phenylalanine derivatives as inhibitors of alpha4 integrins |
US6521626B1 (en) | 1998-03-24 | 2003-02-18 | Celltech R&D Limited | Thiocarboxamide derivatives |
GB9811159D0 (en) | 1998-05-22 | 1998-07-22 | Celltech Therapeutics Ltd | Chemical compounds |
GB9811969D0 (en) * | 1998-06-03 | 1998-07-29 | Celltech Therapeutics Ltd | Chemical compounds |
US6685617B1 (en) | 1998-06-23 | 2004-02-03 | Pharmacia & Upjohn Company | Inhibitors of α4β1 mediated cell adhesion |
GB9814414D0 (en) | 1998-07-03 | 1998-09-02 | Celltech Therapeutics Ltd | Chemical compounds |
US6339101B1 (en) * | 1998-08-14 | 2002-01-15 | Gpi Nil Holdings, Inc. | N-linked sulfonamides of N-heterocyclic carboxylic acids or isosteres for vision and memory disorders |
US6333340B1 (en) * | 1998-08-14 | 2001-12-25 | Gpi Nil Holdings, Inc. | Small molecule sulfonamides for vision and memory disorders |
GB9821061D0 (en) | 1998-09-28 | 1998-11-18 | Celltech Therapeutics Ltd | Chemical compounds |
GB9821222D0 (en) | 1998-09-30 | 1998-11-25 | Celltech Therapeutics Ltd | Chemical compounds |
US7396526B1 (en) | 1998-11-12 | 2008-07-08 | Johnson & Johnson Consumer Companies, Inc. | Skin care composition |
GB9825652D0 (en) | 1998-11-23 | 1999-01-13 | Celltech Therapeutics Ltd | Chemical compounds |
GB9826174D0 (en) | 1998-11-30 | 1999-01-20 | Celltech Therapeutics Ltd | Chemical compounds |
WO2000048994A1 (en) * | 1999-02-18 | 2000-08-24 | F. Hoffmann-La Roche Ag | Thioamide derivatives |
US6518283B1 (en) | 1999-05-28 | 2003-02-11 | Celltech R&D Limited | Squaric acid derivatives |
EP1741428A3 (en) * | 1999-08-13 | 2007-05-09 | Biogen Idec MA, Inc. | Cell adhesion inhibitors |
US6534513B1 (en) | 1999-09-29 | 2003-03-18 | Celltech R&D Limited | Phenylalkanoic acid derivatives |
US6455539B2 (en) | 1999-12-23 | 2002-09-24 | Celltech R&D Limited | Squaric acid derivates |
JP2003519697A (en) | 1999-12-28 | 2003-06-24 | ファイザー・プロダクツ・インク | Non-peptide VLA-4-dependent cell binding inhibitors useful for the treatment of inflammatory diseases, autoimmune diseases and respiratory diseases |
WO2001068586A2 (en) * | 2000-03-14 | 2001-09-20 | Novartis Ag | α4β1 AND α4β7 INTEGRIN INHIBITORS |
ATE375330T1 (en) | 2000-04-17 | 2007-10-15 | Ucb Pharma Sa | ENAMINE DERIVATIVES AS CELL ADHESION MOLECULES |
US6545013B2 (en) | 2000-05-30 | 2003-04-08 | Celltech R&D Limited | 2,7-naphthyridine derivatives |
US6403608B1 (en) | 2000-05-30 | 2002-06-11 | Celltech R&D, Ltd. | 3-Substituted isoquinolin-1-yl derivatives |
JP2004502762A (en) | 2000-07-07 | 2004-01-29 | セルテック アール アンド ディ リミテッド | Squaric acid derivatives as integrin antagonists containing bicyclic heteroaromatic rings |
AU2001275724A1 (en) | 2000-08-02 | 2002-02-13 | Celltech R&D Limited | 3-substituted isoquinolin-1-yl derivatives |
ATE497385T1 (en) | 2000-08-18 | 2011-02-15 | Ajinomoto Kk | NEW PHENYLALANINE DERIVATIVES |
MY129000A (en) | 2000-08-31 | 2007-03-30 | Tanabe Seiyaku Co | INHIBITORS OF a4 MEDIATED CELL ADHESION |
US6607735B2 (en) | 2000-12-21 | 2003-08-19 | Johnson & Johnson Consumer Companies, Inc. | Method for reducing the appearance of dark circles under the eyes |
JP2004526733A (en) | 2001-03-20 | 2004-09-02 | メルク エンド カムパニー インコーポレーテッド | Substituted N-arylsulfonyl-proline derivatives as potent cell adhesion inhibitors |
US6559174B2 (en) | 2001-03-20 | 2003-05-06 | Merck & Co., Inc. | N-arylsulfonyl aryl aza-bicyclic derivatives as potent cell adhesion inhibitors |
US6855708B2 (en) | 2001-03-20 | 2005-02-15 | Merck & Co., Inc. | N-arylsulfonyl aza-bicyclic derivatives as potent cell adhesion inhibitors |
EP1477482B1 (en) * | 2002-02-20 | 2010-04-14 | Ajinomoto Co., Inc. | Novel phenylalanine derivative |
EP1592386A4 (en) * | 2003-01-24 | 2007-06-13 | Elan Pharm Inc | Composition for and treatment of demyelinating diseases and paralysis by administration of remyelinating agents |
UY28391A1 (en) * | 2003-06-25 | 2004-12-31 | Elan Pharm Inc | METHODS AND COMPOSITIONS TO TREAT REUMATOID ARTHRITIS |
EP1683525B1 (en) * | 2003-11-14 | 2017-05-17 | EA Pharma Co., Ltd. | Sustained-release phenylalanine derivative preparation for oral administration |
ES2360064T3 (en) * | 2003-11-14 | 2011-05-31 | Ajinomoto Co., Inc. | SOLID DISPERSION OR MEDICINAL SOLID DISPERSION PREPARATION OF A PHENYLALANINE DERIVATIVE. |
EP1968635B1 (en) * | 2005-12-14 | 2014-09-17 | Ambrx, Inc. | Compositions containing, methods involving, and uses of non-natural amino acids and polypeptides |
US20100150915A1 (en) | 2007-02-20 | 2010-06-17 | Stewart Edward J | Methods of treating multiple sclerosis by administration of alpha-fetoprotein in combination with an integrin antagonist |
CA2721093A1 (en) | 2008-04-11 | 2009-10-15 | Merrimack Pharmaceuticals, Inc. | Human serum albumin linkers and conjugates thereof |
JP6007417B2 (en) | 2011-05-31 | 2016-10-12 | レセプトス エルエルシー | Novel GLP-1 receptor stabilizer and modulator |
AU2012352349B2 (en) * | 2011-12-12 | 2017-08-17 | Receptos Llc | Carboxylic acid derivatives comprising four cycles acting as GLP-1 receptor modulators for therapy of diseases such as diabetes |
KR102271179B1 (en) | 2013-06-11 | 2021-07-01 | 셀진 인터내셔널 Ii 에스에이알엘 | Novel glp-1 receptor modulators |
MX2017000972A (en) | 2014-07-25 | 2017-07-27 | Celgene Int Ii Sarl | Novel glp-1 receptor modulators. |
WO2016094729A1 (en) | 2014-12-10 | 2016-06-16 | Celgene International Ii Sarl | Glp-1 receptor modulators |
US10308677B2 (en) * | 2014-12-19 | 2019-06-04 | Cem Corporation | Coupling method for peptide synthesis at elevated temperatures |
US9969769B2 (en) | 2014-12-19 | 2018-05-15 | Cem Corporation | Coupling method for peptide synthesis at elevated temperatures |
JP7189369B2 (en) | 2018-10-30 | 2022-12-13 | ギリアード サイエンシーズ, インコーポレイテッド | Compounds for inhibition of alpha4beta7 integrin |
US11116760B2 (en) | 2018-10-30 | 2021-09-14 | Gilead Sciences, Inc. | Quinoline derivatives |
JP7189368B2 (en) | 2018-10-30 | 2022-12-13 | ギリアード サイエンシーズ, インコーポレイテッド | Compounds for inhibition of alpha4beta7 integrin |
JP7214882B2 (en) | 2018-10-30 | 2023-01-30 | ギリアード サイエンシーズ, インコーポレイテッド | Imidazopyridine derivatives as alpha4beta7 integrin inhibitors |
US11578069B2 (en) | 2019-08-14 | 2023-02-14 | Gilead Sciences, Inc. | Compounds for inhibition of α4 β7 integrin |
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FR2679903B1 (en) * | 1991-08-02 | 1993-12-03 | Elf Sanofi | DERIVATIVES OF N-SULFONYL INDOLINE CARRYING AN AMIDIC FUNCTION, THEIR PREPARATION, THE PHARMACEUTICAL COMPOSITIONS CONTAINING SAME. |
JPH04154732A (en) * | 1990-10-18 | 1992-05-27 | Nippon Kayaku Co Ltd | Optical resolution method |
WO1994007815A2 (en) * | 1992-09-25 | 1994-04-14 | Abbott Laboratories | Small peptide anaphylatoxin receptor ligands |
US5648368A (en) * | 1992-12-01 | 1997-07-15 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
AU693143B2 (en) * | 1993-12-06 | 1998-06-25 | Cytel Corporation | CS-1 peptidomimetics, compositions and methods of using the same |
JPH0873422A (en) * | 1994-09-07 | 1996-03-19 | Kdk Corp | New amino acid ester and method for detecting leukocyte, esterase or protease |
US6306840B1 (en) * | 1995-01-23 | 2001-10-23 | Biogen, Inc. | Cell adhesion inhibitors |
-
1998
- 1998-07-31 KR KR1020007000985A patent/KR20010022405A/en not_active Application Discontinuation
- 1998-07-31 CN CN98807721A patent/CN1265672A/en active Pending
- 1998-07-31 AU AU88234/98A patent/AU8823498A/en not_active Abandoned
- 1998-07-31 WO PCT/US1998/016070 patent/WO1999006437A1/en not_active Application Discontinuation
- 1998-07-31 IL IL13363798A patent/IL133637A0/en unknown
- 1998-07-31 JP JP2000505192A patent/JP2001512139A/en not_active Withdrawn
- 1998-07-31 EP EP98939871A patent/EP0994896A1/en not_active Withdrawn
- 1998-07-31 HU HU0003921A patent/HUP0003921A3/en unknown
- 1998-07-31 BR BR9811594-4A patent/BR9811594A/en not_active IP Right Cessation
- 1998-07-31 CA CA002290748A patent/CA2290748A1/en not_active Abandoned
- 1998-07-31 PL PL98338457A patent/PL338457A1/en not_active Application Discontinuation
-
2000
- 2000-01-28 NO NO20000452A patent/NO20000452L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IL133637A0 (en) | 2001-04-30 |
KR20010022405A (en) | 2001-03-15 |
PL338457A1 (en) | 2000-11-06 |
HUP0003921A2 (en) | 2001-02-28 |
EP0994896A1 (en) | 2000-04-26 |
WO1999006437A1 (en) | 1999-02-11 |
CA2290748A1 (en) | 1999-02-11 |
JP2001512139A (en) | 2001-08-21 |
NO20000452D0 (en) | 2000-01-28 |
AU8823498A (en) | 1999-02-22 |
NO20000452L (en) | 2000-03-27 |
CN1265672A (en) | 2000-09-06 |
HUP0003921A3 (en) | 2001-03-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 5A,6A,7A E 8A ANUIDADES. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 1890 DE 27/03/2007. |