ZA200303357B - LFA-1 antagonist compounds. - Google Patents
LFA-1 antagonist compounds. Download PDFInfo
- Publication number
- ZA200303357B ZA200303357B ZA200303357A ZA200303357A ZA200303357B ZA 200303357 B ZA200303357 B ZA 200303357B ZA 200303357 A ZA200303357 A ZA 200303357A ZA 200303357 A ZA200303357 A ZA 200303357A ZA 200303357 B ZA200303357 B ZA 200303357B
- Authority
- ZA
- South Africa
- Prior art keywords
- compound according
- optionally substituted
- hydroxyl
- amino
- halogen
- Prior art date
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Classifications
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- 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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- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
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- C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D277/06—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Furan Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
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| US25368200P | 2000-11-28 | 2000-11-28 |
Publications (1)
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| ZA200303357B true ZA200303357B (en) | 2004-04-30 |
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| JP (1) | JP2004517928A (de) |
| KR (1) | KR20030051882A (de) |
| CN (1) | CN1592746A (de) |
| AU (1) | AU2002248142B2 (de) |
| CA (1) | CA2429353A1 (de) |
| CZ (1) | CZ20031380A3 (de) |
| HU (1) | HUP0402305A2 (de) |
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| RU (1) | RU2003114422A (de) |
| WO (1) | WO2002059114A1 (de) |
| ZA (1) | ZA200303357B (de) |
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| CZ20031380A3 (cs) * | 2000-11-28 | 2003-10-15 | Genentech, Inc. | LFA-1 Antagonistické sloučeniny |
| WO2004032861A2 (en) | 2002-10-11 | 2004-04-22 | Bristol-Myers Squibb Company | Hexahydro-benzimidazolone compounds useful as anti-inflammatory agents |
| TWI311557B (en) | 2003-01-23 | 2009-07-01 | Novartis A | Pharmaceutically active diazepanes |
| CA2544678C (en) | 2003-11-05 | 2013-12-31 | Sunesis Pharmaceuticals, Inc. | Modulators of cellular adhesion |
| WO2005113003A2 (en) * | 2004-04-16 | 2005-12-01 | Genentech, Inc. | Method for augmenting b cell depletion |
| WO2006023491A2 (en) | 2004-08-16 | 2006-03-02 | The Cbr Institute For Biomedical Research, Inc. | Method of delivering rna interference and uses thereof |
| WO2006029385A2 (en) * | 2004-09-08 | 2006-03-16 | Chelsea Therapeutics, Inc. | Quinazoline derivatives as metabolically inert antifolate compounds. |
| TW200616634A (en) | 2004-10-01 | 2006-06-01 | Bristol Myers Squibb Co | Crystalline forms and process for preparing spiro-hydantoin compounds |
| US7186727B2 (en) | 2004-12-14 | 2007-03-06 | Bristol-Myers Squibb Company | Pyridyl-substituted spiro-hydantoin compounds and use thereof |
| DK1881823T3 (en) | 2005-05-17 | 2015-03-02 | Sarcode Bioscience Inc | COMPOSITION AND PROCEDURES FOR TREATMENT OF EYE DISORDERS |
| WO2007127272A2 (en) * | 2006-04-24 | 2007-11-08 | The Cbr Institute For Biomedical Research | Method of producing immunoliposomes and compositions thereof |
| WO2007127219A2 (en) * | 2006-04-25 | 2007-11-08 | Immune Disease Institute, Inc. | Targeted delivery to leukocytes using protein carriers |
| CN101652366A (zh) * | 2007-01-19 | 2010-02-17 | 切尔西治疗公司 | 新型抗叶酸剂 |
| MX2010004281A (es) * | 2007-10-19 | 2010-09-10 | Sarcode Corp | Composiciones y metodos para el tratamiento de la retinopatia diabetica. |
| AU2009233829A1 (en) * | 2008-04-07 | 2009-10-15 | Chelsea Therapeutics, Inc. | Crystalline salt forms of antifolate compounds and methods of manufacturing thereof |
| WO2009139817A2 (en) | 2008-04-15 | 2009-11-19 | Sarcode Corporation | Crystalline pharmaceutical and methods of preparation and use thereof |
| JP2011521896A (ja) | 2008-04-15 | 2011-07-28 | サーコード コーポレイション | 免疫関連障害に対する局部治療に使用するための局所ｌｆａ−１アンタゴニスト |
| CN105943534A (zh) * | 2008-04-15 | 2016-09-21 | 萨可德生物科学公司 | 用于局部治疗免疫相关疾病的局部lfa-1拮抗剂 |
| EP2276508A4 (de) * | 2008-04-15 | 2011-12-28 | Sarcode Bioscience Inc | Freisetzung von lfa-1-antagonisten gegen das magen-darm-system |
| EP2265124A4 (de) * | 2008-04-15 | 2011-12-28 | Sarcode Bioscience Inc | Aerosolisierte lfa-1-antagonisten zur verwendung bei der lokalen behandlung von immunerkrankungen |
| JP2012532877A (ja) * | 2009-07-08 | 2012-12-20 | チェルシー・セラピューティクス，インコーポレイテッド | （ｓ）−２−｛４−［２−（２，４−ジアミノ−キナゾリン−６−イル）−エチル］−ベンゾイルアミノ｝−４−メチレン−ペンタン二酸の二カリウム塩の安定な結晶多形 |
| US8378105B2 (en) | 2009-10-21 | 2013-02-19 | Sarcode Bioscience Inc. | Crystalline pharmaceutical and methods of preparation and use thereof |
| JP2013510163A (ja) * | 2009-11-06 | 2013-03-21 | チェルシー・セラピューティクス，インコーポレイテッド | 酵素阻害化合物 |
| WO2012064377A1 (en) * | 2010-03-29 | 2012-05-18 | Chelsea Therapeutics, Inc. | Antifolate compositions |
| WO2012078708A1 (en) | 2010-12-07 | 2012-06-14 | Chelsea Therapeutics, Inc. | Combination comprising methotrexate and an antifolate compound |
| WO2012174392A1 (en) | 2011-06-17 | 2012-12-20 | Cytodyn, Inc. | Methods of treating retroviral infections in felines |
| JP6607780B2 (ja) | 2012-07-25 | 2019-11-20 | サルコード・バイオサイエンス・インコーポレイテッド | Ｌｆａ−１阻害剤およびその多形 |
| CA2944989A1 (en) | 2013-04-08 | 2014-10-16 | Cytodyn Inc. | Felinized antibodies and methods of treating retroviral infections in felines |
| WO2019246455A1 (en) | 2018-06-20 | 2019-12-26 | Progenity, Inc. | Treatment of a disease of the gastrointestinal tract with an integrin inhibitor |
| US20230107927A1 (en) | 2020-02-28 | 2023-04-06 | First Wave Bio, Inc. | Methods of treating iatrogenic autoimmune colitis |
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| IL47062A (en) * | 1975-04-10 | 1979-07-25 | Yeda Res & Dev | Process for diminishing antigenicity of tissues to be usedas transplants by treatment with glutaraldehyde |
| US4665077A (en) | 1979-03-19 | 1987-05-12 | The Upjohn Company | Method for treating rejection of organ or skin grafts with 6-aryl pyrimidine compounds |
| US5424399A (en) * | 1988-06-28 | 1995-06-13 | The Children's Medical Center Corporation | Human CR3α/β heterodimers |
| US5149780A (en) * | 1988-10-03 | 1992-09-22 | The Scripps Research Institute | Peptides and antibodies that inhibit integrin-ligand binding |
| EP0546077A1 (de) * | 1990-08-27 | 1993-06-16 | Chiron Corporation | Cd18-peptid arzneimittel zur behandlung von krankheiten |
| US5288854A (en) * | 1990-11-28 | 1994-02-22 | Center For Blood Research, Inc. | Functional derivatives of ICAM-1 which are substantially capable of binding to LFA-1 but are substantially incapable of binding to MAC-1 |
| US5472973A (en) * | 1991-12-12 | 1995-12-05 | Scios Nova Inc. | Fluorenyl derivatives as anti-inflammatory agents |
| US5470953A (en) * | 1993-12-23 | 1995-11-28 | Icos Corporation | Human β2 integrin α subunit |
| DE69634822T2 (de) | 1995-08-22 | 2006-04-27 | Japan Tobacco Inc. | Amid-verbindungen und ihre anwendung |
| JP2000516596A (ja) * | 1996-07-25 | 2000-12-12 | バイオジェン，インコーポレイテッド | 細胞接着インヒビター |
| UA74531C2 (en) | 1998-03-27 | 2006-01-16 | Genentech Inc | Antagonsists for treating disorders mediated by cd11/cd18 adhesion receptors |
| US6331640B1 (en) * | 1998-10-13 | 2001-12-18 | Hoffmann-La Roche Inc. | Diaminopropionic acid derivatives |
| US6110922A (en) * | 1998-12-29 | 2000-08-29 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory and immune-suppressive compounds |
| CZ20031380A3 (cs) * | 2000-11-28 | 2003-10-15 | Genentech, Inc. | LFA-1 Antagonistické sloučeniny |
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2001
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- 2001-11-26 NZ NZ525573A patent/NZ525573A/en unknown
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- 2001-11-26 EP EP01997016A patent/EP1347968A1/de not_active Withdrawn
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2003
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2005
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Also Published As
| Publication number | Publication date |
|---|---|
| EP1347968A1 (de) | 2003-10-01 |
| US20020119994A1 (en) | 2002-08-29 |
| WO2002059114A1 (en) | 2002-08-01 |
| NO20032382L (no) | 2003-07-09 |
| HUP0402305A2 (hu) | 2005-02-28 |
| KR20030051882A (ko) | 2003-06-25 |
| RU2003114422A (ru) | 2004-11-20 |
| WO2002059114A9 (en) | 2002-10-17 |
| US6872735B2 (en) | 2005-03-29 |
| US20040058968A1 (en) | 2004-03-25 |
| US20050148588A1 (en) | 2005-07-07 |
| AU2002248142B2 (en) | 2007-11-01 |
| AU2002248142B8 (en) | 2002-08-06 |
| CA2429353A1 (en) | 2002-08-01 |
| CZ20031380A3 (cs) | 2003-10-15 |
| PL363962A1 (en) | 2004-11-29 |
| IL155683A0 (en) | 2003-11-23 |
| NO20032382D0 (no) | 2003-05-27 |
| CN1592746A (zh) | 2005-03-09 |
| JP2004517928A (ja) | 2004-06-17 |
| MXPA03004527A (es) | 2003-09-10 |
| US6667318B2 (en) | 2003-12-23 |
| NZ525573A (en) | 2005-08-26 |
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