MA28170A1 - Nouveaux derives de ceto-oxadiazole comme inhibiteurs de la cathepsine - Google Patents
Nouveaux derives de ceto-oxadiazole comme inhibiteurs de la cathepsineInfo
- Publication number
- MA28170A1 MA28170A1 MA29048A MA29048A MA28170A1 MA 28170 A1 MA28170 A1 MA 28170A1 MA 29048 A MA29048 A MA 29048A MA 29048 A MA29048 A MA 29048A MA 28170 A1 MA28170 A1 MA 28170A1
- Authority
- MA
- Morocco
- Prior art keywords
- novel
- ceto
- oxadiazole derivatives
- cathepsin inhibitors
- inhibitors
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
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- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/10—Seven-membered rings having the hetero atoms in positions 1 and 4 not condensed with other rings
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- C—CHEMISTRY; METALLURGY
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- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
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- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/107—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with two aryl or substituted aryl radicals attached in positions 2 and 5
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- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/195—Radicals derived from nitrogen analogues of carboxylic acids
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen 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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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Urology & Nephrology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Obesity (AREA)
Abstract
Nouveaux inhibiteurs des cathepsines S, K, B, et L, sels pharmaceutiquement acceptables et N-oxvdes de ceux-ci, leurs utilisations comme agents thérapeutiques et méthodes pour leur production.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51437303P | 2003-10-24 | 2003-10-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA28170A1 true MA28170A1 (fr) | 2006-09-01 |
Family
ID=34520197
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA29048A MA28170A1 (fr) | 2003-10-24 | 2006-05-23 | Nouveaux derives de ceto-oxadiazole comme inhibiteurs de la cathepsine |
Country Status (19)
Country | Link |
---|---|
US (1) | US7482448B2 (fr) |
EP (1) | EP1682524A1 (fr) |
JP (1) | JP4769192B2 (fr) |
KR (1) | KR20070008517A (fr) |
CN (1) | CN100543017C (fr) |
AU (1) | AU2004284089B2 (fr) |
BR (1) | BRPI0415826A (fr) |
CA (1) | CA2547591C (fr) |
HK (1) | HK1101871A1 (fr) |
IL (1) | IL175106A0 (fr) |
MA (1) | MA28170A1 (fr) |
ME (1) | MEP39608A (fr) |
MX (1) | MXPA06004422A (fr) |
NO (1) | NO20062150L (fr) |
NZ (1) | NZ546504A (fr) |
RS (1) | RS20060280A (fr) |
RU (1) | RU2346943C2 (fr) |
WO (1) | WO2005040142A1 (fr) |
ZA (1) | ZA200603183B (fr) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5154944B2 (ja) | 2004-12-02 | 2013-02-27 | ビロベイ,インコーポレイティド | システインプロテアーゼインヒビターとしてのスルホンアミド含有化合物 |
EA017874B1 (ru) | 2005-03-21 | 2013-03-29 | Вайробей, Инк. | Производные альфа-кетоамидов в качестве ингибиторов цистеинпротеаз |
JP5215167B2 (ja) | 2005-03-22 | 2013-06-19 | ビロベイ,インコーポレイティド | システインプロテアーゼ阻害剤としてのスルホニル基含有化合物 |
UA100669C2 (ru) | 2006-06-01 | 2013-01-25 | Санофі-Авентіс | Спироциклические нитрилы как ингибиторы протеазы, способ их получения (варианты) и лекарственное средство на их основе |
NZ576105A (en) * | 2006-10-04 | 2012-01-12 | Virobay Inc | Di-fluoro containing compounds as cysteine protease inhibitors |
US7893112B2 (en) | 2006-10-04 | 2011-02-22 | Virobay, Inc. | Di-fluoro containing compounds as cysteine protease inhibitors |
JP2010519320A (ja) * | 2007-02-28 | 2010-06-03 | サノフィ−アベンティス | イメージングプローブ |
JP5497732B2 (ja) * | 2008-04-01 | 2014-05-21 | ビロベイ,インコーポレイティド | システインプロテアーゼ阻害剤としてのジフルオロ含有化合物 |
US7741327B2 (en) | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
WO2010070615A1 (fr) * | 2008-12-19 | 2010-06-24 | Medivir Uk Ltd | Inhibiteurs de cystéine protéase |
US7893099B2 (en) * | 2009-06-11 | 2011-02-22 | Hoffman-La Roche Inc. | Cyclopentane derivatives |
US20110021570A1 (en) | 2009-07-23 | 2011-01-27 | Nancy-Ellen Haynes | Pyridone glucokinase activators |
US8324417B2 (en) * | 2009-08-19 | 2012-12-04 | Virobay, Inc. | Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof |
WO2011069149A2 (fr) | 2009-12-04 | 2011-06-09 | Dcb-Usa Llc | Inhibiteurs de la cathépsine s |
US8500766B2 (en) * | 2009-12-18 | 2013-08-06 | Colgate-Palmolive Company | Oral care implement multiple soft tissue cleaner components |
US8178689B2 (en) | 2010-06-17 | 2012-05-15 | Hoffman-La Roche Inc. | Tricyclic compounds |
NZ704666A (en) * | 2012-08-23 | 2018-05-25 | Alios Biopharma Inc | Compounds for the treatment of paramoxyvirus viral infections |
US20220193048A1 (en) | 2019-04-05 | 2022-06-23 | Universite De Bretagne Occidentale | Protease-activated receptor-2 inhibitors for the treatment of sensory neuropathy induced by a marine neurotoxic poisoning |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2381023A1 (fr) * | 1977-02-18 | 1978-09-15 | Delalande Sa | Nouveaux oligopeptides trifluoromethyles derives de la l-alanine, leur procede de preparation et leur application en therapeutique |
FR2605009B1 (fr) * | 1986-06-13 | 1989-06-09 | Ayi Ayicoue | Nouveaux peptides contenant un acide a-amine b-monofluore ou b,b-difluore dans leur structure dont des enkephalines et derives d'enkephalines |
WO1990009162A2 (fr) * | 1989-01-31 | 1990-08-23 | Abbott Laboratories | Ligands de recepteurs d'anaphylatoxines |
US5223485A (en) | 1989-01-31 | 1993-06-29 | Abbott Laboratories | Anaphylatoxin-receptor ligands |
JPH0449298A (ja) | 1990-06-19 | 1992-02-18 | Univ New York State | 新規なエンケファリン誘導体および鎮痛剤 |
JP3605158B2 (ja) * | 1994-12-09 | 2004-12-22 | 塩野義製薬株式会社 | Hivプロテアーゼ阻害剤 |
US6403587B1 (en) * | 1997-02-26 | 2002-06-11 | Pfizer Inc. | Heteroaryl-hexanoic acid amide derivatives, their preparation and their use as selective inhibitors of MIP-1-α binding to its CCR 1 receptor |
ID20812A (id) * | 1997-07-09 | 1999-03-11 | Takeda Chemical Industries Ltd | Senyawa polyol, produk dan penggunaannya |
CN1297354A (zh) * | 1998-03-16 | 2001-05-30 | 西托维亚公司 | 二肽卡斯帕酶抑制剂及其用途 |
GB9812523D0 (en) | 1998-06-10 | 1998-08-05 | Angeletti P Ist Richerche Bio | Peptide inhibitors of hepatitis c virus ns3 protease |
TW200404789A (en) | 1999-03-15 | 2004-04-01 | Axys Pharm Inc | Novel compounds and compositions as protease inhibitors |
EP1178958B1 (fr) * | 1999-03-15 | 2004-02-18 | Axys Pharmaceuticals, Inc. | N-cyanomethyl amides utilises en qualite d'inhibiteurs de proteases |
US7012075B2 (en) | 2001-03-02 | 2006-03-14 | Merck & Co., Inc. | Cathepsin cysteine protease inhibitors |
GB0107924D0 (en) | 2001-03-29 | 2001-05-23 | Angeletti P Ist Richerche Bio | Inhibitor of hepatitis C virus NS3 protease |
KR20040015725A (ko) | 2001-06-01 | 2004-02-19 | 액시스 파마슈티컬스 인코포레이티드 | 카텝신 s 억제제로서의 화합물 및 약제학적 조성물 |
US6982263B2 (en) | 2001-06-08 | 2006-01-03 | Boehringer Ingelheim Pharmaceuticals, Inc. | Nitriles useful as reversible inhibitors of cysteine proteases |
CA2477657C (fr) * | 2002-03-05 | 2011-04-26 | Merck Frosst Canada & Co./Merck Frosst Canada & Cie | Inhibiteurs de cathepsine cysteine protease |
WO2003087069A2 (fr) * | 2002-04-09 | 2003-10-23 | Eli Lilly And Company | Secretagogues d'hormone de croissance |
WO2003097617A1 (fr) * | 2002-05-14 | 2003-11-27 | Axys Pharmaceuticals, Inc. | Inhibiteurs de la cysteine protease |
-
2004
- 2004-10-22 WO PCT/US2004/035282 patent/WO2005040142A1/fr active Application Filing
- 2004-10-22 BR BRPI0415826-1A patent/BRPI0415826A/pt not_active Application Discontinuation
- 2004-10-22 JP JP2006536882A patent/JP4769192B2/ja not_active Expired - Fee Related
- 2004-10-22 RU RU2006117788/04A patent/RU2346943C2/ru not_active IP Right Cessation
- 2004-10-22 ME MEP-396/08A patent/MEP39608A/xx unknown
- 2004-10-22 CA CA2547591A patent/CA2547591C/fr not_active Expired - Fee Related
- 2004-10-22 AU AU2004284089A patent/AU2004284089B2/en not_active Ceased
- 2004-10-22 RS YUP-2006/0280A patent/RS20060280A/sr unknown
- 2004-10-22 MX MXPA06004422A patent/MXPA06004422A/es active IP Right Grant
- 2004-10-22 KR KR1020067008096A patent/KR20070008517A/ko not_active IP Right Cessation
- 2004-10-22 CN CNB2004800389122A patent/CN100543017C/zh not_active Expired - Fee Related
- 2004-10-22 NZ NZ546504A patent/NZ546504A/en not_active IP Right Cessation
- 2004-10-22 EP EP04796294A patent/EP1682524A1/fr not_active Withdrawn
-
2006
- 2006-04-20 ZA ZA200603183A patent/ZA200603183B/en unknown
- 2006-04-23 IL IL175106A patent/IL175106A0/en unknown
- 2006-04-24 US US11/409,601 patent/US7482448B2/en not_active Expired - Fee Related
- 2006-05-12 NO NO20062150A patent/NO20062150L/no unknown
- 2006-05-23 MA MA29048A patent/MA28170A1/fr unknown
-
2007
- 2007-06-25 HK HK07106732.3A patent/HK1101871A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2547591C (fr) | 2010-08-17 |
WO2005040142B1 (fr) | 2005-07-14 |
CN100543017C (zh) | 2009-09-23 |
RS20060280A (en) | 2008-08-07 |
AU2004284089A1 (en) | 2005-05-06 |
RU2346943C2 (ru) | 2009-02-20 |
RU2006117788A (ru) | 2007-11-27 |
KR20070008517A (ko) | 2007-01-17 |
WO2005040142A9 (fr) | 2005-06-09 |
JP2007509175A (ja) | 2007-04-12 |
EP1682524A1 (fr) | 2006-07-26 |
IL175106A0 (en) | 2006-09-05 |
NO20062150L (no) | 2006-05-12 |
US20060189657A1 (en) | 2006-08-24 |
ZA200603183B (en) | 2007-09-26 |
CN1898219A (zh) | 2007-01-17 |
AU2004284089B2 (en) | 2009-11-26 |
MXPA06004422A (es) | 2006-07-03 |
BRPI0415826A (pt) | 2007-01-02 |
HK1101871A1 (en) | 2007-10-26 |
MEP39608A (en) | 2011-02-10 |
JP4769192B2 (ja) | 2011-09-07 |
WO2005040142A1 (fr) | 2005-05-06 |
CA2547591A1 (fr) | 2005-05-06 |
NZ546504A (en) | 2009-01-31 |
US7482448B2 (en) | 2009-01-27 |
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