ZA983843B - Protease inhibitors - Google Patents
Protease inhibitorsInfo
- Publication number
- ZA983843B ZA983843B ZA983843A ZA983843A ZA983843B ZA 983843 B ZA983843 B ZA 983843B ZA 983843 A ZA983843 A ZA 983843A ZA 983843 A ZA983843 A ZA 983843A ZA 983843 B ZA983843 B ZA 983843B
- Authority
- ZA
- South Africa
- Prior art keywords
- protease inhibitors
- protease
- inhibitors
- Prior art date
Links
Classifications
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/99—Enzyme inactivation by chemical treatment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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
-
- 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
-
- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Genetics & Genomics (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Wood Science & Technology (AREA)
- Biophysics (AREA)
- Zoology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- General Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4686597P | 1997-05-08 | 1997-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA983843B true ZA983843B (en) | 1998-11-09 |
Family
ID=21945814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA983843A ZA983843B (en) | 1997-05-08 | 1998-05-07 | Protease inhibitors |
Country Status (18)
Country | Link |
---|---|
US (1) | US6369077B1 (fr) |
EP (1) | EP0991753A4 (fr) |
JP (1) | JP2001525809A (fr) |
KR (1) | KR20010012316A (fr) |
CN (1) | CN1255162A (fr) |
AU (1) | AU7288598A (fr) |
BR (1) | BR9808502A (fr) |
CA (1) | CA2289010A1 (fr) |
CO (1) | CO4950617A1 (fr) |
HU (1) | HUP0001285A3 (fr) |
IL (1) | IL131661A0 (fr) |
MA (1) | MA26494A1 (fr) |
NO (1) | NO995433L (fr) |
PE (1) | PE73799A1 (fr) |
PL (1) | PL336625A1 (fr) |
TR (1) | TR199902752T2 (fr) |
WO (1) | WO1998050534A1 (fr) |
ZA (1) | ZA983843B (fr) |
Families Citing this family (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL135488A0 (en) | 1997-11-18 | 2001-05-20 | Teijin Ltd | Cyclic amine derivatives |
CO5150165A1 (es) * | 1998-11-13 | 2002-04-29 | Smithkline Beecham Plc | Inhibidores de proteasa: tipo catepsina k |
CO5180541A1 (es) * | 1998-12-23 | 2002-07-30 | Smithkline Beechman Corp | Inhibidores de proteasa del tipo de 1,3-diaminocetonas con anillo de 8-14 miembros |
AU4796700A (en) * | 1999-05-13 | 2000-12-05 | Dupont Pharmaceuticals Research Laboratories, Inc. | Ureido-substituted cyclic amine derivatives and their use as drug |
EP1181278B1 (fr) * | 1999-05-14 | 2004-09-29 | Bristol-Myers Squibb Pharma Research Labs, Inc. | Derives d'amine cycliques et leurs utilisations |
CN1240699C (zh) * | 1999-05-18 | 2006-02-08 | 帝人株式会社 | 与趋化因子有关的疾病的治疗或预防药物 |
CA2378499A1 (fr) * | 1999-08-04 | 2001-02-15 | Teijin Limited | Antagonistes d'amine cyclique ccr3 |
ATE346042T1 (de) * | 1999-12-08 | 2006-12-15 | Teijin Ltd | Zyklische aminverbindungen als ccr5-rezeptor antagonisten |
WO2001045700A1 (fr) * | 1999-12-21 | 2001-06-28 | Smithkline Beecham Corporation | Antagonistes des recepteurs de l'urotensine ii |
IL151164A0 (en) | 2000-03-06 | 2003-04-10 | Acadia Pharm Inc | Azacyclic compounds for use in the treatment of serotonin related diseases |
HUP0300068A2 (en) * | 2000-03-21 | 2003-05-28 | Smithkline Beecham Corp | Protease inhibitors, their preparation, their use and pharmaceutical compositions containing them |
US6410566B1 (en) | 2000-05-16 | 2002-06-25 | Teijin Limited | Cyclic amine derivatives and their use as drugs |
US8211916B2 (en) | 2000-06-20 | 2012-07-03 | Wayne State University | N- and O-substituted 4-[2-(diphenylmethoxy)-ethyl]-1-[(phenyl)methyl]piperidine analogs and methods of treating CNS disorders therewith |
US6995268B2 (en) | 2000-06-20 | 2006-02-07 | Wayne State University | N- and O-substituted 4-[2-(diphenylmethoxy)-ethyl]-1- (phenyl) methyl) piperidine analogs and methods of treating CNS disorders therewith |
US6395753B1 (en) * | 2001-08-30 | 2002-05-28 | Kowa Co., Ltd. | Cyclic amine compounds and pharmaceutical composition containing the same |
WO2003057698A2 (fr) | 2001-12-28 | 2003-07-17 | Acadia Pharmaceuticals, Inc. | Composes spiroazacycliques utilises comme modulateurs du recepteur de monoamine |
EP1465862A1 (fr) | 2002-01-17 | 2004-10-13 | SmithKline Beecham Corporation | Derives de cetoamides a substitution cycloalkyle, utiles comme inhibiteurs de cathepsine k |
RU2320646C2 (ru) | 2002-06-24 | 2008-03-27 | Акадиа Фармасьютикалз Инк. | N-замещенные производные пиперидина в качестве агентов серотонинового рецептора |
US7253186B2 (en) | 2002-06-24 | 2007-08-07 | Carl-Magnus Andersson | N-substituted piperidine derivatives as serotonin receptor agents |
US7538222B2 (en) | 2002-06-24 | 2009-05-26 | Acadia Pharmaceuticals, Inc. | N-substituted piperidine derivatives as serotonin receptor agents |
KR100962972B1 (ko) | 2002-07-26 | 2010-06-09 | 주식회사유한양행 | 1-페닐피페리딘-3-온 유도체 및 그의 제조방법 |
CN1816524B (zh) | 2003-01-16 | 2012-06-27 | 阿卡蒂亚药品公司 | 用于神经退行性疾病的治疗的选择性五羟色胺2a/2c受体反向激动剂 |
US20040192674A1 (en) * | 2003-02-14 | 2004-09-30 | Marquis Robert W. | Cathepsin L inhibitors |
US7109243B2 (en) | 2003-03-24 | 2006-09-19 | Irm Llc | Inhibitors of cathepsin S |
US7384970B2 (en) * | 2003-03-24 | 2008-06-10 | Irm Llc | Inhibitors of cathepsin S |
US8017791B2 (en) | 2003-03-28 | 2011-09-13 | Wayne State University | Tri-substituted 2-benzhydryl-5-benzylamino-tetrahydro-pyran-4-ol and 6-benzhydryl-4-benzylamino-tetrahydro-pyran-3-ol analogues, and novel, 3,6-disubstituted pyran derivatives |
US7173051B2 (en) * | 2003-06-13 | 2007-02-06 | Irm, Llc | Inhibitors of cathepsin S |
US7256207B2 (en) * | 2003-08-20 | 2007-08-14 | Irm Llc | Inhibitors of cathepsin S |
CA2563161C (fr) | 2004-04-16 | 2017-01-24 | Wayne State University | Analogues de 2-benzhydryl-5-benzylamino-tetrahydro-pyran-4-ol et 6-benzhydryl-4-benzylamino-tetrahydro-pyran-3-ol trisubstitues et nouveaux derives de pirane disubstitues en positions 3 et 6 |
US7820695B2 (en) | 2004-05-21 | 2010-10-26 | Acadia Pharmaceuticals, Inc. | Selective serotonin receptor inverse agonists as therapeutics for disease |
US20050261278A1 (en) | 2004-05-21 | 2005-11-24 | Weiner David M | Selective serotonin receptor inverse agonists as therapeutics for disease |
EP1796793A4 (fr) * | 2004-09-07 | 2009-08-05 | Smithkline Beecham Corp | Nouveaux composes |
BRPI0516063A (pt) | 2004-09-27 | 2008-08-19 | Acadia Pharm Inc | sìntese de n-(4-fluorbenzil)-n-(1-metilpiperidin-4-il)-n'-(4-(2-metilp ropi-loxi)fenilmetil)carbamida e seu sal tartarato e formas cristalinas |
US7790899B2 (en) | 2004-09-27 | 2010-09-07 | Acadia Pharmaceuticals, Inc. | Synthesis of N-(4-fluorobenzyl)-N-(1-methylpiperidin-4-yl)-N′-(4-(2-methylpropyloxy)phenylmethyl)carbamide and its tartrate salt and crystalline forms |
KR101351209B1 (ko) | 2004-12-03 | 2014-02-06 | 머크 샤프 앤드 돔 코포레이션 | Cb1 길항제로서 치환된 피페라진 |
MX2008002363A (es) * | 2005-08-17 | 2008-03-18 | Schering Corp | Ligandos novedosos de cinasa basados en quinolina de alta afinidad. |
US8067457B2 (en) | 2005-11-01 | 2011-11-29 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of CCR2 |
WO2007053499A2 (fr) * | 2005-11-01 | 2007-05-10 | Millennium Pharmaceuticals, Inc. | Composés pouvant être employés en tant qu'antagonistes de ccr2 |
WO2007053495A2 (fr) * | 2005-11-01 | 2007-05-10 | Millennium Pharmaceuticals, Inc. | Composes utiles en tant qu’antagonistes de ccr2 |
EP1987000A2 (fr) * | 2006-01-13 | 2008-11-05 | Schering Corporation | Utilisation de diaryle pipéridines comme modulateurs de cb1 |
US7897601B2 (en) * | 2006-01-18 | 2011-03-01 | Intervet, Inc. | Cannabinoid receptor modulators |
JPWO2008029924A1 (ja) * | 2006-09-08 | 2010-01-21 | 大日本住友製薬株式会社 | 環状アミノアルキルカルボキサミド誘導体 |
PL2134330T3 (pl) | 2007-03-19 | 2013-10-31 | Acadia Pharm Inc | Kombinacje odwrotnych agonistów i antagonistów 5-HT2A z antypsychotykami |
WO2008130616A2 (fr) * | 2007-04-19 | 2008-10-30 | Schering Corporation | Diaryl morpholines comme modulateurs des récepteurs cb1 |
CN101790521A (zh) * | 2007-06-28 | 2010-07-28 | 英特维特国际股份有限公司 | 作为cb1拮抗剂的取代哌嗪 |
CA2692268A1 (fr) * | 2007-06-28 | 2009-01-08 | Intervet International B.V. | Piperazines a substitution servant d'antagonistes des recepteurs cb1 |
ES2532763T3 (es) * | 2010-03-10 | 2015-03-31 | Janssen Pharmaceutica Nv | Derivados de piperidina 4,4-disustituidos útiles como inhibidores de la dipeptidil peptidasa-1 (DPP-1) |
US8686152B2 (en) | 2010-03-10 | 2014-04-01 | Janssen Pharmaceutica Nv | 4,4-disubstituted piperidine derivatives useful as inhibitors of dipeptidyl peptidase-1 (DPP-1) |
CU24442B1 (es) | 2014-04-04 | 2019-09-04 | X Rx Inc | Derivados de n-(1-(espirocíclico)oxo) amida sustituidos como inhibidores de autotaxina |
SI3325444T1 (sl) | 2015-07-20 | 2021-11-30 | Acadia Pharmaceuticals Inc. | Postopki za pripravo N-(4-fluorobenzil)-N-(1-metilpiperidin-4-il)-N'- (4-(2-metilpropiloksi)fenilmetil)karbamida in njegove tartratne soli in polimorfne oblike C |
US10953000B2 (en) | 2016-03-25 | 2021-03-23 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome P450 modulators |
WO2017165635A1 (fr) | 2016-03-25 | 2017-09-28 | Acadia Pharmaceuticals Inc. | Association de pimavansérine et de modulateurs du cytochrome p450 |
US11464768B2 (en) | 2016-12-20 | 2022-10-11 | Acadia Pharmaceuticals Inc. | Pimavanserin alone or in combination for use in the treatment of Alzheimer's disease psychosis |
EP3615028A1 (fr) | 2017-04-28 | 2020-03-04 | Acadia Pharmaceuticals Inc. | Pimavansérine pour le traitement d'un trouble de contrôle des impulsions |
US20210077479A1 (en) | 2017-08-30 | 2021-03-18 | Acadia Pharmaceuticals Inc. | Formulations of pimavanserin |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2804416A1 (de) | 1978-02-02 | 1979-08-09 | Boehringer Mannheim Gmbh | Neue purin-derivate, verfahren zu deren herstellung sowie diese verbindungen enthaltende arzneimittel |
ES8100016A1 (es) | 1978-07-18 | 1980-04-01 | Hoechst Ag | Procedimiento para la preparacion de nuevos derivados de 1-(4-aminopiperidino)-3,4-dihidroisoquinoleina. |
US4301151A (en) * | 1979-11-27 | 1981-11-17 | Merck & Co., Inc. | Long-lasting agonists of enkephalin |
US4443461A (en) | 1981-09-10 | 1984-04-17 | John Wyeth & Brother Limited | N-[2-[[1-[1H-Indolylalkyl- or oxoalkyl]-4-piperidinyl]-amino]-2-oxoethyl]-arylcarboxamide derivatives |
US4680283A (en) * | 1984-09-26 | 1987-07-14 | Merck & Co., Inc. | Analogs of substance P and eledoisin |
DK386089A (da) | 1988-08-12 | 1990-02-13 | Japan Tobacco Inc | Katekolderivater |
IE903196A1 (en) | 1989-09-05 | 1991-03-13 | Searle & Co | Substituted n-benzylpiperidine amides |
EP0480044A4 (en) | 1990-03-30 | 1993-06-09 | Japan Tobacco Inc. | Novel 4h-3,1-benzoxazin-4-one derivative |
US5514694A (en) | 1992-09-21 | 1996-05-07 | Georgia Tech Research Corp | Peptidyl ketoamides |
JPH09501404A (ja) * | 1993-05-26 | 1997-02-10 | スミスクライン・ビーチャム・ラボラトワール・ファルマソーティク | 新規化合物 |
US5827866A (en) * | 1995-06-07 | 1998-10-27 | Ortho Pharmaceutical Corporation | Peptidyl heterocycles useful in the treatment of thrombin related disorders |
DZ2285A1 (fr) | 1996-08-08 | 2002-12-25 | Smithkline Beecham Corp | Inhibiteurs de protéase de la cystéine. |
-
1998
- 1998-05-06 TR TR1999/02752T patent/TR199902752T2/xx unknown
- 1998-05-06 CA CA002289010A patent/CA2289010A1/fr not_active Abandoned
- 1998-05-06 HU HU0001285A patent/HUP0001285A3/hu unknown
- 1998-05-06 AU AU72885/98A patent/AU7288598A/en not_active Abandoned
- 1998-05-06 US US09/423,325 patent/US6369077B1/en not_active Expired - Fee Related
- 1998-05-06 BR BR9808502-6A patent/BR9808502A/pt not_active Application Discontinuation
- 1998-05-06 WO PCT/US1998/009192 patent/WO1998050534A1/fr not_active Application Discontinuation
- 1998-05-06 CN CN98804794A patent/CN1255162A/zh active Pending
- 1998-05-06 MA MA25064A patent/MA26494A1/fr unknown
- 1998-05-06 KR KR1019997010268A patent/KR20010012316A/ko not_active Application Discontinuation
- 1998-05-06 IL IL13166198A patent/IL131661A0/xx unknown
- 1998-05-06 PL PL98336625A patent/PL336625A1/xx not_active Application Discontinuation
- 1998-05-06 JP JP54841898A patent/JP2001525809A/ja not_active Ceased
- 1998-05-06 EP EP98920274A patent/EP0991753A4/fr not_active Withdrawn
- 1998-05-06 PE PE1998000344A patent/PE73799A1/es not_active Application Discontinuation
- 1998-05-07 ZA ZA983843A patent/ZA983843B/xx unknown
- 1998-05-08 CO CO98025629A patent/CO4950617A1/es unknown
-
1999
- 1999-11-05 NO NO995433A patent/NO995433L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0991753A1 (fr) | 2000-04-12 |
CO4950617A1 (es) | 2000-09-01 |
PL336625A1 (en) | 2000-07-03 |
PE73799A1 (es) | 1999-10-22 |
EP0991753A4 (fr) | 2001-07-11 |
WO1998050534A1 (fr) | 1998-11-12 |
TR199902752T2 (xx) | 2000-06-21 |
CN1255162A (zh) | 2000-05-31 |
NO995433D0 (no) | 1999-11-05 |
JP2001525809A (ja) | 2001-12-11 |
IL131661A0 (en) | 2001-01-28 |
AU7288598A (en) | 1998-11-27 |
KR20010012316A (ko) | 2001-02-15 |
CA2289010A1 (fr) | 1998-11-12 |
HUP0001285A2 (hu) | 2000-09-28 |
US6369077B1 (en) | 2002-04-09 |
BR9808502A (pt) | 2000-05-23 |
MA26494A1 (fr) | 2004-12-20 |
HUP0001285A3 (en) | 2000-10-30 |
NO995433L (no) | 1999-11-05 |
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PL349192A1 (en) | Protease inhibitors | |
ZA98376B (en) | Sulfamide-metalloprotease inhibitors | |
EP0744948A4 (fr) | Inhibiteurs de protease | |
GB2321641B (en) | Sulfamide-metalloprotease inhibitors | |
PL328307A1 (en) | Serinic protease inhibitors | |
HUP0002247A3 (en) | Protease inhibitors | |
IL132630A0 (en) | Protease inhibitors | |
EP1093367A4 (fr) | Inhibiteurs de proteases | |
ZA983522B (en) | Protease inhibitors | |
ZA988479B (en) | Protease inhibitors | |
PL328875A1 (en) | Serinic protease inhibitors | |
PL328223A1 (en) | Aspartil protease inhibitors | |
EP1067894A4 (fr) | Inhibiteurs de protease | |
EP1079821A4 (fr) | Inhibiteurs de la protease | |
ZA988064B (en) | Protease inhibitors | |
HK1041690A1 (zh) | 蛋白酶抑制劑 | |
EP1086083A4 (fr) | Inhibiteurs de proteases | |
EP0975612A4 (fr) | Inhibiteurs de proteases | |
ZA983097B (en) | Protease inhibitors | |
ZA977032B (en) | Protease inhibitors | |
GB9420277D0 (en) | Protease inhibitors | |
GB9727371D0 (en) | Inhibitors | |
GB9725783D0 (en) | Inhibitors |