NO995433L - Protease-inhibitorer - Google Patents
Protease-inhibitorerInfo
- Publication number
- NO995433L NO995433L NO995433A NO995433A NO995433L NO 995433 L NO995433 L NO 995433L NO 995433 A NO995433 A NO 995433A NO 995433 A NO995433 A NO 995433A NO 995433 L NO995433 L NO 995433L
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- het
- 6alkyl
- 6alkenyl
- cycloalkyl
- 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)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Genetics & Genomics (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Immunology (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)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
Abstract
Foreliggende oppfinnelse angår forbindelser med formel (I): R4 R3 R1 N-f)n O hvor: d) YerArellerNR1R2; R1 er R", R"C(O), R"C(S), R"SO2, R"OC(O), R"R'NC(O) eller R"R'NC(S); R2 er H, Ci-ealkyl, C2-6alkenyl, Ar-Co-6alkyl eller Hel-CQ.Qa\ky\; R3 er H, C2-6alkenyl, C2-6alkynyl, Het, Ar eller Ci-ealkyl eventuelt substituert med OR1, SR1, NR'2, N(R')C(O)OR", CO2R', CO2NR'2, N(C=NH)NH2, Het eller Ar; _ R4 er H, Ci.ealkyl, C2-6alkenyl, Ar-Co-6alkyl eller Het-Cn-ealkyl; R5, R-V2' er - Ar-CO-6alkyl, Het-C0.6alkyl, adamantyl-C(O)- Ar-C(O)-. Het-C(O)- eller; R6 er R", R"C(0), R"C(S), R"SO2, R"OC(O), R"R'NC(O). R"R'NC(S),eller R"OC(O)NR'CH(R*)C(O); R7 er Ca.gcykloalkyl-Co-ealkyl, Ar-Crj-ealkyl, Het-Cø-ealkyl, Ar- Crj.ealkoksy, Het-Crj-ealkoksy eller C-|-6alkyl eventuelt substituert med OR1, SR', NR'2, N(R')C(O)OR", C02R1, CO2NR'2, N(C=NH)NH2, Het eller Ar; R* er H, Ci^alkyl. C2-6alkenyl, Cs^cykloalkyl-CQ-S-alkyl, Ar-Co_6alkyl, Het-Crj-6alkyl; hver R' er uavhengig H, C-i^alkyl, C2-ealkenyl, Ar-Co-6alkyl eller Het-Co-ealkyl; hver R" er uavhengig C-i^alkyl, C3_6cykloalkyl-Co-6-alkyl, Ar-Co-6alkyl eller Het-Crj-ealkyl; R1" er H, C^øalkyl, Ca-scykloalkyl-Co-ealkyl, Ar-Cø-ealkyl eller Het- Z er C(O) eller CH2; og ner 1, 2 eller 3; eller et farmasøytisk godtagbart salt derav, som er inhibitorer av cystein- proteaser, spesielt cathepsin K og er nyttige ved behandling av sykdommer hvor hemning av bentap er en faktor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4686597P | 1997-05-08 | 1997-05-08 | |
PCT/US1998/009192 WO1998050534A1 (en) | 1997-05-08 | 1998-05-06 | Protease inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
NO995433L true NO995433L (no) | 1999-11-05 |
NO995433D0 NO995433D0 (no) | 1999-11-05 |
Family
ID=21945814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO995433A NO995433D0 (no) | 1997-05-08 | 1999-11-05 | Protease-inhibitorer |
Country Status (18)
Country | Link |
---|---|
US (1) | US6369077B1 (no) |
EP (1) | EP0991753A4 (no) |
JP (1) | JP2001525809A (no) |
KR (1) | KR20010012316A (no) |
CN (1) | CN1255162A (no) |
AU (1) | AU7288598A (no) |
BR (1) | BR9808502A (no) |
CA (1) | CA2289010A1 (no) |
CO (1) | CO4950617A1 (no) |
HU (1) | HUP0001285A3 (no) |
IL (1) | IL131661A0 (no) |
MA (1) | MA26494A1 (no) |
NO (1) | NO995433D0 (no) |
PE (1) | PE73799A1 (no) |
PL (1) | PL336625A1 (no) |
TR (1) | TR199902752T2 (no) |
WO (1) | WO1998050534A1 (no) |
ZA (1) | ZA983843B (no) |
Families Citing this family (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUP0004200A3 (en) * | 1997-11-18 | 2001-04-28 | Dupont Pharmaceuticals Res Lab | Cyclic amine derivatives and their use as drugs |
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 |
AU5011300A (en) | 1999-05-14 | 2000-12-05 | Combichem, Inc. | Cyclic amine derivatives and their uses |
ES2250132T3 (es) | 1999-05-18 | 2006-04-16 | Teijin Limited | Remedios preventivos para enfermedades asociadas a quimioquinas. |
WO2001010439A1 (fr) * | 1999-08-04 | 2001-02-15 | Teijin Limited | Antagonistes d'amine cyclique ccr3 |
CN1208318C (zh) * | 1999-12-08 | 2005-06-29 | 帝人株式会社 | 环胺ccr5受体拮抗剂 |
ES2225297T3 (es) | 1999-12-21 | 2005-03-16 | Smithkline Beecham Corporation | Antagonistas del receptor de urotensina ii. |
AU780006B2 (en) | 2000-03-06 | 2005-02-24 | Acadia Pharmaceuticals, Inc. | Azacyclic compounds for use in the treatment of serotonin related diseases |
MXPA02009305A (es) * | 2000-03-21 | 2003-03-12 | Smithkline Beecham Corp | Inhibidores de proteasa. |
US6410566B1 (en) | 2000-05-16 | 2002-06-25 | Teijin Limited | Cyclic amine derivatives and their use as drugs |
AU2001275537A1 (en) | 2000-06-20 | 2002-01-02 | Wayne State University | N-and o-substituted 4-(2-(diphenylmethoxy)-ethyl)-1-((phenyl)methyl)piperidine analogs and methods of treating cns disorders therewith |
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 |
US6395753B1 (en) * | 2001-08-30 | 2002-05-28 | Kowa Co., Ltd. | Cyclic amine compounds and pharmaceutical composition containing the same |
DE60236206D1 (de) | 2001-12-28 | 2010-06-10 | Acadia Pharm Inc | Spiroazacyclische verbindungen als monoaminrezeptormodulatoren |
JP2005515254A (ja) | 2002-01-17 | 2005-05-26 | スミスクライン ビーチャム コーポレーション | カテプシンk阻害剤として有用なシクロアルキルケトアミド誘導体 |
US7538222B2 (en) | 2002-06-24 | 2009-05-26 | Acadia Pharmaceuticals, Inc. | N-substituted piperidine derivatives as serotonin receptor agents |
EP1562937A2 (en) | 2002-06-24 | 2005-08-17 | Acadia Pharmaceuticals Inc. | N-substituted piperidine derivatives as serotonin receptor agents |
US7253186B2 (en) | 2002-06-24 | 2007-08-07 | Carl-Magnus Andersson | 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 |
BRPI0406591B8 (pt) | 2003-01-16 | 2021-05-25 | Acadia Pharm Inc | composto e composição farmacêutica |
US20040192674A1 (en) * | 2003-02-14 | 2004-09-30 | Marquis Robert W. | Cathepsin L inhibitors |
US7384970B2 (en) | 2003-03-24 | 2008-06-10 | Irm Llc | Inhibitors of cathepsin S |
US7109243B2 (en) * | 2003-03-24 | 2006-09-19 | Irm Llc | Inhibitors of cathepsin S |
WO2005105075A1 (en) | 2004-04-16 | 2005-11-10 | Wayne State University | Tri-substitued 2-benzhydryl-5-benzlamino-tetrahydro-pyran-4-ol and 6-benzhydryl-4-benzylamino-tetrahydro-pyran-3-ol analogues, and novel 3,6-disubstituted pyran derivatives |
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 |
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 |
JP2008512461A (ja) * | 2004-09-07 | 2008-04-24 | スミスクライン・ビーチャム・コーポレイション | 新規化合物 |
EP1794126B1 (en) | 2004-09-27 | 2013-03-20 | Acadia Pharmaceuticals Inc. | Crystalline form of n-(4-fluorobenzyl)-n-(1-methylpiperidin-4-yl)-n'-(4-(2-methylpropyloxy)phenylmethyl)carbamide hemi-tartrate |
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 |
CN101287727A (zh) * | 2005-08-17 | 2008-10-15 | 先灵公司 | 新的高亲和力喹啉基激酶配体 |
US8067457B2 (en) | 2005-11-01 | 2011-11-29 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of CCR2 |
US8067415B2 (en) * | 2005-11-01 | 2011-11-29 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of CCR2 |
US20100016289A1 (en) * | 2005-11-01 | 2010-01-21 | Kevin Sprott | Compounds Useful as Antagonists of CCR2 |
CA2637057A1 (en) * | 2006-01-13 | 2007-07-26 | Schering Corporation | Diaryl piperidines as cb1 modulators |
EP1973877A2 (en) * | 2006-01-18 | 2008-10-01 | Schering Corporation | Cannibinoid receptor modulators |
US20100179118A1 (en) * | 2006-09-08 | 2010-07-15 | Dainippon Sumitomo Pharma Co., Ltd. | Cyclic aminoalkylcarboxamide derivative |
US20090053329A1 (en) | 2007-03-19 | 2009-02-26 | Acadia Pharmaceuticals, Inc. | Combinations of 5-ht2a inverse agonists and antagonists with antipsychotics |
WO2008130616A2 (en) * | 2007-04-19 | 2008-10-30 | Schering Corporation | Diaryl morpholines as cb1 modulators |
RU2010102478A (ru) * | 2007-06-28 | 2011-08-10 | Интэрвэт Интэрнэшнл Б.Ф. (NL) | Замещенные пиперазины как антагонисты св1 |
WO2009005671A2 (en) * | 2007-06-28 | 2009-01-08 | Schering Corporation | Substituted piperazines as cb1 antagonists |
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) |
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) |
MX2016013049A (es) | 2014-04-04 | 2017-04-27 | X-Rx Inc | Inhibidores de autotaxina espirociclicos sustituidos. |
WO2017015272A1 (en) | 2015-07-20 | 2017-01-26 | Acadia Pharmaceuticals Inc. | Methods for preparing n-(4-fluorobenzyl)-n-(1-methylpiperidin-4-yl)-n'-(4-(2-methylpropyloxy)phenylmethyl)carbamide and its tartrate salt and polymorphic form c |
US10953000B2 (en) | 2016-03-25 | 2021-03-23 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome P450 modulators |
WO2017165635A1 (en) | 2016-03-25 | 2017-09-28 | Acadia Pharmaceuticals Inc. | Combination of pimavanserin and cytochrome p450 modulators |
EP3558311A1 (en) | 2016-12-20 | 2019-10-30 | Acadia Pharmaceuticals Inc. | Pimavanserin alone or in combination for use in the treatment of alzheimer's disease psychosis |
US11135211B2 (en) | 2017-04-28 | 2021-10-05 | Acadia Pharmaceuticals Inc. | Pimavanserin for treating impulse control disorder |
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 |
ES482439A0 (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 |
WO1994027967A1 (en) | 1993-05-26 | 1994-12-08 | Smithkline Beecham Laboratoires Pharmaceutiques | Novel compounds |
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 HU HU0001285A patent/HUP0001285A3/hu unknown
- 1998-05-06 WO PCT/US1998/009192 patent/WO1998050534A1/en 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 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 TR TR1999/02752T patent/TR199902752T2/xx unknown
- 1998-05-06 KR KR1019997010268A patent/KR20010012316A/ko not_active Application Discontinuation
- 1998-05-06 PE PE1998000344A patent/PE73799A1/es not_active Application Discontinuation
- 1998-05-06 JP JP54841898A patent/JP2001525809A/ja not_active Ceased
- 1998-05-06 PL PL98336625A patent/PL336625A1/xx not_active Application Discontinuation
- 1998-05-06 IL IL13166198A patent/IL131661A0/xx unknown
- 1998-05-06 CA CA002289010A patent/CA2289010A1/en not_active Abandoned
- 1998-05-06 EP EP98920274A patent/EP0991753A4/en not_active Withdrawn
- 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/NO995433D0/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0991753A1 (en) | 2000-04-12 |
AU7288598A (en) | 1998-11-27 |
WO1998050534A1 (en) | 1998-11-12 |
JP2001525809A (ja) | 2001-12-11 |
HUP0001285A3 (en) | 2000-10-30 |
EP0991753A4 (en) | 2001-07-11 |
CN1255162A (zh) | 2000-05-31 |
ZA983843B (en) | 1998-11-09 |
MA26494A1 (fr) | 2004-12-20 |
TR199902752T2 (xx) | 2000-06-21 |
HUP0001285A2 (hu) | 2000-09-28 |
PE73799A1 (es) | 1999-10-22 |
BR9808502A (pt) | 2000-05-23 |
US6369077B1 (en) | 2002-04-09 |
CO4950617A1 (es) | 2000-09-01 |
PL336625A1 (en) | 2000-07-03 |
NO995433D0 (no) | 1999-11-05 |
CA2289010A1 (en) | 1998-11-12 |
IL131661A0 (en) | 2001-01-28 |
KR20010012316A (ko) | 2001-02-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO995433L (no) | Protease-inhibitorer | |
CA2262668A1 (en) | Inhibitors of cathepsin k | |
PT87454A (pt) | Heterocyclic ketones | |
WO1996016981A3 (en) | Peptide compounds for prevention and/or treatment of no-mediated diseases | |
DE69720773T2 (de) | SAUERSTOFF ODER SCHWEFEL ENTHALTENDE 5-GLIEDRIGE HETEROAROMATISHE DERIVATIVE ALS FACTOR Xa HEMMER | |
BG106867A (en) | Non-peptidyl inhibitors of vla-4 dependent cell binding useful in treating inflammatory autoimmune and respiratory diseases | |
FI915819A0 (fi) | Hiv- proteas-inhibitorer. | |
NO20013254D0 (no) | Nye difenylureaforbindelser, fremgangsmåte ved deres fremstilling og farmasöytiske samensetninger som inneholder dem | |
DK0759919T3 (da) | Azolidindioner som antihyperglykæmiske midler | |
AP9901578A0 (en) | Sulfonylbenzene compounds as anti-inflammatory/analgesic agents. | |
DE60330758D1 (de) | Bestimmte pharmazeutisch wertvolle substituierte aminoalkyl-heterocyclen | |
ID24846A (id) | Turunan-turunan bifenilamidina | |
ATE99934T1 (de) | Heteroaryl-3-oxo-propannitril-derivate, nuetzlich zur behandlung von rheumatoider arthritis und anderen autoimmunkrankheiten. | |
DE69810800D1 (de) | Azetidinonderivate zur behandlung von hcmv entzündungen | |
AR043271A1 (es) | Compuestos de dihidropironas con heterociclos unidos y su uso en composicines farmaceuticas que poseen actividad inhibidora de hiv proteasa | |
DK0871626T3 (da) | Triazoloner som apolipoprotein-B syntheseinhibitorer | |
NO20001200L (no) | Pyrrolopyrrolonderivater som inhibitorer av nøyrofil elastase | |
NO940019L (no) | Fremgangsmåte for fremstilling av svovelholdige imidazolderivater | |
DE69813554D1 (de) | Cyclische harnstoff- und lactamderivate von benzo(5,6)cycloheptapyridinen zur verwendung als farnesyl-protein-transferase-hemmer | |
UA26459C2 (uk) | Іhгібітор впливу амілоїдhих білків | |
ATE58135T1 (de) | 1,3-oxathianderivate. | |
JPS6422898A (en) | 2-alanyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivative | |
ECSP982497A (es) | Inhibidores de proteasas v | |
TH61368A (th) | สารยับยั้งธรอมบินที่ประกอบด้วยกลุ่มอะมิโนไอโซควิโนลีน | |
HU217345B (hu) | Helyettesített dihidro-piridin ftálamidsav származéka, és eljárás előállítására |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC2A | Withdrawal, rejection or dismissal of laid open patent application |