JP4604161B2 - フェニルアラニン誘導体 - Google Patents
フェニルアラニン誘導体 Download PDFInfo
- Publication number
- JP4604161B2 JP4604161B2 JP2000606620A JP2000606620A JP4604161B2 JP 4604161 B2 JP4604161 B2 JP 4604161B2 JP 2000606620 A JP2000606620 A JP 2000606620A JP 2000606620 A JP2000606620 A JP 2000606620A JP 4604161 B2 JP4604161 B2 JP 4604161B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- group
- compound
- formula
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 C[C@@](C(O[C@@](*)[C@@]1C2C*C2)=O)N1P Chemical compound C[C@@](C(O[C@@](*)[C@@]1C2C*C2)=O)N1P 0.000 description 4
- SBADAGQWPXHNAC-KKFHFHRHSA-N CC(C)(C)OC(CN[C@@H](Cc1ccc(C(C(OC(C)(C)[O]2C(C)(C)C)=O)C2=O)cc1)C(N)=O)=O Chemical compound CC(C)(C)OC(CN[C@@H](Cc1ccc(C(C(OC(C)(C)[O]2C(C)(C)C)=O)C2=O)cc1)C(N)=O)=O SBADAGQWPXHNAC-KKFHFHRHSA-N 0.000 description 1
Images
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
- C07K5/08—Tripeptides
- C07K5/0819—Tripeptides with the first amino acid being acidic
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
- C07D265/32—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings with oxygen atoms directly attached to ring carbon atoms
-
- 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
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- 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
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Child & Adolescent Psychology (AREA)
- Oncology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12604799P | 1999-03-23 | 1999-03-23 | |
| US60/126,047 | 1999-03-23 | ||
| PCT/US2000/008231 WO2000056760A1 (en) | 1999-03-23 | 2000-03-23 | Phenylalanine derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002544119A JP2002544119A (ja) | 2002-12-24 |
| JP2002544119A5 JP2002544119A5 (https=) | 2007-04-19 |
| JP4604161B2 true JP4604161B2 (ja) | 2010-12-22 |
Family
ID=22422719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000606620A Expired - Fee Related JP4604161B2 (ja) | 1999-03-23 | 2000-03-23 | フェニルアラニン誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7825216B2 (https=) |
| EP (1) | EP1163262B1 (https=) |
| JP (1) | JP4604161B2 (https=) |
| AT (1) | ATE509026T1 (https=) |
| AU (1) | AU770920C (https=) |
| CA (2) | CA2368733C (https=) |
| WO (1) | WO2000056760A1 (https=) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001028577A2 (en) * | 1999-10-22 | 2001-04-26 | The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Inhibition of cell motility and angiogenesis by inhibitors of the grb2 sh2-domain |
| US7871981B2 (en) | 1999-10-22 | 2011-01-18 | The United States Of America As Represented By The Department Of Health And Human Services | Inhibition of cell motility, angiogenesis, and metastasis |
| US7425537B2 (en) | 2000-08-22 | 2008-09-16 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | SH2 domain binding inhibitors |
| US6977241B2 (en) | 2000-08-22 | 2005-12-20 | The United States Of America As Represented By The Department Of Health & Human Services | SH2 domain binding inhibitors |
| US6821979B2 (en) | 2002-03-07 | 2004-11-23 | Blanchette Rockefeller Neurosciences Institute | Synergistic enhancement of cognitive ability |
| TW201206425A (en) | 2004-05-18 | 2012-02-16 | Brni Neurosciences Inst | Treatment of depressive disorders |
| CN115192564B (zh) * | 2022-05-23 | 2023-11-17 | 四川大学华西医院 | 一种苯丙氨酸衍生物、药物组合物及其在肿瘤治疗中的应用 |
| CN117603075B (zh) * | 2024-01-18 | 2024-04-12 | 深圳创元生物医药科技有限公司 | 一种碳13标记的3-羧酸苯丙氨酸的制备方法 |
Family Cites Families (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1883113A (en) * | 1932-10-18 | new yoek | ||
| US3906031A (en) | 1971-03-15 | 1975-09-16 | Research Corp | Novel 9-fluorenylmethoxycarbonyl compounds |
| US4394519A (en) | 1982-01-19 | 1983-07-19 | Research Corporation | Amino acid blocking agents |
| US4879398A (en) | 1987-12-31 | 1989-11-07 | Monsanto Company | Process for producing 2,6-disubstituted tyrosine |
| US5296608A (en) | 1988-04-25 | 1994-03-22 | Hoffman-La Roche Inc. | Intermediates for analogs of tyrosine sulfate or tyrosine phosphate containing peptides |
| US5182263A (en) | 1988-04-25 | 1993-01-26 | Hoffmann-La Roche Inc. | Analogs of tyrosine sulfate or tyrosine phosphate containing peptides |
| US5272268A (en) | 1990-06-28 | 1993-12-21 | Shionogi & Co., Ltd. | Dipeptide derivatives |
| US5679842A (en) | 1990-08-17 | 1997-10-21 | Hoechst Aktiengesellschaft | Process for the preparation of aminomethanephosphonic acid and aminomethylphosphinic acids |
| AU687754B2 (en) | 1990-08-31 | 1998-03-05 | Warner-Lambert Company | Tachykinin antagonists |
| AU657498B2 (en) | 1990-12-14 | 1995-03-16 | Novartis Ag | Biphenylyl compounds |
| DE4115468A1 (de) | 1991-05-11 | 1992-11-12 | Behringwerke Ag | Amidinophenylalaninderivate, verfahren zu deren herstellung, deren verwendung und diese enthaltende mittel als antikoagulantien |
| US5200546A (en) | 1991-09-30 | 1993-04-06 | The United States Of America As Represented By The Department Of Health And Human Services | Phosphonoalkyl phenylalanine compounds suitably protected for use in peptide synthesis |
| US5587372A (en) | 1991-12-12 | 1996-12-24 | Roussel Uclaf | Cephalosporins |
| TW399041B (en) | 1992-09-09 | 2000-07-21 | Hoechst Ag | Substituted cyclohexane derivatives, the preparation and the use for treating diseases |
| WO1994007913A1 (en) | 1992-09-25 | 1994-04-14 | Warner-Lambert Company | Peptide antagonists of sh2 binding and therapeutic uses thereof |
| US5981569A (en) | 1992-11-13 | 1999-11-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Substituted phenylacrylonitrile compounds and compositions thereof for the treatment of disease |
| US5792771A (en) | 1992-11-13 | 1998-08-11 | Sugen, Inc. | Quinazoline compounds and compositions thereof for the treatment of disease |
| US5712395A (en) | 1992-11-13 | 1998-01-27 | Yissum Research Development Corp. | Compounds for the treatment of disorders related to vasculogenesis and/or angiogenesis |
| JPH08503217A (ja) | 1992-11-18 | 1996-04-09 | ザ・デュポン・メルク・ファーマシュウティカル・カンパニー | 血小板糖タンパク質▲II▼b/▲III▼aの阻害剤として有用な複素環式環により結合された環状化合物 |
| GB9302331D0 (en) | 1993-02-05 | 1993-03-24 | Smithkline Beecham Plc | Process |
| WO1995001376A1 (en) | 1993-06-30 | 1995-01-12 | Pharmacia S.P.A. | Peptide inhibitors of mitogenesis and motogenesis |
| EP0677581A4 (en) | 1993-08-19 | 1995-12-06 | Japan Tobacco Inc | DNA WHICH CODES THE PLANT-BASED ATP-DEPENDENT FRUCTOSE-6-PHOSPHATE-1-PHOSPHOTRANSFERASE, A RECOMBINANT VECTOR CONTAINING THE SAME, AND A METHOD FOR CHANGING THE SUGAR CONTENT OF A PLANT PLANT THROUGH PLANT. |
| US5491253A (en) | 1993-10-22 | 1996-02-13 | Abbott Laboratories | Process for the preparation of a substituted 2,5-diamino-3-hydroxyhexane |
| KR100378615B1 (ko) | 1993-10-25 | 2003-10-10 | 파크데이비스앤드캄파니 | 단백질:파르네실트랜스퍼라제의치환된테트라및펜타펩티드억제제 |
| US5576323A (en) | 1993-12-03 | 1996-11-19 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
| US6037134A (en) | 1994-03-07 | 2000-03-14 | New York University Medical Center | Methods that detect compounds that disrupt receptor tyrosine kinase/GRB-7 complexes |
| WO1995024190A2 (en) | 1994-03-07 | 1995-09-14 | Sugen, Inc. | Receptor tyrosine kinase inhibitors for inhibiting cell proliferative disorders and compositions thereof |
| US5580979A (en) | 1994-03-15 | 1996-12-03 | Trustees Of Tufts University | Phosphotyrosine peptidomimetics for inhibiting SH2 domain interactions |
| US5849510A (en) | 1994-04-26 | 1998-12-15 | Selectide Corporation | Factor Xa inhibitors |
| US5707624A (en) | 1994-06-03 | 1998-01-13 | The Regents Of The University Of Michigan | Treatment of Kaposi's sarcoma by inhibition of scatter factor |
| US5786454A (en) | 1994-09-16 | 1998-07-28 | Washington University School Of Medicine | Modified SH2 domains |
| WO1996023813A1 (en) * | 1995-02-01 | 1996-08-08 | Affymax Technologies N.V. | Peptides and compounds that bind to sh2 domains |
| US5756817C1 (en) | 1995-02-11 | 2001-04-17 | Sk Corp | O-carbamoyl-phenylananinol compounds their pharmaceutically useful salts and process for preparing the same |
| US5710129A (en) | 1995-02-23 | 1998-01-20 | Ariad Pharmaceuticals, Inc. | Inhibitors of SH2-mediated processes |
| US5688992A (en) | 1995-03-31 | 1997-11-18 | The United States Of America As Represented By The Department Of Health And Human Services | O-malonyltryrosyl compounds, O-malonyltryrosyl compound-containing peptides, and use thereof |
| US5646036A (en) | 1995-06-02 | 1997-07-08 | Genentech, Inc. | Nucleic acids encoding hepatocyte growth factor receptor antagonist antibodies |
| US5686292A (en) | 1995-06-02 | 1997-11-11 | Genentech, Inc. | Hepatocyte growth factor receptor antagonist antibodies and uses thereof |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| US5612370A (en) | 1995-06-07 | 1997-03-18 | Bristol-Myers Squibb Company | Phenylglycine and phenylalaninen amido benzopyran derivatives |
| US5798374A (en) | 1995-06-07 | 1998-08-25 | Sugen Inc. | Methods of inhibiting phosphatase activity and treatment of disorders associated therewith |
| WO1996040115A1 (en) | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions |
| US5710173A (en) | 1995-06-07 | 1998-01-20 | Sugen, Inc. | Thienyl compounds for inhibition of cell proliferative disorders |
| WO1996040629A1 (en) | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Tyrphostin-like compounds for the treatment of cell proliferative disorders or cell differentiation disorders |
| US5965558A (en) | 1995-06-19 | 1999-10-12 | Ontogen Corporation | Modulators of proteins with phosphotyrosine recognition units |
| US5753687A (en) | 1995-06-19 | 1998-05-19 | Ontogen Corporation | Modulators of proteins with phosphotryrosine recognition units |
| IT1282022B1 (it) | 1995-07-06 | 1998-03-06 | Mini Ricerca Scient Tecnolog | Procedimento per la produzione di carbammati aromatici |
| GB9517060D0 (en) | 1995-08-17 | 1995-10-25 | Ciba Geigy Ag | Acylated oligopeptide derivatives |
| WO1997012903A1 (en) * | 1995-10-04 | 1997-04-10 | Warner-Lambert Company | Compounds, compositions and methods for inhibiting the binding of proteins containing an sh2 domain to cognate phosphorylated proteins |
| US5958957A (en) | 1996-04-19 | 1999-09-28 | Novo Nordisk A/S | Modulators of molecules with phosphotyrosine recognition units |
| US5948658A (en) | 1996-06-25 | 1999-09-07 | The Trustees Of Columbia University In The City Of New York | Anti-cocaine catalytic antibody |
| US5922697A (en) | 1996-10-02 | 1999-07-13 | Warner-Lambert Company | Compounds, compositions and methods for inhibiting the binding of proteins containing an SH2 domain to cognate phosphorylated proteins |
| SE9701718D0 (sv) | 1997-05-07 | 1997-05-07 | Astra Ab | Analgesic peptidomimetic compounds |
| EP1019364B1 (en) * | 1997-08-28 | 2004-06-09 | Biovitrum Ab | Inhibitors of protein tyrosine phosphatase |
| US6410585B1 (en) | 1997-08-28 | 2002-06-25 | Scott D. Larsen | Inhibitors of protein tyrosine phosphatase |
| US6022696A (en) | 1998-04-02 | 2000-02-08 | Washington State University Research Foundation | Methods of identifying agonists or antagonists of angiotensin IV |
| US6228986B1 (en) | 1998-04-13 | 2001-05-08 | Ortho-Mcneil Pharmaceutical, Inc. | Solid-phase synthesis of novel 14-membered macroycles for high throughput screening |
| US6307090B1 (en) | 1999-01-22 | 2001-10-23 | The United States Of America As Represented By The Department Of Health And Human Services | Acylated oligopeptide derivatives having cell signal inhibiting activity |
| WO2000073326A2 (en) | 1999-06-02 | 2000-12-07 | The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Redox-stable, non-phosphorylated cyclic peptide inhibitors of sh2 domain binding to target protein, conjugates thereof, compositions and methods of synthesis and use |
-
2000
- 2000-03-23 EP EP00918474A patent/EP1163262B1/en not_active Expired - Lifetime
- 2000-03-23 CA CA2368733A patent/CA2368733C/en not_active Expired - Fee Related
- 2000-03-23 AU AU39276/00A patent/AU770920C/en not_active Ceased
- 2000-03-23 AT AT00918474T patent/ATE509026T1/de not_active IP Right Cessation
- 2000-03-23 JP JP2000606620A patent/JP4604161B2/ja not_active Expired - Fee Related
- 2000-03-23 WO PCT/US2000/008231 patent/WO2000056760A1/en not_active Ceased
- 2000-03-23 CA CA2855415A patent/CA2855415A1/en not_active Abandoned
-
2007
- 2007-05-16 US US11/749,499 patent/US7825216B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AU3927600A (en) | 2000-10-09 |
| CA2368733C (en) | 2014-10-07 |
| ATE509026T1 (de) | 2011-05-15 |
| AU770920B2 (en) | 2004-03-11 |
| EP1163262B1 (en) | 2011-05-11 |
| AU770920C (en) | 2004-10-07 |
| CA2368733A1 (en) | 2000-09-28 |
| EP1163262A1 (en) | 2001-12-19 |
| JP2002544119A (ja) | 2002-12-24 |
| US7825216B2 (en) | 2010-11-02 |
| US20070219194A1 (en) | 2007-09-20 |
| WO2000056760A1 (en) | 2000-09-28 |
| CA2855415A1 (en) | 2000-09-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP7823181B2 (ja) | Hrasおよびnrasに対して選択的なkras阻害作用を有する環状化合物 | |
| JP6871310B2 (ja) | ジペプチド及びトリペプチドエポキシケトンプロテアーゼ阻害剤 | |
| AU772024B2 (en) | Inhibitors of urokinase and blood vessel formation | |
| US7825216B2 (en) | Phenylanine derivatives | |
| US6933290B2 (en) | 2-{N-(2-amino-3-(heteroaryl or aryl)propionyl)-aminoacyl}-amino}-alkylboronic acid derivatives | |
| JPH05230095A (ja) | 治療薬としての新規5−アミノ−4−ヒドロキシヘキサン酸誘導体 | |
| RO119413B1 (ro) | Derivaţi izosteri ai substratului aspartat proteazei, sărurile lor, compoziţii farmaceutice şi utilizare | |
| KR19980703151A (ko) | 락탐-함유 히드록삼산 유도체, 그의 제조 그리고 매트릭스 메탈로프로테아제의 억제제로서의 그의 용도 | |
| JPH02212434A (ja) | レトロウイルスプロテアーゼインヒビターとしてのペプチドアイソスターの使用 | |
| WO2023155808A1 (zh) | 抗体-艾日布林或其衍生物的偶联物、其中间体、制备方法、药物组合物和用途 | |
| JP2024088768A (ja) | カンナビノイドプロドラッグ化合物 | |
| JP2002503714A (ja) | 抗腫瘍剤 | |
| JP2016501848A (ja) | 大環状化合物及びその使用 | |
| KR102413079B1 (ko) | 돌라프로인-돌라이소류인 펩타이드의 유도체 | |
| US6977241B2 (en) | SH2 domain binding inhibitors | |
| US7226991B1 (en) | Phenylalanine derivatives | |
| US20030166572A1 (en) | 2-Amino-3-hydroxy-4-tert-leucyl-amino-5 phenyl-pentanoic acid amide derivatives | |
| KR101264934B1 (ko) | 아미도메틸-치환1-(카르복시알킬)-시클로펜틸카보닐아미노-벤자제핀-n-아세트산 유도체, 그것의 제조를 위한 공정 및 중간체 생성물및 이들 화합물을 포함하는 의약품 | |
| CN109796519A (zh) | 一类甾体化合物及其应用 | |
| US7425537B2 (en) | SH2 domain binding inhibitors | |
| WO2019061812A1 (zh) | 氨基酸骨架类新型cxcr4拮抗剂及其制备与生物医学应用 | |
| WO2004003005A2 (en) | Sh2 domain binding inhibitors | |
| KR20250001962A (ko) | 신규한 헤미아스텔린 유도체 및 이의 용도 | |
| HK1243085A1 (en) | Derivatives of dolaproine-dolaisoleuine peptides | |
| JPH093095A (ja) | 新規なフエネチルアミド誘導体 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070129 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070129 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20100210 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100223 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100520 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20100607 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100615 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20100713 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100812 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20100817 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20100902 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20100901 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20131015 Year of fee payment: 3 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |