WO2008140782A3 - Composés d'inhibition enzymatique - Google Patents
Composés d'inhibition enzymatique Download PDFInfo
- Publication number
- WO2008140782A3 WO2008140782A3 PCT/US2008/005997 US2008005997W WO2008140782A3 WO 2008140782 A3 WO2008140782 A3 WO 2008140782A3 US 2008005997 W US2008005997 W US 2008005997W WO 2008140782 A3 WO2008140782 A3 WO 2008140782A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- peptide
- based compounds
- compounds
- enzyme inhibition
- proteasome
- Prior art date
Links
Classifications
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- 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
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/081—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- C07K5/10—Tetrapeptides
- C07K5/1024—Tetrapeptides with the first amino acid being heterocyclic
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)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
L'invention concerne des composés à base de peptides comprenant des noyaux à trois chaînons contenant des hétéroatomes, qui inhibent de manière efficace et sélective des activités spécifiques de N-terminal nucléophile (Ntn) hydrolases associées au protéasome. Ces composés à base de peptides comprennent un époxide ou une aziridine, et une fonctionnalisation à l'extrémité N. Entre autres applications thérapeutiques, les composés à base de peptides peuvent présenter des propriétés anti-inflammatoires et d'inhibition de la prolifération cellulaire. L'administration par voie orale de ces inhibiteurs de protéasome à base de peptides est possible en raison de leur profil de biodisponibilité.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92875807P | 2007-05-10 | 2007-05-10 | |
US60/928,758 | 2007-05-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008140782A2 WO2008140782A2 (fr) | 2008-11-20 |
WO2008140782A3 true WO2008140782A3 (fr) | 2008-12-31 |
Family
ID=39743821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2008/005997 WO2008140782A2 (fr) | 2007-05-10 | 2008-05-09 | Composés d'inhibition enzymatique |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008140782A2 (fr) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102174076A (zh) | 2004-04-15 | 2011-09-07 | 普罗特奥里克斯公司 | 用于抑制蛋白酶体酶的化合物 |
US8198270B2 (en) | 2004-04-15 | 2012-06-12 | Onyx Therapeutics, Inc. | Compounds for proteasome enzyme inhibition |
DK2030981T3 (da) | 2004-05-10 | 2014-10-13 | Onyx Therapeutics Inc | Forbindelser til proteasom-enzymhæmning |
PL1948678T3 (pl) | 2005-11-09 | 2013-09-30 | Onyx Therapeutics Inc | Związki do hamowania enzymów |
DK2041158T3 (da) | 2006-06-19 | 2013-06-24 | Onyx Therapeutics Inc | Peptid-epoxidketoner til proteasom inhibering |
KR20150131405A (ko) | 2007-10-04 | 2015-11-24 | 오닉스 세라퓨틱스, 인크. | 결정형 펩티드 에폭시 케톤 프로테아제 저해제 및 아미노산 케토-에폭시드의 합성 |
US7635773B2 (en) | 2008-04-28 | 2009-12-22 | Cydex Pharmaceuticals, Inc. | Sulfoalkyl ether cyclodextrin compositions |
EP2349313A4 (fr) | 2008-10-21 | 2012-08-29 | Onyx Therapeutics Inc | Thérapie de combinaison avec des peptides époxycétones |
AP2912A (en) * | 2009-03-20 | 2014-05-31 | Onyx Therapeutics Inc | Crystalline tripeptide epoxy protease inhibitors |
AU2013203857B2 (en) * | 2009-03-20 | 2016-05-19 | Onyx Therapeutics, Inc. | Crystalline tripeptide epoxy ketone protease inhibitors |
AR075899A1 (es) * | 2009-03-20 | 2011-05-04 | Onyx Therapeutics Inc | Tripeptidos epoxicetonas cristalinos inhibidores de proteasa |
US8853147B2 (en) | 2009-11-13 | 2014-10-07 | Onyx Therapeutics, Inc. | Use of peptide epoxyketones for metastasis suppression |
MX2012010017A (es) | 2010-03-01 | 2012-10-01 | Onyx Therapeutics Inc | Compuestos de para la inhibicion de inmunoproteasomas. |
DK3702374T3 (da) | 2012-02-15 | 2022-06-27 | Cydex Pharmaceuticals Inc | Fremsgangsmåde til fremstilling for cyclodextrin-derivater |
US20140105921A1 (en) | 2012-07-09 | 2014-04-17 | Onyx Therapeutics, Inc. | Prodrugs of Peptide Epoxy Ketone Protease Inhibitors |
CN109096370B (zh) * | 2012-07-26 | 2022-03-18 | 圣特莱国际公司 | 多肽环氧酮化合物 |
CA2888822C (fr) | 2012-10-22 | 2021-01-26 | Cydex Pharmaceuticals, Inc. | Compositions de cyclodextrine alkylee et procedes de preparation et d'utilisation de celles-ci |
TW201422255A (zh) | 2012-10-24 | 2014-06-16 | Onyx Therapeutics Inc | 用於蛋白酶體抑制劑之調整釋放製劑 |
KR102360356B1 (ko) | 2014-07-14 | 2022-02-08 | 센트랙스 인터내셔널, 아이엔씨. | 효소 억제를 위한 에폭시케톤 화합물 |
WO2016029179A1 (fr) | 2014-08-22 | 2016-02-25 | Cydex Pharmaceuticals, Inc. | Compositions de cyclodextrine alkylée fractionnées et leurs procédés de préparation et d'utilisation |
CN105949279A (zh) * | 2016-04-27 | 2016-09-21 | 浙江大学 | 蛋白酶体抑制剂Oprozomib及其类似物的制备方法 |
CN110092813B (zh) * | 2019-06-05 | 2021-05-11 | 南京师范大学 | 一种三肽环氧丙烷衍生物及其制备方法和用途 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005111008A2 (fr) * | 2004-05-10 | 2005-11-24 | Proteolix, Inc. | Composes d'inhibition enzymatique |
WO2006045066A2 (fr) * | 2004-10-20 | 2006-04-27 | Proteolix, Inc. | Composes pour inhibition d'enzymes |
WO2007056464A1 (fr) * | 2005-11-09 | 2007-05-18 | Proteolix, Inc. | Composés pour l'inhibition d'enzymes |
-
2008
- 2008-05-09 WO PCT/US2008/005997 patent/WO2008140782A2/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005111008A2 (fr) * | 2004-05-10 | 2005-11-24 | Proteolix, Inc. | Composes d'inhibition enzymatique |
WO2006045066A2 (fr) * | 2004-10-20 | 2006-04-27 | Proteolix, Inc. | Composes pour inhibition d'enzymes |
WO2007056464A1 (fr) * | 2005-11-09 | 2007-05-18 | Proteolix, Inc. | Composés pour l'inhibition d'enzymes |
Also Published As
Publication number | Publication date |
---|---|
WO2008140782A2 (fr) | 2008-11-20 |
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