UY30391A1 - HEPATITIS C PROTEASE INHIBITORS ACICLIC OXYM COMPOUND - Google Patents
HEPATITIS C PROTEASE INHIBITORS ACICLIC OXYM COMPOUNDInfo
- Publication number
- UY30391A1 UY30391A1 UY30391A UY30391A UY30391A1 UY 30391 A1 UY30391 A1 UY 30391A1 UY 30391 A UY30391 A UY 30391A UY 30391 A UY30391 A UY 30391A UY 30391 A1 UY30391 A1 UY 30391A1
- Authority
- UY
- Uruguay
- Prior art keywords
- hepatitis
- aciclic
- oxym
- compound
- protease inhibitors
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 title 1
- 208000006454 hepatitis Diseases 0.000 title 1
- 231100000283 hepatitis Toxicity 0.000 title 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 title 1
- 241000711549 Hepacivirus C Species 0.000 abstract 5
- 230000000694 effects Effects 0.000 abstract 2
- 208000015181 infectious disease Diseases 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 108091005804 Peptidases Proteins 0.000 abstract 1
- 239000004365 Protease Substances 0.000 abstract 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 abstract 1
- 102000012479 Serine Proteases Human genes 0.000 abstract 1
- 108010022999 Serine Proteases Proteins 0.000 abstract 1
- 239000003443 antiviral agent Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compuestos de formula I o sus sales aceptables para uso farmacéutico, ésteres, o prodrogas: que inhiben la actividad de la serina proteasa, particularmente la actividad de la proteasa del virus de la hepatitis C (HCV) NS3-NS4A. En consecuencia, interfieren con el ciclo de vida del virus de la hepatitis C y también son utiles como agentes antivirales. Composiciones farmacéuticas que comprenden los compuestos mencionados para su administracion a un sujeto que sufra de una infeccion por HCV. Métodos para tratar una infeccion por HCV en un sujeto administrando una composicion farmacéutica que comprende los compuestos de la presente invencion.Compounds of formula I or their salts acceptable for pharmaceutical use, esters, or prodrugs: which inhibit the activity of serine protease, particularly hepatitis C virus (HCV) NS3-NS4A protease activity. Consequently, they interfere with the life cycle of the hepatitis C virus and are also useful as antiviral agents. Pharmaceutical compositions comprising the compounds mentioned for administration to a subject suffering from an HCV infection. Methods for treating an HCV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81146406P | 2006-06-06 | 2006-06-06 | |
| US50338506A | 2006-08-11 | 2006-08-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UY30391A1 true UY30391A1 (en) | 2008-01-31 |
Family
ID=38832101
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UY30391A UY30391A1 (en) | 2006-06-06 | 2007-06-06 | HEPATITIS C PROTEASE INHIBITORS ACICLIC OXYM COMPOUND |
Country Status (5)
| Country | Link |
|---|---|
| AR (1) | AR063942A1 (en) |
| CL (1) | CL2007001630A1 (en) |
| TW (1) | TW200815481A (en) |
| UY (1) | UY30391A1 (en) |
| WO (1) | WO2007146695A1 (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008070358A2 (en) * | 2006-11-16 | 2008-06-12 | Phenomix Corporation | N-cyclopropyl-hydroxyproline-based tripeptidic hepatitis c serine protease inhibitors containing an isoindole, pyrrolopyridine, pyrrolopyrimidine or pyrrolopyrazine heterocycle in the side chain |
| US8426360B2 (en) | 2007-11-13 | 2013-04-23 | Enanta Pharmaceuticals, Inc. | Carbocyclic oxime hepatitis C virus serine protease inhibitors |
| WO2009073713A1 (en) | 2007-12-05 | 2009-06-11 | Enanta Pharmaceuticals, Inc. | Oximyl macrocyclic derivatives |
| WO2009076166A2 (en) | 2007-12-05 | 2009-06-18 | Enanta Pharmaceuticals, Inc. | Oximyl hcv serine protease inhibitors |
| WO2009073780A1 (en) | 2007-12-06 | 2009-06-11 | Enanta Pharmaceuticals, Inc. | Process for making macrocyclic oximyl hepatitis c protease inhibitors |
| MX2010006518A (en) | 2007-12-14 | 2010-08-10 | Enanta Pharm Inc | Macrocyclic oximyl hepatitis c serine protease inhibitors. |
| US8283309B2 (en) | 2007-12-20 | 2012-10-09 | Enanta Pharmaceuticals, Inc. | Bridged carbocyclic oxime hepatitis C virus serine protease inhibitors |
| WO2009117594A1 (en) | 2008-03-20 | 2009-09-24 | Enanta Pharmaceuticals, Inc. | Fluorinated macrocyclic compounds as hepatitis c virus inhibitors |
| TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
| CA2769652A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
| TW201309690A (en) | 2011-02-10 | 2013-03-01 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections |
| EP2850059A4 (en) | 2012-05-15 | 2016-06-29 | Concortis Biosystems Corp | Drug-conjugates, conjugation methods, and uses thereof |
| EP2899207A1 (en) | 2014-01-28 | 2015-07-29 | Amikana.Biologics | New method for testing HCV protease inhibition |
| EP3472151A4 (en) | 2016-06-21 | 2020-03-04 | Orion Ophthalmology LLC | CARBOCYCLIC PROLINAMIDE DERIVATIVES |
| KR102595723B1 (en) | 2016-06-21 | 2023-10-27 | 오리온 옵탈몰로지 엘엘씨 | Heterocyclic Prolinamide Derivatives |
| CN110904121B (en) * | 2019-12-17 | 2022-11-29 | 南京农业大学 | Application of susceptibility gene SR30 in improving crop resistance |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7273851B2 (en) * | 2003-06-05 | 2007-09-25 | Enanta Pharmaceuticals, Inc. | Tri-peptide hepatitis C serine protease inhibitors |
-
2007
- 2007-06-06 AR ARP070102426A patent/AR063942A1/en unknown
- 2007-06-06 CL CL200701630A patent/CL2007001630A1/en unknown
- 2007-06-06 WO PCT/US2007/070481 patent/WO2007146695A1/en not_active Ceased
- 2007-06-06 UY UY30391A patent/UY30391A1/en not_active Application Discontinuation
- 2007-06-06 TW TW096120284A patent/TW200815481A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007146695A1 (en) | 2007-12-21 |
| AR063942A1 (en) | 2009-03-04 |
| CL2007001630A1 (en) | 2008-02-08 |
| TW200815481A (en) | 2008-04-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| UY30527A1 (en) | TETRAZOLILOS MACROCICLICOS AS INHIBITORS OF SERINE PROTEASE OF HEPATITIS C | |
| UY30392A1 (en) | HEPATITIS C PROTEASE INHIBITING MACROCICLIC OXIMYL COMPOUNDS | |
| DOP2019000218A (en) | INHIBITORS OF MACROCYCLIC PROLINES DERIVED HCV SERINE PROTEASES | |
| ECSP077649A (en) | PIRIDAZINONILOS MACROCICLICOS AS INHIBITORS OF SERINE PROTEASE OF HEPATITIS C | |
| UY30391A1 (en) | HEPATITIS C PROTEASE INHIBITORS ACICLIC OXYM COMPOUND | |
| UY30437A1 (en) | QUINOXALINIL MACROCECLIC INHIBITORS OF SERINE PROTEASE VIRUS OF HEPATITIS C | |
| ECSP10010254A (en) | COMPOUNDS CONTAINING QUINOXALINE AS INHIBITORS OF THE HEPATITIS C VIRUS | |
| CO6571891A2 (en) | Hepatitis C virus inhibitors | |
| CO2020002980A2 (en) | Antiviral agents against hepatitis b. | |
| MX2010010276A (en) | Fluorinated macrocyclic compounds as hepatitis c virus inhibitors. | |
| UY28423A1 (en) | INHIBITORS OF SERINE PROTEASES, IN SPECIAL PROTEASA NS3-NS4A OF HCV.- | |
| ECSP088258A (en) | SERINA PROTEASAS INHIBITORS | |
| MX2010006210A (en) | Fluorinated tripeptide hcv serine protease inhibitors. | |
| MX2010006518A (en) | Macrocyclic oximyl hepatitis c serine protease inhibitors. | |
| MX2010006209A (en) | Quinoxalinyl derivatives. | |
| MX2011012155A (en) | Macrocyclic compounds as hepatitis c virus inhibitors. | |
| MX2010008109A (en) | Difluorinated tripeptides as hcv serine protease inhibitors. | |
| MX2010008108A (en) | Heteroaryl-containing tripeptide hcv serine protease inhibitors. | |
| TH139657A (en) | HCV serine protease inhibitors that provide macro-cyclic proline. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 109 | Application deemed to be withdrawn |
Effective date: 20170627 |