AU2001236623A1 - Hydantoin c-proteinase inhibitors - Google Patents
Hydantoin c-proteinase inhibitorsInfo
- Publication number
- AU2001236623A1 AU2001236623A1 AU2001236623A AU3662301A AU2001236623A1 AU 2001236623 A1 AU2001236623 A1 AU 2001236623A1 AU 2001236623 A AU2001236623 A AU 2001236623A AU 3662301 A AU3662301 A AU 3662301A AU 2001236623 A1 AU2001236623 A1 AU 2001236623A1
- Authority
- AU
- Australia
- Prior art keywords
- hydantoin
- proteinase inhibitors
- proteinase
- inhibitors
- 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.)
- Abandoned
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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/76—Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
- C07D233/78—Radicals substituted by oxygen atoms
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/497,946 US6462063B1 (en) | 2000-02-04 | 2000-02-04 | C-proteinase inhibitors |
US09497946 | 2000-02-04 | ||
PCT/US2001/003410 WO2001056996A1 (en) | 2000-02-04 | 2001-02-02 | Hydantoin c-proteinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001236623A1 true AU2001236623A1 (en) | 2001-08-14 |
Family
ID=23978983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001236623A Abandoned AU2001236623A1 (en) | 2000-02-04 | 2001-02-02 | Hydantoin c-proteinase inhibitors |
Country Status (3)
Country | Link |
---|---|
US (1) | US6462063B1 (en) |
AU (1) | AU2001236623A1 (en) |
WO (1) | WO2001056996A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2001261519A1 (en) * | 2000-05-12 | 2001-11-26 | Fibrogen, Inc. | Methods of affecting laminin 5 processing |
JP4711523B2 (en) * | 2001-02-13 | 2011-06-29 | 日本臓器製薬株式会社 | Hypoalbuminemia improving agent |
US7354933B2 (en) | 2003-01-31 | 2008-04-08 | Aventis Pharma Sa | Cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors |
DOP2005000123A (en) | 2004-07-02 | 2011-07-15 | Merck Sharp & Dohme | CETP INHIBITORS |
JP5186384B2 (en) | 2005-12-14 | 2013-04-17 | メディヴィル・アクチボラグ | (2,5-Dioxoimidazolidin-1-yl) -N-hydroxy-acetamide as a metalloproteinase inhibitor |
GB0625283D0 (en) * | 2006-12-19 | 2007-01-24 | Cyclacel Ltd | Combination |
US20090163494A1 (en) * | 2007-12-19 | 2009-06-25 | Pao-Chiung Hong | Protein kinase inhibitors |
WO2009085040A1 (en) * | 2007-12-27 | 2009-07-09 | Dcb-Usa Llc | Protein kinase inhibitors |
AU2009259136B2 (en) | 2008-06-09 | 2014-09-25 | Cyclacel Limited | Combinations of sapacitabine or CNDAC with DNA methyltransferase inhibitors such as decitabine and procaine |
TW201031650A (en) | 2008-12-02 | 2010-09-01 | Organon Nv | 1-(biphenyl-4-ylmethyl)imidazolidine-2,4-dione |
TW201031649A (en) | 2008-12-02 | 2010-09-01 | Organon Nv | 1-(4-(pyridin-2-yl)benzyl)imidazolidine-2,4-dione derivatives |
EP2696878B1 (en) | 2011-04-14 | 2019-07-10 | Cyclacel Limited | Dosage regimen for sapacitabine and decitabine in combination for treating acute myeloid leukemia |
EP2664616A1 (en) * | 2012-05-15 | 2013-11-20 | Vivalis | Hydantoin and thiohydantoin derivatives as antiviral drugs |
CN110143925B (en) * | 2019-06-05 | 2022-10-25 | 山东大学 | Hydantoin hydroxamic acid histone deacetylase 6 subtype selective inhibitor, and preparation method and application thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0640594A1 (en) | 1993-08-23 | 1995-03-01 | Fujirebio Inc. | Hydantoin derivative as metalloprotease inhibitor |
GB9411088D0 (en) | 1994-06-03 | 1994-07-27 | Hoffmann La Roche | Hydroxylamine derivatives |
WO1997005865A1 (en) | 1995-08-08 | 1997-02-20 | Fibrogen, Inc. | C-proteinase inhibitors for the treatment of disorders related to the overproduction of collagen |
BR9807678A (en) | 1997-02-11 | 2000-02-15 | Pfizer | Derivatives of arylsulfonyl hydroxamic acids |
-
2000
- 2000-02-04 US US09/497,946 patent/US6462063B1/en not_active Expired - Lifetime
-
2001
- 2001-02-02 WO PCT/US2001/003410 patent/WO2001056996A1/en active Application Filing
- 2001-02-02 AU AU2001236623A patent/AU2001236623A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US6462063B1 (en) | 2002-10-08 |
WO2001056996A1 (en) | 2001-08-09 |
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