CA2458040A1 - Inhibiteurs de protease antivirale - Google Patents
Inhibiteurs de protease antivirale Download PDFInfo
- Publication number
- CA2458040A1 CA2458040A1 CA002458040A CA2458040A CA2458040A1 CA 2458040 A1 CA2458040 A1 CA 2458040A1 CA 002458040 A CA002458040 A CA 002458040A CA 2458040 A CA2458040 A CA 2458040A CA 2458040 A1 CA2458040 A1 CA 2458040A1
- Authority
- CA
- Canada
- Prior art keywords
- compound according
- phenyl
- mmol
- compound
- alkyl
- 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
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/16—Ring systems of three rings containing carbocyclic rings other than six-membered
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/36—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- AIDS & HIV (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
Abstract
L'invention concerne des composés de la formule (I) où X et Y représentent hydroxy ou H. A' et A'' sont des fonctions amine terminale telles que valinamide ou indanolamine. Z', Z'' et les ( )n groupes adjacents représentent indépendamment alkylaryle. Ces composés sont utiles comme inhibiteurs d'aspartyle sida-protéase ayant une activité particulièrement bonne en présence de sérum humain.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE0102892-7 | 2001-08-29 | ||
SE0102892A SE0102892D0 (sv) | 2001-08-29 | 2001-08-29 | Antivirals I |
PCT/SE2002/001549 WO2003018537A1 (fr) | 2001-08-29 | 2002-08-29 | Inhibiteurs de protease antivirale |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2458040A1 true CA2458040A1 (fr) | 2003-03-06 |
Family
ID=20285183
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002458040A Abandoned CA2458040A1 (fr) | 2001-08-29 | 2002-08-29 | Inhibiteurs de protease antivirale |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1421060A1 (fr) |
JP (1) | JP2005501118A (fr) |
CA (1) | CA2458040A1 (fr) |
IL (1) | IL160626A0 (fr) |
SE (1) | SE0102892D0 (fr) |
WO (1) | WO2003018537A1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014169456A1 (fr) * | 2013-04-18 | 2014-10-23 | 西安力邦医药科技有限责任公司 | Utilisation de 7-a-[9-(4,4,5,5,5-pentafluoro-pentyl-sulfinyl)nonyl]-estra-1,3,5(10)-triène-3,17b-diol et de ses dérivés |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9701245D0 (sv) * | 1997-04-04 | 1997-04-04 | Bjoern Classon | Antivirals |
-
2001
- 2001-08-29 SE SE0102892A patent/SE0102892D0/xx unknown
-
2002
- 2002-08-29 JP JP2003523202A patent/JP2005501118A/ja active Pending
- 2002-08-29 EP EP02763160A patent/EP1421060A1/fr not_active Withdrawn
- 2002-08-29 CA CA002458040A patent/CA2458040A1/fr not_active Abandoned
- 2002-08-29 WO PCT/SE2002/001549 patent/WO2003018537A1/fr not_active Application Discontinuation
- 2002-08-29 IL IL16062602A patent/IL160626A0/xx unknown
Also Published As
Publication number | Publication date |
---|---|
WO2003018537A1 (fr) | 2003-03-06 |
IL160626A0 (en) | 2004-07-25 |
JP2005501118A (ja) | 2005-01-13 |
EP1421060A1 (fr) | 2004-05-26 |
SE0102892D0 (sv) | 2001-08-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4237224B2 (ja) | ノイラミニダーゼ阻害剤r6を調製するためのアジドを含まない方法 | |
AU2200199A (en) | Substituted cyclopentane and cyclopentene compounds useful as neuraminidase inhibitors | |
RU2382029C2 (ru) | Новые производные циклогексана | |
JPH1180156A (ja) | 1−(置換アリール)アルキル−1h−イミダゾピリジン−4−アミン誘導体 | |
MX2015003637A (es) | Piridinonas biciclicas novedosas. | |
WO2008134036A1 (fr) | DÉRIVÉS D'AMIDE PYRIMIDE ARYLMETHYL PYRAZOLO[1,5-α ] À SUBSTITUTION ALPHA | |
AU2022328556A1 (en) | Prodrugs and derivatives of psilocin and uses thereof | |
US9629824B2 (en) | Indole derivatives and process for their preparation | |
NZ505086A (en) | Dipeptide and tripeptide hemiasterlin analogs | |
KR20240031347A (ko) | 아제티디닐 피리미딘 및 그의 용도 | |
JP4068639B2 (ja) | 抗hcv作用を有する化合物およびその製法 | |
CN103265487A (zh) | 截短侧耳素扩环衍生物及其制备方法和用途 | |
CN108558808B (zh) | 一种酰胺类衍生物或其药学上可接受的盐及其制备方法和应用 | |
CA2458040A1 (fr) | Inhibiteurs de protease antivirale | |
US6489364B2 (en) | Antiviral protease inhibitors | |
CA3016086A1 (fr) | Composes inhibiteurs de cyclophilines et leurs utilisations | |
AU2002327997A1 (en) | Antiviral protease inhibitors | |
JP2001501213A (ja) | スワインソニンの新規な3,5,および/または6置換された同族体、それらの製造方法および治療剤としてのそれらの使用 | |
AU2002301207B2 (en) | Antiviral protease inhibitors | |
US20230331667A1 (en) | Process for making a pharmaceutical compound | |
WO2022119928A1 (fr) | Composés d'imidazole en tant qu'inhibiteurs d'enpp1 | |
MXPA99009084A (en) | Antiviral protease inhibitors | |
US20040063696A1 (en) | 1,1-dioxo-2h-1,2-benzothiazine-3-carboxamide derivatives,method for preparing same and pharmaceutical compositions comprising same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued |