NO20005795L - Antiviral compounds - Google Patents
Antiviral compoundsInfo
- Publication number
- NO20005795L NO20005795L NO20005795A NO20005795A NO20005795L NO 20005795 L NO20005795 L NO 20005795L NO 20005795 A NO20005795 A NO 20005795A NO 20005795 A NO20005795 A NO 20005795A NO 20005795 L NO20005795 L NO 20005795L
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- hydrogen
- halo
- formula
- pyridyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 230000000840 anti-viral effect Effects 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 150000002431 hydrogen Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004076 pyridyl group Chemical group 0.000 abstract 3
- 101100295741 Gallus gallus COR4 gene Chemical group 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 241000710190 Cardiovirus Species 0.000 abstract 1
- 241000709687 Coxsackievirus Species 0.000 abstract 1
- 241001466953 Echovirus Species 0.000 abstract 1
- 241000709661 Enterovirus Species 0.000 abstract 1
- 241000991587 Enterovirus C Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 241000710185 Mengo virus Species 0.000 abstract 1
- 241000709664 Picornaviridae Species 0.000 abstract 1
- 241000700605 Viruses Species 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 208000006454 hepatitis Diseases 0.000 abstract 1
- 231100000283 hepatitis Toxicity 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Gastroenterology & Hepatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Den foreliggende oppfinnelsen vedrører forbindelser med formel (I) Som hemmer veksten av pikornavirus, Hepatitt virus, enterovirus, kardiovirus, poliovirus, coxsackievirus av A og B gruppene, echovirus og Mengo virus. I nevnte formel er A fenyl, pyridyl, substituert fenyl, substituert pyridyl eller benzyl; R er hydrogen, COR4, eller COCF3; X er N-OH, O eller CHR1; R1 er hydrogen, halo, CN, C,-Q alkyl, -C=CH, CO(Ci-C» alkyl), CO2(C,-C4 alkyl) eller CONR2R3; R2 og R3 er uavhengig av hverandre hydrogen eller Q-C4 alkyl; A' er hydrogen, halo, Cj-Ce alkyl, benzyl, naftyl, tienyl, furyl, pyridyl, pyrollyl, COR4, S(O)nR4, eller en gruppe med formel (II) (RS)m R6 (10 R4 er Ci-C6 alkyl, fenyl eller substituert fenyl; n er O, l eller 2; R5 er uavhengig av hver forekomst hydrogen eller halo; m er l, 2, 3 eller 4; og R6 er hydrogen, halo, CF3, OH, CO2H, NH2, N02, CONHOCHj, C,-C4 alkyl, eller CO2(Ci-C4 alkyl), C,-C4 alkoksy; eller farmasøytisk akseptable salter derav.The present invention relates to compounds of formula (I) which inhibit the growth of picornavirus, hepatitis virus, enterovirus, cardiovirus, poliovirus, coxsackie virus of the A and B groups, echovirus and Mengo virus. In said formula, A is phenyl, pyridyl, substituted phenyl, substituted pyridyl or benzyl; R is hydrogen, COR4, or COCF3; X is N-OH, O or CHR 1; R 1 is hydrogen, halo, CN, C 1 -Q alkyl, -C = CH, CO (C 1 -C 4 alkyl), CO 2 (C 1 -C 4 alkyl) or CONR 2 R 3; R 2 and R 3 are independently hydrogen or C 1 -C 4 alkyl; A 'is hydrogen, halo, C1-C6 alkyl, benzyl, naphthyl, thienyl, furyl, pyridyl, pyrollyl, COR4, S (O) nR4, or a group of formula (II) (RS) m R6 (R4 is C1 -C6 alkyl, phenyl or substituted phenyl; n is 0, 1 or 2; R5 is independently hydrogen or halo; m is 1, 2, 3 or 4; and R6 is hydrogen, halo, CF3, OH, CO2H, NH 2, NO 2, CONHOCH 2, C 1 -C 4 alkyl, or CO 2 (C 1 -C 4 alkyl), C 1 -C 4 alkoxy, or pharmaceutically acceptable salts thereof.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US1998/010299 WO1999059587A1 (en) | 1998-05-20 | 1998-05-20 | Anti-viral compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO20005795D0 NO20005795D0 (en) | 2000-11-16 |
| NO20005795L true NO20005795L (en) | 2001-01-18 |
Family
ID=22267098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20005795A NO20005795L (en) | 1998-05-20 | 2000-11-16 | Antiviral compounds |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP1077701A4 (en) |
| JP (1) | JP2002515433A (en) |
| KR (1) | KR20010025055A (en) |
| CN (1) | CN1292697A (en) |
| AU (1) | AU7583098A (en) |
| BR (1) | BR9815899A (en) |
| CA (1) | CA2332403A1 (en) |
| CZ (1) | CZ289425B6 (en) |
| EA (1) | EA200001208A1 (en) |
| HU (1) | HUP0102117A2 (en) |
| IL (1) | IL139166A0 (en) |
| NO (1) | NO20005795L (en) |
| SK (1) | SK17482000A3 (en) |
| TR (1) | TR200003414T2 (en) |
| WO (1) | WO1999059587A1 (en) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AUPR213700A0 (en) | 2000-12-18 | 2001-01-25 | Biota Scientific Management Pty Ltd | Antiviral agents |
| AR048650A1 (en) * | 2004-05-04 | 2006-05-10 | Tibotec Pharm Ltd | DERIVATIVES OF (1,10B-DIHIDRO-2- (AMINOCARBONIL-PHENYL) -5H-PIRAZOLO [1,5 C] [1,3] BENZOXAZIN-5-IL) METHANONE PHENYL AS INHIBITORS OF HIV VIRAL REPLICATION |
| ES2343640T3 (en) | 2004-08-12 | 2010-08-05 | Amgen Inc. | BISARIL-SULFONAMIDS. |
| US7666880B2 (en) | 2005-03-21 | 2010-02-23 | S*Bio Pte Ltd. | Imidazo[1,2-A]pyridine derivatives: preparation and pharmaceutical applications |
| MX2007011710A (en) * | 2005-03-21 | 2007-11-20 | S Bio Pte Ltd | Imidazo[1,2-a]pyridine derivatives: preparation and pharmaceutical applications. |
| US7910595B2 (en) | 2005-12-21 | 2011-03-22 | Abbott Laboratories | Anti-viral compounds |
| US7915411B2 (en) | 2005-12-21 | 2011-03-29 | Abbott Laboratories | Anti-viral compounds |
| CN102702194A (en) | 2005-12-21 | 2012-10-03 | 雅培制药有限公司 | Anti-viral compounds |
| US8236950B2 (en) | 2006-12-20 | 2012-08-07 | Abbott Laboratories | Anti-viral compounds |
| MX2010013019A (en) * | 2008-05-27 | 2011-03-21 | Biota Scient Management Pty Ltd | Antiviral salts. |
| WO2010075380A1 (en) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Anti-viral compounds |
| WO2010075376A2 (en) | 2008-12-23 | 2010-07-01 | Abbott Laboratories | Anti-viral compounds |
| EP2419404B1 (en) * | 2009-04-15 | 2015-11-04 | AbbVie Inc. | Anti-viral compounds |
| WO2014060381A1 (en) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclic compounds as pesticides |
| CN104884449A (en) | 2012-10-31 | 2015-09-02 | 拜尔农作物科学股份公司 | Novel heterocyclic compounds as pest control agents |
| CN104370732B (en) * | 2014-01-26 | 2015-08-19 | 山东信立泰药业有限公司 | The preparation method of a kind of clopidogrel and intermediate thereof |
| CN109535405B (en) * | 2017-09-21 | 2021-07-30 | 宁波聚嘉新材料科技有限公司 | A kind of preparation method of polyarylate based on 2-(4-carboxyphenyl)-5-hydroxypyridoimidazole |
| CN109810085B (en) * | 2019-04-19 | 2019-07-19 | 上海皓元生物医药科技有限公司 | The preparation method of ACC inhibitor and its intermediate |
| CN110746450A (en) * | 2019-09-17 | 2020-02-04 | 济南康和医药科技有限公司 | Synthetic method of beraprost sodium key intermediate |
| CN117902992A (en) * | 2024-01-04 | 2024-04-19 | 浙江永太科技股份有限公司 | A preparation method of 2,4-difluorophenylglycine |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4096264A (en) * | 1975-12-09 | 1978-06-20 | Merck & Co., Inc. | Certain substituted imidazo [1,2-a] pyridines |
| US4250174A (en) * | 1979-05-02 | 1981-02-10 | Merck & Co., Inc. | 3-Substituted imidazo [1,2-A] pyridines |
| US5693661A (en) * | 1995-06-07 | 1997-12-02 | Eli Lilly And Company | Anti-viral compounds |
| US5891874A (en) * | 1996-06-05 | 1999-04-06 | Eli Lilly And Company | Anti-viral compound |
| JP2000511899A (en) * | 1996-06-05 | 2000-09-12 | イーライ・リリー・アンド・カンパニー | Anti-viral compounds |
| US5821242A (en) * | 1996-06-06 | 1998-10-13 | Eli Lilly And Company | Anti-viral compounds |
-
1998
- 1998-05-20 KR KR1020007012999A patent/KR20010025055A/en not_active Withdrawn
- 1998-05-20 BR BR9815899-6A patent/BR9815899A/en not_active IP Right Cessation
- 1998-05-20 JP JP2000549252A patent/JP2002515433A/en not_active Withdrawn
- 1998-05-20 WO PCT/US1998/010299 patent/WO1999059587A1/en not_active Ceased
- 1998-05-20 HU HU0102117A patent/HUP0102117A2/en unknown
- 1998-05-20 IL IL13916698A patent/IL139166A0/en unknown
- 1998-05-20 SK SK1748-2000A patent/SK17482000A3/en unknown
- 1998-05-20 EA EA200001208A patent/EA200001208A1/en unknown
- 1998-05-20 CN CN988140519A patent/CN1292697A/en active Pending
- 1998-05-20 CZ CZ20004278A patent/CZ289425B6/en unknown
- 1998-05-20 CA CA002332403A patent/CA2332403A1/en not_active Abandoned
- 1998-05-20 TR TR2000/03414T patent/TR200003414T2/en unknown
- 1998-05-20 EP EP98923565A patent/EP1077701A4/en not_active Withdrawn
- 1998-05-20 AU AU75830/98A patent/AU7583098A/en not_active Abandoned
-
2000
- 2000-11-16 NO NO20005795A patent/NO20005795L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002515433A (en) | 2002-05-28 |
| CA2332403A1 (en) | 1999-11-25 |
| IL139166A0 (en) | 2001-11-25 |
| KR20010025055A (en) | 2001-03-26 |
| EP1077701A1 (en) | 2001-02-28 |
| HUP0102117A2 (en) | 2001-12-28 |
| CZ20004278A3 (en) | 2001-05-16 |
| CN1292697A (en) | 2001-04-25 |
| NO20005795D0 (en) | 2000-11-16 |
| TR200003414T2 (en) | 2001-03-21 |
| AU7583098A (en) | 1999-12-06 |
| EA200001208A1 (en) | 2001-06-25 |
| BR9815899A (en) | 2001-02-20 |
| EP1077701A4 (en) | 2002-03-20 |
| CZ289425B6 (en) | 2002-01-16 |
| SK17482000A3 (en) | 2005-03-04 |
| WO1999059587A1 (en) | 1999-11-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |