ES2130269T3 - Oximas sustituidas con piridina, pirrolidina y azepina utiles como agentes contra la aterosclerosis y antihipercolesterolemicos. - Google Patents
Oximas sustituidas con piridina, pirrolidina y azepina utiles como agentes contra la aterosclerosis y antihipercolesterolemicos.Info
- Publication number
- ES2130269T3 ES2130269T3 ES93912362T ES93912362T ES2130269T3 ES 2130269 T3 ES2130269 T3 ES 2130269T3 ES 93912362 T ES93912362 T ES 93912362T ES 93912362 T ES93912362 T ES 93912362T ES 2130269 T3 ES2130269 T3 ES 2130269T3
- Authority
- ES
- Spain
- Prior art keywords
- hypercholesterolemics
- pirrolidine
- piridine
- azepine
- useful
- 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.)
- Expired - Lifetime
Links
- 201000001320 Atherosclerosis Diseases 0.000 title abstract 2
- 150000002923 oximes Chemical class 0.000 title abstract 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 title 2
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 title 1
- 208000035150 Hypercholesterolemia Diseases 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Urology & Nephrology (AREA)
- Pharmacology & Pharmacy (AREA)
- Vascular Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Steroid Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
OXIMAS SUSTITUIDAS DE IMIDAZOPIRIDINO-, PIRAZOLOPIRIDINO-, PIRAZOLAPIRRALIDINO Y PIROZOLOAZEPINO, TENIENDO FORMULAS (I), (II), (III), (IV), (V), EN LAS QUE R1, R2, R3, R4, R5 Y A SON CONFORME SE DESCRIBEN EN LAS REIVINDICACIONES. ESTOS COMPUESTOS SON UTILES EN EL TRATAMIENETO DE LA ATEROESCLEROSIS Y LA HIPERCOLESTEROLEMIA.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90022992A | 1992-06-17 | 1992-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2130269T3 true ES2130269T3 (es) | 1999-07-01 |
Family
ID=25412199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES93912362T Expired - Lifetime ES2130269T3 (es) | 1992-06-17 | 1993-05-05 | Oximas sustituidas con piridina, pirrolidina y azepina utiles como agentes contra la aterosclerosis y antihipercolesterolemicos. |
Country Status (13)
Country | Link |
---|---|
US (3) | US5565468A (es) |
EP (1) | EP0649425B1 (es) |
JP (1) | JPH07507796A (es) |
CN (1) | CN1081678A (es) |
AT (1) | ATE177426T1 (es) |
AU (1) | AU4293393A (es) |
DE (1) | DE69323883T2 (es) |
DK (1) | DK0649425T3 (es) |
ES (1) | ES2130269T3 (es) |
GR (1) | GR3029946T3 (es) |
IL (1) | IL105693A0 (es) |
MX (1) | MX9303594A (es) |
WO (1) | WO1993025553A1 (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI312347B (en) | 2001-02-08 | 2009-07-21 | Eisai R&D Man Co Ltd | Bicyclic nitrogen-containing condensed ring compounds |
KR100881647B1 (ko) * | 2001-04-27 | 2009-02-04 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 피라졸로[1,5-a]피리딘 화합물 및 그 의약 |
PL221339B1 (pl) * | 2001-05-24 | 2016-03-31 | Lilly Co Eli | Nowe pochodne pirolu jako środki farmaceutyczne |
US7176216B2 (en) * | 2002-10-22 | 2007-02-13 | Eisai Co., Ltd. | 7-phenylpyrazolopyridine compounds |
ATE426600T1 (de) * | 2002-10-22 | 2009-04-15 | Eisai R&D Man Co Ltd | 7-phenylpyrazolopyridinverbindungen |
WO2007008529A2 (en) * | 2005-07-08 | 2007-01-18 | Kalypsys, Inc | Celullar cholesterol absorption modifiers |
US7501438B2 (en) | 2006-07-07 | 2009-03-10 | Forest Laboratories Holdings Limited | Pyridoimidazole derivatives |
AU2008273050A1 (en) * | 2007-07-11 | 2009-01-15 | Auckland Uniservices Limited | Pyrazolo[1,5-a]pyridines and their use in cancer therapy |
NZ588376A (en) * | 2008-04-15 | 2011-06-30 | Eisai R&D Man Co Ltd | 3-phenylpyrazolo[5,1-b]thiazole compound having antagonism against corticotropin-releasing factor (CRF) receptor |
AR078521A1 (es) * | 2009-10-08 | 2011-11-16 | Eisai R&D Man Co Ltd | Compuesto pirazolotiazol |
EP2487177A1 (en) * | 2009-10-08 | 2012-08-15 | Eisai R&D Management Co., Ltd. | Pyrazoloxazole compound |
TW201613860A (en) | 2014-02-13 | 2016-04-16 | Incyte Corp | Cyclopropylamines as LSD1 inhibitors |
MX2016010395A (es) | 2014-02-13 | 2017-02-28 | Incyte Corp | Ciclopropilamina como inhibidor de la desmetilasa 1 especifica de lisinas (lsd1). |
EP3626714A1 (en) | 2014-02-13 | 2020-03-25 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
CN103980281B (zh) * | 2014-05-27 | 2016-06-08 | 天津市斯芬克司药物研发有限公司 | 一种咪唑吡嗪化合物及其制备方法 |
TWI687419B (zh) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | 作為lsd1抑制劑之咪唑并吡啶及咪唑并吡嗪 |
US9695180B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors |
US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
TWI714567B (zh) | 2015-04-03 | 2021-01-01 | 美商英塞特公司 | 作為lsd1抑制劑之雜環化合物 |
UA126277C2 (uk) | 2015-08-12 | 2022-09-14 | Інсайт Корпорейшн | Солі інгібітору lsd1 |
EP3445339B1 (en) | 2016-04-22 | 2023-08-23 | Incyte Corporation | Formulations of an lsd1 inhibitor |
US10968200B2 (en) | 2018-08-31 | 2021-04-06 | Incyte Corporation | Salts of an LSD1 inhibitor and processes for preparing the same |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1600969A (en) * | 1977-01-07 | 1981-10-21 | Acf Chemiefarma Nv | Heterocyclic compounds |
US4352804A (en) * | 1978-07-25 | 1982-10-05 | Acf Chemiefarma Nv | Oxime ethers, their preparation and pharmaceutical compositions containing them |
US4925849A (en) * | 1987-06-15 | 1990-05-15 | Fujisawa Pharmaceutical Company, Ltd. | Pharmaceutically useful pyrazolopyridines |
-
1993
- 1993-05-05 AU AU42933/93A patent/AU4293393A/en not_active Abandoned
- 1993-05-05 AT AT93912362T patent/ATE177426T1/de not_active IP Right Cessation
- 1993-05-05 JP JP6501458A patent/JPH07507796A/ja active Pending
- 1993-05-05 EP EP93912362A patent/EP0649425B1/en not_active Expired - Lifetime
- 1993-05-05 DE DE69323883T patent/DE69323883T2/de not_active Expired - Fee Related
- 1993-05-05 ES ES93912362T patent/ES2130269T3/es not_active Expired - Lifetime
- 1993-05-05 DK DK93912362T patent/DK0649425T3/da active
- 1993-05-05 WO PCT/US1993/004059 patent/WO1993025553A1/en active IP Right Grant
- 1993-05-13 IL IL105693A patent/IL105693A0/xx unknown
- 1993-06-16 MX MX9303594A patent/MX9303594A/es unknown
- 1993-06-17 CN CN93107183A patent/CN1081678A/zh active Pending
-
1994
- 1994-09-27 US US08/313,684 patent/US5565468A/en not_active Expired - Fee Related
-
1995
- 1995-06-06 US US08/466,181 patent/US5523318A/en not_active Expired - Fee Related
- 1995-06-06 US US08/468,158 patent/US5597816A/en not_active Expired - Fee Related
-
1999
- 1999-04-13 GR GR990401036T patent/GR3029946T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
WO1993025553A1 (en) | 1993-12-23 |
DE69323883D1 (de) | 1999-04-15 |
MX9303594A (es) | 1994-01-31 |
DE69323883T2 (de) | 1999-07-22 |
EP0649425B1 (en) | 1999-03-10 |
GR3029946T3 (en) | 1999-07-30 |
IL105693A0 (en) | 1993-09-22 |
US5597816A (en) | 1997-01-28 |
US5523318A (en) | 1996-06-04 |
ATE177426T1 (de) | 1999-03-15 |
CN1081678A (zh) | 1994-02-09 |
AU4293393A (en) | 1994-01-04 |
JPH07507796A (ja) | 1995-08-31 |
DK0649425T3 (da) | 1999-09-27 |
EP0649425A1 (en) | 1995-04-26 |
US5565468A (en) | 1996-10-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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