CO5011072A1 - Etanolaminas pirazinil substituidas como agfonistas de los receptores - Google Patents
Etanolaminas pirazinil substituidas como agfonistas de los receptoresInfo
- Publication number
- CO5011072A1 CO5011072A1 CO98071198A CO98071198A CO5011072A1 CO 5011072 A1 CO5011072 A1 CO 5011072A1 CO 98071198 A CO98071198 A CO 98071198A CO 98071198 A CO98071198 A CO 98071198A CO 5011072 A1 CO5011072 A1 CO 5011072A1
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- aryl
- optionally substituted
- heterocycle
- hydrogen
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000003107 substituted aryl group Chemical group 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 101150003374 sor2 gene Proteins 0.000 abstract 1
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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
- C07D231/18—One oxygen or sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
en donde:X1 es -OCH2 -, -SCH2 -, ó un enlace;R1 es un heterociclo de la fórmula:R2 y R3 son independientemente hidrógeno, alquil C1 -C4 , ó aril;R4 es un heterociclo opcionalmente sustituido ó una mitad seleccionada del grupo conformado por:X2 es un enlace, ó un alquileno de 1 a 5 carbonos de cadena recta o ramificada;R5 es hidrógeno ó alquil C1 -C4 ;R6 es hidrógeno ó alquil C1 -C4 ;ó R5 y R6 combinados con el carbono al cual van ligados forman un cicloalquil C3 -C6 ;ó R6 combinado con X2 y el carbono al cual van ligados forman un cicloalquil C3 -C8 ; - 2 -ó R6 se combina con X2 , R4 , y el carbono al cual van ligados, para formar:a condición de que R5 sea hidrógeno;R7 es hidrógeno, hidroxi, ciano, oxo, COn R2 , CONHR2 , alquil C1 -C4 , alcoxi C1 -C4 , haloalquil C1 -C4 , alquil C1 -C4 opcionalmente sustituido, (CH2 )n aril, (CH2 )n heterociclo, (CH2 )n aril opcionalmente sustituido, ó (CH2 )n heterocicloopcionalmente sustituido;R8 es independientemente hidrógeno, halo, ó alquil C1 -C4 ;R9 es halo, CN, OR10 , alquil C1 -C4 , haloalquil C1 -C4 , CO2 R2 , CONR11 R12 , CONH(alquil C1 -C4 ó alcoxi C1 -C4 ), SR2 , CSNHR2 , CSNR11 R12 , SO2 R2 ,SOR2 , NR11 R12 , aril opcionalmente sustituido, heterociclo opcionalmente sustituido, ó alquenil C2 -C4 sustituido con CN, CO2 R2 , ó CONR11 R12 ;R10 es alquil C1 -C4 , haloalquil C1 -C4 , (CH2 )n -cicloalquil C3 -C8 , (CH2 )n aril, (CH2 )n heterociclo, (CH2 )n cicloalquil C3 -C8 opcionalmente sustituido, (CH2 )n aril opcionalmente sustituido, ó (CH2 )n heterociclo opcionalmente sustituido;R11 y R12 son independientemente hidrógeno, alquil C1 -C4 , aril, (CH2 )n aril, ó combinados con el nitrógeno al cual cada uno van ligados forman un anillo morfolinil, piperidinil, pirrolidinil, ó piperazinil;R13 es hidrógeno, halo, aril, ó alquil C1 -C4 ;m es 0 ó 1 ;n es 0, 1, 2, ó 3;ó una sal farmacéuticamente aceptable de éste.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6759997P | 1997-12-05 | 1997-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5011072A1 true CO5011072A1 (es) | 2001-02-28 |
Family
ID=22077113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO98071198A CO5011072A1 (es) | 1997-12-05 | 1998-12-01 | Etanolaminas pirazinil substituidas como agfonistas de los receptores |
Country Status (11)
Country | Link |
---|---|
US (2) | US6046227A (es) |
EP (1) | EP0921120A1 (es) |
JP (1) | JP2001525399A (es) |
AR (1) | AR017798A1 (es) |
AU (1) | AU1628199A (es) |
CA (1) | CA2312987A1 (es) |
CO (1) | CO5011072A1 (es) |
PE (1) | PE132699A1 (es) |
SV (1) | SV1998000142A (es) |
WO (1) | WO1999029673A1 (es) |
ZA (1) | ZA9811026B (es) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6133409A (en) * | 1996-12-19 | 2000-10-17 | Aventis Pharmaceuticals Products Inc. | Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds |
US6392010B1 (en) | 1996-12-19 | 2002-05-21 | Aventis Pharmaceuticals Inc. | Process for the solid phase synthesis of aldehyde, ketone, oxime, amine, hydroxamic acid and αβ-unsaturated carboxylic acid and aldehyde compounds |
CO5011072A1 (es) * | 1997-12-05 | 2001-02-28 | Lilly Co Eli | Etanolaminas pirazinil substituidas como agfonistas de los receptores |
AU1572701A (en) * | 1999-11-15 | 2001-05-30 | Eli Lilly And Company | Treating wasting syndromes with aryloxy propanolamines |
JP2003514801A (ja) | 1999-11-15 | 2003-04-22 | イーライ・リリー・アンド・カンパニー | 家畜の生産を改善するためのインダゾリルオキシプロパノールアミン |
US6841563B1 (en) * | 1999-11-15 | 2005-01-11 | Eli Lilly And Company | Aryloxy propanolamines for improving livestock production |
BR0015578A (pt) * | 1999-11-15 | 2002-07-09 | Lilly Co Eli | Arilóxi propanolaminas para melhorar a produção de rebanhos |
WO2001036412A1 (en) * | 1999-11-15 | 2001-05-25 | Eli Lilly And Company | Process for the preparation of aryloxy propanolamines |
KR100816527B1 (ko) * | 2001-09-12 | 2008-04-10 | 한국화학연구원 | 페닐테트라졸 유도체로 치환된 β-아미노알코올 화합물 |
HRP20050253B1 (hr) * | 2002-09-19 | 2013-11-08 | Eli Lilly And Company | Diaril eteri kao opioid antagonisti opioidnih receptora |
CA2662766C (en) | 2006-09-08 | 2011-08-09 | Pfizer Products Inc. | Diaryl ether derivatives and uses thereof |
JP5886121B2 (ja) * | 2011-07-01 | 2016-03-16 | 花王株式会社 | メラニン生成抑制剤 |
RU2014111079A (ru) * | 2011-08-25 | 2015-09-27 | Когнишн Терапьютикс, Инк. | Композиции и способы для лечения нейродегенеративного заболевания |
WO2015025960A1 (ja) * | 2013-08-23 | 2015-02-26 | 石原産業株式会社 | 有害生物防除剤 |
ES2915833T3 (es) | 2014-01-31 | 2022-06-27 | Cognition Therapeutics Inc | Composiciones de isoindolina y métodos para tratar una enfermedad neurodegenerativa y una degeneración macular |
US10626096B2 (en) | 2015-11-24 | 2020-04-21 | Sanford Burnham Prebys Medical Discovery Institute | Azole derivatives as apelin receptor agonist |
CN105837500A (zh) * | 2016-03-31 | 2016-08-10 | 常州大学 | 一种n-(2-(3-(三氟甲基)苯氧基)-4-吡啶基)甲亚胺的合成方法 |
KR102614814B1 (ko) | 2017-05-15 | 2023-12-20 | 카그니션 테라퓨틱스, 인코퍼레이티드 | 신경변성 질환 치료용 조성물 |
US10865163B2 (en) | 2017-12-20 | 2020-12-15 | The University Of Toledo | Carbon dioxide as a directing group for C—H functionalization reactions involving Lewis basic amines, alcohols, thiols, and phosphines for the synthesis of compounds |
Family Cites Families (86)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE379196B (es) * | 1971-06-24 | 1975-09-29 | Sandoz Ag | |
DE2815926A1 (de) * | 1978-04-13 | 1979-10-18 | Boehringer Mannheim Gmbh | Neue carbazolyl-(4)-oxy-propanolamin-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
CA1001161A (en) * | 1972-05-05 | 1976-12-07 | Burton K. Wasson | 5-(3-substituted amino-2-hydroxypropoxy)1,3-disubstituted pyrazoles and method of preparation |
JPS5310974B2 (es) * | 1974-06-10 | 1978-04-18 | ||
CH624395A5 (es) * | 1976-01-08 | 1981-07-31 | Ciba Geigy Ag | |
DE2609645A1 (de) * | 1976-03-09 | 1977-09-15 | Boehringer Sohn Ingelheim | Aminoalkylheterocyclen |
DE2645710C2 (de) * | 1976-10-09 | 1985-06-27 | Merck Patent Gmbh, 6100 Darmstadt | Phenoxy-amino-propanole, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitung |
US4235919A (en) * | 1977-07-21 | 1980-11-25 | Sandoz Ltd. | 1-(Indol-4-yloxy)-3-(2-substituted amino)-2-propanols and pharmaceutical use thereof |
CA1108619A (en) * | 1977-08-12 | 1981-09-08 | Carl H. Ross | 4-hydroxy-2-benzimidazolinone derivatives and the preparation thereof |
DE2805404A1 (de) * | 1978-02-09 | 1979-08-16 | Merck Patent Gmbh | 1-aryloxy-3-nitratoalkylamino-2-propanole und verfahren zu ihrer herstellung |
DE2965655D1 (en) * | 1978-06-28 | 1983-07-21 | Beecham Group Plc | Secondary amines, their preparation, pharmaceutical compositions containing them and their use |
US4391826A (en) * | 1978-07-03 | 1983-07-05 | Eli Lilly And Company | Phenethanolamines, compositions containing the same, and method for effecting weight control |
CH636856A5 (en) * | 1978-07-17 | 1983-06-30 | Sandoz Ag | 4-(3-Aminopropoxy)indole derivatives, their preparation and medicines containing them |
US4751246A (en) * | 1978-08-30 | 1988-06-14 | Sterling Drug Inc. | Compositions and method |
DE2905877A1 (de) * | 1979-02-16 | 1980-08-28 | Boehringer Mannheim Gmbh | Neue aminopropanolderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
DD150456A5 (de) * | 1979-03-01 | 1981-09-02 | Ciba Geigy Ag | Verfahren zur herstellung von derivaten des 3-amino-1,2-propandiols |
DE3061334D1 (en) * | 1979-06-16 | 1983-01-20 | Beecham Group Plc | Ethanamine derivatives, their preparation and use in pharmaceutical compositions |
ATE1899T1 (de) * | 1979-06-16 | 1982-12-15 | Beecham Group Plc | Sekundaere amine, ihre herstellung und verwendung in pharmazeutischen zusammensetzungen. |
DE3062216D1 (en) * | 1979-09-06 | 1983-04-07 | Beecham Group Plc | Cinnamic acid derivatives, their preparation, and pharmaceutical compositions containing them |
EP0040000B1 (en) * | 1980-05-08 | 1983-10-12 | Beecham Group Plc | Arylethanolamine derivatives, their preparation and use in pharmaceutical compositions |
EP0040915B1 (en) * | 1980-05-22 | 1984-03-21 | Beecham Group Plc | Arylethanolamine derivatives, their preparation and use in pharmaceutical compositions |
CA1175851A (en) * | 1980-09-26 | 1984-10-09 | Beecham Group Limited | Secondary amines |
DE3169094D1 (en) * | 1980-11-20 | 1985-03-28 | Beecham Group Plc | Secondary amines |
DE3264364D1 (en) * | 1981-03-06 | 1985-08-01 | Beecham Group Plc | Arylethanol amine derivatives, their preparation and use in pharmaceutical compositions |
DE3260490D1 (en) * | 1981-03-31 | 1984-09-06 | Beecham Group Plc | Secondary amines, their preparation, pharmaceutical compositions containing them and their use |
EP0063004A1 (en) * | 1981-04-09 | 1982-10-20 | Beecham Group Plc | Secondary amines, processes for their preparation, and pharmaceutical compositions containing them |
EP0068669A1 (en) * | 1981-06-20 | 1983-01-05 | Beecham Group Plc | Secondary phenylethanol amines, processes for their preparation and their pharmaceutical application |
EP0070134B1 (en) * | 1981-07-11 | 1985-11-13 | Beecham Group Plc | Secondary phenyl ethanol amines and their pharmaceutical use |
IE54220B1 (en) * | 1981-12-23 | 1989-07-19 | Ici Plc | Phenol esters |
EP0089154A3 (en) * | 1982-03-12 | 1984-08-08 | Beecham Group Plc | Ethanolamine derivatives, their preparation and use in pharmaceutical compositions |
FR2523965B1 (fr) * | 1982-03-24 | 1985-09-27 | Bellon Labor Sa Roger | (benzimidazolyl-1)-1, n-((hydroxy-4 methoxy-3 phenyl)-2 hydroxy-2 ethyl) amino-3 butane et ses sels a activite b-adrenergique, leurs applications therapeutiques, et procede pour les preparer |
EP0095827B1 (en) * | 1982-04-08 | 1985-07-24 | Beecham Group Plc | N-substituted derivatives of ethanol amine |
EP0091749A3 (en) * | 1982-04-08 | 1984-12-05 | Beecham Group Plc | Ethanolamine derivatives, process for their preparation and pharmaceutical compositions containing them |
CA1219865A (en) * | 1982-05-14 | 1987-03-31 | Leo Alig | Aziridine phenethanolamine derivatives |
DE3368258D1 (en) * | 1982-07-16 | 1987-01-22 | Beecham Group Plc | 2-aminoethyl ether derivatives, processes for their preparation and pharmaceutical compositions containing them |
EP0102213A1 (en) | 1982-08-21 | 1984-03-07 | Beecham Group Plc | Ethanolamine derivatives, pharmaceutical compositions containing them, and processes for preparing them |
DE3319027A1 (de) * | 1983-05-26 | 1984-11-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur herstellung von optisch aktiven carbazol-derivaten, neue r- und s-carbazol-derivate, sowie arzneimittel, die diese verbindungen enthalten |
US5166218A (en) * | 1983-10-19 | 1992-11-24 | Hoffmann-La Roche Inc. | Phenoxypropanolamines and pharmaceutical compositions thereof |
CA1262729A (en) * | 1983-10-19 | 1989-11-07 | Leo Alig | Phenoxypropanolamines |
GB8419797D0 (en) * | 1984-08-03 | 1984-09-05 | Beecham Group Plc | Compounds |
GB8507942D0 (en) * | 1985-03-27 | 1985-05-01 | Beecham Group Plc | Compounds |
IL79323A (en) * | 1985-07-10 | 1990-03-19 | Sanofi Sa | Phenylethanolaminotetralines,their preparation and pharmaceutical compositions containing them |
GB8519154D0 (en) * | 1985-07-30 | 1985-09-04 | Ici Plc | Aromatic ethers |
GB8528633D0 (en) * | 1985-11-21 | 1985-12-24 | Beecham Group Plc | Compounds |
GB8714901D0 (en) * | 1986-07-23 | 1987-07-29 | Ici Plc | Amide derivatives |
EP0300290B1 (de) * | 1987-07-21 | 1991-12-18 | F. Hoffmann-La Roche Ag | Phenoxypropanolamine |
DE3800096A1 (de) * | 1988-01-05 | 1989-07-13 | Bayer Ag | Verwendung von benzimidazolderivaten als leistungsfoerderer |
GB8801306D0 (en) * | 1988-01-21 | 1988-02-17 | Ici Plc | Chemical compounds |
US5013761A (en) * | 1988-06-03 | 1991-05-07 | Eli Lilly And Company | Serotonin antagonists |
ATE117980T1 (de) * | 1988-06-03 | 1995-02-15 | Lilly Co Eli | Serotonin-antagonisten. |
IT1226726B (it) * | 1988-07-29 | 1991-02-05 | Zambon Spa | Composti attivi come inibitori della biosintesi del colesterolo. |
US5254595A (en) * | 1988-12-23 | 1993-10-19 | Elf Sanofi | Aryloxypropanolaminotetralins, a process for their preparation and pharmaceutical compositions containing them |
GB8905336D0 (en) * | 1989-03-08 | 1989-04-19 | Ici Plc | Chemical compounds |
DE4040186A1 (de) * | 1989-12-20 | 1991-06-27 | Hoechst Ag | Hypoglykaemisch aktive propandiolaminderivate mit insulin-aehnlicher wirkung und deren verwendung, neue propandiolaminderivate, diese substanzen enthaltende pharmazeutische zubereitungen und ihre verwendung zur behandlung von krankheiten |
IE65511B1 (en) * | 1989-12-29 | 1995-11-01 | Sanofi Sa | New phenylethanolaminomethyltetralins |
US5360811A (en) * | 1990-03-13 | 1994-11-01 | Hoechst-Roussel Pharmaceuticals Incorporated | 1-alkyl-, 1-alkenyl-, and 1-alkynylaryl-2-amino-1,3-propanediols and related compounds as anti-inflammatory agents |
US5061727A (en) * | 1990-05-04 | 1991-10-29 | American Cyanamid Company | Substituted 5-(2-((2-aryl-2-hydroxyethyl)amino)propyl)-1,3-benzodioxoles |
EP0499755A1 (fr) * | 1991-02-18 | 1992-08-26 | MIDY S.p.A. | Nouvelles phényléthanolaminotétralines, procédé pour leur préparation, intermédiaires dans ce procédé et compositions pharmaceutiques les contenant |
GB9107827D0 (en) * | 1991-04-12 | 1991-05-29 | Fujisawa Pharmaceutical Co | New ethanolamine derivatives,processes for the preparation thereof and pharmaceutical composition comprising the same |
GB9207964D0 (en) * | 1992-04-10 | 1992-05-27 | Ici Plc | Chemical compounds |
GB9209076D0 (en) * | 1992-04-27 | 1992-06-10 | Ici Plc | Chemical compounds |
GB9215844D0 (en) * | 1992-07-25 | 1992-09-09 | Smithkline Beecham Plc | Novel compounds |
WO1994003425A2 (en) * | 1992-07-31 | 1994-02-17 | Syntex (U.S.A.) Inc. | Carbostyril derivatives for the treatment of arrhythmia |
US5451677A (en) * | 1993-02-09 | 1995-09-19 | Merck & Co., Inc. | Substituted phenyl sulfonamides as selective β 3 agonists for the treatment of diabetes and obesity |
US5321036A (en) * | 1993-02-10 | 1994-06-14 | Bristol-Myers Squibb Company | Thiazole and oxazole-based β3 adrenergic receptor agonists |
US5308862A (en) * | 1993-03-05 | 1994-05-03 | Boehringer Mannheim Pharmaceuticals Corporation - Smithkline Beecham Corp., Ltd. Partnership No. 1 | Use of, and method of treatment using, carbazolyl-(4)-oxypropanolamine compounds for inhibition of smooth muscle cell proliferation |
EP0627407A1 (fr) * | 1993-05-28 | 1994-12-07 | MIDY S.p.A. | Acide (7S)-7-[(2R)-2(3-chlorophényl)-2-hydroxyéthylamino]-5,6,7,8-tétrahydronaphtalèn-2-yloxy acétique, ses sels pharmaceutiquement acceptables, à action agoniste bêta-3 adrénergique et compositions pharmaceutiques le contenant |
CA2164009A1 (en) * | 1993-06-14 | 1994-12-22 | Robert L. Dow | Secondary amines as antidiabetic and antiobesity agents |
GB9313574D0 (en) * | 1993-07-01 | 1993-08-18 | Glaxo Group Ltd | Medicaments |
AU7532294A (en) * | 1993-07-31 | 1995-02-28 | Smithkline Beecham Plc | 2-benzoheterocyclyloxy or thiopropanolamine derivatives with adreno receptor agonist activity |
IL110857A0 (en) * | 1993-09-09 | 1994-11-28 | Lilly Co Eli | Cessation of tobacco use |
US5393772A (en) * | 1993-11-24 | 1995-02-28 | Boehringer Mannheim Pharmaceuticals Corporation | Use of, and method of treatment using, hydroxycarbazole compounds for inhibition of smooth muscle migration and proliferation |
US5776983A (en) * | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
US5561142A (en) * | 1994-04-26 | 1996-10-01 | Merck & Co., Inc. | Substituted sulfonamides as selective β3 agonists for the treatment of diabetes and obesity |
US5541197A (en) * | 1994-04-26 | 1996-07-30 | Merck & Co., Inc. | Substituted sulfonamides as selective β3 agonists for the treatment of diabetes and obesity |
US5488064A (en) * | 1994-05-02 | 1996-01-30 | Bristol-Myers Squibb Company | Benzo 1,3 dioxole derivatives |
CA2134038C (en) * | 1994-06-16 | 1997-06-03 | David Taiwai Wong | Potentiation of drug response |
US5726165A (en) | 1994-07-29 | 1998-03-10 | Smithkline Beecham P.L.C. | Derivatives of 4-(2-aminoethyl)phenoxymethyl-phosphonic and -phosphinic acid and pharmaceutical and veterinary uses therefor |
JPH10503507A (ja) * | 1994-07-29 | 1998-03-31 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | ベータ3−アドレナリン受容体アゴニストおよびベータ1およびベータ2−アドレナリン受容体アンタゴニストとして有用なアリールオキシおよびアリールチオプロパノールアミン誘導体、およびその医薬組成物 |
US5648091A (en) * | 1994-08-03 | 1997-07-15 | The Proctor & Gamble Company | Stable vitamin A encapsulated |
EP0714663A3 (en) * | 1994-11-28 | 1997-01-15 | Lilly Co Eli | Potentiation of drug responses by serotonin 1A receptor antagonists |
US5541204A (en) * | 1994-12-02 | 1996-07-30 | Bristol-Myers Squibb Company | Aryloxypropanolamine β 3 adrenergic agonists |
ZA967892B (en) * | 1995-09-21 | 1998-03-18 | Lilly Co Eli | Selective β3 adrenergic agonists. |
EP0827746B1 (en) * | 1996-09-05 | 2002-04-03 | Eli Lilly And Company | Carbazole analogues as selective beta3 adrenergic agonists |
CO5011072A1 (es) * | 1997-12-05 | 2001-02-28 | Lilly Co Eli | Etanolaminas pirazinil substituidas como agfonistas de los receptores |
FR2801398B1 (fr) * | 1999-11-22 | 2002-01-11 | Claude Ricard | Procede pour securiser le fonctionnement du capteur electronique associe a un taximetre |
-
1998
- 1998-12-01 CO CO98071198A patent/CO5011072A1/es unknown
- 1998-12-02 EP EP98309868A patent/EP0921120A1/en not_active Withdrawn
- 1998-12-02 ZA ZA9811026A patent/ZA9811026B/xx unknown
- 1998-12-03 SV SV1998000142A patent/SV1998000142A/es unknown
- 1998-12-03 AR ARP980106149A patent/AR017798A1/es unknown
- 1998-12-03 PE PE1998001178A patent/PE132699A1/es not_active Application Discontinuation
- 1998-12-04 WO PCT/US1998/025831 patent/WO1999029673A1/en active Application Filing
- 1998-12-04 JP JP2000524270A patent/JP2001525399A/ja not_active Withdrawn
- 1998-12-04 CA CA002312987A patent/CA2312987A1/en not_active Abandoned
- 1998-12-04 US US09/206,107 patent/US6046227A/en not_active Expired - Fee Related
- 1998-12-04 AU AU16281/99A patent/AU1628199A/en not_active Abandoned
-
1999
- 1999-11-18 US US09/443,272 patent/US6617347B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0921120A1 (en) | 1999-06-09 |
US6046227A (en) | 2000-04-04 |
WO1999029673A1 (en) | 1999-06-17 |
SV1998000142A (es) | 1999-10-06 |
AU1628199A (en) | 1999-06-28 |
PE132699A1 (es) | 1999-12-21 |
US6617347B1 (en) | 2003-09-09 |
CA2312987A1 (en) | 1999-06-17 |
ZA9811026B (en) | 2000-06-02 |
AR017798A1 (es) | 2001-10-24 |
JP2001525399A (ja) | 2001-12-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO5011072A1 (es) | Etanolaminas pirazinil substituidas como agfonistas de los receptores | |
AR040475A1 (es) | Espiropiperidinas o espiropirrolidinas triciclicas | |
CO5680412A2 (es) | Agonistas del receptor adrenergico etilamino beta 2 sustituido con amino | |
AR016666A1 (es) | Derivados de pirimidinona, un procedimiento para su preparacion y una composicion farmaceutica que los contiene | |
AR046615A1 (es) | Pirrolidinas 3-(benzoil)-n-aciladas, como inhibidores de 11-beta-hsd1, utiles en el tratamiento de desordenes metabolicos | |
CO5080767A1 (es) | Derivados sulfonamida | |
CO4970713A1 (es) | Derivados de carboxamidotiazoles, su preparacion, composiciones farmaceuticas que los contienen | |
ES2186253T3 (es) | Un metodo para controlar la reologia de un fluido acuoso y agente gelificante para dicho control. | |
CO5261601A1 (es) | Indolilquinolinonas utiles como inhibidores de la tirosinoquinasa | |
CO5601018A2 (es) | Derivados de n-fenil-2-pirimidin-amina | |
AR068413A2 (es) | Derivados 8-amino, metodos de preparacion, composiciones farmaceuticas y su uso en terapia | |
AR051202A1 (es) | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa | |
PE20030808A1 (es) | Derivados triciclicos heterociclicos como antagonistas receptores de trombina | |
AR037907A1 (es) | Derivados de azaindolilalquilamina como ligandos de 5-hidroxitriptamina-6 | |
CO5650164A2 (es) | Hetrociclil-3-sulfonilindazoles como ligandos de 5-hidroxitriptamina-6 | |
HN1998000034A (es) | Quinoxalinadionas | |
AR012622A1 (es) | Inhibidores de proteasas, procedimiento para su preparacion, composicion farmaceutica que los comprende y el uso de los mismos en la fabricacion de unmedicamento | |
MY128442A (en) | Diphenyl ether compounds useful in therapy | |
AR072045A1 (es) | Derivados heterociclicos de urea y metodos para utilizarlos | |
MX9304151A (es) | Nuevas ciclobut-3-en-1,2-dionas substituidas, proceso para su preparacion y composiciones farmaceuticas que las contienen. | |
ES2038678T3 (es) | Procedimiento para la preparacion de n-(2-alquil-3-mercapto-glutaril)-alfamino-acidos. | |
ES2164881T3 (es) | Derivados de 6-carboxamido dihidropirano. | |
ES2317103T3 (es) | Derivados de c-ciclohexilmetilamina sustituidos. | |
PE20020194A1 (es) | 2,3,7,8,9,10,11,12-OCTAHIDROAZEPINO[4,5-b]PIRANO[3,2-e)INDOLES SUSTITUIDOS | |
ECSP045121A (es) | Agonistas del receptor activado por proliferador de peroxisoma |