CO5150220A1 - 4-carboxiamino-2- metil-1,2,3,4-tetrahidroquinolinas - Google Patents
4-carboxiamino-2- metil-1,2,3,4-tetrahidroquinolinasInfo
- Publication number
- CO5150220A1 CO5150220A1 CO99057639A CO99057639A CO5150220A1 CO 5150220 A1 CO5150220 A1 CO 5150220A1 CO 99057639 A CO99057639 A CO 99057639A CO 99057639 A CO99057639 A CO 99057639A CO 5150220 A1 CO5150220 A1 CO 5150220A1
- Authority
- CO
- Colombia
- Prior art keywords
- substituted
- optionally
- mono
- carbon
- oxo
- Prior art date
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 27
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 22
- 229910052757 nitrogen Chemical group 0.000 abstract 22
- 125000004043 oxo group Chemical group O=* 0.000 abstract 19
- 229910052799 carbon Inorganic materials 0.000 abstract 16
- 229920006395 saturated elastomer Polymers 0.000 abstract 16
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 15
- 229910052717 sulfur Inorganic materials 0.000 abstract 15
- 239000011593 sulfur Chemical group 0.000 abstract 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 11
- 229910052760 oxygen Inorganic materials 0.000 abstract 11
- 239000001301 oxygen Substances 0.000 abstract 11
- 125000005842 heteroatom Chemical group 0.000 abstract 10
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000004414 alkyl thio group Chemical group 0.000 abstract 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 6
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000002619 bicyclic group Chemical group 0.000 abstract 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 3
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229940002612 prodrug Drugs 0.000 abstract 2
- 239000000651 prodrug Substances 0.000 abstract 2
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 150000003973 alkyl amines Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 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
- A61P3/06—Antihyperlipidemics
-
- 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
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Un compuesto de la fórmula I<EMI FILE="99057639_1" ID="1" IMF=JPEG >uno de sus profármacos, una sal farmacéuticamente aceptable de dicho compuesto o de dicho profármaco;en la que R1 es hidrógeno, Y, W-X, W-Y;en el que W es un carbonilo, tiocarbonilo, sulfinilo o sulfonilo;X es -a-Y, -S-Y, -N(H)-Y o -N-(Y)2;Y en cada caso es independientemente Z o una cadena de carbonos, lineal o ramificada, de uno a diez miembros, totalmente saturada, parcialmente insaturada o totalmente insaturada, en la que los carbonos, distintos del carbono de unión, pueden estar reemplazados opcionalmente por uno o dos heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno, y dicho carbono está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, dicho carbono está opcionalmente mono- sustituido con hidroxi, dicho carbono está opcionalmente mono-sustituido con oxo, dicho azufre está opcionalmente mono- o di-sustituido con oxo, dicho nitrógeno está opcionalmente mono- o di-sustituido con oxo y dicha cadena de carbonos está opcionalmente mono-sustituida con Z; en el que Z es un anillo, de tres a doce miembros, parcialmente saturado, totalmente saturado o totalmente insaturado, que tiene opcionalmente uno a cuatro heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno, o un anillo bicíclico que consiste en dos anillos, de tres a seis miembros, fusionados, parcialmente saturados, totalmente saturados o totalmente insaturados, considerados independientemente, teniendo opcionalmente de uno a cuatro heteroátomos seleccionados independientemente de nitrógeno, azufre y oxígeno;en el que dicho sustituyente Z está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, alquenilo(C2-C6), alquilo(C1-C6), hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxi, alquiloxi (C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6) en el que dicho sustituyente alquilo(C1-C6) está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxi, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6), estando dicho alquilo(C1-6) opcionalmente sustituido con uno a nueve átomos de flúor; R3 es hidrógeno o Q; en el que Q es una cadena de carbonos, lineal o ramificada, de uno a seis miembros, totalmente saturada, parcialmente insaturada o totalmente insaturada, en la que los carbonos, distintos del carbono de unión, pueden estar reemplazados opcionalmente por un heteroátomo- 2 - seleccionado de oxígeno, azufre y nitrógeno, y dicho carbono está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, dicho carbono está opcionalmente mono-sustituido con hidroxi, dicho carbono está opcionalmente mono-sustituido con oxo, dicho azufre está opcionalmente mono- o di-sustituido con oxo, dicho nitrógeno está opcionalmente mono- o di-sustituido con oxo y dicha cadena de carbonos está opcionalmente mono-sustituida con V; en el que V es un anillo, de tres a doce miembros parcialmente saturado, totalmente saturado o totalmente insaturado, que tiene opcionalmente de uno a cuatro heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno, o un anillo bicíclico que consiste en dos anillos, de tres a seis miembros, fusionados, parcialmente saturados, totalmente saturados o totalmente insaturados, considerados independientemente, que tienen opcionalmente de uno a cuatro heteroátomos seleccionados independientemente de nitrógeno, azufre y oxígeno; en el que dicho sustituyente V está opcionalmente mono-, di-, tri o tetra-sustituido independientemente con halógeno, alquilo(C1-C6), alquenilo(C2-C6), hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxamoilo, mono-N- o di-N,N-alquil(C1-C6)-carboxamoilo, carboxi, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6), en el que dicho sustituyente alquilo(C1-C6) o alquenilo(C2-C6) está opcionalmente mono-, di- o tri-sustituido independientemente con hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxi, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N- alquilamillo(C1-C6), estando dicho alquilo(C1-C6) o alquenilo(C2-C6) opcionalmente sustituido con uno a nueve átomos de flúor; R4 esQ1 oV1; en el que Q1 es una cadena de carbonos, lineal o ramificada, de uno a seis miembros, totalmente saturada, parcialmente insaturada o totalmente insaturada, en la que los carbonos, distintos del carbono de unión, pueden estar reemplazados opcionalmente por un heteroátomo seleccionado de oxígeno, azufre y nitrógeno, y dicho carbono está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, dicho carbono está opcionalmente mono-sustituido con hidroxi, dicho carbono está opcionalmente mono-sustituido con oxo, dicho azufre está opcionalmente mono- o di-sustituido con oxo, dicho nitrógeno está opcionalmentc mono- o di-sustituido con oxo, y dicha cadena de carbonos está opcionalmente mono- sustituida con V1; en el que V1 es un anillo, de tres a seis miembros, parcialmente saturado, totalmente saturado o totalmente insaturado, que tiene uno a dos heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno; en el que dicho sustituyente V1 está opcionalmente mono-, di-, tri- o tetra-sustituido independientemente con halógeno, alquilo(C1-C6), alcoxi(C1-C6), amino, nitro, ciano, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6), en el que dicho sustituyente alquilo(C1-C6) está opcionalmente mono-sustituido con oxo, teniendo opcionalmente dicho sustituyente alquilo(C1-C6) de uno a nueve átomos de flúor; en la que R3 debe contener V o R4 debe contener V1; y R5, R6, R7, y R8 son cada uno independientemente hidrógeno, un enlace, nitro o halo, en el que dicho enlace está sustituido con T o una cadena de carbonos lineal o ramificada de (C1-C12) parcial o completamente saturada, o completamente insaturada, reemplazándose opcionalmente dicho carbono con uno o dos heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno, en el que dichos átomos de carbono están mono-, di- o tri-sustituidos independientemente con halo, dicho carbono está mono-sustituido con hidroxi, dicho carbono está mono-sustituido con oxo, dicho azufre está opcionalmente mono- o di-sustituido con oxo, dicho nitrógeno está opcionalmente mono- o di-sustituido con oxo, y dicho carbono está mono-sustituido con T; en el que T es un anillo de tres a doce miembros parcial o completamente saturado o completamente insaturado, que tiene opcionalmente uno a cuatro heteroátomos seleccionados independientemente de oxígeno, azufre y nitrógeno; o un anillo bicíclico que comprende dos anillos condensados de tres a seis miembros parcial o completamente saturado, o completamente insaturado, tomados independientemente, teniendo opcionalmente uno a cuatro heteroátomos seleccionados independientemente de nitrógeno, azufre y oxígeno; en la que dicho sustituyente T está opcionalmente mono-, di- o tri-sustituido independientemente con halógeno, alquilo(C1-C6), alquenilo(C2-C6), hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxi, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6) en el que dicho sustituyente alquilo(C1-C6) está opcionalmente mono-, di- o tri-sustituido independientemente con hidroxi, alcoxi(C1-C6), alquiltio(C1-C4), amino, nitro, ciano, oxo, carboxi, alquiloxi(C1-C6)-carbonilo, mono-N- o di-N,N-alquilamino(C1-C6), o teniendo dicho alquilo(C1-C6) opcionalmente uno a nueve átomos de flúor; con la condición de que R5, R6, R7 y R8 no sea hidrógeno y no esté enlazado al resto de quinolina a través de oxi.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10092998P | 1998-09-17 | 1998-09-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5150220A1 true CO5150220A1 (es) | 2002-04-29 |
Family
ID=22282259
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO99057639A CO5150220A1 (es) | 1998-09-17 | 1999-09-10 | 4-carboxiamino-2- metil-1,2,3,4-tetrahidroquinolinas |
Country Status (25)
Country | Link |
---|---|
US (2) | US6147090A (es) |
EP (1) | EP1114033B1 (es) |
JP (1) | JP3655193B2 (es) |
AR (1) | AR021482A1 (es) |
AT (1) | ATE277906T1 (es) |
AU (1) | AU5439899A (es) |
BR (1) | BR9913842A (es) |
CA (1) | CA2344556A1 (es) |
CO (1) | CO5150220A1 (es) |
DE (1) | DE69920727T2 (es) |
DK (1) | DK1114033T3 (es) |
DZ (1) | DZ2889A1 (es) |
ES (1) | ES2228086T3 (es) |
GT (1) | GT199900149A (es) |
HN (1) | HN1999000155A (es) |
MA (1) | MA26687A1 (es) |
MY (1) | MY121838A (es) |
PA (1) | PA8481501A1 (es) |
PE (1) | PE20001048A1 (es) |
PT (1) | PT1114033E (es) |
SI (1) | SI1114033T1 (es) |
SV (1) | SV1999000149A (es) |
TN (1) | TNSN99172A1 (es) |
TW (1) | TWI232859B (es) |
WO (1) | WO2000017166A1 (es) |
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USRE44578E1 (en) | 2000-04-10 | 2013-11-05 | Teva Pharmaceutical Industries, Ltd. | Stable pharmaceutical compositions containing 7-substituted-3,5-dihydroxyheptanoic acids or 7-substituted-3,5-dihydroxyheptenoic acids |
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US6982251B2 (en) * | 2000-12-20 | 2006-01-03 | Schering Corporation | Substituted 2-azetidinones useful as hypocholesterolemic agents |
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AR038375A1 (es) | 2002-02-01 | 2005-01-12 | Pfizer Prod Inc | Composiciones farmaceuticas de inhibidores de la proteina de transferencia de esteres de colesterilo |
PL371416A1 (en) * | 2002-02-01 | 2005-06-13 | Pfizer Products Inc. | Controlled release pharmaceutical dosage forms of a cholesteryl ester transfer protein inhibitor |
MXPA04007438A (es) | 2002-02-01 | 2004-10-11 | Pfizer Prod Inc | Composiciones farmaceuticas de dispersiones amorfas de farmacos y materiales que forman microfases lipofilas. |
US20040053842A1 (en) * | 2002-07-02 | 2004-03-18 | Pfizer Inc. | Methods of treatment with CETP inhibitors and antihypertensive agents |
US7071210B2 (en) * | 2002-07-02 | 2006-07-04 | Pfizer Inc. | CETP inhibitors in combination with antihypertensive agents and uses thereof |
IL161559A0 (en) | 2002-08-30 | 2004-09-27 | Japan Tobacco Inc | Dibenzylamine derivatives and pharmaceutical compositions containing the same |
JP2006508077A (ja) | 2002-10-04 | 2006-03-09 | ミレニアム・ファーマシューティカルズ・インコーポレイテッド | 炎症疾患を治療するためのpgd2レセプタアンタゴニスト |
US7504508B2 (en) | 2002-10-04 | 2009-03-17 | Millennium Pharmaceuticals, Inc. | PGD2 receptor antagonists for the treatment of inflammatory diseases |
US20090181966A1 (en) * | 2002-10-04 | 2009-07-16 | Millennium Pharmaceuticals, Inc. | PGD2 receptor antagonists for the treatment of inflammatory diseases |
ES2263015T3 (es) * | 2002-10-21 | 2006-12-01 | Warner-Lambert Company Llc | Derivados de tetrahidroquinolina como antagonistas de crth2. |
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- 1999-09-10 PE PE1999000923A patent/PE20001048A1/es not_active Application Discontinuation
- 1999-09-10 DK DK99940421T patent/DK1114033T3/da active
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- 1999-09-10 TW TW088115690A patent/TWI232859B/zh not_active IP Right Cessation
- 1999-09-10 AT AT99940421T patent/ATE277906T1/de not_active IP Right Cessation
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- 1999-09-10 WO PCT/IB1999/001529 patent/WO2000017166A1/en active IP Right Grant
- 1999-09-10 SV SV1999000149A patent/SV1999000149A/es not_active Application Discontinuation
- 1999-09-10 CA CA002344556A patent/CA2344556A1/en not_active Abandoned
- 1999-09-10 BR BR9913842-5A patent/BR9913842A/pt not_active Application Discontinuation
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- 1999-09-10 AU AU54398/99A patent/AU5439899A/en not_active Abandoned
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- 1999-09-13 TN TNTNSN99172A patent/TNSN99172A1/fr unknown
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DZ2889A1 (fr) | 2003-12-15 |
SV1999000149A (es) | 2000-07-06 |
AR021482A1 (es) | 2002-07-24 |
TWI232859B (en) | 2005-05-21 |
US6395751B1 (en) | 2002-05-28 |
ES2228086T3 (es) | 2005-04-01 |
DE69920727T2 (de) | 2006-03-09 |
CA2344556A1 (en) | 2000-03-30 |
GT199900149A (es) | 2001-03-03 |
HN1999000155A (es) | 2000-01-12 |
WO2000017166A1 (en) | 2000-03-30 |
PT1114033E (pt) | 2004-12-31 |
BR9913842A (pt) | 2001-06-12 |
US6147090A (en) | 2000-11-14 |
ATE277906T1 (de) | 2004-10-15 |
AU5439899A (en) | 2000-04-10 |
MA26687A1 (fr) | 2004-12-20 |
EP1114033A1 (en) | 2001-07-11 |
JP2002526477A (ja) | 2002-08-20 |
DE69920727D1 (en) | 2004-11-04 |
SI1114033T1 (en) | 2005-02-28 |
TNSN99172A1 (fr) | 2005-11-10 |
JP3655193B2 (ja) | 2005-06-02 |
PE20001048A1 (es) | 2000-10-17 |
MY121838A (en) | 2006-02-28 |
DK1114033T3 (da) | 2004-12-20 |
EP1114033B1 (en) | 2004-09-29 |
PA8481501A1 (es) | 2001-12-14 |
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