CO5011105A1 - ORGANIC COMPOUNDS TO TREAT OBESITY AND RELATED DISORDERS, PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND AND PROCESSES FOR THEIR PREPARATION - Google Patents
ORGANIC COMPOUNDS TO TREAT OBESITY AND RELATED DISORDERS, PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND AND PROCESSES FOR THEIR PREPARATIONInfo
- Publication number
- CO5011105A1 CO5011105A1 CO98075202A CO98075202A CO5011105A1 CO 5011105 A1 CO5011105 A1 CO 5011105A1 CO 98075202 A CO98075202 A CO 98075202A CO 98075202 A CO98075202 A CO 98075202A CO 5011105 A1 CO5011105 A1 CO 5011105A1
- Authority
- CO
- Colombia
- Prior art keywords
- carbon atoms
- atoms
- carbon
- alkoxy
- alkyl
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/88—Nitrogen atoms, e.g. allantoin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
- C07D249/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole 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
- C07D277/38—Nitrogen atoms
- C07D277/42—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Child & Adolescent Psychology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente invención se relaciona con un compuesto de lafórmula I: donde X es S ó NH, e Y y Z son cada uno CH; o X es NH, es una de las variables Y y Z es N, y la otra es CH; R1 y R2 , independientemente uno del otro, representan hidrógeno, alquilo de 1 a 7 átomos de carbono, o alquilo de 1 a 7 átomos de carbono sustituido por hidroxi, halógeno, alcoxi de 1 a 7 átomos de carbono, carboxi, alcoxi, de 1 a 7 átomos de carbono-carbonilo, carbamoílo, alquilo de 1 a 7 átomos de carbono-carbamoílo, dialquilo de 1 a 7 átomos de carbono-carbamoílo, cicloalquilo de 3 a 8 átomos de carbono, por cicloalquilo de 3 a 8 átomos de carbono que está sustituido por alcoxi de 1 a 7 átomos de carbono-carbonilo, o representan alcanoílo de 2 a 7 átomos de carbono; mientras que cuando menos una de las variables R1 y R2 es diferente de hidrógeno; o el grupo NR1 R2 alquileno de 2 a 6 átomos de carbono-amino lineal que está insustituido a sustituido por alquilo de 1 a 7 átomos de carbono, hidroxialquilo de 1 a 7 átomos de carbono, alcoxi de 1 a 7 átomos de carbono, alcoxi de 1 a 7 átomos de carbono, alcoxi de 1 a 7 átomos de carbono-alcoxi de 1 a 7 átomos de carbono-alquilo de 1 a 7 átomos de carbono, tioalquilo de 1 a 7 átomos de carbono-alquilo de 1 a 7 átomos de carbono, alcano 1 a 7 átomos de carbono, alcano de 1 a 7 átomos de carbono-sulfonialquilo de 1 a 7 átomos de carbono, aminoalquilo de 1 a 7 átomos de carbono, alquilo de 1 a 7 átomos de carbono-aminoalquilo de 1 a 7 átomos de carbono, dialquilo de 1 a 7 átomos de carbono-aminoalquilo de 1 a 7 átomos de carbono, hidroxi, ciano, amino, alquilo de 1 a 7 átomos de carbono-amino, dialquilo de 1 a 7 átomos de carbono-amino, alcanoílo de 1 a 7 átomos de carbono, hidroxiliminoalquilo de 2 a 7 átomos de carbono, carboxi, alcoxi de 1 a 7 átomos de carbono-carbamoílo, dialquilo de 1 a 7 átomos de carbono-carbamoílo, o por oxo, ...The present invention relates to a compound of the formula I: where X is S or NH, and Y and Z are each CH; or X is NH, is one of the variables Y and Z is N, and the other is CH; R1 and R2, independently of each other, represent hydrogen, alkyl of 1 to 7 carbon atoms, or alkyl of 1 to 7 carbon atoms substituted by hydroxy, halogen, alkoxy of 1 to 7 carbon atoms, carboxy, alkoxy, of 1 to 7 carbon-carbonyl atoms, carbamoyl, alkyl of 1 to 7 carbon-carbamoyl atoms, dialkyl of 1 to 7 carbon-carbamoyl atoms, cycloalkyl of 3 to 8 carbon atoms, per cycloalkyl of 3 to 8 atoms of carbon which is substituted by alkoxy of 1 to 7 carbon-carbonyl atoms, or represent alkanoyl of 2 to 7 carbon atoms; while at least one of the variables R1 and R2 is different from hydrogen; or the NR1 R2 alkylene group of 2 to 6 carbon-linear amino atoms which is unsubstituted to substituted by alkyl of 1 to 7 carbon atoms, hydroxyalkyl of 1 to 7 carbon atoms, alkoxy of 1 to 7 carbon atoms, alkoxy from 1 to 7 carbon atoms, alkoxy of 1 to 7 carbon atoms-alkoxy of 1 to 7 carbon atoms-alkyl of 1 to 7 carbon atoms, thioalkyl of 1 to 7 carbon atoms-alkyl of 1 to 7 atoms carbon, alkane 1 to 7 carbon atoms, alkane of 1 to 7 carbon atoms-sulfonyalkyl of 1 to 7 carbon atoms, aminoalkyl of 1 to 7 carbon atoms, alkyl of 1 to 7 carbon atoms-aminoalkyl of 1 at 7 carbon atoms, dialkyl of 1 to 7 carbon-aminoalkyl atoms of 1 to 7 carbon atoms, hydroxy, cyano, amino, alkyl of 1 to 7 carbon-amino atoms, dialkyl of 1 to 7 carbon atoms- amino, alkanoyl of 1 to 7 carbon atoms, hydroxyiminoalkyl of 2 to 7 carbon atoms, carboxy, alkoxy of 1 to 7 carbon atoms o-carbamoyl, dialkyl of 1 to 7 carbon-carbamoyl atoms, or by oxo, ...
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19757248 | 1997-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5011105A1 true CO5011105A1 (en) | 2001-02-28 |
Family
ID=7853006
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO98075202A CO5011105A1 (en) | 1997-12-22 | 1998-12-17 | ORGANIC COMPOUNDS TO TREAT OBESITY AND RELATED DISORDERS, PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND AND PROCESSES FOR THEIR PREPARATION |
Country Status (6)
Country | Link |
---|---|
AR (1) | AR014406A1 (en) |
AU (1) | AU2415299A (en) |
CO (1) | CO5011105A1 (en) |
PE (1) | PE20000127A1 (en) |
WO (1) | WO1999032466A1 (en) |
ZA (1) | ZA9811705B (en) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU756797B2 (en) | 1998-11-10 | 2003-01-23 | Banyu Pharmaceutical Co., Ltd. | Spiro-indolines as Y5 receptor antagonists |
FR2792314B1 (en) * | 1999-04-15 | 2001-06-01 | Adir | NOVEL AMINOTRIAZOLE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
US6218408B1 (en) | 1999-06-30 | 2001-04-17 | Synaptic Pharmaceutical Corporation | Selective NPY (Y5) antagonists (bicyclics) |
US6989379B1 (en) | 1999-04-22 | 2006-01-24 | H. Lundbick A/S | Selective NPY (Y5) antagonists |
US6340683B1 (en) | 1999-04-22 | 2002-01-22 | Synaptic Pharmaceutical Corporation | Selective NPY (Y5) antagonists (triazines) |
CA2371274A1 (en) * | 1999-04-22 | 2000-11-02 | Synaptic Pharmaceutical Corporation | Selective npy (y5) antagonists |
US6222040B1 (en) | 1999-06-30 | 2001-04-24 | Synaptic Pharmaceutical Corporation | Selective NPY (Y5) antagonists (tricyclics) |
US6225330B1 (en) | 1999-06-30 | 2001-05-01 | Synaptic Pharmaceutical Corporation | Selective NPY (Y5) antagonists (tricyclics) |
US6214853B1 (en) | 1999-06-30 | 2001-04-10 | Synaptic Pharmaceutical Corporation | Selective NPY (Y5) antagonists (bicyclics) |
US7273880B2 (en) | 1999-06-30 | 2007-09-25 | H. Lunbeck A/S | Selective NPY (Y5) antagonists |
SI2014285T1 (en) * | 1999-11-26 | 2010-08-31 | Shionogi & Co | NPYY5 antagonists |
ES2317889T3 (en) * | 2000-03-01 | 2009-05-01 | Janssen Pharmaceutica Nv | DERIVATIVES OF TIAZOLIL 2,4-DISPOSED. |
FR2815346B1 (en) * | 2000-10-13 | 2004-02-20 | Servier Lab | NOVEL AMINOTRIAZOLONE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
JP2005508841A (en) * | 2001-03-29 | 2005-04-07 | スミスクライン・ビーチャム・コーポレイション | Compounds and methods |
CA2403307A1 (en) | 2001-10-23 | 2003-04-23 | Neurogen Corporation | Substituted 2-cyclohexyl-4-phenyl-1h-imidazole derivatives |
TW200303742A (en) * | 2001-11-21 | 2003-09-16 | Novartis Ag | Organic compounds |
WO2004092146A2 (en) * | 2003-04-14 | 2004-10-28 | The Institutes For Pharmaceutical Discovery, Llc | N- (((((1,3-thiazol-2-yl) amino) carbonyl) phenyl) sulfonyl) phenylalanine derivatives and related compounds for the treatment of diabetes |
EP1620420A2 (en) | 2003-04-30 | 2006-02-01 | The Institutes for Pharmaceutical Discovery, LLC | Substituted carboxylic acids |
WO2006042215A1 (en) * | 2004-10-08 | 2006-04-20 | Janssen Pharmaceutica, N.V. | 1,2,4-triazolylaminoaryl (heteroaryl) sulfonamide derivatives |
GB0526257D0 (en) | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
US9353078B2 (en) * | 2013-10-01 | 2016-05-31 | New York University | Amino, amido and heterocyclic compounds as modulators of rage activity and uses thereof |
JP2023508909A (en) * | 2019-12-20 | 2023-03-06 | イケナ オンコロジー, インコーポレイテッド | 4-Phenyl-N-(phenyl)thiazol-2-amine Derivatives and Related Compounds as Aryl Hydrocarbon Receptor (AHR) Agonists, For example, for the Treatment of Angiogenesis-Related Disorders or Inflammatory Diseases |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3776765A (en) * | 1972-02-28 | 1973-12-04 | Cities Service Co | Process for protecting a substrate with an n{11 substituted aminoarylsulfonamide intumescent agent |
FR2701480B1 (en) * | 1993-02-15 | 1995-05-24 | Sanofi Elf | Compounds with a sulfamoyl and amidino group, process for their preparation and pharmaceutical compositions containing them. |
AU3201095A (en) * | 1994-07-27 | 1996-02-22 | G.D. Searle & Co. | Substituted thiazoles for the treatment of inflammation |
-
1998
- 1998-12-17 CO CO98075202A patent/CO5011105A1/en unknown
- 1998-12-17 PE PE1998001240A patent/PE20000127A1/en not_active Application Discontinuation
- 1998-12-18 AU AU24152/99A patent/AU2415299A/en not_active Abandoned
- 1998-12-18 WO PCT/EP1998/008333 patent/WO1999032466A1/en active Application Filing
- 1998-12-18 AR ARP980106523A patent/AR014406A1/en unknown
- 1998-12-21 ZA ZA9811705A patent/ZA9811705B/en unknown
Also Published As
Publication number | Publication date |
---|---|
AR014406A1 (en) | 2001-02-28 |
ZA9811705B (en) | 1999-09-07 |
WO1999032466A1 (en) | 1999-07-01 |
AU2415299A (en) | 1999-07-12 |
PE20000127A1 (en) | 2000-03-14 |
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