CO4990966A1 - Compuestos de tiourea y benzamida, composiciones y metodos para tratar y prevenir enfermedades inflamatorias y arteros- clerosis - Google Patents
Compuestos de tiourea y benzamida, composiciones y metodos para tratar y prevenir enfermedades inflamatorias y arteros- clerosisInfo
- Publication number
- CO4990966A1 CO4990966A1 CO98076093A CO98076093A CO4990966A1 CO 4990966 A1 CO4990966 A1 CO 4990966A1 CO 98076093 A CO98076093 A CO 98076093A CO 98076093 A CO98076093 A CO 98076093A CO 4990966 A1 CO4990966 A1 CO 4990966A1
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- substituted
- aryl
- cycloalkyl
- heteroaryl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having carbon atoms of carboxamide groups, amino groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
- C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
- C07C311/44—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
- C07C311/46—Y being a hydrogen or a carbon atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/62—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/63—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/38—Amides of thiocarboxylic acids
- C07C327/48—Amides of thiocarboxylic acids having carbon atoms of thiocarboxamide groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C335/20—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C335/22—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by carboxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Quinoline Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
Compuestos CARACTERIZADOS porque tienen la Fórmula Idondecada n es independientemente 0 a 3;Q es alquilo C1 -C6 ,heteroarilo, heteroarilo sustituido, -NR´, o cicloalquilo; cada R´ es independientemente hidrógeno o alquilo C1 -C6 ;Re es - 2 -heteroarilo sustituido, naftilo, bencilo o dansilo;cada uno de R1 , R2 , R3 , R4 , R5 , R7 , R8 , Ra , Rb , Rc , y Rd es independientemente hidrógeno, -O alquilo, C1 -C6 , -S alquilo C1 -C6 , hidrógeno, alquilo C1 -C6 , -OH, CF3 , -NO2 , -CN, CO2 H, OCF3 , -CO2 , alquilo C1 -C6 , SO3 H, -SO3 -metal alcalino -NH2 , -NH alquilo C1 -C6 O O ½ ½-N(C alquilo C1 -C6 )2 -OC alquilo C1 -C6 , -CO2 alquilo C1 -C6 -SO3 H,-SO3 metal alcalino, -CN -CH2 -halógeno, CH2 -CH2 ½ ½O O ½ ½heteroarilo, heteroarilo sustituido, arilo, arilo sustituido, cicloalquilo, cicloalquilo sustituido, heterocicloalquilo, heterocicloalquilo sustituido, benzoilo, O½C alquilo C1 -C6 O O½ ½ -OCH, -OC alquilo C1 -C6 -SO3 H, -SO3 NR´R´, -CHO, -SO2 NH2 o -NR´R´; o las sales farmacéuticamente aceptables de ellos.O½siempre que cuando Y es -CO-,Q no sea alquilo C1 -C6 ; además siempre que cuando X es O½-CNH- e Y es NH, Rb no sea -OH; además siempre que cuando X e Y sonO½-NHC- Re y Q no sean fenilo sin sustituir; además siempre que O O½ ½ cuando Y es -NHC- y X es -NHCO-, Re y Q no sean ambos arilo; además siempre que cuando Y es SO2 NH- o -SO2 N alquilo C1 -C6 yO O½ ½X es CNH ó CN alquilo C1 -C6 , Q y Re no sean ambos fenilo sin sustituir; además siempre que cuando Y esO O O½ ½ ½-CNH ó -CN alquilo C1 -C6 y X es-NC, ½HRe sea fenilo sin sustituir fenilo di- o tri-sustituido; siempre además que cuando Y esO½-NR´CNR´-,Q no sea arilo sin sustituir.donde heteroarilo ó arilo cicloalquilo o heterocicloalquilo sustituido significa que dichos ciclos tienen uno o más sustituyentes seleccionados entre halógeno, alquilo C1 -C8 , -CN, CF3 , -NO2 -NH2 , -NH(alquilo C1 -C8 ), -N(alquilo C1 -C8 ),-O-(alquilo C1 -C8 ) y -OH.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6860497P | 1997-12-23 | 1997-12-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO4990966A1 true CO4990966A1 (es) | 2000-12-26 |
Family
ID=22083601
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO98076093A CO4990966A1 (es) | 1997-12-23 | 1998-12-22 | Compuestos de tiourea y benzamida, composiciones y metodos para tratar y prevenir enfermedades inflamatorias y arteros- clerosis |
Country Status (17)
Country | Link |
---|---|
US (2) | US6268387B1 (es) |
EP (1) | EP1042276B1 (es) |
JP (1) | JP2001526255A (es) |
KR (1) | KR20010033470A (es) |
AR (1) | AR024826A1 (es) |
AT (1) | ATE282591T1 (es) |
AU (1) | AU1529799A (es) |
BR (1) | BR9814327A (es) |
CA (1) | CA2300197A1 (es) |
CO (1) | CO4990966A1 (es) |
DE (1) | DE69827664T2 (es) |
ES (1) | ES2234169T3 (es) |
NZ (1) | NZ502963A (es) |
PE (1) | PE20000064A1 (es) |
UY (1) | UY25322A1 (es) |
WO (1) | WO1999032433A1 (es) |
ZA (1) | ZA9811805B (es) |
Families Citing this family (70)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6563802B2 (en) | 1998-06-22 | 2003-05-13 | Intel Corporation | Echo cancellation with dynamic latency adjustment |
AU747663B2 (en) | 1998-09-23 | 2002-05-16 | Tularik Inc. | Arylsulfonanilide ureas |
AU2735201A (en) * | 1999-12-28 | 2001-07-09 | Pharmacopeia, Inc. | Pyrimidine and triazine kinase inhibitors |
AU2001261269A1 (en) * | 2000-06-14 | 2001-12-24 | Warner Lambert Company | 1,2,4-trisubstituted benzenes as inhibitors of 15-lipoxygenase |
UA76977C2 (en) | 2001-03-02 | 2006-10-16 | Icos Corp | Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers |
BR0212189A (pt) | 2001-08-15 | 2004-07-13 | Du Pont | Composto, método para controle de pragas invertebradas e composição para controle de pragas invertebradas |
CN100349890C (zh) | 2002-01-22 | 2007-11-21 | 纳幕尔杜邦公司 | 用于防治无脊椎害虫的喹唑啉(二)酮 |
RU2319483C2 (ru) * | 2002-02-08 | 2008-03-20 | Ф.Хоффманн-Ля Рош Аг | Способ лечения и предупреждения потери костной ткани |
US7238717B2 (en) | 2002-05-24 | 2007-07-03 | Millennium Pharmaceuticals, Inc. | CCR9 inhibitors and methods of use thereof |
KR20040018295A (ko) * | 2002-08-22 | 2004-03-03 | 임철부 | 항암 활성을 갖는 티오우레이도 세라마이드 유도체 및 이화합물을 함유하는 약학적 조성물 |
US6812355B2 (en) | 2002-10-22 | 2004-11-02 | Sekhsaria Chemicals Limited | Process for the manufacture of citalopram hydrobromide from 5-bromophthalide |
FR2846326A1 (fr) * | 2002-10-29 | 2004-04-30 | Isochem Sa | Procede de purification des n-carboxyanhydrides |
US7741519B2 (en) | 2007-04-23 | 2010-06-22 | Chemocentryx, Inc. | Bis-aryl sulfonamides |
US7420055B2 (en) | 2002-11-18 | 2008-09-02 | Chemocentryx, Inc. | Aryl sulfonamides |
EP1798223B2 (en) | 2002-11-18 | 2014-07-30 | ChemoCentryx, Inc. | Aryl sulfonamides |
US7227035B2 (en) | 2002-11-18 | 2007-06-05 | Chemocentryx | Bis-aryl sulfonamides |
OA12961A (en) | 2002-11-19 | 2006-10-13 | Achillion Pharmaceuticals Inc | Substituted aryl thioureas and related compounds, inhibitors of viral replication. |
KR100555655B1 (ko) * | 2002-11-20 | 2006-03-03 | 임철부 | 항암 활성을 갖는 우레이도 또는 티오우레이도 유도체 및이 화합물을 함유하는 약학조성물 |
CA2515544A1 (en) * | 2003-02-11 | 2004-08-26 | Kemia Inc. | Compounds for the treatment of viral infection |
TW200529812A (en) | 2003-12-26 | 2005-09-16 | Chugai Pharmaceutical Co Ltd | Benzamide derivatives |
US7262318B2 (en) * | 2004-03-10 | 2007-08-28 | Pfizer, Inc. | Substituted heteroaryl- and phenylsulfamoyl compounds |
TW200600492A (en) * | 2004-05-18 | 2006-01-01 | Achillion Pharmaceuticals Inc | Substituted aryl acylthioureas and related compounds; inhibitors of viral replication |
US20050288340A1 (en) * | 2004-06-29 | 2005-12-29 | Pfizer Inc | Substituted heteroaryl- and phenylsulfamoyl compounds |
EP1775283A4 (en) * | 2004-07-14 | 2008-12-10 | Japan Tobacco Inc | 3-AMINOBENZAMIDE COMPOUND AND INHIBITORS OF THE ACTIVITY OF VANILLOID RECEPTOR 1 (VR1) |
EP2314585B1 (en) * | 2004-07-15 | 2012-09-12 | Japan Tobacco, Inc. | Condensed benzamide compounds as inhibitors of vanilloid receptor subtype 1 (VR1) activity |
DE602006014139D1 (de) * | 2005-06-06 | 2010-06-17 | Hoffmann La Roche | Sulfonamid-derivate als lebercarnitin-palmitoyl-transferase-hemmer |
EP1911751A4 (en) | 2005-06-21 | 2010-10-20 | Mitsui Chemicals Agro Inc | AMIDE DERIVATIVE AND PESTICIDE CONTAINING SUCH A COMPOUND |
US7754717B2 (en) | 2005-08-15 | 2010-07-13 | Amgen Inc. | Bis-aryl amide compounds and methods of use |
US7464565B2 (en) | 2005-11-29 | 2008-12-16 | Maytag Corporation | Rapid temperature change device for a refrigerator |
US20070155746A1 (en) * | 2005-12-23 | 2007-07-05 | Kalypsys, Inc. | Novel substituted pyridinyloxy and pyrimidinyloxy amides useful as inhibitors of protein kinases |
US7906508B2 (en) * | 2005-12-28 | 2011-03-15 | Japan Tobacco Inc. | 3,4-dihydrobenzoxazine compounds and inhibitors of vanilloid receptor subtype 1 (VRI) activity |
EP2069287A1 (en) | 2006-09-11 | 2009-06-17 | Syngeta Participations AG | Insecticidal compounds |
WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
MX2010000617A (es) | 2007-07-17 | 2010-05-17 | Plexxikon Inc | Compuestos y metodos para modulacion de cinasa, e indicaciones de estos. |
FR2926297B1 (fr) | 2008-01-10 | 2013-03-08 | Centre Nat Rech Scient | Molecules chimiques inhibitrices du mecanisme d'epissage pour traiter des maladies resultant d'anomalies d'epissage. |
FR2930552B1 (fr) * | 2008-04-24 | 2012-10-12 | Centre Nat Rech Scient | N-acylthiourees et n-acylurees inhibiteurs de la voie de signalisation des proteines hedgehog |
GB0813403D0 (en) | 2008-07-22 | 2008-08-27 | Lectus Therapeutics Ltd | Potassium ion channel modulators & uses thereof |
CN101367749B (zh) * | 2008-09-28 | 2013-04-24 | 中国医学科学院医药生物技术研究所 | 一组胺基苯酰衍生物及其制备方法和应用 |
NZ594398A (en) | 2009-04-03 | 2014-03-28 | Plexxikon Inc | Propane-1-sulfonic acid (3-[5-(4-chloro-phenyl)-1h-pyrrol [2, 3-b] pyridine-3-carbonyl]-2,4-difluoro-phenyl} -amide compositions and uses thereof |
KR20120083905A (ko) | 2009-10-09 | 2012-07-26 | 자프겐 코포레이션 | 비만의 치료에 사용하기 위한 설폰 화합물 |
KR20120102669A (ko) | 2009-11-06 | 2012-09-18 | 플렉시콘, 인코퍼레이티드 | 키나제 조정을 위한 화합물 및 방법, 및 이를 위한 적응증 |
CA2804593C (en) | 2010-07-09 | 2015-11-24 | Pfizer Limited | Biphenyloxybenzensulphonamide derivatives useful as sodium channel inhibitors |
EP2595988B1 (en) | 2010-07-22 | 2014-12-17 | Zafgen, Inc. | Tricyclic compounds and methds of making and using same |
EP2611778B1 (en) * | 2010-09-03 | 2015-08-05 | Forma TM, LLC. | Guanidine compounds and compositions for the inhibition of nampt |
BR112013018771A2 (pt) | 2011-01-26 | 2019-09-17 | Zafgen Inc | compostos de tetrazol e métodos para fazer e usar os mesmos |
US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
TWI558702B (zh) | 2011-02-21 | 2016-11-21 | 普雷辛肯公司 | 醫藥活性物質的固態形式 |
EP2505198A1 (en) | 2011-04-01 | 2012-10-03 | Société Splicos | Compounds for use as therapeutic agents affecting p53 expression and/or activity |
US9290472B2 (en) | 2011-05-06 | 2016-03-22 | Zafgen, Inc. | Partially saturated tricyclic compounds and methods of making and using same |
JP5941981B2 (ja) | 2011-05-06 | 2016-06-29 | ザフゲン,インコーポレイテッド | 三環式スルホンアミド化合物ならびにその製造および使用方法 |
US9242997B2 (en) | 2011-05-06 | 2016-01-26 | Zafgen, Inc. | Tricyclic pyrazole sulphonamide compunds and methods of making and using same |
CN104169268A (zh) | 2012-01-18 | 2014-11-26 | 扎夫根股份有限公司 | 三环砜化合物及其制备和使用方法 |
MX2014008706A (es) | 2012-01-18 | 2015-03-05 | Zafgen Inc | Compuestos tricíclicos de sulfonamida y métodos para elaborarlos y usarlos. |
US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
KR20150079952A (ko) | 2012-11-05 | 2015-07-08 | 자프겐 인크. | 트리시클릭 화합물 및 그의 제조 및 사용 방법 |
BR112015010223A2 (pt) | 2012-11-05 | 2017-07-11 | Zafgen Inc | compostos tricíclicos para o uso no tratamento e/ou controle de obesidade |
KR20150079951A (ko) | 2012-11-05 | 2015-07-08 | 자프겐 인크. | 간 질환의 치료 방법 |
GB201317609D0 (en) | 2013-10-04 | 2013-11-20 | Cancer Rec Tech Ltd | Inhibitor compounds |
JP6156846B2 (ja) * | 2014-03-04 | 2017-07-05 | 株式会社島津製作所 | マトリックス支援レーザ脱離イオン化質量分析用マトリックス |
WO2015184405A1 (en) * | 2014-05-30 | 2015-12-03 | Medivation Technologies, Inc. | Aromatic compounds, compositions and uses thereof |
WO2016029136A1 (en) * | 2014-08-21 | 2016-02-25 | Northwestern University | 3-amidobenzamides and uses thereof for increasing cellular levels of a3g |
EP3227262B1 (en) * | 2014-12-02 | 2020-05-13 | Novira Therapeutics Inc. | Sulfide alkyl and pyridyl reverse sulfonamide compounds for hbv treatment |
US9597332B2 (en) | 2014-12-02 | 2017-03-21 | Novira Therapeutics, Inc. | Sulfide alkyl compounds for HBV treatment |
US9765050B2 (en) | 2014-12-30 | 2017-09-19 | Novira Therapeutics, Inc. | Pyridyl reverse sulfonamides for HBV treatment |
GB201505658D0 (en) | 2015-04-01 | 2015-05-13 | Cancer Rec Tech Ltd | Inhibitor compounds |
EP3108883A1 (en) * | 2015-06-22 | 2016-12-28 | Fundació Institut de Recerca Biomèdica de Bellvitge | Therapeutic uses of non-peptide inhibitors of the calcineurin - nfat signalling pathway |
GB201617103D0 (en) | 2016-10-07 | 2016-11-23 | Cancer Research Technology Limited | Compound |
CN109503518B (zh) * | 2018-11-15 | 2021-03-30 | 中国医学科学院医药生物技术研究所 | 一种取代的双芳香基酰胺化合物及其制备方法和应用 |
WO2021026257A1 (en) * | 2019-08-06 | 2021-02-11 | Empirico Inc. | Prodrugs of alox-15 inhibitors and methods of using the same |
US20230117592A1 (en) * | 2019-12-23 | 2023-04-20 | Sri International | Lipoxygenase inhibitors |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH373028A (de) * | 1960-08-29 | 1963-11-15 | Geigy Ag J R | Verfahren zur Herstellung neuer Aminobenzoesäurederivate |
DE3743517A1 (de) | 1987-12-22 | 1989-07-06 | Basf Ag | Verfahren zur herstellung von aromatischen hydroxycarbonsaeuren |
DE3816703A1 (de) | 1988-05-17 | 1989-11-30 | Hoechst Ag | Heterocyclisch substituierte phenoxysulfonylharnstoffe, verfahren zu ihrer herstellung und ihre verwendung als herbizide oder pflanzenwachstumsregulatoren |
US5041545A (en) | 1989-04-06 | 1991-08-20 | Atochem North America, Inc. | 2-hydroxybenzophenone hydrazides and derivatives thereof |
US5256686A (en) * | 1989-06-27 | 1993-10-26 | Ono Pharmaceutical Co., Ltd. | Phenylalkan(en)oic acid |
US5177246A (en) | 1989-10-02 | 1993-01-05 | Ciba-Geigy Corporation | Hydroxphenylcarboxylic acid esters as stabilizers |
AU648359B2 (en) | 1990-11-22 | 1994-04-21 | Janssen Pharmaceutica N.V. | Isonicotinic acid derivatives |
US5049496A (en) | 1990-12-24 | 1991-09-17 | General Electric Company | Method for microbiologically hydroxylating biphenyl and terphenyl compounds |
US5382690A (en) | 1992-08-11 | 1995-01-17 | Mitsui Toatsu Chemicals, Incorporated | Method for preparing aromatic secondary amino compound |
DE4238994A1 (de) | 1992-11-19 | 1994-05-26 | Basf Ag | Aniline als Markierungsmittel für Mineralöle |
DE4331416A1 (de) | 1993-12-09 | 1995-06-14 | Bayer Ag | Verwendung von Phenylcarbonsäure-amiden als Kristallisationsinhibitoren |
-
1998
- 1998-11-20 KR KR1020007006971A patent/KR20010033470A/ko not_active Application Discontinuation
- 1998-11-20 AT AT98959510T patent/ATE282591T1/de not_active IP Right Cessation
- 1998-11-20 AU AU15297/99A patent/AU1529799A/en not_active Abandoned
- 1998-11-20 NZ NZ502963A patent/NZ502963A/en unknown
- 1998-11-20 BR BR9814327-1A patent/BR9814327A/pt not_active IP Right Cessation
- 1998-11-20 WO PCT/US1998/024688 patent/WO1999032433A1/en active IP Right Grant
- 1998-11-20 US US09/529,135 patent/US6268387B1/en not_active Expired - Fee Related
- 1998-11-20 ES ES98959510T patent/ES2234169T3/es not_active Expired - Lifetime
- 1998-11-20 EP EP98959510A patent/EP1042276B1/en not_active Expired - Lifetime
- 1998-11-20 JP JP2000525370A patent/JP2001526255A/ja not_active Withdrawn
- 1998-11-20 CA CA002300197A patent/CA2300197A1/en not_active Abandoned
- 1998-11-20 DE DE69827664T patent/DE69827664T2/de not_active Expired - Fee Related
- 1998-12-22 CO CO98076093A patent/CO4990966A1/es unknown
- 1998-12-22 ZA ZA9811805A patent/ZA9811805B/xx unknown
- 1998-12-22 UY UY25322A patent/UY25322A1/es unknown
- 1998-12-22 AR ARP980106614A patent/AR024826A1/es unknown
- 1998-12-22 PE PE1998001268A patent/PE20000064A1/es not_active Application Discontinuation
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2001
- 2001-05-15 US US09/858,089 patent/US6528528B2/en not_active Expired - Fee Related
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ES2234169T3 (es) | 2005-06-16 |
US6268387B1 (en) | 2001-07-31 |
US20010031874A1 (en) | 2001-10-18 |
EP1042276A1 (en) | 2000-10-11 |
DE69827664D1 (de) | 2004-12-23 |
KR20010033470A (ko) | 2001-04-25 |
AU1529799A (en) | 1999-07-12 |
ATE282591T1 (de) | 2004-12-15 |
ZA9811805B (en) | 1999-06-29 |
WO1999032433A1 (en) | 1999-07-01 |
EP1042276B1 (en) | 2004-11-17 |
JP2001526255A (ja) | 2001-12-18 |
AR024826A1 (es) | 2002-10-30 |
UY25322A1 (es) | 2004-07-30 |
CA2300197A1 (en) | 1999-07-01 |
US6528528B2 (en) | 2003-03-04 |
DE69827664T2 (de) | 2005-12-08 |
BR9814327A (pt) | 2000-10-03 |
PE20000064A1 (es) | 2000-02-11 |
NZ502963A (en) | 2002-06-28 |
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