ES2181052T3 - Fenilacetamidas como inhibidores de la spla2. - Google Patents

Fenilacetamidas como inhibidores de la spla2.

Info

Publication number
ES2181052T3
ES2181052T3 ES97952228T ES97952228T ES2181052T3 ES 2181052 T3 ES2181052 T3 ES 2181052T3 ES 97952228 T ES97952228 T ES 97952228T ES 97952228 T ES97952228 T ES 97952228T ES 2181052 T3 ES2181052 T3 ES 2181052T3
Authority
ES
Spain
Prior art keywords
phenylacetamids
spla2
inhibitors
septi
phenylacetamides
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES97952228T
Other languages
English (en)
Inventor
Theodore Goodson Jr
Richard W Harper
David K Herron
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Application granted granted Critical
Publication of ES2181052T3 publication Critical patent/ES2181052T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C07C233/04Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C233/05Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C07C233/11Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/32Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C07C235/34Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Obesity (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

LA PRESENTE INVENCION SE REFIERE A UNA CLASE DE NUEVAS FENILACETAMIDAS ASI COMO AL USO DE ESTOS COMPUESTOS TRATANDOSE DE INHIBIR LA LIBERACION DE LOS ACIDOS GRASOS CON MEDIACION SPLA 2 DE FORMA QUE SE TRATEN LOS TRASTORNOS COMO, POR EJEMPLO, UN CHOQUE SEPTICO.
ES97952228T 1996-12-03 1997-11-25 Fenilacetamidas como inhibidores de la spla2. Expired - Lifetime ES2181052T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3250896P 1996-12-03 1996-12-03

Publications (1)

Publication Number Publication Date
ES2181052T3 true ES2181052T3 (es) 2003-02-16

Family

ID=21865299

Family Applications (1)

Application Number Title Priority Date Filing Date
ES97952228T Expired - Lifetime ES2181052T3 (es) 1996-12-03 1997-11-25 Fenilacetamidas como inhibidores de la spla2.

Country Status (12)

Country Link
US (1) US6353128B1 (es)
EP (1) EP0946495B1 (es)
JP (1) JP2001505575A (es)
KR (1) KR20000069248A (es)
AU (1) AU5589298A (es)
BR (1) BR9713987A (es)
CA (1) CA2273995A1 (es)
DE (1) DE69714289T2 (es)
ES (1) ES2181052T3 (es)
HU (1) HUP9904172A2 (es)
IL (1) IL130200A0 (es)
WO (1) WO1998024756A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20010042307A (ko) 1998-03-31 2001-05-25 시오노 요시히코 피롤로[1,2-a]피라진 sPLA2 억제제
EP1085021A4 (en) 1998-05-21 2003-01-08 Shionogi & Co DERIVATIVES OF PYRROLO 1,2-B] PYRIDAZINE, WITH INHIBITOR EFFECT ON SPLA 2?
ATE329619T1 (de) 1998-10-14 2006-07-15 Shionogi & Co Spla2-inhibitoren zur behandlung von ischämischen reperfusionsschäden
FR2793791B1 (fr) * 1999-05-19 2002-01-25 Univ Paris 7 Denis Diderot Nouveaux composes inhibiteurs specifiques de phospholipases a2
AU6015600A (en) 1999-07-19 2001-02-05 Shionogi & Co., Ltd. Tricyclic compounds having spla2-inhibitory activities
JP4636522B2 (ja) 1999-08-02 2011-02-23 塩野義製薬株式会社 sPLA2阻害作用を有する三環式化合物
WO2001014378A1 (fr) 1999-08-23 2001-03-01 Shionogi & Co., Ltd. DERIVES DE PYRROLOTRIAZINE A ACTIVITES INHIBANT sPLA¿2?
SE0000754D0 (sv) * 2000-03-07 2000-03-07 Amersham Pharm Biotech Ab Mass spectral peak identification
US6967200B2 (en) 2000-06-29 2005-11-22 Shionogi & Co., Ltd. Remedies for cirrhosis
AU2001267823A1 (en) 2000-06-29 2002-01-08 Shionogi And Co., Ltd. Compounds exhibiting x-type spla2 inhibiting effect
TWI314457B (es) 2001-03-19 2009-09-11 Shionogi & Co
EP2424521A4 (en) 2009-04-29 2015-03-04 Amarin Pharmaceuticals Ie Ltd PHARMACEUTICAL COMPOSITIONS COMPRISING EPA AND CARDIOVASCULAR AGENT AND METHODS OF USE
WO2015026990A2 (en) * 2013-08-20 2015-02-26 University Of Washington Through Its Center For Commercialization Novel and specific inhibitors of cytochrome p450 26 retinoic acid hydrolase

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1584246A (en) 1976-06-16 1981-02-11 Ici Ltd Carboxamidoesters
US4256758A (en) 1979-06-11 1981-03-17 Merck & Co., Inc. 4-Substituted-3-hydroxy-3-pyrroline-2,5-dione inhibitors of glycolic acid oxidase
EP0161529B1 (en) 1984-05-18 1989-07-12 Asahi Kasei Kogyo Kabushiki Kaisha 2-nitro-5-(2'-chloro-4'trifluoromethylphenoxy)phenylacetic ester, thioester and amide, process for preparation therof, herbicidal composition, and method for destruction of undesirable weeds
DE3812768A1 (de) 1988-04-16 1989-10-26 Bayer Ag Halogensubstituierte phenoxybenzylverbindungen
BR9612347A (pt) 1995-12-13 1999-07-13 Lilly Co Eli Naftil acetamidas como inibidores de spla2

Also Published As

Publication number Publication date
US6353128B1 (en) 2002-03-05
EP0946495B1 (en) 2002-07-24
CA2273995A1 (en) 1998-06-11
EP0946495A1 (en) 1999-10-06
EP0946495A4 (en) 2000-04-12
KR20000069248A (ko) 2000-11-25
DE69714289D1 (en) 2002-08-29
WO1998024756A1 (en) 1998-06-11
BR9713987A (pt) 2000-02-08
HUP9904172A2 (hu) 2000-05-28
AU5589298A (en) 1998-06-29
IL130200A0 (en) 2000-06-01
DE69714289T2 (de) 2003-01-16
JP2001505575A (ja) 2001-04-24

Similar Documents

Publication Publication Date Title
ES2179088T3 (es) Inhibidores de flsa2 1h-indol-3-glioxilamida.
ES2181052T3 (es) Fenilacetamidas como inhibidores de la spla2.
BR9714002A (pt) Pirróis como inibidores de spla2
ES2162198T3 (es) Agentes estrogenos.
RU94012931A (ru) Гидразиды 1н-индол-3-уксусной кислоты как ингибиторы spla2
EA199900301A2 (ru) Замещенные трициклические соединения
ATE347362T1 (de) Bicyclische spla 2-inhibitoren
BR9713261A (pt) Tricìclicos substituìdos
ES2159347T3 (es) Naftil-acetamidas como inhibidores de spla2.
ES2195182T3 (es) Fenil glioxamidas como inhibidores de spla2.
SV1999000052A (es) Triciclicos substituidos ref. x-12144
ATE326963T1 (de) Indolverbindungen als spla2 inhibitoren
GR3031602T3 (en) Novel 2-substituted indane-2-mercaptoacetylamide tricyclic derivatives useful as inhibitors of enkephalinase.
ES2174034T3 (es) Naftilglioxamidas como inhibidores de spla2
ATE247119T1 (de) Substituierte pyrroloindole
DE60032774D1 (de) Spla2 inhibitoren
ES2184192T3 (es) Procedimiento microbiologico para la transformacion de 3-oxo-4-azaesteroides 17beta-carboxisustituidos y uso de tales productos como inhibidores de la enzima 5alfa-reductasa.
ECSP982563A (es) Procedimiento para la preparacion de 4- sustituido -1h- indol -3-glioxamidas
AR013802A1 (es) Inhibidores de angiogenesis de triazina