PE20091473A1 - Heterociclos como inhibidores de esteaoril-coa desaturasa - Google Patents

Heterociclos como inhibidores de esteaoril-coa desaturasa

Info

Publication number
PE20091473A1
PE20091473A1 PE2009000239A PE2009000239A PE20091473A1 PE 20091473 A1 PE20091473 A1 PE 20091473A1 PE 2009000239 A PE2009000239 A PE 2009000239A PE 2009000239 A PE2009000239 A PE 2009000239A PE 20091473 A1 PE20091473 A1 PE 20091473A1
Authority
PE
Peru
Prior art keywords
oxo
methyl
alkyl
inhibitors
thiazol
Prior art date
Application number
PE2009000239A
Other languages
English (en)
Inventor
Sultan Chowdhury
Natalie Dales
Julia Fonarev
Jianmin Fu
Duanjie Hou
Qi Jia
Vishnumurthy Kodumuru
Natalia Pokrovskaia
Shaoyi Sun
Zaihui Zhang
Original Assignee
Novartis Ag
Xenon Pharmaceuticals Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40740143&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20091473(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag, Xenon Pharmaceuticals Inc filed Critical Novartis Ag
Publication of PE20091473A1 publication Critical patent/PE20091473A1/es

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/10—Anti-acne agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • 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
    • 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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
    • 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
    • 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

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Dermatology (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

REFERIDA A COMPUESTOS DERIVADOS DE FORMULA (I) DONDE Q ES DE PREFERENCIA 2-OXO-IMIDAZOLIDIN-1-IL, 5-OXO-1H-1,2,4-TRIAZOL-4(5H)-IL; W ES -N(R6)C(O)-, -R8-C(O)N(R6)-, -R8-OC(O)N(R6)-, ENTRE OTROS; R6 ES H, ALQUILO, HIDROXIALQUILO, ENTRE OTROS; R8 ES UN ENLACE, ALQUILENO, ALQUENILENO, ENTRE OTROS; V ES -C(O)N(R6)-, S(O)t-, -C(O)-, ENTRE OTROS; R1 ES H, HALO, ALQUILO, ENTRE OTROS; R2 ES H, ALQUILO, ALQUENILO, ENTRE OTROS; R3 ES H O ALQUILO; t ES 1-2. SON COMPUESTOS SELECCIONADOS: 2-(1-(4-FLUORO-BENCIL)-5-OXO-1H-1,2,4-TRIAZOL-4(5H)-IL)-4-METIL-TIAZOL-5-CARBOXAMIDA; 2-[1-(CICLOPROPIL-METIL)-5-OXO-1H-1,2,4-TRIAZOL-4(5H)-IL]-4-METIL-TIAZOL-5-CARBOXAMIDA; 4-METIL-2-{2-OXO-3-[4-(TRIFLUORO-METIL)-BENCIL]-IMIDAZOLIDIN-1-IL}TIAZOL-5-CARBOXAMIDA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE ESTEAROIL-CoA-DESATURASA, UTILES PARA EL TRATAMIENTO DE LA DISLIPIDEMIA, DIABETES, OBESIDAD, ENTRE OTROS
PE2009000239A 2008-02-20 2009-02-18 Heterociclos como inhibidores de esteaoril-coa desaturasa PE20091473A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3013708P 2008-02-20 2008-02-20

Publications (1)

Publication Number Publication Date
PE20091473A1 true PE20091473A1 (es) 2009-10-23

Family

ID=40740143

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2009000239A PE20091473A1 (es) 2008-02-20 2009-02-18 Heterociclos como inhibidores de esteaoril-coa desaturasa

Country Status (29)

Country Link
US (2) US8049016B2 (es)
EP (1) EP2245029B1 (es)
JP (2) JP5507474B2 (es)
KR (1) KR101584826B1 (es)
CN (1) CN102007123B (es)
AR (1) AR070429A1 (es)
AU (1) AU2009216769A1 (es)
BR (1) BRPI0907826A2 (es)
CA (1) CA2715947C (es)
CL (1) CL2009000381A1 (es)
CO (1) CO6290655A2 (es)
CR (1) CR11629A (es)
CU (1) CU23890B1 (es)
EA (1) EA022797B1 (es)
EC (1) ECSP10010411A (es)
HK (1) HK1144808A1 (es)
HN (1) HN2010001647A (es)
IL (1) IL207578A (es)
JO (1) JO3014B1 (es)
MA (1) MA32150B1 (es)
MX (1) MX2010009158A (es)
MY (1) MY156317A (es)
NZ (1) NZ587350A (es)
PE (1) PE20091473A1 (es)
SV (1) SV2010003650A (es)
TW (1) TWI457338B (es)
UA (1) UA105000C2 (es)
WO (1) WO2009103739A1 (es)
ZA (1) ZA201005725B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2660201C (en) 2006-08-15 2016-05-03 Novartis Ag Organic compounds
BRPI0720452A2 (pt) * 2006-12-20 2014-01-14 Novartis Ag Compostos orgânicos
NZ587350A (en) 2008-02-20 2012-07-27 Novartis Ag Thiazole derivatives featuring an imidazolidine or triazole derivative as inhibitors of stearoyl-CoA desaturase
US8168794B2 (en) 2008-03-03 2012-05-01 Novartis Ag Pim kinase inhibitors and methods of their use
EA201200545A1 (ru) * 2009-10-01 2012-12-28 Новартис Аг Производные пиразола, которые модулируют стеароил-соа десатуразу
AR091022A1 (es) * 2012-05-11 2014-12-30 Abbvie Inc Inhibidores del nampt
CA2873672A1 (en) 2012-05-21 2013-11-28 Novartis Ag Novel ring-substituted n-pyridinyl amides as kinase inhibitors
US20190315771A1 (en) * 2016-09-08 2019-10-17 Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. Novel 2-acylaminothiazole derivative and preparation method therefor and use thereof
WO2018081167A1 (en) 2016-10-24 2018-05-03 Yumanity Therapeutics Compounds and uses thereof
EP3566055A4 (en) 2017-01-06 2020-12-02 Yumanity Therapeutics, Inc. TREATMENT METHODS FOR NEUROLOGICAL DISORDERS
CA3083000A1 (en) 2017-10-24 2019-05-02 Yumanity Therapeutics, Inc. Compounds and uses thereof
CN114222732B (zh) * 2019-10-28 2023-04-04 南京明德新药研发有限公司 一种尿酸促排剂及其合成方法和其在医药上的应用

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH590267A5 (es) * 1972-10-04 1977-07-29 Ciba Geigy Ag
US4058617A (en) * 1972-10-04 1977-11-15 Ciba-Geigy Corporation Imidazoles and pharmaceutical composition
IL44282A (en) 1974-02-25 1979-01-31 Ciba Geigy Ag 1-(1-alkyl-4(5)nitro-imidazol-2-yl)-2-oxo-tetrahydroimidazole derivatives, their manufacture and pharmaceutical compositions containing them
CA2302417A1 (en) 1997-10-27 1999-05-06 Takeda Chemical Industries, Ltd. Adenosine a3 receptor antagonists
WO2001010865A1 (fr) 1999-08-06 2001-02-15 Takeda Chemical Industries, Ltd. INHIBITEURS DE p38MAP KINASE
EP1268474A2 (en) 2000-03-30 2003-01-02 Takeda Chemical Industries, Ltd. Substituted 1,3-thiazole compounds, their production and use
CA2436739A1 (en) 2000-12-26 2002-07-04 Takeda Chemical Industries, Ltd. Combination agent
CA2450400A1 (en) 2001-06-11 2002-12-19 Takeda Chemical Industries, Ltd. Medicinal compositions
WO2005077937A1 (en) 2004-01-09 2005-08-25 Cadila Healthcare Limited Substituted hydroxamic acid derivatives as tnf inhibitors
EP1621539A1 (en) 2004-07-27 2006-02-01 Aventis Pharma S.A. Heterocycle -substituted cyclic urea derivatives, preparation thereof and pharmaceutical use thereof as kinase inhibitors
CN101083992A (zh) * 2004-09-20 2007-12-05 泽农医药公司 抑制人硬脂酰CoA去饱和酶的哒嗪衍生物
AR051092A1 (es) * 2004-09-20 2006-12-20 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como inhibidores de la estearoil-coa
CA2618646A1 (en) * 2005-06-03 2007-11-15 Xenon Pharmaceuticals Inc. Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors
CN101460476B (zh) 2006-06-05 2013-12-04 诺瓦提斯公司 有机化合物
CA2660201C (en) * 2006-08-15 2016-05-03 Novartis Ag Organic compounds
MX2009002019A (es) 2006-08-24 2009-03-09 Novartis Ag Derivados de 2-(pirazin-2-il)-tiazol y 2-(1h-pirazol-3-il)-tiazol asi como compuestos relacionados como inhibidores de la estearoil-coa-desaturasa (scd) para el tratamiento de trastornos metabolicos, cardiovasculares, y otros.
EP2066664A1 (en) * 2006-09-22 2009-06-10 Novartis AG Heterocyclic organic compounds
GB0621452D0 (en) * 2006-10-27 2006-12-06 Ucl Business Plc Therapy for liver disease
BRPI0720452A2 (pt) * 2006-12-20 2014-01-14 Novartis Ag Compostos orgânicos
US8252810B2 (en) * 2008-02-13 2012-08-28 Eisai R&D Management Co., Ltd. Bicycloamine derivatives
NZ587350A (en) 2008-02-20 2012-07-27 Novartis Ag Thiazole derivatives featuring an imidazolidine or triazole derivative as inhibitors of stearoyl-CoA desaturase
MX2010014572A (es) 2008-06-27 2011-03-24 Novartis Ag Compuestos organicos.

Also Published As

Publication number Publication date
JP5813162B2 (ja) 2015-11-17
AR070429A1 (es) 2010-04-07
BRPI0907826A2 (pt) 2019-12-10
MA32150B1 (fr) 2011-03-01
TWI457338B (zh) 2014-10-21
KR20100117677A (ko) 2010-11-03
CO6290655A2 (es) 2011-06-20
CL2009000381A1 (es) 2010-09-10
EP2245029A1 (en) 2010-11-03
MX2010009158A (es) 2010-09-24
ECSP10010411A (es) 2010-09-30
JP2011512384A (ja) 2011-04-21
MY156317A (en) 2016-02-15
TW200942534A (en) 2009-10-16
CA2715947C (en) 2016-10-25
SV2010003650A (es) 2011-07-05
US8049016B2 (en) 2011-11-01
HK1144808A1 (en) 2011-03-11
AU2009216769A1 (en) 2009-08-27
NZ587350A (en) 2012-07-27
JO3014B1 (ar) 2016-09-05
US20090264444A1 (en) 2009-10-22
WO2009103739A1 (en) 2009-08-27
JP2014132025A (ja) 2014-07-17
CR11629A (es) 2010-11-16
KR101584826B1 (ko) 2016-01-18
CN102007123B (zh) 2014-04-30
CU20100170A7 (es) 2011-10-31
ZA201005725B (en) 2011-04-28
JP5507474B2 (ja) 2014-05-28
IL207578A (en) 2014-11-30
CN102007123A (zh) 2011-04-06
EA022797B1 (ru) 2016-03-31
CU23890B1 (es) 2013-04-19
CA2715947A1 (en) 2009-08-27
UA105000C2 (uk) 2014-04-10
IL207578A0 (en) 2010-12-30
HN2010001647A (es) 2013-11-11
US8318949B2 (en) 2012-11-27
EP2245029B1 (en) 2015-04-15
US20120014906A1 (en) 2012-01-19
EA201001315A1 (ru) 2011-06-30

Similar Documents

Publication Publication Date Title
PE20091473A1 (es) Heterociclos como inhibidores de esteaoril-coa desaturasa
PE20211375A1 (es) Compuestos de 4-aminoisoindolina-1,3-diona sustituidos y su uso para el tratamiento de linfoma
PE20090773A1 (es) Derivados de morfolina pirimidina
PE20120008A1 (es) Derivados de fenoxi bencenosulfonamida
PE20050874A1 (es) Compuestos de bencimidazolona que tienen actividad agonista del receptor 5-ht4
PE20120690A1 (es) Derivados de 5-fluoropirimidinona
PE20051173A1 (es) Compuestos azabiciclico (3.1.0) hexanos como moduladores de receptores de dopamina d3
PE20160843A1 (es) Pirrolidinonas herbicidas
PE20091816A1 (es) Inhibidores de bace
PE20080056A1 (es) Derivados de cromencarboxamida como antagonistas del receptor s1p1
PE20120693A1 (es) Compuestos heterociclos como moduladores de la piruvato cinasa m2 (pkm2)
PE20140102A1 (es) Compuestos de piperidina puenteada tipo quinoxalina sustituida con actividad sobre el receptor orl-1
PE20110433A1 (es) Antagonistas de la via hedgehog de ftalazina disustituida
PE20090895A1 (es) Derivados de triazol como inhibidores de la jak quinasa
PE20080065A1 (es) Compuestos derivados de bencimidazol como moduladores del receptor vainilloide vr1
PE20110341A1 (es) COMPUESTOS HETEROCICLICOS QUE MODULAN LA ACTIVIDAD DE LA ESTEROIL-CoA-DESATURASA
PE20121506A1 (es) Compuestos triazolopiridinas como inhibidores de c-met
PE20060736A1 (es) DERIVADOS DE PIRROL COMO ANTAGONISTAS DE CRTh2
PE20121695A1 (es) 5-alquinil-pirimidinas
PE20141203A1 (es) Benzilindazoles sustituidos para uso como inhibidores de la quinasa bub1 en el tratamiento de enfermedades hiperproliferativas
PE20121159A1 (es) DERIVADOS DE PIRIDINA, PIRAZINA Y QUINOLINA COMO INHIBIDORES DE LA FOSFOINOSITIDA 3 CINASA Y LA mTOR
PE20090904A1 (es) ARILOXAZOLES SUSTITUIDOS COMO LIGANDOS DE LOS RECEPTORES DE ADENOSINA A1 Y/O A2b
PE20080925A1 (es) DERIVADOS DE PIRROLO[2,3-b]PIRIDINA COMO INHIBIDORES DE QUINASA, EN PARTICULAR INHIBIDORES IKK2 (O IKK BETA)
PE20090041A1 (es) Derivados de triazol como inhibidores de la biosintesis de leucotrienos
PE20090160A1 (es) COMPUESTOS AMINO-5-[4-(DIFLUOROMETOXI)FENIL SUSTITUIDO]-5-FENILIMIDAZOLONA COMO INHIBIDORES DE ß-SECRETASA

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed