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CR6963A - Formas de sal de amida de acido 3.(4-bromo-2,6-difluoro-benciloxi)-5-(3-(4-piprolidin-1-ilbutil)ureido)isotiazol-4-carboxilico y metodo de produccion - Google Patents

Formas de sal de amida de acido 3.(4-bromo-2,6-difluoro-benciloxi)-5-(3-(4-piprolidin-1-ilbutil)ureido)isotiazol-4-carboxilico y metodo de produccion

Info

Publication number
CR6963A
CR6963A CR6963A CR6963A CR6963A CR 6963 A CR6963 A CR 6963A CR 6963 A CR6963 A CR 6963A CR 6963 A CR6963 A CR 6963A CR 6963 A CR6963 A CR 6963A
Authority
CR
Costa Rica
Prior art keywords
isotiazol
carboxilico
amida
ureido
bromo
Prior art date
Application number
CR6963A
Other languages
English (en)
Inventor
G Gant Thomas
Robert Williams Glenn
Original Assignee
Pfizer Prod 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
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of CR6963A publication Critical patent/CR6963A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Dermatology (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Ophthalmology & Optometry (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

LA INVENCION SE REFIERE A LAS FORMAS DE SAL HIDROCLORURO, HIDROBROMURO, HEMICITRATO, ACETATO, P-TOSILATO, HEMISUCCINATO Y MESILATO DE AMIDA DE ACIDO 3-(4-BROMO-2,6-DIFLUOROBENCILOXI)-5-(3-(PIRROLIDIN-1-ILBUTIL)UREIDO)ISOTIAZOL-4-CARBOXILICO.LA INVENCION TAMBIEN SE REFIERE A COMPOSICIONES FARMACEUTICAS QUE CONTIENEN SALES HIDROCLORURO, HIDROBROMURO, HEMICITRATO, ACETATO, P-TOSILATO, L-TARTRATO, HEMISUCCINATO Y MESILATO DE FORMULA I. LA INVENCION SE REFIERE ADEMAS A METODOS PARA TRATAR ENFERMEDADES HIPERPROLIFERATIVAS, TALES COMO CANCERES, EN MAMIFERS ESPECIALMENTE SERES HUMANOS, POR ADMINISTRACION DE LAS SALES ANTERIORES Y LOS METODOS PARA PREPARAR LAS FORMAS CRISTALINAS DE LAS SALES ANTERIORES.
CR6963A 2000-11-28 2003-04-24 Formas de sal de amida de acido 3.(4-bromo-2,6-difluoro-benciloxi)-5-(3-(4-piprolidin-1-ilbutil)ureido)isotiazol-4-carboxilico y metodo de produccion CR6963A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US25351300P 2000-11-28 2000-11-28

Publications (1)

Publication Number Publication Date
CR6963A true CR6963A (es) 2003-11-25

Family

ID=22960587

Family Applications (1)

Application Number Title Priority Date Filing Date
CR6963A CR6963A (es) 2000-11-28 2003-04-24 Formas de sal de amida de acido 3.(4-bromo-2,6-difluoro-benciloxi)-5-(3-(4-piprolidin-1-ilbutil)ureido)isotiazol-4-carboxilico y metodo de produccion

Country Status (49)

Country Link
US (1) US6831091B2 (es)
EP (1) EP1337521B1 (es)
JP (2) JP2004514714A (es)
KR (2) KR20050116401A (es)
CN (1) CN1231474C (es)
AP (1) AP2001002358A0 (es)
AR (1) AR031512A1 (es)
AT (1) ATE340786T1 (es)
AU (2) AU2002214204B2 (es)
BG (1) BG107752A (es)
BR (1) BR0115621A (es)
CA (1) CA2430065C (es)
CR (1) CR6963A (es)
CY (1) CY1106240T1 (es)
CZ (1) CZ20031315A3 (es)
DE (1) DE60123461T2 (es)
DK (1) DK1337521T3 (es)
DO (1) DOP2001000288A (es)
EA (1) EA005859B1 (es)
EC (1) ECSP034628A (es)
EE (1) EE200300247A (es)
ES (1) ES2271086T3 (es)
GE (1) GEP20053652B (es)
GT (1) GT200100237A (es)
HN (1) HN2001000268A (es)
HR (1) HRP20030408A2 (es)
HU (1) HUP0302553A3 (es)
IL (1) IL155371A0 (es)
IS (1) IS6788A (es)
MA (1) MA26960A1 (es)
MX (1) MXPA03004714A (es)
MY (1) MY136686A (es)
NO (1) NO325187B1 (es)
NZ (1) NZ525788A (es)
OA (1) OA12532A (es)
PA (1) PA8533801A1 (es)
PE (1) PE20020591A1 (es)
PL (1) PL362079A1 (es)
PT (1) PT1337521E (es)
SI (1) SI1337521T1 (es)
SK (1) SK5862003A3 (es)
SV (1) SV2002000748A (es)
TN (1) TNSN01167A1 (es)
TW (1) TWI287542B (es)
UA (1) UA74221C2 (es)
UY (1) UY27039A1 (es)
WO (1) WO2002044158A1 (es)
YU (1) YU36403A (es)
ZA (1) ZA200303341B (es)

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ME00275B (me) 1999-01-13 2011-02-10 Bayer Corp ω-KARBOKSIARIL SUPSTITUISANI DIFENIL KARBAMIDI KAO INHIBITORI RAF KINAZE
JP2002534468A (ja) 1999-01-13 2002-10-15 バイエル コーポレイション p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
PT1478358E (pt) 2002-02-11 2013-09-11 Bayer Healthcare Llc Tosilato de sorafenib para o tratamento de doenças caracterizadas por angiogénese anormal
US20030216396A1 (en) 2002-02-11 2003-11-20 Bayer Corporation Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
CA2493701A1 (en) * 2002-07-25 2004-02-05 Pfizer Products Inc. Isothiazole derivatives useful as anticancer agents
BR0313593A (pt) * 2002-08-19 2005-07-12 Pfizer Prod Inc Terapia de combinação para doenças hiperproliferativas
DK1636585T3 (da) 2003-05-20 2008-05-26 Bayer Pharmaceuticals Corp Diarylurinstoffer med kinasehæmmende aktivitet
PT1663978E (pt) 2003-07-23 2008-02-15 Bayer Pharmaceuticals Corp Omega-carboxiaril difenil ureia substituída por flúor para o tratamento e a prevenção de doenças e estados patológicos
CA2543201C (en) * 2003-10-27 2010-12-21 Merck & Co., Inc. ((ir, 3s)-3-isopropyl-3-{ [3-(trifluoromethyl)-7, 8-dihydro-1, 6-naphthyridin-6 (5h)-yl] carbonyl} cyclopentyl) [(3s, 4s)-3-methoxytetrahydro-2h-pyran-4-yl] amine succinate salt, composition thereof, and its use in the treatment of inflammatory diseases
EP1694686A1 (en) 2003-12-19 2006-08-30 Takeda San Diego, Inc. Kinase inhibitors
WO2005102327A1 (en) * 2004-04-20 2005-11-03 Pfizer Products Inc. Dosage forms and methods of treatment using vegfr inhibitors
MXPA06012394A (es) 2004-04-30 2007-01-31 Bayer Pharmaceuticals Corp Derivados de pirazolilurea sustituidos utiles en el tratamiento de cancer.
TW200538104A (en) * 2004-05-17 2005-12-01 Pfizer Prod Inc Phenyl derivatives for the treatment of abnormal cell growth
EP1778669A2 (en) 2004-08-18 2007-05-02 Takeda San Diego, Inc. Kinase inhibitors
DE602005023333D1 (de) 2004-10-15 2010-10-14 Takeda Pharmaceutical Kinaseinhibitoren
US8119655B2 (en) 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
ZA200810017B (en) 2006-06-16 2010-04-28 Lundbeck & Co As H 1- [2- (2, 4-Dimethylphenylsulfanyl) -phenyl] piperazine as a compound with combined serotonin Reuptake, 5-HT3 and 5-HT1A activity for the treatment of cognitive impairment
US7932390B2 (en) 2006-06-29 2011-04-26 Hoffman-La Roche Inc. Substituted thieno[3,2-C]pyridine carboxylic acid derivatives
EA200970361A1 (ru) 2006-10-09 2010-02-26 Такеда Фармасьютикал Компани Лимитед Ингибиторы киназы
MX2010001636A (es) 2007-08-14 2010-03-15 Hoffmann La Roche Derivados de pirazolo[3,4-d]-pirimidina como agentes antiproliferativos.
WO2011073521A1 (en) 2009-12-15 2011-06-23 Petri Salven Methods for enriching adult-derived endothelial progenitor cells and uses thereof
SG187592A1 (en) 2010-07-23 2013-03-28 Univ Boston Anti-despr inhibitors as therapeutics for inhibition of pathological angiogenesis and tumor cell invasiveness and for molecular imaging and targeted delivery
TR201901462T4 (tr) 2013-03-14 2019-02-21 Panoptica Inc Gözün posterior segmentine ilaç uygulanması için oküler formülasyonlar.
AU2015317531B2 (en) * 2014-09-17 2020-11-19 Panoptica, Inc. Ocular formulations for drug-delivery and protection of the anterior segment of the eye
AU2023416218A1 (en) * 2022-12-28 2025-07-10 Beyang Therapeutics Co., Ltd. Protein tyrosine kinase inhibitor and medical use thereof
WO2026002142A1 (zh) * 2024-06-27 2026-01-02 苏州必扬医药科技有限公司 一种蛋白酪氨酸激酶抑制剂的半琥珀酸盐晶型
WO2026002133A1 (zh) * 2024-06-27 2026-01-02 苏州必扬医药科技有限公司 一种蛋白酪氨酸激酶抑制剂的盐型
WO2026002126A1 (zh) * 2024-06-27 2026-01-02 苏州必扬医药科技有限公司 一种蛋白酪氨酸激酶抑制剂及其眼用制剂

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Publication number Priority date Publication date Assignee Title
UA60365C2 (uk) * 1998-06-04 2003-10-15 Пфайзер Продактс Інк. Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця

Also Published As

Publication number Publication date
UA74221C2 (uk) 2005-11-15
PA8533801A1 (es) 2002-10-31
ES2271086T3 (es) 2007-04-16
MY136686A (en) 2008-11-28
ATE340786T1 (de) 2006-10-15
JP2008056692A (ja) 2008-03-13
GT200100237A (es) 2002-07-03
HN2001000268A (es) 2002-01-30
DE60123461D1 (de) 2006-11-09
EA005859B1 (ru) 2005-06-30
MXPA03004714A (es) 2003-08-19
DOP2001000288A (es) 2002-12-15
BR0115621A (pt) 2003-09-02
AU1420402A (en) 2002-06-11
DE60123461T2 (de) 2007-02-15
NO20032388L (no) 2003-07-18
KR20050116401A (ko) 2005-12-12
CN1231474C (zh) 2005-12-14
AP2001002358A0 (en) 2001-12-31
UY27039A1 (es) 2002-07-31
SV2002000748A (es) 2002-12-02
IL155371A0 (en) 2003-11-23
OA12532A (en) 2006-06-02
IS6788A (is) 2003-04-14
JP2004514714A (ja) 2004-05-20
NO325187B1 (no) 2008-02-11
SI1337521T1 (sl) 2006-12-31
PL362079A1 (en) 2004-10-18
HK1059085A1 (en) 2004-06-18
AU2002214204B2 (en) 2007-05-24
YU36403A (sh) 2006-08-17
NZ525788A (en) 2004-11-26
NO20032388D0 (no) 2003-05-27
US6831091B2 (en) 2004-12-14
TNSN01167A1 (fr) 2005-11-10
EP1337521A1 (en) 2003-08-27
HUP0302553A3 (en) 2009-03-30
CN1476439A (zh) 2004-02-18
HRP20030408A2 (en) 2003-08-31
CZ20031315A3 (cs) 2004-04-14
PT1337521E (pt) 2006-12-29
HUP0302553A2 (hu) 2003-11-28
PE20020591A1 (es) 2002-07-06
DK1337521T3 (da) 2007-01-29
WO2002044158A1 (en) 2002-06-06
EE200300247A (et) 2003-10-15
CY1106240T1 (el) 2011-06-08
KR20030059275A (ko) 2003-07-07
JP4971946B2 (ja) 2012-07-11
GEP20053652B (en) 2005-11-10
ECSP034628A (es) 2003-07-25
MA26960A1 (fr) 2004-12-20
BG107752A (bg) 2004-01-30
CA2430065A1 (en) 2002-06-06
SK5862003A3 (en) 2004-05-04
US20020151573A1 (en) 2002-10-17
CA2430065C (en) 2008-05-20
EA200300424A1 (ru) 2003-10-30
TWI287542B (en) 2007-10-01
ZA200303341B (en) 2004-04-30
EP1337521B1 (en) 2006-09-27
AR031512A1 (es) 2003-09-24

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