BR9609989A - Compostos de benzilaminopiperidina substituídos - Google Patents

Compostos de benzilaminopiperidina substituídos

Info

Publication number
BR9609989A
BR9609989A BR9609989A BR9609989A BR9609989A BR 9609989 A BR9609989 A BR 9609989A BR 9609989 A BR9609989 A BR 9609989A BR 9609989 A BR9609989 A BR 9609989A BR 9609989 A BR9609989 A BR 9609989A
Authority
BR
Brazil
Prior art keywords
compounds
substituted
substituted benzylaminopiperidine
benzylaminopiperidine compounds
benzylaminopiperidine
Prior art date
Application number
BR9609989A
Other languages
English (en)
Inventor
Kunio Satake
Yuji Shishido
Hiroaki Wakabayashi
Original Assignee
Pfizer
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 filed Critical Pfizer
Publication of BR9609989A publication Critical patent/BR9609989A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/56—Nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • 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
    • 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
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
BR9609989A 1995-08-24 1996-06-10 Compostos de benzilaminopiperidina substituídos BR9609989A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IB9500683 1995-08-24
PCT/IB1996/000572 WO1997008144A1 (en) 1995-08-24 1996-06-10 Substituted benzylaminopiperidine compounds

Publications (1)

Publication Number Publication Date
BR9609989A true BR9609989A (pt) 1999-07-06

Family

ID=11004362

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9609989A BR9609989A (pt) 1995-08-24 1996-06-10 Compostos de benzilaminopiperidina substituídos

Country Status (42)

Country Link
US (1) US6506775B1 (pt)
EP (2) EP1114817B1 (pt)
JP (1) JP3084069B2 (pt)
KR (1) KR100288673B1 (pt)
CN (1) CN1153764C (pt)
AP (1) AP643A (pt)
AR (1) AR006305A1 (pt)
AT (2) ATE258166T1 (pt)
AU (1) AU702698B2 (pt)
BG (1) BG64126B1 (pt)
BR (1) BR9609989A (pt)
CA (1) CA2227814C (pt)
CO (1) CO4480738A1 (pt)
CZ (1) CZ297543B6 (pt)
DE (2) DE69616817T2 (pt)
DK (2) DK1114817T3 (pt)
DZ (1) DZ2086A1 (pt)
ES (2) ES2163017T3 (pt)
HK (1) HK1014935A1 (pt)
HR (1) HRP960386B1 (pt)
HU (1) HU225480B1 (pt)
IL (1) IL119078A (pt)
IS (1) IS1947B (pt)
MA (1) MA23961A1 (pt)
MX (1) MX9801467A (pt)
MY (1) MY114800A (pt)
NO (1) NO310720B1 (pt)
NZ (1) NZ308207A (pt)
OA (1) OA10666A (pt)
PE (2) PE20010700A1 (pt)
PL (1) PL186773B1 (pt)
PT (2) PT1114817E (pt)
RO (1) RO119299B1 (pt)
RU (1) RU2152930C2 (pt)
SI (2) SI1114817T1 (pt)
SK (1) SK282925B6 (pt)
TN (1) TNSN96107A1 (pt)
TR (1) TR199800300T1 (pt)
TW (1) TW340842B (pt)
UA (1) UA48981C2 (pt)
WO (1) WO1997008144A1 (pt)
YU (1) YU49122B (pt)

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TW426667B (en) * 1997-11-19 2001-03-21 Pfizer Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists
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CA2373079A1 (en) * 1999-05-06 2000-11-16 Susan Beth Sobolov-Jaynes Substituted benzolactam compounds
RS49964B (sr) 1999-05-17 2008-09-29 Pfizer Products Inc., Postupak za dobijanje 2-fenil-3-aminopiridina,njegovih supstituisanih fenil derivata, i njegovih soli
WO2000071538A2 (en) 1999-05-21 2000-11-30 Pfizer Products Inc. 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives
JP2001172178A (ja) * 1999-10-25 2001-06-26 Pfizer Prod Inc 偏頭痛治療用のｎｋ−１レセプターアンタゴニスト及びエレトリプタン
US20020049211A1 (en) * 2000-09-06 2002-04-25 Sobolov-Jaynes Susan Beth Combination treatment for depression and anxiety
EP1192952A3 (en) * 2000-09-28 2003-03-26 Pfizer Products Inc. Combination, for treating depression and anxiety, containing an NK-3 receptor antagonist and a CNS penetrant NK-1 receptor antagonist
US6911544B2 (en) 2002-10-23 2005-06-28 Pfizer Inc. Process for the preparation of (S,S)-cis-2-phenyl-3-aminopiperidine
EP1626958B1 (en) 2003-04-18 2012-06-27 Eli Lilly And Company (piperidinyloxy)phenyl, (piperidinyloxy)pyridinyl, (piperidinylsulfanyl)phenyl and (piperidinylsulfanyl)pyridinyl compounds as 5-ht 1f agonists
MXPA06013484A (es) * 2004-05-21 2007-01-23 Pfizer Prod Inc Metabolitos de (+)-(2s, 3s)-3-(2- metoxi-5- trifluorometoxibencilamino) -2-fenil- piperidina.
MX2007000428A (es) 2004-07-15 2008-03-05 Amr Technology Inc Tetrahidroisoquinolinas sustituidas con arilo y heteroarilo y uso de las mismas para bloquear la captacion de norepinefrina, dopamina y serotonina.
ATE550019T1 (de) 2005-05-17 2012-04-15 Merck Sharp & Dohme Cis-4-ä(4-chlorophenyl)sulfonylü-4-(2,5- difluorophenyl)cyclohexanepropansäure zur behandlug von krebs
CA2615403C (en) 2005-07-15 2015-06-16 Amr Technology, Inc. Aryl-and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin
AU2006297443B2 (en) 2005-09-29 2010-08-12 Merck Sharp & Dohme Corp. Acylated spiropiperidine derivatives as melanocortin-4 receptor modulators
GB0603041D0 (en) 2006-02-15 2006-03-29 Angeletti P Ist Richerche Bio Therapeutic compounds
CA2664113C (en) 2006-09-22 2013-05-28 Merck & Co., Inc. Use of platencin and platensimycin as fatty acid synthesis inhibitors to treat obesity, diabetes and cancer
US20110218176A1 (en) 2006-11-01 2011-09-08 Barbara Brooke Jennings-Spring Compounds, methods, and treatments for abnormal signaling pathways for prenatal and postnatal development
EP2109608B1 (en) 2007-01-10 2011-03-23 Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. Amide substituted indazoles as poly(adp-ribose)polymerase (parp) inhibitors
US8106086B2 (en) 2007-04-02 2012-01-31 Msd K.K. Indoledione derivative
JP5501227B2 (ja) 2007-06-27 2014-05-21 メルク・シャープ・アンド・ドーム・コーポレーション ヒストンデアセチラーゼ阻害剤としての４−カルボキシベンジルアミノ誘導体
AU2009222122A1 (en) 2008-03-03 2009-09-11 Tiger Pharmatech Tyrosine kinase inhibitors
EP2264029A4 (en) 2008-03-31 2011-08-24 Kowa Co 1,3-dihydroisobenzofuran DERIVATIVE
US9156812B2 (en) 2008-06-04 2015-10-13 Bristol-Myers Squibb Company Crystalline form of 6-[(4S)-2-methyl-4-(2-naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine
EP2413932A4 (en) 2009-04-01 2012-09-19 Merck Sharp & Dohme INHIBITORS OF AKT ACTIVITY
KR20120034644A (ko) 2009-05-12 2012-04-12 알바니 몰레큘라 리써치, 인크. 아릴, 헤테로아릴, 및 헤테로사이클 치환된 테트라하이드로이소퀴놀린 및 이의 용도
EP2429293B1 (en) 2009-05-12 2014-10-29 Bristol-Myers Squibb Company CRYSTALLINE FORMS OF (S)-7-([1,2,4]TRIAZOLO[1,5-a]PYRIDIN-6-YL)-4-(3,4-DICHLOROHPHENYL)-1,2,3,4-TETRAHYDROISOQUINOLINE AND USE THEREOF
ES2662072T3 (es) 2009-05-12 2018-04-05 Albany Molecular Research, Inc. 7-([1,2,4]triazolo[1,5-a]piridin-6-il)-4-(3,4-diclorofenil)-1,2,3,4-tetrahidroisoquinolina y uso de la misma
KR101485645B1 (ko) 2009-10-14 2015-01-22 머크 샤프 앤드 돔 코포레이션 ｐ53 활성을 증가시키는 치환된 피페리딘 및 그의 용도
WO2011163330A1 (en) 2010-06-24 2011-12-29 Merck Sharp & Dohme Corp. Novel heterocyclic compounds as erk inhibitors
CN107090456B (zh) 2010-08-02 2022-01-18 瑟纳治疗公司 使用短干扰核酸的RNA干扰介导的联蛋白（钙粘蛋白关联蛋白质），β1基因表达的抑制
HUE044815T2 (hu) 2010-08-17 2019-11-28 Sirna Therapeutics Inc Hepatitisz B vírus (HBV) génexpressziójának RNS-interferencia közvetített gátlása, rövid interferáló nukleinsav (SINS) alkalmazásával
US8883801B2 (en) 2010-08-23 2014-11-11 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors
WO2012030685A2 (en) 2010-09-01 2012-03-08 Schering Corporation Indazole derivatives useful as erk inhibitors
US9242981B2 (en) 2010-09-16 2016-01-26 Merck Sharp & Dohme Corp. Fused pyrazole derivatives as novel ERK inhibitors
WO2012058210A1 (en) 2010-10-29 2012-05-03 Merck Sharp & Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACIDS (siNA)
US9351965B2 (en) 2010-12-21 2016-05-31 Merck Sharp & Dohme Corp. Indazole derivatives useful as ERK inhibitors
CN103732592A (zh) 2011-04-21 2014-04-16 默沙东公司 胰岛素样生长因子-1受体抑制剂
US9023865B2 (en) 2011-10-27 2015-05-05 Merck Sharp & Dohme Corp. Compounds that are ERK inhibitors
EP3919620A1 (en) 2012-05-02 2021-12-08 Sirna Therapeutics, Inc. Short interfering nucleic acid (sina) compositions
CA2882950A1 (en) 2012-09-28 2014-04-03 Merck Sharp & Dohme Corp. Novel compounds that are erk inhibitors
EP2919788A4 (en) 2012-11-14 2016-05-25 Univ Johns Hopkins METHODS AND COMPOSITIONS FOR THE TREATMENT OF SCHIZOPHRENIA
LT2925888T (lt) 2012-11-28 2018-01-10 Merck Sharp & Dohme Corp. Vėžio gydymo kompozicijos ir būdai
BR112015013611A2 (pt) 2012-12-20 2017-11-14 Merck Sharp & Dohme composto, e, composição farmacêutica
WO2014120748A1 (en) 2013-01-30 2014-08-07 Merck Sharp & Dohme Corp. 2,6,7,8 substituted purines as hdm2 inhibitors
US20160194368A1 (en) 2013-09-03 2016-07-07 Moderna Therapeutics, Inc. Circular polynucleotides
US10947234B2 (en) 2017-11-08 2021-03-16 Merck Sharp & Dohme Corp. PRMT5 inhibitors
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Also Published As

Publication number Publication date
IL119078A (en) 2003-11-23
DE69631390T2 (de) 2004-11-25
HRP960386B1 (en) 2002-04-30
HUP9901159A3 (en) 2000-05-29
US6506775B1 (en) 2003-01-14
CZ297543B6 (cs) 2007-02-07
EP0861235A1 (en) 1998-09-02
WO1997008144A1 (en) 1997-03-06
CN1193961A (zh) 1998-09-23
CA2227814A1 (en) 1997-03-06
BG64126B1 (bg) 2004-01-30
AU5776996A (en) 1997-03-19
NZ308207A (en) 1998-07-28
AP9600850A0 (en) 1996-10-31
DZ2086A1 (fr) 2002-07-22
HUP9901159A2 (hu) 1999-07-28
SI1114817T1 (en) 2004-06-30
PL186773B1 (pl) 2004-02-27
PE1398A1 (es) 1998-02-27
EP1114817A1 (en) 2001-07-11
ATE208377T1 (de) 2001-11-15
DK1114817T3 (da) 2004-04-26
MY114800A (en) 2003-01-31
SK20798A3 (en) 1999-03-12
MA23961A1 (fr) 1997-04-01
EP1114817B1 (en) 2004-01-21
AR006305A1 (es) 1999-08-25
YU49122B (sh) 2004-03-12
NO310720B1 (no) 2001-08-20
NO980751D0 (no) 1998-02-23
SI0861235T1 (en) 2002-04-30
SK282925B6 (sk) 2003-01-09
AU702698B2 (en) 1999-03-04
JPH10510554A (ja) 1998-10-13
UA48981C2 (uk) 2002-09-16
TNSN96107A1 (fr) 2005-03-15
ES2163017T3 (es) 2002-01-16
DE69616817T2 (de) 2002-04-04
HRP960386A2 (en) 1998-04-30
DE69616817D1 (de) 2001-12-13
NO980751L (no) 1998-02-23
ATE258166T1 (de) 2004-02-15
PL325332A1 (en) 1998-07-20
PT861235E (pt) 2002-03-28
PE20010700A1 (es) 2001-07-09
YU47896A (sh) 1998-12-23
CA2227814C (en) 2002-12-31
AP643A (en) 1998-04-24
MX9801467A (es) 1998-05-31
RU2152930C2 (ru) 2000-07-20
EP0861235B1 (en) 2001-11-07
ES2211684T3 (es) 2004-07-16
IS4644A (is) 1997-12-30
IS1947B (is) 2004-10-13
KR19990044077A (ko) 1999-06-25
TR199800300T1 (xx) 1998-06-22
CO4480738A1 (es) 1997-07-09
DE69631390D1 (de) 2004-02-26
HU225480B1 (en) 2006-12-28
TW340842B (en) 1998-09-21
OA10666A (en) 2002-11-25
CZ52198A3 (cs) 1999-01-13
DK0861235T3 (da) 2001-12-27
BG102288A (en) 1998-09-30
CN1153764C (zh) 2004-06-16
PT1114817E (pt) 2004-05-31
JP3084069B2 (ja) 2000-09-04
KR100288673B1 (ko) 2001-05-02
RO119299B1 (ro) 2004-07-30
IL119078A0 (en) 1996-11-14
HK1014935A1 (en) 1999-10-08

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Legal Events

Date Code Title Description
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B09B Patent application refused [chapter 9.2 patent gazette]

Free format text: INDEFIRO O PEDIDO DE PATENTE COM BASE NOS ARTIGOS 8, 11, 13 E 24 DA LPI NO 9.279/1.996.