DZ3453A1 - Compose lactame - Google Patents

Compose lactame

Info

Publication number
DZ3453A1
DZ3453A1 DZ013453A DZ013453A DZ3453A1 DZ 3453 A1 DZ3453 A1 DZ 3453A1 DZ 013453 A DZ013453 A DZ 013453A DZ 013453 A DZ013453 A DZ 013453A DZ 3453 A1 DZ3453 A1 DZ 3453A1
Authority
DZ
Algeria
Prior art keywords
lactame
compound
lactame compound
Prior art date
Application number
DZ013453A
Other languages
English (en)
Inventor
James Edmund Audia
Varghese John
Lee H Latimer
Stacey Leigh Mcdaniel
Jeffrey Scott Nissen
Eugene D Thorsett
Jay S Tung
Original Assignee
Lilly Co Eli
Elan Pharm 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 Lilly Co Eli, Elan Pharm Inc filed Critical Lilly Co Eli
Application granted granted Critical
Publication of DZ3453A1 publication Critical patent/DZ3453A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16—Benzazepines; Hydrogenated benzazepines
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
DZ013453A 2000-11-17 2001-11-05 Compose lactame DZ3453A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US24955200P 2000-11-17 2000-11-17
PCT/US2001/027799 WO2002047671A2 (fr) 2000-11-17 2001-11-05 Composé de lactam

Publications (1)

Publication Number Publication Date
DZ3453A1 true DZ3453A1 (fr) 2002-06-20

Family

ID=22943982

Family Applications (1)

Application Number Title Priority Date Filing Date
DZ013453A DZ3453A1 (fr) 2000-11-17 2001-11-05 Compose lactame

Country Status (34)

Country Link
US (1) US20050261495A1 (fr)
EP (1) EP1341531B1 (fr)
JP (1) JP4116437B2 (fr)
KR (1) KR100819679B1 (fr)
CN (1) CN1486184A (fr)
AR (1) AR035927A1 (fr)
AU (2) AU2002243192B2 (fr)
BR (1) BR0115427A (fr)
CA (1) CA2427227C (fr)
CY (1) CY1106366T1 (fr)
CZ (1) CZ20031351A3 (fr)
DE (1) DE60126132T2 (fr)
DK (1) DK1341531T3 (fr)
DZ (1) DZ3453A1 (fr)
EA (1) EA005954B1 (fr)
EC (1) ECSP034600A (fr)
ES (1) ES2278804T3 (fr)
HK (1) HK1059731A1 (fr)
HR (1) HRP20030383B1 (fr)
HU (1) HU228117B1 (fr)
IL (2) IL155960A0 (fr)
MX (1) MXPA03004292A (fr)
MY (1) MY134559A (fr)
NO (1) NO324324B1 (fr)
NZ (1) NZ525854A (fr)
PE (1) PE20020802A1 (fr)
PL (1) PL212199B1 (fr)
PT (1) PT1341531E (fr)
SI (1) SI1341531T1 (fr)
SK (1) SK288065B6 (fr)
TW (1) TWI305204B (fr)
UA (1) UA74849C2 (fr)
WO (1) WO2002047671A2 (fr)
ZA (1) ZA200303789B (fr)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA74849C2 (en) * 2000-11-17 2006-02-15 Lilly Co Eli Lactam
US7468365B2 (en) 2000-11-17 2008-12-23 Eli Lilly And Company Lactam compound
WO2006109729A1 (fr) 2005-04-08 2006-10-19 Daiichi Sankyo Company, Limited Dérivé de pyridylméthylsulfone
US8362075B2 (en) 2005-05-17 2013-01-29 Merck Sharp & Dohme Corp. Cyclohexyl sulphones for treatment of cancer
EP1985615A4 (fr) * 2006-01-31 2011-12-14 Api Corp Procédé de production de benzazépinone
EP2121633A2 (fr) 2007-02-12 2009-11-25 Merck & Co., Inc. Dérivés de pipérazine pour le traitement de la maladie d'alzheimer et des conditions apparentées
CL2008002060A1 (es) * 2007-07-16 2008-11-21 Wyeth Corp Compuestos derivados de sulfonamida, inhibidores de la produccion de beta amiloide; metodo de preparacion; composicion farmaceutica; kit farmaceutico; y uso en el tratamiento de enfermedades tales como alzheimer, angiopatia amiloide, sindrome de down, entre otras.
US8188069B2 (en) 2007-08-14 2012-05-29 Eli Lilly And Company Azepine derivatives as gamma-secretase inhibitors
TW200920362A (en) 2007-09-11 2009-05-16 Daiichi Sankyo Co Ltd Alkylsulfone derivatives
PT2222636E (pt) 2007-12-21 2013-07-16 Ligand Pharm Inc Moduladores seletivos de recetores de andrógeno (sarms) e suas utilizações
WO2009128057A2 (fr) 2008-04-18 2009-10-22 UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN et al Produits psycho-pharmaceutiques
WO2010114780A1 (fr) 2009-04-01 2010-10-07 Merck Sharp & Dohme Corp. Inhibiteurs de l'activité akt
NZ599343A (en) 2009-10-14 2014-05-30 Merck Sharp & Dohme Substituted piperidines that increase p53 activity and the uses thereof
WO2011163330A1 (fr) 2010-06-24 2011-12-29 Merck Sharp & Dohme Corp. Nouveaux composés hétérocycliques utilisés comme inhibiteurs de erk
US8518907B2 (en) 2010-08-02 2013-08-27 Merck Sharp & Dohme Corp. RNA interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (CTNNB1) gene expression using short interfering nucleic acid (siNA)
RU2624045C2 (ru) 2010-08-17 2017-06-30 Сирна Терапьютикс,Инк ОПОСРЕДУЕМОЕ РНК-ИНТЕРФЕРЕНЦИЕЙ ИНГИБИРОВАНИЕ ЭКСПРЕССИИ ГЕНОВ ВИРУСА ГЕПАТИТА B (HBV) С ПРИМЕНЕНИЕМ МАЛОЙ ИНТЕРФЕРИРУЮЩЕЙ НУКЛЕИНОВОЙ КИСЛОТЫ (миНК)
WO2012030685A2 (fr) 2010-09-01 2012-03-08 Schering Corporation Dérivés d'indazole utilisables en tant qu'inhibiteurs de la voie erk
WO2012036997A1 (fr) 2010-09-16 2012-03-22 Schering Corporation Dérivés condensés de pyrazole utilisés comme nouveaux inhibiteurs erk
WO2012040444A2 (fr) * 2010-09-24 2012-03-29 Bristol-Myers Squibb Company Traitement de patients présentant un début de maladie d'alzheimer
WO2012058210A1 (fr) 2010-10-29 2012-05-03 Merck Sharp & Dohme Corp. INHIBITION FACILITÉE PAR L'INTERFÉRENCE D'ARN DE L'EXPRESSION D'UN GÈNE AU MOYEN D'ACIDES NUCLÉIQUES INTERFÉRENTS COURTS (siNA)
EP2654748B1 (fr) 2010-12-21 2016-07-27 Merck Sharp & Dohme Corp. Dérivés d'indazole utiles en tant qu'inhibiteurs de erk
WO2013063214A1 (fr) 2011-10-27 2013-05-02 Merck Sharp & Dohme Corp. Nouveaux composés qui sont des inhibiteurs d'erk
CN102690231B (zh) * 2012-04-11 2014-07-09 南京友杰医药科技有限公司 治疗阿尔茨海默病潜在药物司马西特的合成方法
EP3358013B1 (fr) 2012-05-02 2020-06-24 Sirna Therapeutics, Inc. Compositions d'acide nucléique interférent court (sina)
EP3970725A1 (fr) 2012-09-07 2022-03-23 Massachusetts Eye & Ear Infirmary Un inhibiteur de la gamma-sécrétase pour le traitement de la perte auditive
US9233979B2 (en) 2012-09-28 2016-01-12 Merck Sharp & Dohme Corp. Compounds that are ERK inhibitors
PT2925888T (pt) 2012-11-28 2017-12-13 Merck Sharp & Dohme Composições e métodos para tratamento do cancro
CA2895504A1 (fr) 2012-12-20 2014-06-26 Merck Sharp & Dohme Corp. Imidazopyridines substituees en tant qu'inhibiteurs de hdm2
WO2014120748A1 (fr) 2013-01-30 2014-08-07 Merck Sharp & Dohme Corp. Purines 2,6,7,8-substituées utilisées en tant qu'inhibiteurs de hdm2
WO2014171434A1 (fr) 2013-04-19 2014-10-23 国立大学法人岡山大学 Agent de traitement des troubles cognitifs, basé sur la protéine bêta-amyloïde, agent thérapeutique contre la maladie d'alzheimer et procédé de traitement et procédé d'analyse pathologique correspondants
US20160194368A1 (en) 2013-09-03 2016-07-07 Moderna Therapeutics, Inc. Circular polynucleotides
EP3613418A1 (fr) 2014-01-17 2020-02-26 Ligand Pharmaceuticals, Inc. Procédés et compositions de modulation des niveaux d'hormones
US11370823B2 (en) 2014-10-29 2022-06-28 Massachusetts Eye And Ear Infirmary Efficient delivery of therapeutic molecules to cells of the inner ear
EP3458076A4 (fr) 2016-05-16 2020-01-22 The General Hospital Corporation Cellules souches de voies respiratoires humaines en ingénierie épithéliale pulmonaire
US10947234B2 (en) 2017-11-08 2021-03-16 Merck Sharp & Dohme Corp. PRMT5 inhibitors
US11590152B2 (en) 2018-01-26 2023-02-28 Massachusetts Eye And Ear Infirmary Treatment of hearing loss
WO2020033282A1 (fr) 2018-08-07 2020-02-13 Merck Sharp & Dohme Corp. Inhibiteurs de prmt5
EP3833667B1 (fr) 2018-08-07 2024-03-13 Merck Sharp & Dohme LLC Inhibiteurs de prmt5
KR20220123229A (ko) 2019-12-17 2022-09-06 머크 샤프 앤드 돔 엘엘씨 Prmt5 억제제
US20240116945A1 (en) 2022-09-02 2024-04-11 Merck Sharp & Dohme Llc Exatecan-derived topoisomerase-1 inhibitors pharmaceutical compositions, and uses thereof
WO2024091437A1 (fr) 2022-10-25 2024-05-02 Merck Sharp & Dohme Llc Charges utiles de lieur adc dérivées d'exatécan, compositions pharmaceutiques et leurs utilisations

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20000069654A (ko) * 1996-12-23 2000-11-25 엘란 파마슈티칼스, 인크. 시클로알킬, 락탐, 락톤 및 관련 화합물, 그의 약제학적 조성물및 그를 사용한 β-아밀로이드 펩티드의 방출 및(또는) 합성억제 방법
JP2002518481A (ja) * 1998-06-22 2002-06-25 エラン ファーマシューティカルズ，インコーポレイテッド β−アミロイドペプチドの放出および／またはその合成を阻害するための化合物
EP1230220A1 (fr) * 1999-11-09 2002-08-14 Eli Lilly And Company COMPOSES CONTENANT DES $g(b)-ACIDES AMINES UTILES POUR INHIBER LA LIBERATION ET/OU LA SYNTHESE DU PEPTIDE $g(b)-AMYLOIDE
UA74849C2 (en) * 2000-11-17 2006-02-15 Lilly Co Eli Lactam
UA77165C2 (en) * 2000-11-17 2006-11-15 Lilly Co Eli (n)-((s)-2-hydroxy-3-methyl-butyryl)-1-(l-alaninyl)-(s)-1-amino-3-methyl-4,5,6,7-tetrahydro-2h-3-benzazepin-2-one dihydrate, processes for manufacturing and pharmaceutical composition
ATE405577T1 (de) * 2000-11-17 2008-09-15 Lilly Co Eli Lactam dipeptid und dessen verwendung zur inhibierung der beta-amyloid peptid frisetzung

Also Published As

Publication number Publication date
HUP0301842A3 (en) 2010-03-29
DE60126132T2 (de) 2007-10-18
NO20032236D0 (no) 2003-05-16
HK1059731A1 (en) 2004-07-16
HU228117B1 (en) 2012-11-28
PL362688A1 (en) 2004-11-02
MXPA03004292A (es) 2004-02-12
JP4116437B2 (ja) 2008-07-09
EP1341531A2 (fr) 2003-09-10
CZ20031351A3 (cs) 2003-11-12
CN1486184A (zh) 2004-03-31
UA74849C2 (en) 2006-02-15
EA200300580A1 (ru) 2003-10-30
AU2002243192B2 (en) 2006-07-20
EP1341531B1 (fr) 2007-01-17
PL212199B1 (pl) 2012-08-31
PT1341531E (pt) 2007-04-30
NZ525854A (en) 2004-06-25
MY134559A (en) 2007-12-31
NO324324B1 (no) 2007-09-24
SK288065B6 (sk) 2013-04-03
US20050261495A1 (en) 2005-11-24
HRP20030383B1 (en) 2007-12-31
DK1341531T3 (da) 2007-05-14
SI1341531T1 (sl) 2007-06-30
JP2004517090A (ja) 2004-06-10
EA005954B1 (ru) 2005-08-25
HRP20030383A2 (en) 2005-10-31
DE60126132D1 (de) 2007-03-08
PE20020802A1 (es) 2002-09-10
ES2278804T3 (es) 2007-08-16
IL155960A0 (en) 2003-12-23
SK5592003A3 (en) 2003-12-02
ECSP034600A (es) 2003-06-25
AR035927A1 (es) 2004-07-28
CA2427227A1 (fr) 2002-06-20
HUP0301842A2 (hu) 2003-09-29
AU4319202A (en) 2002-06-24
ZA200303789B (en) 2004-08-16
WO2002047671A3 (fr) 2003-03-06
NO20032236L (no) 2003-07-10
KR20030051846A (ko) 2003-06-25
CY1106366T1 (el) 2011-10-12
TWI305204B (en) 2009-01-11
CA2427227C (fr) 2010-08-17
WO2002047671A2 (fr) 2002-06-20
IL155960A (en) 2009-06-15
BR0115427A (pt) 2003-10-07
KR100819679B1 (ko) 2008-04-04

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