ME00585A - Smac peptidomimetics useful as iap inhibitors - Google Patents

Smac peptidomimetics useful as iap inhibitors

Info

Publication number
ME00585A
ME00585A MEP-19/09A MEP1909A ME00585A ME 00585 A ME00585 A ME 00585A ME P1909 A MEP1909 A ME P1909A ME 00585 A ME00585 A ME 00585A
Authority
ME
Montenegro
Prior art keywords
iap inhibitors
peptidomimetics useful
smac peptidomimetics
smac
useful
Prior art date
Application number
MEP-19/09A
Other languages
Bosnian (bs)
English (en)
Croatian (hr)
Inventor
Mark G Charest
Christine Hiu-Tung Chen
Zhuoliang Chen
Miao Dai
Feng He
Huangshu Lei
Ly Luu Pham
Sushil Kumar Sharma
Christopher Sean Straub
Run-Ming David Wang
Fan Yang
Leigh Zawel
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=38686647&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ME00585(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed filed Critical
Publication of ME00585A publication Critical patent/ME00585A/xx
Publication of ME00585B publication Critical patent/ME00585B/me

Links

Classifications

    • 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
    • C07D417/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/427Thiazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06191Dipeptides containing heteroatoms different from O, S, or N

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Pyrrole Compounds (AREA)
MEP-2009-19A 2006-08-02 2007-07-31 Smac peptidomimetici koji se mogu koristiti kao inhibitori aktivnosti iap ME00585B (me)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US83500006P 2006-08-02 2006-08-02
PCT/US2007/074790 WO2008016893A1 (en) 2006-08-02 2007-07-31 Smac peptidomimetics useful as iap inhibitors

Publications (2)

Publication Number Publication Date
ME00585A true ME00585A (en) 2011-12-20
ME00585B ME00585B (me) 2011-12-20

Family

ID=38686647

Family Applications (1)

Application Number Title Priority Date Filing Date
MEP-2009-19A ME00585B (me) 2006-08-02 2007-07-31 Smac peptidomimetici koji se mogu koristiti kao inhibitori aktivnosti iap

Country Status (42)

Country Link
US (3) US8552003B2 (pt)
EP (3) EP2051990B1 (pt)
JP (1) JP4875749B2 (pt)
KR (2) KR101245945B1 (pt)
CN (2) CN101511860B (pt)
AR (3) AR062159A1 (pt)
AU (1) AU2007281230B2 (pt)
BR (1) BRPI0714803B8 (pt)
CA (1) CA2658525C (pt)
CL (1) CL2007002234A1 (pt)
CR (2) CR10567A (pt)
CU (2) CU23866B1 (pt)
DK (1) DK2051990T3 (pt)
DO (1) DOP2013000084A (pt)
EA (2) EA021671B1 (pt)
ES (2) ES2559042T3 (pt)
GE (1) GEP20115251B (pt)
GT (2) GT200900019A (pt)
HK (2) HK1176613A1 (pt)
HN (1) HN2009000214A (pt)
HR (1) HRP20130373T1 (pt)
IL (3) IL196596A (pt)
JO (1) JO2848B1 (pt)
MA (1) MA30652B1 (pt)
ME (1) ME00585B (pt)
MX (1) MX2009001212A (pt)
MY (1) MY150460A (pt)
NI (2) NI200900008A (pt)
NO (1) NO342230B1 (pt)
NZ (1) NZ574393A (pt)
PA (1) PA8740901A1 (pt)
PE (5) PE20110220A1 (pt)
PL (1) PL2051990T3 (pt)
PT (1) PT2051990E (pt)
SI (1) SI2051990T1 (pt)
SM (1) SMP200900013B (pt)
SV (1) SV2009003160A (pt)
TN (1) TN2009000034A1 (pt)
TW (1) TWI408133B (pt)
UA (1) UA95485C2 (pt)
WO (1) WO2008016893A1 (pt)
ZA (1) ZA200900371B (pt)

Families Citing this family (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2253614B1 (en) 2004-04-07 2012-09-19 Novartis AG Inhibitors of IAP
ES2475207T3 (es) 2004-07-15 2014-07-10 Tetralogic Pharmaceuticals Corporation Compuestos de unión a IAP
KR20120127754A (ko) 2004-12-20 2012-11-23 제넨테크, 인크. Iap의 피롤리딘 억제제
KR101317661B1 (ko) 2005-02-25 2013-10-15 테트랄로직 파마슈티칼스 코포레이션 이량체성 iap 억제제
CA2607940C (en) 2005-05-18 2009-12-15 Aegera Therapeutics Inc. Bir domain binding compounds
CA2564872C (en) 2005-10-25 2010-12-21 Aegera Therapeutics Inc. Iap bir domain binding compounds
TWI543988B (zh) 2006-03-16 2016-08-01 科學製藥股份有限公司 結合於細胞凋亡抑制蛋白(iap)之桿狀病毒iap重複序列(bir)區域之化合物
KR101506466B1 (ko) 2006-05-16 2015-03-27 파마사이언스 인크. Iap bir 도메인 결합 화합물
US20100056495A1 (en) * 2006-07-24 2010-03-04 Tetralogic Pharmaceuticals Corporation Dimeric iap inhibitors
WO2008014263A2 (en) 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Dimeric iap antagonists
CL2007002166A1 (es) 2006-07-24 2008-01-25 Tetralogic Pharm Corp Compuestos derivados de heterociclos de nitrogeno, antagonistas de los inhibidores de las proteinas de la apoptosis; sus composiciones farmaceuticas; y uso de dichos compuestos para el tratamiento del cancer.
CA2665838A1 (en) * 2006-10-19 2008-05-15 Novartis Ag Organic compounds
KR20090083412A (ko) * 2006-11-28 2009-08-03 노파르티스 아게 급성 골수성 백혈병의 치료를 위한 iap 억제제의 용도
PL2089024T3 (pl) * 2006-11-28 2011-10-31 Novartis Ag Kombinacja inhibitorów IAP i inhibitorów FLT3
CN101605786A (zh) * 2006-12-19 2009-12-16 健泰科生物技术公司 细胞凋亡抑制剂的咪唑并吡啶抑制剂
PE20130150A1 (es) 2007-04-30 2013-02-27 Genentech Inc Inhibidores de las iap
US9750729B2 (en) * 2008-05-16 2017-09-05 Dana-Farber Cancer Institute, Inc. Immunomodulation by IAP inhibitors
WO2010017035A2 (en) 2008-08-02 2010-02-11 Genentech, Inc. Inhibitors of iap
US8841067B2 (en) 2009-01-09 2014-09-23 Dana-Farber Cancer Institute, Inc. NOL3 is a predictor of patient outcome
US8283372B2 (en) 2009-07-02 2012-10-09 Tetralogic Pharmaceuticals Corp. 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic
WO2011016576A1 (en) 2009-08-04 2011-02-10 Takeda Pharmaceutical Company Limited Alanine derivatives as inhibitors of apoptosis proteins
WO2011019782A1 (en) * 2009-08-11 2011-02-17 Novartis Ag Combinations of vascular disrupting agents with inhibitor of apoptosis proteins antagonists
BR112012003118A2 (pt) 2009-08-12 2016-02-23 Novartis Ag formulações orais sólidas e formas cristalinas de um inibidor de proteína apoptose
KR20120140658A (ko) 2010-02-12 2012-12-31 파마사이언스 인크. Iap bir 도메인 결합 화합물
UY33236A (es) * 2010-02-25 2011-09-30 Novartis Ag Inhibidores dimericos de las iap
KR101560227B1 (ko) * 2010-08-31 2015-10-14 한미사이언스 주식회사 세포사멸 유도 활성을 갖는 퀴놀린 또는 퀴나졸린 유도체
WO2012052758A1 (en) 2010-10-22 2012-04-26 Astrazeneca Ab Response biomarkers for iap antagonists in human cancers
UY33794A (es) 2010-12-13 2012-07-31 Novartis Ag Inhibidores diméricos de las iap
EP2731942B1 (en) 2011-07-13 2015-09-23 Novartis AG Novel 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
US9227982B2 (en) 2011-07-13 2016-01-05 Novartis Ag 4-oxo-3,5,7,8-tetrahydro-4H-pyrano[4,3-d]pyrminidinyl compounds for use as tankyrase inhibitors
EP2760446A1 (en) 2011-09-30 2014-08-06 Tetralogic Pharmaceuticals Corporation Smac mimetic (birinapant) for use in the treatment of proliferative diseases (cancer)
US8859541B2 (en) * 2012-02-27 2014-10-14 Boehringer Ingelheim International Gmbh 6-alkynylpyridines
WO2013174780A1 (en) * 2012-05-22 2013-11-28 F. Hoffmann-La Roche Ag Substituted dipyridylamines and uses thereof
KR20140011773A (ko) * 2012-07-19 2014-01-29 한미약품 주식회사 이중 저해 활성을 갖는 헤테로고리 유도체
EP2991977B1 (en) 2013-05-01 2020-07-22 F.Hoffmann-La Roche Ag C-linked heterocycloalkyl substituted pyrimidines and their uses
WO2014205516A1 (en) 2013-06-25 2014-12-31 The Walter And Eliza Hall Institute Of Medical Research Method of treating intracellular infection
US10570204B2 (en) 2013-09-26 2020-02-25 The Medical College Of Wisconsin, Inc. Methods for treating hematologic cancers
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
JOP20200096A1 (ar) 2014-01-31 2017-06-16 Children’S Medical Center Corp جزيئات جسم مضاد لـ tim-3 واستخداماتها
AU2015229103C9 (en) 2014-03-14 2020-11-26 Immutep S.A.S Antibody molecules to LAG-3 and uses thereof
WO2016040882A1 (en) 2014-09-13 2016-03-17 Novartis Ag Combination therapies of egfr inhibitors
BR112017006664A2 (pt) 2014-10-03 2017-12-26 Novartis Ag terapias de combinação
MA41044A (fr) 2014-10-08 2017-08-15 Novartis Ag Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer
UY36351A (es) 2014-10-14 2016-06-01 Novartis Ag Moléculas de anticuerpo que se unen a pd-l1 y usos de las mismas
WO2016079527A1 (en) 2014-11-19 2016-05-26 Tetralogic Birinapant Uk Ltd Combination therapy
WO2016097773A1 (en) 2014-12-19 2016-06-23 Children's Cancer Institute Therapeutic iap antagonists for treating proliferative disorders
SG11201706756VA (en) 2015-03-10 2017-09-28 Aduro Biotech Inc Compositions and methods for activating "stimulator of interferon gene" -dependent signalling
GB201506871D0 (en) 2015-04-22 2015-06-03 Glaxosmithkline Ip Dev Ltd Novel compounds
US20180340025A1 (en) 2015-07-29 2018-11-29 Novartis Ag Combination therapies comprising antibody molecules to lag-3
CN114272371A (zh) 2015-07-29 2022-04-05 诺华股份有限公司 包含抗pd-1抗体分子的联合疗法
EP3316902A1 (en) 2015-07-29 2018-05-09 Novartis AG Combination therapies comprising antibody molecules to tim-3
CN108697791B (zh) 2015-11-03 2022-08-23 詹森生物科技公司 特异性结合pd-1的抗体及其用途
WO2017106656A1 (en) 2015-12-17 2017-06-22 Novartis Ag Antibody molecules to pd-1 and uses thereof
BR112018071408A2 (pt) 2016-04-20 2019-02-05 Glaxosmithkline Ip Dev Ltd “composto inibidor de rip2 quinase, composição farmacêutica, usos de um composto e de uma combinação, e, combinação
GB201610147D0 (en) 2016-06-10 2016-07-27 Glaxosmithkline Ip Dev Ltd Novel compounds
WO2018009466A1 (en) 2016-07-05 2018-01-11 Aduro Biotech, Inc. Locked nucleic acid cyclic dinucleotide compounds and uses thereof
CN106496213B (zh) * 2016-09-30 2019-08-20 东南大学 Lcl161前药及其制备方法和应用
JP6899993B2 (ja) * 2016-10-04 2021-07-07 国立医薬品食品衛生研究所長 複素環化合物
CN110475567A (zh) 2017-03-31 2019-11-19 勃林格殷格翰国际有限公司 抗癌组合疗法
UY37695A (es) 2017-04-28 2018-11-30 Novartis Ag Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
EP3642240A1 (en) 2017-06-22 2020-04-29 Novartis AG Antibody molecules to cd73 and uses thereof
CN118307674A (zh) 2017-06-22 2024-07-09 诺华股份有限公司 针对cd73的抗体分子及其用途
KR20200089286A (ko) 2017-11-16 2020-07-24 노파르티스 아게 조합 요법
CN108484640B (zh) * 2018-05-22 2020-09-15 南京华威医药科技集团有限公司 一种抗肿瘤的细胞凋亡蛋白抑制剂
UY38247A (es) 2018-05-30 2019-12-31 Novartis Ag Anticuerpos frente a entpd2, terapias de combinación y métodos de uso de los anticuerpos y las terapias de combinación
WO2019232244A2 (en) 2018-05-31 2019-12-05 Novartis Ag Antibody molecules to cd73 and uses thereof
JP7133043B2 (ja) 2018-06-09 2022-09-07 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Dll3-cd3二重特異性抗体
JP7515175B2 (ja) 2018-07-31 2024-07-12 ファイメクス株式会社 複素環化合物
US20220096436A1 (en) 2019-01-17 2022-03-31 Debiopharm International S.A. Combination product for the treatment of cancer
TW202043466A (zh) 2019-01-25 2020-12-01 德商百靈佳殷格翰國際股份有限公司 編碼ccl21之重組棒狀病毒
EP3947368A4 (en) 2019-04-04 2023-01-04 Dana-Farber Cancer Institute, Inc. CDK2/5 DEGRADING AGENTS AND ASSOCIATED USES
CN114728076A (zh) 2019-05-20 2022-07-08 诺华股份有限公司 Mcl-1抑制剂抗体-药物缀合物及使用方法
JPWO2021020585A1 (pt) 2019-07-31 2021-02-04
JP2022548881A (ja) 2019-09-18 2022-11-22 ノバルティス アーゲー Entpd2抗体、組合せ療法並びに抗体及び組合せ療法を使用する方法
CN114727984A (zh) 2019-09-25 2022-07-08 德彪药业国际股份公司 治疗患有局部晚期鳞状细胞癌的患者的给药方案
CA3166980A1 (en) 2020-01-20 2021-07-29 Astrazeneca Ab Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer
IL298648A (en) 2020-06-03 2023-01-01 Boehringer Ingelheim Int Recombinant rhabdovirus coding for a fc fusion protein with a cd80 extracellular site
AU2021385349A1 (en) 2020-11-24 2023-06-22 Les Laboratoires Servier Mcl-1 inhibitor antibody-drug conjugates and methods of use
EP4251648A2 (en) 2020-11-24 2023-10-04 Novartis AG Anti-cd48 antibodies, antibody drug conjugates, and uses thereof
IL304891A (en) 2021-02-02 2023-10-01 Servier Lab Selective Protech BCL-XL compounds and methods of use
WO2023225336A1 (en) 2022-05-20 2023-11-23 Novartis Ag Met bcl-xl inhibitor antibody-drug conjugates and methods of use thereof
WO2023225320A1 (en) 2022-05-20 2023-11-23 Novartis Ag Epha2 bcl-xl inhibitor antibody-drug conjugates and methods of use thereof

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2714880A1 (de) * 1977-04-02 1978-10-26 Hoechst Ag Cephemderivate und verfahren zu ihrer herstellung
JPS59141547A (ja) * 1983-02-01 1984-08-14 Eisai Co Ltd 鎮痛作用を有する新規ペプタイドおよび製法
FR2575753B1 (fr) * 1985-01-07 1987-02-20 Adir Nouveaux derives peptidiques a structure polycyclique azotee, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
DK167813B1 (da) * 1989-12-07 1993-12-20 Carlbiotech Ltd As Pentapeptidderivat, farmaceutisk acceptable salte heraf, fremgangsmaade til fremstilling deraf og farmaceutisk praeparat indeholdende et saadant derivat
US5559209A (en) * 1993-02-18 1996-09-24 The General Hospital Corporation Regulator regions of G proteins
US6472172B1 (en) * 1998-07-31 2002-10-29 Schering Aktiengesellschaft DNA encoding a novel human inhibitor-of-apoptosis protein
TR200200767T1 (tr) 2000-05-23 2002-09-23 Vertex Pharmaceuticals Incorporated Kaspaz engelleyiciler ve kullanımları
US6608026B1 (en) * 2000-08-23 2003-08-19 Board Of Regents, The University Of Texas System Apoptotic compounds
US20020160975A1 (en) * 2001-02-08 2002-10-31 Thomas Jefferson University Conserved XIAP-interaction motif in caspase-9 and Smac/DIABLO for mediating apoptosis
US20030157522A1 (en) * 2001-11-09 2003-08-21 Alain Boudreault Methods and reagents for peptide-BIR interaction screens
WO2004005248A1 (en) 2002-07-02 2004-01-15 Novartis Ag Peptide inhibitors of smac protein binding to inhibitor of apoptosis proteins (iap)
DE60324964D1 (de) * 2002-07-15 2009-01-08 Univ Princeton Iap-bindende verbindungen
US20040171554A1 (en) * 2003-02-07 2004-09-02 Genentech, Inc. Compositions and methods for enhancing apoptosis
EP1687431A2 (en) * 2003-11-13 2006-08-09 Genentech, Inc. Compositions and methods for screening pro-apoptotic compounds
JP2007523061A (ja) * 2004-01-16 2007-08-16 ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン Smacペプチドミメティクスおよびその使用法
SE527038C2 (sv) * 2004-02-26 2005-12-13 Ingenjoers N Per Oskar Persson Kassett och apparat för vätskefrysning
CN1926118A (zh) * 2004-03-01 2007-03-07 德克萨斯大学董事会 二聚的小分子细胞凋亡增强剂
EP2253614B1 (en) * 2004-04-07 2012-09-19 Novartis AG Inhibitors of IAP
WO2006014361A1 (en) 2004-07-02 2006-02-09 Genentech, Inc. Inhibitors of iap
KR20120127754A (ko) * 2004-12-20 2012-11-23 제넨테크, 인크. Iap의 피롤리딘 억제제
US20060218632A1 (en) * 2005-03-28 2006-09-28 Cisco Technology, Inc.; Method and system for installing premise equipment
MX2009003834A (es) * 2006-10-12 2009-04-22 Novartis Ag Derivados de pirrolidina como inhibidores de iap.
JP2010512322A (ja) * 2006-12-07 2010-04-22 ノバルティス アーゲー 有機化合物

Also Published As

Publication number Publication date
GT200900019A (es) 2010-06-01
MA30652B1 (fr) 2009-08-03
NO342230B1 (no) 2018-04-23
MY150460A (en) 2014-01-30
KR101087878B1 (ko) 2011-11-30
NI200900008A (es) 2010-01-07
IL236883A0 (en) 2015-03-31
ES2559042T3 (es) 2016-02-10
NO20090878L (no) 2009-04-27
SMAP200900013A (it) 2009-05-11
US8552003B2 (en) 2013-10-08
ZA200900371B (en) 2009-12-30
CN102558165A (zh) 2012-07-11
EP2537846B1 (en) 2015-09-16
AU2007281230B2 (en) 2011-09-08
SMP200900013B (it) 2010-01-19
EA200900227A1 (ru) 2009-08-28
DK2051990T3 (da) 2013-05-13
HRP20130373T1 (en) 2013-05-31
IL196596A0 (en) 2009-11-18
CN101511860B (zh) 2013-05-01
CU20090017A7 (es) 2011-03-21
UA95485C2 (uk) 2011-08-10
EA201401247A1 (ru) 2015-07-30
KR101245945B1 (ko) 2013-03-22
KR20110030667A (ko) 2011-03-23
PE20110218A1 (es) 2011-04-01
JP2009545613A (ja) 2009-12-24
WO2008016893A1 (en) 2008-02-07
HN2009000214A (es) 2011-10-11
IL231079A0 (en) 2014-03-31
IL196596A (en) 2014-09-30
IL231079A (en) 2015-02-26
CA2658525C (en) 2013-02-19
CU23866B1 (es) 2013-03-27
PE20110220A1 (es) 2011-04-11
EP2537850A1 (en) 2012-12-26
KR20090038479A (ko) 2009-04-20
AR112816A2 (es) 2019-12-18
JP4875749B2 (ja) 2012-02-15
BRPI0714803A2 (pt) 2013-05-21
ME00585B (me) 2011-12-20
GT200900019AA (es) 2015-11-24
CR10567A (es) 2009-02-18
EP2051990B1 (en) 2013-02-06
ES2405947T3 (es) 2013-06-04
US20130005663A1 (en) 2013-01-03
MX2009001212A (es) 2009-02-11
US20140004101A1 (en) 2014-01-02
NZ574393A (en) 2012-03-30
CL2007002234A1 (es) 2008-06-13
CU24004B1 (es) 2014-06-27
SV2009003160A (es) 2010-04-13
TWI408133B (zh) 2013-09-11
PL2051990T3 (pl) 2013-07-31
NI200900081A (es) 2010-01-07
PE20110217A1 (es) 2011-04-01
BRPI0714803B1 (pt) 2021-03-09
US20110065726A1 (en) 2011-03-17
CU20110027A7 (es) 2011-12-28
CA2658525A1 (en) 2008-02-07
AU2007281230A1 (en) 2008-02-07
AR062159A1 (es) 2008-10-22
GEP20115251B (en) 2011-07-11
DOP2013000084A (es) 2013-06-15
JO2848B1 (en) 2014-09-15
EP2537846A1 (en) 2012-12-26
HK1176613A1 (en) 2013-08-02
BRPI0714803B8 (pt) 2021-05-25
HK1127616A1 (en) 2009-10-02
AR110313A2 (es) 2019-03-13
PE20110224A1 (es) 2011-04-05
EP2051990A1 (en) 2009-04-29
TN2009000034A1 (en) 2010-08-19
TW200815399A (en) 2008-04-01
SI2051990T1 (sl) 2013-06-28
US8546336B2 (en) 2013-10-01
EA021671B1 (ru) 2015-08-31
PA8740901A1 (es) 2009-04-23
CN102558165B (zh) 2014-08-13
CN101511860A (zh) 2009-08-19
PT2051990E (pt) 2013-05-10
PE20080951A1 (es) 2008-09-11
CR20140555A (es) 2015-01-14

Similar Documents

Publication Publication Date Title
ME00585A (en) Smac peptidomimetics useful as iap inhibitors
RS52823B (en) NEW UNITS USEFUL FOR TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES
BR112015022861A8 (pt) inibidores de bromodomínio
CL2011000504A1 (es) Compuestos derivados de piridin-4-il-tiazol-2il-amida 2-amida-pirrolidin-1,2-dicarboxilico, inhibidores de quinasa de fosfatidil-inositol-3; composicion farmaceutica que comprende a uno de los compuestos; y uso de los compuestos en la preparacion de un medicamento para el tratamiento del cancer.
BR112015018663A2 (pt) derivados de piridazinona-amidas
EA201001772A1 (ru) Производные 3,5-диамино-6-хлорпиразин-2-карбоновой кислоты и их применение в качестве блокаторов эпителиальных натриевых каналов для лечения заболеваний дыхательных путей
EA201100613A1 (ru) Конденсированные, спироциклические гетероароматические соединения для лечения бактериальных инфекций
EA201490971A1 (ru) Производные урацила в качестве ингибиторов axl и c-met киназы
EA201200049A1 (ru) 1,3-дизамещенные производные имидазолидин-2-она в качестве ингибиторов cyp 17
HK1131146A1 (en) Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors
UA111770C2 (uk) Інгібітори бромдомену
EA201001455A1 (ru) Пиридины и пиразины в качестве ингибиторов pi3k (фосфатидилинозиткиназы-3)
RS53617B1 (en) NEW UNITS USEFUL FOR TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES
EA201290183A1 (ru) Бензодиазепиновый ингибитор бромодомена
EA200801996A1 (ru) 2-замещенные производные 4-бензилфталазинонов в качестве гистаминовых h1- и h3-антагонистов
EA201100750A1 (ru) Замещенные диоксопиперидинилфталимидные производные
EA200900924A1 (ru) Циклизованные производные как ингибиторы eg-5
EA201001196A1 (ru) Соединения 4-пиридинона и их применение для лечения рака
EA201590021A1 (ru) Новые замещенные производные 1,3-дигидро-2h-бензимидазол-2-она, замещенные гетероциклами, в качестве противовирусных средств против респираторного синцитиального вируса
ATE517873T1 (de) 6-oxo-1,6-dihydropyrimidin-2-yle bei der behandlung proliferativer krankheiten
CA2929436C (en) Compounds, pharmaceutical composition and methods for use in treating inflammatory diseases
NO20085317L (no) Imidazoazepinonforbindelser
ATE502935T1 (de) C-met-proteinkinasehemmer
EA201000703A1 (ru) Производные пиразола в качестве ингибиторов 5-lo
EA201100350A1 (ru) Противогрибковые средства