AR110313A2 - Derivados de tiazol-2-il-pirrolidina - Google Patents

Derivados de tiazol-2-il-pirrolidina

Info

Publication number
AR110313A2
AR110313A2 ARP170103398A ARP170103398A AR110313A2 AR 110313 A2 AR110313 A2 AR 110313A2 AR P170103398 A ARP170103398 A AR P170103398A AR P170103398 A ARP170103398 A AR P170103398A AR 110313 A2 AR110313 A2 AR 110313A2
Authority
AR
Argentina
Prior art keywords
pirrolidina
tiazol
derivatives
fluoro
phenyl
Prior art date
Application number
ARP170103398A
Other languages
English (en)
Original Assignee
Novartis Ag
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=AR110313(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR110313A2 publication Critical patent/AR110313A2/es

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)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (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)

Abstract

Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1), en donde Ar = 4-fluoro-fenilo.
ARP170103398A 2006-08-02 2017-12-04 Derivados de tiazol-2-il-pirrolidina AR110313A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US83500006P 2006-08-02 2006-08-02

Publications (1)

Publication Number Publication Date
AR110313A2 true AR110313A2 (es) 2019-03-13

Family

ID=38686647

Family Applications (3)

Application Number Title Priority Date Filing Date
ARP070103375A AR062159A1 (es) 2006-08-02 2007-07-31 Compuestos que inhiben el enlace de la proteina smac al inhibidor de proteinas de apoptosis (iap)
ARP170103398A AR110313A2 (es) 2006-08-02 2017-12-04 Derivados de tiazol-2-il-pirrolidina
ARP180102641A AR112816A2 (es) 2006-08-02 2018-09-17 Compuestos que inhiben el enlace de la proteína smac al inhibidor de proteínas de apoptosis (iap)

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ARP070103375A AR062159A1 (es) 2006-08-02 2007-07-31 Compuestos que inhiben el enlace de la proteina smac al inhibidor de proteinas de apoptosis (iap)

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP180102641A AR112816A2 (es) 2006-08-02 2018-09-17 Compuestos que inhiben el enlace de la proteína smac al inhibidor de proteínas de apoptosis (iap)

Country Status (41)

Country Link
US (3) US8552003B2 (es)
EP (3) EP2051990B1 (es)
JP (1) JP4875749B2 (es)
KR (2) KR101087878B1 (es)
CN (2) CN101511860B (es)
AR (3) AR062159A1 (es)
AU (1) AU2007281230B2 (es)
BR (1) BRPI0714803B8 (es)
CA (1) CA2658525C (es)
CL (1) CL2007002234A1 (es)
CR (2) CR10567A (es)
CU (2) CU23866B1 (es)
DK (1) DK2051990T3 (es)
DO (1) DOP2013000084A (es)
EA (2) EA201401247A1 (es)
ES (2) ES2405947T3 (es)
GE (1) GEP20115251B (es)
GT (2) GT200900019A (es)
HN (1) HN2009000214A (es)
HR (1) HRP20130373T1 (es)
IL (3) IL196596A (es)
JO (1) JO2848B1 (es)
MA (1) MA30652B1 (es)
ME (1) ME00585B (es)
MX (1) MX2009001212A (es)
MY (1) MY150460A (es)
NI (2) NI200900008A (es)
NO (1) NO342230B1 (es)
NZ (1) NZ574393A (es)
PA (1) PA8740901A1 (es)
PE (5) PE20110220A1 (es)
PL (1) PL2051990T3 (es)
PT (1) PT2051990E (es)
SI (1) SI2051990T1 (es)
SM (1) SMP200900013B (es)
SV (1) SV2009003160A (es)
TN (1) TN2009000034A1 (es)
TW (1) TWI408133B (es)
UA (1) UA95485C2 (es)
WO (1) WO2008016893A1 (es)
ZA (1) ZA200900371B (es)

Families Citing this family (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG152225A1 (en) 2004-04-07 2009-05-29 Novartis Ag Inhibitors of iap
JP5230865B2 (ja) 2004-07-15 2013-07-10 テトラロジック ファーマシューティカルズ コーポレーション Iap結合性化合物
KR20120127754A (ko) 2004-12-20 2012-11-23 제넨테크, 인크. Iap의 피롤리딘 억제제
US7517906B2 (en) 2005-02-25 2009-04-14 Tetralogic Pharmaceuticals Corporation Dimeric IAP inhibitors
CA2607940C (en) 2005-05-18 2009-12-15 Aegera Therapeutics Inc. Bir domain binding compounds
BRPI0617751A2 (pt) 2005-10-25 2011-08-02 Aegera Therapeutics Inc compostos de ligação do domìnio iap bir
TWI504597B (zh) 2006-03-16 2015-10-21 Pharmascience Inc 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
EP2024362A4 (en) 2006-05-16 2012-01-25 Pharmascience Inc BINDING COMPOUNDS TO THE IAP BIR DOMAIN
WO2008014236A1 (en) * 2006-07-24 2008-01-31 Tetralogic Pharmaceuticals Corporation Dimeric iap inhibitors
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.
BRPI0715195A2 (pt) 2006-07-24 2013-06-11 Tetralogic Pharm Corp composto, mÉtodos para induzir e para estimular a apoptose em uma cÉlula, para intensificar a apoptose de cÉlulas patogÊnicas in vivo em um indivÍduo, e para tratar uma doenÇa, e, composiÇço farmacÊutica
BRPI0717411A2 (pt) * 2006-10-19 2013-11-12 Novartis Ag Uso de inibidores de iap
KR20090087094A (ko) * 2006-11-28 2009-08-14 노파르티스 아게 Iap 억제제 및 flt3 억제제의 조합물
WO2008085610A1 (en) * 2006-11-28 2008-07-17 Novartis Ag Use of iap inhibitors for the treatment of acute myeloid leukemia
BRPI0719481A2 (pt) * 2006-12-19 2014-02-11 Genentech Inc " composto, método de indução de apoptose em uma célula, de sensibilização de uma célula, para inibir a ligação de uma proteína iap a uma proteína caspase, para tratar uma doença ou condição associada com a superexpressão de uma proteína iap e para tratar câncer"
RU2491276C2 (ru) 2007-04-30 2013-08-27 Дженентек, Инк. Ингибиторы iap
WO2009140447A1 (en) * 2008-05-16 2009-11-19 Novartis Ag Immunomodulation by iap inhibitors
US8835393B2 (en) 2008-08-02 2014-09-16 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
US20110034469A1 (en) 2009-08-04 2011-02-10 Takeda Pharmaceutical Company Limited Heterocyclic Compound
EP2464347A1 (en) * 2009-08-11 2012-06-20 Novartis AG Combinations of vascular disrupting agents with inhibitor of apoptosis proteins antagonists
CN105646471A (zh) * 2009-08-12 2016-06-08 诺华股份有限公司 细胞凋亡蛋白抑制剂的固体口服制剂和晶形
US9284350B2 (en) 2010-02-12 2016-03-15 Pharmascience Inc. IAP BIR domain binding compounds
UY33236A (es) 2010-02-25 2011-09-30 Novartis Ag Inhibidores dimericos de las iap
HUE031420T2 (en) * 2010-08-31 2017-07-28 Hanmi Science Co Ltd Quinoline or quinazoline derivatives having apoptosis-inducing effect on cells
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
CN103814032A (zh) 2011-07-13 2014-05-21 诺华股份有限公司 用作端锚聚合酶抑制剂的4-氧代-3,5,7,8-四氢-4H-吡喃并[4,3-d]嘧啶基化合物
US9181266B2 (en) 2011-07-13 2015-11-10 Novartis Ag 2-piperidin-1-yl-acetamide 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
CA2871695A1 (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
KR20160002850A (ko) 2013-05-01 2016-01-08 에프. 호프만-라 로슈 아게 C-연결된 헤테로사이클로알킬 치환된 피리미딘 및 이의 용도
ES2828642T3 (es) 2013-06-25 2021-05-27 Walter & Eliza Hall Inst Medical Res Miméticos Smac para el tratamiento de una infección intracelular persistente de VHB
WO2015048312A1 (en) 2013-09-26 2015-04-02 Costim Pharmaceuticals 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
RS59853B1 (sr) 2014-03-14 2020-02-28 Novartis Ag Molekuli anti-lag-3 antitela i njihove upotrebe
KR20170060042A (ko) 2014-09-13 2017-05-31 노파르티스 아게 Alk 억제제의 조합 요법
CA2963281A1 (en) 2014-10-03 2016-04-07 Novartis Ag Combination therapies
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
TWI716362B (zh) 2014-10-14 2021-01-21 瑞士商諾華公司 針對pd-l1之抗體分子及其用途
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
KR20170129802A (ko) 2015-03-10 2017-11-27 아두로 바이오테크, 인코포레이티드 "인터페론 유전자의 자극인자"-의존적 신호전달을 활성화하는 조성물 및 방법
GB201506871D0 (en) 2015-04-22 2015-06-03 Glaxosmithkline Ip Dev Ltd Novel compounds
EP3316902A1 (en) 2015-07-29 2018-05-09 Novartis AG Combination therapies comprising antibody molecules to tim-3
EP4378957A3 (en) 2015-07-29 2024-08-07 Novartis AG Combination therapies comprising antibody molecules to pd-1
SI3317301T1 (sl) 2015-07-29 2021-10-29 Novartis Ag Kombinirane terapije, ki obsegajo molekule protitelesa na LAG-3
EP3370768B9 (en) 2015-11-03 2022-03-16 Janssen Biotech, Inc. Antibodies specifically binding pd-1 and their uses
EP3389712B1 (en) 2015-12-17 2024-04-10 Novartis AG Antibody molecules to pd-1 and uses thereof
WO2017182418A1 (en) 2016-04-20 2017-10-26 Glaxosmithkline Intellectual Property Development Limited Conjugates comprising ripk2 inhibitors
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
KR20190130644A (ko) 2017-03-31 2019-11-22 베링거 인겔하임 인터내셔날 게엠베하 항암 조합 요법
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
US20200172628A1 (en) 2017-06-22 2020-06-04 Novartis Ag Antibody molecules to cd73 and uses thereof
WO2018237157A1 (en) 2017-06-22 2018-12-27 Novartis Ag CD73 BINDING ANTIBODY MOLECULES AND USES THEREOF
WO2019099838A1 (en) 2017-11-16 2019-05-23 Novartis Ag Combination therapies
US12398209B2 (en) 2018-01-22 2025-08-26 Janssen Biotech, Inc. Methods of treating cancers with antagonistic anti-PD-1 antibodies
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
TWI848953B (zh) 2018-06-09 2024-07-21 德商百靈佳殷格翰國際股份有限公司 針對癌症治療之多特異性結合蛋白
JP7515175B2 (ja) 2018-07-31 2024-07-12 ファイメクス株式会社 複素環化合物
EP3911316A1 (en) 2019-01-17 2021-11-24 Debiopharm International SA Combination product for the treatment of cancer
TWI894135B (zh) 2019-01-25 2025-08-21 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
CA3130706A1 (en) 2019-04-04 2020-10-08 Dana-Farber Cancer Institute, Inc. Cdk2/5 degraders and uses thereof
WO2020236817A2 (en) 2019-05-20 2020-11-26 Novartis Ag Mcl-1 inhibitor antibody-drug conjugates and methods of use
US20220402935A1 (en) 2019-07-31 2022-12-22 Fimecs, Inc. Heterocyclic compound
WO2021053559A1 (en) 2019-09-18 2021-03-25 Novartis Ag Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies
MX2022003628A (es) 2019-09-25 2022-07-21 Debiopharm Int Sa Regímenes de dosificación para el tratamiento de pacientes con carcinoma de células escamosas avanzado localmente.
AU2021211871A1 (en) 2020-01-20 2022-09-08 Astrazeneca Ab Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer
JP7565384B2 (ja) 2020-06-03 2024-10-10 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 CD80細胞外ドメインFc融合タンパク質をコードするリコンビナントラブドウイルス
KR20230138444A (ko) 2020-11-24 2023-10-05 노파르티스 아게 Mcl-1 억제제 항체-약물 접합체 및 사용 방법
IL303059A (en) 2020-11-24 2023-07-01 Novartis Ag Antibodies against CD48, antibody-drug conjugates and uses thereof
EP4288434A1 (en) 2021-02-02 2023-12-13 Les Laboratoires Servier Selective bcl-xl protac compounds and methods of use
KR20250027281A (ko) 2022-05-20 2025-02-25 노파르티스 아게 Epha2 bcl-xl 억제제 항체-약물 접합체 및 그의 사용 방법
CA3256012A1 (en) 2022-05-20 2023-11-23 Les Laboratoires Servier ANTIBODY-DRUG CONJUGATES, MET INHIBITORS BCL-XL, AND THEIR METHODS OF USE
EP4676540A1 (en) 2023-03-10 2026-01-14 Novartis AG Panras inhibitor antibody-drug conjugates and methods of use thereof
WO2024240858A1 (en) 2023-05-23 2024-11-28 Valerio Therapeutics Protac molecules directed against dna damage repair system and uses thereof
TW202540185A (zh) 2023-11-22 2025-10-16 法商施維雅藥廠 抗cd74抗體藥物結合物及其使用方法
WO2025215536A1 (en) 2024-04-10 2025-10-16 Novartis Ag Macrocyclic panras inhibitors for the treatment of cancer

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
EP1283827A2 (en) 2000-05-23 2003-02-19 Vertex Pharmaceuticals Incorporated Caspase inhibitors and uses thereof
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
CA2491041A1 (en) 2002-07-02 2004-01-15 Novartis Ag Peptide inhibitors of smac protein binding to inhibitor of apoptosis proteins (iap)
AU2003265276A1 (en) * 2002-07-15 2004-02-02 The Trustees Of Princeton University Iap binding compounds
US20040171554A1 (en) * 2003-02-07 2004-09-02 Genentech, Inc. Compositions and methods for enhancing apoptosis
AU2004291936A1 (en) * 2003-11-13 2005-06-02 Burnham Institute Compositions and methods for screening pro-apoptotic compounds
CN1933847A (zh) * 2004-01-16 2007-03-21 密歇根大学董事会 Smac肽模拟物及其应用
SE527038C2 (sv) * 2004-02-26 2005-12-13 Ingenjoers N Per Oskar Persson Kassett och apparat för vätskefrysning
JP4674231B2 (ja) * 2004-03-01 2011-04-20 ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム 2量体小分子アポトーシス増強剤
SG152225A1 (en) 2004-04-07 2009-05-29 Novartis Ag Inhibitors of iap
RS53734B1 (sr) 2004-07-02 2015-06-30 Genentech Inc. Inhibitori 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
AU2007307763A1 (en) * 2006-10-12 2008-04-17 Novartis Ag Pyrrolydine derivatives as IAP inhibitors
BRPI0720049A2 (pt) * 2006-12-07 2014-01-07 Novartis Ag Derivados de piridina utilizados como inibidores de xiap

Also Published As

Publication number Publication date
PE20110224A1 (es) 2011-04-05
BRPI0714803B1 (pt) 2021-03-09
BRPI0714803A2 (pt) 2013-05-21
CN102558165B (zh) 2014-08-13
SV2009003160A (es) 2010-04-13
DK2051990T3 (da) 2013-05-13
PA8740901A1 (es) 2009-04-23
DOP2013000084A (es) 2013-06-15
CU23866B1 (es) 2013-03-27
CU20090017A7 (es) 2011-03-21
HK1127616A1 (en) 2009-10-02
PE20110217A1 (es) 2011-04-01
MA30652B1 (fr) 2009-08-03
HRP20130373T1 (en) 2013-05-31
IL231079A (en) 2015-02-26
CR10567A (es) 2009-02-18
ZA200900371B (en) 2009-12-30
US20110065726A1 (en) 2011-03-17
IL231079A0 (en) 2014-03-31
AU2007281230A1 (en) 2008-02-07
CA2658525A1 (en) 2008-02-07
GT200900019A (es) 2010-06-01
US20140004101A1 (en) 2014-01-02
IL196596A (en) 2014-09-30
AR062159A1 (es) 2008-10-22
US8552003B2 (en) 2013-10-08
AR112816A2 (es) 2019-12-18
ME00585A (en) 2011-12-20
KR101245945B1 (ko) 2013-03-22
KR20110030667A (ko) 2011-03-23
ES2405947T3 (es) 2013-06-04
PE20080951A1 (es) 2008-09-11
ME00585B (me) 2011-12-20
EA201401247A1 (ru) 2015-07-30
SMP200900013B (it) 2010-01-19
SI2051990T1 (sl) 2013-06-28
GEP20115251B (en) 2011-07-11
CR20140555A (es) 2015-01-14
CA2658525C (en) 2013-02-19
CL2007002234A1 (es) 2008-06-13
MX2009001212A (es) 2009-02-11
EP2051990B1 (en) 2013-02-06
EP2537850A1 (en) 2012-12-26
HN2009000214A (es) 2011-10-11
AU2007281230B2 (en) 2011-09-08
US20130005663A1 (en) 2013-01-03
CN101511860A (zh) 2009-08-19
US8546336B2 (en) 2013-10-01
MY150460A (en) 2014-01-30
HK1176613A1 (en) 2013-08-02
PT2051990E (pt) 2013-05-10
TN2009000034A1 (en) 2010-08-19
TW200815399A (en) 2008-04-01
EA200900227A1 (ru) 2009-08-28
BRPI0714803B8 (pt) 2021-05-25
NO20090878L (no) 2009-04-27
TWI408133B (zh) 2013-09-11
CN101511860B (zh) 2013-05-01
EP2537846A1 (en) 2012-12-26
WO2008016893A1 (en) 2008-02-07
NZ574393A (en) 2012-03-30
UA95485C2 (uk) 2011-08-10
ES2559042T3 (es) 2016-02-10
NI200900081A (es) 2010-01-07
PL2051990T3 (pl) 2013-07-31
KR101087878B1 (ko) 2011-11-30
CU24004B1 (es) 2014-06-27
NO342230B1 (no) 2018-04-23
IL196596A0 (en) 2009-11-18
PE20110218A1 (es) 2011-04-01
KR20090038479A (ko) 2009-04-20
EA021671B1 (ru) 2015-08-31
PE20110220A1 (es) 2011-04-11
EP2051990A1 (en) 2009-04-29
JO2848B1 (en) 2014-09-15
IL236883A0 (en) 2015-03-31
EP2537846B1 (en) 2015-09-16
CN102558165A (zh) 2012-07-11
NI200900008A (es) 2010-01-07
SMAP200900013A (it) 2009-05-11
JP4875749B2 (ja) 2012-02-15
GT200900019AA (es) 2015-11-24
CU20110027A7 (es) 2011-12-28
JP2009545613A (ja) 2009-12-24

Similar Documents

Publication Publication Date Title
AR110313A2 (es) Derivados de tiazol-2-il-pirrolidina
CY1112467T1 (el) Παραγωγα 1-θειο-d-γλυκιτολης
HRP20120323T1 (en) Diarylhydantoin compounds
ATE481383T1 (de) 3-aza-bicycloä3.1.0ühexanderivate
HUS1900034I1 (hu) 6,7-telítetlen-7-karbamoil-szubsztituált morfinán-származékok
CY1118343T1 (el) Αντισωματα συνδεσης twεακ
ATE469145T1 (de) 4-ä5-methoxy-6-(2-methyl-6-ä1,2,4ütriazol-1-yl-
DK1902037T3 (da) 2,4-diamino-pyrimidiner som auroainhibitorer
CY1110064T1 (el) Παραγωγα φαινυλ-πιπεραζινης ως αναστολεις επαναπροσληψης σεροτονινης
TW200730490A (en) Photoactive compounds
BRPI0411897A (pt) pirroldihidroisoquinolinas como inibidores de pde10
NL1031385A1 (nl) Gesubstitueerde sulfonylaminoarylmethylcyclopropaancarbonamideverbindingen.
UY31688A1 (es) Plaguicidas
TW200637837A (en) Fungicides
DE602007001681D1 (de) 1,3-dioxan-carboxylsäuren
CO6241120A2 (es) (DIHIDRO)PIRROLO[2,1-á]ISOQUINOLINAS.
ATE483000T1 (de) Naphtalin-amidin-imide
NL1031335A1 (nl) Gesubstitueerde N-sulfonylaminofenylethyl-2-fenoxyaceetamideverbindingen.
NL1032046A1 (nl) Prostaglandinederivaten.
IL198571A0 (en) 5,6 or 7-substituted-s-(hetero)arylisoquinolinamine derivatives as antitumor agents
RU2012137206A (ru) Лигнангидроксилаза
NL1030010A1 (nl) 4-Amino-gesubstitueerde-2-gesubstitueerde-1,2,3,4- tetrahydrochinolineverbindingen.
NO20091386L (no) Fenyloksyanilinderivater
ATE473233T1 (de) Neue morphinderivate
FR2910232B1 (fr) Machine pour la fenaison, notamment andaineuse.

Legal Events

Date Code Title Description
FB Suspension of granting procedure