HN2009000214A - Peptidomimeticos de smac utiles como inhibidores de proteinas de apoptosis (iap) - Google Patents
Peptidomimeticos de smac utiles como inhibidores de proteinas de apoptosis (iap)Info
- Publication number
- HN2009000214A HN2009000214A HN2009000214A HN2009000214A HN2009000214A HN 2009000214 A HN2009000214 A HN 2009000214A HN 2009000214 A HN2009000214 A HN 2009000214A HN 2009000214 A HN2009000214 A HN 2009000214A HN 2009000214 A HN2009000214 A HN 2009000214A
- Authority
- HN
- Honduras
- Prior art keywords
- smac
- iap
- peptidomimetics
- inhibitors
- useful
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/02—Heterocyclic 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
- C07D417/04—Heterocyclic 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic 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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (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)
- Pyrrole Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A UN COMPUESTO DE LA FORMULA (I); O SALES FARMACEUTICAMENTE ACEPTABLES DE MISMO, Y AL USO DE ESTOS COMPUESTOS PARA EL TRATAMIENTO DE ENFERMEDADES PROLIFERATIVAS, TALES COMO CANCER, EN MAMIFEROS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83500006P | 2006-08-02 | 2006-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
HN2009000214A true HN2009000214A (es) | 2011-10-11 |
Family
ID=38686647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HN2009000214A HN2009000214A (es) | 2006-08-02 | 2009-01-30 | Peptidomimeticos de smac utiles como inhibidores de proteinas de apoptosis (iap) |
Country Status (42)
Families Citing this family (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG152225A1 (en) | 2004-04-07 | 2009-05-29 | Novartis Ag | Inhibitors of iap |
ES2475207T3 (es) | 2004-07-15 | 2014-07-10 | Tetralogic Pharmaceuticals Corporation | Compuestos de unión a IAP |
DK1836201T4 (da) | 2004-12-20 | 2013-11-11 | Genentech Inc | Pyrrolidininhibitorer af IAP. |
CN103083644B (zh) | 2005-02-25 | 2014-05-28 | 泰特拉洛吉克药业公司 | Iap二聚体抑制剂 |
EP1883627B1 (en) | 2005-05-18 | 2018-04-18 | Pharmascience Inc. | Bir domain binding compounds |
AU2006308453B9 (en) | 2005-10-25 | 2011-12-01 | Pharmascience Inc. | IAP BIR domain binding compounds |
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 |
NZ572836A (en) | 2006-05-16 | 2011-12-22 | Pharmascience Inc | Iap bir domain binding compounds |
AU2007276760B2 (en) | 2006-07-24 | 2012-01-19 | Tetralogic Pharmaceuticals Corporation | Dimeric IAP antagonists |
US20100056495A1 (en) * | 2006-07-24 | 2010-03-04 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
AR064235A1 (es) | 2006-07-24 | 2009-03-25 | Tetralogic Pharmaceuticals Cor | Dipeptidos antagonistas de iap, una composicion farmaceutica que los comprende y el uso de los mismos para el tratamiento del cancer |
MX2009004061A (es) * | 2006-10-19 | 2009-04-27 | Novartis Ag | Compuestos organicos. |
CA2670270A1 (en) * | 2006-11-28 | 2008-07-17 | Novartis Ag | Use of iap inhibitors for the treatment of acute myeloid leukemia |
AU2007325280B2 (en) * | 2006-11-28 | 2011-03-10 | Dana-Farber Cancer Institute, Inc. | Combination of IAP inhibitors and FLT3 inhibitors |
WO2008079735A1 (en) * | 2006-12-19 | 2008-07-03 | Genentech, Inc. | Imidazopyridine inhibitors of iap |
NZ580226A (en) | 2007-04-30 | 2012-11-30 | Genentech Inc | Dimer compounds as inhibitors of iap |
US9750729B2 (en) * | 2008-05-16 | 2017-09-05 | Dana-Farber Cancer Institute, Inc. | Immunomodulation by IAP inhibitors |
CA2730448A1 (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 |
UY32826A (es) | 2009-08-04 | 2011-02-28 | Takeda Pharmaceutical | Compuestos heterocíclicos |
US20120129895A1 (en) * | 2009-08-11 | 2012-05-24 | Colleen Conway | Methods of treatment |
MX351274B (es) * | 2009-08-12 | 2017-10-06 | Novartis Ag | Formulaciones orales sólidas y formas cristalinas de un inhibidor de la proteína de apoptosis. |
SG10201501095WA (en) | 2010-02-12 | 2015-04-29 | Pharmascience Inc | Iap bir domain binding compounds |
UY33236A (es) | 2010-02-25 | 2011-09-30 | Novartis Ag | Inhibidores dimericos de las iap |
PT2611797T (pt) | 2010-08-31 | 2017-02-07 | Hanmi Science Co Ltd | Derivados de quinolina ou de quinazolina com atividade indutora de apoptose nas células |
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 |
JP2014520858A (ja) | 2011-07-13 | 2014-08-25 | ノバルティス アーゲー | タンキラーゼ阻害剤として用いるための新規な2−ピペリジン−1−イル−アセトアミド化合物 |
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 |
US20140243276A1 (en) | 2011-09-30 | 2014-08-28 | 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 |
BR112014026176A2 (pt) * | 2012-05-22 | 2017-06-27 | Hoffmann La Roche | dipiridilaminas substituídas e usos das mesmas |
KR20140011773A (ko) * | 2012-07-19 | 2014-01-29 | 한미약품 주식회사 | 이중 저해 활성을 갖는 헤테로고리 유도체 |
RU2015147601A (ru) | 2013-05-01 | 2017-06-05 | Ф. Хоффманн-Ля Рош Аг | С-связанные гетероциклоалкилзамещенные пиримидины и их применения |
JP6785653B2 (ja) | 2013-06-25 | 2020-11-18 | ザ・ウォルター・アンド・エリザ・ホール・インスティテュート・オブ・メディカル・リサーチ | 細胞内感染の処置方法 |
EP3049442A4 (en) | 2013-09-26 | 2017-06-28 | 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 |
SI3116909T1 (sl) | 2014-03-14 | 2020-03-31 | Novartis Ag | Molekule protiteles na LAG-3 in njih uporaba |
CA2960824A1 (en) | 2014-09-13 | 2016-03-17 | Novartis Ag | Combination therapies of alk inhibitors |
JP2017535528A (ja) | 2014-10-03 | 2017-11-30 | ノバルティス アーゲー | 組み合わせ治療 |
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 |
PE20171067A1 (es) | 2014-10-14 | 2017-07-24 | Novartis Ag | Moleculas 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 |
WO2016145102A1 (en) | 2015-03-10 | 2016-09-15 | 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 |
EP3878465A1 (en) | 2015-07-29 | 2021-09-15 | Novartis AG | Combination therapies comprising antibody molecules to tim-3 |
EP3317301B1 (en) | 2015-07-29 | 2021-04-07 | Novartis AG | Combination therapies comprising antibody molecules to lag-3 |
JP6878405B2 (ja) | 2015-07-29 | 2021-05-26 | ノバルティス アーゲー | Pd−1に対する抗体分子を含む組み合わせ治療 |
CR20180234A (es) | 2015-11-03 | 2018-09-11 | Janssen Biotech Inc | Anticuerpos que se unen especificamente a pd-1 y sus usos |
JP2019503349A (ja) | 2015-12-17 | 2019-02-07 | ノバルティス アーゲー | Pd−1に対する抗体分子およびその使用 |
JP2019514878A (ja) | 2016-04-20 | 2019-06-06 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Ripk2阻害剤を含むコンジュゲート |
GB201610147D0 (en) | 2016-06-10 | 2016-07-27 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
US11098077B2 (en) | 2016-07-05 | 2021-08-24 | Chinook Therapeutics, 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 |
WO2018237173A1 (en) | 2017-06-22 | 2018-12-27 | Novartis Ag | ANTIBODY MOLECULES DIRECTED AGAINST CD73 AND CORRESPONDING USES |
MA49457A (fr) | 2017-06-22 | 2020-04-29 | Novartis Ag | Molécules d'anticorps se liant à cd73 et leurs utilisations |
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 |
AR126019A1 (es) | 2018-05-30 | 2023-09-06 | 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 |
EP3831811A4 (en) | 2018-07-31 | 2022-04-20 | Fimecs, Inc. | HETEROCYCLIC COMPOUND |
EP3911316A1 (en) | 2019-01-17 | 2021-11-24 | Debiopharm International SA | 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 |
WO2020206137A1 (en) | 2019-04-04 | 2020-10-08 | Dana-Farber Cancer Institute, Inc. | Cdk2/5 degraders and uses thereof |
TW202100184A (zh) | 2019-05-20 | 2021-01-01 | 瑞士商諾華公司 | Mcl-1抑制劑抗體-藥物結合物及使用方法 |
EP4006037A4 (en) | 2019-07-31 | 2023-12-13 | Fimecs, Inc. | HETEROCYCLIC COMPOUND |
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 |
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. |
KR20220130190A (ko) | 2020-01-20 | 2022-09-26 | 아스트라제네카 아베 | 암 치료를 위한 표피성장인자 수용체 티로신 키나제 억제제 |
CR20220606A (es) | 2020-06-03 | 2023-01-23 | Boehringer Ingelheim Int | Rhabdovirus recombinante que codifica una proteína de fusión fc de dominio extracelular cd80 |
CN117136076A (zh) | 2020-11-24 | 2023-11-28 | 诺华股份有限公司 | Mcl-1抑制剂抗体药物缀合物和使用方法 |
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 |
WO2024189481A1 (en) | 2023-03-10 | 2024-09-19 | Novartis Ag | Panras inhibitor antibody-drug conjugates and methods of use thereof |
Family Cites Families (23)
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 |
CA2380935A1 (en) | 2000-05-23 | 2001-11-29 | 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 |
US20060128632A1 (en) | 2002-07-02 | 2006-06-15 | Sharma Sushil K | Peptide inhibitors of smac protein binding to inhibitor of apoptosis proteins (iap) |
ES2318167T3 (es) * | 2002-07-15 | 2009-05-01 | The Trustees Of Princeton University | Compuestos de union a iap. |
US20040171554A1 (en) * | 2003-02-07 | 2004-09-02 | Genentech, Inc. | Compositions and methods for enhancing apoptosis |
WO2005049853A2 (en) * | 2003-11-13 | 2005-06-02 | Genentech, Inc. | Compositions and methods for screening pro-apoptotic compounds |
WO2005069888A2 (en) * | 2004-01-16 | 2005-08-04 | The Regents Of The University Of Michigan | Smac peptidomimetics and the uses thereof |
SE527038C2 (sv) * | 2004-02-26 | 2005-12-13 | Ingenjoers N Per Oskar Persson | Kassett och apparat för vätskefrysning |
US7309792B2 (en) * | 2004-03-01 | 2007-12-18 | Board Of Regents, The University Of Texas System | Dimeric small molecule potentiators of apoptosis |
SG152225A1 (en) * | 2004-04-07 | 2009-05-29 | Novartis Ag | Inhibitors of iap |
US7244851B2 (en) | 2004-07-02 | 2007-07-17 | Genentech, Inc. | Inhibitors of IAP |
DK1836201T4 (da) | 2004-12-20 | 2013-11-11 | Genentech Inc | Pyrrolidininhibitorer af IAP. |
US20060218632A1 (en) * | 2005-03-28 | 2006-09-28 | Cisco Technology, Inc.; | Method and system for installing premise equipment |
BRPI0719221A2 (pt) * | 2006-10-12 | 2014-03-18 | Novartis Ag | Derivados de pirrolidina como inibidores de iap |
CN101595093A (zh) * | 2006-12-07 | 2009-12-02 | 诺瓦提斯公司 | 有机化合物 |
-
2007
- 2007-07-26 PE PE2007000978A patent/PE20080951A1/es active IP Right Grant
- 2007-07-26 PE PE2011000111A patent/PE20110217A1/es not_active Application Discontinuation
- 2007-07-26 PE PE2011000113A patent/PE20110220A1/es not_active Application Discontinuation
- 2007-07-26 PE PE2011000112A patent/PE20110218A1/es not_active Application Discontinuation
- 2007-07-26 PE PE2011000114A patent/PE20110224A1/es active IP Right Grant
- 2007-07-31 CA CA2658525A patent/CA2658525C/en active Active
- 2007-07-31 CN CN2007800329568A patent/CN101511860B/zh active Active
- 2007-07-31 AU AU2007281230A patent/AU2007281230B2/en active Active
- 2007-07-31 EA EA200900227A patent/EA021671B1/ru not_active IP Right Cessation
- 2007-07-31 KR KR1020097004264A patent/KR101087878B1/ko active IP Right Grant
- 2007-07-31 SI SI200731218T patent/SI2051990T1/sl unknown
- 2007-07-31 EA EA201401247A patent/EA201401247A1/ru unknown
- 2007-07-31 CN CN201110446951.8A patent/CN102558165B/zh active Active
- 2007-07-31 JP JP2009523001A patent/JP4875749B2/ja active Active
- 2007-07-31 UA UAA200900768A patent/UA95485C2/uk unknown
- 2007-07-31 BR BRPI0714803A patent/BRPI0714803B8/pt active IP Right Grant
- 2007-07-31 WO PCT/US2007/074790 patent/WO2008016893A1/en active Application Filing
- 2007-07-31 MX MX2009001212A patent/MX2009001212A/es active IP Right Grant
- 2007-07-31 EP EP12184747.9A patent/EP2537846B1/en active Active
- 2007-07-31 EP EP12184700A patent/EP2537850A1/en not_active Withdrawn
- 2007-07-31 AR ARP070103375A patent/AR062159A1/es not_active Application Discontinuation
- 2007-07-31 ME MEP-19/09A patent/ME00585A/xx unknown
- 2007-07-31 DK DK07813569.6T patent/DK2051990T3/da active
- 2007-07-31 NZ NZ574393A patent/NZ574393A/en not_active IP Right Cessation
- 2007-07-31 MY MYPI20090334 patent/MY150460A/en unknown
- 2007-07-31 US US12/376,057 patent/US8552003B2/en active Active
- 2007-07-31 PL PL07813569T patent/PL2051990T3/pl unknown
- 2007-07-31 KR KR1020117002855A patent/KR101245945B1/ko active IP Right Grant
- 2007-07-31 PT PT78135696T patent/PT2051990E/pt unknown
- 2007-07-31 EP EP07813569A patent/EP2051990B1/en active Active
- 2007-07-31 ES ES07813569T patent/ES2405947T3/es active Active
- 2007-07-31 ES ES12184747.9T patent/ES2559042T3/es active Active
- 2007-07-31 GE GEAP200711084A patent/GEP20115251B/en unknown
- 2007-08-01 CL CL200702234A patent/CL2007002234A1/es unknown
- 2007-08-01 TW TW096128289A patent/TWI408133B/zh not_active IP Right Cessation
- 2007-08-02 PA PA20078740901A patent/PA8740901A1/es unknown
- 2007-08-02 JO JO2007318A patent/JO2848B1/en active
-
2009
- 2009-01-16 CR CR10567A patent/CR10567A/es unknown
- 2009-01-16 ZA ZA2009/00371A patent/ZA200900371B/en unknown
- 2009-01-19 IL IL196596A patent/IL196596A/en active IP Right Grant
- 2009-01-22 NI NI200900008A patent/NI200900008A/es unknown
- 2009-01-22 NI NI2009000081A patent/NI200900081A/es unknown
- 2009-01-29 CU CU20090017A patent/CU23866B1/es active IP Right Grant
- 2009-01-30 HN HN2009000214A patent/HN2009000214A/es unknown
- 2009-01-30 GT GT200900019A patent/GT200900019A/es unknown
- 2009-01-30 TN TN2009000034A patent/TN2009000034A1/fr unknown
- 2009-02-02 SV SV2009003160A patent/SV2009003160A/es active IP Right Grant
- 2009-02-17 MA MA31648A patent/MA30652B1/fr unknown
- 2009-02-25 NO NO20090878A patent/NO342230B1/no not_active IP Right Cessation
- 2009-02-26 SM SM200900013T patent/SMP200900013B/it unknown
- 2009-07-22 HK HK13103786.7A patent/HK1176613A1/xx not_active IP Right Cessation
- 2009-07-22 HK HK09106712.5A patent/HK1127616A1/xx not_active IP Right Cessation
-
2011
- 2011-02-02 CU CU2011000027A patent/CU24004B1/es active IP Right Grant
-
2012
- 2012-09-07 US US13/606,676 patent/US8546336B2/en active Active
-
2013
- 2013-04-16 DO DO2013000084A patent/DOP2013000084A/es unknown
- 2013-04-29 HR HRP20130373TT patent/HRP20130373T1/hr unknown
- 2013-08-29 US US14/013,666 patent/US20140004101A1/en not_active Abandoned
- 2013-10-23 GT GT200900019AK patent/GT200900019AA/es unknown
-
2014
- 2014-02-20 IL IL231079A patent/IL231079A/en active IP Right Grant
- 2014-12-03 CR CR20140555A patent/CR20140555A/es unknown
-
2015
- 2015-01-22 IL IL236883A patent/IL236883A0/en unknown
-
2017
- 2017-12-04 AR ARP170103398A patent/AR110313A2/es unknown
-
2018
- 2018-09-17 AR ARP180102641A patent/AR112816A2/es unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HN2009000214A (es) | Peptidomimeticos de smac utiles como inhibidores de proteinas de apoptosis (iap) | |
PA8852901A1 (es) | Inhibidores de proteina cinasa | |
GT201400057A (es) | 3-pirmidin-4-il-oxazolidin-2-onas como inhibidores de la idh mutante | |
ECSP12012318A (es) | Inhibidores de pirazolil quinazolina cinasa | |
CL2010001426A1 (es) | Compuestos derivados de triciclos, inhibidores de la proteina quinasa; composicion farmaceutica que los comprende; utiles en el tratamiento de enfermedades oncologicas e inmunologicas. | |
PE20151939A1 (es) | 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de idh mutante | |
CL2011001967A1 (es) | Compuestos derivados de carboxamida-azaheterociclica sustituida, inhibidores de p70s6k, proceso de preparacion de estos; composicion farmaceutica que los comprende; y su uso en el tratamiento de enfermedades inflamatorias y cancer; kit farmaceutico. | |
BRPI0815708A8 (pt) | composto derivado de benzilbenzeno como inibidor de sglt, composição farmacêutica, e, uso de um composto | |
ECSP066893A (es) | Inhibidores de proteínas de apoptosis (iap) | |
GT200800184A (es) | Aminotetrahidropiranos como inhibidores de dipeptidil peptidasa-iv para el tratamiento o prevencion de diabetes. | |
ECSP099445A (es) | Quinazolinas para la inhibición de pdk1 | |
CL2007001995A1 (es) | Compuestos derivados de pirrolotriazina; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar el cancer. | |
CL2012001821A1 (es) | Compuestos derivados de 5-alquinil-pirimidinas, inhibidores de quinasas; composiciones farmaceuticas que los contienen; y su uso para el tratamiento y/o prevencion de cancer, infecciones, enfermedades inflamatorias y autoinmunitarias. | |
GT201400111A (es) | Triazolopiridinas sustituidas | |
CR11427A (es) | 2-fluoro-2 - desoxitetrahidrouridinas como inhibidores de citidina desaminasa | |
CL2011000691A1 (es) | Compuestos derivados de nicotinamida sustituida; composicion farmaceutica que los comprende; uso para el tratamiento y/o prevencion de cancer, infecciones, enfermedades inflamatorias y autoinmunitarias. | |
UY33616A (es) | Compuestos con estructura de imidazotriazinona | |
CL2009000402A1 (es) | Compuestos derivados de 2-amino-acetamida sustituida; composicion farmaceutica; utiles en el tratamiento de enfermedades pulmonares, enfermedad reumatica, enfermedad autoinmune, entre otras. | |
UY32052A (es) | 5-aminopirazoles sustituidos y uso de los mismos | |
CO6341625A2 (es) | Derivados de indol como agentes anticáncer | |
CL2011000168A1 (es) | Compuestos derivados de narciclasina y pancratistatina; procedimiento de preparación; composición farmacéutica; combinación farmacéutica; y su uso para el tratamiento del cáncer. | |
SV2011003784A (es) | Nifurtimox para el tratamiento de enfermedades causadas por trichomonadida | |
CL2011001850A1 (es) | Uso de un compuesto nitrogenado heterociclico sustituido para el tratamiento de cánceres tales como cáncer de colon o mieloma múltiple;composición farmacéutica que comprende al compuesto. | |
UY30514A1 (es) | Compuestos organicos | |
NI201200162A (es) | Inhibidores de pirazolil quinoxalina cinasa |