AR062159A1 - Compuestos que inhiben el enlace de la proteina smac al inhibidor de proteinas de apoptosis (iap) - Google Patents
Compuestos que inhiben el enlace de la proteina smac al inhibidor de proteinas de apoptosis (iap)Info
- Publication number
- AR062159A1 AR062159A1 ARP070103375A ARP070103375A AR062159A1 AR 062159 A1 AR062159 A1 AR 062159A1 AR P070103375 A ARP070103375 A AR P070103375A AR P070103375 A ARP070103375 A AR P070103375A AR 062159 A1 AR062159 A1 AR 062159A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- carbon atoms
- aryl
- substituted
- lower alkyl
- 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)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (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)
Abstract
La presente invencion se refiere a un compuesto de la formula (1) o sales farmacéuticamente aceptables del mismo, y al uso de estos compuestos para el tratamiento de enfermedades proliferativas, tales como cáncer, en mamíferos. Reivindicacion 1: Un compuesto de la formula (1): o sales farmacéuticamente aceptables del mismo, en donde: R1 es H, alquilo de 1 a 4 átomos de carbono, alquenilo de 2 a 4 átomos de carbono, alquinilo de 2 a 4 átomos de carbono, o cicloalquilo de 3 a 10 átomos de carbono, cuyo R1 puede estar insustituido o sustituido; R2 es H, alquilo de 1 a 4 átomos de carbono, alquenilo de 2 a 4 átomos de carbono, alquinilo de 2 a 4 átomos de carbono, cicloalquilo de 3 a 10 átomos de carbono, cuyo R2 puede estar insustituido o sustituido; R3 es H, CF3, C2F5, alquilo de 1 a 4 átomos de carbono, alquenilo de 2 a 4 átomos de carbono, alquinilo de 2 a 4 átomos de carbono, CH2-Z, o R2 y R3, tomados junto con el átomo de nitrogeno con el que están unidos, forman un anillo heterocíclico, cuyo alquilo, alquenilo, alquinilo, o anillo heterociclico puede estar insustituido o sustituido; Z es H, OH, F, CI, CH3, CH2Cl, CH2F o CH2OH; R4 es alquilo de 0 a 10 átomos de carbono, alquenilo de 0 a 10 átomos de carbono, alquinilo de 0 e 10 átomos de carbono, cicloalquilo de 3 a 10 átomos de carbono, en donde el grupo alquilo de 0 a 10 átomos de carbono, o cicloalquilo está insustituido o sustituido; A es hel, el cual puede estar sustituido o insustituido; D es alquileno de 1 a 7 átomos de carbono o alquenileno de 2 a 9 átomos de carbono, C(O), O. NR7, S(O)r, C(O)-alquilo de 1 a 10 átomos de carbono, O-alquilo de 1 a 10 átomos de carbono, S(O)r-alquilo de 1 a 10 átomos de carbono, C(O)-arilalquilo de 0 a 10 átomos de carbono, O-arialquiIo de 0 a 10 átomos de carbono, o S(O)r-arilalquilo de 0 a 10 átomos de carbono, cuyos grupos alquilo y arilo pueden estar insustituidos o sustituidos; r es 0, 1, o 2; A1 es un arilo sustituido o insustituido o het insustituido o sustituido, cuyos sustituyentes sobre arilo y het son halogeno, alquilo, alcoxilo interior, NR5R6, CN, NO2 o SR5; cada Q es independientemente H, alquilo de 1 a 10 átomos de carbono, alcoxilo de 1 a 10 átomos de carbono, aril-alcoxilo de 1 a 10 átomos de carbono, OH, O-alquilo de 1 a 10 átomos de carbono, (CH2)0-6-cicloalquilo de 3 a 7 átomos de carbono, arilo, aril-alquilo de 1 a 10 átomos de carbono, O-(CH2)0-6 arilo, (CH2)1-6 het, het, O-(CH2)1-6, het, OR11, C(O)R11, - C(O)N(R11)(R12), N(R11)(R12), SR11, S(O)R11,S(O)2R11, S(O)2-N(R11)(R12), o NR11-S(O)2-(R12), en donde alquilo, cicloalquilo y arilo están insustituidos o sustituidos; n es 0, 1, 2 o 3, 4, 5, 6 o 7; het es un anillo heterocíclico monocíclico de 5 a 7 miembros que contiene de 1 a 4 heteroátomos del anillo seleccionados a partir de N, O y S, o un sistema de anillo fusionado de 8 a 12 miembros que incluye un anillo heterocíclico monocíclico de 5 a 7 miembros que contiene 1, 2, o 3 heteroátomos del arillo seleccionados a partir de N, O y S, cuyo het está insustituido o sustituido; R11 y R12, son independientemente H, alquilo de 1 a 10 átomos de carbono, (CH2)0-6-cicIoalquiIo de 3 a 7 átomos de carbono, (CH2)0-6-(CH)0-1(arilo)1-2,C(O)-aIquilo de 1 a 10 átomos de carbono, -C(O)-(CH2)1-6-cicIoaIquiIo de 3 a 7 átomos de carbono, -C(O)-O(CH2)0-6-arilo, -C(O)-(CH2)0-6-O-fluorenilo, C(O)-NH-(CH2)0-6-arilo, C(O)-(CH2)0-6-arilo, C(O)-(CH2)1-6-het, -C(S)-alquilo de 1 a 10 átomos de carbono, -C(S)- (CH2)1-6-cicloalquilo de 3 a 7 átomos de carbono, -C(S)-O-(CH2)0-6-arilo, -C(S)-(CH2)0-6-O-fluorenilo, C(S)-NH-(CH2)0-6-arilo, -C(S)-(CH2)0-6-arilo, o C(S)-(CH2)1-6-het, C(O)R11, C(O)NR11R12, C(O)OR11, S(O)nR11, S(O)mNR11R12, m = 1 o 2, C(S)R11, C(S)NR11R12, C(S)OR11, en donde alquilo, cicloalquilo y arilo están insustituidos o sustituidos; o R11 y R12 son un sustituyente que facilita el transporte de la molécula a través de una rnembrana celular, o R11 y R12, junto con el átomo de nitrogeno, forman het, en donde: los sustituyentes de alquilo de R11 y R12 pueden estar insustituidos o sustituidos por uno o mis sustituyentes seleccionados a partir de alquilo de 1 a 10 átomos de carbono, halogeno, OH, O-alquilo de 1 a 6 átomos de carbono, -S-alquilo de 1 a 6 átomos de carbono, CF3 o NR11R12; los sustituyentes de cicloalquilo sustituido de R11 y R12 están sustituídos por uno o más sustituyentes seleccionados a partir de un alqueno de 2 a 10 átomos de carbono; alquilo de 1 a 6 átomos de carbono; halogeno; OH; O-alquilo de 1 a 6 átomos de carbono; S-alquilo de 1 a 6 átomos de carbono, CF3; o NR11R12 y het sustituido o arilo sustituido de R11 y R12 están sustituidos por uno o más sustituyentes seleccionados a partir de halogeno, hidroxilo, alquilo de 1 a 4 átomos de carbono, alcoxilo de 1 a 4 átomos de carbono, nitro, CNO-C(O)-alquilo de 1 a 4 átomos de carbono, y C(O)-O-alquilo de 1 a 4 átomos de carbono; R5, R6 y R7 son independientemente hidrogeno, alquilo inferior, arilo. aril-alquilo inferior, cicloalquilo, o cicloalquilo alquilo inferior C(O)R5, S(O)R5, C(O)OR5, C(O)NR5R6; y los sustituyentes sobre R1, R2, R3, R4, Q, y A y los grupos A1 son independientemente halogeno, hidroxilo, alquilo inferior, alquenilo inferior, alquinilo inferior, alcanoílo inferior, alcoxilo inferior, arilo, aril-alquilo inferior, amino, amino-alquilo interior, di-alquilo inferior-amino, alcanoílo inferior, amino-alcoxilo inferior, nitro, ciano, ciano-alquilo inferior, carboxilo, carbalcoxilo inferior, alcanoílo inferior, ariloílo, arilo inferior-alcanoílo, carbamoílo, N-mono- o N,N-di-alquilo inferior-carbamoílo, éster del ácido alquilo inferior-carbámico, amidino, guanidina, ureido, mercapto, sulfo, tioalquilo inferior, sulfoamino, sulfonamida, benzo-sulfonamida, sulfonato, sulfanil-alquilo inferior, aril-sulfonamida. aril-sulfonato sustituido por halogeno, alquilo inferior-sulfinilo, aril-sulfinilo; aril-alquilo inferior-sulfinilo, alquilo interior- arilsulfinilo, alquilo inferior-sulfonilo, aril-sulfonilo, aril-alquilo inferior-sulfonilo, aril-alquilo inferior-alquilo inferior-aril-sulfonilo, halogeno-alquilo inferior-mercapto. halogeno-alquilo inferior-sulfonilo, fosfono (-P(=O){OH)2), hidroxi-alcoxilo inferior-fosforilo, o di-alcoxilo inferior-fosforilo, (R9)NC(O)-NR10R13, éster del ácido alquilo inferior-carbámico o carbamatos o -NR8R14, en donde: R8 y R14 pueden ser iguales o diferentes, y son independientemente H o alquilo inferior, o R8 y R14, junto con el átomo de nitrogeno, forman un anillo heterocíclico de 3 a 8 miembros que contiene un heteroátorno de nitrogeno del anillo, y que opcionalmente puede contener uno o dos heteroátomos adicionales del anillo seleccionados a partir de nitrogeno, oxigeno, y azufre, cuyo anillo heterocíclico puede estar insustituido o sustituido con alquilo inferior, halogeno, alquenilo inferior, alquinilo inferior, hidroxilo, alcoxilo inferior, nitro, amino, alquilo inferior, amino, di-alquilo inferior-amino, ciano, carboxilo, carbalcoxilo inferior, formilo, alcanoílo inferior, oxo, carbarmoílo, N- o N,N-di-alquilo inferior-carbamoílo, mercapto, o tioalquilo inferior; y R9, R10 y R13 son independientemente hidrogeno, alquilo inferior, alquilo inferior sustituido por halogeno, arilo, aril-alquilo inferior, arilo sustituido por halogeno, aril-alquilo inferior sustituido por halogeno.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83500006P | 2006-08-02 | 2006-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR062159A1 true AR062159A1 (es) | 2008-10-22 |
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 After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
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) |
Country Status (42)
Families Citing this family (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20080083220A (ko) | 2004-04-07 | 2008-09-16 | 노파르티스 아게 | Iap 억제제 |
EP1773766B1 (en) | 2004-07-15 | 2014-04-02 | Tetralogic Pharmaceuticals Corporation | Iap binding compounds |
ES2349110T5 (es) | 2004-12-20 | 2013-11-27 | Genentech, Inc. | Inhibidores de IAP derivados de pirrolidina |
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 |
KR20080067357A (ko) | 2005-10-25 | 2008-07-18 | 에게라 쎄라퓨틱스 인코포레이티드 | Iap bir 도메인 결합 화합물 |
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 |
US8163792B2 (en) | 2006-05-16 | 2012-04-24 | Pharmascience Inc. | IAP BIR domain binding compounds |
KR20090041391A (ko) | 2006-07-24 | 2009-04-28 | 테트랄로직 파마슈티칼스 | 이량체성 iap 길항제 |
WO2008014236A1 (en) * | 2006-07-24 | 2008-01-31 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
JP5452223B2 (ja) | 2006-07-24 | 2014-03-26 | 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阻害剤 |
US20100316573A1 (en) * | 2006-10-19 | 2010-12-16 | Larry Alexander Gaither | Organic Compounds |
US20100076013A1 (en) * | 2006-11-28 | 2010-03-25 | Novartis Ag | Methods of Treatment |
PT2089024E (pt) * | 2006-11-28 | 2011-08-31 | Novartis Ag | Combinação de inibidores de iap e inibidores de flt3 |
KR20090094461A (ko) * | 2006-12-19 | 2009-09-07 | 제넨테크, 인크. | Iap의 이미다조피리딘 억제제 |
TWI432212B (zh) | 2007-04-30 | 2014-04-01 | Genentech Inc | Iap抑制劑 |
BRPI0912692A2 (pt) * | 2008-05-16 | 2017-03-21 | Dana Farber Cancer Inst Inc | imunomodulação através de inibidores de iap |
EP2318395A4 (en) | 2008-08-02 | 2011-10-26 | Genentech Inc | IPA INHIBITORS |
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 |
EP2464347A1 (en) * | 2009-08-11 | 2012-06-20 | 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 |
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 |
PL2611797T3 (pl) * | 2010-08-31 | 2017-05-31 | Hanmi Science Co., Ltd. | Pochodne chinoliny lub chinazoliny o aktywności wywoływania apoptozy wobec komórek |
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 |
US9181266B2 (en) | 2011-07-13 | 2015-11-10 | Novartis Ag | 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors |
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 |
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 |
JP6267193B2 (ja) * | 2012-05-22 | 2018-01-24 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 置換ジピリジルアミン類及びそれらの使用 |
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 |
NZ714347A (en) | 2013-06-25 | 2020-01-31 | Walter & Eliza Hall Inst Medical Res | Method of treating intracellular infection |
EP3757130A1 (en) | 2013-09-26 | 2020-12-30 | 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 |
CU24481B1 (es) | 2014-03-14 | 2020-03-04 | Immutep Sas | Moléculas de anticuerpo que se unen a lag-3 |
JP6681905B2 (ja) | 2014-09-13 | 2020-04-15 | ノバルティス アーゲー | Alk阻害剤の併用療法 |
AU2015327868A1 (en) | 2014-10-03 | 2017-04-20 | 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 |
CR20170143A (es) | 2014-10-14 | 2017-06-19 | Dana Farber Cancer Inst Inc | 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 |
TN2017000375A1 (en) | 2015-03-10 | 2019-01-16 | 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 |
WO2017019896A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to pd-1 |
PT3317301T (pt) | 2015-07-29 | 2021-07-09 | Novartis Ag | Terapias de associação compreendendo moléculas de anticorpo contra lag-3 |
US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
SG11201803520PA (en) | 2015-11-03 | 2018-05-30 | Janssen Biotech Inc | Antibodies specifically binding pd-1 and their uses |
AU2016369537B2 (en) | 2015-12-17 | 2024-03-14 | Novartis Ag | Antibody molecules to PD-1 and uses thereof |
EP3445759A1 (en) | 2016-04-20 | 2019-02-27 | GlaxoSmithKline Intellectual Property Development Ltd | 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 |
MX2019011572A (es) | 2017-03-31 | 2019-11-18 | Boehringer Ingelheim Int | Tratamiento conjunto antineoplasico. |
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 |
SG11201912473PA (en) | 2017-06-22 | 2020-01-30 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
WO2018237173A1 (en) | 2017-06-22 | 2018-12-27 | Novartis Ag | ANTIBODY MOLECULES DIRECTED AGAINST CD73 AND CORRESPONDING USES |
CN111655288A (zh) | 2017-11-16 | 2020-09-11 | 诺华股份有限公司 | 组合疗法 |
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 |
US20210214459A1 (en) | 2018-05-31 | 2021-07-15 | 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 |
KR20220017931A (ko) | 2019-05-20 | 2022-02-14 | 노파르티스 아게 | Mcl-1 억제제 항체-약물 접합체 및 사용 방법 |
JPWO2021020585A1 (es) | 2019-07-31 | 2021-02-04 | ||
EP4031578A1 (en) | 2019-09-18 | 2022-07-27 | 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. |
KR20220130190A (ko) | 2020-01-20 | 2022-09-26 | 아스트라제네카 아베 | 암 치료를 위한 표피성장인자 수용체 티로신 키나제 억제제 |
CA3185332A1 (en) | 2020-06-03 | 2021-12-09 | Boehringer Ingelheim International Gmbh | Recombinant rhabdovirus encoding for a cd80 extracellular domain fc-fusion protein |
WO2022115451A1 (en) | 2020-11-24 | 2022-06-02 | Novartis Ag | Mcl-1 inhibitor antibody-drug conjugates and methods of use |
WO2022112942A2 (en) | 2020-11-24 | 2022-06-02 | Novartis Ag | Anti-cd48 antibodies, antibody drug conjugates, and uses thereof |
CN117794929A (zh) | 2021-02-02 | 2024-03-29 | 法国施维雅药厂 | 选择性bcl-xl protac化合物及使用方法 |
AR129382A1 (es) | 2022-05-20 | 2024-08-21 | Novartis Ag | Conjugados de anticuerpo-fármaco inhibidores de bcl-xl y met y sus métodos de uso |
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 |
MXPA02000823A (es) | 2000-05-23 | 2002-07-30 | Vertex Pharma | Inhibidores de caspasa y uso de los mismos. |
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 |
WO2003040172A2 (en) | 2001-11-09 | 2003-05-15 | Aegera Therapeutics, Inc. | Methods and reagents for peptide-bir interaction screens |
AU2003249920A1 (en) | 2002-07-02 | 2004-01-23 | Novartis Ag | 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 |
CA2543897A1 (en) | 2003-11-13 | 2005-06-02 | Genentech, Inc. | Compositions and methods for screening pro-apoptotic compounds |
US20100093645A1 (en) | 2004-01-16 | 2010-04-15 | Shaomeng Wang | SMAC Peptidomimetics and the Uses Thereof |
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 |
KR20080083220A (ko) | 2004-04-07 | 2008-09-16 | 노파르티스 아게 | Iap 억제제 |
WO2006014361A1 (en) | 2004-07-02 | 2006-02-09 | Genentech, Inc. | Inhibitors of iap |
ES2349110T5 (es) | 2004-12-20 | 2013-11-27 | Genentech, Inc. | Inhibidores de IAP derivados de pirrolidina |
US20060218632A1 (en) * | 2005-03-28 | 2006-09-28 | Cisco Technology, Inc.; | Method and system for installing premise equipment |
KR20090065548A (ko) * | 2006-10-12 | 2009-06-22 | 노파르티스 아게 | Iap 억제제로서의 피롤리딘 유도체 |
BRPI0720049A2 (pt) * | 2006-12-07 | 2014-01-07 | Novartis Ag | Derivados de piridina utilizados como inibidores de xiap |
-
2007
- 2007-07-26 PE PE2011000111A patent/PE20110217A1/es not_active Application Discontinuation
- 2007-07-26 PE PE2011000114A patent/PE20110224A1/es active IP Right Grant
- 2007-07-26 PE PE2007000978A patent/PE20080951A1/es active IP Right Grant
- 2007-07-26 PE PE2011000113A patent/PE20110220A1/es not_active Application Discontinuation
- 2007-07-26 PE PE2011000112A patent/PE20110218A1/es not_active Application Discontinuation
- 2007-07-31 ME MEP-19/09A patent/ME00585A/xx unknown
- 2007-07-31 EP EP12184700A patent/EP2537850A1/en not_active Withdrawn
- 2007-07-31 ES ES12184747.9T patent/ES2559042T3/es active Active
- 2007-07-31 SI SI200731218T patent/SI2051990T1/sl unknown
- 2007-07-31 MY MYPI20090334 patent/MY150460A/en unknown
- 2007-07-31 PT PT78135696T patent/PT2051990E/pt unknown
- 2007-07-31 EP EP07813569A patent/EP2051990B1/en active Active
- 2007-07-31 JP JP2009523001A patent/JP4875749B2/ja active Active
- 2007-07-31 KR KR1020097004264A patent/KR101087878B1/ko active IP Right Grant
- 2007-07-31 EP EP12184747.9A patent/EP2537846B1/en active Active
- 2007-07-31 BR BRPI0714803A patent/BRPI0714803B8/pt active IP Right Grant
- 2007-07-31 MX MX2009001212A patent/MX2009001212A/es active IP Right Grant
- 2007-07-31 CN CN2007800329568A patent/CN101511860B/zh active Active
- 2007-07-31 EA EA201401247A patent/EA201401247A1/ru unknown
- 2007-07-31 PL PL07813569T patent/PL2051990T3/pl unknown
- 2007-07-31 AU AU2007281230A patent/AU2007281230B2/en active Active
- 2007-07-31 CA CA2658525A patent/CA2658525C/en active Active
- 2007-07-31 KR KR1020117002855A patent/KR101245945B1/ko active IP Right Grant
- 2007-07-31 US US12/376,057 patent/US8552003B2/en active Active
- 2007-07-31 UA UAA200900768A patent/UA95485C2/uk unknown
- 2007-07-31 NZ NZ574393A patent/NZ574393A/en not_active IP Right Cessation
- 2007-07-31 AR ARP070103375A patent/AR062159A1/es not_active Application Discontinuation
- 2007-07-31 WO PCT/US2007/074790 patent/WO2008016893A1/en active Application Filing
- 2007-07-31 EA EA200900227A patent/EA021671B1/ru not_active IP Right Cessation
- 2007-07-31 CN CN201110446951.8A patent/CN102558165B/zh active Active
- 2007-07-31 GE GEAP200711084A patent/GEP20115251B/en unknown
- 2007-07-31 DK DK07813569.6T patent/DK2051990T3/da active
- 2007-07-31 ES ES07813569T patent/ES2405947T3/es active Active
- 2007-08-01 TW TW096128289A patent/TWI408133B/zh not_active IP Right Cessation
- 2007-08-01 CL CL200702234A patent/CL2007002234A1/es unknown
- 2007-08-02 JO JO2007318A patent/JO2848B1/en active
- 2007-08-02 PA PA20078740901A patent/PA8740901A1/es unknown
-
2009
- 2009-01-16 ZA ZA2009/00371A patent/ZA200900371B/en unknown
- 2009-01-16 CR CR10567A patent/CR10567A/es unknown
- 2009-01-19 IL IL196596A patent/IL196596A/en active IP Right Grant
- 2009-01-22 NI NI2009000081A patent/NI200900081A/es unknown
- 2009-01-22 NI NI200900008A patent/NI200900008A/es unknown
- 2009-01-29 CU CU20090017A patent/CU23866B1/es active IP Right Grant
- 2009-01-30 GT GT200900019A patent/GT200900019A/es unknown
- 2009-01-30 HN HN2009000214A patent/HN2009000214A/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 |
---|---|---|
AR062159A1 (es) | Compuestos que inhiben el enlace de la proteina smac al inhibidor de proteinas de apoptosis (iap) | |
PE20210640A1 (es) | Inhibidores pd-1/pd-l1 | |
UY28756A1 (es) | Compuestos | |
ES2570127T3 (es) | Compuestos y composiciones como inhibidores de la proteína quinasa | |
ECSP105253A (es) | Derivados de 5-feniltiazol y uso como inhibidores de pi3 cinasa | |
GT200700036A (es) | Compuestos fenil amido heterociclicos condensados | |
AR061840A1 (es) | Compuestos fosfinatos antivirales | |
UY28936A1 (es) | Grupo de compuestos benzoil-amino-heterociclilo y composiciones farmaceuticas que los comprenden, utiles para tratamiento de enfermedades mediadas por glucoquinasa (gq) | |
AR060768A1 (es) | Compuestos de imidazol sustituidos inhibidores del factor x, composiciones farmaceuticas que los contienen y usos como agentes antitromboticos. | |
PE20081447A1 (es) | Compuestos y composiciones como inhibidores de la proteina cinasa | |
AR056185A1 (es) | Derivados de (hetero)ariletinilbencil)benceno sustituidos con glucopiranosilo, composicion farmaceutica y proceso de preparacion del compuesto | |
AR062282A1 (es) | Composiciones colorantes | |
AR071644A1 (es) | Plaguicidas mesoionicos | |
AR064876A1 (es) | Composiciones de amino alcohol y biocidas para sistemas de base acuosa | |
AR054799A1 (es) | Derivados de oxindol | |
UY28755A1 (es) | Compuestos | |
RS53638B1 (en) | CRYSTAL SOLVATES OF DERIVATIVES (1S) -1,5-ANHYDRO-1-C- (3 - ((PHENYL) METHYL) PHENYL) -D-GLUCITOL WITH ALCOHOLS AS INHIBITORS OF SGLT2 FOR TREATMENT OF DIABETES | |
AR051388A1 (es) | Analogos de 17-hidroxiwortmanina como inhibidores de pi3k | |
RU2008129683A (ru) | Ингибиторы iap | |
AR056888A1 (es) | Derivados de heterociclil imidazol | |
AR074670A1 (es) | Inhibidores de la proteasa ns3 del vhc virus de la hepatitis c | |
AR067008A1 (es) | Derivados 3- amino-6-(1- amino - etil)-tetrahidropirano | |
GT200400146A (es) | Derivados sustituidos del dioxido de tiazol-benzoisotiazol, procedimiento para su preparacion y su uso | |
AR056702A1 (es) | Inhibidores de derivados de naftilo de la agregacion de beta -amiloide | |
PE20061362A1 (es) | Derivados de tetrahidronaftalina, procedimientos para su preparacion y su uso como inhibidor de la inflamacion |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |