AR077080A1 - Compuestos de 2,3-dihidro-1h-indeno - Google Patents
Compuestos de 2,3-dihidro-1h-indenoInfo
- Publication number
- AR077080A1 AR077080A1 ARP100102082A ARP100102082A AR077080A1 AR 077080 A1 AR077080 A1 AR 077080A1 AR P100102082 A ARP100102082 A AR P100102082A AR P100102082 A ARP100102082 A AR P100102082A AR 077080 A1 AR077080 A1 AR 077080A1
- Authority
- AR
- Argentina
- Prior art keywords
- compounds
- dihidro
- indeno
- cycloalkyl
- alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- 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
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Compuestos de 2,3-dihidro-1H-indeno, métodos para obtener dichos compuestos y composiciones farmacéuticas que los contienen. Los compuestos que se describen inhiben a las proteínas IAP (proteínas inhibidoras de la apoptosis) y se pueden utilizar en el tratamiento de diversos tipos de cáncer. Reivindicacion 1: Un compuesto caracterizado porque tiene la formula (1) donde R1 y R2 son, independientemente, H o alquilo C1-6; R3 es H o cicloalquilo C3-8; R4 es -OC-alquil C3-10-O-, -OC-alquenil C3-10-O- u -OC-alquinil C3-10-O-, R5 es H o cicloalquilo C3-8; y R6 y R7 son, independientemente, H o alquilo C1-6; o una sal del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US18659409P | 2009-06-12 | 2009-06-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR077080A1 true AR077080A1 (es) | 2011-07-27 |
Family
ID=42630911
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP100102082A AR077080A1 (es) | 2009-06-12 | 2010-06-11 | Compuestos de 2,3-dihidro-1h-indeno |
Country Status (11)
Country | Link |
---|---|
US (1) | US20100317593A1 (es) |
EP (1) | EP2440549A1 (es) |
JP (1) | JP2012529482A (es) |
KR (1) | KR20120046162A (es) |
CN (1) | CN102459238A (es) |
AR (1) | AR077080A1 (es) |
AU (1) | AU2010258437A1 (es) |
CA (1) | CA2765150A1 (es) |
TW (1) | TW201103536A (es) |
UY (1) | UY32704A (es) |
WO (1) | WO2010142994A1 (es) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
CA2974651A1 (en) | 2014-01-24 | 2015-07-30 | Children's Hospital Of Eastern Ontario Research Institute Inc. | Smc combination therapy for the treatment of cancer |
US11639354B2 (en) | 2018-07-31 | 2023-05-02 | Fimecs, Inc. | Heterocyclic compound |
WO2020046941A1 (en) * | 2018-08-28 | 2020-03-05 | Arbutus Biopharma Corporation | Crystalline forms of substituted dihydroindene-4-carboxamide compounds and methods of preparing and using same |
WO2020109328A1 (en) | 2018-11-26 | 2020-06-04 | Debiopharm International S.A. | Combination treatment of hiv infections |
US10870663B2 (en) | 2018-11-30 | 2020-12-22 | Glaxosmithkline Intellectual Property Development Limited | Compounds useful in HIV therapy |
MX2021006156A (es) * | 2018-11-30 | 2021-09-08 | Glaxosmithkline Ip Dev Ltd | Compuestos utiles en la terapia para el vih. |
CN113573707A (zh) | 2019-01-17 | 2021-10-29 | 德彪药业国际股份公司 | 用于治疗癌症的组合产品 |
EP4006037A4 (en) | 2019-07-31 | 2023-12-13 | Fimecs, Inc. | HETEROCYCLIC COMPOUND |
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 |
WO2023230432A1 (en) | 2022-05-23 | 2023-11-30 | Inhibrx, Inc. | Dr5 agonist and iap antagonist combination therapy |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2078258T3 (es) * | 1989-04-28 | 1995-12-16 | Sclavo Spa | Mutantes de toxina pertussica, cepas de bordetella capaces de producir tales mutantes y su uso en el desarrollo de vacunas antipertussicas. |
US5508272A (en) * | 1993-06-15 | 1996-04-16 | Bristol-Myers Squibb Company | Compounds containing a fused bicycle ring and processes therefor |
US6187557B1 (en) * | 1995-08-08 | 2001-02-13 | Tularik Inc. | c-IAP1 and c-IAP2: inhibitors of apoptosis |
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
ES2194181T3 (es) | 1996-02-13 | 2003-11-16 | Astrazeneca Ab | Derivados de quinazolina como inhibidores de vegf. |
CA2244897C (en) | 1996-03-05 | 2006-04-11 | Zeneca Limited | 4-anilinoquinazoline derivatives |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
US6242569B1 (en) * | 1997-02-05 | 2001-06-05 | Tularik, Inc. | Regulators of apoptosis |
US6162965A (en) * | 1997-06-02 | 2000-12-19 | Novartis Ag | Plant transformation methods |
GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
US6162913A (en) * | 1998-07-15 | 2000-12-19 | Bristol-Myers Squibb Co. | Preparation of [4S-(4α,7α,10aβ)]-4-amino-octahydro-5-oxo-7H-pyrido[2,1 -b] [1,3]thiazepine-7-carboxylic acid, methyl ester and salts thereof via novel disulfides |
GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
SI1553097T1 (sl) | 1999-02-10 | 2010-12-31 | Astrazeneca Ab | Kinazolinski derivati kot inhibitorji angiogeneze in intermediati za to |
AU2001258628A1 (en) | 2000-05-31 | 2001-12-11 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
UA73993C2 (uk) | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
AU6623301A (en) | 2000-07-07 | 2002-01-21 | Angiogene Pharm Ltd | Colchinol derivatives as vascular damaging agents |
WO2002008213A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
US20040171554A1 (en) * | 2003-02-07 | 2004-09-02 | Genentech, Inc. | Compositions and methods for enhancing apoptosis |
US20080199439A1 (en) * | 2003-02-12 | 2008-08-21 | Mclendon George L | IAP-binding cargo molecules and peptidomimetics for use in diagnostic and therapeutic methods |
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 |
WO2005092326A1 (en) * | 2004-03-22 | 2005-10-06 | The Regents Of The University Of Michigan | Small molecule antagonists of xiap family proteins |
WO2006014361A1 (en) * | 2004-07-02 | 2006-02-09 | Genentech, Inc. | Inhibitors of iap |
EP2457895A1 (en) * | 2004-07-12 | 2012-05-30 | Idun Pharmaceuticals, Inc. | Tetrapeptide analogs |
EP1773766B1 (en) * | 2004-07-15 | 2014-04-02 | Tetralogic Pharmaceuticals Corporation | Iap binding compounds |
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 |
DE102005017116A1 (de) * | 2005-04-13 | 2006-10-26 | Novartis Ag | Hemmstoffe für Inhibitoren von Apoptose Proteinen (IAP) |
CA2607940C (en) * | 2005-05-18 | 2009-12-15 | Aegera Therapeutics Inc. | Bir domain binding compounds |
MX2007015419A (es) * | 2005-06-08 | 2008-02-21 | Novartis Ag | Compuestos organicos. |
US20100256046A1 (en) * | 2009-04-03 | 2010-10-07 | Tetralogic Pharmaceuticals Corporation | Treatment of proliferative disorders |
JP2009512719A (ja) * | 2005-10-25 | 2009-03-26 | アエゲラ セラピューティクス インコーポレイテッド | Iapbirドメイン結合化合物 |
CA2632256A1 (en) * | 2005-12-20 | 2007-07-05 | Novartis Ag | Combination of an iap-inhibitor and a taxane7 |
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 |
US20090043099A1 (en) * | 2006-03-17 | 2009-02-12 | The Burnham Institute | Methods and compositions for derepression of IAP-inhibited caspase |
US8202902B2 (en) * | 2006-05-05 | 2012-06-19 | The Regents Of The University Of Michigan | Bivalent SMAC mimetics and the uses thereof |
SG10201407457UA (en) * | 2006-05-16 | 2014-12-30 | Pharmascience Inc | Iap bir domain binding compounds |
WO2008014236A1 (en) * | 2006-07-24 | 2008-01-31 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
KR20090041391A (ko) * | 2006-07-24 | 2009-04-28 | 테트랄로직 파마슈티칼스 | 이량체성 iap 길항제 |
US20100143499A1 (en) * | 2006-07-24 | 2010-06-10 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
EP2049524A2 (en) * | 2006-07-24 | 2009-04-22 | Tetralogic Pharmaceuticals Corporation | Iap inhibitors |
US20100144650A1 (en) * | 2006-07-24 | 2010-06-10 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
WO2008014240A2 (en) * | 2006-07-24 | 2008-01-31 | Tetralogic Pharmaceuticals Corporation | Dimeric iap inhibitors |
KR20090065548A (ko) * | 2006-10-12 | 2009-06-22 | 노파르티스 아게 | Iap 억제제로서의 피롤리딘 유도체 |
JP2010511057A (ja) * | 2006-11-28 | 2010-04-08 | ノバルティス アーゲー | 急性骨髄性白血病の処置のためのiap阻害剤の使用 |
PT2089024E (pt) * | 2006-11-28 | 2011-08-31 | Novartis Ag | Combinação de inibidores de iap e inibidores de flt3 |
AU2007332862A1 (en) * | 2006-12-07 | 2008-06-19 | Novartis Ag | Organic compounds |
ES2370536T3 (es) * | 2006-12-07 | 2011-12-19 | Novartis Ag | 6-oxo-1,6-dihidropirimidín-2-ils en el tratamiento de enfermedades proliferativas. |
US20110008802A1 (en) * | 2007-05-07 | 2011-01-13 | Tetralogic Pharmaceuticals Corp. | TNFalpha GENE EXPRESSION AS A BIOMARKER OF SENSITIVITY TO ANTAGONISTS OF INHIBITOR OF APOPTOSIS PROTEINS |
US20100203012A1 (en) * | 2007-05-30 | 2010-08-12 | Aegera Therapeutics, Inc. | Iap bir domain binding compounds |
US20110117081A1 (en) * | 2008-05-05 | 2011-05-19 | Aegera Therapeutics, Inc. | Functionalized pyrrolidines and use thereof as iap inhibitors |
CA2728933A1 (en) * | 2008-06-27 | 2009-12-30 | Aegera Therapeutics Inc. | Bridged secondary amines and use thereof as iap bir domain binding compounds |
US20110177060A1 (en) * | 2008-09-19 | 2011-07-21 | Aegera Therapeutics, Inc. | Iap bir domain binding compounds |
US8088890B2 (en) * | 2008-09-26 | 2012-01-03 | Fibrex Medical Research & Development Gmbh | Peptides and peptidomimetic compounds, the manufacturing thereof as well as their use for preparing a therapeutically and/or preventively active pharmaceutical composition |
US8283372B2 (en) * | 2009-07-02 | 2012-10-09 | Tetralogic Pharmaceuticals Corp. | 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic |
US8440693B2 (en) * | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
UY33236A (es) * | 2010-02-25 | 2011-09-30 | Novartis Ag | Inhibidores dimericos de las iap |
-
2010
- 2010-06-08 US US12/796,089 patent/US20100317593A1/en not_active Abandoned
- 2010-06-10 JP JP2012514539A patent/JP2012529482A/ja active Pending
- 2010-06-10 KR KR1020127000831A patent/KR20120046162A/ko not_active Application Discontinuation
- 2010-06-10 CA CA2765150A patent/CA2765150A1/en not_active Abandoned
- 2010-06-10 AU AU2010258437A patent/AU2010258437A1/en not_active Abandoned
- 2010-06-10 WO PCT/GB2010/050973 patent/WO2010142994A1/en active Application Filing
- 2010-06-10 CN CN2010800362040A patent/CN102459238A/zh active Pending
- 2010-06-10 EP EP10725266A patent/EP2440549A1/en not_active Withdrawn
- 2010-06-11 AR ARP100102082A patent/AR077080A1/es unknown
- 2010-06-11 TW TW099119151A patent/TW201103536A/zh unknown
- 2010-06-11 UY UY0001032704A patent/UY32704A/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
TW201103536A (en) | 2011-02-01 |
EP2440549A1 (en) | 2012-04-18 |
WO2010142994A1 (en) | 2010-12-16 |
CN102459238A (zh) | 2012-05-16 |
CA2765150A1 (en) | 2010-12-16 |
KR20120046162A (ko) | 2012-05-09 |
US20100317593A1 (en) | 2010-12-16 |
AU2010258437A1 (en) | 2012-01-12 |
UY32704A (es) | 2011-01-31 |
JP2012529482A (ja) | 2012-11-22 |
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