MX2011006959A - Compuestos substituidos de 5,6-dihidro-6-fenilbenzo [f] isoquinolina-2-amina. - Google Patents
Compuestos substituidos de 5,6-dihidro-6-fenilbenzo [f] isoquinolina-2-amina.Info
- Publication number
- MX2011006959A MX2011006959A MX2011006959A MX2011006959A MX2011006959A MX 2011006959 A MX2011006959 A MX 2011006959A MX 2011006959 A MX2011006959 A MX 2011006959A MX 2011006959 A MX2011006959 A MX 2011006959A MX 2011006959 A MX2011006959 A MX 2011006959A
- Authority
- MX
- Mexico
- Prior art keywords
- phenylbenzo
- isoquinolin
- dihydro
- substituted
- amine compounds
- Prior art date
Links
- IKLWZGVCUZDMEL-UHFFFAOYSA-N 6-phenyl-5,6-dihydrobenzo[f]isoquinolin-2-amine Chemical class C1=NC(N)=CC(C2=CC=CC=C22)=C1CC2C1=CC=CC=C1 IKLWZGVCUZDMEL-UHFFFAOYSA-N 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/06—Ring systems of three rings
- C07D221/10—Aza-phenanthrenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oncology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Hematology (AREA)
- Pest Control & Pesticides (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La presente invención se relaciona con compuestos sustituidos de 5,6-dihidro-6-fenilbenzo (f) isoquinolina2- amino y métodos para sintetizar estos compuestos. La presente invención también se relaciona con composiciones farmacéuticas que contienen compuestos sustituidos de 5,6-dihidro-6-fenilbenzo (f) isoquinolina2-amino y métodos para el tratamiento de desordenes celulares proliferativos tales como el cáncer, mediante la administración de estos compuestos y composiciones farmacéuticos a sujetos que tienen necesidad de los mismos.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14143908P | 2008-12-30 | 2008-12-30 | |
US26050509P | 2009-11-12 | 2009-11-12 | |
PCT/US2009/069813 WO2010078421A1 (en) | 2008-12-30 | 2009-12-30 | Substituted 5,6-dihydro-6-phenylbenzo[f] isoquinolin-2-amine compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2011006959A true MX2011006959A (es) | 2011-12-06 |
Family
ID=41682678
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2011006959A MX2011006959A (es) | 2008-12-30 | 2009-12-30 | Compuestos substituidos de 5,6-dihidro-6-fenilbenzo [f] isoquinolina-2-amina. |
Country Status (14)
Country | Link |
---|---|
US (1) | US8357694B2 (es) |
EP (1) | EP2379506B1 (es) |
JP (1) | JP5739820B2 (es) |
KR (1) | KR101714799B1 (es) |
CN (1) | CN102325755B (es) |
BR (1) | BRPI0923786C8 (es) |
CA (1) | CA2748491C (es) |
DK (1) | DK2379506T3 (es) |
ES (1) | ES2554623T3 (es) |
IL (1) | IL213787A (es) |
MX (1) | MX2011006959A (es) |
TW (1) | TWI461410B (es) |
WO (1) | WO2010078421A1 (es) |
ZA (1) | ZA201104706B (es) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
EP2731953A1 (en) * | 2011-07-15 | 2014-05-21 | Abbvie Inc. | Tricyclic inhibitors of kinases useful for the treatment of proliferative diseases |
GB2499666A (en) * | 2012-02-27 | 2013-08-28 | Nanyang Polytechnic | Mcl-1 inhibitors for the treatment of conditions associated with proliferative disorders |
DK2861595T5 (en) | 2012-06-13 | 2018-01-15 | Incyte Holdings Corp | Substituted tricyclic compounds as FGFR inhibitors |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
MY181497A (en) | 2013-04-19 | 2020-12-23 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
MX369646B (es) | 2014-08-18 | 2019-11-15 | Eisai R&D Man Co Ltd | Sal de derivado de piridina monociclico y su cristal. |
US9949981B2 (en) * | 2014-09-05 | 2018-04-24 | Arqule, Inc. | Compositions and methods for treating proliferation disorders |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
RU2712222C2 (ru) | 2015-03-25 | 2020-01-27 | Нэшнл Кэнсер Сентер | Терапевтическое средство против рака желчных протоков |
TWI771280B (zh) * | 2015-12-17 | 2022-07-21 | 美商亞闊股份有限公司 | 經取代之5,6-二氫-6-苯基苯并[f]異喹啉-2-胺化合物之固體形式 |
HK1255014A1 (zh) * | 2015-12-17 | 2019-08-02 | Arqule, Inc. | 制备取代5,6-二氢-6-苯基苯并[f]异喹啉-2-胺的方法 |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
JPWO2019189241A1 (ja) | 2018-03-28 | 2021-03-18 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 肝細胞癌治療剤 |
MA52493A (fr) | 2018-05-04 | 2021-03-10 | Incyte Corp | Sels d'un inhibiteur de fgfr |
JP2021523121A (ja) | 2018-05-04 | 2021-09-02 | インサイト・コーポレイションIncyte Corporation | Fgfr阻害剤の固体形態及びその調製プロセス |
CN110669015A (zh) * | 2018-07-03 | 2020-01-10 | 上海喀露蓝科技有限公司 | 一种fgfr抑制剂的制备方法 |
JP7446287B2 (ja) * | 2018-09-27 | 2024-03-08 | 貝達薬業股▲ふん▼有限公司 | Fgfr4阻害剤及びその使用 |
WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
AU2020366006A1 (en) | 2019-10-14 | 2022-04-21 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CN115151539A (zh) | 2019-12-04 | 2022-10-04 | 因赛特公司 | Fgfr抑制剂的衍生物 |
EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
CN116547280A (zh) * | 2020-10-08 | 2023-08-04 | 雷多纳治疗公司 | 用于治疗癌症的苯并[h]喹唑啉-4-胺和噻吩并[3,2-h]喹唑啉-4-胺衍生物 |
CN116601155A (zh) * | 2020-11-26 | 2023-08-15 | 成都赛璟生物医药科技有限公司 | 杂芳基并喹唑啉类化合物作为蛋白激酶抑制剂 |
US12065494B2 (en) | 2021-04-12 | 2024-08-20 | Incyte Corporation | Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent |
WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
CN113354630B (zh) * | 2021-06-30 | 2022-11-01 | 江南大学 | 一种5,6-二氢苯并[h]喹唑啉类化合物及其应用 |
WO2023072913A1 (en) * | 2021-10-25 | 2023-05-04 | Twentyeight-Seven, Inc. | Benzo[h]quinazoline-4-amine derivatives for the treatment of cancer |
WO2023196629A1 (en) * | 2022-04-07 | 2023-10-12 | Redona Therapeutics, Inc. | Benzo[h]quinazoline-4-amine derivatives for the treatment of cancer |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2623846A1 (de) * | 1976-05-28 | 1977-12-15 | Hoechst Ag | 4-chinazolinyl-guanidine und verfahren zu ihrer herstellung |
US4522811A (en) * | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
IT1154024B (it) | 1982-09-22 | 1987-01-21 | Lepetit Spa | Derivati pridinici e procedimento per la loro produzione |
US4814335A (en) | 1982-12-30 | 1989-03-21 | Biomeasure, Incorporated | Antiviral compounds |
US4625026A (en) | 1982-12-30 | 1986-11-25 | Biomeasure, Inc. | 2-amino-4-oxo-tricyclicpyrimidines having antiviral activities against herpes simplex virus type II infections |
DD240010A1 (de) | 1985-03-22 | 1986-10-15 | Univ Berlin Humboldt | Verfahren zur herstellung von substituierten 2-imino-1h-pyridin-1-aminen |
SU1540240A1 (ru) | 1988-05-16 | 1995-09-10 | Институт Тонкой Органической Химии Им.А.Л.Мнджояна | 5-ЗАМЕЩЕННЫЕ 1-АМИНО -8,9-ДИГИДРО -8,8-ДИМЕТИЛ-3, 6Н- ПИРАЗОЛО [3,4-B] ПИРАНО[[4′,3′-d]] ПИРИДИНА ИЛИ ИХ ГИДРОХЛОРИДЫ, ОБЛАДАЮЩИЕ ПРОТИВОСУДОРОЖНОЙ АКТИВНОСТЬЮ |
DD280109A1 (de) | 1989-02-22 | 1990-06-27 | Univ Berlin Humboldt | Verfahren zur herstellung substituierter 1.2.4-triazolo/1.5-a/-pyridine |
SU1626648A1 (ru) | 1989-07-20 | 1995-09-27 | Институт Тонкой Органической Химии Им.А.Л.Мнджояна | 1-амино-8,9- дигидро-5,8,8- триметил-3,6н- пиразоло[3,4-b] тиопирано [4,3-d]пиридин или его гидрохлорид, обладающие противосудорожной активностью |
DE4117802A1 (de) | 1991-05-30 | 1992-12-03 | Berlin Chemie Ag | 2-aminopyridin-3-carbonitrile als selektive hemmstoffe des humanen cytomegalievirus |
AU7831694A (en) | 1993-09-24 | 1995-04-10 | Du Pont Merck Pharmaceutical Company, The | Improved methods for preparing bis-imide compounds |
US6046206A (en) * | 1995-06-07 | 2000-04-04 | Cell Pathways, Inc. | Method of treating a patient having a precancerous lesions with amide quinazoline derivatives |
US6262059B1 (en) * | 1995-06-07 | 2001-07-17 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with quinazoline derivatives |
EP0856001B1 (en) * | 1995-10-02 | 2002-08-28 | F. Hoffmann-La Roche Ag | Pyrimidine derivatives as 5ht2c receptor antagonists |
EP0946523A1 (en) * | 1996-12-23 | 1999-10-06 | Celltech Therapeutics Limited | Fused polycyclic 2-aminopyrimidine derivatives, their preparation and their use as protein tyrosine kinase inhibitors |
GB9713087D0 (en) | 1997-06-20 | 1997-08-27 | Celltech Therapeutics Ltd | Chemical compounds |
US6191123B1 (en) | 1999-03-19 | 2001-02-20 | Parker Hughes Institute | Organic-arsenic compounds |
GB9929685D0 (en) | 1999-12-15 | 2000-02-09 | Merck Sharp & Dohme | Therapeutic agents |
KR20020083533A (ko) | 2000-03-31 | 2002-11-02 | 니뽄 신야쿠 가부시키가이샤 | 복소환 유도체 및 의약 |
WO2002074341A1 (fr) | 2001-03-19 | 2002-09-26 | Nippon Shinyaku Co., Ltd. | Antiprurigineux |
WO2005014727A1 (en) * | 2003-07-17 | 2005-02-17 | Ciba Specialty Chemicals Holding Inc. | Black pigment compositions |
EP1648455A4 (en) | 2003-07-23 | 2009-03-04 | Exelixis Inc | MODULATORS OF ALK PROTEIN (ANAPLASTIC LYMPHOMA KINASE) AND METHODS OF USE |
CN1897950A (zh) * | 2003-10-14 | 2007-01-17 | 惠氏公司 | 稠合芳基和杂芳基衍生物及其使用方法 |
JP4733047B2 (ja) | 2003-12-02 | 2011-07-27 | テバ ファーマシューティカル インダストリーズ リミティド | ロスバスタチンの特性評価のためのリファレンス・スタンダード |
US7169802B2 (en) * | 2003-12-23 | 2007-01-30 | Cephalon, Inc. | Fused pyrrolocarbazoles |
WO2006010567A1 (de) | 2004-07-23 | 2006-02-02 | Curacyte Discovery Gmbh | INHIBITOREN DER PHOSPHODIESTERASE 4 UND TNFα-FREISETZUNG |
RU2547148C2 (ru) | 2005-02-09 | 2015-04-10 | Аркьюл, Инк. | Композиции и способы лечения рака |
EP1917027A2 (en) | 2005-08-24 | 2008-05-07 | Protherics Medicines Development Limited | Cleavage of antifolate compounds |
RU2008136784A (ru) | 2006-02-15 | 2010-03-20 | Абботт Лаборэтриз (Us) | Пиразолохинолоновые соединения, фармацевтическая композиция на их основе, способ ингибирования поли(адф-рибоза)полимеразы (parp) и способы лечения воспаления, сепсиса, септического шока и рака |
US8735411B2 (en) | 2006-10-02 | 2014-05-27 | Abbvie Inc. | Macrocyclic benzofused pyrimidine derivatives |
EP2476679B1 (en) | 2006-12-29 | 2015-10-14 | Rigel Pharmaceuticals, Inc. | Substituted triazoles useful as AXL inhibitors |
-
2009
- 2009-12-30 CN CN200980156889.XA patent/CN102325755B/zh active Active
- 2009-12-30 DK DK09793690.0T patent/DK2379506T3/en active
- 2009-12-30 ES ES09793690.0T patent/ES2554623T3/es active Active
- 2009-12-30 BR BRPI0923786A patent/BRPI0923786C8/pt active IP Right Grant
- 2009-12-30 JP JP2011544603A patent/JP5739820B2/ja active Active
- 2009-12-30 TW TW098145881A patent/TWI461410B/zh active
- 2009-12-30 WO PCT/US2009/069813 patent/WO2010078421A1/en active Application Filing
- 2009-12-30 KR KR1020117017777A patent/KR101714799B1/ko active Active
- 2009-12-30 US US12/649,573 patent/US8357694B2/en active Active
- 2009-12-30 EP EP09793690.0A patent/EP2379506B1/en active Active
- 2009-12-30 CA CA2748491A patent/CA2748491C/en active Active
- 2009-12-30 MX MX2011006959A patent/MX2011006959A/es active IP Right Grant
-
2011
- 2011-06-24 ZA ZA2011/04706A patent/ZA201104706B/en unknown
- 2011-06-27 IL IL213787A patent/IL213787A/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CA2748491A1 (en) | 2010-07-08 |
TWI461410B (zh) | 2014-11-21 |
TW201035055A (en) | 2010-10-01 |
IL213787A (en) | 2014-08-31 |
CN102325755A (zh) | 2012-01-18 |
IL213787A0 (en) | 2011-07-31 |
ES2554623T3 (es) | 2015-12-22 |
CA2748491C (en) | 2019-08-06 |
US8357694B2 (en) | 2013-01-22 |
WO2010078421A8 (en) | 2011-10-27 |
BRPI0923786A2 (pt) | 2016-07-26 |
JP5739820B2 (ja) | 2015-06-24 |
CN102325755B (zh) | 2015-07-01 |
KR101714799B1 (ko) | 2017-03-09 |
KR20110099790A (ko) | 2011-09-08 |
ZA201104706B (en) | 2012-08-29 |
WO2010078421A1 (en) | 2010-07-08 |
JP2012514045A (ja) | 2012-06-21 |
BRPI0923786B1 (pt) | 2020-11-24 |
EP2379506A1 (en) | 2011-10-26 |
AU2009335010A1 (en) | 2011-07-21 |
EP2379506B1 (en) | 2015-09-02 |
BRPI0923786C8 (pt) | 2021-05-25 |
US20100239525A1 (en) | 2010-09-23 |
DK2379506T3 (en) | 2015-12-14 |
BRPI0923786C1 (pt) | 2021-05-11 |
AU2009335010A8 (en) | 2011-08-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2011006959A (es) | Compuestos substituidos de 5,6-dihidro-6-fenilbenzo [f] isoquinolina-2-amina. | |
MY157124A (en) | Substituted imidazopyridinyl-aminopyridine compounds | |
PH12012501337A1 (en) | Substituted pyrrolo-aminopyrimidine compounds | |
WO2011082267A3 (en) | Substituted triazolo-pyrazine compounds | |
WO2011082266A3 (en) | Substituted heterocyclic compounds | |
PH12013502565A1 (en) | Substituted imidazopyridinyl-aminopyridine compounds | |
MX2007009649A (es) | Derivados de meleimida, composiciones farmaceuticas y metodos para el tratamiento del cancer. | |
WO2011123678A3 (en) | Substituted benzo-pyrido-triazolo-diazepine compounds | |
WO2012118812A3 (en) | Substituted 6,5-fused bicyclic heteroaryl compounds | |
PH12012501556A1 (en) | Substituted naphthalenyl-pyrimidine compounds | |
PL1951729T3 (pl) | Pochodne pirymidyny połączone przez atom tlenu | |
PH12013502369A1 (en) | Diazacarbazoles and methods of use | |
UA98804C2 (ru) | Катехоламиновые производные и фармацевтическая композиция на их основе | |
TNSN08370A1 (en) | Tetrahydropyridothienopyrimidine compounds and methods of use thereof | |
WO2007076085A3 (en) | Fused pyrimidones and thiopyrimidones, and uses thereof | |
MX2011006006A (es) | Compuestos, composicion farmaceutica y metodos para utilizarse en el tratamiento de trastornos metabolicos. | |
MX370721B (es) | Compuestos y composiciones novedosas para atacar las células madre del cáncer. | |
MX2009013815A (es) | Compuestos de quinazolinona y metodos de uso para los mismos. | |
MX342924B (es) | Nuevos compuestos disustituidos de 3,4-diamino-3-ciclobuteno-1,2-d iona para uso en el tratamiento de patologias mediadas por quimiocinas. | |
WO2007076087A3 (en) | 3-aryl-substituted quinazolones, and uses thereof | |
MX2010009147A (es) | Derivados de pirrolidinilo y usos de los mismos. | |
WO2012061342A3 (en) | Substituted benzo-imidazo-pyrido-diazepine compounds | |
WO2011082271A3 (en) | Substituted triazolo-pyrimidine compounds | |
WO2012088491A3 (en) | Pyrroloquinolinyl-pyrrolidine-2,5-dione compositions and methods for preparing and using same | |
WO2009151495A3 (en) | Oxazole compounds, compositions and methods of use |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant or registration |