PE20091720A1 - Compuestos de benzopirano y benzoxepina como inhibidores de pi3k - Google Patents
Compuestos de benzopirano y benzoxepina como inhibidores de pi3kInfo
- Publication number
- PE20091720A1 PE20091720A1 PE2009000466A PE2009000466A PE20091720A1 PE 20091720 A1 PE20091720 A1 PE 20091720A1 PE 2009000466 A PE2009000466 A PE 2009000466A PE 2009000466 A PE2009000466 A PE 2009000466A PE 20091720 A1 PE20091720 A1 PE 20091720A1
- Authority
- PE
- Peru
- Prior art keywords
- compounds
- oxepine
- dihydrobenzo
- chlorophenyl
- benzopyrane
- Prior art date
Links
- KYNSBQPICQTCGU-UHFFFAOYSA-N Benzopyrane Chemical compound C1=CC=C2C=CCOC2=C1 KYNSBQPICQTCGU-UHFFFAOYSA-N 0.000 title 1
- 239000012828 PI3K inhibitor Substances 0.000 title 1
- 150000005119 benzoxepines Chemical class 0.000 title 1
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 title 1
- -1 BENZOXEPINE DERIVATIVE COMPOUNDS Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 206010006187 Breast cancer Diseases 0.000 abstract 1
- 208000026310 Breast neoplasm Diseases 0.000 abstract 1
- 206010009944 Colon cancer Diseases 0.000 abstract 1
- 208000009956 adenocarcinoma Diseases 0.000 abstract 1
- 208000029742 colonic neoplasm Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- GWWYCZYBZIMLGT-UHFFFAOYSA-N oxepine-2-carboxamide Chemical compound NC(=O)C1=CC=CC=CO1 GWWYCZYBZIMLGT-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002685 pulmonary effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered 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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non 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
- A61K31/41—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
- A61K31/4196—1,2,4-Triazoles
-
- 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
- A61K31/4245—Oxadiazoles
-
- 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
- A61K31/41—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
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
- A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material 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)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE BENZOXEPINA DE FORMULA (I) DONDE Z1 ES CR1 O N; Z2 ES CR2 O N; Z3 ES CR3 O N; Z4 ES CR4 O N; X1 Y X2 SON CADA UNO N, S O CR7, EN DONDE R1, R2, R3, R4 Y R7 SON CADA UNO H, F, -CN, -CF3, -NO2, ENTRE OTROS; A ES -C(=O)NR5R6, HETEROCICLILO(C3-C20), HETEROARILO(C6-C20), ENTRE OTROS, DONDE R5 ES H O ALQUILO(C1-C12); R6 ES ALQUILO(C1-C12), CARBOCICLILO(C3-C12), HETEROCICLILO(C3-C20), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N2-(2-CLOROFENIL-N2,N8,N8-TRIMETIL-4,5-DIHIDROBENZO[b]TIENO[2,3-d]OXEPINA-2,8-DICARBOXAMIDA, 7-ACETAMIDO-N-(2-CLOROFENIL-N-METIL-4,5-DIHIDROBENZO[b]TIENO[2,3-d]OXEPINA-2-CARBOXAMIDA, N2-(2-CLOROFENIL-N8-(3-(DIETILAMINO)PROPIL)-N2-METIL-4,5-DIHIDROBENZO[b]TIENO[2,3-d]OXEPINA-2,8-DICARBOXAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA FOSFATIDILINOSITOL 3-CINASA (PI3K) SIENDO UTILES PARA EL TRATAMIENTO DE CANCER DE MAMA, ADENOCARCINOMA PULMONAR, CANCER DE COLON
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4082708P | 2008-03-31 | 2008-03-31 | |
| US10222008P | 2008-10-02 | 2008-10-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20091720A1 true PE20091720A1 (es) | 2009-11-26 |
Family
ID=40790991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2009000466A PE20091720A1 (es) | 2008-03-31 | 2009-03-30 | Compuestos de benzopirano y benzoxepina como inhibidores de pi3k |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US7928248B2 (es) |
| EP (1) | EP2276767B1 (es) |
| JP (1) | JP5511786B2 (es) |
| KR (1) | KR101626996B1 (es) |
| CN (1) | CN102333779B (es) |
| AR (1) | AR071112A1 (es) |
| AU (1) | AU2009231885B2 (es) |
| BR (1) | BRPI0910346A2 (es) |
| CA (1) | CA2719032C (es) |
| CL (1) | CL2009000780A1 (es) |
| DK (1) | DK2276767T3 (es) |
| ES (1) | ES2480994T3 (es) |
| IL (1) | IL208359A (es) |
| MX (1) | MX2010010659A (es) |
| PE (1) | PE20091720A1 (es) |
| PL (1) | PL2276767T3 (es) |
| RU (1) | RU2506267C2 (es) |
| SI (1) | SI2276767T1 (es) |
| TW (1) | TWI443102B (es) |
| WO (1) | WO2009123971A1 (es) |
| ZA (1) | ZA201007218B (es) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2250160B1 (en) | 2008-01-25 | 2015-11-11 | Millennium Pharmaceuticals, Inc. | Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors |
| PE20091720A1 (es) | 2008-03-31 | 2009-11-26 | Genentech Inc | Compuestos de benzopirano y benzoxepina como inhibidores de pi3k |
| US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9139589B2 (en) | 2009-01-30 | 2015-09-22 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| US20100233733A1 (en) * | 2009-02-10 | 2010-09-16 | Nodality, Inc., A Delaware Corporation | Multiple mechanisms for modulation of the pi3 kinase pathway |
| UY32748A (es) * | 2009-07-02 | 2011-01-31 | Novartis Ag | 2-carboxamida-cicloamino-ureas |
| US8242104B2 (en) * | 2009-09-28 | 2012-08-14 | F. Hoffman-La Roche Ag | Benzoxazepin P13K inhibitor compounds and methods of use |
| PH12012500608A1 (en) * | 2009-09-28 | 2017-08-09 | Hoffmann La Roche | Benzoxepin pi3k inhibitor compounds and methods of use |
| WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
| AU2010319879A1 (en) * | 2009-10-29 | 2012-06-14 | Bristol-Myers Squibb Company | Tricyclic heterocyclic compounds |
| SI2496567T1 (en) | 2009-11-05 | 2018-01-31 | Rhizen Pharmaceuticals S.A. | Novel benzopyran kinase modulators |
| AU2010317883B2 (en) * | 2009-11-13 | 2015-08-06 | Merck Serono S.A. | Tricyclic pyrazol amine derivatives |
| US9072783B2 (en) | 2009-11-18 | 2015-07-07 | Aridis Pharmaceuticals | Highly dispersible powders, compositions and methods for preparation |
| JP2013536193A (ja) | 2010-08-11 | 2013-09-19 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | ヘテロアリール類およびその使用 |
| WO2012021611A1 (en) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| WO2012021615A1 (en) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| EA201390539A1 (ru) * | 2010-10-13 | 2013-09-30 | Милленниум Фармасьютикалз, Инк. | Гетероарилы и их применение |
| CA2825966A1 (en) | 2011-03-21 | 2012-09-27 | F. Hoffmann-La Roche Ag | Benzoxazepin compounds selective for pi3k p110 delta and methods of use |
| PL2705029T3 (pl) | 2011-05-04 | 2019-04-30 | Rhizen Pharmaceuticals S A | Nowe związki jako modulatory kinaz białkowych |
| CN103649072A (zh) | 2011-05-27 | 2014-03-19 | 莱西肯医药有限公司 | 基于4h-噻吩并[3,2-c]色烯的背板胶质乙酰酯酶抑制剂及其用法 |
| RU2014136578A (ru) * | 2012-02-17 | 2016-04-10 | Ф. Хоффманн-Ля Рош Аг | Трициклические соединения и способы их применения |
| US8940742B2 (en) * | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| EP2852661A1 (en) | 2012-05-23 | 2015-04-01 | F. Hoffmann-La Roche AG | Compositions and methods of obtaining and using endoderm and hepatocyte cells |
| EP3260455B1 (en) | 2012-07-04 | 2019-03-20 | Rhizen Pharmaceuticals S.A. | Selective pi3k delta inhibitors |
| EP2914260A1 (en) | 2012-10-31 | 2015-09-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
| JP6363120B2 (ja) | 2013-03-13 | 2018-07-25 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | ベンゾオキサゼピン化合物の作製方法 |
| HK1214533A1 (zh) | 2013-03-15 | 2016-07-29 | 基因泰克公司 | 治疗癌症和预防癌症耐药性的方法 |
| WO2014168986A1 (en) | 2013-04-08 | 2014-10-16 | Brown Dennis M | Therapeutic benefit of suboptimally administered chemical compounds |
| US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| US9359365B2 (en) | 2013-10-04 | 2016-06-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| JP6701088B2 (ja) | 2014-03-19 | 2020-05-27 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | Pi3k−ガンマ媒介障害の治療で使用するための複素環式化合物 |
| US9708348B2 (en) | 2014-10-03 | 2017-07-18 | Infinity Pharmaceuticals, Inc. | Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof |
| HUE047144T2 (hu) | 2014-12-11 | 2020-04-28 | Natco Pharma Ltd | 7-(morfolinil)-2-(N-piperazinil) metil-tieno-[2,3-C]piridin-származékok mint rákellenes gyógyszerek |
| ES2911886T3 (es) * | 2015-03-30 | 2022-05-23 | Jubilant Biosys Ltd | Derivados condensados tricíclicos de 1-(ciclo)alquilpiridin-2-ona útiles para el tratamiento del cáncer |
| EP4585268A3 (en) | 2015-09-14 | 2025-10-15 | Twelve Therapeutics, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
| US10759806B2 (en) | 2016-03-17 | 2020-09-01 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors |
| WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| HUE070253T2 (hu) | 2016-07-29 | 2025-05-28 | Janssen Pharmaceutica Nv | Niraparib a prosztatarák kezelésére szolgáló eljárásban való felhasználásra |
| US10633354B2 (en) | 2016-09-02 | 2020-04-28 | Bristol-Myers Squibb Company | Substituted tricyclic heterocyclic compounds |
| TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| TW201815787A (zh) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
| SG11202000431PA (en) | 2017-07-18 | 2020-02-27 | Nuvation Bio Inc | 1,8-naphthyridinone compounds and uses thereof |
| KR20200041315A (ko) | 2017-07-18 | 2020-04-21 | 누베이션 바이오 인크. | 아데노신 길항제로서의 헤테로시클릭 화합물 |
| US11046646B2 (en) | 2017-08-09 | 2021-06-29 | Bristol-Myers Squibb Company | Alkylphenyl compounds |
| WO2019032631A1 (en) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | Oxime ether compounds |
| CN107805255B (zh) * | 2017-09-22 | 2020-06-16 | 中国药科大学 | 呋喃[3,2-b]吡啶-2(1H)-酮类化合物、制备方法和医药用途 |
| CA3093189A1 (en) | 2018-03-07 | 2019-09-12 | Bayer Aktiengesellschaft | Identification and use of erk5 inhibitors |
| CN110467629B (zh) * | 2018-05-09 | 2022-04-08 | 上海迪诺医药科技有限公司 | 苯醌衍生物、其药物组合物及应用 |
| CN113924095A (zh) | 2019-01-18 | 2022-01-11 | 诺维逊生物股份有限公司 | 作为腺苷拮抗剂的杂环化合物 |
| EP3911324A4 (en) | 2019-01-18 | 2022-08-17 | Nuvation Bio Inc. | 1,8-NAPHTHYRIDINONE COMPOUNDS AND THEIR USES |
| CN114156414B (zh) * | 2021-11-30 | 2024-05-31 | 合肥工业大学 | 一种高效稳定CsPbI3无机钙钛矿电池的制备方法 |
| CN117209457B (zh) * | 2022-06-09 | 2025-08-15 | 四川师范大学 | 一种α-手性脒化合物的合成 |
| CN115403591A (zh) * | 2022-10-08 | 2022-11-29 | 河南师范大学 | 一种合成萘并噻吩并奥塞平并异喹啉酮类化合物的方法 |
| WO2025082467A1 (zh) * | 2023-10-19 | 2025-04-24 | 成都先导药物开发股份有限公司 | 一种免疫调节剂 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8504702D0 (en) | 1985-02-23 | 1985-03-27 | Zyma Sa | Tricyclic compounds |
| FR2677356B1 (fr) | 1991-06-05 | 1995-03-17 | Sanofi Sa | Derives heterocycliques d'acylamino-2 thiazoles-5 substitues, leur preparation et compositions pharmaceutiques en contenant. |
| DE69309670T2 (de) | 1992-12-28 | 1997-11-20 | Eisai Co Ltd | Heterocyclische carbonsäure-derivate, die an rar rezeptoren binden können |
| WO1997019087A1 (en) | 1995-11-17 | 1997-05-29 | E.I. Du Pont De Nemours And Company | Tricyclic herbicidal heterocycles |
| DE19831878C2 (de) * | 1998-07-17 | 2001-05-17 | Aventis Pharma Gmbh | Polycyclische Thiazolidin-2-yliden Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| DE19908533A1 (de) | 1999-02-26 | 2000-08-31 | Aventis Pharma Gmbh | Polycyclische Thiazol-Systeme, Verfahren zu ihrer Herstellung und Arzneimittel enthaltend diese Verbindungen |
| DE19908537A1 (de) | 1999-02-26 | 2000-08-31 | Aventis Pharma Gmbh | Verwendung von polycyclischen 2-Amino-Thiazol Systemen zur Herstellung von Medikamenten zur Prophylaxe oder Behandlung von Obesitas |
| DE19908535A1 (de) | 1999-02-26 | 2000-08-31 | Aventis Pharma Gmbh | Verwendung von polycyclischen Thiazol-Systemen zur Herstellung von Medikamenten zur Prophylaxe oder Behandlung von Obesitas |
| DE19908538A1 (de) | 1999-02-26 | 2000-08-31 | Aventis Pharma Gmbh | Polycyclische 2-Amino-Thiazol Systeme, Verfahren zu ihrer Herstellung und Arzneimittel enthaltend diese Verbindungen |
| US7273880B2 (en) | 1999-06-30 | 2007-09-25 | H. Lunbeck A/S | Selective NPY (Y5) antagonists |
| WO2001064675A1 (en) | 2000-03-03 | 2001-09-07 | Novartis Ag | Condensed thiazolamines and their use as neuropeptide y5 antagonists |
| EP1403256A4 (en) * | 2001-06-05 | 2004-10-20 | Fujisawa Pharmaceutical Co | FUSED IMIDAZOLE DERIVATIVE |
| MXPA05000381A (es) | 2002-07-19 | 2005-03-31 | Pharmacia Corp | Compuestos de carboxamida tiofeno sustituido para el tratamiento de inflamacion. |
| BRPI0407335A (pt) | 2003-02-07 | 2006-01-10 | Warner Lambert Co | Agentes antibacterianos |
| RU2403258C2 (ru) * | 2004-10-07 | 2010-11-10 | Бёрингер Ингельхайм Интернациональ Гмбх | Тиазолилдигидроиндазолы |
| CN101039667A (zh) * | 2004-10-15 | 2007-09-19 | 辉瑞大药厂 | 双相性精神障碍和相关症状的治疗 |
| RU2281947C1 (ru) * | 2005-07-05 | 2006-08-20 | Общество С Ограниченной Ответственностью "Исследовательский Институт Химического Разнообразия" | Аннелированные карбамоилазагетероциклы, фокусированная библиотека, фармацевтическая композиция и способ получения |
| US8877791B2 (en) | 2006-08-04 | 2014-11-04 | Beth Israel Deaconess Medical Center, Inc. | Inhibitors of pyruvate kinase and methods of treating disease |
| US8779154B2 (en) * | 2006-09-26 | 2014-07-15 | Qinglin Che | Fused ring compounds for inflammation and immune-related uses |
| PE20091720A1 (es) | 2008-03-31 | 2009-11-26 | Genentech Inc | Compuestos de benzopirano y benzoxepina como inhibidores de pi3k |
-
2009
- 2009-03-30 PE PE2009000466A patent/PE20091720A1/es not_active Application Discontinuation
- 2009-03-30 PL PL09726963T patent/PL2276767T3/pl unknown
- 2009-03-30 TW TW098110447A patent/TWI443102B/zh not_active IP Right Cessation
- 2009-03-30 RU RU2010143319/04A patent/RU2506267C2/ru not_active IP Right Cessation
- 2009-03-30 MX MX2010010659A patent/MX2010010659A/es active IP Right Grant
- 2009-03-30 KR KR1020107024488A patent/KR101626996B1/ko not_active Expired - Fee Related
- 2009-03-30 EP EP09726963.3A patent/EP2276767B1/en active Active
- 2009-03-30 CN CN200980120112.8A patent/CN102333779B/zh active Active
- 2009-03-30 WO PCT/US2009/038795 patent/WO2009123971A1/en not_active Ceased
- 2009-03-30 CA CA2719032A patent/CA2719032C/en not_active Expired - Fee Related
- 2009-03-30 AR ARP090101126A patent/AR071112A1/es not_active Application Discontinuation
- 2009-03-30 JP JP2011503076A patent/JP5511786B2/ja active Active
- 2009-03-30 BR BRPI0910346A patent/BRPI0910346A2/pt not_active IP Right Cessation
- 2009-03-30 DK DK09726963.3T patent/DK2276767T3/da active
- 2009-03-30 ES ES09726963.3T patent/ES2480994T3/es active Active
- 2009-03-30 SI SI200930981T patent/SI2276767T1/sl unknown
- 2009-03-30 CL CL2009000780A patent/CL2009000780A1/es unknown
- 2009-03-30 US US12/414,403 patent/US7928248B2/en active Active
- 2009-03-30 AU AU2009231885A patent/AU2009231885B2/en not_active Ceased
-
2010
- 2010-10-03 IL IL208359A patent/IL208359A/en not_active IP Right Cessation
- 2010-10-08 ZA ZA2010/07218A patent/ZA201007218B/en unknown
-
2011
- 2011-01-31 US US13/018,068 patent/US8399690B2/en active Active
-
2013
- 2013-01-10 US US13/738,846 patent/US8846762B2/en active Active
-
2014
- 2014-07-29 US US14/446,154 patent/US9309265B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20091720A1 (es) | Compuestos de benzopirano y benzoxepina como inhibidores de pi3k | |
| CY1124117T1 (el) | Ετεροκυκλικες αλκυνυλοβενζολικες ενωσεις και ιατρικες συνθεσεις και χρησεις αυτων | |
| PE20191817A1 (es) | Tienopiridinas y benzotiofenos utiles como inhibidores de cinasa 4 asociada al receptor de interleucina 1 (irak4) | |
| CY1121265T1 (el) | Παραγωγα πιπεριδινονης ως αναστολεις της mdm2 για την θεραπευτικη αγωγη του καρκινου | |
| PE20160844A1 (es) | Compuestos triciclicos como agentes anticancerigenos | |
| MX352672B (es) | Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer. | |
| CR20110013A (es) | Derivados de Heteroarilo como Inhibidores de DGAT1 | |
| EA201101650A1 (ru) | Новые производные пиримидина и их применение в лечении злокачественных новообразований и последующих заболеваний | |
| EA201290260A1 (ru) | Бензимидазол-имидазольные производные | |
| PE20160540A1 (es) | Inhibidores de bromodominios | |
| NI201000107A (es) | Derivados de tiazol utilizados como inhibidores de pi 3 - cinasa. | |
| EA201200176A1 (ru) | Производные оксазина и их применение для лечения неврологических нарушений | |
| CR11803A (es) | Pirrolopiridinas como inhibidores de cinasa | |
| EA201001683A1 (ru) | Производные фенил- или пиридинилзамещенных индазолов | |
| EA201101583A1 (ru) | Ингибиторы pi3 киназы или mtor | |
| PE20091486A1 (es) | Derivado de pirrolopirimidina como inhibidor de la enzima pi3k | |
| GEP20146146B (en) | Pyrrolopyrimidine compounds as inhibitors of cdk4/6 | |
| PE20140918A1 (es) | Compuestos de benzoxepina inhibidores de la pi3k | |
| EA201270339A1 (ru) | Замещенные производные ксантина | |
| EA201400338A1 (ru) | Производные аминопиримидина для применения в качестве модуляторов киназной активности | |
| EA201101566A1 (ru) | Производные имидазола и их применение в качестве модуляторов циклинзависимых киназ | |
| EA201390163A1 (ru) | Гетеробициклические производные в качетстве ингибиторов hcv | |
| EA201170997A1 (ru) | Производные индола в качестве противораковых агентов | |
| EA201200247A1 (ru) | Новые азагетероциклические соединения | |
| EA201101621A1 (ru) | Производные бензоксазолона в качестве ингибиторов альдостеронсинтазы |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration | ||
| FD | Application declared void or lapsed |