MA38208B1 - Inhibiteurs de bmi-1 pyrimidines inversés substitués - Google Patents
Inhibiteurs de bmi-1 pyrimidines inversés substituésInfo
- Publication number
- MA38208B1 MA38208B1 MA38208A MA38208A MA38208B1 MA 38208 B1 MA38208 B1 MA 38208B1 MA 38208 A MA38208 A MA 38208A MA 38208 A MA38208 A MA 38208A MA 38208 B1 MA38208 B1 MA 38208B1
- Authority
- MA
- Morocco
- Prior art keywords
- bmi
- inhibitors
- substituted
- inhibit
- function
- Prior art date
Links
- 101100058550 Mus musculus Bmi1 gene Proteins 0.000 title abstract 5
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 241000713869 Moloney murine leukemia virus Species 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000010354 integration Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 150000003230 pyrimidines Chemical class 0.000 abstract 1
Classifications
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- 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
- 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
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Pathology (AREA)
- Radiology & Medical Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hematology (AREA)
- Oncology (AREA)
Abstract
L'invention concerne des composés pyrimidines inversés substitués aminés et des formes de ceux-ci qui inhibent la fonction et réduisent le taux d'une protéine de site 1 d'intégration du virus de la leucémie murine de moloney spécifique des lymphocytes b (bmi-1) et leurs procédés d'utilisation pour inhiber la fonction de bmi-1 et réduire le taux de bmi-1 pour traiter un cancer à médiation par bmi-1.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261728907P | 2012-11-21 | 2012-11-21 | |
| PCT/US2013/071132 WO2014081906A2 (fr) | 2012-11-21 | 2013-11-21 | Inhibiteurs de bmi-1 pyrimidines inversés substitués |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA38208B1 true MA38208B1 (fr) | 2021-12-31 |
Family
ID=50776672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38208A MA38208B1 (fr) | 2012-11-21 | 2013-11-21 | Inhibiteurs de bmi-1 pyrimidines inversés substitués |
Country Status (32)
| Country | Link |
|---|---|
| US (3) | US10428050B2 (fr) |
| EP (1) | EP2922828B1 (fr) |
| JP (3) | JP6412503B2 (fr) |
| KR (4) | KR20220143164A (fr) |
| CN (2) | CN104918919A (fr) |
| AR (1) | AR093579A1 (fr) |
| AU (1) | AU2013348009C1 (fr) |
| BR (1) | BR112015011760B1 (fr) |
| CA (1) | CA2892045C (fr) |
| CL (1) | CL2015001377A1 (fr) |
| CR (1) | CR20150294A (fr) |
| CU (1) | CU24387B1 (fr) |
| DK (1) | DK2922828T3 (fr) |
| EA (2) | EA035349B1 (fr) |
| EC (1) | ECSP15019948A (fr) |
| ES (1) | ES2821529T3 (fr) |
| HK (1) | HK1215032A1 (fr) |
| IL (2) | IL238871B (fr) |
| MA (1) | MA38208B1 (fr) |
| MX (2) | MX385385B (fr) |
| NI (1) | NI201500072A (fr) |
| NZ (2) | NZ746607A (fr) |
| PE (1) | PE20151413A1 (fr) |
| PH (1) | PH12015501130B1 (fr) |
| PL (1) | PL2922828T3 (fr) |
| PT (1) | PT2922828T (fr) |
| SA (1) | SA517381847B1 (fr) |
| SG (2) | SG11201503982XA (fr) |
| TW (1) | TWI623531B (fr) |
| UA (1) | UA118094C2 (fr) |
| WO (1) | WO2014081906A2 (fr) |
| ZA (1) | ZA201503642B (fr) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20220143164A (ko) | 2012-11-21 | 2022-10-24 | 피티씨 테라퓨틱스, 인크. | 치환된 리버스 피리미딘 bmi-1 저해제 |
| US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| CN105593215B (zh) * | 2013-07-11 | 2019-01-15 | 安吉奥斯医药品有限公司 | 用于治疗癌症的作为idh2突变体抑制剂的2,4-或4,6-二氨基嘧啶化合物 |
| WO2015003355A2 (fr) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Composés thérapeutiquement actifs et leurs méthodes d'utilisation |
| WO2015003360A2 (fr) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Composés thérapeutiquement actifs et leurs méthodes d'utilisation |
| AR093580A1 (es) * | 2013-08-30 | 2015-06-10 | Ptc Therapeutics Inc | Inhibidores bmi-1 de pirimidina sustituidos |
| WO2015076800A1 (fr) | 2013-11-21 | 2015-05-28 | Ptc Therapeutics, Inc. | Inhibiteurs de bmi-1 à base de pyridine et de pyrazine substituées |
| US10874355B2 (en) | 2014-04-24 | 2020-12-29 | Cognoa, Inc. | Methods and apparatus to determine developmental progress with artificial intelligence and user input |
| US10851082B2 (en) | 2015-10-28 | 2020-12-01 | Northwestern University | Substituted aromatic n-heterocyclic compounds as inhibitors of mitogen-activated protein kinase interacting kinase 1 (MNK1) and 2 (MNK2) |
| US11972336B2 (en) | 2015-12-18 | 2024-04-30 | Cognoa, Inc. | Machine learning platform and system for data analysis |
| CN108602775B (zh) * | 2016-01-14 | 2022-04-29 | 贝思以色列女会吏医学中心公司 | 肥大细胞调节剂及其用途 |
| CN118609834A (zh) | 2016-11-14 | 2024-09-06 | 科格诺亚公司 | 用于评估发育状况并提供覆盖度和可靠性控制的方法和装置 |
| CA3053245A1 (fr) | 2017-02-09 | 2018-08-16 | Cognoa, Inc. | Plate-forme et systeme de medecine personnalisee numerique |
| WO2019028171A1 (fr) | 2017-08-01 | 2019-02-07 | Ptc Therapeutics, Inc. | Inhibiteur de dhodh pour utilisation dans le traitement de cancers hématologiques |
| EP3564235A1 (fr) * | 2018-05-03 | 2019-11-06 | Northwestern University | Dérivés n-hétérocycliques aromatiques en tant qu'inhibiteurs de kinase de protéine kinase activée par mitogène interagissant sur la kinase 1 (mnk1) et 2 (mnk2) |
| CN113164479A (zh) * | 2018-08-17 | 2021-07-23 | Ptc医疗公司 | 用于治疗胰腺癌的方法 |
| CN109988172B (zh) * | 2019-01-10 | 2020-09-29 | 石家庄学院 | 一种吡唑并[1,5-a]嘧啶类杂环化合物及衍生物的合成方法 |
| WO2020150326A1 (fr) * | 2019-01-15 | 2020-07-23 | Ptc Therapeutics, Inc. | Méthode de traitement d'une leucémie aiguë myéloïde |
| EA202192117A1 (ru) * | 2019-02-28 | 2021-11-23 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Способ лечения множественной миеломы |
| SG11202109503TA (en) * | 2019-03-11 | 2021-09-29 | Ptc Therapeutics Inc | Compound form having enhanced bioavailability and formulations thereof |
| CA3134521A1 (fr) | 2019-03-22 | 2020-10-01 | Cognoa, Inc. | Procedes et dispositifs de therapie numerique personnalisee |
| MX2021011688A (es) * | 2019-03-27 | 2022-01-24 | Ptc Therapeutics Inc | Combinaciones utiles en un metodo para tratar sarcoma. |
| US20220177459A1 (en) * | 2019-04-02 | 2022-06-09 | Hinova Pharmaceuticals Inc. | Aromatic amine compound and use thereof in preparation of ar and brd4 dual inhibitors and regulators |
| US12564342B2 (en) | 2019-09-06 | 2026-03-03 | Cognoa, Inc. | Methods, systems, and devices for the diagnosis of behavioral disorders, developmental delays, and neurologic impairments |
| JP2024511277A (ja) | 2021-02-19 | 2024-03-13 | メビオン・メディカル・システムズ・インコーポレーテッド | 粒子線治療システムのためのガントリー |
| US20240120050A1 (en) * | 2022-10-07 | 2024-04-11 | Insight Direct Usa, Inc. | Machine learning method for predicting a health outcome of a patient using video and audio analytics |
Family Cites Families (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH593266A5 (fr) * | 1973-09-20 | 1977-11-30 | Delalande Sa | |
| JP2896532B2 (ja) | 1994-08-13 | 1999-05-31 | ユーハン コーポレーション | 新規なピリミジン誘導体およびその製造方法 |
| IN188411B (fr) | 1997-03-27 | 2002-09-21 | Yuhan Corp | |
| KR100272471B1 (ko) | 1998-11-17 | 2000-11-15 | 김선진 | 신규의 피리미딘 유도체 및 그의 제조방법 |
| GB9905075D0 (en) * | 1999-03-06 | 1999-04-28 | Zeneca Ltd | Chemical compounds |
| AU5636900A (en) | 1999-06-30 | 2001-01-31 | Merck & Co., Inc. | Src kinase inhibitor compounds |
| GB9919778D0 (en) | 1999-08-21 | 1999-10-27 | Zeneca Ltd | Chemical compounds |
| WO2001025220A1 (fr) | 1999-10-07 | 2001-04-12 | Amgen Inc. | Inhibiteurs de triazine kinase |
| ATE311385T1 (de) | 1999-10-27 | 2005-12-15 | Novartis Pharma Gmbh | Thiazol und imidazo(4,5-b)pyridin verbindungen und ihre verwendung als pharmazeutika |
| EP1257546A1 (fr) | 2000-02-17 | 2002-11-20 | Amgen Inc. | Inhibiteurs de kinases |
| EP1274705A1 (fr) | 2000-03-29 | 2003-01-15 | Cyclacel Limited | 4-heteroaryle-pyrimidines substituees en 2 et leur utilisation dans le traitement de troubles proliferants |
| EP1317450B1 (fr) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Composes de pyrazole utiles comme inhibiteurs de proteine kinase |
| CA2423050A1 (fr) | 2000-09-20 | 2002-03-28 | Ortho-Mcneil Pharmaceutical, Inc. | Derives de pyrazine tenant lieu de modulateurs de tyrosine kinase |
| AU2002228922A1 (en) * | 2000-12-12 | 2002-06-24 | Cytovia, Inc. | Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| US6716851B2 (en) * | 2000-12-12 | 2004-04-06 | Cytovia, Inc. | Substituted 2-aryl-4-arylaminopyrimidines and analogs as activators or caspases and inducers of apoptosis and the use thereof |
| DE60112330T2 (de) | 2000-12-15 | 2006-04-13 | Glaxo Group Ltd., Greenford | Pyrazolopyridinderivate |
| GB0103926D0 (en) | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
| EP1423388B1 (fr) | 2001-02-20 | 2008-12-03 | AstraZeneca AB | 2-arylamino-pyrimidines pour le traitement de troubles associes a gsk3 |
| DE60239097D1 (de) | 2001-03-02 | 2011-03-17 | Gpc Biotech Ag | Drei-hybrid-assaysystem |
| CA2450555A1 (fr) | 2001-06-25 | 2003-01-03 | Merck & Co., Inc. | Composes d'heteroaryle fondus (pyrimidyle)(phenyle) substitues inhibiteurs de p38 et de la kinase pkg |
| WO2003004492A1 (fr) | 2001-07-03 | 2003-01-16 | Vertex Pharmaceuticals Incorporated | Isoxazolyl-pyrimidines utilisees en tant qu'inhibiteurs des proteines kinases src et lck |
| WO2003011837A1 (fr) | 2001-08-01 | 2003-02-13 | Merck & Co., Inc. | Inhibiteurs de la tyrosine kinase |
| WO2003075828A2 (fr) | 2002-03-11 | 2003-09-18 | Zetiq Technologies Ltd. | Composes utiles pour le traitement du cancer |
| NZ537156A (en) | 2002-05-23 | 2007-06-29 | Cytopia Pty Ltd | Kinase inhibitors |
| WO2004002963A1 (fr) | 2002-06-28 | 2004-01-08 | Nippon Shinyaku Co., Ltd. | Derive d'amide |
| GB0215844D0 (en) | 2002-07-09 | 2002-08-14 | Novartis Ag | Organic compounds |
| WO2004007407A2 (fr) | 2002-07-11 | 2004-01-22 | Fluorous Technologies Incorporated | Nouveau reactifs de marquage au fluor et de piegeage et procedes de synthese et d'utilisation correspondants |
| US20040110821A1 (en) * | 2002-08-07 | 2004-06-10 | Konkel Michael J. | GAL3 receptor antagonists for the treatment of affective disorders |
| UA80296C2 (en) | 2002-09-06 | 2007-09-10 | Biogen Inc | Imidazolopyridines and methods of making and using the same |
| EP1551842A1 (fr) | 2002-10-15 | 2005-07-13 | Smithkline Beecham Corporation | Composes de pyradazine utiles comme inhibiteurs de gsk-3 |
| US7169781B2 (en) | 2003-10-17 | 2007-01-30 | Hoffmann-La Roche Inc. | Imidazole derivatives and their use as pharmaceutical agents |
| NZ546058A (en) | 2004-01-12 | 2010-09-30 | Ym Biosciences Australia Pty | Benzimidazole and other fused ring derivatives as selective janus kinase inhibitors |
| JP2007520558A (ja) | 2004-02-04 | 2007-07-26 | スミスクライン・ビーチャム・コーポレイション | キナーゼ阻害剤として有用なピリミジノン化合物 |
| TWI372624B (en) * | 2004-03-30 | 2012-09-21 | Vertex Pharma | Azaindoles useful as inhibitors of jak and other protein kinases |
| JP2006045119A (ja) | 2004-08-04 | 2006-02-16 | Toray Ind Inc | ピラジン誘導体及びそれを有効成分とする腎炎治療薬 |
| US7855205B2 (en) | 2004-10-29 | 2010-12-21 | Janssen Pharmaceutica Nv | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
| WO2006093247A1 (fr) | 2005-02-28 | 2006-09-08 | Japan Tobacco Inc. | NOUVEAU COMPOSÉ AMINOPYRIDINE AYANT UNE ACTIVITÉ D'INHIBITION DE LA Syk |
| KR20080004488A (ko) | 2005-03-10 | 2008-01-09 | 바이엘 파마슈티칼스 코포레이션 | 과다증식성 장애 치료용 피리미딘 유도체 |
| CA2654358A1 (fr) | 2006-06-22 | 2007-12-27 | Biovitrum Ab (Publ) | Derives de pyridine et de pyrazine utilises en tant qu'inhibiteurs de la kinase mnk |
| CA2665398A1 (fr) | 2006-10-03 | 2008-04-10 | Neurosearch A/S | Derives d'indazolyle utiles en tant qu'agents modulant les canaux potassiques |
| CN101516873A (zh) * | 2006-10-03 | 2009-08-26 | 神经研究公司 | 用作钾通道调节剂的吲唑基衍生物 |
| US7968556B2 (en) * | 2006-10-19 | 2011-06-28 | Signal Pharmaceuticals, Llc | Heteroaryl compounds, compositions thereof, and methods of treatment therewith |
| CA2672518A1 (fr) | 2006-12-22 | 2008-07-03 | Novartis Ag | Composes organiques et leurs utilisations |
| AR065015A1 (es) | 2007-01-26 | 2009-05-13 | Smithkline Beecham Corp | Derivados de antranilamida, composiciones farmaceuticas que los contienen, y usos para el tratamiento del cancer |
| CA2676715A1 (fr) | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Derives de piperazine pour le traitement de la maladie d'alzheimer et des conditions apparentees |
| WO2008132502A1 (fr) | 2007-04-25 | 2008-11-06 | Astrazeneca Ab | Pyrimidines substitués par pyrazolyle-amino et leur utilisation dans le traitement du cancer |
| GB0714573D0 (en) | 2007-07-26 | 2007-09-05 | Imp Innovations Ltd | Marker gene |
| WO2009037247A1 (fr) | 2007-09-17 | 2009-03-26 | Neurosearch A/S | Dérivés de pyrazine et leur utilisation en tant que modulateurs des canaux potassiques |
| WO2009064835A1 (fr) | 2007-11-16 | 2009-05-22 | Incyte Corporation | 4-pyrazolyl-n-arylpyrimidin-2-amines et 4-pyrazolyl-n-hétéroarylpyrimidin-2-amines en tant qu'inhibiteurs de janus kinase |
| CA2707989A1 (fr) | 2007-12-07 | 2009-06-11 | Novartis Ag | Derives de pyrazole et leur utilisation comme inhibiteurs de kinases dependantes des cyclines |
| DE102008005493A1 (de) | 2008-01-22 | 2009-07-23 | Merck Patent Gmbh | 4-(Pyrrolo[2,3-c] pyridine-3-yl)-pyrimidin-2-yl-amin-derivate |
| GB0801416D0 (en) | 2008-01-25 | 2008-03-05 | Piramed Ltd | Pharmaceutical compounds |
| NZ588830A (en) | 2008-04-22 | 2012-11-30 | Portola Pharm Inc | Inhibitors of protein kinases |
| ES2605815T3 (es) | 2008-07-01 | 2017-03-16 | Ptc Therapeutics, Inc. | Moduladores de la expresión de la proteína Bmi-1 |
| ES2378513T3 (es) | 2008-08-06 | 2012-04-13 | Pfizer Inc. | Compuestos 2-heterociclilamino piracinas sustituidas en posición 6 como inhibidores de CHK-1 |
| CN102177154A (zh) | 2008-09-02 | 2011-09-07 | 神经研究公司 | 吡唑基-嘧啶衍生物及其作为钾通道调节剂的应用 |
| WO2010061903A1 (fr) * | 2008-11-27 | 2010-06-03 | 塩野義製薬株式会社 | Dérivé de pyrimidine et dérivé de pyridine présentant tous deux une activité inhibitrice de pi3k |
| US20120165309A1 (en) | 2009-02-12 | 2012-06-28 | Astellas Pharma Inc. | Hetero ring derivative |
| SG174527A1 (en) | 2009-03-27 | 2011-11-28 | Pathway Therapeutics Inc | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
| US8536180B2 (en) | 2009-05-27 | 2013-09-17 | Abbvie Inc. | Pyrimidine inhibitors of kinase activity |
| TW201102387A (en) | 2009-06-08 | 2011-01-16 | Medicinova Inc | Substituted pyrazolo[1,5-a]pyridine compounds having multi-target activity |
| RS57869B1 (sr) | 2009-06-17 | 2018-12-31 | Vertex Pharma | Inhibitori replikacije virusa gripa |
| US8486939B2 (en) | 2009-07-07 | 2013-07-16 | Pathway Therapeutics Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy |
| CA2767091A1 (fr) | 2009-07-15 | 2011-01-20 | Abbott Laboratories | Inhibiteurs des pyrrolopyrazines kinases |
| CA2767089A1 (fr) | 2009-07-15 | 2011-01-20 | Abbott Laboratories | Pyrrolopyridines inhibiteurs de kinases |
| JP2011136925A (ja) * | 2009-12-28 | 2011-07-14 | Dainippon Sumitomo Pharma Co Ltd | 含窒素二環性化合物 |
| MX2012008083A (es) | 2010-01-12 | 2012-08-15 | Ab Science | Inhibidores de triazol y oxazol quinaza. |
| UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
| ES2365960B1 (es) * | 2010-03-31 | 2012-06-04 | Palobiofarma, S.L | Nuevos antagonistas de los receptores de adenosina. |
| BR112013003031A2 (pt) * | 2010-08-19 | 2016-06-14 | Hoffmann La Roche | método de produção de células hastes neurais (chn), células hastes neurais e seu uso, composição terapêutica e banco biológico de nscs |
| CN103221408A (zh) | 2010-09-13 | 2013-07-24 | 诺瓦提斯公司 | 三嗪-*二唑类化合物 |
| WO2012050884A2 (fr) | 2010-09-28 | 2012-04-19 | President And Fellows Of Harvard College | Glycosides cardiaques qui sont de puissants inhibiteurs de l'expression du gène de l'interféron bêta |
| CA2819373A1 (fr) | 2010-12-09 | 2012-06-14 | Amgen Inc. | Composes bicycliques en tant qu'inhibiteurs de pim |
| PL2678332T3 (pl) | 2011-02-25 | 2016-12-30 | Pochodne diaminopirymidyny i sposoby ich wytwarzania | |
| JP6116554B2 (ja) | 2011-07-07 | 2017-04-19 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | がんの処置のための置換されたアザ複素環 |
| US9695228B2 (en) | 2012-11-21 | 2017-07-04 | Janssen Biotech, Inc. | EGFR and c-Met fibronectin type III domain binding molecules |
| UY35148A (es) | 2012-11-21 | 2014-05-30 | Amgen Inc | Immunoglobulinas heterodiméricas |
| KR20220143164A (ko) * | 2012-11-21 | 2022-10-24 | 피티씨 테라퓨틱스, 인크. | 치환된 리버스 피리미딘 bmi-1 저해제 |
| CA2905435A1 (fr) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions utiles pour le traitement de troubles gastro-intestinaux |
| SG11202109503TA (en) * | 2019-03-11 | 2021-09-29 | Ptc Therapeutics Inc | Compound form having enhanced bioavailability and formulations thereof |
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2013
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