UY33131A - Isoquinolinonas y quinazolinonas sustituidas - Google Patents
Isoquinolinonas y quinazolinonas sustituidasInfo
- Publication number
- UY33131A UY33131A UY33131A UY33131A UY33131A UY 33131 A UY33131 A UY 33131A UY 33131 A UY33131 A UY 33131A UY 33131 A UY33131 A UY 33131A UY 33131 A UY33131 A UY 33131A
- Authority
- UY
- Uruguay
- Prior art keywords
- isoquinolinones
- quinazolinones
- replaced
- replaced quinazolinones
- Prior art date
Links
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
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/80—Oxygen atoms
- C07D239/82—Oxygen atoms with an aryl radical attached in position 4
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US28899209P | 2009-12-22 | 2009-12-22 | |
CN2010078927 | 2010-11-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY33131A true UY33131A (es) | 2011-07-29 |
Family
ID=43530866
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY33131A UY33131A (es) | 2009-12-22 | 2010-12-22 | Isoquinolinonas y quinazolinonas sustituidas |
Country Status (41)
Families Citing this family (114)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2118123B1 (fr) | 2007-01-31 | 2015-10-14 | Dana-Farber Cancer Institute, Inc. | Peptides p53 stabilises et utilisations de ceux-ci |
WO2008121767A2 (fr) | 2007-03-28 | 2008-10-09 | President And Fellows Of Harvard College | Polypeptides cousus |
GB0811643D0 (en) | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
US20100317593A1 (en) * | 2009-06-12 | 2010-12-16 | Astrazeneca Ab | 2,3-dihydro-1h-indene compounds |
US8440693B2 (en) * | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
EP3378854B1 (fr) | 2010-01-27 | 2022-12-21 | Arena Pharmaceuticals, Inc. | Procédés de préparation d'acide (r)-2-(7-(4-cyclopentyl-3-(trifluorométhyl)benzyloxy)-1,2,3,4-tétrahydrocyclopenta[b]indol-3-yl) acétique et de ses sels |
JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
WO2012021876A2 (fr) | 2010-08-13 | 2012-02-16 | Aileron Therapeutics, Inc. | Macrocycles peptidomimétiques |
BR112013008100A2 (pt) | 2010-09-22 | 2016-08-09 | Arena Pharm Inc | "moduladores do receptor de gpr19 e o tratamento de distúrbios relacionados a eles." |
CA2828378C (fr) * | 2011-03-16 | 2017-11-14 | Mitsubishi Tanabe Pharma Corporation | Compose heterocyclique sature contenant de l'azote |
US20140066369A1 (en) * | 2011-04-19 | 2014-03-06 | Arena Pharmaceuticals, Inc. | Modulators Of The GPR119 Receptor And The Treatment Of Disorders Related Thereto |
US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone compounds |
EP2721008B1 (fr) * | 2011-06-20 | 2015-04-29 | Novartis AG | Dérivés de isoquinolinone substitués par un radical hydroxylé en tant que inhibiteurs de p53 (mdm2 or mdm4) |
MX352672B (es) | 2011-09-27 | 2017-12-04 | Amgen Inc | Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer. |
AU2012326026B2 (en) | 2011-10-18 | 2017-04-13 | Aileron Therapeutics, Inc. | Peptidomimetic macrocyles |
WO2013080141A1 (fr) | 2011-11-29 | 2013-06-06 | Novartis Ag | Composés pyrazolopyrrolidine |
US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
UY34591A (es) * | 2012-01-26 | 2013-09-02 | Novartis Ag | Compuestos de imidazopirrolidinona |
KR102112373B1 (ko) | 2012-02-15 | 2020-05-18 | 에일러론 테라퓨틱스 인코포레이티드 | 펩티드모방체 마크로사이클 |
US8987414B2 (en) | 2012-02-15 | 2015-03-24 | Aileron Therapeutics, Inc. | Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles |
JP6171003B2 (ja) * | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
PL2880447T3 (pl) | 2012-07-31 | 2019-10-31 | Novartis Ag | Markery związane z wrażliwością na inhibitory ludzkiego białka „double minute " 2 (mdm2) |
JP5764628B2 (ja) * | 2012-09-14 | 2015-08-19 | 田辺三菱製薬株式会社 | 医薬組成物 |
SG11201503052RA (en) | 2012-11-01 | 2015-05-28 | Aileron Therapeutics Inc | Disubstituted amino acids and methods of preparation and use thereof |
WO2014100065A1 (fr) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Imidazopyridines substituées en tant qu'inhibiteurs de hdm2 |
BG111378A (bg) | 2013-01-14 | 2015-01-30 | Николай Цветков | Субституирани индазолови производни като in-vitro mao-b инхибитори |
EP2948453B1 (fr) | 2013-01-22 | 2017-08-02 | Novartis AG | Composés pyrazolo[3,4-d]pyrimidinone utilisés en tant qu'inhibiteurs de l'interaction p53/mdm2 |
EP2948451B1 (fr) | 2013-01-22 | 2017-07-12 | Novartis AG | Composés de purinone substitués |
US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
MX368703B (es) | 2013-02-28 | 2019-10-11 | Amgen Inc | Un inhibidor de mdm2 derivado de acido benzoico para el tratamiento del cancer. |
CA2906538C (fr) | 2013-03-14 | 2021-02-02 | Ana Gonzalez Buenrostro | Composes morpholinone d'acide heteroaryle utilises comme inhibiteurs de mdm2 pour le traitement du cancer |
CN103232400B (zh) * | 2013-04-26 | 2015-01-21 | 苏州大学 | 一种制备喹唑啉-2-硫酮的方法 |
US8975417B2 (en) | 2013-05-27 | 2015-03-10 | Novartis Ag | Pyrazolopyrrolidine derivatives and their use in the treatment of disease |
EP3412675A1 (fr) | 2013-05-27 | 2018-12-12 | Novartis AG | Dérivés d'imidazopyrrolidinone et leur utilisation dans le traitement d'une maladie |
US9624247B2 (en) | 2013-05-28 | 2017-04-18 | Novartis Ag | Pyrazolo-pyrrolidin-4-one derivatives as bet inhibitors and their use in the treatment of disease |
PT3004112T (pt) | 2013-05-28 | 2017-12-11 | Novartis Ag | Derivados de pirazolo-pirrolidin-4-ona e sua utilização no tratamento de doença |
JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
EP3757130A1 (fr) | 2013-09-26 | 2020-12-30 | Costim Pharmaceuticals Inc. | Méthodes de traitement de cancers hématologiques |
CN105916857B (zh) | 2013-11-21 | 2018-06-22 | 诺华股份有限公司 | 吡咯并吡咯酮衍生物及其作为bet抑制剂的用途 |
TW201605450A (zh) | 2013-12-03 | 2016-02-16 | 諾華公司 | Mdm2抑制劑與BRAF抑制劑之組合及其用途 |
AU2014372166B2 (en) | 2013-12-23 | 2017-10-26 | Novartis Ag | Pharmaceutical combinations |
AU2014372167A1 (en) * | 2013-12-23 | 2016-06-09 | Novartis Ag | Pharmaceutical combinations |
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 |
PL3157915T3 (pl) * | 2014-06-17 | 2019-07-31 | Pfizer Inc. | Podstawione związki dihydroizochinolinonowe |
TW201613576A (en) * | 2014-06-26 | 2016-04-16 | Novartis Ag | Intermittent dosing of MDM2 inhibitor |
WO2016035023A1 (fr) | 2014-09-03 | 2016-03-10 | Novartis Ag | Combinaisons pharmaceutiques et leur utilisation |
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 |
CN107106642B (zh) | 2014-09-24 | 2021-02-26 | 艾瑞朗医疗公司 | 拟肽大环化合物及其制剂 |
WO2016049359A1 (fr) | 2014-09-24 | 2016-03-31 | Aileron Therapeutics, Inc. | Macrocycles peptidomimétiques et leurs utilisations |
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 |
WO2016057322A1 (fr) * | 2014-10-08 | 2016-04-14 | Salk Institute For Biological Studies | Agonistes de ppar et leurs méthodes d'utilisation |
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 |
CN116850181A (zh) | 2015-01-06 | 2023-10-10 | 艾尼纳制药公司 | 治疗与s1p1受体有关的病症的方法 |
TN2017000375A1 (en) | 2015-03-10 | 2019-01-16 | Aduro Biotech Inc | Compositions and methods for activating "stimulator of interferon gene" -dependent signalling |
AU2016235424A1 (en) | 2015-03-20 | 2017-10-05 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles and uses thereof |
MX2017016530A (es) | 2015-06-22 | 2018-03-12 | Arena Pharm Inc | Sal cristalina de l-arginina del acido (r)-2-(7-(4-ciclopentil-3-( trifluorometil)benciloxi)-1,2,3,4-tetrahidrociclopenta[b]indol-3- il)acetico (compuesto1) para ser utilizada en transtornos asociados con el receptor de esfingosina-1-fosfato 1 (s1p1). |
US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
PT3317301T (pt) | 2015-07-29 | 2021-07-09 | Novartis Ag | Terapias de associação compreendendo moléculas de anticorpo contra lag-3 |
WO2017019896A1 (fr) | 2015-07-29 | 2017-02-02 | Novartis Ag | Traitements combinés comprenant des molécules d'anticorps qui se lient à pd-1 |
TWI804010B (zh) | 2015-08-03 | 2023-06-01 | 瑞士商諾華公司 | 作為血液學毒性生物標記之gdf-15 |
RU2018108804A (ru) | 2015-08-14 | 2019-09-16 | Новартис Аг | Фармацевтические комбинации и их применение |
CN111821306A (zh) * | 2015-08-28 | 2020-10-27 | 诺华股份有限公司 | Mdm2抑制剂和其组合 |
WO2017037586A1 (fr) | 2015-08-28 | 2017-03-09 | Novartis Ag | Polythérapie utilisant un inhibiteur de pi3k et un inhibiteur de mdm2 |
CN108368161A (zh) | 2015-09-10 | 2018-08-03 | 艾瑞朗医疗公司 | 作为mcl-1调节剂的拟肽大环化合物 |
GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
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 |
US11001582B2 (en) * | 2016-03-10 | 2021-05-11 | Assia Chemical Industries Ltd. | Solid state forms of Venetoclax and processes for preparation of Venetoclax |
CR20180443A (es) | 2016-03-17 | 2018-11-21 | Hoffmann La Roche | Derivado de morfolina |
WO2017201449A1 (fr) | 2016-05-20 | 2017-11-23 | Genentech, Inc. | Conjugués anticorps-protac et procédés d'utilisation |
WO2018009466A1 (fr) | 2016-07-05 | 2018-01-11 | Aduro Biotech, Inc. | Composés dinucléotidiques cycliques d'acide nucléique bloqué et leurs utilisations |
CA3043004A1 (fr) * | 2016-11-15 | 2018-05-24 | Novartis Ag | Dose et regime posologique pour inhibiteurs d'interaction hdm2-p53 |
WO2018092064A1 (fr) | 2016-11-18 | 2018-05-24 | Novartis Ag | Combinaisons d'inhibiteurs de mdm2 et d'inhibiteurs de bcl-xl |
EP3689868B1 (fr) * | 2016-12-01 | 2023-09-27 | Arvinas Operations, Inc. | Dérivés de tétrahydronaphtalène et de tétrahydroisoquinoléine en tant qu'agents de dégradation des récepteurs des oestrogènes |
US11173211B2 (en) | 2016-12-23 | 2021-11-16 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of rapidly accelerated Fibrosarcoma polypeptides |
CN110520124A (zh) | 2017-02-16 | 2019-11-29 | 艾尼纳制药公司 | 用于治疗原发性胆汁性胆管炎的化合物和方法 |
GB201704966D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
EP3606556A1 (fr) | 2017-04-05 | 2020-02-12 | Boehringer Ingelheim International GmbH | Polythérapie anticancéreuse |
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 |
WO2018237173A1 (fr) | 2017-06-22 | 2018-12-27 | Novartis Ag | Molécules d'anticorps dirigées contre cd73 et utilisations correspondantes |
US11413284B2 (en) | 2017-09-12 | 2022-08-16 | Novartis Ag | Protein kinase C inhibitors for treatment of uveal melanoma |
US11406627B2 (en) | 2017-10-12 | 2022-08-09 | Novartis Ag | Combinations of MDM2 inhibitors with inhibitors of ERK for treating cancers |
CN111655288A (zh) | 2017-11-16 | 2020-09-11 | 诺华股份有限公司 | 组合疗法 |
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 |
AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
WO2020041331A1 (fr) | 2018-08-20 | 2020-02-27 | Arvinas Operations, Inc. | Composé chimère ciblant la protéolyse (protac) ayant une activité de liaison à l'ubiquitine ligase e3 et ciblant une protéine alpha-synucléine pour le traitement de maladies neurodégénératives |
KR20210106437A (ko) | 2018-12-20 | 2021-08-30 | 노파르티스 아게 | 3-(1-옥소이소인돌린-2-일)피페리딘-2,6-디온 유도체를 포함하는 투약 요법 및 약학적 조합물 |
EP3924055B1 (fr) | 2019-02-15 | 2024-04-03 | Novartis AG | Dérivés de 3-(1-oxoisoindoline-2-yl)pipéridine-2,6-dione substitués et leurs utilisations |
CN113490528A (zh) | 2019-02-15 | 2021-10-08 | 诺华股份有限公司 | 3-(1-氧代-5-(哌啶-4-基)异吲哚啉-2-基)哌啶-2,6-二酮衍生物及其用途 |
KR20220017931A (ko) | 2019-05-20 | 2022-02-14 | 노파르티스 아게 | Mcl-1 억제제 항체-약물 접합체 및 사용 방법 |
CN114450008A (zh) | 2019-09-16 | 2022-05-06 | 诺华股份有限公司 | Mdm2抑制剂用于治疗骨髓纤维化的用途 |
EP4031578A1 (fr) | 2019-09-18 | 2022-07-27 | Novartis AG | Anticorps d'entpd2, polythérapies, et procédés d'utilisation des anticorps et des polythérapies |
MX2022007759A (es) | 2019-12-20 | 2022-07-19 | Novartis Ag | Combinacion del anticuerpo anti tim-3 mbg453 y anticuerpo anti tgf-beta nis793, con o sin decitabina o el anticuerpo anti pd-1 spartalizumab, para el tratamiento de mielofibrosis y sindrome mielodisplasico. |
GB201919219D0 (en) | 2019-12-23 | 2020-02-05 | Otsuka Pharma Co Ltd | Cancer biomarkers |
CN115916199A (zh) | 2020-06-23 | 2023-04-04 | 诺华股份有限公司 | 包含3-(1-氧代异吲哚啉-2-基)哌啶-2,6-二酮衍生物的给药方案 |
WO2022043930A2 (fr) | 2020-08-27 | 2022-03-03 | Otsuka Pharmaceutical Co., Ltd. | Biomarqueurs pour la thérapie anticancéreuse utilisant des antagonistes de mdm2 |
WO2022112942A2 (fr) | 2020-11-24 | 2022-06-02 | Novartis Ag | Anticorps anti-cd48, conjugués anticorps-médicament et leurs utilisations |
WO2022115451A1 (fr) | 2020-11-24 | 2022-06-02 | Novartis Ag | Conjugués anticorps-médicament inhibiteurs de mcl-1 et procédés d'utilisation |
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 |
GB202103080D0 (en) | 2021-03-04 | 2021-04-21 | Otsuka Pharma Co Ltd | Cancer biomarkers |
TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
AR125874A1 (es) | 2021-05-18 | 2023-08-23 | Novartis Ag | Terapias de combinación |
WO2023056069A1 (fr) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation |
WO2023225320A1 (fr) | 2022-05-20 | 2023-11-23 | Novartis Ag | Conjugués anticorps-médicament inhibiteurs de bcl-xl et méthodes d'utilisation associées |
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 |
WO2024054591A1 (fr) | 2022-09-07 | 2024-03-14 | Arvinas Operations, Inc. | Composés de dégradation de fibrosarcome rapidement accéléré (raf) et procédés d'utilisation associés |
WO2024126453A1 (fr) | 2022-12-15 | 2024-06-20 | Boehringer Ingelheim International Gmbh | Nouveaux indole-2-carboxamides substitués utilisés comme inhibiteurs de phgdh |
WO2024189481A1 (fr) | 2023-03-10 | 2024-09-19 | Novartis Ag | Conjugués anticorps-médicament inhibiteurs de panras et leurs procédés d'utilisation |
Family Cites Families (101)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR901228A (fr) | 1943-01-16 | 1945-07-20 | Deutsche Edelstahlwerke Ag | Système d'aimant à entrefer annulaire |
US3829420A (en) | 1970-07-13 | 1974-08-13 | Sumitomo Chemical Co | 3,4-dihydro-2(1h)-quinazolinones and preparation thereof |
US4099002A (en) | 1970-12-23 | 1978-07-04 | Sumitomo Chemical Company, Limited | Quinazolinone derivatives and a process for production thereof |
JPS4822715B1 (fr) | 1970-12-28 | 1973-07-07 | ||
JPS5427356B2 (fr) | 1972-03-31 | 1979-09-10 | ||
GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
US4258187A (en) | 1977-06-16 | 1981-03-24 | E. I. Du Pont De Nemours And Company | Process for preparing quinazolinone oxides |
US4335127A (en) | 1979-01-08 | 1982-06-15 | Janssen Pharmaceutica, N.V. | Piperidinylalkyl quinazoline compounds, composition and method of use |
PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
ATE28864T1 (de) | 1982-07-23 | 1987-08-15 | Ici Plc | Amide-derivate. |
GB8327256D0 (en) | 1983-10-12 | 1983-11-16 | Ici Plc | Steroid derivatives |
DE3420799A1 (de) | 1984-06-04 | 1985-12-05 | Bayer Ag, 5090 Leverkusen | Chromogene 4,4-diaryl-dihydrochinazolone, ihre herstellung und verwendung |
US5010099A (en) | 1989-08-11 | 1991-04-23 | Harbor Branch Oceanographic Institution, Inc. | Discodermolide compounds, compositions containing same and method of preparation and use |
US5395855A (en) | 1990-05-07 | 1995-03-07 | Ciba-Geigy Corporation | Hydrazones |
NZ243082A (en) | 1991-06-28 | 1995-02-24 | Ici Plc | 4-anilino-quinazoline derivatives; pharmaceutical compositions, preparatory processes, and use thereof |
AU2436792A (en) | 1991-08-16 | 1993-03-16 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
TW225528B (fr) | 1992-04-03 | 1994-06-21 | Ciba Geigy Ag | |
DE69233803D1 (de) | 1992-10-28 | 2011-03-31 | Genentech Inc | Verwendung von vaskulären Endothelwachstumsfaktor-Antagonisten |
GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
US5508300A (en) | 1994-01-14 | 1996-04-16 | Pfizer Inc. | Dihydro pyrazolopyrroles, compositions and use |
EP3103799B1 (fr) | 1995-03-30 | 2018-06-06 | OSI Pharmaceuticals, LLC | Derives de quinazoline |
GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
US5843901A (en) | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
CA2224435C (fr) | 1995-07-06 | 2008-08-05 | Novartis Ag | Pyrrolopyrimidines et leurs procedes de preparation |
US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
IL126351A0 (en) | 1996-04-12 | 1999-05-09 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
JP2000512990A (ja) | 1996-06-24 | 2000-10-03 | ファイザー・インク | 過増殖性疾患を処置するためのフェニルアミノ置換三環式誘導体 |
CA2259149A1 (fr) | 1996-07-05 | 1998-01-15 | Novartis Ag | Inhibiteurs de l'interaction entre p53 et mdm2 |
NZ334821A (en) | 1996-08-30 | 2000-12-22 | Novartis Ag | Method for producing epothilones |
DE69724269T2 (de) | 1996-09-06 | 2004-06-09 | Obducat Ab | Verfahren für das anisotrope ätzen von strukturen in leitende materialien |
DE19638745C2 (de) | 1996-09-11 | 2001-05-10 | Schering Ag | Monoklonale Antikörper gegen die extrazelluläre Domäne des menschlichen VEGF - Rezeptorproteins (KDR) |
CA2265630A1 (fr) | 1996-09-13 | 1998-03-19 | Gerald Mcmahon | Utilisation de derives de la quinazoline pour la fabrication d'un medicament destine au traitement de troubles cutanes hyperproliferatifs |
EP0837063A1 (fr) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | Dérivés de 4-aminoquinazoline |
EP0882314B1 (fr) | 1996-10-28 | 1999-10-06 | Abb Power Systems Ab | Electrode pour eau de mer utilisee dans un systeme de transmission a courant continu a haute tension |
DK1367057T3 (da) | 1996-11-18 | 2009-01-19 | Biotechnolog Forschung Gmbh | Epothiloner E og F |
US6441186B1 (en) | 1996-12-13 | 2002-08-27 | The Scripps Research Institute | Epothilone analogs |
CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
HRP980143A2 (en) | 1997-04-09 | 1999-02-28 | Soo Sung Ko | 4,4-disubstituted-3,4-dihydro-2 (1h)-quinazolinones useful as hiv reverse transcriptase inhibitors |
CO4940418A1 (es) | 1997-07-18 | 2000-07-24 | Novartis Ag | Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso |
GB9721069D0 (en) | 1997-10-03 | 1997-12-03 | Pharmacia & Upjohn Spa | Polymeric derivatives of camptothecin |
US6194181B1 (en) | 1998-02-19 | 2001-02-27 | Novartis Ag | Fermentative preparation process for and crystal forms of cytostatics |
CA2322157C (fr) | 1998-02-25 | 2012-05-29 | Sloan-Kettering Institute For Cancer Research | Synthese d'epothilones, de leurs intermediaires et de leurs analogues |
BR9912938B1 (pt) | 1998-08-11 | 2011-06-28 | derivados de isoquinolina, composição que os compreende, processo para preparação e uso dos mesmos. | |
GB9824579D0 (en) | 1998-11-10 | 1999-01-06 | Novartis Ag | Organic compounds |
UA71587C2 (uk) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Аміди антранілової кислоти та їхнє застосування як лікарських засобів |
EP1135470A2 (fr) | 1998-11-20 | 2001-09-26 | Kosan Biosciences, Inc. | Matieres et procedes recombinants destines a la production d'epothilone et de derives d'epothilone |
EP2016953A3 (fr) | 1998-12-22 | 2009-04-15 | Genentech, Inc. | Antagonistes de facteur de croissance cellulaire endothéliale vasculaire et utilisations associées |
PT1165085E (pt) | 1999-03-30 | 2006-10-31 | Novartis Ag | Derivados de ftalazina para tratar doencas inflamatorias |
WO2000066560A1 (fr) | 1999-05-04 | 2000-11-09 | American Home Products Corporation | Derives de quinazolinone et de benzoxazine tenant lieu de modulateurs du recepteur de progesterone |
JP2001302515A (ja) | 2000-04-18 | 2001-10-31 | Sumitomo Pharmaceut Co Ltd | ポリ(adp−リボース)ポリメラーゼ阻害剤 |
US6479499B1 (en) | 2000-06-28 | 2002-11-12 | National Science Council | 2-phenyl-4-quinazolinone compounds, 2-phenyl-4-alkoxy-quinazoline compounds and their pharmaceutical compositions |
JP4555547B2 (ja) | 2000-08-10 | 2010-10-06 | ファイザー イタリア ソシエタ ア レスポンサビリタ リミタータ | キナーゼ阻害剤としての二環式ピラゾール、それらを製造するための方法およびそれらを含む医薬組成物 |
PE20020354A1 (es) | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
AR035885A1 (es) | 2001-05-14 | 2004-07-21 | Novartis Ag | Derivados de 4-amino-5-fenil-7-ciclobutilpirrolo (2,3-d)pirimidina, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos derivados para la preparacion de una composicion farmaceutica |
GB0119249D0 (en) | 2001-08-07 | 2001-10-03 | Novartis Ag | Organic compounds |
WO2003051359A1 (fr) | 2001-12-18 | 2003-06-26 | F.Hoffmann-La Roche Ag | Cis-2,4,5- triphenyl-imidazolines et leurs utilisations dans le traitement des tumeurs |
WO2003062392A2 (fr) | 2002-01-18 | 2003-07-31 | Ceretek Llc | Procedes pour traiter des pathologies associees a un recepteur d'edg |
US20060189511A1 (en) | 2002-05-13 | 2006-08-24 | Koblish Holly K | Method for cytoprotection through mdm2 and hdm2 inhibition |
US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
JP2007524596A (ja) | 2003-02-28 | 2007-08-30 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | 共結晶医薬組成物 |
US20040213264A1 (en) | 2003-04-25 | 2004-10-28 | Nortel Networks Limited | Service class and destination dominance traffic management |
CA2536313A1 (fr) | 2003-08-22 | 2005-03-03 | Takeda Pharmaceutical Company Limited | Derive de pyrimidine fusionne et utilisation associee |
DK1663185T3 (da) | 2003-09-22 | 2009-04-06 | Onepharm Res & Dev Gmbh | Forebyggelse og behandling af inflammationsinduceret og/eller immun-medieret knogletab |
CN1886384A (zh) | 2003-11-25 | 2006-12-27 | 希龙公司 | 喹唑酮化合物作为抗癌药剂 |
KR20080027969A (ko) | 2004-05-18 | 2008-03-28 | 에프. 호프만-라 로슈 아게 | 신규 cis-이미다졸린 |
ES2604197T3 (es) | 2004-06-01 | 2017-03-03 | University Of Virginia Patent Foundation | Inhibidores dobles de molécula pequeña de cáncer y angiogénesis |
GB0419481D0 (en) | 2004-09-02 | 2004-10-06 | Cancer Rec Tech Ltd | Isoindolin-1-one derivatives |
US20060069085A1 (en) | 2004-09-28 | 2006-03-30 | Rulin Zhao | Preparation of 4,5-dihydro-pyrazolo[3,4-c]pyrid-2-ones |
US20060160869A1 (en) | 2005-01-05 | 2006-07-20 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase inhibitors |
EP1868685A2 (fr) | 2005-03-18 | 2007-12-26 | onepharm GmbH | INHIBITEURS DE LA 11ßG(B)-HYDROXYSTEROIDE DESHYDROGENASES |
US7576082B2 (en) | 2005-06-24 | 2009-08-18 | Hoffman-La Roche Inc. | Oxindole derivatives |
WO2007068637A1 (fr) | 2005-12-12 | 2007-06-21 | Nerviano Medical Sciences S.R.L. | Derives de pyrrolo-pyrazole substitues agissant comme inhibiteurs de kinase |
WO2007096334A1 (fr) | 2006-02-24 | 2007-08-30 | Pfizer Italia Srl | Pyrrolopyrrolones fonctionnant comme inhibiteurs de kinase |
DE102006016426A1 (de) | 2006-04-07 | 2007-10-11 | Merck Patent Gmbh | Neuartige Cyclobutyl-Verbindungen als Kinase-Inhibitoren |
US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
WO2008034039A2 (fr) | 2006-09-15 | 2008-03-20 | Nexuspharma Inc. | Tétrahydro-isoquinolines innovantes |
CN101679246A (zh) | 2007-03-30 | 2010-03-24 | 盐野义制药株式会社 | 新型吡咯啉酮衍生物以及包含其的药物组合物 |
WO2008130614A2 (fr) | 2007-04-20 | 2008-10-30 | University Of Pittsburg-Of The Commonwealth System Of Higher Education | Antagonistes p53/mdm2/mdm4 sélectifs et à action double |
WO2009086303A2 (fr) | 2007-12-21 | 2009-07-09 | University Of Rochester | Procédé permettant de modifier la durée de vie d'organismes eucaryotes |
UY31982A (es) | 2008-07-16 | 2010-02-26 | Boehringer Ingelheim Int | Derivados de 1,2-dihidropiridin-3-carboxamidas n-sustituidas |
TW201016702A (en) | 2008-09-25 | 2010-05-01 | Shionogi & Co | Novel pyrrolinone derivative and pharmaceutical composition comprising the same |
WO2010077680A2 (fr) | 2008-12-08 | 2010-07-08 | Vm Discovery Inc. | Compositions d'inhibiteurs de tyrosine kinase de récepteur protéique |
US20120208204A1 (en) | 2009-06-03 | 2012-08-16 | The Brigham And Women's Hospital, Inc. | Compositions and Methods for Inhibiting Tumor Growth |
US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
CU24130B1 (es) | 2009-12-22 | 2015-09-29 | Novartis Ag | Isoquinolinonas y quinazolinonas sustituidas |
WO2011161031A1 (fr) | 2010-06-22 | 2011-12-29 | Glaxosmithkline Llc | Composés de benzotriazolodiazépine inhibiteurs de bromodomaines |
US20120065210A1 (en) | 2010-09-15 | 2012-03-15 | Xin-Jie Chu | Substituted hexahydropyrrolo[1,2-c]imidazolones |
GB201016880D0 (en) | 2010-10-07 | 2010-11-17 | Riotech Pharmaceuticals Ltd | Phosphodiesterase inhibitors |
UY33725A (es) | 2010-11-12 | 2012-06-29 | Sanofi Sa | Antagonistas de mdm2 de espiro-oxindol |
US9422292B2 (en) | 2011-05-04 | 2016-08-23 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
WO2012174487A2 (fr) | 2011-06-17 | 2012-12-20 | Constellation Pharmaceuticals, Inc. | Inhibiteurs à bromodomaine et leurs utilisations |
EP2721008B1 (fr) | 2011-06-20 | 2015-04-29 | Novartis AG | Dérivés de isoquinolinone substitués par un radical hydroxylé en tant que inhibiteurs de p53 (mdm2 or mdm4) |
US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone compounds |
WO2013033268A2 (fr) | 2011-08-29 | 2013-03-07 | Coferon, Inc. | Ligands bromodomaines bivalents et procédés d'utilisation de ceux-ci |
WO2013080141A1 (fr) | 2011-11-29 | 2013-06-06 | Novartis Ag | Composés pyrazolopyrrolidine |
UY34591A (es) | 2012-01-26 | 2013-09-02 | Novartis Ag | Compuestos de imidazopirrolidinona |
JP6171003B2 (ja) | 2012-05-24 | 2017-07-26 | ノバルティス アーゲー | ピロロピロリジノン化合物 |
-
2010
- 2010-12-20 US US12/973,474 patent/US8440693B2/en active Active
- 2010-12-21 WO PCT/EP2010/070364 patent/WO2011076786A1/fr active Application Filing
- 2010-12-21 AR ARP100104820A patent/AR079663A1/es active IP Right Grant
- 2010-12-21 AU AU2010334890A patent/AU2010334890B2/en not_active Ceased
- 2010-12-21 EA EA201200920A patent/EA021126B1/ru not_active IP Right Cessation
- 2010-12-21 IN IN5467DEN2012 patent/IN2012DN05467A/en unknown
- 2010-12-21 CA CA2785340A patent/CA2785340C/fr active Active
- 2010-12-21 SG SG2012044244A patent/SG181734A1/en unknown
- 2010-12-21 MX MX2012007336A patent/MX2012007336A/es active IP Right Grant
- 2010-12-21 EP EP10792944.0A patent/EP2516009B1/fr active Active
- 2010-12-21 NZ NZ600716A patent/NZ600716A/xx not_active IP Right Cessation
- 2010-12-21 PL PL10792944T patent/PL2516009T3/pl unknown
- 2010-12-21 BR BR112012018412-1A patent/BR112012018412B1/pt not_active IP Right Cessation
- 2010-12-21 KR KR20147029863A patent/KR20140140602A/ko not_active Application Discontinuation
- 2010-12-21 JO JO2010470A patent/JO2974B1/en active
- 2010-12-21 JP JP2012545293A patent/JP5542962B2/ja active Active
- 2010-12-21 PE PE2012000866A patent/PE20121510A1/es active IP Right Grant
- 2010-12-21 RS RS20140667A patent/RS53676B1/en unknown
- 2010-12-21 TW TW099145068A patent/TWI629264B/zh not_active IP Right Cessation
- 2010-12-21 GE GEAP201012760A patent/GEP20146042B/en unknown
- 2010-12-21 MY MYPI2012002732A patent/MY156438A/en unknown
- 2010-12-21 ES ES10792944T patent/ES2527001T3/es active Active
- 2010-12-21 DK DK10792944.0T patent/DK2516009T3/en active
- 2010-12-21 SI SI201030821T patent/SI2516009T1/sl unknown
- 2010-12-21 PT PT107929440T patent/PT2516009E/pt unknown
- 2010-12-21 KR KR1020127019166A patent/KR101473068B1/ko active IP Right Grant
- 2010-12-22 UY UY33131A patent/UY33131A/xx not_active Application Discontinuation
-
2012
- 2012-06-15 MA MA34976A patent/MA33832B1/fr unknown
- 2012-06-18 IL IL220492A patent/IL220492A/en active IP Right Grant
- 2012-06-18 ZA ZA2012/04467A patent/ZA201204467B/en unknown
- 2012-06-19 CR CR20120333A patent/CR20120333A/es unknown
- 2012-06-19 DO DO2012000172A patent/DOP2012000172A/es unknown
- 2012-06-20 EC ECSP12011990 patent/ECSP12011990A/es unknown
- 2012-06-20 TN TNP2012000309A patent/TN2012000309A1/en unknown
- 2012-06-21 NI NI201200111A patent/NI201200111A/es unknown
- 2012-06-21 CL CL2012001688A patent/CL2012001688A1/es unknown
- 2012-06-22 CO CO12105263A patent/CO6561772A2/es unknown
- 2012-06-22 GT GT201200208A patent/GT201200208A/es unknown
- 2012-06-22 HN HN2012001332A patent/HN2012001332A/es unknown
- 2012-11-19 HK HK12111771.8A patent/HK1170972A1/xx not_active IP Right Cessation
-
2013
- 2013-02-27 US US13/778,910 patent/US9051279B2/en active Active
-
2014
- 2014-12-22 SM SM201400193T patent/SMT201400193B/xx unknown
- 2014-12-24 HR HRP20141259AT patent/HRP20141259T1/hr unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY33131A (es) | Isoquinolinonas y quinazolinonas sustituidas | |
NL350111I2 (nl) | fenpicoxamid en prothioconazool | |
BRPI1004907A2 (pt) | unidade principal e unidade subordinada | |
BRPI1014404A2 (pt) | cânula dotada de recurso de cânula e recurso de encaixe em sobreposição | |
BRPI1012760A2 (pt) | métodos e arranjo de filtro | |
NO20092808A (no) | Hårføner | |
DK2417204T3 (da) | Piezokromt sikkerhedselement | |
BR112012010242A2 (pt) | derivados de heteroarilpiperidina e heteroarilpiperazina | |
DK2318378T3 (da) | Quinazolin-derivater | |
FI20090134A0 (fi) | Hissijärjestely ja menetelmä | |
BR112013002544A2 (pt) | seção de armario e armario | |
DK2373644T3 (da) | Pyridazinonderivater | |
BRPI0911977A2 (pt) | quinazolinas substituídas | |
FI20095671A0 (fi) | Lukitusjärjestely | |
BR112012010524A2 (pt) | compostos derivados de quinazolina | |
BR112012003603A2 (pt) | [4-(5-aminometil-fenil)-piperidin-1il]-1hindol-3-il]-metanonas dissubstituídas | |
BRPI0911967A2 (pt) | quinazolinas substituídas | |
BRPI0914735A2 (pt) | isoquinolinas e isoquinolinonas 6-substituídas | |
ES1071902Y (es) | Mecanismo de termosoldadura y precorte | |
BRPI0912672A2 (pt) | quinazolinas substituídas | |
DK2310037T3 (da) | Conglutin-gamma as-medikament og -kosttilskudpatentkrav | |
DK2386008T3 (da) | Gelænderkonstruktion | |
DK2373647T3 (da) | Pyridazinonderivater | |
FI20090462A0 (fi) | Kaiderakenne | |
FI20096360A0 (fi) | Bioliima ja puulevy |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20181127 |