CO2021017504A2 - Derivados de benzisoxazol sulfonamida - Google Patents
Derivados de benzisoxazol sulfonamidaInfo
- Publication number
- CO2021017504A2 CO2021017504A2 CONC2021/0017504A CO2021017504A CO2021017504A2 CO 2021017504 A2 CO2021017504 A2 CO 2021017504A2 CO 2021017504 A CO2021017504 A CO 2021017504A CO 2021017504 A2 CO2021017504 A2 CO 2021017504A2
- Authority
- CO
- Colombia
- Prior art keywords
- compounds
- sulfonamide derivatives
- patients
- cell growth
- abnormal cell
- Prior art date
Links
Classifications
-
- 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
- C07D413/06—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 only aliphatic carbon atoms
-
- 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
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic 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
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
La presente invención se relaciona con los compuestos de la fórmula (I) o sales farmacéuticamente aceptables de los mismos, en donde el Anillo A, R1-R8, y n se definen en la presente. Los derivados de benzisoxazol sulfonamida novedosos son útiles para el tratamiento de crecimiento celular anormal, tal como cáncer, en pacientes. Las modalidades adicionales relacionadas con las composiciones farmacéuticas que contienen los compuestos y a métodos de utilización los compuestos y composiciones en el tratamiento de crecimiento celular anormal en pacientes.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962863199P | 2019-06-18 | 2019-06-18 | |
US201962953223P | 2019-12-24 | 2019-12-24 | |
US202063025278P | 2020-05-15 | 2020-05-15 | |
PCT/IB2020/055589 WO2020254946A1 (en) | 2019-06-18 | 2020-06-16 | Benzisoxazole sulfonamide derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
CO2021017504A2 true CO2021017504A2 (es) | 2022-01-17 |
Family
ID=71738189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CONC2021/0017504A CO2021017504A2 (es) | 2019-06-18 | 2021-12-21 | Derivados de benzisoxazol sulfonamida |
Country Status (29)
Country | Link |
---|---|
US (2) | US11492346B2 (es) |
EP (2) | EP3986890B1 (es) |
JP (2) | JP7352662B2 (es) |
KR (1) | KR20220024671A (es) |
CN (1) | CN114364672A (es) |
AU (2) | AU2020296361A1 (es) |
BR (1) | BR112021025528A2 (es) |
CA (1) | CA3143666A1 (es) |
CL (1) | CL2021003372A1 (es) |
CO (1) | CO2021017504A2 (es) |
CR (1) | CR20210627A (es) |
DK (1) | DK3986890T3 (es) |
EC (1) | ECSP21091615A (es) |
ES (1) | ES2969616T3 (es) |
FI (1) | FI3986890T3 (es) |
HR (1) | HRP20231501T1 (es) |
HU (1) | HUE064683T2 (es) |
IL (1) | IL288802A (es) |
LT (1) | LT3986890T (es) |
MD (1) | MD3986890T2 (es) |
MX (1) | MX2021016085A (es) |
PE (1) | PE20220808A1 (es) |
PL (1) | PL3986890T3 (es) |
PT (1) | PT3986890T (es) |
RS (1) | RS64931B1 (es) |
SI (1) | SI3986890T1 (es) |
TW (1) | TWI787620B (es) |
UY (1) | UY38752A (es) |
WO (1) | WO2020254946A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201810092D0 (en) * | 2018-06-20 | 2018-08-08 | Ctxt Pty Ltd | Compounds |
MX2021014441A (es) | 2019-05-31 | 2022-01-06 | Ikena Oncology Inc | Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos. |
LT3986890T (lt) * | 2019-06-18 | 2023-12-11 | Pfizer Inc. | Benzizoksazolo sulfonamido dariniai |
JP2022019654A (ja) * | 2020-07-15 | 2022-01-27 | ファイザー・インク | がん処置のためのkat6阻害剤方法および組合せ |
WO2022187688A1 (en) * | 2021-03-05 | 2022-09-09 | Umbra Therapeutics Inc. | Covalent kras-binding compounds for therapeutic purposes |
WO2022187693A1 (en) * | 2021-03-05 | 2022-09-09 | Umbra Therapeutics Inc. | Covalent cdk2-binding compounds for therapeutic purposes |
CN117881677A (zh) * | 2021-05-21 | 2024-04-12 | 奥瑞基尼肿瘤有限公司 | 作为KAT6Aw抑制剂的稠合异噁唑基化合物 |
EP4368620A1 (en) * | 2021-07-05 | 2024-05-15 | Hangzhou Innogate Pharma Co., Ltd. | Compound serving as kat6 inhibitor |
CA3228411A1 (en) | 2021-08-10 | 2023-02-16 | Xiaomin Zhang | Sulfonamide derivative, preparation method therefor and medical use thereof |
CA3237830A1 (en) * | 2021-11-16 | 2023-05-25 | Insilico Medicine Ip Limited | Lysine acetyltransferase 6a (kat6a) inhibitors and uses thereof |
WO2023114710A1 (en) * | 2021-12-13 | 2023-06-22 | Aurigene Oncology Limited | Fused benzoisoxazolyl compounds as kat6a inhibitors |
TW202400593A (zh) * | 2022-03-28 | 2024-01-01 | 美商艾索司特瑞克斯公司 | Myst家族離胺酸乙醯轉移酶之抑制劑 |
WO2023245150A1 (en) * | 2022-06-16 | 2023-12-21 | Prelude Therapeutics Incorporated | Kat6 targeting compounds with ubiquitin ligase binding moiety |
WO2024023703A1 (en) | 2022-07-29 | 2024-02-01 | Pfizer Inc. | Dosing regimens comprising a kat6 inhibitor for the treatment of cancer |
Family Cites Families (91)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3064003A (en) | 1962-11-13 | Carboxylic acid derivatives of sub- | ||
US2358031A (en) | 1944-09-12 | Substituted thiadiazoles | ||
US2525321A (en) | 1949-01-07 | 1950-10-10 | American Cyanamid Co | Hydroxybenzenesulfonamidoisoxazoles and preparation of same |
GB689281A (en) | 1950-02-18 | 1953-03-25 | Lunbeck Corp | Improvements in or relating to the production of sulphanilamido-thiadiazoles |
DE1102745B (de) | 1959-06-06 | 1961-03-23 | Boehringer & Soehne Gmbh | Verfahren zur Herstellung von 5-Sulfanilamidoisoxazolen |
BE617370A (fr) | 1961-05-09 | 1962-11-08 | Ciba Geigy | Procédé de préparation du 2,5-di-[benzoxazolyl-(2')]-thiofène |
US3332942A (en) | 1962-11-02 | 1967-07-25 | White Lab Inc | Substituted thiadiazoles |
JPS498255B1 (es) | 1970-10-08 | 1974-02-25 | ||
US3951967A (en) | 1972-03-20 | 1976-04-20 | Merck & Co., Inc. | 7-Mercapto(or thio)-benzothiadiazine products |
US3960854A (en) | 1972-03-20 | 1976-06-01 | Merck & Co., Inc. | 7-Mercapto(or thio)-benzothiadiazine products |
DE2617809C2 (de) | 1976-04-23 | 1984-09-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Stabilisierung von Chromdioxid-Magnetpigmenten und seine Verwendung |
JPS6042794B2 (ja) | 1977-09-27 | 1985-09-25 | 三共株式会社 | イソオキサゾリウム塩,およびその製造方法 |
US4251664A (en) | 1978-05-24 | 1981-02-17 | Henkel Corporation | Sulfonamidothiadiazoles, metal complexes thereof, and solutions containing such compounds for use in extraction of metal values |
US4172896A (en) | 1978-06-05 | 1979-10-30 | Dainippon Pharmaceutical Co., Ltd. | Methane-sulfonamide derivatives, the preparation thereof and composition comprising the same |
JPS603685B2 (ja) | 1980-04-15 | 1985-01-30 | 日本コロムビア株式会社 | 絵入りレコ−ド盤の製造方法 |
GB8427618D0 (en) | 1984-11-01 | 1984-12-05 | Shell Int Research | Anticoccidial compositions |
GB8607683D0 (en) | 1986-03-27 | 1986-04-30 | Ici Plc | Anti-tumor agents |
JPS63238006A (ja) | 1987-03-26 | 1988-10-04 | Shionogi & Co Ltd | イモチ防除剤 |
US5591761A (en) | 1993-05-20 | 1997-01-07 | Texas Biotechnology Corporation | Thiophenyl-, furyl-and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5962490A (en) | 1987-09-25 | 1999-10-05 | Texas Biotechnology Corporation | Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
NZ231534A (en) | 1988-11-29 | 1992-02-25 | Warner Lambert Co | 3,5-di-t-butyl-4-hydroxyphenyl-triazoles, oxadiazoles and thiadiazoles; anti-inflammatory compositions |
JPH03258771A (ja) | 1990-03-09 | 1991-11-19 | Tosoh Corp | スルホンアミド誘導体、その製法及びそれを有効成分として含有する除草剤 |
TW224462B (es) | 1992-02-24 | 1994-06-01 | Squibb & Sons Inc | |
FR2690160A1 (fr) | 1992-04-15 | 1993-10-22 | Rhone Poulenc Rorer Sa | Application de dérivés d'acide 2H-1,2,4-benzothiadiazine-1,1-dioxyde-3-carboxylique à la préparation de médicaments, les produits nouveaux, leur préparation et les médicaments les contenant. |
NZ247440A (en) | 1992-05-06 | 1995-04-27 | Squibb & Sons Inc | Phenyl sulphonamide derivatives, preparation and pharmaceutical compositions thereof |
CA2121724A1 (en) | 1993-04-21 | 1994-10-22 | Toshifumi Watanabe | Methods and compositions for the prophylactic and/or therapeutic treatment of organ hypofunction |
JP3901229B2 (ja) | 1994-05-13 | 2007-04-04 | Ntn株式会社 | 耐熱・潤滑性樹脂組成物 |
DE69628740T2 (de) | 1995-04-04 | 2004-05-13 | Encysive Pharmaceuticals Inc., Bellaire | Thienyl-, furyl-, pyrrolyl- und biphenylsulfonamide und derivate zur modulation der endothelin-aktivität |
US5804585A (en) | 1996-04-15 | 1998-09-08 | Texas Biotechnology Corporation | Thieno-pyridine sulfonamides derivatives thereof and related compounds that modulate the activity of endothelin |
CA2271116A1 (en) | 1996-11-13 | 1998-05-22 | Gregory J. Wells | Benzothiazo and related heterocyclic group-containing cysteine and serine protease inhibitors |
US5783705A (en) | 1997-04-28 | 1998-07-21 | Texas Biotechnology Corporation | Process of preparing alkali metal salys of hydrophobic sulfonamides |
NZ336898A (en) | 1997-04-28 | 2001-10-26 | Texas Biotechnology Corp | Sulfonamides for treatment of endothelin-mediated disorders |
HUP0203954A2 (hu) | 1999-09-17 | 2003-03-28 | Millennium Pharmaceuticals, Inc. | Xa faktor inhibitorok |
AU2456701A (en) | 1999-12-31 | 2001-07-16 | Texas Biotechnology Corporation | Pharmaceutical and veterinary uses of endothelin antagonists |
ATE311366T1 (de) | 2000-02-29 | 2005-12-15 | Millennium Pharm Inc | Benzamide und ähnliche inhibitoren vom faktor xa |
GB0127344D0 (en) | 2001-11-14 | 2002-01-02 | Cancer Res Ventures Ltd | Assay method |
AU2002353717B2 (en) | 2001-11-22 | 2006-08-03 | Biovitrum Ab | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1 |
JP2003292485A (ja) | 2002-04-01 | 2003-10-15 | Yamanouchi Pharmaceut Co Ltd | スルホンアミド誘導体 |
TW200505902A (en) | 2003-03-20 | 2005-02-16 | Schering Corp | Cannabinoid receptor ligands |
EP1631558A1 (en) | 2003-05-21 | 2006-03-08 | Biovitrum Ab | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type i |
WO2004113310A1 (en) | 2003-06-25 | 2004-12-29 | Biovitrum Ab | Use of an inhibitor of 11-b-hydroxysteroid dehydrogenase type 1 compounds for promoting wound healing |
BRPI0412876A (pt) | 2003-07-22 | 2006-10-03 | Janssen Pharmaceutica Nv | derivados de quinolinona como inibidores de c-fms quinase |
TW200524888A (en) | 2003-08-08 | 2005-08-01 | Vertex Pharma | Compositions useful as inhibitors of voltage-gated ion channels |
US7615563B2 (en) | 2003-08-08 | 2009-11-10 | Gonzalez Iii Jesus E | Compositions useful as inhibitors of voltage-gated sodium channels |
WO2005049593A2 (en) | 2003-11-13 | 2005-06-02 | Abbott Laboratories | N-acylsulfonamide apoptosis promoters |
US7642260B2 (en) | 2003-11-13 | 2010-01-05 | Abbott Laboratories, Inc. | Apoptosis promoters |
US7767684B2 (en) | 2003-11-13 | 2010-08-03 | Abbott Laboratories | Apoptosis promoters |
US8614318B2 (en) | 2003-11-13 | 2013-12-24 | Abbvie Inc. | Apoptosis promoters |
US7973161B2 (en) | 2003-11-13 | 2011-07-05 | Abbott Laboratories | Apoptosis promoters |
KR20070085340A (ko) | 2004-10-12 | 2007-08-27 | 디코드 제네틱스, 아이엔씨. | 폐쇄성 동맥 질환용의 아릴 설폰아미드 주변 치환된바이사이클릭 화합물 |
JP2008540661A (ja) | 2005-05-16 | 2008-11-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | イオンチャネルのモジュレーターとしての二環式の誘導体 |
DE102005038947A1 (de) | 2005-05-18 | 2006-11-30 | Grünenthal GmbH | Substituierte Benzo[d]isoxazol-3-yl-amin-Verbindungen und deren Verwendung in Arzneimitteln |
ATE513829T1 (de) | 2005-10-06 | 2011-07-15 | Sanofi Aventis | Bicyclische arylsulfonsäureä1,3,4ü-thiadiazol-2- yl-amide, verfahren zu ihrer herstellung und ihre verwendung als pharmazeutika |
WO2007039175A1 (en) | 2005-10-06 | 2007-04-12 | Sanofi-Aventis | N-[1 ,3,4]-thiadiazol-2-yl-benzene sulfonamides, processes for their preparation and their use as pharmaceuticals |
DE102005055355A1 (de) | 2005-11-21 | 2007-10-31 | Merck Patent Gmbh | 3,6-Dihydro-2-oxo-6H-[1,3,4]thiadiazinderivate |
TW200740803A (en) | 2005-12-21 | 2007-11-01 | Vertex Pharma | Heterocyclic derivatives as modulators of ion channels |
EP2054056A4 (en) | 2006-08-16 | 2010-08-25 | J David Gladstone Inst A Testa | SMALL MOLECULAR INHIBITORS OF KYNURENINE-3-MONOOXYGENASE |
WO2008064116A2 (en) | 2006-11-16 | 2008-05-29 | Abbott Laboratories | Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection |
EP2094671A1 (en) | 2006-11-20 | 2009-09-02 | Alantos Pharmaceuticals Holding, Inc. | Heterobicyclic metalloprotease inhibitors |
WO2008089307A2 (en) | 2007-01-18 | 2008-07-24 | Lexicon Pharmaceuticals, Inc. | Delta 5 desaturase inhibitors for the treatment of pain, inflammation and cancer |
EP2173743A2 (en) | 2007-07-13 | 2010-04-14 | Icagen, Inc. | Sodium channel inhibitors |
US20110039847A1 (en) | 2007-11-01 | 2011-02-17 | Sirtris Pharmaceuticals, Inc | Amide derivatives as sirtuin modulators |
WO2009086303A2 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
EP2240474B1 (en) | 2007-12-26 | 2012-03-14 | Sanofi | Cyclic pyridyl-n-(1,3,4)-thiadiazol-2-yl-benzene sulfonamides, processes for their preparation and their use as pharmaceuticals |
US8475505B2 (en) | 2008-08-13 | 2013-07-02 | Smed-Ta/Td, Llc | Orthopaedic screws |
WO2010046780A2 (en) | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Anti viral compounds |
JP5731479B2 (ja) | 2009-04-21 | 2015-06-10 | ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ | Hsp90阻害剤としてのレゾルシノール誘導体 |
UA107360C2 (en) | 2009-08-05 | 2014-12-25 | Biogen Idec Inc | Bicyclic aryl sphingosine 1-phosphate analogs |
US20130022629A1 (en) | 2010-01-04 | 2013-01-24 | Sharpe Arlene H | Modulators of Immunoinhibitory Receptor PD-1, and Methods of Use Thereof |
WO2011085575A1 (zh) | 2010-01-15 | 2011-07-21 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
CN101845043A (zh) | 2010-01-15 | 2010-09-29 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
CN101747325A (zh) | 2010-01-15 | 2010-06-23 | 江苏省农药研究所股份有限公司 | 邻杂环甲酰苯胺类化合物及其合成方法和应用 |
EP2563761A1 (en) | 2010-04-29 | 2013-03-06 | The U.S.A. As Represented By The Secretary, Department Of Health And Human Services | Activators of human pyruvate kinase |
TW201210597A (en) | 2010-06-09 | 2012-03-16 | Gilead Sciences Inc | Inhibitors of hepatitis C virus |
CA2804716A1 (en) | 2010-07-12 | 2012-01-19 | Pfizer Limited | Chemical compounds |
DK2835131T3 (en) | 2010-12-14 | 2017-12-04 | Electrophoretics Ltd | Casein kinase 1 delta inhibitors (CK1 delta) |
WO2012088438A1 (en) | 2010-12-22 | 2012-06-28 | Eutropics Pharmaceuticals, Inc. | Compositions and methods useful for treating diseases |
WO2012129562A2 (en) | 2011-03-24 | 2012-09-27 | The Scripps Research Institute | Compounds and methods for inducing chondrogenesis |
PL220630B1 (pl) | 2012-12-28 | 2015-11-30 | Inst Immunologii I Terapii Doświadczalnej Pan | Nowe sulfonamidowe pochodne izoksazolo[5,4-b]pirydyny o aktywności przeciwbakteryjnej, sposób ich wytwarzania oraz nowe zastosowanie 3-aminoizoksazolo[5,4-b]pirydyny |
WO2014144545A2 (en) | 2013-03-15 | 2014-09-18 | Genentech, Inc. | Substituted benzoxazoles and methods of use thereof |
WO2015102929A1 (en) | 2013-12-30 | 2015-07-09 | Novartis Ag | Tricyclic sulfonamide derivatives |
EP3097101B1 (en) | 2014-01-24 | 2020-12-23 | Merck Sharp & Dohme Corp. | Isoquinoline derivatives as mgat2 inhibitors |
GB201510019D0 (en) | 2015-06-09 | 2015-07-22 | Cancer Therapeutics Crc Pty Ltd | Compounds |
WO2017002120A1 (en) | 2015-07-02 | 2017-01-05 | Yeda Research And Development Co. Ltd. | Selective inhibitors of senescent cells and uses thereof |
WO2017098421A1 (en) | 2015-12-08 | 2017-06-15 | Glaxosmithkline Intellectual Property Development Limited | Benzothiadiazine compounds |
CN107098846B (zh) * | 2016-02-26 | 2020-10-09 | 中国医学科学院药物研究所 | N-酰基磺酰胺类FBPase抑制剂、其制备方法、药物组合物及用途 |
WO2018081167A1 (en) | 2016-10-24 | 2018-05-03 | Yumanity Therapeutics | Compounds and uses thereof |
EP3548480A1 (en) * | 2016-11-29 | 2019-10-09 | Epizyme, Inc. | Compounds containing a sulfonic group as kat inhibitors |
US11542248B2 (en) | 2017-06-08 | 2023-01-03 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
GB201810092D0 (en) * | 2018-06-20 | 2018-08-08 | Ctxt Pty Ltd | Compounds |
LT3986890T (lt) | 2019-06-18 | 2023-12-11 | Pfizer Inc. | Benzizoksazolo sulfonamido dariniai |
-
2020
- 2020-06-16 LT LTEPPCT/IB2020/055589T patent/LT3986890T/lt unknown
- 2020-06-16 WO PCT/IB2020/055589 patent/WO2020254946A1/en active Application Filing
- 2020-06-16 KR KR1020227001722A patent/KR20220024671A/ko not_active Application Discontinuation
- 2020-06-16 UY UY0001038752A patent/UY38752A/es unknown
- 2020-06-16 DK DK20743773.2T patent/DK3986890T3/da active
- 2020-06-16 CR CR20210627A patent/CR20210627A/es unknown
- 2020-06-16 PL PL20743773.2T patent/PL3986890T3/pl unknown
- 2020-06-16 EP EP20743773.2A patent/EP3986890B1/en active Active
- 2020-06-16 MD MDE20220478T patent/MD3986890T2/ro unknown
- 2020-06-16 JP JP2021574753A patent/JP7352662B2/ja active Active
- 2020-06-16 ES ES20743773T patent/ES2969616T3/es active Active
- 2020-06-16 US US16/902,515 patent/US11492346B2/en active Active
- 2020-06-16 HR HRP20231501TT patent/HRP20231501T1/hr unknown
- 2020-06-16 CA CA3143666A patent/CA3143666A1/en active Pending
- 2020-06-16 EP EP23203023.9A patent/EP4299135A3/en active Pending
- 2020-06-16 HU HUE20743773A patent/HUE064683T2/hu unknown
- 2020-06-16 FI FIEP20743773.2T patent/FI3986890T3/fi active
- 2020-06-16 AU AU2020296361A patent/AU2020296361A1/en not_active Abandoned
- 2020-06-16 PT PT207437732T patent/PT3986890T/pt unknown
- 2020-06-16 MX MX2021016085A patent/MX2021016085A/es unknown
- 2020-06-16 PE PE2021002180A patent/PE20220808A1/es unknown
- 2020-06-16 BR BR112021025528A patent/BR112021025528A2/pt unknown
- 2020-06-16 SI SI202030335T patent/SI3986890T1/sl unknown
- 2020-06-16 RS RS20231177A patent/RS64931B1/sr unknown
- 2020-06-16 CN CN202080057621.7A patent/CN114364672A/zh active Pending
- 2020-06-17 TW TW109120469A patent/TWI787620B/zh active
-
2021
- 2021-12-08 IL IL288802A patent/IL288802A/en unknown
- 2021-12-16 CL CL2021003372A patent/CL2021003372A1/es unknown
- 2021-12-17 EC ECSENADI202191615A patent/ECSP21091615A/es unknown
- 2021-12-21 CO CONC2021/0017504A patent/CO2021017504A2/es unknown
-
2022
- 2022-09-16 US US17/946,101 patent/US20230174522A1/en active Pending
-
2023
- 2023-09-15 JP JP2023149699A patent/JP2023175821A/ja active Pending
- 2023-11-30 AU AU2023274178A patent/AU2023274178A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO2021017504A2 (es) | Derivados de benzisoxazol sulfonamida | |
CL2019000368A1 (es) | Inhibidores de cdk2/4/6. | |
UY38553A (es) | Inhibidores de cdk2 | |
DOP2020000191A (es) | Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de cinasa dependientes de ciclina | |
CL2021001190A1 (es) | Compuestos de azalactam como inhibidores de hpk1 | |
UY37900A (es) | Nuevos derivados de rapamicina | |
UY35845A (es) | ?derivados de purina?. | |
CL2022003007A1 (es) | Compuestos de azalactama como inhibidores de hpk1 | |
ECSP22038509A (es) | Aminas de heteroaril-bifenilo para el tratamiento de enfermedades pd-l1 | |
ECSP22038478A (es) | Heteroaril bifenil amidas para el tratamiento de enfermedades relacionadas con el ligando pd-l1 | |
DOP2023000281A (es) | Inhibidores de mutación de her2 | |
DOP2016000293A (es) | Derivados de diheterociclo enlazado a cicloalquilo | |
UY36074A (es) | ?derivados de dihidropirrolopirimidina? . | |
CO2023012702A2 (es) | Derivados de diazepina útiles en el tratamiento de clostridium difficile | |
CL2023001277A1 (es) | Derivados de pirazol como inhibidores de la ret-cinasa | |
UY39303A (es) | Inhibidores de mutación her2 | |
CU20140033A7 (es) | Derivados de pirrolopirimidina y purina | |
AR122805A1 (es) | Inhibidores de mutación her2 |