PE20251399A1 - Derivados de tetrahidrotiazepina biciclicos - Google Patents
Derivados de tetrahidrotiazepina biciclicosInfo
- Publication number
- PE20251399A1 PE20251399A1 PE2024003152A PE2024003152A PE20251399A1 PE 20251399 A1 PE20251399 A1 PE 20251399A1 PE 2024003152 A PE2024003152 A PE 2024003152A PE 2024003152 A PE2024003152 A PE 2024003152A PE 20251399 A1 PE20251399 A1 PE 20251399A1
- Authority
- PE
- Peru
- Prior art keywords
- pharmaceutically acceptable
- compound
- acceptable salt
- optionally substituted
- halogen
- Prior art date
Links
Classifications
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
-
- 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
- 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La presente invencion se refiere a compuesto de formula (I) o una sal farmaceuticamente aceptable de este, en donde Y es S(O), S(O)2, entre otros; R1 es heteroarilo de 5 miembros, en donde R1 se sustituye opcionalmente con uno o mas R10 que pueden ser iguales o diferentes; R10 es -C(R10aR10b)2-S(O)2(R10c); R10a, R10b, R10c, se seleccionan cada uno independientemente de hidrogeno, alquil C1-6, entre otros; R2 se selecciona de hidrogeno y halogeno; R4 se selecciona de aril C5-14 y heteroarilo de 5-14 miembros, en donde R4 se sustituye opcionalmente con uno o mas R11 que pueden ser iguales o diferentes; R11 se selecciona de halogeno; heterociclilo de 3-10 miembros, opcionalmente sustituido con uno o mas haloalquil C1-6, cicloalquil C3-10, entre otros. La invencion tambien se refiere al procedimiento para preparar dicho compuesto o una sal farmaceuticamente aceptable del mismo; a una composicion farmaceutica que comprende el compuesto o una sal farmaceuticamente aceptable de este, junto a un excipiente farmaceuticamente aceptable y, adicionalmente, un agente terapeutico. La administracion a un sujeto de una cantidad terapeuticamente eficaz del compuesto o una sal farmaceuticamente aceptable de este, permite el tratamiento, prevencion y/o retraso de la progresion de un cancer asociado a una senalizacion anomala de diacilglicerol quinasa, como la leucemia linfoide aguda de linfocitos B, la macroglobulinemia de Waldenstrom, entre otros.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP22189817 | 2022-08-11 | ||
| PCT/EP2023/071988 WO2024033388A1 (en) | 2022-08-11 | 2023-08-09 | Bicyclic tetrahydrothiazepine derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20251399A1 true PE20251399A1 (es) | 2025-05-22 |
Family
ID=82898783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2024003152A PE20251399A1 (es) | 2022-08-11 | 2023-08-09 | Derivados de tetrahidrotiazepina biciclicos |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP4568958A1 (es) |
| JP (1) | JP2025526727A (es) |
| KR (1) | KR20250038674A (es) |
| CN (1) | CN119698413A (es) |
| AR (1) | AR130194A1 (es) |
| AU (1) | AU2023322637A1 (es) |
| CL (1) | CL2025000379A1 (es) |
| CO (1) | CO2025001103A2 (es) |
| CR (1) | CR20250042A (es) |
| IL (1) | IL318163A (es) |
| MA (1) | MA71727A (es) |
| MX (1) | MX2025000918A (es) |
| PE (1) | PE20251399A1 (es) |
| TW (1) | TW202417438A (es) |
| WO (1) | WO2024033388A1 (es) |
| ZA (1) | ZA202408363B (es) |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CU22545A1 (es) | 1994-11-18 | 1999-03-31 | Centro Inmunologia Molecular | Obtención de un anticuerpo quimérico y humanizado contra el receptor del factor de crecimiento epidérmico para uso diagnóstico y terapéutico |
| US4943533A (en) | 1984-03-01 | 1990-07-24 | The Regents Of The University Of California | Hybrid cell lines that produce monoclonal antibodies to epidermal growth factor receptor |
| JP2975679B2 (ja) | 1989-09-08 | 1999-11-10 | ザ・ジョーンズ・ホプキンス・ユニバーシティ | ヒト神経膠腫のegf受容体遺伝子の構造変化 |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| EP0659439B1 (en) | 1993-12-24 | 2001-10-24 | MERCK PATENT GmbH | Immunoconjugates |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| US5679683A (en) | 1994-01-25 | 1997-10-21 | Warner-Lambert Company | Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family |
| IL112249A (en) | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
| PL179659B1 (pl) | 1994-07-21 | 2000-10-31 | Akzo Nobel Nv | Kompozycja cyklicznych nadtlenków ketonów sluzaca do modyfikowania (ko)polimerów zwlaszcza do degradacji polipropylenu PL PL PL PL PL PL PL |
| US5804396A (en) | 1994-10-12 | 1998-09-08 | Sugen, Inc. | Assay for agents active in proliferative disorders |
| ATE205483T1 (de) | 1995-03-30 | 2001-09-15 | Pfizer | Chinazolinderivate |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| GB9508565D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quiazoline derivative |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| EP0831880A4 (en) | 1995-06-07 | 2004-12-01 | Imclone Systems Inc | ANTIBODIES AND FRAGMENTS OF ANTIBODIES INHIBITING TUMOR GROWTH |
| HUP9900330A3 (en) | 1995-07-06 | 2001-08-28 | Novartis Ag | Pyrrolopyrimidines and processes for the preparation thereof |
| 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 |
| PT892789E (pt) | 1996-04-12 | 2002-07-31 | Warner Lambert Co | Inibidores irreversiveis de quinases de tirosina |
| AR007857A1 (es) | 1996-07-13 | 1999-11-24 | Glaxo Group Ltd | Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen. |
| ID18494A (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
| US6002008A (en) | 1997-04-03 | 1999-12-14 | American Cyanamid Company | Substituted 3-cyano quinolines |
| UA73073C2 (uk) | 1997-04-03 | 2005-06-15 | Уайт Холдінгз Корпорейшн | Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція |
| US6235883B1 (en) | 1997-05-05 | 2001-05-22 | Abgenix, Inc. | Human monoclonal antibodies to epidermal growth factor receptor |
| DE69815340T2 (de) | 1997-05-06 | 2004-05-06 | Wyeth Holdings Corp. | Verwendung von chinazolin verbindungen zur behandlung von polyzystischer nierenkrankheit |
| ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
| ZA986729B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
| TW436485B (en) | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
| JP2001522802A (ja) | 1997-11-06 | 2001-11-20 | アメリカン・サイアナミド・カンパニー | 大腸ポリープを治療するためのチロシンキナーゼインヒビターとしてのキナゾリン誘導体の使用 |
| SK283688B6 (sk) | 1998-11-19 | 2003-12-02 | Warner-Lambert Company | N-[4-(3-chlór-4-fluór-fenylamino)-7-(3-morfolín-4-yl-propoxy)- chinazolín-6-yl]-akrylamid jeho použitie a farmaceutický prípravok na jeho báze |
| TWI380996B (zh) | 2004-09-17 | 2013-01-01 | Hoffmann La Roche | 抗ox40l抗體 |
| JP5238936B2 (ja) | 2005-03-25 | 2013-07-17 | ジーアイティーアール,インク. | Gitr結合分子およびその使用 |
| PL1879573T3 (pl) | 2005-05-10 | 2013-05-31 | Incyte Holdings Corp | Modulatory 2,3-dioksygenazy indoloaminy i sposoby ich zastosowania |
| AU2006265108C1 (en) | 2005-07-01 | 2013-01-17 | E. R. Squibb & Sons, L.L.C. | Human monoclonal antibodies to programmed death ligand 1 (PD-L1) |
| ES2540561T3 (es) | 2005-12-20 | 2015-07-10 | Incyte Corporation | N-hidroxiamidinoheterociclos como moduladores de indolamina 2,3-dioxigenasa |
| JP5319532B2 (ja) | 2006-09-19 | 2013-10-16 | インサイト・コーポレイション | インドールアミン2,3−ジオキシゲナーゼのモジュレーターとしてのn−ヒドロキシアミジノヘテロサイクル |
| CL2007002650A1 (es) | 2006-09-19 | 2008-02-08 | Incyte Corp | Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras. |
| EP1987839A1 (en) | 2007-04-30 | 2008-11-05 | I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale | Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease |
| US8591886B2 (en) | 2007-07-12 | 2013-11-26 | Gitr, Inc. | Combination therapies employing GITR binding molecules |
| EP2044949A1 (en) | 2007-10-05 | 2009-04-08 | Immutep | Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response |
| EP2227233B1 (en) | 2007-11-30 | 2013-02-13 | Newlink Genetics | Ido inhibitors |
| CN103372215B (zh) | 2008-01-03 | 2016-03-09 | 艾克斯-马赛大学 | 抗hiv治疗期间使用的组合物和方法 |
| AR072999A1 (es) | 2008-08-11 | 2010-10-06 | Medarex Inc | Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos |
| SMT202400136T1 (it) | 2008-12-09 | 2024-05-14 | Hoffmann La Roche | Anticorpi anti-pd-l1 e loro uso per potenziare la funzione dei linfociti t |
| US8709424B2 (en) | 2009-09-03 | 2014-04-29 | Merck Sharp & Dohme Corp. | Anti-GITR antibodies |
| CA2778115C (en) | 2009-10-28 | 2016-04-05 | Newlink Genetics Corporation | Imidazole derivatives as ido inhibitors |
| SG10201604336VA (en) | 2010-03-04 | 2016-07-28 | Macrogenics Inc | Antibodies Reactive With B7-H3, Immunologically Active Fragments Thereof And Uses Thereof |
| MX374682B (es) | 2010-09-09 | 2025-03-06 | Pfizer | Moléculas de unión a 4-1bb. |
| NO2694640T3 (es) | 2011-04-15 | 2018-03-17 | ||
| SI2699264T1 (en) | 2011-04-20 | 2018-08-31 | Medimmune Llc | Antibodies and other molecules that bind b7-h1 and pd-1 |
| EA036814B9 (ru) | 2011-11-28 | 2021-12-27 | Мерк Патент Гмбх | Антитело против pd-l1 (варианты), композиция, содержащая это антитело, и их применение |
| UY34887A (es) | 2012-07-02 | 2013-12-31 | Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware | Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos |
| US9394263B2 (en) * | 2012-08-09 | 2016-07-19 | F. Hoffmann-La Roche Ag | Substituted hetero-azepinones |
| EP3265463B1 (en) | 2015-03-02 | 2018-12-19 | Apeiron Biologics AG | Bicyclic tetrahydrothiazepine derivatives useful for the treatment of neoplastic and/or infectious diseases |
| MX2023009379A (es) * | 2021-02-12 | 2023-10-10 | Hoffmann La Roche | Derivados de tetrahidroazepina biciclicos para el tratamiento del cancer. |
-
2023
- 2023-08-09 CN CN202380058973.8A patent/CN119698413A/zh active Pending
- 2023-08-09 EP EP23754298.0A patent/EP4568958A1/en active Pending
- 2023-08-09 KR KR1020257004160A patent/KR20250038674A/ko active Pending
- 2023-08-09 WO PCT/EP2023/071988 patent/WO2024033388A1/en not_active Ceased
- 2023-08-09 PE PE2024003152A patent/PE20251399A1/es unknown
- 2023-08-09 CR CR20250042A patent/CR20250042A/es unknown
- 2023-08-09 AU AU2023322637A patent/AU2023322637A1/en active Pending
- 2023-08-09 IL IL318163A patent/IL318163A/en unknown
- 2023-08-09 MA MA71727A patent/MA71727A/fr unknown
- 2023-08-09 JP JP2025507470A patent/JP2025526727A/ja active Pending
- 2023-08-10 TW TW112130045A patent/TW202417438A/zh unknown
- 2023-08-11 AR ARP230102135A patent/AR130194A1/es unknown
-
2024
- 2024-11-05 ZA ZA2024/08363A patent/ZA202408363B/en unknown
-
2025
- 2025-01-23 MX MX2025000918A patent/MX2025000918A/es unknown
- 2025-01-30 CO CONC2025/0001103A patent/CO2025001103A2/es unknown
- 2025-02-10 CL CL2025000379A patent/CL2025000379A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL318163A (en) | 2025-03-01 |
| MA71727A (fr) | 2025-05-30 |
| MX2025000918A (es) | 2025-03-07 |
| CN119698413A (zh) | 2025-03-25 |
| CR20250042A (es) | 2025-03-25 |
| AU2023322637A1 (en) | 2024-11-14 |
| CO2025001103A2 (es) | 2025-02-13 |
| TW202417438A (zh) | 2024-05-01 |
| EP4568958A1 (en) | 2025-06-18 |
| ZA202408363B (en) | 2025-10-29 |
| WO2024033388A1 (en) | 2024-02-15 |
| KR20250038674A (ko) | 2025-03-19 |
| JP2025526727A (ja) | 2025-08-15 |
| CL2025000379A1 (es) | 2025-04-11 |
| AR130194A1 (es) | 2024-11-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US10947213B1 (en) | TLR7/8 antagonists and uses thereof | |
| PE20230249A1 (es) | Compuestos de heteroarilo biciclicos y usos de estos | |
| PE20191260A1 (es) | Compuestos inhibidores del vih | |
| PE20211655A1 (es) | Compuestos de 6-azabencimidazol sustituidos como inhibidores de hpk1 | |
| PE20200937A1 (es) | Compuestos macrociclicos para tratar enfermedades | |
| PE20240775A1 (es) | Compuestos antivirales | |
| PE20200834A1 (es) | Derivados acetamida de biciclo[1.1.1]pentano sustituidos como moduladores del factor de iniciacion eucariota 2b y composiciones farmaceuticas de las mismas | |
| UY37133A (es) | Derivados de pirazolo[1,5-a]pirazin-4-ilo | |
| AR046297A1 (es) | Inhibidores de la dpp - iv metodos para prepararlos y composiciones farmaceuticas que los contienen como agente activo | |
| DE60331056D1 (de) | 6-11 bicyclische ketolidderivate | |
| PH12019550083A1 (en) | Inhibitors of bruton's tyrosine kinase | |
| CL2023000670A1 (es) | Compuestos heterocíclicos como inhibidores del bromodominio cbp/ep300 | |
| UY39799A (es) | Compuestos de pirrolil–sulfonamida | |
| RU2018106498A (ru) | Производные 5-(N-конденсированный трициклический арил-тетрагидроизохинолин-6-ил) пиридин-3-ил-уксусной кислоты в качестве ингибиторов репликации вируса иммунодефицита человека | |
| MX384072B (es) | Compuesto derivado de pirrolo-piridina, metodo para preparar el mismo y composicion farmaceutica que contiene el mismo como ingrediente activo para la prevencion o el tratamiento de enfermedades relacionadas con la proteina cinasa. | |
| MX2019006942A (es) | Agonistas de receptores de oxitocina no peptidicos. | |
| CL2024001922A1 (es) | Compuesto de indazol y composición farmacéutica | |
| PE20251389A1 (es) | Compuestos de piridinona sustituida como inhibidores de cbl-b | |
| AR042284A1 (es) | Derivados de piperidina, preparacion y composiciones farmaceuticas que las contienen; y uso de los mismos para la fabricacion de medicamentos | |
| PE20251399A1 (es) | Derivados de tetrahidrotiazepina biciclicos | |
| CO2023000854A2 (es) | Nuevo derivado de pirazol | |
| AR051686A1 (es) | Derivados de piridotienopirimidina; composiciones farmaceuticas que los contienen y su empleo en la fabricacion de un medicamento para el tratamiento de enfermedaes mediadas por inhibicion de pde4. | |
| PE20201148A1 (es) | Compuestos biciclicos 5,6-fusionados y composiciones para el tratamiento de enfermedades parasitarias | |
| RU2018106501A (ru) | Производные 5-(N-[6,5]-конденсированный бицикличный арил-тетрагидроизохинолин-6-ил)-пиридин-3-ил-уксусной кислоты в качестве ингибиторов репликации вируса иммунодефицита человека | |
| RU2018103266A (ru) | Производные пиридин-3-ил-уксусной кислоты в качестве ингибиторов репликации вируса иммунодефицита человека |