MX2019009653A - Inhibidores de mnk sustituidos con piperidina y metodos relacionados con los mismos. - Google Patents
Inhibidores de mnk sustituidos con piperidina y metodos relacionados con los mismos.Info
- Publication number
- MX2019009653A MX2019009653A MX2019009653A MX2019009653A MX2019009653A MX 2019009653 A MX2019009653 A MX 2019009653A MX 2019009653 A MX2019009653 A MX 2019009653A MX 2019009653 A MX2019009653 A MX 2019009653A MX 2019009653 A MX2019009653 A MX 2019009653A
- Authority
- MX
- Mexico
- Prior art keywords
- formula
- piperidine
- substituted
- methods related
- compounds
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/20—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Epidemiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
La presente invención se refiere a compuestos de acuerdo con la Fórmula (I): VER FORMULA (I), o un estereoisómero, tautómero o una sal farmacéuticamente aceptable del mismo en el que X1, X2, R1, R2, R3 y n son como se definen en el presente documento; también se describen composiciones farmacéuticamente aceptables de compuestos de la Fórmula (I), así como métodos para utilizar los compuestos de la Fórmula (I) y las composiciones farmacéuticamente aceptables de compuestos de la Fórmula (I) como inhibidores de Mnk, así como productos terapéuticos para el tratamiento de enfermedades tales como cáncer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762458671P | 2017-02-14 | 2017-02-14 | |
| PCT/US2018/018022 WO2018152117A1 (en) | 2017-02-14 | 2018-02-13 | Piperidine-substituted mnk inhibitors and methods related thereto |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2019009653A true MX2019009653A (es) | 2019-12-19 |
| MX394700B MX394700B (es) | 2025-03-24 |
Family
ID=63106539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2019009653A MX394700B (es) | 2017-02-14 | 2018-02-13 | Inhibidores de mnk sustituidos con piperidina y métodos relacionados con los mismos. |
Country Status (22)
| Country | Link |
|---|---|
| US (3) | US20180228803A1 (es) |
| EP (1) | EP3582776B1 (es) |
| JP (2) | JP2020507588A (es) |
| KR (1) | KR20190117013A (es) |
| CN (1) | CN110719781A (es) |
| AU (2) | AU2018220840A1 (es) |
| BR (1) | BR112019016707A2 (es) |
| CA (1) | CA3053493A1 (es) |
| CL (1) | CL2019002297A1 (es) |
| CO (1) | CO2019009423A2 (es) |
| DK (1) | DK3582776T3 (es) |
| EA (1) | EA201991894A1 (es) |
| ES (1) | ES2969988T3 (es) |
| FI (1) | FI3582776T3 (es) |
| IL (1) | IL268619B (es) |
| MX (1) | MX394700B (es) |
| MY (1) | MY199730A (es) |
| PE (1) | PE20191349A1 (es) |
| PH (1) | PH12019550140A1 (es) |
| SG (1) | SG11201907356SA (es) |
| TW (1) | TWI762579B (es) |
| WO (1) | WO2018152117A1 (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA201991894A1 (ru) | 2017-02-14 | 2020-02-05 | Эффектор Терапьютикс, Инк. | ПИПЕРИДИН-ЗАМЕЩЕННЫЕ ИНГИБИТОРЫ Mnk И СВЯЗАННЫЕ С НИМИ СПОСОБЫ |
| JP2022505846A (ja) | 2018-10-24 | 2022-01-14 | イーフェクター セラピューティクス， インコーポレイテッド | Ｍｎｋ阻害剤の結晶形態 |
| CN111484494B (zh) * | 2019-01-29 | 2022-09-13 | 诺沃斯达药业(上海)有限公司 | 抑制mnk1和mnk2的多环化合物 |
| AU2020387982B2 (en) | 2019-11-18 | 2023-08-03 | Jumbo Drug Bank Co., Ltd. | Pyrrolotriazine compounds acting as MNK inhibitor |
| EP4200296A1 (en) * | 2020-08-20 | 2023-06-28 | Hepagene Therapeutics (HK) Limited | Mnk inhibitors |
| KR20240004828A (ko) * | 2021-05-08 | 2024-01-11 | 점보 드러그 뱅크 컴퍼니 리미티드 | 피롤로트리아진 화합물의 염 형태, 이의 결정형 및 이의 제조 방법 |
| CN114853756B (zh) * | 2022-03-31 | 2023-03-28 | 武汉九州钰民医药科技有限公司 | 化合物Tomivosertib的制备工艺 |
| CN114736205B (zh) * | 2022-03-31 | 2023-03-03 | 武汉九州钰民医药科技有限公司 | 化合物Tomivosertib的制备方法 |
| CN118785912A (zh) * | 2022-07-19 | 2024-10-15 | 成都嘉葆药银医药科技有限公司 | 一种吡咯并三嗪类化合物在制备抗肿瘤药物中的应用 |
| CN116425750A (zh) * | 2023-02-10 | 2023-07-14 | 诺沃斯达药业(上海)有限公司 | 一种mnk抑制剂化合物的盐、晶体及其制备方法 |
| AU2024265078A1 (en) | 2023-05-04 | 2025-12-11 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| AR133696A1 (es) * | 2023-09-02 | 2025-10-22 | Bristol Myers Squibb Co | Compuestos de fenil oxooxazolil piperidinadiona sustituida |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025137653A1 (en) * | 2023-12-20 | 2025-06-26 | Mellicell, Inc. | Methods and compositions of polycyclic and a dual acting nitroxide compounds for treatment of fat cell associated diseases |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5491144A (en) | 1991-05-30 | 1996-02-13 | Ciba-Geigy Corporation | Substituted diaminophthalimides and analogues |
| ATE360422T1 (de) | 2001-06-05 | 2007-05-15 | Lilly Icos Llc | Tetrazyklische verbindungen als pde5-inhibitoren |
| ES2359233T3 (es) | 2001-10-29 | 2011-05-19 | Boehringer Ingelheim International Gmbh | Proteínas homólogas de la quinasa mnk implicadas en la regulación de la homeostasis energética y en el metabolismo organular. |
| US20050012622A1 (en) | 2003-05-19 | 2005-01-20 | Sutton William R. | Monitoring and control of sleep cycles |
| TWI301760B (en) | 2004-02-27 | 2008-10-11 | Merz Pharma Gmbh & Co Kgaa | Tetrahydroquinolinones and their use as antagonists of metabotropic glutamate receptors |
| US7488745B2 (en) | 2004-07-16 | 2009-02-10 | Schering Corporation | Compounds for the treatment of inflammatory disorders |
| TW200613272A (en) | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
| WO2006135783A2 (en) | 2005-06-10 | 2006-12-21 | Wisconsin Alumni Research Foundation | Compositions and methods for modulating angiogenesis |
| CN101309905A (zh) | 2005-08-12 | 2008-11-19 | 阿斯利康(瑞典)有限公司 | 取代的异吲哚酮及其作为代谢型谷氨酸受体增效剂的用途 |
| ES2340093T3 (es) | 2006-06-22 | 2010-05-28 | Biovitrum Ab (Publ) | Derivados pirazina y piridina como inhibidores de cinasa mnk. |
| EP1889847A1 (en) | 2006-07-10 | 2008-02-20 | DeveloGen Aktiengesellschaft | Pyrrolopyrimidines for pharmaceutical compositions |
| DK2134689T3 (da) | 2007-03-16 | 2014-06-30 | Scripps Research Inst | Inhibitorer af fokal adhæsionskinase |
| GB0706072D0 (en) | 2007-03-28 | 2007-05-09 | Sterix Ltd | Compound |
| US20100247517A1 (en) | 2007-11-22 | 2010-09-30 | Boehringer Ingelheim Internationational GmbH | Use of mnk inhibitors for the treatment of alzheimer's disease |
| JP2009173629A (ja) | 2007-12-21 | 2009-08-06 | Banyu Pharmaceut Co Ltd | Ｒｓｋ１阻害作用を有する新規スピロインダン誘導体 |
| WO2009112445A1 (en) | 2008-03-10 | 2009-09-17 | Novartis Ag | Method of increasing cellular phosphatidyl choline by dgat1 inhibition |
| NZ591113A (en) * | 2008-08-26 | 2012-07-27 | Boehringer Ingelheim Int | Thienopyrimidine linked to phenyl or pyridine via an nh amine for pharmaceutical compositions |
| WO2010055072A2 (en) | 2008-11-12 | 2010-05-20 | Novartis Forschungsstiftung, Zweigniederlassung, Friedrich Miescher Institute For Biomedical Research | Treating cancer by modulating a mnk |
| US8637525B2 (en) | 2009-07-31 | 2014-01-28 | Bristol-Myers Squibb Company | Compounds for the reduction of beta-amyloid production |
| TWI468402B (zh) | 2009-07-31 | 2015-01-11 | 必治妥美雅史谷比公司 | 降低β－類澱粉生成之化合物 |
| WO2011017296A1 (en) | 2009-08-04 | 2011-02-10 | Schering Corporation | 4, 5, 6-trisubstituted pyrimidine derivatives as factor ixa inhibitors |
| US8604217B2 (en) | 2009-11-12 | 2013-12-10 | Selvita S.A. | Compound, a process for its preparation, a pharmaceutical composition, use of a compound, a method for modulating or regulating serine/threonine kinases and a serine/threonine kinases modulating agent |
| WO2011106168A1 (en) | 2010-02-24 | 2011-09-01 | Dcam Pharma Inc | Purine compounds for treating autoimmune and demyelinating diseases |
| AU2011310532B2 (en) | 2010-10-01 | 2016-01-14 | Bayer Intellectual Property Gmbh | Substituted N-(2-arylamino)aryl sulfonamide-containing combinations |
| CA2818853A1 (en) | 2010-11-30 | 2012-06-07 | Gilead Pharmasset Llc | 2'-spirocyclo-nucleosides for use in therapy of hcv or dengue virus |
| US9938269B2 (en) | 2011-06-30 | 2018-04-10 | Abbvie Inc. | Inhibitor compounds of phosphodiesterase type 10A |
| US9447087B2 (en) | 2011-09-23 | 2016-09-20 | University Of Utah Research Foundation | Galactokinase inhibitors for the treatment and prevention of associated diseases and disorders |
| US9156852B2 (en) | 2011-12-30 | 2015-10-13 | Hanmi Pharm. Co., Ltd | Thieno[3,2-D]pyrimidine derivatives having inhibitory activity for protein kinases |
| WO2013148748A1 (en) | 2012-03-29 | 2013-10-03 | Francis Xavier Tavares | Lactam kinase inhibitors |
| GB201205669D0 (en) | 2012-03-30 | 2012-05-16 | Agency Science Tech & Res | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
| US10280168B2 (en) | 2012-03-30 | 2019-05-07 | Agency For Science, Technology And Research | Bicyclic heteroaryl derivatives as MNK1 and MNK2 modulators and uses thereof |
| WO2013151975A1 (en) | 2012-04-02 | 2013-10-10 | Northeastern University | Compositions and methods for the inhibition of methyltransferases |
| CA2873971A1 (en) | 2012-05-21 | 2013-11-28 | Bayer Pharma Aktiengesellschaft | Substituted pyrrolopyrimidines |
| TW201412740A (zh) | 2012-09-20 | 2014-04-01 | Bayer Pharma AG | 經取代之吡咯并嘧啶胺基苯并噻唑酮 |
| EP2917185B1 (en) | 2012-11-09 | 2017-05-10 | Evotec International GmbH | Sulfoximine substituted quinazolines for pharmaceutical compositions |
| GB2508652A (en) | 2012-12-07 | 2014-06-11 | Agency Science Tech & Res | Heterocyclic piperazine derivatives |
| WO2014099941A1 (en) | 2012-12-19 | 2014-06-26 | Idenix Pharmaceuticals, Inc. | 4'-fluoro nucleosides for the treatment of hcv |
| CA2901527A1 (en) | 2013-02-20 | 2014-08-28 | Bayer Pharma Aktiengesellschaft | Substituted-imidazo[1,2-b]pyridazines as mknk1 inhibitors |
| TW201605867A (zh) | 2013-11-20 | 2016-02-16 | 拜耳製藥公司 | 噻吩并嘧啶 |
| TWI713455B (zh) * | 2014-06-25 | 2020-12-21 | 美商伊凡克特治療公司 | ＭｎＫ抑制劑及其相關方法 |
| KR20170095985A (ko) | 2014-12-19 | 2017-08-23 | 바이엘 파마 악티엔게젤샤프트 | Mknk1 및 mknk2 억제제로서의 피라졸로피리딘아민 |
| CA2982984C (en) * | 2015-04-20 | 2023-10-17 | Effector Therapeutics, Inc. | Inhibitors of immune checkpoint modulators for use in treating cancer and infections |
| EP3368533A1 (en) | 2015-10-29 | 2018-09-05 | Effector Therapeutics Inc. | Pyrrolo-, pyrazolo-, imidazo-pyrimidine and pyridine compounds that inhibit mnk1 and mnk2 |
| EP3368530A1 (en) | 2015-10-29 | 2018-09-05 | Effector Therapeutics Inc. | Isoindoline, azaisoindoline, dihydroindenone and dihydroazaindenone inhibitors of mnk1 and mnk2 |
| US10000487B2 (en) | 2015-11-20 | 2018-06-19 | Effector Therapeutics, Inc. | Heterocyclic compounds that inhibit the kinase activity of Mnk useful for treating various cancers |
| GB201520499D0 (en) | 2015-11-20 | 2016-01-06 | Medical Res Council Technology | Compounds |
| GB201520500D0 (en) | 2015-11-20 | 2016-01-06 | Medical Res Council Technology | Compounds |
| WO2017117052A1 (en) | 2015-12-31 | 2017-07-06 | Effector Therapeutics, Inc. | Mnk biomarkers and uses thereof |
| TWI808067B (zh) * | 2016-12-19 | 2023-07-11 | 美商雅酶股份有限公司 | 作為ehmt2抑制劑之胺取代的雜環化合物及其使用方法 |
| EA201991894A1 (ru) | 2017-02-14 | 2020-02-05 | Эффектор Терапьютикс, Инк. | ПИПЕРИДИН-ЗАМЕЩЕННЫЕ ИНГИБИТОРЫ Mnk И СВЯЗАННЫЕ С НИМИ СПОСОБЫ |
| US10780119B2 (en) | 2017-05-24 | 2020-09-22 | Effector Therapeutics Inc. | Methods and compositions for cellular immunotherapy |
| WO2019099838A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
| US20200297696A1 (en) | 2017-11-21 | 2020-09-24 | Saint Louis University | P38 inhibitors for the treatment of fshd |
| JP2022505846A (ja) | 2018-10-24 | 2022-01-14 | イーフェクター セラピューティクス， インコーポレイテッド | Ｍｎｋ阻害剤の結晶形態 |
-
2018
- 2018-02-13 EA EA201991894A patent/EA201991894A1/ru unknown
- 2018-02-13 ES ES18754330T patent/ES2969988T3/es active Active
- 2018-02-13 PE PE2019001676A patent/PE20191349A1/es unknown
- 2018-02-13 US US15/895,523 patent/US20180228803A1/en not_active Abandoned
- 2018-02-13 MY MYPI2019004638A patent/MY199730A/en unknown
- 2018-02-13 SG SG11201907356SA patent/SG11201907356SA/en unknown
- 2018-02-13 BR BR112019016707A patent/BR112019016707A2/pt not_active Application Discontinuation
- 2018-02-13 TW TW107105327A patent/TWI762579B/zh active
- 2018-02-13 KR KR1020197026790A patent/KR20190117013A/ko not_active Ceased
- 2018-02-13 CN CN201880011685.6A patent/CN110719781A/zh active Pending
- 2018-02-13 WO PCT/US2018/018022 patent/WO2018152117A1/en not_active Ceased
- 2018-02-13 MX MX2019009653A patent/MX394700B/es unknown
- 2018-02-13 CA CA3053493A patent/CA3053493A1/en active Pending
- 2018-02-13 FI FIEP18754330.1T patent/FI3582776T3/fi active
- 2018-02-13 JP JP2019543809A patent/JP2020507588A/ja active Pending
- 2018-02-13 DK DK18754330.1T patent/DK3582776T3/da active
- 2018-02-13 AU AU2018220840A patent/AU2018220840A1/en not_active Abandoned
- 2018-02-13 EP EP18754330.1A patent/EP3582776B1/en active Active
- 2018-12-27 US US16/233,507 patent/US11083727B2/en not_active Expired - Fee Related
-
2019
- 2019-08-09 PH PH12019550140A patent/PH12019550140A1/en unknown
- 2019-08-11 IL IL268619A patent/IL268619B/en unknown
- 2019-08-13 CL CL2019002297A patent/CL2019002297A1/es unknown
- 2019-08-29 CO CONC2019/0009423A patent/CO2019009423A2/es unknown
-
2021
- 2021-08-06 US US17/396,187 patent/US11878015B2/en active Active
-
2022
- 2022-04-29 AU AU2022202864A patent/AU2022202864B2/en not_active Ceased
- 2022-09-29 JP JP2022156442A patent/JP2022185050A/ja active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CO2019009423A2 (es) | Inhibidores de mnk sustituidos con piperidina y métodos relacionados con los mismos | |
| CO2017000399A2 (es) | Inhibidores de cinasa de interacción con proteína cinasa activada por mitógeno (mnk) y métodos relacionados con los mismos | |
| CL2019002204A1 (es) | Compuestos inhibidores del vih. | |
| MX2021005898A (es) | Terapia de combinacion que incluye un inhibidor de krasg12c y uno o mas agentes farmaceuticamente activos adicionales para el tratamiento de canceres. | |
| MX2019010541A (es) | Compuestos de imidazo-piperidina fusionada como inhibidores de jak. | |
| CL2019000221A1 (es) | Compuestos de tiazolo-piridina sustituida como inhibidores de malt1. | |
| CO2018006475A2 (es) | Compuestos que inhiben eif4a y métodos relacionados a los mismos | |
| NI201600165A (es) | Inhibidores de desmetilasa 1 específica a lisina | |
| MX2016011038A (es) | Compuestos para el tratamiento de trastornos mediados por complemento. | |
| MX2017015211A (es) | Compuestos de naftiridina como inhibidores de quinasa jak. | |
| MX2024008886A (es) | Sulfonamida sustituida con trifluorometilo como inhibidor selectivo de bcl-2. | |
| CU20160111A7 (es) | Compuestos de heterociclilo bicíclico como inhibidores de irak4 | |
| CO2018000589A2 (es) | Oxiesteroles y composiciones farmacéuticas que los contienen | |
| CO2019009722A2 (es) | Dendrímeros terapéuticos | |
| SV2017005381A (es) | Compuestos de imidazopiridazina | |
| MX2020003732A (es) | Derivado de anillo fusionado como inhibidor del receptor a2a. | |
| MX2019008436A (es) | Inhibidores del inmunoproteasoma. | |
| EA201891319A1 (ru) | Соединения алкилдигидрохинолинсульфонамида | |
| CO2018013828A2 (es) | Composiciones farmacéuticas de oligómero de morfolino fósforodiamidato | |
| SV2016005310A (es) | Derivados de diheterociclo enlazado a cicloalquilo | |
| CU20200020A7 (es) | Composición farmacéutica que comprende abx196 | |
| EA201892188A1 (ru) | Соединения пирролотриазина в качестве ингибиторов tam |