CL2023003327A1 - Inhibidores de la interaccion de menina-mll - Google Patents
Inhibidores de la interaccion de menina-mllInfo
- Publication number
- CL2023003327A1 CL2023003327A1 CL2023003327A CL2023003327A CL2023003327A1 CL 2023003327 A1 CL2023003327 A1 CL 2023003327A1 CL 2023003327 A CL2023003327 A CL 2023003327A CL 2023003327 A CL2023003327 A CL 2023003327A CL 2023003327 A1 CL2023003327 A1 CL 2023003327A1
- Authority
- CL
- Chile
- Prior art keywords
- menin
- inhibitors
- mll
- mll interaction
- interaction
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 230000003993 interaction Effects 0.000 title abstract 2
- 101710169972 Menin Proteins 0.000 abstract 1
- 102100030550 Menin Human genes 0.000 abstract 1
- 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
- 102000037865 fusion proteins Human genes 0.000 abstract 1
- 108020001507 fusion proteins Proteins 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La presente invención se refiere a inhibidores de la Fórmula (0), o u estereoisómero de ellos o una sal farmacéuticamente aceptable de ellos, de la interacción de la menina con la MLL y las proteínas de fusión de la MLL, composiciones farmacéuticas que las contienen y su uso en el tratamiento del cáncer y de otras enfermedades
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163188704P | 2021-05-14 | 2021-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2023003327A1 true CL2023003327A1 (es) | 2024-05-03 |
Family
ID=84029448
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2023003327A CL2023003327A1 (es) | 2021-05-14 | 2023-11-08 | Inhibidores de la interaccion de menina-mll |
Country Status (14)
Country | Link |
---|---|
US (1) | US11919901B2 (es) |
EP (1) | EP4337203A1 (es) |
JP (1) | JP2024517945A (es) |
KR (1) | KR20240047338A (es) |
CN (1) | CN117956992A (es) |
AR (1) | AR125866A1 (es) |
AU (1) | AU2022274325A1 (es) |
BR (1) | BR112023023463A2 (es) |
CA (1) | CA3213074A1 (es) |
CL (1) | CL2023003327A1 (es) |
IL (1) | IL308476A (es) |
MX (1) | MX2023013515A (es) |
TW (1) | TW202311262A (es) |
WO (1) | WO2022241265A1 (es) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11919901B2 (en) | 2021-05-14 | 2024-03-05 | Syndax Pharmaceuticals, Inc. | Inhibitors of the menin-MLL interaction |
WO2024046457A1 (en) * | 2022-09-02 | 2024-03-07 | Hutchmed Limited | Triazine compounds and uses thereof |
WO2024110649A1 (en) | 2022-11-24 | 2024-05-30 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors and menin inhibitors for treating cancer |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6124477A (en) | 1996-06-27 | 2000-09-26 | Bioavailability Systems, Llc | Anti-first-pass effect compounds |
US5820915A (en) | 1996-06-27 | 1998-10-13 | Bioavailability Systems, L.L.C. | Method for the preparation of a first-pass effective citrus-derived substance and product thereof |
US5990154A (en) | 1997-05-30 | 1999-11-23 | Bioavailability Systems, L.L.C. | Anti-first-pass effect compounds and citrus extract |
US6248776B1 (en) | 1997-08-26 | 2001-06-19 | Bioavailability Systems, L.L.C. | Anti-first-pass effect compounds |
US20040058982A1 (en) | 1999-02-17 | 2004-03-25 | Bioavailability System, Llc | Pharmaceutical compositions |
US6063809A (en) | 1997-08-26 | 2000-05-16 | Bioavailability Systems, Llc | Anti-first-pass effect compounds |
US5993887A (en) | 1998-06-29 | 1999-11-30 | Bioavailability Systems, L.L.C. | Safe citrus juice and process for preparation |
WO2004037827A1 (en) | 2000-10-20 | 2004-05-06 | Bioavailability Systems, Llc | Synthesis of spiro ortho esters, spiro ortho carbonates, and intermediates |
EP1732891A4 (en) | 2004-03-11 | 2009-05-06 | Sequoia Pharmaceuticals Inc | RESISTANT PREVENTIVE INHIBITORS FOR RETROVIRAL PROTEASES |
EP2422780A1 (en) | 2004-05-07 | 2012-02-29 | Sequoia Pharmaceuticals, Inc. | Resistance-repellent retroviral protease inhibitors |
US20090281114A1 (en) | 2008-05-08 | 2009-11-12 | Fabre-Kramer Pharmaceuticals, Inc. | Indolylalkyl derivatives of pyrimidinylpiperazine and metabolites thereof for treatment of anxiety, depression, and sexual dysfunction |
CL2009001152A1 (es) | 2008-05-13 | 2009-10-16 | Array Biopharma Inc | Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa. |
SG194219A1 (en) | 2011-06-10 | 2013-11-29 | Merck Patent Gmbh | Compositions and methods for the production of pyrimidine and pyridine compounds with btk inhibitory activity |
US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
US9216993B2 (en) | 2013-03-13 | 2015-12-22 | The Regents Of The University Of Michigan | Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof |
WO2015108940A2 (en) | 2014-01-14 | 2015-07-23 | The Trustees Of The University Of Pennsylvania | Tailored combinatorial epigenetic therapies for p53 gain-of-function tumors |
US20170119769A1 (en) | 2014-06-10 | 2017-05-04 | The Trustees Of The University Of Pennsylvania | Scaffolds for inhibitors of menin-mll interactions |
CA2956962A1 (en) | 2014-08-13 | 2016-02-18 | Epizyme, Inc. | Combination therapy for treating cancer |
CN105732636B (zh) | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
RU2018126774A (ru) | 2015-12-22 | 2020-01-23 | Витэ Фармасьютикалз, Инк. | Ингибиторы менин-mll взаимодействия |
EP3407884A4 (en) | 2016-01-26 | 2019-09-11 | Memorial Sloan-Kettering Cancer Center | TARGETING OF CHROMATIN REGULATORS FOR THE INHIBITION OF LEUKEMOGENIC GENE EXPRESSION INNPM1 |
JP7000333B2 (ja) | 2016-03-16 | 2022-02-10 | クラ オンコロジー,インク. | メニン-mllの架橋された二環式阻害剤及びその使用方法 |
EP3454862B1 (en) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
MX2018015252A (es) | 2016-06-10 | 2019-04-25 | Vitae Pharmaceuticals Inc | Inhibidores de la interaccion de menina-leucemia de linaje mixto. |
IL265028B (en) | 2016-09-16 | 2022-09-01 | Vitae Pharmaceuticals Llc | Inhibitors of the menin-mil interaction |
EP3728260A4 (en) | 2017-12-20 | 2021-08-11 | Janssen Pharmaceutica NV | SPIRO EXO-AZA INHIBITORS OF MENIN-MLL INTERACTION |
CN111971286B (zh) | 2018-01-18 | 2023-04-14 | 阿雷生物药品公司 | 作为RET激酶抑制剂的取代的吡咯并[2,3-d]嘧啶化合物 |
BR112020020059A2 (pt) | 2018-03-30 | 2021-03-30 | The Regents Of The University Of Michigan | Compostos de piperidina como inibidores de menin covalentes |
CA3111066A1 (en) | 2018-09-13 | 2020-03-19 | Merck Sharp & Dohme Corp. | Combination therapy of a pd-1 antagonist and lag3 antagonist for treating patients with non-microsatellite instability-high or proficient mismatch repair colorectal cancer |
JP2022503792A (ja) | 2018-09-26 | 2022-01-12 | クラ オンコロジー,インク. | メニン阻害剤を用いた血液悪性腫瘍の処置 |
JP7536767B2 (ja) | 2018-12-31 | 2024-08-20 | バイオメア フュージョン,インコーポレイテッド | メニン-mll相互作用の不可逆的阻害剤 |
EP4132932A4 (en) | 2020-04-07 | 2024-04-17 | Syndax Pharmaceuticals, Inc. | COMBINATIONS OF MENIN INHIBITORS AND CYP3A4 INHIBITORS AND METHODS OF USE THEREOF |
US11919901B2 (en) | 2021-05-14 | 2024-03-05 | Syndax Pharmaceuticals, Inc. | Inhibitors of the menin-MLL interaction |
TW202320796A (zh) | 2021-08-11 | 2023-06-01 | 美商拜歐米富士恩股份有限公司 | 用於糖尿病的menin-mll相互作用之共價抑制劑 |
-
2022
- 2022-05-13 US US17/744,249 patent/US11919901B2/en active Active
- 2022-05-13 AU AU2022274325A patent/AU2022274325A1/en active Pending
- 2022-05-13 JP JP2023569958A patent/JP2024517945A/ja active Pending
- 2022-05-13 EP EP22808443.0A patent/EP4337203A1/en active Pending
- 2022-05-13 TW TW111118095A patent/TW202311262A/zh unknown
- 2022-05-13 MX MX2023013515A patent/MX2023013515A/es unknown
- 2022-05-13 WO PCT/US2022/029271 patent/WO2022241265A1/en active Application Filing
- 2022-05-13 BR BR112023023463A patent/BR112023023463A2/pt unknown
- 2022-05-13 CN CN202280034670.8A patent/CN117956992A/zh active Pending
- 2022-05-13 AR ARP220101276A patent/AR125866A1/es unknown
- 2022-05-13 IL IL308476A patent/IL308476A/en unknown
- 2022-05-13 CA CA3213074A patent/CA3213074A1/en active Pending
- 2022-05-13 KR KR1020237043336A patent/KR20240047338A/ko unknown
-
2023
- 2023-11-08 CL CL2023003327A patent/CL2023003327A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
IL308476A (en) | 2024-01-01 |
AU2022274325A1 (en) | 2023-10-05 |
WO2022241265A1 (en) | 2022-11-17 |
US20230021684A1 (en) | 2023-01-26 |
TW202311262A (zh) | 2023-03-16 |
KR20240047338A (ko) | 2024-04-12 |
CN117956992A (zh) | 2024-04-30 |
US11919901B2 (en) | 2024-03-05 |
EP4337203A1 (en) | 2024-03-20 |
CA3213074A1 (en) | 2022-11-17 |
AR125866A1 (es) | 2023-08-23 |
BR112023023463A2 (pt) | 2024-01-30 |
MX2023013515A (es) | 2024-02-29 |
JP2024517945A (ja) | 2024-04-23 |
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