JP6991585B2 - メニン阻害剤としてのピペリジン - Google Patents
メニン阻害剤としてのピペリジン Download PDFInfo
- Publication number
- JP6991585B2 JP6991585B2 JP2018557418A JP2018557418A JP6991585B2 JP 6991585 B2 JP6991585 B2 JP 6991585B2 JP 2018557418 A JP2018557418 A JP 2018557418A JP 2018557418 A JP2018557418 A JP 2018557418A JP 6991585 B2 JP6991585 B2 JP 6991585B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl
- optionally substituted
- pharmaceutically acceptable
- cancer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 0 CC(C)C(C)NC(C)* Chemical compound CC(C)C(C)NC(C)* 0.000 description 22
- XILPCSMEKCBYFO-UHFFFAOYSA-N C[n]1cnnc1 Chemical compound C[n]1cnnc1 XILPCSMEKCBYFO-UHFFFAOYSA-N 0.000 description 2
- MHFBISFDLRWTLQ-UHFFFAOYSA-N N#CC(C1CCN(Cc2ccccc2)CC1)c1ccccc1 Chemical compound N#CC(C1CCN(Cc2ccccc2)CC1)c1ccccc1 MHFBISFDLRWTLQ-UHFFFAOYSA-N 0.000 description 2
- RTKAORMIRLPJCV-UBFHEZILSA-N N#CC([C@@H](CCC1)[C@H]1O)(C1CCNCC1)c1ccccc1 Chemical compound N#CC([C@@H](CCC1)[C@H]1O)(C1CCNCC1)c1ccccc1 RTKAORMIRLPJCV-UBFHEZILSA-N 0.000 description 2
- BHHGXPLMPWCGHP-UHFFFAOYSA-N NCCc1ccccc1 Chemical compound NCCc1ccccc1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 2
- QKOISEJYYVTTLJ-LVGUHPFSSA-N C/C=C(\C=C/N=C)/S(c(cc1)ccc1N1CC(CN(CC2)CCC2C(C2=CCC[C@@H]2OC(NC)=O)(c2ccccc2)C#N)C1)(=O)=O Chemical compound C/C=C(\C=C/N=C)/S(c(cc1)ccc1N1CC(CN(CC2)CCC2C(C2=CCC[C@@H]2OC(NC)=O)(c2ccccc2)C#N)C1)(=O)=O QKOISEJYYVTTLJ-LVGUHPFSSA-N 0.000 description 1
- CFBNLHMUKNJENC-UHFFFAOYSA-N CC(C)(C)OC(N1C2C1CCC2)=O Chemical compound CC(C)(C)OC(N1C2C1CCC2)=O CFBNLHMUKNJENC-UHFFFAOYSA-N 0.000 description 1
- LYFGHAXJURULLN-FEVNIDIWSA-N CC(C)(C)OC(N[C@@H](CCC1)[C@H]1[C@@](C1CCN(Cc2ccccc2)CC1)(c1ccccc1)C#N)=O Chemical compound CC(C)(C)OC(N[C@@H](CCC1)[C@H]1[C@@](C1CCN(Cc2ccccc2)CC1)(c1ccccc1)C#N)=O LYFGHAXJURULLN-FEVNIDIWSA-N 0.000 description 1
- IOILKZYWNMYWJY-UHFFFAOYSA-N CC(C)c1ncc[n]1C Chemical compound CC(C)c1ncc[n]1C IOILKZYWNMYWJY-UHFFFAOYSA-N 0.000 description 1
- KDISMIMTGUMORD-UHFFFAOYSA-N CC(N1CCCCC1)=O Chemical compound CC(N1CCCCC1)=O KDISMIMTGUMORD-UHFFFAOYSA-N 0.000 description 1
- YSDBJKNOEWSFGA-UHFFFAOYSA-N CC(N1CCN(C)CC1)=O Chemical compound CC(N1CCN(C)CC1)=O YSDBJKNOEWSFGA-UHFFFAOYSA-N 0.000 description 1
- WHTUWYBGTLLCKF-UHFFFAOYSA-N CC(NC1CCN(C)CC1)=O Chemical compound CC(NC1CCN(C)CC1)=O WHTUWYBGTLLCKF-UHFFFAOYSA-N 0.000 description 1
- WCKJDCHROXGPFH-JCEITLPESA-N CC(c1ccc([C@](C2CCN(Cc3ccccc3)CC2)([C@@](C2)(CCC3)[C@@]23NC(OC(C)(C)C)=O)C#N)cc1)S Chemical compound CC(c1ccc([C@](C2CCN(Cc3ccccc3)CC2)([C@@](C2)(CCC3)[C@@]23NC(OC(C)(C)C)=O)C#N)cc1)S WCKJDCHROXGPFH-JCEITLPESA-N 0.000 description 1
- SPCLFRMQZOAHLD-UHFFFAOYSA-N CCC1(CC1)C1(C)CCCC1 Chemical compound CCC1(CC1)C1(C)CCCC1 SPCLFRMQZOAHLD-UHFFFAOYSA-N 0.000 description 1
- XFOKTRRRNKDGNB-UHFFFAOYSA-N CCCC1=C(C(C2CCCC2)(C2CCN(Cc3ccccc3)CC2)N)C=CCC1 Chemical compound CCCC1=C(C(C2CCCC2)(C2CCN(Cc3ccccc3)CC2)N)C=CCC1 XFOKTRRRNKDGNB-UHFFFAOYSA-N 0.000 description 1
- HFAJKGQCFGQDTQ-UHFFFAOYSA-N CCc1ncc[n]1C(C)C Chemical compound CCc1ncc[n]1C(C)C HFAJKGQCFGQDTQ-UHFFFAOYSA-N 0.000 description 1
- GZXCSMZEPVRSLL-KKUQBAQOSA-N CN[C@](CCC1)([C@H]1N)[C@](C1CCN(Cc2ccccc2)CC1)(c1ccccc1)C#N Chemical compound CN[C@](CCC1)([C@H]1N)[C@](C1CCN(Cc2ccccc2)CC1)(c1ccccc1)C#N GZXCSMZEPVRSLL-KKUQBAQOSA-N 0.000 description 1
- NRPFIGRDAIKDCK-UHFFFAOYSA-N CS(C1CCOCC1)(=O)=O Chemical compound CS(C1CCOCC1)(=O)=O NRPFIGRDAIKDCK-UHFFFAOYSA-N 0.000 description 1
- PANWHYHNSGYWAG-UHFFFAOYSA-N CS(CC1CCCCC1)(=O)=O Chemical compound CS(CC1CCCCC1)(=O)=O PANWHYHNSGYWAG-UHFFFAOYSA-N 0.000 description 1
- DSZYFHYERQIEAF-UHFFFAOYSA-N C[n]1c(CC(F)(F)F)nnc1 Chemical compound C[n]1c(CC(F)(F)F)nnc1 DSZYFHYERQIEAF-UHFFFAOYSA-N 0.000 description 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N C[n]1cncc1 Chemical compound C[n]1cncc1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-N Cc1ncc[n]1C Chemical compound Cc1ncc[n]1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 description 1
- XKIHZSIFRKRCKY-SKCDSABHSA-N N#CC(C1CCN(Cc2ccccc2)CC1)(C1=CCC[C@@H]1O)c1ccccc1 Chemical compound N#CC(C1CCN(Cc2ccccc2)CC1)(C1=CCC[C@@H]1O)c1ccccc1 XKIHZSIFRKRCKY-SKCDSABHSA-N 0.000 description 1
- NECGMGJIOIEQNL-KOPQTXDBSA-N N#CC([C@@H](CCC1)[C@H]1O)(C1CCN(CC(C2)CN2c(cc2)ccc2S(c2ccncc2)(=O)=O)CC1)c1ccccc1 Chemical compound N#CC([C@@H](CCC1)[C@H]1O)(C1CCN(CC(C2)CN2c(cc2)ccc2S(c2ccncc2)(=O)=O)CC1)c1ccccc1 NECGMGJIOIEQNL-KOPQTXDBSA-N 0.000 description 1
- WUAHWFBUFSMXMG-LGTSYYJHSA-N N#CC([C@@H](CCC1)[C@H]1O)(C1CCN(CC2CNC2)CC1)c1ccccc1 Chemical compound N#CC([C@@H](CCC1)[C@H]1O)(C1CCN(CC2CNC2)CC1)c1ccccc1 WUAHWFBUFSMXMG-LGTSYYJHSA-N 0.000 description 1
- JWTYDFNVTXWZAZ-AEAWWFNXSA-N N#CC([C@H](CCC1)[C@@H]1O)(C1CCN(Cc2ccccc2)CC1)c1ccccc1 Chemical compound N#CC([C@H](CCC1)[C@@H]1O)(C1CCN(Cc2ccccc2)CC1)c1ccccc1 JWTYDFNVTXWZAZ-AEAWWFNXSA-N 0.000 description 1
- GYGWKIHINPEOAM-UHFFFAOYSA-N O=S(C(F)(F)F)(c(cc1)ccc1F)=O Chemical compound O=S(C(F)(F)F)(c(cc1)ccc1F)=O GYGWKIHINPEOAM-UHFFFAOYSA-N 0.000 description 1
- GVMCBTFAQSEFQY-UHFFFAOYSA-N O=S(c(cc1)ccc1F)(c1ccncc1)=O Chemical compound O=S(c(cc1)ccc1F)(c1ccncc1)=O GVMCBTFAQSEFQY-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- 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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- 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
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/34—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
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)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662330350P | 2016-05-02 | 2016-05-02 | |
| US62/330,350 | 2016-05-02 | ||
| PCT/US2017/030577 WO2017192543A1 (en) | 2016-05-02 | 2017-05-02 | Piperidines as menin inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019514950A JP2019514950A (ja) | 2019-06-06 |
| JP2019514950A5 JP2019514950A5 (enExample) | 2020-06-18 |
| JP6991585B2 true JP6991585B2 (ja) | 2022-01-12 |
Family
ID=58699299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018557418A Expired - Fee Related JP6991585B2 (ja) | 2016-05-02 | 2017-05-02 | メニン阻害剤としてのピペリジン |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US10899738B2 (enExample) |
| EP (1) | EP3452461B1 (enExample) |
| JP (1) | JP6991585B2 (enExample) |
| KR (1) | KR20190015275A (enExample) |
| CN (1) | CN109415337B (enExample) |
| AU (1) | AU2017259436B2 (enExample) |
| BR (1) | BR112018072570A2 (enExample) |
| CA (1) | CA3022868A1 (enExample) |
| ES (1) | ES2899936T3 (enExample) |
| IL (2) | IL262697B (enExample) |
| MX (1) | MX384087B (enExample) |
| SG (1) | SG11201809714TA (enExample) |
| WO (1) | WO2017192543A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2020515571A (ja) * | 2017-03-31 | 2020-05-28 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | 共有結合性メニン阻害剤としてのピペリジン |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE49687E1 (en) | 2014-09-09 | 2023-10-10 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| TWI703150B (zh) | 2015-06-04 | 2020-09-01 | 美商庫拉腫瘤技術股份有限公司 | 用於抑制menin及mll蛋白之交互作用的方法及組合物 |
| HK1246593A1 (zh) | 2015-06-04 | 2018-09-14 | Kura Oncology, Inc. | 用於抑制menin蛋白与mll蛋白的相互作用的方法及组合物 |
| PH12018501955B1 (en) | 2016-03-16 | 2024-01-24 | Kura Oncology Inc | Bridged bicyclic inhibitors of menin-mll and methods of use |
| PL3429591T3 (pl) | 2016-03-16 | 2023-07-17 | Kura Oncology, Inc. | Podstawione pochodne tieno[2,3-d]pirymidyny jako inhibitory meniny-mll i metody ich zastosowania |
| JP6991585B2 (ja) | 2016-05-02 | 2022-01-12 | ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン | メニン阻害剤としてのピペリジン |
| WO2017214367A1 (en) | 2016-06-10 | 2017-12-14 | Vitae Pharmaceuticals, Inc. | Inhibitors of the menin-mll interaction |
| EP3512857B1 (en) | 2016-09-14 | 2021-02-24 | Janssen Pharmaceutica NV | Spiro bicyclic inhibitors of menin-mll interaction |
| CA3033020A1 (en) | 2016-09-14 | 2018-03-22 | Janssen Pharmaceutica Nv | Fused bicyclic inhibitors of menin-mll interaction |
| US12084462B2 (en) | 2016-09-14 | 2024-09-10 | Janssen Pharmaceutica Nv | Spiro bicyclic inhibitors of menin-MLL interaction |
| CN110248946B (zh) | 2016-12-15 | 2023-05-23 | 詹森药业有限公司 | Menin-MLL相互作用的氮杂环庚烷抑制剂 |
| WO2018175746A1 (en) | 2017-03-24 | 2018-09-27 | Kura Oncology, Inc. | Methods for treating hematological malignancies and ewing's sarcoma |
| WO2018226976A1 (en) | 2017-06-08 | 2018-12-13 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with mll proteins |
| EP3684361A4 (en) | 2017-09-20 | 2021-09-08 | Kura Oncology, Inc. | SUBSTITUTED INHIBITORS OF MENIN-MLL AND METHOD OF USING |
| US11396517B1 (en) | 2017-12-20 | 2022-07-26 | Janssen Pharmaceutica Nv | Exo-aza spiro inhibitors of menin-MLL interaction |
| JP7307729B2 (ja) | 2017-12-20 | 2023-07-12 | ヤンセン ファーマシューティカ エヌ.ベー. | メニン-mll相互作用のエキソ-アザスピロ阻害剤 |
| EP3774731A4 (en) * | 2018-03-30 | 2021-11-24 | The Regents Of The University Of Michigan | PIPERIDINE COMPOUNDS AS COVALENT MENINE INHIBITORS |
| US11325921B2 (en) | 2018-03-30 | 2022-05-10 | Sumitomo Dainippon Pharma Co., Ltd. | Optically active crosslinked cyclic secondary amine derivative |
| 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 |
| CA3112340A1 (en) * | 2018-10-03 | 2020-04-09 | The Regents Of The University Of Michigan | Small molecule menin inhibitors |
| US11174263B2 (en) | 2018-12-31 | 2021-11-16 | Biomea Fusion, Inc. | Inhibitors of menin-MLL interaction |
| SG11202106304RA (en) * | 2018-12-31 | 2021-07-29 | Biomea Fusion Llc | Irreversible inhibitors of menin-mll interaction |
| WO2021067215A1 (en) | 2019-09-30 | 2021-04-08 | Agios Pharmaceuticals, Inc. | Piperidine compounds as menin inhibitors |
| TW202525813A (zh) | 2019-12-19 | 2025-07-01 | 比利時商健生藥品公司 | 經取代之直鏈螺環接衍生物 |
| EP4132932A4 (en) | 2020-04-07 | 2024-04-17 | Syndax Pharmaceuticals, Inc. | COMBINATIONS OF MENIN INHIBITORS AND CYP3A4 INHIBITORS AND METHODS OF USE THEREOF |
| TW202204333A (zh) | 2020-04-08 | 2022-02-01 | 美商阿吉歐斯製藥公司 | Menin抑制劑及治療癌症之使用方法 |
| WO2021207310A1 (en) | 2020-04-08 | 2021-10-14 | Agios Pharmaceuticals, Inc. | Menin inhibitors and methods of use for treating cancer |
| US20240417405A1 (en) | 2021-05-08 | 2024-12-19 | Janssen Pharmaceutica Nv | Substituted Spiro Derivatives |
| CA3215379A1 (en) | 2021-05-08 | 2022-11-17 | Olivier Alexis Georges Querolle | Substituted spiro derivatives |
| US20240238291A1 (en) * | 2021-05-12 | 2024-07-18 | Syndax Pharmaceuticals, Inc. | Combinations for treatment of cancer |
| IL308862A (en) | 2021-06-01 | 2024-01-01 | Janssen Pharmaceutica Nv | Altered phenyl-1H-pyrrolo[3,2-c]pyridine histories |
| JP2024521902A (ja) | 2021-06-03 | 2024-06-04 | ヤンセン ファーマシューティカ エヌ.ベー. | スピロ環状アミンで置換されたピリダジン又は1,2,4-トリアジン |
| WO2022262796A1 (en) | 2021-06-17 | 2022-12-22 | Janssen Pharmaceutica Nv | (r)-n-ethyl-5-fluoro-n-isopropyl-2-((5-(2-(6-((2-methoxyethyl)(methyl)amino)-2-m ethylhexan-3-yl)-2,6-diazaspiro[3.4]octan-6-yl)-1,2,4-triazin-6-yl)oxy)benzamide besylate salt for the treatment of diseases such as cancer |
| 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 |
| US12018032B2 (en) | 2021-08-20 | 2024-06-25 | Biomea Fusion, Inc. | Crystalline forms of N-[4-[4-(4-morpholinyl)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]phenyl]-4-[[3(r)-[(1-oxo-2-propen-1-yl)amino]-1-piperidinyl]methyl]-2-pyridinecarboxamide as an irreversible inhibitor of menin-MLL interaction |
| WO2023056589A1 (en) | 2021-10-08 | 2023-04-13 | Servier Pharmaceuticals Llc | Menin inhibitors and methods of use for treating cancer |
| WO2023225005A1 (en) * | 2022-05-17 | 2023-11-23 | Biomea Fusion, Inc. | Flt3 combination therapy for cancer and compositions therefor |
| CN120529900A (zh) | 2022-11-24 | 2025-08-22 | 奥莱松基因组股份有限公司 | 用于治疗癌症的LSD1抑制剂和Menin抑制剂的组合 |
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| JP2020515571A (ja) * | 2017-03-31 | 2020-05-28 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | 共有結合性メニン阻害剤としてのピペリジン |
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| IL281182A (en) | 2021-04-29 |
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| AU2017259436A1 (en) | 2018-12-20 |
| US20190152947A1 (en) | 2019-05-23 |
| SG11201809714TA (en) | 2018-11-29 |
| WO2017192543A1 (en) | 2017-11-09 |
| CN109415337A (zh) | 2019-03-01 |
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