JP2022509206A - Magl阻害剤による疾病の治療方法 - Google Patents
Magl阻害剤による疾病の治療方法 Download PDFInfo
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- JP2022509206A JP2022509206A JP2021529827A JP2021529827A JP2022509206A JP 2022509206 A JP2022509206 A JP 2022509206A JP 2021529827 A JP2021529827 A JP 2021529827A JP 2021529827 A JP2021529827 A JP 2021529827A JP 2022509206 A JP2022509206 A JP 2022509206A
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- 0 CC(C)C=CCC(*)=C[C@](C)(*)N=*C Chemical compound CC(C)C=CCC(*)=C[C@](C)(*)N=*C 0.000 description 67
- KAUMXIFOBGXMIF-UHFFFAOYSA-N CN(C1)CC2C1COC2 Chemical compound CN(C1)CC2C1COC2 KAUMXIFOBGXMIF-UHFFFAOYSA-N 0.000 description 3
- SNEQGKPWXUJUIG-UHFFFAOYSA-N CN(CC1)CCN1C1CC1 Chemical compound CN(CC1)CCN1C1CC1 SNEQGKPWXUJUIG-UHFFFAOYSA-N 0.000 description 2
- MCBFNYVOJAYSCR-UHFFFAOYSA-N CN1C2COCC1CC2 Chemical compound CN1C2COCC1CC2 MCBFNYVOJAYSCR-UHFFFAOYSA-N 0.000 description 2
- LNJMHEJAYSYZKK-UHFFFAOYSA-N Cc1ncccn1 Chemical compound Cc1ncccn1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 2
- ZEKBKTMMBLWNGK-UHFFFAOYSA-N CC(C)(C)c1nnn[nH]1 Chemical compound CC(C)(C)c1nnn[nH]1 ZEKBKTMMBLWNGK-UHFFFAOYSA-N 0.000 description 1
- AWYOANDNNWXEQT-LNSVPDHHSA-N CC(C)COC(C1C2[IH]C2)C=CC=C1O[C@@H](C1)C[C@@H](C2)[C@H]1CN2C(N(CC1)N=C1C(O)=O)=O Chemical compound CC(C)COC(C1C2[IH]C2)C=CC=C1O[C@@H](C1)C[C@@H](C2)[C@H]1CN2C(N(CC1)N=C1C(O)=O)=O AWYOANDNNWXEQT-LNSVPDHHSA-N 0.000 description 1
- HXAWMZDJHKRLOX-UHFFFAOYSA-N CC(C)N(CC1)CCC1OC Chemical compound CC(C)N(CC1)CCC1OC HXAWMZDJHKRLOX-UHFFFAOYSA-N 0.000 description 1
- OQFWCGBXTIYRKF-UHFFFAOYSA-N CC(C)N1CC(CC2)OC2C1 Chemical compound CC(C)N1CC(CC2)OC2C1 OQFWCGBXTIYRKF-UHFFFAOYSA-N 0.000 description 1
- ZQXGZHHTOWJJLB-JTQLQIEISA-N CC(C)N1C[C@H](CCC2)N2CC1 Chemical compound CC(C)N1C[C@H](CCC2)N2CC1 ZQXGZHHTOWJJLB-JTQLQIEISA-N 0.000 description 1
- IYKCETRGBFKTRU-UHFFFAOYSA-N CC(C)c1nnc[o]1 Chemical compound CC(C)c1nnc[o]1 IYKCETRGBFKTRU-UHFFFAOYSA-N 0.000 description 1
- RFFXUEDBNNOGDO-UHFFFAOYSA-N CC(C)c1nnn[nH]1 Chemical compound CC(C)c1nnn[nH]1 RFFXUEDBNNOGDO-UHFFFAOYSA-N 0.000 description 1
- KHSBHAPEBURECN-COYMHYPVSA-N CC(C1)C(C(O)=O)=NN1C(N1[C@@H](C)CN(Cc2cccc(Oc(cc3)ccc3Cl)c2)CC1)O Chemical compound CC(C1)C(C(O)=O)=NN1C(N1[C@@H](C)CN(Cc2cccc(Oc(cc3)ccc3Cl)c2)CC1)O KHSBHAPEBURECN-COYMHYPVSA-N 0.000 description 1
- JFGXGAPLZJVGNF-IGSZECBISA-N CC(CC(C1)C(C2)[O]2c(cccc2OC)c2Cl)(C2)[C@H]1CN2C([n](cc1)nc1C(O)=O)=O Chemical compound CC(CC(C1)C(C2)[O]2c(cccc2OC)c2Cl)(C2)[C@H]1CN2C([n](cc1)nc1C(O)=O)=O JFGXGAPLZJVGNF-IGSZECBISA-N 0.000 description 1
- UYGVTUDOXLXEGH-GQCTYLIASA-N CC/C(/C)=N/N=N\N Chemical compound CC/C(/C)=N/N=N\N UYGVTUDOXLXEGH-GQCTYLIASA-N 0.000 description 1
- NNWUEBIEOFQMSS-UHFFFAOYSA-N CC1NCCCC1 Chemical compound CC1NCCCC1 NNWUEBIEOFQMSS-UHFFFAOYSA-N 0.000 description 1
- SNALRIFMJPORKB-VIFPVBQESA-N CCN1C[C@H](CCC2)N2CC1 Chemical compound CCN1C[C@H](CCC2)N2CC1 SNALRIFMJPORKB-VIFPVBQESA-N 0.000 description 1
- DHNLWBALDJWTTH-UHFFFAOYSA-N CCc1nnc[o]1 Chemical compound CCc1nnc[o]1 DHNLWBALDJWTTH-UHFFFAOYSA-N 0.000 description 1
- LFHMKODCPPOLIB-UHFFFAOYSA-N CN(CC1)CCC1(F)F Chemical compound CN(CC1)CCC1(F)F LFHMKODCPPOLIB-UHFFFAOYSA-N 0.000 description 1
- YNJUHLCZQTYQIS-UHFFFAOYSA-N CN(CC1)CCC1(F)[F]C Chemical compound CN(CC1)CCC1(F)[F]C YNJUHLCZQTYQIS-UHFFFAOYSA-N 0.000 description 1
- JZTHADLNXYYKRA-UHFFFAOYSA-N CN(CC1)CCC1F Chemical compound CN(CC1)CCC1F JZTHADLNXYYKRA-UHFFFAOYSA-N 0.000 description 1
- KHMVSJKIXGNZTN-UHFFFAOYSA-N CN(CC1)CCC1S(C)(=O)=O Chemical compound CN(CC1)CCC1S(C)(=O)=O KHMVSJKIXGNZTN-UHFFFAOYSA-N 0.000 description 1
- HJUXLQPJJHRLCR-UHFFFAOYSA-N CN1C2=CCC1COC2 Chemical compound CN1C2=CCC1COC2 HJUXLQPJJHRLCR-UHFFFAOYSA-N 0.000 description 1
- XJZDIZQNHVHDKM-UHFFFAOYSA-N CN1CC(CC2)OC2C1 Chemical compound CN1CC(CC2)OC2C1 XJZDIZQNHVHDKM-UHFFFAOYSA-N 0.000 description 1
- SJRJJKPEHAURKC-UHFFFAOYSA-N CN1CCOCC1 Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 1
- XJRPIZCHFSKXPJ-UHFFFAOYSA-N CNCCNC1CC1 Chemical compound CNCCNC1CC1 XJRPIZCHFSKXPJ-UHFFFAOYSA-N 0.000 description 1
- PYKOUNQHZVLMLL-NVHKAFQKSA-N C[C@@H](CN(Cc1cccc(Oc(cc2)ccc2Cl)c1)CC1)N1C(N(CC1C(F)(F)F)N=C1C(O)=O)=C1CC1 Chemical compound C[C@@H](CN(Cc1cccc(Oc(cc2)ccc2Cl)c1)CC1)N1C(N(CC1C(F)(F)F)N=C1C(O)=O)=C1CC1 PYKOUNQHZVLMLL-NVHKAFQKSA-N 0.000 description 1
- DLTHEPWEENQLKV-UHFFFAOYSA-N Cc1cnc2[n]1cccc2 Chemical compound Cc1cnc2[n]1cccc2 DLTHEPWEENQLKV-UHFFFAOYSA-N 0.000 description 1
- VZWOXDYRBDIHMA-UHFFFAOYSA-N Cc1ncc[s]1 Chemical compound Cc1ncc[s]1 VZWOXDYRBDIHMA-UHFFFAOYSA-N 0.000 description 1
- CDDGNGVFPQRJJM-UHFFFAOYSA-N FC1CNCC1 Chemical compound FC1CNCC1 CDDGNGVFPQRJJM-UHFFFAOYSA-N 0.000 description 1
- VLBBFZPUQGSFOX-UHFFFAOYSA-N O=Cc(cc1)n[n]1C(N(CC1)CCC11N(Cc2ccc(C(F)(F)F)cc2N2CCCC2)CCC1)=O Chemical compound O=Cc(cc1)n[n]1C(N(CC1)CCC11N(Cc2ccc(C(F)(F)F)cc2N2CCCC2)CCC1)=O VLBBFZPUQGSFOX-UHFFFAOYSA-N 0.000 description 1
- HDOWRFHMPULYOA-UHFFFAOYSA-N OC1CCNCC1 Chemical compound OC1CCNCC1 HDOWRFHMPULYOA-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
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- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862772554P | 2018-11-28 | 2018-11-28 | |
| US62/772,554 | 2018-11-28 | ||
| PCT/US2019/063451 WO2020112905A1 (en) | 2018-11-28 | 2019-11-26 | Methods of treating disease with magl inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022509206A true JP2022509206A (ja) | 2022-01-20 |
| JP2022509206A5 JP2022509206A5 (https=) | 2022-11-28 |
| JPWO2020112905A5 JPWO2020112905A5 (https=) | 2022-11-28 |
Family
ID=70851863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021529827A Pending JP2022509206A (ja) | 2018-11-28 | 2019-11-26 | Magl阻害剤による疾病の治療方法 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20220031676A1 (https=) |
| EP (1) | EP3886844A4 (https=) |
| JP (1) | JP2022509206A (https=) |
| KR (1) | KR20210097734A (https=) |
| CN (1) | CN113347971A (https=) |
| AU (1) | AU2019389017B2 (https=) |
| BR (1) | BR112020015043A2 (https=) |
| CA (1) | CA3120577A1 (https=) |
| CL (1) | CL2021001363A1 (https=) |
| IL (1) | IL283508A (https=) |
| MA (1) | MA54313A (https=) |
| MX (1) | MX2021006312A (https=) |
| SG (1) | SG11202105320YA (https=) |
| WO (1) | WO2020112905A1 (https=) |
| ZA (1) | ZA202103975B (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK3630744T3 (da) | 2017-05-23 | 2023-03-06 | H Lundbeck As | Pyrazol-magl-inhibitorer |
| US10927105B1 (en) | 2017-05-23 | 2021-02-23 | Lundbeck La Jolla Research Center, Inc. | Pyrazole MAGL inhibitors |
| CN117177744A (zh) | 2021-01-29 | 2023-12-05 | 塞迪拉治疗股份有限公司 | Cdk2抑制剂及其使用方法 |
| MX2023015436A (es) | 2021-06-26 | 2024-02-21 | Cedilla Therapeutics Inc | Inhibidores de cdk2 y metodos de uso de los mismos. |
| WO2023006893A1 (en) | 2021-07-30 | 2023-02-02 | Confo Therapeutics N.V. | Compounds for the treatment of pain, in particular neuropathic pain, and/or other diseases or disorders that are associated with at2r and/or at2r mediated signaling |
| CA3234430A1 (en) * | 2021-11-02 | 2023-05-11 | Samuel George ANDREW | Crystalline forms of a monoacylglycerol lipase inhibitor |
| CA3242372A1 (en) | 2021-12-29 | 2023-07-06 | Psy Therapeutics, Inc. | Inhibiting monoacylglycerol lipase (magl) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017087854A1 (en) * | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
| US20170247387A1 (en) * | 2014-07-25 | 2017-08-31 | Northeastern University | Urea/carbamates faah magl or dual faah/magl inhibitors and uses thereof |
| WO2018134698A1 (en) * | 2017-01-23 | 2018-07-26 | Pfizer Inc. | Heterocyclic spiro compounds as magl inhibitors |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8455476B2 (en) * | 2009-04-22 | 2013-06-04 | Janssen Pharmaceutica, Nv | Azetidinyl diamides as monoacylglycerol lipase inhibitors |
| US10093630B2 (en) * | 2014-05-21 | 2018-10-09 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
| WO2017087858A1 (en) * | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
| KR20170128029A (ko) * | 2016-05-13 | 2017-11-22 | 삼성에스디아이 주식회사 | 태양전지 전극 형성용 조성물 및 이로부터 제조된 전극 |
| DK3630744T3 (da) * | 2017-05-23 | 2023-03-06 | H Lundbeck As | Pyrazol-magl-inhibitorer |
| US10927105B1 (en) * | 2017-05-23 | 2021-02-23 | Lundbeck La Jolla Research Center, Inc. | Pyrazole MAGL inhibitors |
-
2019
- 2019-11-26 KR KR1020217019736A patent/KR20210097734A/ko not_active Ceased
- 2019-11-26 CA CA3120577A patent/CA3120577A1/en active Pending
- 2019-11-26 US US17/296,489 patent/US20220031676A1/en not_active Abandoned
- 2019-11-26 MX MX2021006312A patent/MX2021006312A/es unknown
- 2019-11-26 BR BR112020015043-6A patent/BR112020015043A2/pt unknown
- 2019-11-26 MA MA054313A patent/MA54313A/fr unknown
- 2019-11-26 SG SG11202105320YA patent/SG11202105320YA/en unknown
- 2019-11-26 WO PCT/US2019/063451 patent/WO2020112905A1/en not_active Ceased
- 2019-11-26 EP EP19889241.6A patent/EP3886844A4/en not_active Withdrawn
- 2019-11-26 JP JP2021529827A patent/JP2022509206A/ja active Pending
- 2019-11-26 AU AU2019389017A patent/AU2019389017B2/en not_active Expired - Fee Related
- 2019-11-26 CN CN201980090281.5A patent/CN113347971A/zh active Pending
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2021
- 2021-05-25 CL CL2021001363A patent/CL2021001363A1/es unknown
- 2021-05-27 IL IL283508A patent/IL283508A/en unknown
- 2021-06-09 ZA ZA2021/03975A patent/ZA202103975B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20170247387A1 (en) * | 2014-07-25 | 2017-08-31 | Northeastern University | Urea/carbamates faah magl or dual faah/magl inhibitors and uses thereof |
| WO2017087854A1 (en) * | 2015-11-20 | 2017-05-26 | Abide Therapeutics, Inc. | Pyrazole compounds and methods of making and using same |
| WO2018134698A1 (en) * | 2017-01-23 | 2018-07-26 | Pfizer Inc. | Heterocyclic spiro compounds as magl inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| SG11202105320YA (en) | 2021-06-29 |
| CN113347971A (zh) | 2021-09-03 |
| US20220031676A1 (en) | 2022-02-03 |
| MA54313A (fr) | 2022-03-09 |
| AU2019389017A1 (en) | 2021-06-10 |
| IL283508A (en) | 2021-07-29 |
| WO2020112905A1 (en) | 2020-06-04 |
| CA3120577A1 (en) | 2020-06-04 |
| EP3886844A1 (en) | 2021-10-06 |
| CL2021001363A1 (es) | 2021-11-12 |
| MX2021006312A (es) | 2021-08-11 |
| KR20210097734A (ko) | 2021-08-09 |
| AU2019389017B2 (en) | 2025-01-09 |
| ZA202103975B (en) | 2023-11-29 |
| EP3886844A4 (en) | 2022-08-24 |
| BR112020015043A2 (pt) | 2021-08-31 |
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