JP6936498B2 - 抗アポトーシス性Bcl−2ファミリータンパク質の分解を誘導する化合物及びその使用 - Google Patents
抗アポトーシス性Bcl−2ファミリータンパク質の分解を誘導する化合物及びその使用 Download PDFInfo
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- JP6936498B2 JP6936498B2 JP2018555177A JP2018555177A JP6936498B2 JP 6936498 B2 JP6936498 B2 JP 6936498B2 JP 2018555177 A JP2018555177 A JP 2018555177A JP 2018555177 A JP2018555177 A JP 2018555177A JP 6936498 B2 JP6936498 B2 JP 6936498B2
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- 0 C*C(N[C@@](C(C)(C)C)C(N(C[C@@](C1)O)[C@@]1C(NCc(cc1)ccc1-c1c(C)nc[s]1)=O)=O)=O Chemical compound C*C(N[C@@](C(C)(C)C)C(N(C[C@@](C1)O)[C@@]1C(NCc(cc1)ccc1-c1c(C)nc[s]1)=O)=O)=O 0.000 description 19
- BTODVRFBCGOZGM-UHFFFAOYSA-N CC(C)Nc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O Chemical compound CC(C)Nc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O BTODVRFBCGOZGM-UHFFFAOYSA-N 0.000 description 6
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- SJMJNYOGTSLBHK-UHFFFAOYSA-N CC(CCC1C2=C1)=C2c(cc1)ccc1Cl Chemical compound CC(CCC1C2=C1)=C2c(cc1)ccc1Cl SJMJNYOGTSLBHK-UHFFFAOYSA-N 0.000 description 1
- PDTILPPSUGDTPD-UHFFFAOYSA-N CC1(C)CC(c(cc2)ccc2Cl)=C(CN(CC2)CCN2c(cc2)cc(Oc3cnc4[nH]ccc4c3)c2C(NS(c(cc2)cc([N+]([O-])=O)c2NCC2CCNCC2)(=O)=O)=O)CC1 Chemical compound CC1(C)CC(c(cc2)ccc2Cl)=C(CN(CC2)CCN2c(cc2)cc(Oc3cnc4[nH]ccc4c3)c2C(NS(c(cc2)cc([N+]([O-])=O)c2NCC2CCNCC2)(=O)=O)=O)CC1 PDTILPPSUGDTPD-UHFFFAOYSA-N 0.000 description 1
- DEDUSLXECWIBOP-UHFFFAOYSA-N CCC(CSc1ccccc1)Nc(ccc(S(NC=O)(=O)=O)c1)c1[N+]([O-])=O Chemical compound CCC(CSc1ccccc1)Nc(ccc(S(NC=O)(=O)=O)c1)c1[N+]([O-])=O DEDUSLXECWIBOP-UHFFFAOYSA-N 0.000 description 1
- YUSZWJCZWADDAV-PQRVURBRSA-N CCN(CCN(C)Cc1ccccc1-c(cc1)ccc1Cl)/C(/C1CC1)=C/C=C/C(NS(c(cc1[N+]([O-])=O)ccc1N[C@H](CCN(C)CC(C)=C)CSc1ccccc1)(=O)=O)=O Chemical compound CCN(CCN(C)Cc1ccccc1-c(cc1)ccc1Cl)/C(/C1CC1)=C/C=C/C(NS(c(cc1[N+]([O-])=O)ccc1N[C@H](CCN(C)CC(C)=C)CSc1ccccc1)(=O)=O)=O YUSZWJCZWADDAV-PQRVURBRSA-N 0.000 description 1
- QVCYHOFHQLEWSS-NNYCITFYSA-N CCN(CCN(C)Cc1ccccc1-c(cc1)ccc1Cl)c(cc1)ccc1C(N/S(/c(cc1[N+]([O-])=O)ccc1N[C@H](CCN(CC1)CCN1C(C)C)CSc1ccccc1)=C/C)=O Chemical compound CCN(CCN(C)Cc1ccccc1-c(cc1)ccc1Cl)c(cc1)ccc1C(N/S(/c(cc1[N+]([O-])=O)ccc1N[C@H](CCN(CC1)CCN1C(C)C)CSc1ccccc1)=C/C)=O QVCYHOFHQLEWSS-NNYCITFYSA-N 0.000 description 1
- BSUVNXSGZOFVDR-USYZEHPZSA-N CCNC1CCN(CC[C@H](CSc2ccccc2)Nc(c(S(C(F)(F)F)(=O)=O)c2)ccc2S(Nc(cc2)ccc2N(CC2)CCN2c2cc(F)cc(-c3c(-c(cc4)ccc4Cl)[n](C(C)C)c(C)c3S=O)c2)(=O)=O)CC1 Chemical compound CCNC1CCN(CC[C@H](CSc2ccccc2)Nc(c(S(C(F)(F)F)(=O)=O)c2)ccc2S(Nc(cc2)ccc2N(CC2)CCN2c2cc(F)cc(-c3c(-c(cc4)ccc4Cl)[n](C(C)C)c(C)c3S=O)c2)(=O)=O)CC1 BSUVNXSGZOFVDR-USYZEHPZSA-N 0.000 description 1
- YSWQOCGODHPKED-UHFFFAOYSA-N CN(C(CCC1N(C(c2c3c(N)ccc2)=O)C3=O)=O)C1=O Chemical compound CN(C(CCC1N(C(c2c3c(N)ccc2)=O)C3=O)=O)C1=O YSWQOCGODHPKED-UHFFFAOYSA-N 0.000 description 1
- VIDOWPWTFHJVID-UHFFFAOYSA-N Cc1c(C)[nH]c(C)c1 Chemical compound Cc1c(C)[nH]c(C)c1 VIDOWPWTFHJVID-UHFFFAOYSA-N 0.000 description 1
- WLDYZBODTRKEIC-UHFFFAOYSA-N Cc1c(C2C=CC(Cl)=CC2)cccc1 Chemical compound Cc1c(C2C=CC(Cl)=CC2)cccc1 WLDYZBODTRKEIC-UHFFFAOYSA-N 0.000 description 1
- RQDYUDRHKBUMAQ-UHFFFAOYSA-N Cc1c(C=C)[nH]c(C)c1 Chemical compound Cc1c(C=C)[nH]c(C)c1 RQDYUDRHKBUMAQ-UHFFFAOYSA-N 0.000 description 1
- ALLIZEAXNXSFGD-UHFFFAOYSA-N Cc1ccccc1-c1ccccc1 Chemical compound Cc1ccccc1-c1ccccc1 ALLIZEAXNXSFGD-UHFFFAOYSA-N 0.000 description 1
- DVIAMHFNPKURFJ-UHFFFAOYSA-N ICNC1CCNCC1 Chemical compound ICNC1CCNCC1 DVIAMHFNPKURFJ-UHFFFAOYSA-N 0.000 description 1
- IWCPRLCHJRYTNB-DOZRBHJQSA-O N/C(/COCCOCCOCCNc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)=C\NCCCC(N1CCN(CC[C@H](CSc2ccccc2)Nc(ccc([SH2+])c2)c2S(C(F)(F)F)=O)CC1)=O Chemical compound N/C(/COCCOCCOCCNc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)=C\NCCCC(N1CCN(CC[C@H](CSc2ccccc2)Nc(ccc([SH2+])c2)c2S(C(F)(F)F)=O)CC1)=O IWCPRLCHJRYTNB-DOZRBHJQSA-O 0.000 description 1
- CRAUTELYXAAAPW-UHFFFAOYSA-N O=C(c1cccc(F)c11)N(C(CCC(N2)=O)C2=O)C1=O Chemical compound O=C(c1cccc(F)c11)N(C(CCC(N2)=O)C2=O)C1=O CRAUTELYXAAAPW-UHFFFAOYSA-N 0.000 description 1
- GYVGTEWZTVGKGM-UHFFFAOYSA-N OC(c1c(CCCOc(c(F)c2)ccc2C#CCN2CCNCC2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O Chemical compound OC(c1c(CCCOc(c(F)c2)ccc2C#CCN2CCNCC2)[s]c(N(CCc2ccc3)Cc2c3C(Nc2nc3ccccc3[s]2)=O)n1)=O GYVGTEWZTVGKGM-UHFFFAOYSA-N 0.000 description 1
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- 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
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- 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
- 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
- C07D405/14—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 three or more hetero rings
-
- 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
- C07D471/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662325856P | 2016-04-21 | 2016-04-21 | |
| US62/325,856 | 2016-04-21 | ||
| PCT/US2017/028875 WO2017184995A1 (en) | 2016-04-21 | 2017-04-21 | Compounds that induce degradation of anti-apoptotic bcl-2 family proteins and the uses thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019514877A JP2019514877A (ja) | 2019-06-06 |
| JP2019514877A5 JP2019514877A5 (https=) | 2020-06-11 |
| JP6936498B2 true JP6936498B2 (ja) | 2021-09-15 |
Family
ID=60116391
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018555177A Active JP6936498B2 (ja) | 2016-04-21 | 2017-04-21 | 抗アポトーシス性Bcl−2ファミリータンパク質の分解を誘導する化合物及びその使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10807977B2 (https=) |
| EP (1) | EP3445452A4 (https=) |
| JP (1) | JP6936498B2 (https=) |
| KR (1) | KR102447884B1 (https=) |
| CN (1) | CN109152933B (https=) |
| AU (1) | AU2017254687B2 (https=) |
| WO (2) | WO2017184995A1 (https=) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3139942B1 (en) | 2014-05-05 | 2019-12-18 | Bioventures, Llc | COMPOSITIONS AND METHODS FOR INHIBITING ANTIAPOPTOTIC Bcl-2 PROTEINS AS ANTI-AGING AGENTS |
| WO2016014625A1 (en) | 2014-07-22 | 2016-01-28 | Board Of Trustees Of The University Of Arkansas | Compositions and methods for selectively depleting senescent cells |
| CN109152933B (zh) * | 2016-04-21 | 2022-12-02 | 生物风险投资有限责任公司 | 诱导抗细胞凋亡bcl-2家族蛋白的降解的化合物及其用途 |
| CN110506039A (zh) | 2016-10-11 | 2019-11-26 | 阿尔维纳斯股份有限公司 | 用于雄激素受体靶向降解的化合物和方法 |
| MX2019005007A (es) | 2016-11-01 | 2019-07-18 | Arvinas Inc | Protac dirigidos a la proteína tau y métodos asociados de uso. |
| EP4467143B1 (en) | 2017-07-10 | 2026-03-11 | Celgene Corporation | Method for preparing 4-(4-(4-(((2-(2,6-dioxopiperidin-3-yl)-l-oxoisoindolin-4-yl)oxy)methyl)benzyl)piperazin-l-yl)-3-fluorobenzonitrile |
| KR20200108301A (ko) | 2018-01-10 | 2020-09-17 | 리커리엄 아이피 홀딩스, 엘엘씨 | 벤즈아미드 화합물 |
| ES3041854T3 (en) * | 2018-01-22 | 2025-11-17 | Bioventures Llc | Bcl-2 proteins degraders for cancer treatment |
| US12539292B2 (en) | 2018-04-01 | 2026-02-03 | Arvinas Operations, Inc. | BRM targeting compounds and associated methods of use |
| US12084423B2 (en) | 2018-05-18 | 2024-09-10 | Bioventures, Llc | Piperlongumine analogues and uses thereof |
| WO2019218904A1 (zh) * | 2018-05-18 | 2019-11-21 | 四川科伦博泰生物医药股份有限公司 | 非天然氨基酸类衍生物、其制备方法及用途 |
| US11026963B2 (en) * | 2018-07-11 | 2021-06-08 | Rubedo Life Sciences, Inc. | Senolytic compositions and uses thereof |
| CN113660937A (zh) * | 2019-02-08 | 2021-11-16 | 佛罗里达大学研究基金公司 | 治疗剂和治疗方法 |
| AU2020310147A1 (en) * | 2019-07-10 | 2022-01-06 | Recurium Ip Holdings, Llc | Bcl-2 protein inhibitors |
| EP3999182A1 (en) * | 2019-07-17 | 2022-05-25 | Arvinas Operations, Inc. | Tau-protein targeting compounds and associated methods of use |
| JP7502425B2 (ja) * | 2019-10-01 | 2024-06-18 | アルヴィナス・オペレーションズ・インコーポレイテッド | Brm標的化化合物および関連使用方法 |
| CN112707900B (zh) * | 2019-10-24 | 2022-06-10 | 上海科技大学 | 蛋白降解剂及其在疾病治疗中的应用 |
| WO2021126973A1 (en) * | 2019-12-17 | 2021-06-24 | Orionis Biosciences, Inc. | Compounds modulating protein recruitment and/or degradation |
| US12441722B2 (en) | 2020-01-15 | 2025-10-14 | University Of Florida Research Foundation, Incorporated | Therapeutic agents and methods of treatment |
| US20230128137A1 (en) * | 2020-03-12 | 2023-04-27 | Medshine Discovery Inc. | Benzo five-membered cyclic compound |
| US20230167105A1 (en) * | 2020-04-28 | 2023-06-01 | Recurium Ip Holdings, Llc | Bcl-2 protein inhibitors |
| CR20220630A (es) | 2020-05-09 | 2023-01-23 | Arvinas Operations Inc | Métodos para fabricar un compuesto bifuncional, formas ultrapuras del compuesto bifuncional y formas de dosificación que comprenden el mismo |
| AU2022207648A1 (en) | 2021-01-13 | 2023-07-27 | Monte Rosa Therapeutics Ag | Isoindolinone compounds |
| JP2024505562A (ja) | 2021-02-02 | 2024-02-06 | レス ラボラトイレス セルビエル | 選択的bcl-xl protac化合物及び使用の方法 |
| KR20240020735A (ko) | 2021-05-07 | 2024-02-15 | 카이메라 쎄라퓨틱스 인코포레이티드 | Cdk2 분해제 및 그 용도 |
| WO2022255888A1 (en) * | 2021-06-01 | 2022-12-08 | Captor Therapeutics S.A. | Targeted protein degradation using bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
| JP2024534223A (ja) * | 2021-09-01 | 2024-09-18 | シーザン ハイスーク ファーマシューティカル カンパニー リミテッド | Bcl-2ファミリータンパク質を分解する化合物及びその医薬的な応用 |
| US20250197387A1 (en) * | 2021-09-17 | 2025-06-19 | Kymera Therapeutics, Inc. | Bcl-xl degraders and uses thereof |
| US20250136593A1 (en) * | 2021-11-17 | 2025-05-01 | Hitgen Inc. | Degradation agent and use thereof |
| JP7825122B2 (ja) * | 2022-01-04 | 2026-03-06 | 上海科技大学 | Bcl-2ファミリータンパク質リガンド化合物に基づいて開発したタンパク質分解剤及びそれらの応用 |
| WO2023205802A2 (en) * | 2022-04-22 | 2023-10-26 | Sens Research Foundation | Senolytic targets of senescent cells |
| WO2023215449A1 (en) | 2022-05-06 | 2023-11-09 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-xl degraders |
| EP4519259A1 (en) | 2022-05-06 | 2025-03-12 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-xl degraders |
| EP4519260A1 (en) | 2022-05-06 | 2025-03-12 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-xdegraders |
| TW202402272A (zh) * | 2022-07-12 | 2024-01-16 | 中國商正大天晴藥業集團股份有限公司 | 含有三氟甲基基團的化合物 |
| EP4565236A1 (en) * | 2022-08-02 | 2025-06-11 | Beijing Neox Biotech Limited | Bcl-xl degrading compounds |
| CN115141198A (zh) * | 2022-09-01 | 2022-10-04 | 上海睿跃生物科技有限公司 | 降解蛋白的化合物及其应用和药物 |
| WO2024051741A1 (zh) * | 2022-09-06 | 2024-03-14 | 西藏海思科制药有限公司 | 一种抑制Bcl-2或Bcl-xL的化合物及其在医药上的应用 |
| CN115260191B (zh) * | 2022-09-29 | 2022-12-27 | 上海睿跃生物科技有限公司 | 哌啶类化合物及其制备方法和应用 |
| CN115286689B (zh) * | 2022-09-29 | 2023-01-06 | 上海睿跃生物科技有限公司 | 靶向降解Bcl-2蛋白的化合物及其应用和药物 |
| TW202430522A (zh) * | 2022-09-30 | 2024-08-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 一種用於bcl-2蛋白靶向降解的嵌合體化合物、其製備方法及其在醫藥上的應用 |
| CN115286630B (zh) * | 2022-10-09 | 2022-12-27 | 上海睿跃生物科技有限公司 | 哌嗪类化合物及其制备方法和应用 |
| WO2024078581A1 (en) * | 2022-10-12 | 2024-04-18 | Appicine Therapeutics (Hk) Limited | Selective bcl-xl protac compounds and uses thereof |
| KR20250130610A (ko) * | 2022-12-06 | 2025-09-02 | 캡터 테라퓨틱스 에스.에이. | 유비퀴틴 리가제 및 표적 mcl-1 단백질에 결합하는 이작용성 화합물을 사용하는 표적화된 단백질 분해 |
| WO2024123195A1 (en) * | 2022-12-06 | 2024-06-13 | Captor Therapeutics S.A. | Targeted protein degradation using prodrugs of bifunctional compounds that bind ubiquitin ligase and target mcl-1 protein |
| JP2026507476A (ja) * | 2023-02-17 | 2026-03-04 | チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッド | トリフルオロメタンスルホニル基を含む化合物 |
| EP4719408A1 (en) * | 2023-05-30 | 2026-04-08 | Ascentage Pharma (Suzhou) Co., Ltd. | Bcl-2/bcl-xl protein degrader and use thereof |
| WO2025101575A1 (en) | 2023-11-07 | 2025-05-15 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-x l degraders |
| TW202527930A (zh) | 2023-11-07 | 2025-07-16 | 美商樹線生物科學公司 | 四氫異喹啉異雙功能bcl-xl降解劑 |
| TW202535872A (zh) | 2023-11-07 | 2025-09-16 | 美商樹線生物科學公司 | 四氫異喹啉異雙功能bcl-xl降解劑 |
| WO2025117556A1 (en) * | 2023-11-27 | 2025-06-05 | Rubedo Life Sciences, Inc. | Phosphorous containing bcl inhibitors and senolytic compounds and uses thereof |
| TW202535392A (zh) | 2023-12-08 | 2025-09-16 | 美商亞文納營運公司 | 使用雄性素受體降解劑治療脊髓延髓性肌肉萎縮 |
| WO2025136208A1 (en) | 2023-12-21 | 2025-06-26 | Hadjab Saida | Senolytic compounds for use in the treatment and/or prevention of a headache disorder and/or chronic pain |
| CN117624134B (zh) * | 2024-01-26 | 2024-05-03 | 南昌市第一医院 | 一种靶向降解hdac4的化合物及其制备方法和应用 |
| CN118908940B (zh) * | 2024-10-11 | 2024-12-31 | 齐鲁理工学院 | 一种靶向抗凋亡Bcl-2的蛋白水解靶向嵌合体的制备和应用 |
Family Cites Families (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4394448A (en) | 1978-02-24 | 1983-07-19 | Szoka Jr Francis C | Method of inserting DNA into living cells |
| US4529561A (en) | 1978-03-24 | 1985-07-16 | The Regents Of The University Of California | Method for producing liposomes in selected size range |
| US4241046A (en) | 1978-11-30 | 1980-12-23 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| US4925661A (en) | 1984-04-19 | 1990-05-15 | Leaf Huang | Target-specific cytotoxic liposomes |
| US4957735A (en) | 1984-06-12 | 1990-09-18 | The University Of Tennessee Research Corporation | Target-sensitive immunoliposomes- preparation and characterization |
| US4755388A (en) | 1984-11-09 | 1988-07-05 | The Regents Of The University Of California | Liposome-encapsulated 5-fluoropyrimidines and methods for their use |
| DE3542773A1 (de) | 1985-12-04 | 1987-06-11 | Roehm Pharma Gmbh | Hautwirksame pharmaka mit liposomen als wirkstofftraeger |
| US4828837A (en) | 1987-03-30 | 1989-05-09 | Liposome Technology, Inc. | Non-crystalline minoxidil composition, its production and application |
| US5077211A (en) | 1988-07-06 | 1991-12-31 | Applied Genetics, Inc. | Purification and administration of dna repair enzymes |
| US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
| US5043164A (en) | 1989-01-17 | 1991-08-27 | The University Of Tennessee Research Corporation | Blood-stable, cholesterol-free liposomes |
| US5064655A (en) | 1989-02-24 | 1991-11-12 | Liposome Technology, Inc. | Liposome gel composition and method |
| US5744101A (en) | 1989-06-07 | 1998-04-28 | Affymax Technologies N.V. | Photolabile nucleoside protecting groups |
| US5264618A (en) | 1990-04-19 | 1993-11-23 | Vical, Inc. | Cationic lipids for intracellular delivery of biologically active molecules |
| US5270339A (en) | 1991-04-05 | 1993-12-14 | Kanagafuchi Kagaku Kogyo Kabushiki Kaisha | Phenoxybenzene derivative |
| US5491069A (en) | 1994-02-18 | 1996-02-13 | The Regents Of The University Of California | Biomarkers of cell senescence |
| US5888764A (en) | 1995-01-20 | 1999-03-30 | Uab Research Foundation | Human fas gene promoter region |
| DE19713393C2 (de) | 1997-04-01 | 2002-12-05 | Apotech Res & Dev Ltd | Flip-Gen und Flip-Protein |
| JPH11349568A (ja) | 1998-06-08 | 1999-12-21 | Maruho Co Ltd | ラクタム誘導体及びその医薬用途 |
| CA2338328A1 (en) | 1998-07-21 | 2000-02-03 | Thomas Jefferson University | Small molecule inhibitors of bcl-2 proteins |
| AUPR038200A0 (en) | 2000-09-26 | 2000-10-19 | Beta Peptide Foundation Pty Ltd, The | Compositions and methods for delaying, preventing, rejuvenating or reversing senescence |
| WO2002097053A2 (en) | 2001-05-30 | 2002-12-05 | The Regents Of The University Of Michigan | Small molecule antagonists of bcl2 family proteins |
| ES2276895T3 (es) | 2002-05-07 | 2007-07-01 | Institut Pasteur | Cribado de peptidos qque inhiben la union de pp1c a las proteinas bcl-2, bcl-xi y bcl-w. |
| AU2003245436A1 (en) | 2003-01-23 | 2004-08-23 | The Trustees Of Columbia University In The City Of New York | Old-35, a gene associated with senescence and terminal cell differentiation, and uses thereof |
| ES2382377T3 (es) | 2003-05-30 | 2012-06-07 | Gemin X Pharmaceuticals Canada Inc. | Compuestos triheterocíclicos, composiciones, y métodos para tratar cáncer |
| US20050208151A1 (en) | 2003-10-30 | 2005-09-22 | Entelos, Inc. | Treatment of rheumatoid arthritis with FLIP antagonists |
| US7973161B2 (en) | 2003-11-13 | 2011-07-05 | Abbott Laboratories | Apoptosis promoters |
| JP2007525661A (ja) | 2003-12-12 | 2007-09-06 | セントルイス ユニバーシティー | 大分子その他の分析物の検出用生物センサー |
| RU2361872C2 (ru) | 2004-05-26 | 2009-07-20 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Циннамидное соединение |
| AU2005277223C1 (en) | 2004-08-20 | 2009-05-21 | The Regents Of The University Of Michigan | Small molecule inhibitors of anti-apoptotic Bcl-2 family members and the uses thereof |
| PL1888550T3 (pl) | 2005-05-12 | 2014-12-31 | Abbvie Bahamas Ltd | Promotory apoptozy |
| EP2135078B1 (en) | 2007-03-09 | 2013-08-21 | DiscoveRx Corporation | Methods for identifying agents and their use for the prevention or stabilization of fibrosis |
| EA200901212A1 (ru) | 2007-03-29 | 2010-04-30 | Новартис Аг | 3-имидазолилиндолы, предназначенные для лечения пролиферативных заболеваний |
| US20100310504A1 (en) | 2007-09-26 | 2010-12-09 | Lowe Scott W | Methods for treating fibrosis by modulating cellular senescence |
| US8039668B2 (en) | 2008-10-17 | 2011-10-18 | Burnham Institute For Medical Research | Naphthalene-based inhibitors of anti-apoptotic proteins |
| WO2009085216A2 (en) | 2007-12-20 | 2009-07-09 | Squicor | Compositions and methods for detecting or elimninating senescent cells to diagnose or treat disease |
| US20090312373A1 (en) | 2008-03-11 | 2009-12-17 | The General Hospital Corporation | Methods for the treatment of cancer using piperlongumine and piperlongumine analogs |
| US8168784B2 (en) | 2008-06-20 | 2012-05-01 | Abbott Laboratories | Processes to make apoptosis promoters |
| US20100086941A1 (en) | 2008-10-01 | 2010-04-08 | Adami Guy R | Methods for determining aged based accumulation of senescent cells using senescence specific DNA damage markers |
| NZ593536A (en) | 2008-12-19 | 2013-07-26 | Genentech Inc | Quinoline derivatives and methods of use |
| WO2010080503A1 (en) | 2008-12-19 | 2010-07-15 | Genentech, Inc. | Heterocyclic compounds and methods of use |
| WO2010138588A2 (en) | 2009-05-26 | 2010-12-02 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| EP2289528A1 (en) | 2009-07-21 | 2011-03-02 | DSM IP Assets B.V. | Novel nutraceutical compositions containing black pepper or its constituents improving mental performance |
| US8349832B2 (en) | 2009-09-02 | 2013-01-08 | Canthera Therapeutics | Compounds and compositions for treating cancer |
| US8318737B2 (en) | 2009-09-02 | 2012-11-27 | Canthera Therapeutics Inc. | Compounds and compositions for treating cancer |
| US20120157455A1 (en) | 2009-09-02 | 2012-06-21 | Canthera Therapeutics, Inc. | Compounds And Compositions For Treating Cancer |
| EP2519260A2 (en) | 2009-12-31 | 2012-11-07 | Deutsches Krebsforschungszentrum | Novel modulators of trail signalling |
| CN101774875A (zh) | 2010-01-08 | 2010-07-14 | 北京欧凯纳斯科技有限公司 | 一种荜拔酰胺类化合物的合成方法 |
| CN102125552A (zh) | 2010-01-20 | 2011-07-20 | 李绍路 | 荜茇酰胺衍生物在制备治疗癌症的药物中的用途及其药物组合物 |
| CN102146054A (zh) | 2010-02-10 | 2011-08-10 | 新昌县来益科技开发有限公司 | 荜茇酰胺衍生物及其药物组合物和在制备抑制肿瘤生长的药物中的用途 |
| WO2011130395A1 (en) | 2010-04-13 | 2011-10-20 | University Of Utah Research Foundation | Inhibitors of flip to treat cancer |
| ES2603129T3 (es) | 2010-11-23 | 2017-02-23 | Abbvie Ireland Unlimited Company | Métodos de tratamiento utilizando inhibidores selectivos de Bcl-2 |
| EP2668180B1 (en) * | 2011-01-25 | 2018-08-01 | The Regents of The University of Michigan | Bcl-2/bcl-xl inhibitors for use in the treatment of cancer |
| US8940737B2 (en) | 2011-10-14 | 2015-01-27 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| EP2602330A1 (en) | 2011-12-07 | 2013-06-12 | Palacky University, Olomouc | Method of determination of cancer cell drug sensitivity towards Aurora kinase inhibitors and overcoming their resistance |
| KR102668696B1 (ko) * | 2012-01-12 | 2024-05-29 | 예일 유니버시티 | E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법 |
| US9828344B2 (en) | 2012-06-01 | 2017-11-28 | LEIBNIZ-INSTITUT FÜR ALTERSFORSCHUNG FRITZ-LIPMANN-INSTITUT e.V. (FLI) | Inhibitors of the notch signaling pathway and secretion for use in medicine |
| US9108923B2 (en) | 2012-07-20 | 2015-08-18 | Howard Hughes Medical Institute | Compounds, compositions, and methods for cancer therapy |
| CN103601670B (zh) | 2012-11-20 | 2016-06-15 | 中国人民解放军第二军医大学 | 荜拔酰胺类似物及其制备方法与应用 |
| WO2014089124A1 (en) | 2012-12-03 | 2014-06-12 | Cenexys, Inc. | Immunogenic compositions for inducing an immune response for elimination of senescent cells |
| GB201311910D0 (en) | 2013-07-03 | 2013-08-14 | Glaxosmithkline Ip Dev Ltd | Novel Compounds |
| EP3689886A1 (en) * | 2013-01-16 | 2020-08-05 | The Regents of The University of Michigan | Bcl-2/bcl-xl inhibitors and their use in the treatment of cancer |
| RU2015149680A (ru) | 2013-04-21 | 2017-05-24 | Йеда Ресеарч Энд Девелопмент Ко. Лтд. | Агенты для подавления активности и/или снижения количества bcl-xl и/или bcl-w |
| IL286427B2 (en) | 2014-01-28 | 2024-08-01 | Mayo Found Medical Education & Res | Inhibitors bcl-2 anti-apoptotic protein family members for treatment of non cancer pulmonary disease or an opthalmic disease |
| RU2738833C9 (ru) | 2014-04-14 | 2022-02-28 | Арвинас, Оперэйшнз, Инк. | Имидные модуляторы протеолиза и способы их применения |
| EP3139942B1 (en) | 2014-05-05 | 2019-12-18 | Bioventures, Llc | COMPOSITIONS AND METHODS FOR INHIBITING ANTIAPOPTOTIC Bcl-2 PROTEINS AS ANTI-AGING AGENTS |
| WO2016014625A1 (en) | 2014-07-22 | 2016-01-28 | Board Of Trustees Of The University Of Arkansas | Compositions and methods for selectively depleting senescent cells |
| US10071164B2 (en) | 2014-08-11 | 2018-09-11 | Yale University | Estrogen-related receptor alpha based protac compounds and associated methods of use |
| US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
| WO2016118859A1 (en) | 2015-01-22 | 2016-07-28 | Board Of Trustees Of The University Of Arkansas | Compositions and methods for selectively depleting senescent cells comprising flip |
| WO2016118855A1 (en) | 2015-01-22 | 2016-07-28 | Board Of Trustees Of The University Of Arkansas | Compositions and methods for selectively depleting senescent cells comprising death receptors |
| US20180000816A1 (en) * | 2015-02-06 | 2018-01-04 | Unity Biotechnology, Inc. | Use of a Heterocyclic Bcl-xL Inhibitor and Related Analogs for Removing Senescent Cells in the Treatment of Eye Diseases and Other Age-Related Conditions |
| EP3270917A4 (en) * | 2015-03-18 | 2018-08-08 | Arvinas, Inc. | Compounds and methods for the enhanced degradation of targeted proteins |
| CN105085620B (zh) | 2015-06-25 | 2018-05-08 | 中山大学附属第一医院 | 一种靶向泛素化降解Smad3的化合物 |
| AU2016295984B2 (en) | 2015-07-21 | 2021-05-27 | Fundació Investigació Hospital General Universitari De València Per A La Investigació Biomèdica I Ciències De La Salut | Combination comprising pterostilbene for the treatment of cancer |
| US10772962B2 (en) * | 2015-08-19 | 2020-09-15 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of bromodomain-containing proteins |
| WO2017101851A1 (en) | 2015-12-18 | 2017-06-22 | Unity Biotechnology, Inc. | Acylsulfonamide derivatives for treating senescence-associated diseases and disorders |
| CN109152933B (zh) | 2016-04-21 | 2022-12-02 | 生物风险投资有限责任公司 | 诱导抗细胞凋亡bcl-2家族蛋白的降解的化合物及其用途 |
| US20190054097A1 (en) | 2016-04-21 | 2019-02-21 | Bioventures, Llc | Compositions targeting senescent cells and the uses thereof |
| ES3041854T3 (en) * | 2018-01-22 | 2025-11-17 | Bioventures Llc | Bcl-2 proteins degraders for cancer treatment |
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| EP3445452A1 (en) | 2019-02-27 |
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| JP2019514877A (ja) | 2019-06-06 |
| WO2020081880A1 (en) | 2020-04-23 |
| CN109152933B (zh) | 2022-12-02 |
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