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
- VQMYDHLGMMKVLK-UHFFFAOYSA-N CC(C)(CC1)CC(CN(CC2)CCN2c(cc2)ccc2C(N)=O)=C1c(cc1)ccc1Cl Chemical compound CC(C)(CC1)CC(CN(CC2)CCN2c(cc2)ccc2C(N)=O)=C1c(cc1)ccc1Cl VQMYDHLGMMKVLK-UHFFFAOYSA-N 0.000 description 2
- PJCDQHGMXMZQDS-UHFFFAOYSA-N CC(C)(CCO)OCCNc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O Chemical compound CC(C)(CCO)OCCNc(cccc1C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O PJCDQHGMXMZQDS-UHFFFAOYSA-N 0.000 description 2
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- HIUJBNPXBIRABU-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(CC#CC(C2)C=CC(OCCCc3c(C(O)=O)nc(N(CCc4ccc5)Cc4c5C(Nc4nc5ccccc5[s]4)=O)[s]3)=C2F)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(CC#CC(C2)C=CC(OCCCc3c(C(O)=O)nc(N(CCc4ccc5)Cc4c5C(Nc4nc5ccccc5[s]4)=O)[s]3)=C2F)CC1)=O HIUJBNPXBIRABU-UHFFFAOYSA-N 0.000 description 1
- XRWPQVWKLLRDLM-UHFFFAOYSA-N CC(C)(CC1)CC(CN(CC2)CCN2C(CC2)=CC=C2C(N)=O)=C1c(cc1)ccc1Cl Chemical compound CC(C)(CC1)CC(CN(CC2)CCN2C(CC2)=CC=C2C(N)=O)=C1c(cc1)ccc1Cl XRWPQVWKLLRDLM-UHFFFAOYSA-N 0.000 description 1
- ZTOYAGORZQZBCF-UHFFFAOYSA-N CC(C)Nc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O Chemical compound CC(C)Nc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O ZTOYAGORZQZBCF-UHFFFAOYSA-N 0.000 description 1
- 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
-
- 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)
- 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)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (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 |
| US10071087B2 (en) | 2014-07-22 | 2018-09-11 | Bioventures, Llc | Compositions and methods for selectively depleting senescent cells |
| JP6936498B2 (ja) | 2016-04-21 | 2021-09-15 | バイオベンチャーズ・リミテッド・ライアビリティ・カンパニーBioVentures, LLC | 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 |
| WO2018071606A1 (en) | 2016-10-11 | 2018-04-19 | Arvinas, Inc. | Compounds and methods for the targeted degradation of androgen receptor |
| IL290809B2 (en) | 2016-11-01 | 2024-01-01 | Arvinas Operations Inc | Tau-protein targeting protacs and associated methods of use |
| TWI791552B (zh) | 2017-07-10 | 2023-02-11 | 美商西建公司 | 抗增生化合物及其使用方法 |
| EP3737681A4 (en) | 2018-01-10 | 2022-01-12 | Recurium IP Holdings, LLC | BENZAMIDE COMPOUNDS |
| EP3743069B1 (en) * | 2018-01-22 | 2025-08-06 | 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 |
| IL312612A (en) * | 2018-07-11 | 2024-07-01 | Rubedo Life Sciences Inc | Senolytic compositions and uses thereof |
| WO2020163823A2 (en) * | 2019-02-08 | 2020-08-13 | University Of Florida Research Foundation, Incorporated | Therapeutic agents and methods of treatment |
| WO2021007307A1 (en) * | 2019-07-10 | 2021-01-14 | Recurium Ip Holdings, Llc | Bcl-2 protein inhibitors |
| CN119954801A (zh) | 2019-07-17 | 2025-05-09 | 阿尔维纳斯运营股份有限公司 | Tau蛋白靶向化合物及相关使用方法 |
| EP4038066A1 (en) * | 2019-10-01 | 2022-08-10 | Arvinas Operations, Inc. | Brm targeting compounds and associated methods of use |
| WO2021078301A1 (zh) * | 2019-10-24 | 2021-04-29 | 上海科技大学 | 蛋白降解剂及其在疾病治疗中的应用 |
| JP2023507590A (ja) * | 2019-12-17 | 2023-02-24 | オリオニス バイオサイエンシズ,インコーポレイテッド | タンパク質の動員および/または分解を調節する化合物 |
| AU2021207672A1 (en) | 2020-01-15 | 2022-07-14 | 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 |
| MX2022010512A (es) * | 2020-04-28 | 2022-11-16 | Recurium Ip Holdings Llc | Inhibidores de proteína bcl-2. |
| CN115996918A (zh) | 2020-05-09 | 2023-04-21 | 阿尔维纳斯运营股份有限公司 | 制造双官能团化合物的方法、双官能团化合物的超纯形式以及包括所述双官能团化合物的剂型 |
| JP2024504932A (ja) | 2021-01-13 | 2024-02-02 | モンテ ローザ セラピューティクス, インコーポレイテッド | イソインドリノン化合物 |
| CN117794929A (zh) | 2021-02-02 | 2024-03-29 | 法国施维雅药厂 | 选择性bcl-xl protac化合物及使用方法 |
| AU2022271290A1 (en) | 2021-05-07 | 2023-11-23 | Kymera Therapeutics, Inc. | Cdk2 degraders and uses thereof |
| 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 |
| CA3231175A1 (en) * | 2021-09-01 | 2023-03-09 | Xizang Haisco Pharmaceutical Co., Ltd. | Compound for degradation of bcl-2 family proteins and medical application thereof |
| EP4401729A4 (en) * | 2021-09-17 | 2025-10-01 | Kymera Therapeutics Inc | BCL-XL DEGRADING AGENTS AND THEIR USES |
| WO2023088245A1 (zh) * | 2021-11-17 | 2023-05-25 | 成都先导药物开发股份有限公司 | 一种降解剂及其用途 |
| EP4461730A4 (en) * | 2022-01-04 | 2025-12-24 | Univ Shanghai Technology | PROTEIN DEGRADING AGENTS DEVELOPED BASED ON BCL-2 FAMILY PROTEIN LIGAND COMPOUNDS AND THEIR USE |
| WO2023205802A2 (en) * | 2022-04-22 | 2023-10-26 | Sens Research Foundation | Senolytic targets of senescent cells |
| US20250282771A1 (en) | 2022-05-06 | 2025-09-11 | Treeline Biosciences, Inc. | Tetrahydroisoquinoline heterobifunctional bcl-xl degraders |
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| AU2017254687B2 (en) | 2021-09-30 |
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