TWI755992B - 一種蛋白降解劑化合物的製備方法和應用 - Google Patents
一種蛋白降解劑化合物的製備方法和應用 Download PDFInfo
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- TWI755992B TWI755992B TW109145818A TW109145818A TWI755992B TW I755992 B TWI755992 B TW I755992B TW 109145818 A TW109145818 A TW 109145818A TW 109145818 A TW109145818 A TW 109145818A TW I755992 B TWI755992 B TW I755992B
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- alkyl
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- compound
- pharmaceutically acceptable
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- ZKBOZYAKCJRMSG-UHFFFAOYSA-N CC(C(C1)CN1c(cc1)ccc1-c(cc1)cc(C(C)(C)C2=O)c1N2c(cc1)cc(Cl)c1C#N)N(CC1)CCN1c(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O Chemical compound CC(C(C1)CN1c(cc1)ccc1-c(cc1)cc(C(C)(C)C2=O)c1N2c(cc1)cc(Cl)c1C#N)N(CC1)CCN1c(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O ZKBOZYAKCJRMSG-UHFFFAOYSA-N 0.000 description 1
- GQLMMOYXQAEKEQ-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)cc(F)c2N2CC(CN(CC3)CCN3c(cc3C(N4C(CCC(N5)=O)C5=O)=O)ccc3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)cc(F)c2N2CC(CN(CC3)CCN3c(cc3C(N4C(CCC(N5)=O)C5=O)=O)ccc3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O GQLMMOYXQAEKEQ-UHFFFAOYSA-N 0.000 description 1
- UYKBUPUGWAYSNX-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)ccc2N(C2)CC2(CN(CC2)CCN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)O)c1N1c(cc2)cc(Cl)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)ccc2N(C2)CC2(CN(CC2)CCN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)O)c1N1c(cc2)cc(Cl)c2C#N)C1=O UYKBUPUGWAYSNX-UHFFFAOYSA-N 0.000 description 1
- MARPVFHBQRQWCT-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)ccc2N2CC(COc(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)CC2)c1N1c(cc2)cc(OC)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)ccc2N2CC(COc(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)CC2)c1N1c(cc2)cc(OC)c2C#N)C1=O MARPVFHBQRQWCT-UHFFFAOYSA-N 0.000 description 1
- HQTCTJZGGRZDMH-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)ccc2OCCCOC(CC2)CN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)c1N1c(cc2)cc(OC)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)ccc2OCCCOC(CC2)CN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)c1N1c(cc2)cc(OC)c2C#N)C1=O HQTCTJZGGRZDMH-UHFFFAOYSA-N 0.000 description 1
- ADWHFJBXGQQUPW-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)ccc2OCCOCC(C2)OCCN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)c1N1c(cc2)cc(OC)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)ccc2OCCOCC(C2)OCCN2c(cc2)cc(C(N3C(CCC(N4)=O)C4=O)=O)c2C3=O)c1N1c(cc2)cc(OC)c2C#N)C1=O ADWHFJBXGQQUPW-UHFFFAOYSA-N 0.000 description 1
- HSHUCAWAIZRJFI-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)cnc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)cnc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O HSHUCAWAIZRJFI-UHFFFAOYSA-N 0.000 description 1
- UZRADRIMSKNIBT-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(cc2)nnc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(cc2)nnc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O UZRADRIMSKNIBT-UHFFFAOYSA-N 0.000 description 1
- QQKJEQPOJPLNBE-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c(nc2)ccc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c(nc2)ccc2N2CC(CN(CC3)CCN3c(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)C2)c1N1c(cc2)cc(Cl)c2C#N)C1=O QQKJEQPOJPLNBE-UHFFFAOYSA-N 0.000 description 1
- KTMOJQHAWLPZAG-UHFFFAOYSA-N CC(C)(c(cc(cc1)-c2ccc(N3CC(CCN(CC4)CCN4c(cc4)cc(C(N5C(CCC(N6)=O)C6=O)=O)c4C5=O)C3)nn2)c1N1c(cc2Cl)ccc2C#N)C1=O Chemical compound CC(C)(c(cc(cc1)-c2ccc(N3CC(CCN(CC4)CCN4c(cc4)cc(C(N5C(CCC(N6)=O)C6=O)=O)c4C5=O)C3)nn2)c1N1c(cc2Cl)ccc2C#N)C1=O KTMOJQHAWLPZAG-UHFFFAOYSA-N 0.000 description 1
- DYRHMSXGVHRWDZ-UHFFFAOYSA-N CC(C)(c1cc(-c(cc2)ccc2N2CC(CCOc(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)CC2)ccc1N1c(cc2OC)ccc2C#N)C1=O Chemical compound CC(C)(c1cc(-c(cc2)ccc2N2CC(CCOc(cc3)cc(C(N4C(CCC(N5)=O)C5=O)=O)c3C4=O)CC2)ccc1N1c(cc2OC)ccc2C#N)C1=O DYRHMSXGVHRWDZ-UHFFFAOYSA-N 0.000 description 1
- DIRPUESKCKCQPD-UHFFFAOYSA-N CC(CN(CC1)CCN1c(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)(C1)CN1c(cc1)ccc1-c(cc1)cc(C(C)(C)C2=O)c1N2c(cc1)cc(Cl)c1C#N Chemical compound CC(CN(CC1)CCN1c(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)(C1)CN1c(cc1)ccc1-c(cc1)cc(C(C)(C)C2=O)c1N2c(cc1)cc(Cl)c1C#N DIRPUESKCKCQPD-UHFFFAOYSA-N 0.000 description 1
- IJUMDSZWMBPSHQ-UHFFFAOYSA-N CCN(C)C(COC)=O Chemical compound CCN(C)C(COC)=O IJUMDSZWMBPSHQ-UHFFFAOYSA-N 0.000 description 1
- GPZKSOWOKOABRH-UHFFFAOYSA-N CN(C1)CC1OCC1CN(C)CC1 Chemical compound CN(C1)CC1OCC1CN(C)CC1 GPZKSOWOKOABRH-UHFFFAOYSA-N 0.000 description 1
- GBZLPQFTINJNCL-UHFFFAOYSA-N CN(C1)CC1OCCC1OCCN(C)C1 Chemical compound CN(C1)CC1OCCC1OCCN(C)C1 GBZLPQFTINJNCL-UHFFFAOYSA-N 0.000 description 1
- FUJIHCVOEMIUBC-UHFFFAOYSA-N CN(CC1)CCC1OCCOC Chemical compound CN(CC1)CCC1OCCOC FUJIHCVOEMIUBC-UHFFFAOYSA-N 0.000 description 1
- NFTWWHSKWXOTLL-UHFFFAOYSA-N CN(CCN1C)CC1=O Chemical compound CN(CCN1C)CC1=O NFTWWHSKWXOTLL-UHFFFAOYSA-N 0.000 description 1
- LNGUFNFCCJRSNV-UHFFFAOYSA-N CN(CCOC)C1CN(C)CC1 Chemical compound CN(CCOC)C1CN(C)CC1 LNGUFNFCCJRSNV-UHFFFAOYSA-N 0.000 description 1
- YVMNACVXZIVJDJ-UHFFFAOYSA-N CN1CC(COC2CN(C)CC2)C1 Chemical compound CN1CC(COC2CN(C)CC2)C1 YVMNACVXZIVJDJ-UHFFFAOYSA-N 0.000 description 1
- BGVTUIRPHLSMJU-UHFFFAOYSA-N Cc1ccc(C)nn1 Chemical compound Cc1ccc(C)nn1 BGVTUIRPHLSMJU-UHFFFAOYSA-N 0.000 description 1
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- A61K31/403—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 carbocyclic rings, e.g. carbazole
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- C07D209/04—Indoles; Hydrogenated indoles
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- 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
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Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201911342649 | 2019-12-23 | ||
| CN201911342649.0 | 2019-12-23 | ||
| CN202010200682 | 2020-03-20 | ||
| CN202010200682.6 | 2020-03-20 | ||
| CN202010496353.0 | 2020-06-03 | ||
| CN202010496353 | 2020-06-03 | ||
| CN202011486334.6 | 2020-12-16 | ||
| CN202011486334 | 2020-12-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW202128662A TW202128662A (zh) | 2021-08-01 |
| TWI755992B true TWI755992B (zh) | 2022-02-21 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW109145818A TWI755992B (zh) | 2019-12-23 | 2020-12-23 | 一種蛋白降解劑化合物的製備方法和應用 |
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| EP (1) | EP4083020A4 (enExample) |
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| BR (1) | BR112022012385A2 (enExample) |
| CA (1) | CA3162523A1 (enExample) |
| CL (1) | CL2022001724A1 (enExample) |
| CO (1) | CO2022010305A2 (enExample) |
| EC (1) | ECSP22056811A (enExample) |
| IL (1) | IL294225B2 (enExample) |
| JO (1) | JOP20220159A1 (enExample) |
| MX (1) | MX2022007885A (enExample) |
| PE (1) | PE20230114A1 (enExample) |
| PH (1) | PH12022551571A1 (enExample) |
| TW (1) | TWI755992B (enExample) |
| WO (1) | WO2021129653A1 (enExample) |
| ZA (1) | ZA202208051B (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL319363A (en) | 2017-01-31 | 2025-05-01 | Arvinas Operations Inc | Cervalon ligands and bifunctional compounds containing them |
| WO2021127443A1 (en) | 2019-12-19 | 2021-06-24 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of androgen receptor |
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