KR102301867B1 - Nrf2 조절제 - Google Patents
Nrf2 조절제 Download PDFInfo
- Publication number
- KR102301867B1 KR102301867B1 KR1020167018852A KR20167018852A KR102301867B1 KR 102301867 B1 KR102301867 B1 KR 102301867B1 KR 1020167018852 A KR1020167018852 A KR 1020167018852A KR 20167018852 A KR20167018852 A KR 20167018852A KR 102301867 B1 KR102301867 B1 KR 102301867B1
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- KR
- South Korea
- Prior art keywords
- methyl
- benzo
- mmol
- dioxido
- triazol
- Prior art date
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- UHZFHXHECXKUIN-UHFFFAOYSA-N Cc1c(CN(CCN(C)c2c3cccc2)S3(=O)=O)cc(C(CC(OCCCCN(C)C)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 Chemical compound Cc1c(CN(CCN(C)c2c3cccc2)S3(=O)=O)cc(C(CC(OCCCCN(C)C)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 UHZFHXHECXKUIN-UHFFFAOYSA-N 0.000 description 1
- QHHJBFGEOQGEIC-UHFFFAOYSA-N Cc1c(CN(CCN(C)c2c3cccc2)S3(=O)=O)cc(C(CC(OCCCN2CCOCC2)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 Chemical compound Cc1c(CN(CCN(C)c2c3cccc2)S3(=O)=O)cc(C(CC(OCCCN2CCOCC2)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 QHHJBFGEOQGEIC-UHFFFAOYSA-N 0.000 description 1
- OLHWMXBKPFRTNX-UHFFFAOYSA-N Cc1c(CN(CCN(C)c2c3cncc2)S3(=O)=O)cc(C(CC(O)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 Chemical compound Cc1c(CN(CCN(C)c2c3cncc2)S3(=O)=O)cc(C(CC(O)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 OLHWMXBKPFRTNX-UHFFFAOYSA-N 0.000 description 1
- IOFAJVMIPCXGPX-UHFFFAOYSA-N Cc1c(CN(CCOc2c3cccc2)S3(=O)=O)cc(C(CC(O)=O)c(cc2CCN(C)C)c(C)cc2F)cc1 Chemical compound Cc1c(CN(CCOc2c3cccc2)S3(=O)=O)cc(C(CC(O)=O)c(cc2CCN(C)C)c(C)cc2F)cc1 IOFAJVMIPCXGPX-UHFFFAOYSA-N 0.000 description 1
- CBSAZUJTEVZJBM-UHFFFAOYSA-N Cc1c(CN(CCOc2c3cccc2)S3(=O)=O)cc(C(CC(O)=O)c2ccc(C)c(F)c2)cc1 Chemical compound Cc1c(CN(CCOc2c3cccc2)S3(=O)=O)cc(C(CC(O)=O)c2ccc(C)c(F)c2)cc1 CBSAZUJTEVZJBM-UHFFFAOYSA-N 0.000 description 1
- AXWNWSUHDMQRQP-UHFFFAOYSA-N Cc1c(CNS(c(cccc2)c2NC)(=O)=O)cc(C(CC(OC)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 Chemical compound Cc1c(CNS(c(cccc2)c2NC)(=O)=O)cc(C(CC(OC)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1 AXWNWSUHDMQRQP-UHFFFAOYSA-N 0.000 description 1
- QRSPPCAGWIMSFE-UHFFFAOYSA-N Cc1c(COCc(cc2)ccc2OC)cc(C(c(cc2)c(C)c3c2[n](C)nn3)O)cc1 Chemical compound Cc1c(COCc(cc2)ccc2OC)cc(C(c(cc2)c(C)c3c2[n](C)nn3)O)cc1 QRSPPCAGWIMSFE-UHFFFAOYSA-N 0.000 description 1
- LANPIAKLVSACTR-UHFFFAOYSA-N Cc1c(ccc(Br)c2)[n]2nn1 Chemical compound Cc1c(ccc(Br)c2)[n]2nn1 LANPIAKLVSACTR-UHFFFAOYSA-N 0.000 description 1
- RHAPURYCDOSIKA-UHFFFAOYSA-N Cc1c2N=NC(CCCCCCCC(CN3C4CC5)Oc(cccc6)c6S3(=O)=O)c2ccc1C(CC(O)=O)c1ccc5c4c1 Chemical compound Cc1c2N=NC(CCCCCCCC(CN3C4CC5)Oc(cccc6)c6S3(=O)=O)c2ccc1C(CC(O)=O)c1ccc5c4c1 RHAPURYCDOSIKA-UHFFFAOYSA-N 0.000 description 1
- DHJWAGMDDVEVEK-UHFFFAOYSA-N Cc1ccc(C(CC(OCCN2CCOCC2)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1CNS(c(cccc1)c1NC)(=O)=O Chemical compound Cc1ccc(C(CC(OCCN2CCOCC2)=O)c(cc2)c(C)c3c2[n](C)nn3)cc1CNS(c(cccc1)c1NC)(=O)=O DHJWAGMDDVEVEK-UHFFFAOYSA-N 0.000 description 1
- VDCZKCIEXGXCDJ-UHFFFAOYSA-N Cc1cccc(N)c1[N+]([O-])=O Chemical compound Cc1cccc(N)c1[N+]([O-])=O VDCZKCIEXGXCDJ-UHFFFAOYSA-N 0.000 description 1
- KCNWYJPUGJYMNO-UHFFFAOYSA-N O=S(c(cncc1)c1Cl)(Cl)=O Chemical compound O=S(c(cncc1)c1Cl)(Cl)=O KCNWYJPUGJYMNO-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
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- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
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- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- 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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- 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
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- C07D471/04—Ortho-condensed systems
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361917466P | 2013-12-18 | 2013-12-18 | |
| US61/917,466 | 2013-12-18 | ||
| US201461980091P | 2014-04-16 | 2014-04-16 | |
| US61/980,091 | 2014-04-16 | ||
| PCT/IB2014/067027 WO2015092713A1 (en) | 2013-12-18 | 2014-12-17 | Nrf2 regulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20160098392A KR20160098392A (ko) | 2016-08-18 |
| KR102301867B1 true KR102301867B1 (ko) | 2021-09-15 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020167018852A Active KR102301867B1 (ko) | 2013-12-18 | 2014-12-17 | Nrf2 조절제 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US10144731B2 (enExample) |
| EP (1) | EP3083614B1 (enExample) |
| JP (1) | JP6630671B2 (enExample) |
| KR (1) | KR102301867B1 (enExample) |
| CN (1) | CN105829305B (enExample) |
| AU (2) | AU2014369153B2 (enExample) |
| BR (1) | BR112016014180A2 (enExample) |
| CA (1) | CA2934216C (enExample) |
| CL (1) | CL2016001516A1 (enExample) |
| CR (1) | CR20160272A (enExample) |
| DO (1) | DOP2016000145A (enExample) |
| EA (1) | EA030431B1 (enExample) |
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| PH12017502255B1 (en) * | 2015-06-15 | 2022-07-22 | Astex Therapeutics Ltd | Nrf2 regulators |
| JP2018529744A (ja) * | 2015-10-06 | 2018-10-11 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Nrf2レギュレーターとしてのアリールシクロヘキシルピラゾール |
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| JP2020097526A (ja) * | 2017-03-28 | 2020-06-25 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2019116231A1 (en) | 2017-12-11 | 2019-06-20 | Glaxosmithkline Intellectual Property Development Limited | Nrf2 activator for the treatment of acute lung injury, acute respiratory distress syndrome and multiple organ dysfunction syndrome |
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| US11643407B2 (en) | 2018-05-23 | 2023-05-09 | Glaxosmithkline Intellectual Property Development Limited | Indanes as NRF2 activators |
| US12365677B2 (en) | 2018-07-20 | 2025-07-22 | Dana-Farber Cancer Institute, Inc. | Degraders that target proteins via KEAP1 |
| PT3833662T (pt) * | 2018-08-20 | 2024-03-18 | Janssen Pharmaceutica Nv | Inibidores da interação proteína-proteína keap1-nrf2 |
| JP2022510736A (ja) * | 2018-12-05 | 2022-01-27 | 株式会社スコヒアファーマ | 大環状化合物とその使用 |
| PH12021551873A1 (en) | 2019-02-15 | 2022-05-23 | Glaxosmithkline Ip Dev Ltd | Hydroxypyridoxazepines as nrf2 activators |
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| JP7524899B2 (ja) | 2019-05-31 | 2024-07-30 | Ube株式会社 | ベンゾトリアゾール誘導体 |
| EP3998262A4 (en) * | 2019-07-03 | 2023-07-26 | Senju Pharmaceutical Co., Ltd. | NRF2 ACTIVATING LINK |
| MX2022010673A (es) | 2020-02-28 | 2022-09-23 | Servier Lab | Nuevos compuestos macrociclicos, un proceso para su preparacion y composiciones farmaceuticas que los contienen. |
| PE20231363A1 (es) * | 2020-09-14 | 2023-09-05 | Sanofi Sa | Derivados de tetrahidroisoquinolina para el tratamiento de eritrocitos y enfermedades inflamatorias |
| US20240132519A1 (en) * | 2020-12-28 | 2024-04-25 | Senju Pharmaceutical Co., Ltd. | Nrf2-activating compound |
| TW202404984A (zh) * | 2022-04-28 | 2024-02-01 | 日商第一三共股份有限公司 | 苯并三唑化合物 |
| TW202345792A (zh) | 2022-04-28 | 2023-12-01 | 日商第一三共股份有限公司 | 苯并噻吩化合物 |
| CN117603075B (zh) * | 2024-01-18 | 2024-04-12 | 深圳创元生物医药科技有限公司 | 一种碳13标记的3-羧酸苯丙氨酸的制备方法 |
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| IL245727B (en) | 2019-10-31 |
| MX370410B (es) | 2019-12-11 |
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| BR112016014180A2 (pt) | 2017-09-26 |
| EA030431B1 (ru) | 2018-08-31 |
| ES2784244T3 (es) | 2020-09-23 |
| AU2014369153A1 (en) | 2016-05-26 |
| CN105829305A (zh) | 2016-08-03 |
| JP6630671B2 (ja) | 2020-01-15 |
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