JP2016531870A - Irak阻害剤およびその使用 - Google Patents
Irak阻害剤およびその使用 Download PDFInfo
- Publication number
- JP2016531870A JP2016531870A JP2016517346A JP2016517346A JP2016531870A JP 2016531870 A JP2016531870 A JP 2016531870A JP 2016517346 A JP2016517346 A JP 2016517346A JP 2016517346 A JP2016517346 A JP 2016517346A JP 2016531870 A JP2016531870 A JP 2016531870A
- Authority
- JP
- Japan
- Prior art keywords
- disease
- compound
- irak
- compounds
- ring
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 0 C*C1CCC(CCc2c(c(C(*[*+])I*)n[s]3)c3nc(*)n2)CC1 Chemical compound C*C1CCC(CCc2c(c(C(*[*+])I*)n[s]3)c3nc(*)n2)CC1 0.000 description 5
- QMGUTWWETLCPQJ-UHFFFAOYSA-N NC(C(NC(N1)=O)=O)=C1S Chemical compound NC(C(NC(N1)=O)=O)=C1S QMGUTWWETLCPQJ-UHFFFAOYSA-N 0.000 description 2
- JVSFQJZRHXAUGT-UHFFFAOYSA-N CC(C)(C)C(Cl)=O Chemical compound CC(C)(C)C(Cl)=O JVSFQJZRHXAUGT-UHFFFAOYSA-N 0.000 description 1
- DPJPJABELUIELV-UHFFFAOYSA-N CC(C)(C)c1nc(C(NC(N2)=O)=O)c2[s]1 Chemical compound CC(C)(C)c1nc(C(NC(N2)=O)=O)c2[s]1 DPJPJABELUIELV-UHFFFAOYSA-N 0.000 description 1
- JRMKFMHBKZONMZ-UHFFFAOYSA-N CC(C)(C)c1nc(c(Cl)nc(Cl)n2)c2[s]1 Chemical compound CC(C)(C)c1nc(c(Cl)nc(Cl)n2)c2[s]1 JRMKFMHBKZONMZ-UHFFFAOYSA-N 0.000 description 1
- LMOFVZGEEUOPBO-JOCQHMNTSA-N CC(C)(C)c1nc(c(N[C@H](CC2)CC[C@@H]2N2CCOCC2)nc(Cl)n2)c2[s]1 Chemical compound CC(C)(C)c1nc(c(N[C@H](CC2)CC[C@@H]2N2CCOCC2)nc(Cl)n2)c2[s]1 LMOFVZGEEUOPBO-JOCQHMNTSA-N 0.000 description 1
- ANSLWXNLQTXZKN-SECBINFHSA-N CC(C)CC[C@@H](C)N(C)C Chemical compound CC(C)CC[C@@H](C)N(C)C ANSLWXNLQTXZKN-SECBINFHSA-N 0.000 description 1
- ICLMJTPKXAVFCZ-UHFFFAOYSA-N CC(C)c1nc(c(Cl)ncn2)c2[s]1 Chemical compound CC(C)c1nc(c(Cl)ncn2)c2[s]1 ICLMJTPKXAVFCZ-UHFFFAOYSA-N 0.000 description 1
- UAEPNZWRGJTJPN-UHFFFAOYSA-N CC1CCCCC1 Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
- UWOBQZYJDCGOBT-KAOCOCSGSA-N CCC(C)Sc1nc(Cl)nc(N[C@H](CC2)CC[C@@H]2N2CCOCC2)c1N Chemical compound CCC(C)Sc1nc(Cl)nc(N[C@H](CC2)CC[C@@H]2N2CCOCC2)c1N UWOBQZYJDCGOBT-KAOCOCSGSA-N 0.000 description 1
- FTBYXBQBERZHFG-XYPYZODXSA-N CCc([s]c1ncn2)nc1c2O[C@H](CC1)CC[C@@H]1N(C)C Chemical compound CCc([s]c1ncn2)nc1c2O[C@H](CC1)CC[C@@H]1N(C)C FTBYXBQBERZHFG-XYPYZODXSA-N 0.000 description 1
- OUPDVSZQYIGWHT-UHFFFAOYSA-N CCc1nc(C(NC(N2)=O)=O)c2[s]1 Chemical compound CCc1nc(C(NC(N2)=O)=O)c2[s]1 OUPDVSZQYIGWHT-UHFFFAOYSA-N 0.000 description 1
- QHLZYAIVDXLQRL-UHFFFAOYSA-N CCc1nc(C(OCC)=O)c(N)[s]1 Chemical compound CCc1nc(C(OCC)=O)c(N)[s]1 QHLZYAIVDXLQRL-UHFFFAOYSA-N 0.000 description 1
- ATZUHHWIYWDYRL-HAQNSBGRSA-N CCc1nc(c(N[C@H](CC2)CC[C@@H]2N(CC2)CCC2(F)F)nc(Cl)n2)c2[s]1 Chemical compound CCc1nc(c(N[C@H](CC2)CC[C@@H]2N(CC2)CCC2(F)F)nc(Cl)n2)c2[s]1 ATZUHHWIYWDYRL-HAQNSBGRSA-N 0.000 description 1
- WJRCTOIAZDWFML-JOCQHMNTSA-N CCc1nc(c(O[C@H](CC2)CC[C@@H]2N(C)C(OC(C)(C)C)=O)ncn2)c2[s]1 Chemical compound CCc1nc(c(O[C@H](CC2)CC[C@@H]2N(C)C(OC(C)(C)C)=O)ncn2)c2[s]1 WJRCTOIAZDWFML-JOCQHMNTSA-N 0.000 description 1
- VWQBDQKXACXANE-KOMQPUFPSA-N CCc1nc2c(N[C@H](CC3)CC[C@@H]3N(CC3)CCC3(F)F)nc(Nc3c[n](C)nc3)nc2[s]1 Chemical compound CCc1nc2c(N[C@H](CC3)CC[C@@H]3N(CC3)CCC3(F)F)nc(Nc3c[n](C)nc3)nc2[s]1 VWQBDQKXACXANE-KOMQPUFPSA-N 0.000 description 1
- AOEVMDKTONAGLQ-JCNLHEQBSA-N CCc1nc2c(N[C@H](CC3)CC[C@@H]3N3CCOCC3)nc(Nc3c[n](CCO)nc3)nc2[s]1 Chemical compound CCc1nc2c(N[C@H](CC3)CC[C@@H]3N3CCOCC3)nc(Nc3c[n](CCO)nc3)nc2[s]1 AOEVMDKTONAGLQ-JCNLHEQBSA-N 0.000 description 1
- LBGSWBJURUFGLR-UHFFFAOYSA-N C[n]1ncc(N)c1 Chemical compound C[n]1ncc(N)c1 LBGSWBJURUFGLR-UHFFFAOYSA-N 0.000 description 1
- NWLXFOOZMVQJGB-HDJSIYSDSA-N C[n]1ncc(Nc(nc2N[C@H](CC3)CC[C@@H]3NCCO)nc3c2nc(C2CC2)[s]3)c1 Chemical compound C[n]1ncc(Nc(nc2N[C@H](CC3)CC[C@@H]3NCCO)nc3c2nc(C2CC2)[s]3)c1 NWLXFOOZMVQJGB-HDJSIYSDSA-N 0.000 description 1
- DHNBGVDKUJUKJR-UHFFFAOYSA-N Cc1nc(c(Cl)ncn2)c2[s]1 Chemical compound Cc1nc(c(Cl)ncn2)c2[s]1 DHNBGVDKUJUKJR-UHFFFAOYSA-N 0.000 description 1
- KBDDBVUGXFDYMV-UHFFFAOYSA-N Cc1nc(c(N)ncn2)c2[s]1 Chemical compound Cc1nc(c(N)ncn2)c2[s]1 KBDDBVUGXFDYMV-UHFFFAOYSA-N 0.000 description 1
- FNZAKTNAISILTH-UHFFFAOYSA-N Cc1nc2c(NC(CC3)CCC3N(C)C)ncnc2[s]1 Chemical compound Cc1nc2c(NC(CC3)CCC3N(C)C)ncnc2[s]1 FNZAKTNAISILTH-UHFFFAOYSA-N 0.000 description 1
- CSORXNRVBMFODM-UHFFFAOYSA-N Clc1nc(Cl)nc2c1nc(C1CC1)[s]2 Chemical compound Clc1nc(Cl)nc2c1nc(C1CC1)[s]2 CSORXNRVBMFODM-UHFFFAOYSA-N 0.000 description 1
- FUEVXJKHFCZCJK-ZKCHVHJHSA-N N[C@H](CC1)CC[C@@H]1NCCO Chemical compound N[C@H](CC1)CC[C@@H]1NCCO FUEVXJKHFCZCJK-ZKCHVHJHSA-N 0.000 description 1
- VEHPZWYCFFRGFK-UHFFFAOYSA-N Nc(c(Cl)ncn1)c1S Chemical compound Nc(c(Cl)ncn1)c1S VEHPZWYCFFRGFK-UHFFFAOYSA-N 0.000 description 1
- AXQLNAAVMSWBEQ-UHFFFAOYSA-N Nc1c[n](CCO)nc1 Chemical compound Nc1c[n](CCO)nc1 AXQLNAAVMSWBEQ-UHFFFAOYSA-N 0.000 description 1
- DKRFTVNSGPIYMJ-UHFFFAOYSA-N O=C(c1c(N2)[s]c(C3CC3)n1)NC2=O Chemical compound O=C(c1c(N2)[s]c(C3CC3)n1)NC2=O DKRFTVNSGPIYMJ-UHFFFAOYSA-N 0.000 description 1
- NSFJLZWISHCCPW-XYPYZODXSA-N OCCN[C@H](CC1)CC[C@@H]1Nc1nc(Cl)nc2c1nc(C1CC1)[s]2 Chemical compound OCCN[C@H](CC1)CC[C@@H]1Nc1nc(Cl)nc2c1nc(C1CC1)[s]2 NSFJLZWISHCCPW-XYPYZODXSA-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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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| PCT/US2014/057444 WO2015048281A1 (en) | 2013-09-27 | 2014-09-25 | Irak inhibitors and uses thereof |
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| EP (1) | EP3049086A4 (https=) |
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| JP2021529751A (ja) * | 2018-06-25 | 2021-11-04 | 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Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | IRAK4阻害薬としてのイソチアゾロ[5,4−d]ピリミジン化合物 |
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| CHEMISTRY OF HETEROCYCLIC COMPOUNDS, vol. 40(10), JPN6018016201, 2004, pages 1352 - 1358, ISSN: 0003926598 * |
| JOURNAL OF HETEROCYCLIC CHEMISTRY, vol. 12, JPN6018016203, 1975, pages 883 - 887, ISSN: 0003926599 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2021529751A (ja) * | 2018-06-25 | 2021-11-04 | 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Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | IRAK4阻害薬としてのイソチアゾロ[5,4−d]ピリミジン化合物 |
| JP7511489B2 (ja) | 2018-06-25 | 2024-07-05 | 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 | IRAK4阻害薬としてのイソチアゾロ[5,4-d]ピリミジン化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015048281A1 (en) | 2015-04-02 |
| US9518065B2 (en) | 2016-12-13 |
| KR20160092991A (ko) | 2016-08-05 |
| RU2016110852A3 (https=) | 2018-06-25 |
| TW201522349A (zh) | 2015-06-16 |
| EP3049086A1 (en) | 2016-08-03 |
| BR112016006319A2 (pt) | 2017-08-01 |
| US20170035766A1 (en) | 2017-02-09 |
| RU2016110852A (ru) | 2017-10-30 |
| EP3049086A4 (en) | 2017-02-22 |
| CA2925211A1 (en) | 2015-04-02 |
| US20150094305A1 (en) | 2015-04-02 |
| MX2016003843A (es) | 2017-02-15 |
| CN106232122A (zh) | 2016-12-14 |
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