JP2016536286A5 - - Google Patents
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- Publication number
- JP2016536286A5 JP2016536286A5 JP2016521347A JP2016521347A JP2016536286A5 JP 2016536286 A5 JP2016536286 A5 JP 2016536286A5 JP 2016521347 A JP2016521347 A JP 2016521347A JP 2016521347 A JP2016521347 A JP 2016521347A JP 2016536286 A5 JP2016536286 A5 JP 2016536286A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- compound
- formula
- hdac6
- 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.)
- Granted
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- 150000003839 salts Chemical class 0.000 claims 25
- 102000011427 Histone Deacetylase 6 Human genes 0.000 claims 19
- 108010023925 Histone Deacetylase 6 Proteins 0.000 claims 19
- 239000003112 inhibitor Substances 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 11
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical group C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 6
- 206010006187 Breast cancer Diseases 0.000 claims 5
- 208000026310 Breast neoplasm Diseases 0.000 claims 5
- 102000003964 Histone deacetylase Human genes 0.000 claims 4
- 108090000353 Histone deacetylase Proteins 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 125000001475 halogen functional group Chemical group 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 229940125497 HER2 kinase inhibitor Drugs 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- SJVQHLPISAIATJ-ZDUSSCGKSA-N 8-chloro-2-phenyl-3-[(1S)-1-(7H-purin-6-ylamino)ethyl]-1-isoquinolinone Chemical group C1([C@@H](NC=2C=3N=CNC=3N=CN=2)C)=CC2=CC=CC(Cl)=C2C(=O)N1C1=CC=CC=C1 SJVQHLPISAIATJ-ZDUSSCGKSA-N 0.000 claims 1
- 239000002136 L01XE07 - Lapatinib Substances 0.000 claims 1
- 239000012828 PI3K inhibitor Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 230000004709 cell invasion Effects 0.000 claims 1
- 230000012292 cell migration Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- -1 each of which is OH Chemical group 0.000 claims 1
- 229940121372 histone deacetylase inhibitor Drugs 0.000 claims 1
- 239000003276 histone deacetylase inhibitor Substances 0.000 claims 1
- 229960003445 idelalisib Drugs 0.000 claims 1
- YKLIKGKUANLGSB-HNNXBMFYSA-N idelalisib Chemical compound C1([C@@H](NC=2[C]3N=CN=C3N=CN=2)CC)=NC2=CC=CC(F)=C2C(=O)N1C1=CC=CC=C1 YKLIKGKUANLGSB-HNNXBMFYSA-N 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 229960004891 lapatinib Drugs 0.000 claims 1
- BCFGMOOMADDAQU-UHFFFAOYSA-N lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 claims 1
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 claims 1
- LHNIIDJUOCFXAP-UHFFFAOYSA-N pictrelisib Chemical compound C1CN(S(=O)(=O)C)CCN1CC1=CC2=NC(C=3C=4C=NNC=4C=CC=3)=NC(N3CCOCC3)=C2S1 LHNIIDJUOCFXAP-UHFFFAOYSA-N 0.000 claims 1
- 238000011287 therapeutic dose Methods 0.000 claims 1
- 0 *N(CCCCCCC(NO)=O)C(c1cnc(N(*)C2=CC=CC=CC2)nc1)=O Chemical compound *N(CCCCCCC(NO)=O)C(c1cnc(N(*)C2=CC=CC=CC2)nc1)=O 0.000 description 3
- VLIUIBXPEDFJRF-UHFFFAOYSA-N ONC(CCCCCCNC(c1cnc(N(c2ccccc2)c(cccc2)c2Cl)nc1)=O)=O Chemical compound ONC(CCCCCCNC(c1cnc(N(c2ccccc2)c(cccc2)c2Cl)nc1)=O)=O VLIUIBXPEDFJRF-UHFFFAOYSA-N 0.000 description 2
- QGZYDVAGYRLSKP-UHFFFAOYSA-N ONC(CCCCCCNC(c1cnc(N(c2ccccc2)c2ccccc2)nc1)=O)=O Chemical compound ONC(CCCCCCNC(c1cnc(N(c2ccccc2)c2ccccc2)nc1)=O)=O QGZYDVAGYRLSKP-UHFFFAOYSA-N 0.000 description 2
- LIIWIMDSZVNYHY-UHFFFAOYSA-N ONC(c1cnc(NC2(CC2)c2ccccc2)nc1)=O Chemical compound ONC(c1cnc(NC2(CC2)c2ccccc2)nc1)=O LIIWIMDSZVNYHY-UHFFFAOYSA-N 0.000 description 2
- IYBURCQQEUNLDL-UHFFFAOYSA-N ONC(c1cnc(NC2(CCCCC2)c2cccc(F)c2)nc1)=O Chemical compound ONC(c1cnc(NC2(CCCCC2)c2cccc(F)c2)nc1)=O IYBURCQQEUNLDL-UHFFFAOYSA-N 0.000 description 2
- PQDKJKQGRALNHS-QZQOTICOSA-N CCC/C(/C(NCCCCCCC(NO)=O)=O)=C\N=C(/N)\N(c1ccccc1)c1ccccc1 Chemical compound CCC/C(/C(NCCCCCCC(NO)=O)=O)=C\N=C(/N)\N(c1ccccc1)c1ccccc1 PQDKJKQGRALNHS-QZQOTICOSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361888207P | 2013-10-08 | 2013-10-08 | |
| US61/888,207 | 2013-10-08 | ||
| PCT/US2014/059238 WO2015054099A1 (en) | 2013-10-08 | 2014-10-06 | Combinations of histone deacetylase inhibitors and either her2 inhibitors or pi3k inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016536286A JP2016536286A (ja) | 2016-11-24 |
| JP2016536286A5 true JP2016536286A5 (cg-RX-API-DMAC7.html) | 2017-11-16 |
| JP6626437B2 JP6626437B2 (ja) | 2019-12-25 |
Family
ID=52777441
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016521347A Active JP6626437B2 (ja) | 2013-10-08 | 2014-10-06 | ヒストンデアセチラーゼ阻害剤とHer2阻害剤またはPI3K阻害剤のいずれかの組み合わせ |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US9403779B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3054952B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6626437B2 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2929576T3 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2015054099A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (34)
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| JP6584391B2 (ja) * | 2013-10-10 | 2019-10-02 | アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. | 非ホジキンリンパ腫を治療するための、hdac阻害剤単独またはpi3k阻害剤との組み合わせ |
| US20150105409A1 (en) * | 2013-10-10 | 2015-04-16 | Acetylon Pharmaceticals, Inc. | Hdac inhibitors, alone or in combination with btk inhibitors, for treating nonhodgkin's lymphoma |
| EA201690753A1 (ru) * | 2013-10-11 | 2016-07-29 | Эситайлон Фармасьютикалз, Инк. | Комбинации ингибиторов гистондеацетилазы и иммуномодулирующих лекарственных средств |
| EP3060217B1 (en) | 2013-10-24 | 2022-06-08 | Mayo Foundation for Medical Education and Research | Treatment of polycystic diseases with an hdac6 inhibitor |
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| US20150359794A1 (en) | 2014-06-13 | 2015-12-17 | Buck Institute For Research On Aging | Impairment of the large ribosomal subunit protein rpl24 by depletion or acetylation |
| CN107205988A (zh) * | 2014-07-07 | 2017-09-26 | 埃斯泰隆制药公司 | 利用组蛋白脱乙酰酶抑制剂治疗白血病 |
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| WO2017184774A1 (en) * | 2016-04-19 | 2017-10-26 | Acetylon Pharmaceuticals, Inc. | Hdac inhibitors, alone or in combination with btk inhibitors, for treating chronic lymphocytic leukemia |
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2014
- 2014-10-06 JP JP2016521347A patent/JP6626437B2/ja active Active
- 2014-10-06 EP EP14851657.8A patent/EP3054952B1/en active Active
- 2014-10-06 US US14/506,889 patent/US9403779B2/en active Active
- 2014-10-06 WO PCT/US2014/059238 patent/WO2015054099A1/en not_active Ceased
- 2014-10-06 ES ES14851657T patent/ES2929576T3/es active Active
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2016
- 2016-06-22 US US15/189,554 patent/US10722512B2/en active Active