JP2013529611A5 - - Google Patents
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- Publication number
- JP2013529611A5 JP2013529611A5 JP2013515827A JP2013515827A JP2013529611A5 JP 2013529611 A5 JP2013529611 A5 JP 2013529611A5 JP 2013515827 A JP2013515827 A JP 2013515827A JP 2013515827 A JP2013515827 A JP 2013515827A JP 2013529611 A5 JP2013529611 A5 JP 2013529611A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- triazolo
- chlorophenyl
- ethylacetamide
- 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
Links
- 125000000217 alkyl group Chemical group 0.000 claims 31
- 150000003839 salts Chemical class 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- -1 amino, hydroxyl Chemical group 0.000 claims 5
- 125000004452 carbocyclyl group Chemical group 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 229940125763 bromodomain inhibitor Drugs 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- PJPRMRNFJZOFLA-FQEVSTJZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(1h-pyrazol-4-yl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C2=CNN=C2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 PJPRMRNFJZOFLA-FQEVSTJZSA-N 0.000 claims 1
- WMKQEPQCESYBNS-FQEVSTJZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(1h-pyrazol-5-yl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2NN=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 WMKQEPQCESYBNS-FQEVSTJZSA-N 0.000 claims 1
- HFCOQWDWESZNEW-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-(2-methylphenyl)-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C(=CC=CC=2)C)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 HFCOQWDWESZNEW-DEOSSOPVSA-N 0.000 claims 1
- QKKNSYUKNJSTRL-NDEPHWFRSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[3-(pyrrolidin-1-ylmethyl)phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(CN3CCCC3)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 QKKNSYUKNJSTRL-NDEPHWFRSA-N 0.000 claims 1
- PILKZSVRGDSFDN-LJAQVGFWSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[3-[(4-methylpiperazin-1-yl)methyl]phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(CN3CCN(C)CC3)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 PILKZSVRGDSFDN-LJAQVGFWSA-N 0.000 claims 1
- UCHHERPHYGYXQM-NDEPHWFRSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[4-(pyrrolidin-1-ylmethyl)phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN3CCCC3)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 UCHHERPHYGYXQM-NDEPHWFRSA-N 0.000 claims 1
- DODSTUSXECRXBY-LJAQVGFWSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN3CCN(C)CC3)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 DODSTUSXECRXBY-LJAQVGFWSA-N 0.000 claims 1
- LBNZQYJSQFKTMP-QHCPKHFHSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-phenyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 LBNZQYJSQFKTMP-QHCPKHFHSA-N 0.000 claims 1
- MXNRKTOXHIEBKM-QFIPXVFZSA-N 2-[(4s)-6-(4-chlorophenyl)-1-methyl-8-pyridin-4-yl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CN=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 MXNRKTOXHIEBKM-QFIPXVFZSA-N 0.000 claims 1
- SPAMVIHCDISFJZ-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(3-methoxyphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=C(OC)C=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 SPAMVIHCDISFJZ-DEOSSOPVSA-N 0.000 claims 1
- DBNRUVQIPZTZFK-DEOSSOPVSA-N 2-[(4s)-6-(4-chlorophenyl)-8-(4-methoxyphenyl)-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(OC)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 DBNRUVQIPZTZFK-DEOSSOPVSA-N 0.000 claims 1
- JZVFVHUUEWVBPO-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[3-(ethylaminomethyl)phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound CCNCC1=CC=CC(C=2C=C3C(N4C(C)=NN=C4[C@H](CC(=O)NCC)N=C3C=3C=CC(Cl)=CC=3)=CC=2)=C1 JZVFVHUUEWVBPO-SANMLTNESA-N 0.000 claims 1
- PHVGVVDKYSSPKA-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[4-(ethylaminomethyl)phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound C1=CC(CNCC)=CC=C1C1=CC=C2N3C(C)=NN=C3[C@H](CC(=O)NCC)N=C(C=3C=CC(Cl)=CC=3)C2=C1 PHVGVVDKYSSPKA-SANMLTNESA-N 0.000 claims 1
- USCJQEZHNLJYPQ-SANMLTNESA-N 2-[(4s)-6-(4-chlorophenyl)-8-[4-[(dimethylamino)methyl]phenyl]-1-methyl-4h-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-4-yl]-n-ethylacetamide Chemical compound N([C@H](C1=NN=C(C)N1C1=CC=C(C=C11)C=2C=CC(CN(C)C)=CC=2)CC(=O)NCC)=C1C1=CC=C(Cl)C=C1 USCJQEZHNLJYPQ-SANMLTNESA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 230000001363 autoimmune Effects 0.000 claims 1
- 229940049706 benzodiazepine Drugs 0.000 claims 1
- 150000001557 benzodiazepines Chemical class 0.000 claims 1
- 125000003310 benzodiazepinyl group Chemical group N1N=C(C=CC2=C1C=CC=C2)* 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 230000002757 inflammatory effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1010514.6 | 2010-06-22 | ||
| GBGB1010514.6A GB201010514D0 (en) | 2010-06-22 | 2010-06-22 | Novel compounds |
| GB1106801.2 | 2011-04-21 | ||
| GBGB1106801.2A GB201106801D0 (en) | 2011-04-21 | 2011-04-21 | Novel compounds |
| PCT/EP2011/060179 WO2011161031A1 (en) | 2010-06-22 | 2011-06-20 | Benzotriazolodiazepine compounds inhibitors of bromodomains |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013529611A JP2013529611A (ja) | 2013-07-22 |
| JP2013529611A5 true JP2013529611A5 (cg-RX-API-DMAC10.html) | 2014-06-05 |
| JP5844358B2 JP5844358B2 (ja) | 2016-01-13 |
Family
ID=44310320
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013515827A Expired - Fee Related JP5844358B2 (ja) | 2010-06-22 | 2011-06-20 | ベンゾトリアゾロジアゼピン化合物を含むブロモドメイン阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9085582B2 (cg-RX-API-DMAC10.html) |
| EP (1) | EP2585465B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP5844358B2 (cg-RX-API-DMAC10.html) |
| ES (1) | ES2526671T3 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2011161031A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (81)
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| US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| MX373121B (es) | 2010-05-14 | 2020-04-30 | Dana Farber Cancer Inst Inc | Composiciones y metodos para el tratamiento de leucemia. |
| JP6022442B2 (ja) | 2010-05-14 | 2016-11-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | 男性用避妊組成物および使用方法 |
| CN103037865B (zh) | 2010-05-14 | 2014-10-29 | 达那-法伯癌症研究所 | 用于治疗瘤形成、炎性疾病和其他失调的化合物 |
| US9249161B2 (en) | 2010-12-02 | 2016-02-02 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| AR084070A1 (es) | 2010-12-02 | 2013-04-17 | Constellation Pharmaceuticals Inc | Inhibidores del bromodominio y usos de los mismos |
| EP2705039B1 (en) | 2011-05-04 | 2017-07-26 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| US9328117B2 (en) | 2011-06-17 | 2016-05-03 | Constellation Pharmaceuticals, Inc. | Bromodomain inhibitors and uses thereof |
| WO2013027168A1 (en) | 2011-08-22 | 2013-02-28 | Pfizer Inc. | Novel heterocyclic compounds as bromodomain inhibitors |
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| US9422290B2 (en) | 2012-11-13 | 2016-08-23 | Boehringer Ingelheim International Gmbh | Triazolopyridazine |
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| CN105377851B (zh) | 2013-03-11 | 2018-07-20 | 密执安州立大学董事会 | Bet布罗莫结构域抑制剂和使用这些抑制剂的治疗方法 |
| JP2016516701A (ja) | 2013-03-11 | 2016-06-09 | アッヴィ・インコーポレイテッド | 縮合四環系ブロモドメイン阻害剤 |
| EP2970330B1 (en) * | 2013-03-12 | 2019-04-17 | AbbVie Inc. | Tetracyclic bromodomain inhibitors |
| WO2014159392A1 (en) | 2013-03-14 | 2014-10-02 | Dana-Farber Cancer Institute, Inc. | Bromodomain binding reagents and uses thereof |
| MX366703B (es) | 2013-03-15 | 2019-07-22 | Incyte Holdings Corp | Heterociclos tricíclicos como inhibidores de la proteína bet. |
| MX366623B (es) | 2013-04-26 | 2019-07-16 | Beigene Ltd | 5-(3,5-dimetilisoxazol-4-il)indolina-2-onas sustituidas. |
| CN105209467B (zh) | 2013-05-27 | 2018-06-08 | 诺华股份有限公司 | 咪唑并吡咯烷酮衍生物及其在治疗疾病中的用途 |
| US8975417B2 (en) | 2013-05-27 | 2015-03-10 | Novartis Ag | Pyrazolopyrrolidine derivatives and their use in the treatment of disease |
| CA2912986A1 (en) | 2013-05-28 | 2014-12-04 | Novartis Ag | Pyrazolo-pyrrolidin-4-one derivatives as bet inhibitors and their use in the treatment of disease |
| PL3004112T3 (pl) | 2013-05-28 | 2018-02-28 | Novartis Ag | Pochodne pirazolo-pirolidyn-4-onu oraz ich zastosowanie w leczeniu choroby |
| US9290514B2 (en) | 2013-07-08 | 2016-03-22 | Incyte Holdings Corporation | Tricyclic heterocycles as BET protein inhibitors |
| BR112016001457A2 (pt) | 2013-07-25 | 2017-08-29 | Dana Farber Cancer Inst Inc | Inibidores de fatores de transcrição e usos dos mesmos |
| CA2929652A1 (en) | 2013-11-08 | 2015-05-14 | Dana-Farber Cancer Institute, Inc. | Combination therapy for cancer using bromodomain and extra-terminal (bet) protein inhibitors |
| AU2014351413B2 (en) | 2013-11-21 | 2017-06-01 | Novartis Ag | Pyrrolopyrrolone derivatives and their use as BET inhibitors |
| US9315501B2 (en) | 2013-11-26 | 2016-04-19 | Incyte Corporation | Bicyclic heterocycles as BET protein inhibitors |
| US9399640B2 (en) | 2013-11-26 | 2016-07-26 | Incyte Corporation | Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors |
| GB201320994D0 (en) * | 2013-11-28 | 2014-01-15 | Univ Dundee | Enzyme function probes |
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| EA034972B1 (ru) | 2014-04-23 | 2020-04-13 | Инсайт Корпорейшн | 1h-пирроло[2,3-c]пиридин-7(6h)-оны в качестве ингибиторов белков bet |
| CN106687463B (zh) | 2014-06-20 | 2019-04-09 | 星座制药公司 | 一种乙酰胺类化合物的晶型 |
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| KR20180132861A (ko) | 2016-04-12 | 2018-12-12 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | Bet 단백질 분해제 |
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2011
- 2011-06-20 ES ES11725769.1T patent/ES2526671T3/es active Active
- 2011-06-20 US US13/702,177 patent/US9085582B2/en not_active Expired - Fee Related
- 2011-06-20 WO PCT/EP2011/060179 patent/WO2011161031A1/en not_active Ceased
- 2011-06-20 JP JP2013515827A patent/JP5844358B2/ja not_active Expired - Fee Related
- 2011-06-20 EP EP11725769.1A patent/EP2585465B1/en not_active Not-in-force