JP2015520769A5 - - Google Patents
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- JP2015520769A5 JP2015520769A5 JP2015514535A JP2015514535A JP2015520769A5 JP 2015520769 A5 JP2015520769 A5 JP 2015520769A5 JP 2015514535 A JP2015514535 A JP 2015514535A JP 2015514535 A JP2015514535 A JP 2015514535A JP 2015520769 A5 JP2015520769 A5 JP 2015520769A5
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- JP
- Japan
- Prior art keywords
- group
- alkyl
- substituents
- independently selected
- cycloalkyl
- 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.)
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- 125000001424 substituent group Chemical group 0.000 claims description 112
- 125000000217 alkyl group Chemical group 0.000 claims description 109
- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 55
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 47
- 229910052717 sulfur Inorganic materials 0.000 claims description 38
- 125000000623 heterocyclic group Chemical group 0.000 claims description 37
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 36
- 229910052760 oxygen Inorganic materials 0.000 claims description 36
- 125000001624 naphthyl group Chemical group 0.000 claims description 34
- 125000001072 heteroaryl group Chemical group 0.000 claims description 32
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 30
- 125000005842 heteroatoms Chemical group 0.000 claims description 30
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 29
- 229910052757 nitrogen Inorganic materials 0.000 claims description 28
- 125000004429 atoms Chemical group 0.000 claims description 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 22
- 201000010099 disease Diseases 0.000 claims description 20
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 19
- FDDDEECHVMSUSB-UHFFFAOYSA-N Sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims description 18
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 18
- XPXMKIXDFWLRAA-UHFFFAOYSA-N hydrazinide Chemical compound [NH-]N XPXMKIXDFWLRAA-UHFFFAOYSA-N 0.000 claims description 18
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 18
- 229960001663 sulfanilamide Drugs 0.000 claims description 18
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 18
- 150000003573 thiols Chemical class 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 125000004043 oxo group Chemical group O=* 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 13
- 230000000495 immunoinflammatory Effects 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000011780 sodium chloride Substances 0.000 claims description 9
- 206010011401 Crohn's disease Diseases 0.000 claims description 7
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 7
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 7
- 206010009900 Colitis ulcerative Diseases 0.000 claims description 6
- 206010020751 Hypersensitivity Diseases 0.000 claims description 6
- 206010072736 Rheumatic disease Diseases 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 6
- 201000004681 psoriasis Diseases 0.000 claims description 6
- 201000006704 ulcerative colitis Diseases 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 2
- 230000000240 adjuvant Effects 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 2
- 125000006588 heterocycloalkylene group Chemical group 0.000 claims 1
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 description 6
- 125000001326 naphthylalkyl group Chemical group 0.000 description 6
- 201000005794 allergic hypersensitivity disease Diseases 0.000 description 3
- 0 CC(CC(c1ccccc1)=O)=C(C=CC=C1)C1=CC(SCCN(C)C)=** Chemical compound CC(CC(c1ccccc1)=O)=C(C=CC=C1)C1=CC(SCCN(C)C)=** 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Cc1ccccc1 Chemical compound Cc1ccccc1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 206010009887 Colitis Diseases 0.000 description 1
- XDZBDLYXHMKEPU-UHFFFAOYSA-N Fc1cc(NCc2nc(OCCN3CCCCC3)cc3c2cccc3)cc(F)c1 Chemical compound Fc1cc(NCc2nc(OCCN3CCCCC3)cc3c2cccc3)cc(F)c1 XDZBDLYXHMKEPU-UHFFFAOYSA-N 0.000 description 1
- SOVOWYHTJTWTFL-UHFFFAOYSA-N NCCCc1cc(cccc2)c2c(NC=O)n1 Chemical compound NCCCc1cc(cccc2)c2c(NC=O)n1 SOVOWYHTJTWTFL-UHFFFAOYSA-N 0.000 description 1
- YOEBCMBOBHLGML-UHFFFAOYSA-N O=C(Cc1nc(SCCN2CCCCC2)cc2c1cccc2)c1cc(F)cc(F)c1 Chemical compound O=C(Cc1nc(SCCN2CCCCC2)cc2c1cccc2)c1cc(F)cc(F)c1 YOEBCMBOBHLGML-UHFFFAOYSA-N 0.000 description 1
- ASZRNYIGTQIFJA-UHFFFAOYSA-N O=C(c1ccccc1)Nc1nc(CCCN2CCCC2)cc2c1cccc2 Chemical compound O=C(c1ccccc1)Nc1nc(CCCN2CCCC2)cc2c1cccc2 ASZRNYIGTQIFJA-UHFFFAOYSA-N 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261654385P | 2012-06-01 | 2012-06-01 | |
US61/654,385 | 2012-06-01 | ||
PCT/EP2013/061330 WO2013178816A1 (en) | 2012-06-01 | 2013-05-31 | Heterocycles capable of modulating t-cell responses, and methods of using same |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2015520769A JP2015520769A (ja) | 2015-07-23 |
JP2015520769A5 true JP2015520769A5 (US07714131-20100511-C00001.png) | 2016-07-21 |
JP6167173B2 JP6167173B2 (ja) | 2017-07-19 |
Family
ID=48538006
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015514535A Expired - Fee Related JP6167173B2 (ja) | 2012-06-01 | 2013-05-31 | T細胞受容体を調節することができる複素環およびそれを使用するための方法 |
Country Status (19)
Families Citing this family (42)
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CN113825739A (zh) | 2019-02-08 | 2021-12-21 | 诺格拉制药有限公司 | 制备3-(4’-氨基苯基)-2-甲氧基丙酸及其类似物和中间体的方法 |
JP2022539208A (ja) | 2019-07-03 | 2022-09-07 | スミトモ ファーマ オンコロジー, インコーポレイテッド | チロシンキナーゼ非受容体1(tnk1)阻害剤およびその使用 |
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JP2023526332A (ja) | 2020-05-15 | 2023-06-21 | アルゲン バイオテクノロジーズ,インク. | 特定の化学組成物およびその使用方法 |
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-
2012
- 2012-08-01 US US13/564,118 patent/US9013997B2/en active Active
- 2012-09-12 US US13/611,252 patent/US9325637B2/en not_active Expired - Fee Related
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2013
- 2013-05-31 PL PL13726006T patent/PL2861575T3/pl unknown
- 2013-05-31 SI SI201331441T patent/SI2861575T1/sl unknown
- 2013-05-31 ES ES13726006T patent/ES2726109T3/es active Active
- 2013-05-31 MX MX2014014658A patent/MX366205B/es active IP Right Grant
- 2013-05-31 HU HUE13726006A patent/HUE043201T2/hu unknown
- 2013-05-31 JP JP2015514535A patent/JP6167173B2/ja not_active Expired - Fee Related
- 2013-05-31 CN CN201380033708.0A patent/CN104619691B/zh not_active Expired - Fee Related
- 2013-05-31 AU AU2013269551A patent/AU2013269551B2/en not_active Ceased
- 2013-05-31 CA CA2874938A patent/CA2874938C/en active Active
- 2013-05-31 PT PT13726006T patent/PT2861575T/pt unknown
- 2013-05-31 LT LTEP13726006.3T patent/LT2861575T/lt unknown
- 2013-05-31 WO PCT/EP2013/061330 patent/WO2013178816A1/en active Application Filing
- 2013-05-31 KR KR1020147036727A patent/KR102181914B1/ko active IP Right Grant
- 2013-05-31 BR BR112014030050A patent/BR112014030050A2/pt not_active IP Right Cessation
- 2013-05-31 EP EP13726006.3A patent/EP2861575B1/en active Active
- 2013-05-31 US US14/404,839 patent/US10208017B2/en active Active
- 2013-05-31 DK DK13726006.3T patent/DK2861575T3/da active
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2018
- 2018-12-21 US US16/229,687 patent/US10562883B2/en not_active Expired - Fee Related
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2019
- 2019-04-25 HR HRP20190764 patent/HRP20190764T1/hr unknown
- 2019-05-10 CY CY20191100506T patent/CY1122203T1/el unknown