JP2016530213A5 - - Google Patents
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- Publication number
- JP2016530213A5 JP2016530213A5 JP2016515522A JP2016515522A JP2016530213A5 JP 2016530213 A5 JP2016530213 A5 JP 2016530213A5 JP 2016515522 A JP2016515522 A JP 2016515522A JP 2016515522 A JP2016515522 A JP 2016515522A JP 2016530213 A5 JP2016530213 A5 JP 2016530213A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- sulfonyl
- tetrahydroquinolin
- fluorophenyl
- hexafluoro
- 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
- -1 1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl Chemical group 0.000 claims 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 5
- 125000003118 aryl group Chemical group 0.000 claims 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000003107 substituted aryl group Chemical group 0.000 claims 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 208000030159 metabolic disease Diseases 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims 1
- RBEJZPHWOONGBK-UHFFFAOYSA-N 1-benzyl-3-[[1-(4-fluorophenyl)sulfonyl-6-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-3,4-dihydro-2H-quinolin-2-yl]methyl]urea Chemical compound OC(c1ccc2N(C(CNC(=O)NCc3ccccc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F RBEJZPHWOONGBK-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 208000023275 Autoimmune disease Diseases 0.000 claims 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 1
- MZFZBDFNAPJWGY-PIEWVDTRSA-N C(C)O\N=C(/C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)\C Chemical compound C(C)O\N=C(/C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)\C MZFZBDFNAPJWGY-PIEWVDTRSA-N 0.000 claims 1
- MZFZBDFNAPJWGY-NLQLCTRYSA-N C(C)O\N=C(\C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)/C Chemical compound C(C)O\N=C(\C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)/C MZFZBDFNAPJWGY-NLQLCTRYSA-N 0.000 claims 1
- JCAYOVKPNKUDOP-KQWLVTFDSA-N C1(=CC=CC=C1)O\N=C(\C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)/C Chemical compound C1(=CC=CC=C1)O\N=C(\C[C@H]1N(C2=CC=C(C=C2CC1)C(C(F)(F)F)(C(F)(F)F)O)S(=O)(=O)C1=CC=C(C=C1)F)/C JCAYOVKPNKUDOP-KQWLVTFDSA-N 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 1
- YYLNNBFDGZYCLZ-KRWDZBQOSA-N CC(C)(N)Cc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 Chemical compound CC(C)(N)Cc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 YYLNNBFDGZYCLZ-KRWDZBQOSA-N 0.000 claims 1
- LVYLRMXJXROXMH-INIZCTEOSA-N CC(C)(O)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 Chemical compound CC(C)(O)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 LVYLRMXJXROXMH-INIZCTEOSA-N 0.000 claims 1
- QDZCCHJOVLZIEY-BJQOMGFOSA-N CC(O)(CO)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 Chemical compound CC(O)(CO)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 QDZCCHJOVLZIEY-BJQOMGFOSA-N 0.000 claims 1
- QRVIJCNOXJMAQE-BGERDNNASA-N CCC(O)Cn1ccc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)n1 Chemical compound CCC(O)Cn1ccc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)n1 QRVIJCNOXJMAQE-BGERDNNASA-N 0.000 claims 1
- KOVFYSOWRLIZNN-HNNXBMFYSA-N CSc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)s1 Chemical compound CSc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)s1 KOVFYSOWRLIZNN-HNNXBMFYSA-N 0.000 claims 1
- ORUXJAJOWWWKDP-IBGZPJMESA-N FC(C(C(F)(F)F)(O)C=1C=C2CC[C@H](N(C2=CC=1)S(=O)(=O)C1=CC=C(C=C1)F)CC=1OC(=NN=1)C1=CC=NC=C1)(F)F Chemical compound FC(C(C(F)(F)F)(O)C=1C=C2CC[C@H](N(C2=CC=1)S(=O)(=O)C1=CC=C(C=C1)F)CC=1OC(=NN=1)C1=CC=NC=C1)(F)F ORUXJAJOWWWKDP-IBGZPJMESA-N 0.000 claims 1
- LCTMAKMOTSGICZ-UHFFFAOYSA-N FC1=CC=C(C=C1)S(=O)(=O)N1C(CCC2=CC(=CC=C12)C(C(F)(F)F)(C(F)(F)F)O)CNC(=O)NC1=CC=CC=C1 Chemical compound FC1=CC=C(C=C1)S(=O)(=O)N1C(CCC2=CC(=CC=C12)C(C(F)(F)F)(C(F)(F)F)O)CNC(=O)NC1=CC=CC=C1 LCTMAKMOTSGICZ-UHFFFAOYSA-N 0.000 claims 1
- QBLZQBOPZUOSEP-INIZCTEOSA-N FC1=CC=C(C=C1)S(=O)(=O)N1[C@@H](CCC2=CC(=CC=C12)C(C(F)(F)F)(C(F)(F)F)O)CC(=O)NNC(C(C)(C)O)=O Chemical compound FC1=CC=C(C=C1)S(=O)(=O)N1[C@@H](CCC2=CC(=CC=C12)C(C(F)(F)F)(C(F)(F)F)O)CC(=O)NNC(C(C)(C)O)=O QBLZQBOPZUOSEP-INIZCTEOSA-N 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- YVMCWBSJFQJLMS-INIZCTEOSA-N NC1(CC1)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 Chemical compound NC1(CC1)c1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 YVMCWBSJFQJLMS-INIZCTEOSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- GQGJVWYUFIORRZ-IBGZPJMESA-N OC(c1ccc2N([C@H](CC(=O)NNC(=O)c3ccncc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F Chemical compound OC(c1ccc2N([C@H](CC(=O)NNC(=O)c3ccncc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F GQGJVWYUFIORRZ-IBGZPJMESA-N 0.000 claims 1
- GTDXVWUKRLIACM-NRFANRHFSA-N OC(c1ccc2N([C@H](CNCc3ccccc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F Chemical compound OC(c1ccc2N([C@H](CNCc3ccccc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F GTDXVWUKRLIACM-NRFANRHFSA-N 0.000 claims 1
- MNHHBYVJYTWBGO-INIZCTEOSA-N OC(c1ccc2N([C@H](CNS(=O)(=O)C3CC3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F Chemical compound OC(c1ccc2N([C@H](CNS(=O)(=O)C3CC3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F MNHHBYVJYTWBGO-INIZCTEOSA-N 0.000 claims 1
- WPOUYVFYBNAPSI-DEOSSOPVSA-N OC(c1ccc2N([C@H](Cc3ccnn3Cc3ccc(F)cc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F Chemical compound OC(c1ccc2N([C@H](Cc3ccnn3Cc3ccc(F)cc3)CCc2c1)S(=O)(=O)c1ccc(F)cc1)(C(F)(F)F)C(F)(F)F WPOUYVFYBNAPSI-DEOSSOPVSA-N 0.000 claims 1
- YYGNTJLVXLCHGQ-BHWOMJMDSA-N OCC(O)Cc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 Chemical compound OCC(O)Cc1nnc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)o1 YYGNTJLVXLCHGQ-BHWOMJMDSA-N 0.000 claims 1
- JJGIBUJPPDJWMM-XJDOXCRVSA-N OCC(O)Cn1ccc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)n1 Chemical compound OCC(O)Cn1ccc(C[C@@H]2CCc3cc(ccc3N2S(=O)(=O)c2ccc(F)cc2)C(O)(C(F)(F)F)C(F)(F)F)n1 JJGIBUJPPDJWMM-XJDOXCRVSA-N 0.000 claims 1
- HBNJOSMGIAZNMX-XJDOXCRVSA-N OCC(O)Cn1nccc1C[C@@H]1CCc2cc(ccc2N1S(=O)(=O)c1ccc(F)cc1)C(O)(C(F)(F)F)C(F)(F)F Chemical compound OCC(O)Cn1nccc1C[C@@H]1CCc2cc(ccc2N1S(=O)(=O)c1ccc(F)cc1)C(O)(C(F)(F)F)C(F)(F)F HBNJOSMGIAZNMX-XJDOXCRVSA-N 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 208000026935 allergic disease Diseases 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 239000004202 carbamide Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000016097 disease of metabolism Diseases 0.000 claims 1
- 208000035475 disorder Diseases 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- NKFLEFWUYAUDJV-UHFFFAOYSA-N pyridine-3-sulfonamide Chemical compound NS(=O)(=O)C1=CC=CN=C1 NKFLEFWUYAUDJV-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361880391P | 2013-09-20 | 2013-09-20 | |
| US61/880,391 | 2013-09-20 | ||
| PCT/US2014/056197 WO2015042212A1 (en) | 2013-09-20 | 2014-09-18 | RORγ MODULATORS |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016530213A JP2016530213A (ja) | 2016-09-29 |
| JP2016530213A5 true JP2016530213A5 (enExample) | 2017-10-26 |
| JP6397488B2 JP6397488B2 (ja) | 2018-09-26 |
Family
ID=51726859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016515522A Expired - Fee Related JP6397488B2 (ja) | 2013-09-20 | 2014-09-18 | ＲＯＲγ調節因子 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9725443B2 (enExample) |
| EP (1) | EP3046906B1 (enExample) |
| JP (1) | JP6397488B2 (enExample) |
| CN (1) | CN105555768B (enExample) |
| WO (1) | WO2015042212A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015035278A1 (en) | 2013-09-09 | 2015-03-12 | Bristol-Myers Squibb Company | RORγ MODULATORS |
| EP3046906B1 (en) | 2013-09-20 | 2017-08-16 | Bristol-Myers Squibb Company | Ror gamma modulators |
| JP6463362B2 (ja) * | 2013-12-19 | 2019-01-30 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | ＲＯＲ−ガンマ阻害剤としてのテトラヒドロ−テトラゾロ［１，５−ａ］ピラジン |
| EP3092215B1 (en) | 2014-01-06 | 2018-10-17 | Bristol-Myers Squibb Company | Cyclohexyl sulfone ror gamma modulators |
| US9771320B2 (en) | 2014-01-06 | 2017-09-26 | Bristol-Myers Squibb Company | Carbocyclic sulfone RORγ modulators |
| EP3092221B1 (en) | 2014-01-06 | 2018-10-17 | Bristol-Myers Squibb Company | Heterocyclic sulfones as ror-gamma modulators |
| LT3212641T (lt) | 2014-10-30 | 2019-02-11 | Janssen Pharmaceutica Nv | Tiazolai, kaip roryt moduliatoriai |
| EP3212642B1 (en) | 2014-10-30 | 2019-10-30 | Janssen Pharmaceutica NV | Amide substituted thiazoles as modulators of rorgammat |
| TWI667230B (zh) | 2014-10-30 | 2019-08-01 | 比利時商健生藥品公司 | 用作ＲＯＲγｔ調節劑之三氟甲基醇 |
| KR102114536B1 (ko) * | 2015-05-07 | 2020-05-22 | 브리스톨-마이어스 스큅 컴퍼니 | RORγ 조정제로서의 트리시클릭 술폰 |
| TW201803869A (zh) | 2016-04-27 | 2018-02-01 | 健生藥品公司 | 作為ＲＯＲγＴ調節劑之６－胺基吡啶－３－基噻唑 |
| WO2017213210A1 (ja) * | 2016-06-10 | 2017-12-14 | 武田薬品工業株式会社 | 複素環化合物 |
| KR102506326B1 (ko) * | 2016-10-13 | 2023-03-03 | 브리스톨-마이어스 스큅 컴퍼니 | Ror 감마 조정제로서의 헤테로시클릭 술폰 |
| EP3806958B1 (en) | 2018-06-18 | 2022-09-07 | Janssen Pharmaceutica NV | 6-aminopyridin-3-yl pyrazoles as modulators of roryt |
| CA3103929A1 (en) | 2018-06-18 | 2019-12-26 | Janssen Pharmaceutica Nv | Phenyl substituted pyrazoles as modulators of roryt |
| ES2925473T3 (es) | 2018-06-18 | 2022-10-18 | Janssen Pharmaceutica Nv | Pirazoles de piridinilo como moduladores de RORyt |
| CN112334450A (zh) | 2018-06-18 | 2021-02-05 | 詹森药业有限公司 | 作为RORγt的调节剂的苯基和吡啶基取代的咪唑 |
| CN111635373B (zh) * | 2019-03-01 | 2022-07-12 | 山东轩竹医药科技有限公司 | 多环磺酰胺类RORγ调节剂 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITMI20012060A1 (it) * | 2001-10-05 | 2003-04-05 | Recordati Chem Pharm | Nuovi eterocilcli n-acilati |
| US7741317B2 (en) * | 2005-10-21 | 2010-06-22 | Bristol-Myers Squibb Company | LXR modulators |
| EP2368886A1 (en) * | 2010-03-01 | 2011-09-28 | Phenex Pharmaceuticals AG | Novel compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (ROR gamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune desease |
| JP6063870B2 (ja) | 2010-11-08 | 2017-01-18 | ライセラ・コーポレイション | ＲＯＲγ活性の阻害用のＮ−スルホニル化テトラヒドロキノリンおよび関連二環化合物および病気の治療 |
| WO2013064231A1 (en) * | 2011-10-31 | 2013-05-10 | Phenex Pharmaceuticals Ag | SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3) |
| WO2014062938A1 (en) | 2012-10-19 | 2014-04-24 | Bristol-Myers Squibb Company | Rory modulators |
| WO2015035278A1 (en) | 2013-09-09 | 2015-03-12 | Bristol-Myers Squibb Company | RORγ MODULATORS |
| EP3046906B1 (en) | 2013-09-20 | 2017-08-16 | Bristol-Myers Squibb Company | Ror gamma modulators |
| KR101544975B1 (ko) * | 2013-09-30 | 2015-08-18 | 주식회사 플라즈마트 | 임피던스 매칭 방법 및 임피던스 매칭 시스템 |
| EP3092215B1 (en) | 2014-01-06 | 2018-10-17 | Bristol-Myers Squibb Company | Cyclohexyl sulfone ror gamma modulators |
| EP3092221B1 (en) | 2014-01-06 | 2018-10-17 | Bristol-Myers Squibb Company | Heterocyclic sulfones as ror-gamma modulators |
| CA2936116A1 (en) | 2014-01-06 | 2015-07-09 | Bristol-Myers Squibb Company | Pyrrolidinyl sulfone derivatives and their use as ror gamma modulators |
| US9771320B2 (en) | 2014-01-06 | 2017-09-26 | Bristol-Myers Squibb Company | Carbocyclic sulfone RORγ modulators |
-
2014
- 2014-09-18 EP EP14784387.4A patent/EP3046906B1/en not_active Not-in-force
- 2014-09-18 CN CN201480051836.2A patent/CN105555768B/zh not_active Expired - Fee Related
- 2014-09-18 US US15/022,673 patent/US9725443B2/en active Active
- 2014-09-18 JP JP2016515522A patent/JP6397488B2/ja not_active Expired - Fee Related
- 2014-09-18 WO PCT/US2014/056197 patent/WO2015042212A1/en not_active Ceased