CA3029901A1 - Trpa1 antagonists for treatment of dry eye, ocular pain and inflammation - Google Patents
Trpa1 antagonists for treatment of dry eye, ocular pain and inflammation Download PDFInfo
- Publication number
- CA3029901A1 CA3029901A1 CA3029901A CA3029901A CA3029901A1 CA 3029901 A1 CA3029901 A1 CA 3029901A1 CA 3029901 A CA3029901 A CA 3029901A CA 3029901 A CA3029901 A CA 3029901A CA 3029901 A1 CA3029901 A1 CA 3029901A1
- Authority
- CA
- Canada
- Prior art keywords
- carbonyl
- group
- fluoro
- trifluoromethyl
- pyrazole
- 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.)
- Abandoned
Links
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- 206010015958 Eye pain Diseases 0.000 title claims abstract description 31
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- 206010061218 Inflammation Diseases 0.000 title claims description 36
- 238000011282 treatment Methods 0.000 title claims description 33
- 239000005557 antagonist Substances 0.000 title abstract description 46
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- UKKYZDPIIQYFFN-UHFFFAOYSA-N 1'-(4-fluorophenyl)-8-[1-[3-fluoro-4-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]spiro[8-azabicyclo[3.2.1]octane-3,5'-imidazolidine]-4'-one Chemical compound FC=1C=C(C=CC=1C(F)(F)F)N1N=C(C=C1C=1C=NC=CC=1)C(=O)N1C2CC3(N(CNC3=O)C3=CC=C(C=C3)F)CC1CC2 UKKYZDPIIQYFFN-UHFFFAOYSA-N 0.000 claims 1
- JPWWTDVAVSKWSK-UHFFFAOYSA-N 1'-(4-fluorophenyl)-8-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]spiro[8-azabicyclo[3.2.1]octane-3,5'-imidazolidine]-4'-one Chemical compound FC1=C(C=C(C=C1)N1N=C(C=C1C=1C=NC=CC=1)C(=O)N1C2CC3(N(CNC3=O)C3=CC=C(C=C3)F)CC1CC2)C(F)(F)F JPWWTDVAVSKWSK-UHFFFAOYSA-N 0.000 claims 1
- ZKTKBCKGLVJVBD-UHFFFAOYSA-N 1-(3,5-dichloro-4-fluorophenyl)-8-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound ClC=1C=C(C=C(C=1F)Cl)N1CNC(C11CCN(CC1)C(=O)C1=NN(C(=C1)C=1C=NC=CC=1)C1=CC(=C(C=C1)F)C(F)(F)F)=O ZKTKBCKGLVJVBD-UHFFFAOYSA-N 0.000 claims 1
- NXPDAOKLDWMPEG-UHFFFAOYSA-N 1-(4-fluoro-3,5-dimethylphenyl)-8-[1-[3-fluoro-4-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound FC1=C(C=C(C=C1C)N1CNC(C11CCN(CC1)C(=O)C1=NN(C(=C1)C=1C=NC=CC=1)C1=CC(=C(C=C1)C(F)(F)F)F)=O)C NXPDAOKLDWMPEG-UHFFFAOYSA-N 0.000 claims 1
- NDIKNOFRWJDXNK-UHFFFAOYSA-N 1-(4-fluoro-3,5-dimethylphenyl)-8-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound FC1=C(C=C(C=C1C)N1CNC(C11CCN(CC1)C(=O)C1=NN(C(=C1)C=1C=NC=CC=1)C1=CC(=C(C=C1)F)C(F)(F)F)=O)C NDIKNOFRWJDXNK-UHFFFAOYSA-N 0.000 claims 1
- ITJHHIJGDAYDTJ-UHFFFAOYSA-N 1-(4-fluoro-3,5-dimethylphenyl)-8-[5-pyridin-3-yl-1-(3,4,5-trifluorophenyl)pyrazole-3-carbonyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound FC1=C(C=C(C=C1C)N1CNC(C11CCN(CC1)C(=O)C1=NN(C(=C1)C=1C=NC=CC=1)C1=CC(=C(C(=C1)F)F)F)=O)C ITJHHIJGDAYDTJ-UHFFFAOYSA-N 0.000 claims 1
- AMHQMFAHIHSLDV-UHFFFAOYSA-N 1-(4-fluorophenyl)-8-[1-(4-iodophenyl)-5-pyridin-3-ylpyrazole-3-carbonyl]-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound FC1=CC=C(C=C1)N1CNC(C11CCN(CC1)C(=O)C1=NN(C(=C1)C=1C=NC=CC=1)C1=CC=C(C=C1)I)=O AMHQMFAHIHSLDV-UHFFFAOYSA-N 0.000 claims 1
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- ISGGQJCENPCMHH-UHFFFAOYSA-N 3-[1-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]piperidin-4-yl]-2-oxo-1H-benzimidazole-5-carbonitrile Chemical compound FC1=C(C=C(C=C1)N1N=C(C=C1C=1C=NC=CC=1)C(=O)N1CCC(CC1)N1C(NC2=C1C=C(C=C2)C#N)=O)C(F)(F)F ISGGQJCENPCMHH-UHFFFAOYSA-N 0.000 claims 1
- IFEITTVRIWOATK-UHFFFAOYSA-N 3-[1-[4-bromo-5-pyridin-3-yl-1-(3,4,5-trifluorophenyl)pyrazole-3-carbonyl]piperidin-4-yl]-4,5-difluoro-1H-benzimidazol-2-one Chemical compound BrC=1C(=NN(C=1C=1C=NC=CC=1)C1=CC(=C(C(=C1)F)F)F)C(=O)N1CCC(CC1)N1C(NC2=C1C(=C(C=C2)F)F)=O IFEITTVRIWOATK-UHFFFAOYSA-N 0.000 claims 1
- JLRADJYECXRWJF-UHFFFAOYSA-N 3-[1-[5-(1-benzylimidazol-4-yl)-1-[4-fluoro-3-(trifluoromethyl)phenyl]pyrazole-3-carbonyl]piperidin-4-yl]-4,5-difluoro-1H-benzimidazol-2-one Chemical compound C(C1=CC=CC=C1)N1C=NC(=C1)C1=CC(=NN1C1=CC(=C(C=C1)F)C(F)(F)F)C(=O)N1CCC(CC1)N1C(NC2=C1C(=C(C=C2)F)F)=O JLRADJYECXRWJF-UHFFFAOYSA-N 0.000 claims 1
- IHDPXOBJCHYLMX-UHFFFAOYSA-N 3-[1-[5-(2-chloropyridin-3-yl)-1-[3-fluoro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonyl]piperidin-4-yl]-4,5-difluoro-1H-benzimidazol-2-one Chemical compound ClC1=NC=CC=C1C1=CC(=NN1C1=CC(=C(C=C1)C(F)(F)F)F)C(=O)N1CCC(CC1)N1C(NC2=C1C(=C(C=C2)F)F)=O IHDPXOBJCHYLMX-UHFFFAOYSA-N 0.000 claims 1
- FRFPHRYOGAKFQJ-UHFFFAOYSA-N 3-[1-[5-(6-chloropyridin-3-yl)-1-[3-fluoro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonyl]piperidin-4-yl]-4,5-difluoro-1H-benzimidazol-2-one Chemical compound ClC1=CC=C(C=N1)C1=CC(=NN1C1=CC(=C(C=C1)C(F)(F)F)F)C(=O)N1CCC(CC1)N1C(NC2=C1C(=C(C=C2)F)F)=O FRFPHRYOGAKFQJ-UHFFFAOYSA-N 0.000 claims 1
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- UQGJAQREPBRLBR-UHFFFAOYSA-N 4,5-difluoro-3-[1-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-4,5-dihydropyrazolo[4,3-h]quinoline-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C=3C4=C(CCC2=3)C=CC=N4)C2=CC(=C(C=C2)F)C(F)(F)F)C=1F UQGJAQREPBRLBR-UHFFFAOYSA-N 0.000 claims 1
- DWZCVEGKROROSG-UHFFFAOYSA-N 4,5-difluoro-3-[1-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyrazin-2-ylpyrazole-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C(=C2)C2=NC=CN=C2)C2=CC(=C(C=C2)F)C(F)(F)F)C=1F DWZCVEGKROROSG-UHFFFAOYSA-N 0.000 claims 1
- UHZFMTHVAVWUDU-UHFFFAOYSA-N 4,5-difluoro-3-[1-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]-2-methylpiperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CC(N(CC2)C(=O)C2=NN(C(=C2)C=2C=NC=CC=2)C2=CC(=C(C=C2)F)C(F)(F)F)C)C=1F UHZFMTHVAVWUDU-UHFFFAOYSA-N 0.000 claims 1
- BCJHFNAFVFJEAF-UHFFFAOYSA-N 4,5-difluoro-3-[1-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C(=C2)C=2C=NC=CC=2)C2=CC(=C(C=C2)F)C(F)(F)F)C=1F BCJHFNAFVFJEAF-UHFFFAOYSA-N 0.000 claims 1
- JAVJCSVSXAJEIV-UHFFFAOYSA-N 4,5-difluoro-3-[1-[1-[4-fluoro-3-methyl-5-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C(=C2)C=2C=NC=CC=2)C2=CC(=C(C(=C2)C(F)(F)F)F)C)C=1F JAVJCSVSXAJEIV-UHFFFAOYSA-N 0.000 claims 1
- QJHFXRZMDSAPNQ-UHFFFAOYSA-N 4,5-difluoro-3-[1-[5-(5-fluoropyridin-3-yl)-1-[3-fluoro-4-(trifluoromethyl)phenyl]pyrazole-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C(=C2)C=2C=NC=C(C=2)F)C2=CC(=C(C=C2)C(F)(F)F)F)C=1F QJHFXRZMDSAPNQ-UHFFFAOYSA-N 0.000 claims 1
- XORXFEWGEWTMRE-UHFFFAOYSA-N 4,5-difluoro-3-[1-[5-pyridazin-4-yl-1-(3,4,5-trifluorophenyl)pyrazole-3-carbonyl]piperidin-4-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CCN(CC2)C(=O)C2=NN(C(=C2)C2=CN=NC=C2)C2=CC(=C(C(=C2)F)F)F)C=1F XORXFEWGEWTMRE-UHFFFAOYSA-N 0.000 claims 1
- BVNYQOUIYSOQIZ-UHFFFAOYSA-N 4,5-difluoro-3-[8-[1-[4-fluoro-3-(trifluoromethyl)phenyl]-5-pyridin-3-ylpyrazole-3-carbonyl]-8-azabicyclo[3.2.1]octan-3-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CC3CCC(C2)N3C(=O)C2=NN(C(=C2)C=2C=NC=CC=2)C2=CC(=C(C=C2)F)C(F)(F)F)C=1F BVNYQOUIYSOQIZ-UHFFFAOYSA-N 0.000 claims 1
- AWCBPIOCXSXQKO-UHFFFAOYSA-N 4,5-difluoro-3-[8-[5-pyridin-3-yl-1-(3,4,5-trifluorophenyl)pyrazole-3-carbonyl]-8-azabicyclo[3.2.1]octan-3-yl]-1H-benzimidazol-2-one Chemical compound FC=1C=CC2=C(N(C(N2)=O)C2CC3CCC(C2)N3C(=O)C2=NN(C(=C2)C=2C=NC=CC=2)C2=CC(=C(C(=C2)F)F)F)C=1F AWCBPIOCXSXQKO-UHFFFAOYSA-N 0.000 claims 1
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- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- Medicinal Preparation (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| US201662359122P | 2016-07-06 | 2016-07-06 | |
| US62/359,122 | 2016-07-06 | ||
| PCT/US2017/040976 WO2018009717A1 (en) | 2016-07-06 | 2017-07-06 | Trpa1 antagonists for treatment of dry eye, ocular pain and inflammation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3029901A1 true CA3029901A1 (en) | 2018-01-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3029901A Abandoned CA3029901A1 (en) | 2016-07-06 | 2017-07-06 | Trpa1 antagonists for treatment of dry eye, ocular pain and inflammation |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20200179357A1 (enExample) |
| EP (1) | EP3481808A4 (enExample) |
| JP (1) | JP2019521189A (enExample) |
| CA (1) | CA3029901A1 (enExample) |
| IL (1) | IL264069A (enExample) |
| SG (1) | SG11201811655SA (enExample) |
| WO (1) | WO2018009717A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021228434A1 (en) * | 2020-05-12 | 2021-11-18 | Pharmathen S.A. | Preservative free pharmaceutical composition for ophthalmic administration containing cyclosporine |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2936111C (en) | 2014-01-06 | 2023-03-14 | Algomedix, Inc. | Trpa1 modulators |
| WO2020184479A1 (ja) * | 2019-03-08 | 2020-09-17 | ロート製薬株式会社 | 刺激感が抑制された眼科組成物 |
| US12220396B2 (en) | 2019-05-03 | 2025-02-11 | Zyus Life Sciences Inc. | Formulation for pain management |
| US12178797B2 (en) | 2019-05-03 | 2024-12-31 | Zyus Life Sciences Inc. | Formulation for pain management |
| CA3102473C (en) * | 2019-05-03 | 2021-07-06 | Zyus Life Sciences Inc. | Formulation for pain management |
| IT202100015098A1 (it) | 2021-06-09 | 2022-12-09 | Flonext S R L | Composto antagonista del canale trpa1 per uso in patologie degenerative della retina |
| KR20240032924A (ko) * | 2021-07-12 | 2024-03-12 | 오큐소프트, 인코포레이티드 | 피부 보습 조성물 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CA2331878A1 (en) * | 1998-05-14 | 1999-11-18 | G.D. Searle & Co. | 1,5-diaryl substituted pyrazoles as p38 kinase inhibitors |
| EP1620095A4 (en) * | 2003-04-24 | 2009-04-01 | Merck & Co Inc | HEMMER OF ACT ACTIVITY |
| CA2936111C (en) * | 2014-01-06 | 2023-03-14 | Algomedix, Inc. | Trpa1 modulators |
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2017
- 2017-07-06 JP JP2019520930A patent/JP2019521189A/ja active Pending
- 2017-07-06 US US16/315,113 patent/US20200179357A1/en not_active Abandoned
- 2017-07-06 CA CA3029901A patent/CA3029901A1/en not_active Abandoned
- 2017-07-06 SG SG11201811655SA patent/SG11201811655SA/en unknown
- 2017-07-06 EP EP17824925.6A patent/EP3481808A4/en not_active Ceased
- 2017-07-06 WO PCT/US2017/040976 patent/WO2018009717A1/en not_active Ceased
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2019
- 2019-01-03 IL IL264069A patent/IL264069A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021228434A1 (en) * | 2020-05-12 | 2021-11-18 | Pharmathen S.A. | Preservative free pharmaceutical composition for ophthalmic administration containing cyclosporine |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018009717A1 (en) | 2018-01-11 |
| EP3481808A1 (en) | 2019-05-15 |
| JP2019521189A (ja) | 2019-07-25 |
| EP3481808A4 (en) | 2020-07-15 |
| US20200179357A1 (en) | 2020-06-11 |
| IL264069A (en) | 2019-01-31 |
| SG11201811655SA (en) | 2019-01-30 |
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