JP2017538772A5 - - Google Patents
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- Publication number
- JP2017538772A5 JP2017538772A5 JP2017533502A JP2017533502A JP2017538772A5 JP 2017538772 A5 JP2017538772 A5 JP 2017538772A5 JP 2017533502 A JP2017533502 A JP 2017533502A JP 2017533502 A JP2017533502 A JP 2017533502A JP 2017538772 A5 JP2017538772 A5 JP 2017538772A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- fluoro
- ylidene
- indene
- pyridin
- 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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- -1 phosphonoalkyloxy Chemical group 0.000 claims description 36
- 239000001257 hydrogen Substances 0.000 claims description 19
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 150000002431 hydrogen Chemical class 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 229940002612 prodrug Drugs 0.000 claims description 12
- 239000000651 prodrug Substances 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 206010028980 Neoplasm Diseases 0.000 claims description 7
- 201000011510 cancer Diseases 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- AFWAIGRROIRUIR-CFRMEGHHSA-N N-benzyl-2-[(3Z)-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-6-methoxy-2-methylinden-1-yl]-N-methylacetamide Chemical compound C(C1=CC=CC=C1)N(C(CC1=C(/C(/C2=CC=C(C=C12)OC)=C/C1=CC(=C(C(=C1)OC)O)OC)C)=O)C AFWAIGRROIRUIR-CFRMEGHHSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 4
- 125000001188 haloalkyl group Chemical group 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 3
- 125000005199 aryl carbonyloxy group Chemical group 0.000 claims description 3
- 125000005200 aryloxy carbonyloxy group Chemical group 0.000 claims description 3
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 3
- 125000004193 piperazinyl group Chemical group 0.000 claims description 3
- 125000003386 piperidinyl group Chemical group 0.000 claims description 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 3
- PCFFKTCMQHWBQA-UUYOSTAYSA-N 2-[(3Z)-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-6-methoxy-2-methylinden-1-yl]-N-phenylacetamide Chemical compound OC1=C(C=C(\C=C/2\C(=C(C3=CC(=CC=C\23)OC)CC(=O)NC2=CC=CC=C2)C)C=C1OC)OC PCFFKTCMQHWBQA-UUYOSTAYSA-N 0.000 claims description 2
- TXUHXXCRGBDDLL-FBHDLOMBSA-N 2-[(3Z)-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-6-methoxy-2-methylinden-1-yl]-N-pyridin-3-ylacetamide Chemical compound OC1=C(C=C(\C=C/2\C(=C(C3=CC(=CC=C\23)OC)CC(=O)NC=2C=NC=CC=2)C)C=C1OC)OC TXUHXXCRGBDDLL-FBHDLOMBSA-N 0.000 claims description 2
- QIGYLJLEFBKRPC-NHDPSOOVSA-N 2-[(3Z)-6-fluoro-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-2-methylinden-1-yl]-N-phenylacetamide Chemical compound FC=1C=C2C(=C(/C(/C2=CC=1)=C/C1=CC(=C(C(=C1)OC)O)OC)C)CC(=O)NC1=CC=CC=C1 QIGYLJLEFBKRPC-NHDPSOOVSA-N 0.000 claims description 2
- RBHNASBMHJZBFY-MBTHVWNTSA-N 2-[4-[(Z)-[3-[2-(benzylamino)-2-oxoethyl]-5-fluoro-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl]benzoic acid Chemical compound COc1cc(\C=C2\C(C)=C(CC(=O)NCc3ccccc3)c3cc(F)ccc23)cc(OC)c1-c1ccccc1C(O)=O RBHNASBMHJZBFY-MBTHVWNTSA-N 0.000 claims description 2
- NBXUWTRRDXULPY-WGARJPEWSA-N 2-[4-[(Z)-[3-[2-(benzylamino)-2-oxoethyl]-5-fluoro-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl]pyridine-3-carboxylic acid Chemical compound COc1cc(\C=C2\C(C)=C(CC(=O)NCc3ccccc3)c3cc(F)ccc23)cc(OC)c1-c1ncccc1C(O)=O NBXUWTRRDXULPY-WGARJPEWSA-N 0.000 claims description 2
- NGMARNMVSIRBMW-WKIKZPBSSA-N 2-[4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-3-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl]benzoic acid Chemical compound COc1cc(\C=C2\C(C)=C(CC(=O)NCc3cccnc3)c3cc(F)ccc23)cc(OC)c1-c1ccccc1C(O)=O NGMARNMVSIRBMW-WKIKZPBSSA-N 0.000 claims description 2
- UXBOQICIICVKTQ-ROTLSHHCSA-N 2-[4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-3-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl]pyridine-3-carboxylic acid Chemical compound COc1cc(\C=C2\C(C)=C(CC(=O)NCc3cccnc3)c3cc(F)ccc23)cc(OC)c1-c1ncccc1C(O)=O UXBOQICIICVKTQ-ROTLSHHCSA-N 0.000 claims description 2
- WYGLMMWOUCXDKZ-MXAYSNPKSA-N 3-[4-[(Z)-[3-[2-(benzylamino)-2-oxoethyl]-5-fluoro-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl]morpholine-4-carboxylic acid Chemical compound CC\1=C(C2=C(/C1=C\C3=CC(=C(C(=C3)OC)C4COCCN4C(=O)O)OC)C=CC(=C2)F)CC(=O)NCC5=CC=CC=C5 WYGLMMWOUCXDKZ-MXAYSNPKSA-N 0.000 claims description 2
- MTBULSBBUNXIPE-MYKKPKGFSA-N 3-[4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-3-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl]morpholine-4-carboxylic acid Chemical compound CC\1=C(C2=C(/C1=C\C3=CC(=C(C(=C3)OC)C4COCCN4C(=O)O)OC)C=CC(=C2)F)CC(=O)NCC5=CN=CC=C5 MTBULSBBUNXIPE-MYKKPKGFSA-N 0.000 claims description 2
- SVKMPMCRVTTZDX-FMCGGJTJSA-N C(C1=CC=CC=C1)N(C(CC1=C(/C(/C2=CC=C(C=C12)F)=C/C1=CC(=C(C(=C1)OC)O)OC)C)=O)C Chemical compound C(C1=CC=CC=C1)N(C(CC1=C(/C(/C2=CC=C(C=C12)F)=C/C1=CC(=C(C(=C1)OC)O)OC)C)=O)C SVKMPMCRVTTZDX-FMCGGJTJSA-N 0.000 claims description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
- 101150040459 RAS gene Proteins 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- PSJOJUFEHGAVOJ-YUMHPJSZSA-N [4-[(Z)-[3-[2-(benzylamino)-2-oxoethyl]-5-fluoro-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl] 4-methylpiperazine-1-carboxylate Chemical compound CN1CCN(CC1)C(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(=O)NCC1=CC=CC=C1)C)OC PSJOJUFEHGAVOJ-YUMHPJSZSA-N 0.000 claims description 2
- UNTJZMUWOQKHLZ-JJFYIABZSA-N [4-[(Z)-[3-[2-(benzylamino)-2-oxoethyl]-5-fluoro-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl] dihydrogen phosphate Chemical compound P(=O)(OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(=O)NCC1=CC=CC=C1)C)OC)(O)O UNTJZMUWOQKHLZ-JJFYIABZSA-N 0.000 claims description 2
- QCBZYUZGBWSIQZ-WGARJPEWSA-N [4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-3-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl] 4-methylpiperazine-1-carboxylate Chemical compound CN1CCN(CC1)C(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(NCC=1C=NC=CC=1)=O)C)OC QCBZYUZGBWSIQZ-WGARJPEWSA-N 0.000 claims description 2
- MTFAUHWAFJFHDY-NKVSQWTQSA-N [4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-3-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl] dihydrogen phosphate Chemical compound P(=O)(OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(NCC=1C=NC=CC=1)=O)C)OC)(O)O MTFAUHWAFJFHDY-NKVSQWTQSA-N 0.000 claims description 2
- AVTSZWAGYNVUHA-DICXZTSXSA-N [4-[(Z)-[5-fluoro-3-[2-(3-methoxyanilino)-2-oxoethyl]-2-methylinden-1-ylidene]methyl]-2,6-dimethoxyphenyl] 4-methylpiperazine-1-carboxylate Chemical compound CN1CCN(CC1)C(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(=O)NC1=CC(=CC=C1)OC)C)OC AVTSZWAGYNVUHA-DICXZTSXSA-N 0.000 claims description 2
- 230000003213 activating effect Effects 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 235000013877 carbamide Nutrition 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 2
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 2
- 230000035772 mutation Effects 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 108700042226 ras Genes Proteins 0.000 claims description 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 2
- 229940124530 sulfonamide Drugs 0.000 claims description 2
- 150000003456 sulfonamides Chemical class 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 238000009472 formulation Methods 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- CJBUOVAXMPVXFB-UKWGHVSLSA-N 2-[(3Z)-6-fluoro-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-2-methylinden-1-yl]-N-(furan-2-ylmethyl)acetamide Chemical compound FC=1C=C2C(=C(/C(/C2=CC=1)=C/C1=CC(=C(C(=C1)OC)O)OC)C)CC(=O)NCC=1OC=CC=1 CJBUOVAXMPVXFB-UKWGHVSLSA-N 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 21
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound 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 description 4
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 230000009036 growth inhibition Effects 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- MHQQLIAOAFTDTO-YSMPRRRNSA-N [4-[(Z)-[5-fluoro-2-methyl-3-[2-oxo-2-(pyridin-2-ylmethylamino)ethyl]inden-1-ylidene]methyl]-2,6-dimethoxyphenyl] 4-methylpiperazine-1-carboxylate Chemical compound CN1CCN(CC1)C(=O)OC1=C(C=C(C=C1OC)\C=C/1\C(=C(C2=CC(=CC=C\12)F)CC(NCC1=NC=CC=C1)=O)C)OC MHQQLIAOAFTDTO-YSMPRRRNSA-N 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000005907 cancer growth Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000001394 metastastic effect Effects 0.000 description 1
- 206010061289 metastatic neoplasm Diseases 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14/571,690 | 2014-12-16 | ||
| US14/571,690 US20160168108A1 (en) | 2014-12-16 | 2014-12-16 | Method of treating or preventing ras-mediated diseases |
| PCT/US2015/066154 WO2016100546A1 (en) | 2014-12-16 | 2015-12-16 | Method of treating or preventing ras-mediated diseases |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020005245A Division JP2020055882A (ja) | 2014-12-16 | 2020-01-16 | Ｒａｓ媒介性疾患を処置または予防する方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017538772A JP2017538772A (ja) | 2017-12-28 |
| JP2017538772A5 true JP2017538772A5 (enExample) | 2019-01-24 |
| JP6763858B2 JP6763858B2 (ja) | 2020-09-30 |
Family
ID=55077649
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017533502A Expired - Fee Related JP6763858B2 (ja) | 2014-12-16 | 2015-12-16 | Ｒａｓ媒介性疾患を処置または予防する方法 |
| JP2020005245A Withdrawn JP2020055882A (ja) | 2014-12-16 | 2020-01-16 | Ｒａｓ媒介性疾患を処置または予防する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020005245A Withdrawn JP2020055882A (ja) | 2014-12-16 | 2020-01-16 | Ｒａｓ媒介性疾患を処置または予防する方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (4) | US20160168108A1 (enExample) |
| EP (2) | EP3666268A1 (enExample) |
| JP (2) | JP6763858B2 (enExample) |
| CN (1) | CN107466232B (enExample) |
| DK (1) | DK3233071T3 (enExample) |
| ES (1) | ES2760898T3 (enExample) |
| PT (1) | PT3233071T (enExample) |
| WO (1) | WO2016100546A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9862698B2 (en) | 2014-12-16 | 2018-01-09 | Adt Pharmaceuticals, Inc. | Indenyl compounds, pharmaceutical compositions, and medical uses thereof |
| US20160168108A1 (en) | 2014-12-16 | 2016-06-16 | Adt Pharmaceuticals, Inc. | Method of treating or preventing ras-mediated diseases |
| WO2018170410A1 (en) | 2017-03-17 | 2018-09-20 | University Of South Alabama | Derivatives of sulindac can protect normal cells against oxidative damage |
| AU2018323528B2 (en) * | 2017-08-31 | 2023-01-12 | Leukogene Therapeutics Incorporated | Indene derivatives and uses thereof |
| US11186596B2 (en) | 2018-04-26 | 2021-11-30 | Adt Pharmaceuticals, Llc | Anticancer indenes, indanes, azaindenes, azaindanes, pharmaceutical compositions and uses |
| MX2020011991A (es) * | 2018-05-10 | 2021-04-12 | Univ Louisville Res Found Inc | Inhibidores de la oncoproteina ras, metodos de produccion y metodos de uso de los mismos. |
| US12310986B2 (en) | 2018-08-21 | 2025-05-27 | Board Of Regents, The University Of Texas System | Compositions and methods for the treatment of cancer cells by induction of cytotoxic oxidative stress |
| CN115916194A (zh) | 2020-06-18 | 2023-04-04 | 锐新医药公司 | 用于延迟、预防和治疗针对ras抑制剂的获得性抗性的方法 |
| EP4208261A1 (en) | 2020-09-03 | 2023-07-12 | Revolution Medicines, Inc. | Use of sos1 inhibitors to treat malignancies with shp2 mutations |
| CN113289020B (zh) * | 2021-05-17 | 2023-04-18 | 福州大学 | 蛋白质二硫键异构酶小分子抑制剂及其应用 |
| WO2025006967A1 (en) | 2023-06-30 | 2025-01-02 | Bristol-Myers Squibb Company | Kras inhibitors |
| WO2025148858A1 (zh) * | 2024-01-08 | 2025-07-17 | 应世生物科技(南京)有限公司 | FAK抑制剂和Pan-RAS抑制剂 |
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| NL7200058A (enExample) | 1971-01-21 | 1972-07-25 | ||
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-
2014
- 2014-12-16 US US14/571,690 patent/US20160168108A1/en not_active Abandoned
-
2015
- 2015-12-16 EP EP19197686.9A patent/EP3666268A1/en not_active Withdrawn
- 2015-12-16 WO PCT/US2015/066154 patent/WO2016100546A1/en not_active Ceased
- 2015-12-16 CN CN201580076204.6A patent/CN107466232B/zh not_active Expired - Fee Related
- 2015-12-16 DK DK15821218T patent/DK3233071T3/da active
- 2015-12-16 US US15/537,283 patent/US11104658B2/en not_active Expired - Fee Related
- 2015-12-16 JP JP2017533502A patent/JP6763858B2/ja not_active Expired - Fee Related
- 2015-12-16 PT PT158212183T patent/PT3233071T/pt unknown
- 2015-12-16 EP EP15821218.3A patent/EP3233071B1/en active Active
- 2015-12-16 ES ES15821218T patent/ES2760898T3/es active Active
-
2016
- 2016-02-29 US US15/056,202 patent/US9931315B2/en not_active Expired - Fee Related
-
2020
- 2020-01-16 JP JP2020005245A patent/JP2020055882A/ja not_active Withdrawn
- 2020-04-01 US US16/837,757 patent/US11198679B2/en not_active Expired - Fee Related
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