JP2019523223A5 - - Google Patents
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- Publication number
- JP2019523223A5 JP2019523223A5 JP2018562586A JP2018562586A JP2019523223A5 JP 2019523223 A5 JP2019523223 A5 JP 2019523223A5 JP 2018562586 A JP2018562586 A JP 2018562586A JP 2018562586 A JP2018562586 A JP 2018562586A JP 2019523223 A5 JP2019523223 A5 JP 2019523223A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- optionally substituted
- represented
- heterocyclyl
- 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 description 62
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 45
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 38
- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000000623 heterocyclic group Chemical group 0.000 claims description 34
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 125000004122 cyclic group Chemical group 0.000 claims description 27
- 229910052736 halogen Inorganic materials 0.000 claims description 26
- 150000002367 halogens Chemical class 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 19
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 18
- 125000005842 heteroatom Chemical group 0.000 claims description 18
- 229910052760 oxygen Inorganic materials 0.000 claims description 18
- 239000001301 oxygen Substances 0.000 claims description 18
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 239000011593 sulfur Substances 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- -1 cyano, hydroxyl Chemical group 0.000 claims description 13
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 6
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 6
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 230000000844 anti-bacterial effect Effects 0.000 claims description 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 4
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 4
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 4
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims description 4
- 125000005110 aryl thio group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
- 125000005368 heteroarylthio group Chemical group 0.000 claims description 4
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
- 125000004468 heterocyclylthio group Chemical group 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000001204 N-oxides Chemical class 0.000 claims description 3
- 230000002538 fungal effect Effects 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- 125000006662 (C2-C4) acyloxy group Chemical group 0.000 claims description 2
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 2
- 244000038559 crop plants Species 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical group C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 244000005700 microbiome Species 0.000 claims description 2
- 125000003566 oxetanyl group Chemical group 0.000 claims description 2
- 208000029380 parasitic ectoparasitic infectious disease Diseases 0.000 claims description 2
- 239000000575 pesticide Substances 0.000 claims description 2
- 230000003032 phytopathogenic effect Effects 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 2
- 125000003003 spiro group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 239000003899 bactericide agent Substances 0.000 claims 1
- 238000001356 surgical procedure Methods 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 13
- 241000209140 Triticum Species 0.000 description 5
- 235000021307 Triticum Nutrition 0.000 description 5
- 201000010099 disease Diseases 0.000 description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 241000221785 Erysiphales Species 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241000895502 Blumeria graminis f. sp. tritici Species 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 241001123569 Puccinia recondita Species 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 125000004452 carbocyclyl group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000028644 hyphal growth Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16171966.1 | 2016-05-30 | ||
| EP16171966 | 2016-05-30 | ||
| PCT/EP2017/062443 WO2017207362A1 (en) | 2016-05-30 | 2017-05-23 | Microbiocidal thiazole derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019523223A JP2019523223A (ja) | 2019-08-22 |
| JP2019523223A5 true JP2019523223A5 (enExample) | 2021-10-21 |
| JP7001622B2 JP7001622B2 (ja) | 2022-01-19 |
Family
ID=56087210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018562586A Active JP7001622B2 (ja) | 2016-05-30 | 2017-05-23 | 殺微生物チアゾール誘導体 |
Country Status (27)
| Country | Link |
|---|---|
| US (2) | US10662182B2 (enExample) |
| EP (1) | EP3464284B1 (enExample) |
| JP (1) | JP7001622B2 (enExample) |
| KR (1) | KR102477603B1 (enExample) |
| CN (1) | CN109195966B (enExample) |
| AR (1) | AR108629A1 (enExample) |
| AU (1) | AU2017275603B2 (enExample) |
| BR (1) | BR112018074644B1 (enExample) |
| CA (1) | CA3024528A1 (enExample) |
| CL (1) | CL2018003381A1 (enExample) |
| CO (1) | CO2018012859A2 (enExample) |
| DK (1) | DK3464284T3 (enExample) |
| ES (1) | ES2842550T3 (enExample) |
| HR (1) | HRP20202074T1 (enExample) |
| HU (1) | HUE052020T2 (enExample) |
| IL (1) | IL262938B (enExample) |
| LT (1) | LT3464284T (enExample) |
| MX (1) | MX2018014441A (enExample) |
| PL (1) | PL3464284T3 (enExample) |
| PT (1) | PT3464284T (enExample) |
| RS (1) | RS61298B1 (enExample) |
| SI (1) | SI3464284T1 (enExample) |
| TW (1) | TWI746557B (enExample) |
| UA (1) | UA123515C2 (enExample) |
| UY (1) | UY37265A (enExample) |
| WO (1) | WO2017207362A1 (enExample) |
| ZA (1) | ZA201807659B (enExample) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7250759B2 (ja) * | 2017-08-09 | 2023-04-03 | シンジェンタ パーティシペーションズ アーゲー | 植物病原性微生物によるダイズ植物への侵入を防除又は防止する方法 |
| KR102697953B1 (ko) * | 2017-11-29 | 2024-08-21 | 신젠타 파티서페이션즈 아게 | 살미생물 티아졸 유도체 |
| AU2018390864B9 (en) | 2017-12-20 | 2024-12-12 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of vegetable, tomato and potato plants by phytopathogenic microorganisms |
| AR117183A1 (es) | 2018-11-30 | 2021-07-14 | Syngenta Crop Protection Ag | Derivados de tiazol microbiocidas |
| AR117200A1 (es) * | 2018-11-30 | 2021-07-21 | Syngenta Participations Ag | Derivados de tiazol microbiocidas |
| WO2020193618A1 (en) | 2019-03-27 | 2020-10-01 | Syngenta Crop Protection Ag | Microbiocidal thiazole derivatives |
| CN113924294B (zh) | 2019-05-29 | 2024-12-06 | 先正达农作物保护股份公司 | 杀微生物衍生物 |
| AR119009A1 (es) | 2019-05-29 | 2021-11-17 | Syngenta Crop Protection Ag | Derivados de alcoxipiridina y alcoxipirimidina microbicidas |
| GEP20257723B (en) | 2020-06-03 | 2025-01-27 | Syngenta Crop Protection Ag | Fungicidal compositions |
| AU2021284956A1 (en) * | 2020-06-03 | 2022-12-08 | Syngenta Crop Protection Ag | Fungicidal compositions |
| EP4161924A1 (en) | 2020-06-03 | 2023-04-12 | Syngenta Crop Protection AG | Microbiocidal derivatives |
| IL312654A (en) | 2021-12-02 | 2024-07-01 | Syngenta Crop Protection Ag | Fungicides |
| AR130569A1 (es) | 2022-09-28 | 2024-12-18 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| TW202439972A (zh) | 2022-11-30 | 2024-10-16 | 瑞士商先正達農作物保護股份公司 | 殺真菌組成物 |
| AR131665A1 (es) | 2023-02-01 | 2025-04-16 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| AR132937A1 (es) | 2023-06-14 | 2025-08-13 | Syngenta Crop Protection Ag | Composiciones fungicidas |
| AU2024302452A1 (en) | 2023-06-14 | 2025-12-04 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025031989A1 (en) | 2023-08-04 | 2025-02-13 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
| WO2025031913A1 (en) | 2023-08-04 | 2025-02-13 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
| WO2025031990A1 (en) | 2023-08-04 | 2025-02-13 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of soybean plants by the phytopathogenic microorganism corynespora cassiicola |
| TW202513532A (zh) | 2023-09-15 | 2025-04-01 | 瑞士商先正達農作物保護股份公司 | 用於製備鏡像異構物富集的脂肪族胺之方法 |
| WO2025078263A1 (en) | 2023-10-11 | 2025-04-17 | Syngenta Crop Protection Ag | Microbiocidal pyridyl pyrazole derivatives |
| WO2025104152A1 (en) | 2023-11-15 | 2025-05-22 | Syngenta Crop Protection Ag | Microbiocidal tetrahydroisoquinoline derivatives |
| WO2025114167A1 (en) | 2023-11-28 | 2025-06-05 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025120070A1 (en) | 2023-12-08 | 2025-06-12 | Syngenta Crop Protection Ag | Polymorphs of a methoxyacrylate derivative |
| WO2025163143A1 (en) | 2024-02-02 | 2025-08-07 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025172368A1 (en) | 2024-02-13 | 2025-08-21 | Syngenta Crop Protection Ag | (5-isoxazol-3-yl)-[4-(pyrazol-4-yl)-3,4-dihydro-1h-isoquinolin-2-yl]methanone derivatives for use as fungicides |
| WO2025172374A1 (en) | 2024-02-13 | 2025-08-21 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025191053A1 (en) | 2024-03-14 | 2025-09-18 | Syngenta Crop Protection Ag | Microbiocidal pyrazole derivatives |
| WO2025202482A1 (en) | 2024-03-28 | 2025-10-02 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025202499A1 (en) | 2024-03-28 | 2025-10-02 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025210095A1 (en) | 2024-04-03 | 2025-10-09 | Syngenta Crop Protection Ag | Microbiocidal tetrahydroisoquinoline compounds |
| WO2025210096A1 (en) | 2024-04-03 | 2025-10-09 | Syngenta Crop Protection Ag | Fungicidal compositions |
| WO2025210149A1 (en) | 2024-04-04 | 2025-10-09 | Syngenta Crop Protection Ag | Fungicidal composition |
| WO2025233384A1 (en) | 2024-05-08 | 2025-11-13 | Syngenta Crop Protection Ag | Microbiocidal pyrazole compounds |
| WO2025238048A1 (en) | 2024-05-15 | 2025-11-20 | Syngenta Crop Protection Ag | Fungicidal compositions |
Family Cites Families (37)
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| JPS61107392A (ja) | 1984-10-31 | 1986-05-26 | 株式会社東芝 | 画像処理システム |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| AU613521B2 (en) | 1988-09-02 | 1991-08-01 | Sankyo Company Limited | 13-substituted milbemycin derivatives, their preparation and use |
| US5169629A (en) | 1988-11-01 | 1992-12-08 | Mycogen Corporation | Process of controlling lepidopteran pests, using bacillus thuringiensis isolate denoted b.t ps81gg |
| CA2005658A1 (en) | 1988-12-19 | 1990-06-19 | Eliahu Zlotkin | Insecticidal toxins, genes encoding these toxins, antibodies binding to them and transgenic plant cells and plants expressing these toxins |
| US5015630A (en) | 1989-01-19 | 1991-05-14 | Merck & Co., Inc. | 5-oxime avermectin derivatives |
| NO176766C (no) | 1989-02-07 | 1995-05-24 | Meiji Seika Kaisha | Fremgangsmåte for fremstilling av en forbindelse med anthelmintaktivitet |
| GB8910624D0 (en) | 1989-05-09 | 1989-06-21 | Ici Plc | Bacterial strains |
| CA2015951A1 (en) | 1989-05-18 | 1990-11-18 | Mycogen Corporation | Novel bacillus thuringiensis isolates active against lepidopteran pests, and genes encoding novel lepidopteran-active toxins |
| ES2074547T3 (es) | 1989-11-07 | 1995-09-16 | Pioneer Hi Bred Int | Lectinas larvicidas, y resistencia inducida de las plantas a los insectos. |
| JPH085894B2 (ja) | 1990-03-01 | 1996-01-24 | 三共株式会社 | ミルベマイシンエーテル誘導体 |
| JPH0570366A (ja) | 1991-03-08 | 1993-03-23 | Meiji Seika Kaisha Ltd | 薬用組成物 |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| AU664392B2 (en) * | 1991-10-18 | 1995-11-16 | Monsanto Technology Llc | Fungicides for the control of take-all disease of plants |
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| EP0639572B1 (en) | 1992-04-28 | 1998-07-29 | Yashima Chemical Industry Co., Ltd. | 2-(2,6-difluorophenyl)-4-(2-ethoxy-4-tert-butylphenyl)-2-oxazoline |
| DE4317458A1 (de) | 1992-06-11 | 1993-12-16 | Bayer Ag | Verwendung von cyclischen Depsipeptiden mit 18 Ringatomen zur Bekämpfung von Endoparasiten, neue cyclische Depsipeptide mit 18 Ringatomen und Verfahren zu ihrer Herstellung |
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| DE19520936A1 (de) | 1995-06-08 | 1996-12-12 | Bayer Ag | Ektoparasitizide Mittel |
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| BR0113500A (pt) | 2000-08-25 | 2003-07-01 | Syngenta Participations Ag | Toxinas inseticidas derivadas de proteìnas de cristais inseticidas de bacillus thuringiensis |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
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| EP1916240A1 (en) * | 2006-10-25 | 2008-04-30 | Syngeta Participations AG | Pyridazine derivatives |
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| JP2016512219A (ja) * | 2013-03-15 | 2016-04-25 | シンジェンタ パーティシペーションズ アーゲー | 殺菌活性のあるイミダゾピリジン誘導体 |
| CN106316977B (zh) * | 2015-06-24 | 2018-03-20 | 华中师范大学 | 一种噻唑双酰胺类化合物及其制备方法和应用 |
| CN109923112A (zh) * | 2016-09-23 | 2019-06-21 | 先正达参股股份有限公司 | 杀微生物的噁二唑衍生物 |
-
2017
- 2017-05-23 WO PCT/EP2017/062443 patent/WO2017207362A1/en not_active Ceased
- 2017-05-23 JP JP2018562586A patent/JP7001622B2/ja active Active
- 2017-05-23 HR HRP20202074TT patent/HRP20202074T1/hr unknown
- 2017-05-23 PT PT177271616T patent/PT3464284T/pt unknown
- 2017-05-23 KR KR1020187036958A patent/KR102477603B1/ko active Active
- 2017-05-23 UA UAA201812722A patent/UA123515C2/uk unknown
- 2017-05-23 SI SI201730591T patent/SI3464284T1/sl unknown
- 2017-05-23 MX MX2018014441A patent/MX2018014441A/es unknown
- 2017-05-23 ES ES17727161T patent/ES2842550T3/es active Active
- 2017-05-23 EP EP17727161.6A patent/EP3464284B1/en active Active
- 2017-05-23 DK DK17727161.6T patent/DK3464284T3/da active
- 2017-05-23 RS RS20210016A patent/RS61298B1/sr unknown
- 2017-05-23 US US16/305,452 patent/US10662182B2/en active Active
- 2017-05-23 PL PL17727161T patent/PL3464284T3/pl unknown
- 2017-05-23 CN CN201780033106.3A patent/CN109195966B/zh active Active
- 2017-05-23 HU HUE17727161A patent/HUE052020T2/hu unknown
- 2017-05-23 LT LTEP17727161.6T patent/LT3464284T/lt unknown
- 2017-05-23 AU AU2017275603A patent/AU2017275603B2/en active Active
- 2017-05-23 BR BR112018074644-4A patent/BR112018074644B1/pt active IP Right Grant
- 2017-05-23 CA CA3024528A patent/CA3024528A1/en active Pending
- 2017-05-25 TW TW106117408A patent/TWI746557B/zh active
- 2017-05-29 AR ARP170101462A patent/AR108629A1/es active IP Right Grant
- 2017-05-29 UY UY0001037265A patent/UY37265A/es active IP Right Grant
-
2018
- 2018-11-11 IL IL262938A patent/IL262938B/en unknown
- 2018-11-14 ZA ZA2018/07659A patent/ZA201807659B/en unknown
- 2018-11-27 CO CONC2018/0012859A patent/CO2018012859A2/es unknown
- 2018-11-28 CL CL2018003381A patent/CL2018003381A1/es unknown
-
2020
- 2020-05-14 US US15/931,699 patent/US20200277288A1/en not_active Abandoned
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