AR101316A1 - Moléculas que tienen determinadas utilidades pesticidas, e intermediarios, composiciones y procesos relacionados con ellas - Google Patents
Moléculas que tienen determinadas utilidades pesticidas, e intermediarios, composiciones y procesos relacionados con ellasInfo
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- AR101316A1 AR101316A1 ARP150102370A ARP150102370A AR101316A1 AR 101316 A1 AR101316 A1 AR 101316A1 AR P150102370 A ARP150102370 A AR P150102370A AR P150102370 A ARP150102370 A AR P150102370A AR 101316 A1 AR101316 A1 AR 101316A1
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- alkyl
- alkenyl
- alkynyl
- oxy
- phenyl
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Moléculas que tienen una utilidad pesticida contra plagas en los filos Nematoda, Artropoda y/o Mollusca, a procesos para producir tales moléculas e intermediarios usados en tales procesos, a composiciones que contienen tales moléculas y a procesos de uso de tales moléculas contra tales plagas. Estas moléculas se pueden usar, por ejemplo, como nematicidas, acaricidas, insecticidas, miticidas y/o molusquicidas. Reivindicación 1: Una molécula con la (1) en donde: (A) R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁹ y R¹⁰ están seleccionados cada uno, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi, en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo y cicloalqueniloxi está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi; (B) R⁸ es H; (C) L es un ligador que es (i) un enlace que conecta nitrógeno con el carbono en el anillo o (ii) un alquilo C₁₋₄ que esté opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de F, Cl, CN, OH y oxo; (D) R¹¹ se selecciona de H, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil. C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, alquil C₁₋₄-alcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆, cicloalquenil C₃₋₆-oxi, (alquil C₁₋₄)cicloalquilo C₃₋₆, C₍O₎ₐₗqᵘⁱₗₒ C₁₋₄, C₍O₎ᶠₑₙⁱₗₒ, ₍ₐₗqᵘⁱₗ C₁₋₄)C(O)alquilo C₁₋₄ y (alquil C₁₋₄)C(O)O(alquilo C₁₋₄), en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo, cicloalqueniloxi y fenilo está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, oxo y OC(O)-alquilo C₁₋₄; (E) R¹² se selecciona de (I), H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆, cicloalquenil C₃₋₆-oxi, fenilo, (alquil C₁₋₄)fenilo, O(fenilo), NH(fenilo), heterociclilo y (alquil C₁₋₄)O(heterociclilo), en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo, cicloalqueniloxi, fenilo y heterociclilo está opcionalmente sustituido, con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi; (F) R¹³ se selecciona de (I), (J), H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, (alquil C₁₋₄)(haloalcoxi C₁₋₄), haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆, cicloalquenil C₃₋₆-oxi, (alquil C₁₋₄)fenilo, O(fenilo) y NH(fenilo), en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo, cicloalqueniloxi y fenilo está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆,cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi; (G) R¹⁴ se selecciona de (J), H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆, cicloalquenil C₃₋₆-oxi, fenilo, (alquil C₁₋₄)fenilo, O(fenilo), NH(fenilo), heterociclilo y (alquil C₁₋₄)O(heterociclilo), en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo, cicloalqueniloxi, fenilo y heterociclilo está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi; (H) R¹⁵ y R¹⁶ están seleccionados cada uno, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆, cicloalquenil C₃₋₆-oxi, fenilo, (alquil C₁₋₄)fenilo, O(fenilo), NH(fenilo), heterociclilo y (alquil C₁₋₄)O(heterociclilo), en donde cada alquilo, alquenilo, alqueniloxi, alquinilo, alquiniloxi, haloalquilo, alcoxi, haloalcoxi, cicloalquilo, cicloalcoxi, cicloalquenilo, cicloalqueniloxi, fenilo y heterociclilo está opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN, NO₂, OH, alquilo C₁₋₄, alquenilo C₂₋₄, alquenil C₂₋₄-oxi, alquinilo C₂₋₄, alquinil C₂₋₄-oxi, haloalquilo C₁₋₄, alcoxi C₁₋₄, haloalcoxi C₁₋₄, cicloalquilo C₃₋₆, cicloalcoxi C₃₋₆, cicloalquenilo C₃₋₆ y cicloalquenil C₃₋₆-oxi; (I) R¹² y R¹³ pueden formar juntos opcionalmente un ligador heterohidrocarbilo saturado o insaturado de 2 a 4 miembros, que puede contener uno o varios heteroátomos seleccionados de nitrógeno, azufre y oxígeno, en donde dicho enlace heterohidrocarbilo puede estar opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN y OH; (J) R¹³ y R¹⁴ pueden formar juntos opcionalmente un ligador heterohidrocarbilo saturado o insaturado de 2 a 4 miembros, que puede contener uno o varios heteroátomos seleccionados de nitrógeno, azufre y oxígeno, en donde dicho enlace heterohidrocarbilo puede estar opcionalmente sustituido con uno o varios sustituyentes seleccionados, de modo independiente, de H, F, Cl, Br, I, CN y OH; y (K) Q se selecciona de O y S.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US201462029756P | 2014-07-28 | 2014-07-28 |
Publications (1)
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AR101316A1 true AR101316A1 (es) | 2016-12-07 |
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ARP150102370A AR101316A1 (es) | 2014-07-28 | 2015-07-27 | Moléculas que tienen determinadas utilidades pesticidas, e intermediarios, composiciones y procesos relacionados con ellas |
Country Status (17)
Country | Link |
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US (1) | US9533961B2 (es) |
EP (1) | EP3174865B1 (es) |
JP (1) | JP6646035B2 (es) |
KR (1) | KR20170038782A (es) |
CN (1) | CN106573900B (es) |
AR (1) | AR101316A1 (es) |
AU (1) | AU2015296688B2 (es) |
BR (1) | BR112016031024B8 (es) |
CA (1) | CA2954299A1 (es) |
CO (1) | CO2017000030A2 (es) |
ES (1) | ES2856845T3 (es) |
IL (1) | IL249892B (es) |
MX (1) | MX2016017089A (es) |
NZ (1) | NZ727588A (es) |
RU (1) | RU2016151745A (es) |
TW (1) | TWI670012B (es) |
WO (1) | WO2016018875A1 (es) |
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TW201625563A (zh) * | 2014-07-28 | 2016-07-16 | 陶氏農業科學公司 | 具有某些殺蟲效用之分子及與其相關之中間物、組成物及方法(一) |
CR20170413A (es) | 2015-02-11 | 2018-02-06 | Basf Se | Mezcla plaguicida que comprende un compuesto pirazol, un insecticida y un fungicida |
CN105669576B (zh) * | 2016-02-22 | 2018-12-04 | 浙江博仕达作物科技有限公司 | 一种杀菌化合物、杀菌剂组合物和制剂及其应用 |
CN107094805A (zh) * | 2017-05-02 | 2017-08-29 | 南宁为辰科技有限公司 | 一种包含樟树叶精油的植物源农药组合物及其应用 |
CN111449024A (zh) * | 2020-04-01 | 2020-07-28 | 军事科学院军事医学研究院环境医学与作业医学研究所 | 一种碘吸收抑制大鼠模型的建立方法 |
KR102434595B1 (ko) | 2020-08-06 | 2022-08-22 | 안동대학교 산학협력단 | 아스피린을 유효성분으로 포함하는 모기류 알발육 억제용 조성물 및 이를 이용한 모기류 방제방법 |
CN114436380B (zh) * | 2020-10-31 | 2023-07-28 | 中国石油化工股份有限公司 | 一种木质素基絮凝剂及其制备方法 |
WO2023118434A1 (en) * | 2021-12-22 | 2023-06-29 | Globachem Nv | Pesticidally active amide compounds |
CN118525002A (zh) | 2022-01-14 | 2024-08-20 | 恩科化学公司 | 原卟啉原氧化酶抑制剂 |
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TWI402034B (zh) | 2005-07-28 | 2013-07-21 | Dow Agrosciences Llc | 具有被層狀液晶覆膜包覆之油球之水包油乳化劑之農用組成物 |
DE102005060462A1 (de) * | 2005-12-17 | 2007-06-28 | Bayer Cropscience Ag | Biphenylcarboxamide |
WO2009072621A1 (ja) * | 2007-12-07 | 2009-06-11 | Nissan Chemical Industries, Ltd. | 置換ジヒドロアゾール化合物及び有害生物防除剤 |
WO2009102736A1 (en) | 2008-02-12 | 2009-08-20 | Dow Agrosciences Llc | Pesticidal compositions |
AP3534A (en) * | 2009-08-07 | 2016-01-13 | Dow Agrosciences Llc | Pesticidal compositions |
CA2841450C (en) * | 2011-07-12 | 2019-04-23 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
TWI654180B (zh) * | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | 殺真菌之雜環羧醯胺 |
TW201625563A (zh) * | 2014-07-28 | 2016-07-16 | 陶氏農業科學公司 | 具有某些殺蟲效用之分子及與其相關之中間物、組成物及方法(一) |
WO2016069570A2 (en) * | 2014-10-27 | 2016-05-06 | Fci Asia Pte. Ltd | Circular power connectors |
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2015
- 2015-06-25 TW TW104120569A patent/TWI670012B/zh not_active IP Right Cessation
- 2015-07-27 AR ARP150102370A patent/AR101316A1/es unknown
- 2015-07-28 CA CA2954299A patent/CA2954299A1/en not_active Abandoned
- 2015-07-28 KR KR1020177000209A patent/KR20170038782A/ko not_active Application Discontinuation
- 2015-07-28 CN CN201580034180.8A patent/CN106573900B/zh not_active Expired - Fee Related
- 2015-07-28 EP EP15828280.6A patent/EP3174865B1/en active Active
- 2015-07-28 JP JP2017500039A patent/JP6646035B2/ja not_active Expired - Fee Related
- 2015-07-28 AU AU2015296688A patent/AU2015296688B2/en not_active Ceased
- 2015-07-28 MX MX2016017089A patent/MX2016017089A/es unknown
- 2015-07-28 ES ES15828280T patent/ES2856845T3/es active Active
- 2015-07-28 US US14/810,794 patent/US9533961B2/en active Active
- 2015-07-28 NZ NZ727588A patent/NZ727588A/en not_active IP Right Cessation
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- 2015-07-28 BR BR112016031024A patent/BR112016031024B8/pt not_active IP Right Cessation
- 2015-07-28 RU RU2016151745A patent/RU2016151745A/ru unknown
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2017
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- 2017-01-04 CO CONC2017/0000030A patent/CO2017000030A2/es unknown
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US9533961B2 (en) | 2017-01-03 |
RU2016151745A (ru) | 2018-08-30 |
IL249892A0 (en) | 2017-03-30 |
CN106573900B (zh) | 2018-09-14 |
EP3174865A1 (en) | 2017-06-07 |
BR112016031024B8 (pt) | 2022-08-23 |
KR20170038782A (ko) | 2017-04-07 |
WO2016018875A1 (en) | 2016-02-04 |
AU2015296688B2 (en) | 2018-03-08 |
CA2954299A1 (en) | 2016-02-04 |
US20160024027A1 (en) | 2016-01-28 |
JP2017527534A (ja) | 2017-09-21 |
AU2015296688A1 (en) | 2017-01-12 |
MX2016017089A (es) | 2017-05-10 |
ES2856845T3 (es) | 2021-09-28 |
CO2017000030A2 (es) | 2017-04-28 |
BR112016031024A8 (pt) | 2021-03-30 |
CN106573900A (zh) | 2017-04-19 |
JP6646035B2 (ja) | 2020-02-14 |
EP3174865A4 (en) | 2018-07-11 |
IL249892B (en) | 2018-11-29 |
TWI670012B (zh) | 2019-09-01 |
NZ727588A (en) | 2018-02-23 |
BR112016031024B1 (pt) | 2021-06-08 |
TW201603708A (zh) | 2016-02-01 |
EP3174865B1 (en) | 2020-12-09 |
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