AR099828A1 - Uso de oxotetrahidroquinolinilsulfonamidas sustituidas o sus sales para aumentar la tolerancia al estrés en plantas - Google Patents
Uso de oxotetrahidroquinolinilsulfonamidas sustituidas o sus sales para aumentar la tolerancia al estrés en plantasInfo
- Publication number
- AR099828A1 AR099828A1 ARP150100870A ARP150100870A AR099828A1 AR 099828 A1 AR099828 A1 AR 099828A1 AR P150100870 A ARP150100870 A AR P150100870A AR P150100870 A ARP150100870 A AR P150100870A AR 099828 A1 AR099828 A1 AR 099828A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- alkoxy
- aryl
- amino
- Prior art date
Links
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 35
- 125000000217 alkyl group Chemical group 0.000 abstract 19
- -1 C1−8-aminocarbonyl Chemical group 0.000 abstract 10
- 125000003545 alkoxy group Chemical group 0.000 abstract 10
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 6
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 abstract 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 4
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 4
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 229920006395 saturated elastomer Polymers 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 3
- 125000001769 aryl amino group Chemical group 0.000 abstract 3
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 3
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 abstract 3
- 125000004104 aryloxy group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 3
- 125000005241 heteroarylamino group Chemical group 0.000 abstract 3
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 abstract 3
- 125000005419 heteroarylsulfonylamino group Chemical group 0.000 abstract 3
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 abstract 3
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 239000007983 Tris buffer Substances 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 2
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 2
- 125000005100 aryl amino carbonyl group Chemical group 0.000 abstract 2
- 125000005135 aryl sulfinyl group Chemical group 0.000 abstract 2
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 2
- 125000004447 heteroarylalkenyl group Chemical group 0.000 abstract 2
- 125000005222 heteroarylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000005150 heteroarylsulfinyl group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229940124530 sulfonamide Drugs 0.000 abstract 2
- 150000003456 sulfonamides Chemical class 0.000 abstract 2
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 abstract 1
- 230000036579 abiotic stress Effects 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract 1
- 125000004658 aryl carbonyl amino group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005224 heteroarylcarbonylamino group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 125000004449 heterocyclylalkenyl group Chemical group 0.000 abstract 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 150000002540 isothiocyanates Chemical class 0.000 abstract 1
- 125000004971 nitroalkyl group Chemical group 0.000 abstract 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 125000003544 oxime group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 230000035882 stress Effects 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
Classifications
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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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
-
- 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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Dispersion Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Reivindicación 1: Uso de oxotetrahidroquinolinilsulfonamidas sustituidas de la fórmula general (1) o sus sales para elevar la tolerancia al estrés en plantas frente al estrés abiótico y/o para elevar el rendimiento de la planta, en donde R¹ representa halógeno, ciano, cicloalquilo C₃₋₁₀, halocicloalquilo C₃₋₁₀ cicloalquenilo C₄₋₁₀ halocicloalquenilo C₄₋₁₀, haloalquilo C₁₋₁₀ haloalquenilo C₂₋₈, alcoxi C₁₋₈-haloalquilo C₁₋₈, arilo, aril-alquilo C₁₋₈, heteroarilo, heteroaril-alquilo C₁₋₈, cicloalquil C₃₋₈-alquilo C₁₋₈, haloalquinilo C₂₋₈, heterociclilo, heterociclil-alquilo C₁₋₈, alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-carbonil-alquilo C₁₋₈, hidroxicarbonil-alquilo C₁₋₈, alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, alquenil C₂₋₈-oxicarbonil-alquilo C₁₋₈, alquinil C₂₋₈-oxicarbonil-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, cicloalcoxi C₃₋₈-carbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, aminocarbonil-alquilo C₁₋₈, alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-aminocarbonil-alquilo C₁₋₈, aril-alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, alquil C₁₋₈-tio-alquilo C₁₋₈, cicloalquil C₃₋₈-tio-alquilo C₁₋₈, ariltio-alquilo C₁₋₈, heterocicliltio-alquilo C₁₋₈, heteroariltio-alquilo C₁₋₈, aril-alquil C₁₋₈-tio-alquilo C₁₋₈, alquil C₁₋₈-sulfinil-alquilo C₁₋₈, alquil C₁₋₈-sulfonil-alquilo C₁₋₈, arilsulfinil-alquilo C₁₋₈, arilsulfonil-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfinil-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfonil-alquilo C₁₋₈, alcoxi C₁₋₈-alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-carbonilo, haloalquil C₁₋₈-carbonilo, cicloalquil C₃₋₈-carbonilo, hidroxicarbonilo, alcoxi C₁₋₈-carbonilo, alquenil C₂₋₈-oxicarbonilo, alquinil C₂₋₈-oxicarbonilo, aril-alcoxi C₁₋₈-carbonilo, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonilo, arilcarbonilo, heteroarilcarbonilo, heterociclilcarbonilo, aril-alquil C₁₋₈-carbonilo, alquil C₁₋₈-aminocarbonilo, cicloalquil C₃₋₈-aminocarbonilo, arilaminocarbonilo, aril-alquil C₁₋₈-aminocarbonilo, heteroarilaminocarbonilo, heterociclilaminocarbonilo, heteroaril-alquil C₁₋₈-aminocarbonilo, heterociclil-alquil C₁₋₈-aminocarbonilo, alquil C₁₋₈-sulfonilo, cicloalquil C₃₋₈-sulfonilo, arilsulfonilo, aril-alquil C₁₋₈-sulfonilo, heteroarilsulfonilo, heterociclilsulfonilo, ciano-alquilo C₁₋₈, cicloalquenil C₄₋₈-alquilo C₁₋₈, nitro-alquilo C₁₋₈, haloalcoxi C₁₋₈-alquilo C₁₋₈, haloalquil C₁₋₈-tio-alquilo C₁₋₈, bis-[alquil C₁₋₈]aminocarbonilo, cicloalquil C₃₋₈-[alquil C₁₋₈]aminocarbonilo, aril-[alquil C₁₋₈]aminocarbonilo, aril-alquil C₁₋₈-[alquil C₁₋₈]aminocarbonilo, alquenil C₂₋₈-aminocarbonilo, alquinil C₂₋₈-aminocarbonilo, alquil C₁₋₈-aminosulfonilo, bis-[alquil C₁₋₈]aminosulfonilo, heterociclilsulfinil-alquilo C₁₋₃, heteroarilsulfinil-alquilo C₁₋₈, aril-alquil C₁₋₈-sulfinil-alquilo C₁₋₈, heterociclilsulfonil-alquilo C₁₋₈, heteroarilsulfonil-alquilo C₁₋₈, aril-alquil C₁₋₈-sulfonil-alquilo C₁₋₈, bis-[alquil C₁₋₈]aminocarbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-[alquil C₁₋₈]aminocarbonil-alquilo C₁₋₈, aril-[alquil C₁₋₈]aminocarbonil-alquilo C₁₋₈, aril-alquil C₁₋₈-[alquil C₁₋₈]aminocarbonil-alquilo C₁₋₈, alquenil C₂₋₈-aminocarbonil-alquilo C₁₋₈, alquinil C₂₋₈-aminocarbonilo alquilo C₁₋₈, alquil C₁₋₈-amino, bis-[alquil C₁₋₈]amino, cicloalquil C₃₋₈-[alquil C₁₋₈]amino, amino, alquenil C₂₋₈-amino, alquinil C₂₋₈-amino, arilamino, heteroarilamino, aril-alquil C₁₋₈-amino, heteroaril-alquil C₁₋₈-amino, heterociclilamino, heterociclil-alquil C₁₋₈-amino, alquenil C₂₋₈-carbonil-alquilo C₁₋₈, alquinil C₂₋₈-carbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-alquil C₁₋₈-[alquil C₁₋₈]aminocarbonil-alquilo C₁₋₈, alquenil C₂₋₈-sulfonil-alquilo C₁₋₈, alquinil C₂₋₈-sulfonil-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-sulfonil-alquilo C₁₋₈, heterociclil-alquil C₁₋₈-sulfonil-alquilo C₁₋₈, alquenil C₂₋₈-sulfinil-alquilo C₁₋₈, alquinil C₂₋₈-sulfinil-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-sulfinil-alquilo C₁₋₈, heterociclil-alquil C₁₋₈-sulfinil-alquilo C₁₋₈, alquenil C₂₋₈-oxi-alcoxi C₁₋₈-alquilo C₁₋₈, alquinil C₂₋₈-oxi-alcoxi C₁₋₈-alquilo C₁₋₈, heteroaril-alcoxi C₁₋₈-alquilo C₁₋₈, heterociclil-alcoxi C₁₋₈-alquilo C₁₋₈, tris[alquil C₁₋₈]sililo, tris[alquil C₁₋₈]silil-alquilo C₁₋₈, alcoxi C₁₋₈, haloalcoxi C₁₋₈, alquil C₁₋₈-amino-alquilo C₁₋₈, bis-[alquil C₁₋₈]amino-alquilo C₁₋₈, cicloalquil C₃₋₈-[alquil C₁₋₈]amino-alquilo C₁₋₈, amino-alquilo C₁₋₈, alquenil C₂₋₈-amino-alquilo C₁₋₈, alquinil C₂₋₈-amino-alquilo C₁₋₈, arilamino-alquilo C₁₋₈, heteroarilamino-alquilo C₁₋₈, aril-alquil C₁₋₈-amino-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-amino-alquilo C₁₋₈, heterociclilamino-alquilo C₁₋₈, heterociclil-alquil C₁₋₈-amino-alquilo C₁₋₈, haloalcoxi C₁₋₈-haloalquilo C₁₋₆, alquenil C₂₋₈-oxi-haloalquilo C₁₋₆, alquinil C₂₋₈-oxi-haloalquilo C₁₋₆, alcoxi C₁₋₈-alcoxi C₁₋₈-haloalquilo C₁₋₆, cicloalquil C₃₋₈-alcoxi C₁₋₈-haloalquilo C₁₋₆, cicloalquil C₃₋₈-alcoxi C₁₋₈-alquilo C₁₋₈, alcoxi C₁₋₈-alcoxi C₁₋₈, alcoxi C₁₋₈-carbonil-cicloalquilo C₃₋₈; R², R³, R⁴ representan, de modo independiente entre sí, hidrógeno, halógeno, alcoxi C₁₋₈, alquilo C₁₋₈, haloalquilo C₁₋₈, haloalcoxi C₁₋₈, alquil C₁₋₈-tio, haloalquil C₁₋₈-tio, arilo, aril-alquilo C₁₋₈, heteroarilo, heteroaril-alquilo C₁₋₈, heterociclilo, heterociclil-alquilo C₁₋₈, cicloalquilo C₃₋₈, nitro, amino, hidroxi, alquil C₁₋₈-amino, bis-[alquil C₁₋₈]amino, hidrotio, alquil C₁₋₈-carbonilamino, cicloalquil C₃₋₈-carbonilamino, arilcarbonilamino, heteroarilcarbonilamino, heterociclilcarbonilamino, formilo, hidroxiiminometilo, alcoxi C₁₋₈-iminometilo, cicloalcoxi C₃₋₈-iminometilo, ariloxiiminometilo, cicloalquil C₃₋₈-alcoxi C₁₋₈-iminometilo, tiocianato, isotiocianato, ariloxi, heteroariloxi, cicloalcoxi C₃₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈, aril-alcoxi C₁₋₈, alquinilo C₂₋₈, alquenilo C₂₋₈, aril-alquinilo C₁₋₈, tris-[alquil C₁₋₈]silil-alquinilo C₂₋₈, bis-[alquil C₁₋₈](aril)silil-alquinilo C₂₋₈, bis-aril[alquil C₁₋₈]silil-alquinilo C₂₋₈, cicloalquil C₃₋₈-alquinilo C₂₋₈, aril-alquenilo C₂₋₈, heteroaril-alquenilo C₂₋₈, cicloalquil C₃₋₈-alquenilo C₂₋₈, cicloalquil C₃₋₈-alquilo C₂₋₈, haloalquinilo C₂₋₈, haloalquenilo C₂₋₈, cicloalquenilo C₄₋₈, alcoxi C₁₋₈-alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-sulfonilo, arilsulfonilo, heteroarilsulfonilo, alquil C₁₋₈-sulfonilamino, arilsulfonilamino, aril-alquil C₁₋₈-sulfonilamino, heteroarilsulfonilamino, heteroaril-alquil C₁₋₈-sulfonilamino, bis-[alquil C₁₋₈]aminosulfonilo, cicloalquenil C₄₋₈-alquilo C₁₋₈, alquil C₁₋₈-sulfinilo, arilsulfinilo, heteroarilsulfinilo, haloalquil C₁₋₈-sulfinilo, haloalquil C₁₋₈-sulfonilo, aril-alquil C₁₋₈-sulfonilo, heteroaril-alquil C₁₋₈-sulfonilo, alquil C₁₋₈-aminosulfonilo, alquil C₁₋₈-aminosulfonilamino, bis-[alquil C₁₋₈]aminosulfonilo, cicloalquil C₃₋₈-aminosulfonilamino, alcoxi C₁₋₈-carbonilo, alquenil C₂₋₈-oxicarbonilo, alquinil C₂₋₈-oxicarbonilo, cicloalquil C₃₋₈-oxicarbonilo, aril-alcoxi C₁₋₈-carbonilo, alquil C₁₋₈-aminocarbonilo, cicloalquil C₃₋₈-aminocarbonilo, aril-alquil C₁₋₈-aminocarbonilo; R⁵ representa amino, alquilo C₁₋₈, cicloalquilo C₃₋₈, cicloalquil C₃₋₈-alquilo C₁₋₈, haloalquilo C₁₋₈, halocicloalquilo C₃₋₈, cicloalquenilo C₄₋₈, arilo, heteroarilo, heterociclilo, aril-alquilo C₁₋₈, heteroaril-alquilo C₁₋₈, heterociclil-alquilo C₁₋₈, alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, cicloalcoxi C₃₋₈-carbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, heteroaril-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, aminocarbonil-alquilo C₁₋₈, alquil C₁₋₈-aminocarboniI-alquilo C₁₋₈, cicloalquil C₃₋₈-aminocarbonil-alquilo C₁₋₈, aril-alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, alquil C₁₋₈-amino, arilamino, cicloalquil C₃₋₈-amino, aril-alquil C₁₋₈-amino, heteroaril-alquil C₁₋₈-amino, heteroarilamino, heterociclilamino, ariloxi-alquilo C₁₋₈, alcoxi C₁₋₈-alquilo C₁₋₈, heteroariloxi-alquilo C₁₋₈, alquenilo C₂₋₈, alquinilo C₂₋₈, alquenil C₂₋₈-amino, alquinil C₂₋₈-amino, bis-[alquenil C₁₋₈]amino, ariloxi, bis-[alquil C₁₋₈]amino, aril-alquenilo C₂₋₈, heteroaril-alquenilo C₂₋₈, heterociclil-alquenilo C₂₋₈, ariloxicarbonil-alquilo C₁₋₈, heteroariloxicarbonil-alquilo C₁₋₈, bis[alquil C₁₋₈]aminocarboniI-alquilo C₁₋₈, alquil C₁₋₈-tio-alquilo C₁₋₈, ciano-alquilo C₁₋₈, alcoxi C₁₋₈-alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-sulfonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfonilamino-alquilo C₁₋₈, arilsulfonilamino-alquilo C₁₋₈, heteroarilsulfonilamino-alquilo C₁₋₈, heterociclilsulfonilamino-alquilo C₁₋₈, bis-[alquil C₁₋₈]aminosulfonil-alquilo C₁₋₈; R⁶ representa hidrógeno, alquilo C₁₋₈, cicloalquilo C₃₋₈, ciano-alquilo C₁₋₈, cicloalquil C₃₋₈-alquilo C₁₋₈, alquil C₁₋₈-sulfonilo, arilsulfonilo, heteroarilsulfonilo, cicloalquil C₃₋₈-sulfonilo, heterociclilsulfonilo, aril-alquil C₁₋₈-sulfonilo, alquil C₁₋₈-carbonilo, arilcarbonilo, heteroarilcarbonilo, cicloalquil C₃₋₈-carbonilo, heterociclilcarbonilo, alcoxi C₁₋₈-carbonilo, aril-alcoxi C₁₋₈-carbonilo, haloalquil C₁₋₈-carbonilo, alquenilo C₂₋₈, alquinilo C₂₋₈, haloalquilo C₁₋₈, halo-alquinilo C₂₋₈, halo-alquenilo C₂₋₈, alcoxi C₁₋₈-alquilo C₁₋₈, amino, alcoxi C₁₋₈-alcoxi C₁₋₈-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-sulfonilo, heterociclil-alquil C₁₋₈-sulfonilo, cicloalquenilo C₄₋₈, cicloalquenil C₄₋₈-alquilo C₁₋₈, alquenil C₂₋₈-oxicarbonilo, alquinil C₂₋₈-oxicarbonilo, alquil C₁₋₈-aminocarbonilo, cicloalquil C₃₋₈-aminocarbonilo, bis-[alquil C₁₋₈]aminocarbonilo; R⁷ y R⁸ representan, de modo independiente entre sí, hidrógeno, alquilo C₁₋₈, halógeno, ciano, nitro, hidroxi, amino, hidrotio, alquil C₁₋₈-amino, bis[alquil C₁₋₈)]amino, cicloalquil C₃₋₈-amino, aril-alquil C₁₋₈-amino, heteroaril-alquil C₁₋₈-amino, alquenilo C₂₋₈, alquinilo C₂₋₈, haloalquilo C₁₋₈, hidroxi-alquilo C₁₋₈, ciano-alquilo C₁₋₈, nitro-alquilo C₁₋₈, arilo, heteroarilo, cicloalquilo C₃₋₈, cicloalquenilo C₄₋₈, heterociclilo, alcoxi C₁₋₈, haloalcoxi C₁₋₈, haloalquil C₁₋₈-tio, alquil C₁₋₈-tio, alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-tio-alquilo C₁₋₈, amino-alquilo C₁₋₈, alquil C₁₋₈-amino-alquilo C₁₋₈, cicloalquil C₃₋₈-amino-alquilo C₁₋₈, aril-alquil C₁₋₈-amino-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-amino-alquilo C₁₋₈, heterociclil-alquil C₁₋₈-amino-alquilo C₁₋₈, heterociclilamino-alquilo C₁₋₈, heteroarilamino-alquilo C₁₋₈, alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₃, arilamino-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, cicloalcoxi C₃₋₈-carbonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, heteroaril-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, alquil C₁₋₈-carbonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-carbonilamino-alquilo C₁₋₈, arilcarbonilamino-alquilo C₁₋₈, heteroarilcarbonilamino-alquilo C₁₋₈, heterociclilcarbonilamino-alquilo C₁₋₈, alquenil C₂₋₈-oxicarbonilamino-alquilo C₁₋₈, aril-alquenil C₂₋₈-amino-alquilo C₁₋₈, hidroxicarbonilo, alcoxi C₁₋₈-carbonilo, alquenil C₂₋₈-oxicarbonilo, aril-alcoxi C₁₋₈-carbonilo, aminocarbonilo, alquilaminocarbonilo, cicloalquil C₃₋₈-aminocarbonilo, aril-alquil C₁₋₈-aminocarbonilo, heteroarilaminocarbonilo, arilamino, heteroarilamino, heterociclilamino, alquenil C₂₋₈-amino, alquinil C₂₋₈-amino, alquil C₁₋₈-sulfinilo, alquenil C₂₋₈-sulfinilo, arilsulfinilo, heteroarilsulfinilo, heterociclilsulfinilo, cicloalquil C₃₋₈-sulfinilo, alquil C₁₋₈-sulfonilo, alquenil C₂₋₈-sulfonilo, arilsulfonilo, heteroarilsulfonilo, heterociclilsulfonilo, cicloalquil C₃₋₈-sulfonilo, bis-[alquil C₁₋₈]amino-alquilo C₁₋₈, alquil C₁₋₈-(aril)amino-alquilo C₁₋₈, heteroariloxicarbonilamino-alquilo C₁₋₈, heterocicliloxicarbonilamino-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, arilaminocarbonilo, alquil C₁₋₈-sulfonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfonilamino alquilo C₁₋₈, arilsulfonilamino-alquilo C₁₋₈, heteroarilsulfonilamino-alquilo C₁₋₈, heterociclilsulfonilamino-alquilo C₁₋₈, bis-[alquil C₁₋₈]aminosulfonil-alquilo C₁₋₈, alquil C₁₋₈-sulfonilamino, cicloalquil C₃₋₈-sulfonilamino, arilsulfonilamino, heteroarilsulfonilamino, heterociclilsulfonilamino, alcoxi C₁₋₈-alcoxi C₁₋₈ o R⁷ y R⁸ forman con el átomo de carbono, al que están unidos, un anillo monocíclico o bicíclico de 3 a 10 miembros completamente saturado o parcialmente saturado, dado el caso interrumpido por heteroátomos y dado el caso sustituido o R⁷ y R⁸ forman con el átomo de carbono, al que están unidos, un grupo oxo o R⁷ y R⁸ forman con el átomo de carbono, al que están unidos, un grupo oxima sustituido con hidrógeno, alquilo C₁₋₈, cicloalquilo C₃₋₈, cicloalquil C₃₋₈-alquilo C₁₋₈, arilo, heteroarilo, aril-alquilo C₁₋₈, heteroaril-alquilo C₁₋₈; R⁹, R¹⁰ representan, de modo independiente entre sí, hidrógeno, alquilo C₁₋₈, halógeno, ciano, haloalquilo C₁₋₈, ciano-alquilo C₁₋₈, arilo, heteroarilo, cicloalquilo C₃₋₈, cicloalquenilo C₄₋₈, heterociclilo, alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-tio-alquilo C₁₋₈; W representa oxígeno o azufre; X, Y representan, de modo independiente entre sí, hidrógeno, alquilo C₁₋₈, halógeno, alquenilo C₂₋₈, alquinilo C₂₋₈, haloalquilo C₁₋₈, hidroxi-alquilo C₁₋₈, ciano-alquilo C₁₋₈, arilo, heteroarilo, cicloalquilo C₃₋₈, cicloalquenilo C₄₋₈, heterociclilo, ciano, nitro, hidroxi, alcoxi C₁₋₈, alquil C₁₋₈-tio, alcoxi C₁₋₈-alquilo C₁₋₈, alquil C₁₋₈-tio-alquilo C₁₋₈, ariloxi, aril-alcoxi C₁₋₈, haloalcoxi C₁₋₈, haloalquil C₁₋₃-tio, alquil C₁₋₈-amino, bis-[alquil C₁₋₈]amino, alcoxi C₁₋₈-alcoxi C₁₋₈, amino-alquilo C₁₋₈, alquil C₁₋₈-amino-alquilo C₁₋₈, cicloalquil C₃₋₈-amino-alquilo C₁₋₈, aril-alquil C₁₋₈-amino-alquilo C₁₋₈, heteroaril-alquil C₁₋₈-amino-alquilo C₁₋₈, heterociclil-alquil C₁₋₈-amino-alquilo C₁₋₈, heterociclilamino-alquilo C₁₋₈, heteroarilamino-alquilo C₁₋₈, alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, arilamino-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, cicloalcoxi C₃₋₈-carbonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, heteroaril-alcoxi C₁₋₈-carbonilamino-alquilo C₁₋₈, alquil C₁₋₈-carbonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-carbonilamino-alquilo C₁₋₈, arilcarbonilamino-alquilo C₁₋₈, heteroarilcarbonilamino-alquilo C₁₋₈, heterociclilcarbonilamino-alquilo C₁₋₈, alquenil C₂₋₈-oxicarbonilamino-alquilo C₁₋₈, aril-alquenil C₂₋₈-amino-alquilo C₁₋₈, arilsulfonil-alquilo C₁₋₈, heteroarilsulfonil-alquilo C₁₋₈, alquil C₁₋₈-sulfonil-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfonil-alquilo C₁₋₈, arilsulfinil-alquilo C₁₋₈, heteroarilsulfinil-alquilo C₁₋₈, alquil C₁₋₈-sulfinil-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfinil-alquilo C₁₋₈, bis[alquil C₁₋₈]amino-alquilo C₁₋₈, alcoxi C₁₋₈-carbonilo, aril-alcoxi C₁₋₈-carbonilo, heteroaril-alcoxi C₁₋₈-carbonilo, C₃₋₈-cicloalcoxicarbonilo, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonilo, alquil C₁₋₈-carbonilo, cicloalquil C₃₋₈-carbonilo, arilcarbonilo, heteroarilcarbonilo, heterociclilcarbonilo, alquil C₁₋₈-sulfonilamino-alquilo C₁₋₈, cicloalquil C₃₋₈-sulfonilamino-alquilo C₁₋₈, arilsulfonilamino-alquilo C₁₋₈, heteroarilsulfonilamino-alquilo C₁₋₈, heterociclilsulfonilamino-alquilo C₁₋₈, bis-[alquil C₁₋₈]aminosulfonil-alquilo C₁₋₈, alquil C₁₋₈-sulfonilamino, cicloalquil C₃₋₈-sulfonilamino, arilsulfonilamino, heteroarilsulfonilamino, heterociclilsulfonilamino, heteroariloxicarbonilamino-alquilo C₁₋₈, heterocicliloxicarbonilamino-alquilo C₁₋₈ o X e Y forman con el átomo de carbono, al que están unidos, un anillo monocíclico o bicíclico de 3 a 10 miembros completamente saturado o parcialmente saturado, dado el caso interrumpido por heteroátomos y dado el caso sustituido. Reivindicación 11: Oxotetrahidroquinolinilsulfonamidas sustituidas de la fórmula general (1) o sus sales, en donde R¹ representa halógeno, ciano, cicloalquilo C₃₋₁₀. halocicloalquilo C₃₋₁₀, cicloalquenilo C₄₋₁₀, halocicloalquenilo C₄₋₁₀, haloalquilo C₁₋₁₀, alcoxi C₁₋₈-haloalquilo C₁₋₈, cicloalquil C₃₋₈-alquilo C₁₋₈, alquil C₁₋₈-carbonil-alquilo C₁₋₈, hidroxicarbonil-alquilo C₁₋₈, alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, alquenil C₂₋₈-oxicarbonil-alquilo C₁₋₈, alquinil C₂₋₈-oxicarbonil-alquilo C₁₋₈, aril-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, cicloalcoxi C₃₋₈-carbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-alcoxi C₁₋₈-carbonil-alquilo C₁₋₈, aminocarbonil-alquilo C₁₋₈, alquil C₁₋₈-aminocarbonil-alquilo C₁₋₈, cicloalquil C₃₋₈-aminocarbonil-alquilo C₁₋₈, aril-alquil
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| MX2018002353A (es) * | 2015-08-27 | 2018-09-11 | Univ California | Derivados de halo quinabactina. |
| CN106478499B (zh) * | 2015-08-28 | 2019-08-30 | 中国科学院上海生命科学研究院 | 增强植物抗逆性的小分子化合物 |
| CN106749044B (zh) * | 2015-12-28 | 2020-04-21 | 中国科学院上海生命科学研究院 | 增强植物抗逆性的aba类似物 |
| US11076597B2 (en) * | 2015-12-28 | 2021-08-03 | Cas Center For Excellence In Molecular Plant Sciences | High stress resistant plant growth regulator and preparation method and use thereof |
| WO2019025153A1 (de) | 2017-07-31 | 2019-02-07 | Bayer Cropscience Aktiengesellschaft | Verwendung von substituierten n-sulfonyl-n'-aryldiaminoalkanen und n-sulfonyl-n'-heteroaryldiaminoalkanen oder deren salzen zur steigerung der stresstoleranz in pflanzen |
| WO2022268520A1 (de) | 2021-06-21 | 2022-12-29 | Bayer Aktiengesellschaft | Verwendung von substituierten pyrrolidinonen oder deren salzen zur steigerung der stresstoleranz in pflanzen. |
| CN119824470B (zh) * | 2025-01-16 | 2026-01-06 | 中国林业科学研究院林产化学工业研究所 | 一种利用Bi-(Et3N)催化剂对木质素模型物电催化加氢的方法 |
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| US9345245B2 (en) * | 2012-03-30 | 2016-05-24 | The Regents Of The University Of California | Synthetic compounds for vegetative ABA responses |
| US9321750B2 (en) * | 2012-04-20 | 2016-04-26 | Innov17 Llc | ROR modulators and their uses |
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- 2015-04-07 CN CN201580031074.4A patent/CN106455565A/zh active Pending
- 2015-04-07 US US15/302,867 patent/US20170027172A1/en not_active Abandoned
- 2015-04-07 CA CA2945230A patent/CA2945230A1/en not_active Abandoned
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| BR112016023490A2 (pt) | 2018-05-15 |
| EP3128841A1 (de) | 2017-02-15 |
| AU2015243625A1 (en) | 2016-10-20 |
| WO2015155154A1 (de) | 2015-10-15 |
| MX2016013308A (es) | 2017-01-18 |
| AU2015243625B2 (en) | 2018-11-08 |
| US20170027172A1 (en) | 2017-02-02 |
| EA201692028A1 (ru) | 2017-02-28 |
| CN106455565A (zh) | 2017-02-22 |
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