PT78490B - Process for increasing the commercial value of seeds by producing haploid seeds doubled haploids and of homozygous plant lines obtained therefrom - Google Patents
Process for increasing the commercial value of seeds by producing haploid seeds doubled haploids and of homozygous plant lines obtained therefrom Download PDFInfo
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- PT78490B PT78490B PT78490A PT7849084A PT78490B PT 78490 B PT78490 B PT 78490B PT 78490 A PT78490 A PT 78490A PT 7849084 A PT7849084 A PT 7849084A PT 78490 B PT78490 B PT 78490B
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- Prior art keywords
- group
- alkyl
- plant
- oxo
- apomictic
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 51
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- 238000011161 development Methods 0.000 claims abstract description 14
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- 239000004464 cereal grain Substances 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims description 62
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 49
- -1 1-phenyl-1,4-dihydro-4-oxo-5-carboxymethyl- ethylpyridazine Chemical compound 0.000 claims description 32
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 31
- 150000001875 compounds Chemical class 0.000 claims description 27
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- 125000005843 halogen group Chemical group 0.000 claims description 21
- 235000021307 Triticum Nutrition 0.000 claims description 16
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 15
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- 125000003342 alkenyl group Chemical group 0.000 claims description 6
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- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 6
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- JDEKUYKSOCTBJT-UHFFFAOYSA-N 1-(4-chlorophenyl)-6-methyl-4-oxopyridazine-3-carboxylic acid Chemical compound CC1=CC(=O)C(C(O)=O)=NN1C1=CC=C(Cl)C=C1 JDEKUYKSOCTBJT-UHFFFAOYSA-N 0.000 claims description 3
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- AHRAMVQFCAAISS-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-1-ethyl-6-methyl-4-oxopyridine-3-carboxylic acid Chemical compound CCN1C(C)=CC(=O)C(C(O)=O)=C1C1=CC=C(Cl)C(Cl)=C1 AHRAMVQFCAAISS-UHFFFAOYSA-N 0.000 claims 2
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- HRCFAQWWRUUAMC-UHFFFAOYSA-N ethyl 6-(4-chlorophenyl)-1,2-dimethyl-4-oxopyridine-3-carboxylate Chemical compound O=C1C(C(=O)OCC)=C(C)N(C)C(C=2C=CC(Cl)=CC=2)=C1 HRCFAQWWRUUAMC-UHFFFAOYSA-N 0.000 description 1
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- 229960001340 histamine Drugs 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-O hydron;octadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCC[NH3+] REYJJPSVUYRZGE-UHFFFAOYSA-O 0.000 description 1
- RBLWMQWAHONKNC-UHFFFAOYSA-N hydroxyazanium Chemical compound O[NH3+] RBLWMQWAHONKNC-UHFFFAOYSA-N 0.000 description 1
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- 239000003617 indole-3-acetic acid Substances 0.000 description 1
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- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- KSKLALWRZFODIU-UHFFFAOYSA-N methyl 1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound CCC1=CC(=O)C(C(=O)OC)=NN1C1=CC=C(Cl)C=C1 KSKLALWRZFODIU-UHFFFAOYSA-N 0.000 description 1
- SCQLSRCFARZZAA-UHFFFAOYSA-N methyl 1-(4-chlorophenyl)-6-methyl-4-oxo-5-propylpyridazine-3-carboxylate Chemical compound N1=C(C(=O)OC)C(=O)C(CCC)=C(C)N1C1=CC=C(Cl)C=C1 SCQLSRCFARZZAA-UHFFFAOYSA-N 0.000 description 1
- CKURQPUVUUYRPH-UHFFFAOYSA-N methyl 1-(4-iodophenyl)-6-methyl-4-oxopyridazine-3-carboxylate Chemical compound CC1=CC(=O)C(C(=O)OC)=NN1C1=CC=C(I)C=C1 CKURQPUVUUYRPH-UHFFFAOYSA-N 0.000 description 1
- YAIRSPHHLGCRNO-UHFFFAOYSA-N methyl 2-(4-chlorophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound CCC1=C(C(=O)OC)C(=O)C=NN1C1=CC=C(Cl)C=C1 YAIRSPHHLGCRNO-UHFFFAOYSA-N 0.000 description 1
- LEFHKCWENBVSFU-UHFFFAOYSA-N methyl 5-acetyl-1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound CCC1=C(C(C)=O)C(=O)C(C(=O)OC)=NN1C1=CC=C(Cl)C=C1 LEFHKCWENBVSFU-UHFFFAOYSA-N 0.000 description 1
- NYGDNNQNJLGEBF-UHFFFAOYSA-N methyl 6-bromo-2-(4-chlorophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound CCC1=C(C(=O)OC)C(=O)C(Br)=NN1C1=CC=C(Cl)C=C1 NYGDNNQNJLGEBF-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 230000005404 monopole Effects 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 238000003976 plant breeding Methods 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
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- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- GURNAAYLUXBKGA-UHFFFAOYSA-M potassium;2-(4-chlorophenyl)-5-oxo-3-propylpyridazine-4-carboxylate Chemical compound [K+].CCCC1=C(C([O-])=O)C(=O)C=NN1C1=CC=C(Cl)C=C1 GURNAAYLUXBKGA-UHFFFAOYSA-M 0.000 description 1
- CHWOVEJUIPJPIS-UHFFFAOYSA-M potassium;5-acetyl-1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C=C1 CHWOVEJUIPJPIS-UHFFFAOYSA-M 0.000 description 1
- FZNDOIGSABBARI-UHFFFAOYSA-M potassium;5-acetyl-6-ethyl-4-oxo-1-phenylpyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=CC=C1 FZNDOIGSABBARI-UHFFFAOYSA-M 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 150000005299 pyridinones Chemical class 0.000 description 1
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- 238000000197 pyrolysis Methods 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 230000008117 seed development Effects 0.000 description 1
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- 230000001568 sexual effect Effects 0.000 description 1
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- 150000004760 silicates Chemical class 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- NBNBICNWNFQDDD-UHFFFAOYSA-N sulfuryl dibromide Chemical compound BrS(Br)(=O)=O NBNBICNWNFQDDD-UHFFFAOYSA-N 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- GCRCSLNXFKCFHB-UHFFFAOYSA-N triethyl(hexyl)azanium Chemical compound CCCCCC[N+](CC)(CC)CC GCRCSLNXFKCFHB-UHFFFAOYSA-N 0.000 description 1
- WSFDRHZUAHDHDN-UHFFFAOYSA-N trimethyl-[(4-methylphenyl)methyl]azanium Chemical compound CC1=CC=C(C[N+](C)(C)C)C=C1 WSFDRHZUAHDHDN-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- 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
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H1/00—Processes for modifying genotypes ; Plants characterised by associated natural traits
- A01H1/02—Methods or apparatus for hybridisation; Artificial pollination ; Fertility
- A01H1/022—Genic fertility modification, e.g. apomixis
-
- 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
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Genetics & Genomics (AREA)
- Botany (AREA)
- Developmental Biology & Embryology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48888883A | 1983-04-26 | 1983-04-26 | |
| US58435884A | 1984-02-28 | 1984-02-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PT78490A PT78490A (en) | 1984-05-01 |
| PT78490B true PT78490B (en) | 1987-02-16 |
Family
ID=27049511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT78490A PT78490B (en) | 1983-04-26 | 1984-04-26 | Process for increasing the commercial value of seeds by producing haploid seeds doubled haploids and of homozygous plant lines obtained therefrom |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP0127313B1 (en, 2012) |
| AU (1) | AU562972B2 (en, 2012) |
| BR (1) | BR8401899A (en, 2012) |
| CA (1) | CA1236700A (en, 2012) |
| DE (1) | DE3478985D1 (en, 2012) |
| DK (1) | DK207184A (en, 2012) |
| ES (1) | ES8605139A1 (en, 2012) |
| GR (1) | GR79912B (en, 2012) |
| HU (1) | HU191749B (en, 2012) |
| IL (1) | IL71635A (en, 2012) |
| NO (1) | NO841567L (en, 2012) |
| NZ (1) | NZ207927A (en, 2012) |
| PH (1) | PH23110A (en, 2012) |
| PT (1) | PT78490B (en, 2012) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4623378A (en) * | 1983-08-10 | 1986-11-18 | Ciba-Geigy Corporation | Gametocidal pyridazinylcarboxylic acid derivatives |
| FR2566995B1 (fr) * | 1984-07-04 | 1987-02-13 | Centre Nat Rech Scient | Procede de preparation d'haploides doubles de cereales. |
| DE3843199C2 (de) * | 1988-12-22 | 1998-03-12 | Nunhems Zaden Bv | Verfahren zur Herstellung von doppelt-haploiden Gurken |
| US6706989B2 (en) | 2001-02-02 | 2004-03-16 | Pioneer Hi-Bred International, Inc. | Automated high-throughput seed sample processing system and method |
| US7611842B2 (en) | 2004-08-26 | 2009-11-03 | Monsanto Technology Llc | Automated seed sampler and methods of sampling, testing and bulking seeds |
| US7703238B2 (en) | 2004-08-26 | 2010-04-27 | Monsanto Technology Llc | Methods of seed breeding using high throughput nondestructive seed sampling |
| US7998669B2 (en) | 2006-03-02 | 2011-08-16 | Monsanto Technology Llc | Automated contamination-free seed sampler and methods of sampling, testing and bulking seeds |
| US8028469B2 (en) | 2006-03-02 | 2011-10-04 | Monsanto Technology Llc | Automated high-throughput seed sampler and methods of sampling, testing and bulking seeds |
| MX2013000790A (es) | 2010-07-20 | 2013-03-20 | Monsanto Technology Llc | Sistemas automatizados para extraer muestras de tejidos de semillas y metodos relacionados. |
| US9677082B2 (en) | 2013-03-15 | 2017-06-13 | Syngenta Participations Ag | Haploid induction compositions and methods for use therefor |
| CN115918526B (zh) * | 2015-11-18 | 2024-11-12 | 先正达参股股份有限公司 | 单倍体诱导组合物及其使用方法 |
| EP3451834A1 (en) * | 2016-05-03 | 2019-03-13 | Basf Se | Applications of root-administered chemical hybridizing agents in plant breeding |
| USD1022462S1 (en) * | 2020-02-28 | 2024-04-16 | Rothy's, Inc. | Bag |
| GB202018994D0 (en) * | 2020-12-02 | 2021-01-13 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| GB202018996D0 (en) | 2020-12-02 | 2021-01-13 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| US20250098679A1 (en) | 2021-12-17 | 2025-03-27 | Syngenta Crop Protection Ag | Herbicidal pyridone derivatives |
| WO2023208710A1 (en) | 2022-04-27 | 2023-11-02 | Syngenta Crop Protection Ag | Herbicidal 2-oxo-nicotinic acid derivatives |
| WO2023232676A1 (en) | 2022-06-01 | 2023-12-07 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2023232673A1 (en) | 2022-06-01 | 2023-12-07 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| KR20250019678A (ko) | 2022-06-01 | 2025-02-10 | 신젠타 크롭 프로텍션 아게 | 제초제 유도체 |
| AR130324A1 (es) | 2022-09-01 | 2024-11-27 | Syngenta Crop Protection Ag | Derivados herbicidas |
| AU2023406528A1 (en) | 2022-12-01 | 2025-05-22 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| AR132501A1 (es) | 2023-04-27 | 2025-07-02 | Syngenta Crop Protection Ag | Derivados herbicidas |
| WO2025087845A1 (en) | 2023-10-23 | 2025-05-01 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2025108824A1 (en) | 2023-11-21 | 2025-05-30 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2025119663A1 (en) | 2023-12-05 | 2025-06-12 | Syngenta Crop Protection Ag | Herbicidal derivatives |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4115101A (en) * | 1976-05-24 | 1978-09-19 | Rohm And Haas Company | 1-Aryl-4-pyridones |
| US4345934A (en) * | 1977-03-10 | 1982-08-24 | Rohm And Haas Company | Method of producing hybrid cereal grain seeds by application of 1-aryl-1,4-dihydro-4-oxo(thio)-pyridazines |
| EP0037133A1 (en) * | 1980-03-26 | 1981-10-07 | Shell Internationale Researchmaatschappij B.V. | Pyridazinone compounds, process for their preparation, compositions containing them and a method of regulating the growth of plants, increasing the yield of soya bean plants and sterilizing the male anthers of plants, including small grain cereal plants, using them as well as a method of producing F1 hybrid seed |
| EP0037134A1 (en) * | 1980-03-26 | 1981-10-07 | Shell Internationale Researchmaatschappij B.V. | Pyridazine derivatives, process for their preparation, compositions containing them and methods of regulating the growth of plants, increasing the yield of soya bean plants and sterilizing the male anthers of plants, including small grain cereal plants, using them as well as a method of producing F1 hybrid seed |
| ZA813029B (en) * | 1980-05-12 | 1982-05-26 | Rohm & Haas | Novel substituted oxonicotinates,their use as plant growth regulators and plant growth regulating compositions containing them |
-
1984
- 1984-04-12 CA CA000451846A patent/CA1236700A/en not_active Expired
- 1984-04-18 NO NO841567A patent/NO841567L/no unknown
- 1984-04-18 PH PH30579A patent/PH23110A/en unknown
- 1984-04-19 NZ NZ207927A patent/NZ207927A/en unknown
- 1984-04-24 GR GR74481A patent/GR79912B/el unknown
- 1984-04-24 BR BR8401899A patent/BR8401899A/pt not_active Application Discontinuation
- 1984-04-24 ES ES531843A patent/ES8605139A1/es not_active Expired
- 1984-04-25 HU HU841595A patent/HU191749B/hu not_active IP Right Cessation
- 1984-04-25 IL IL71635A patent/IL71635A/xx unknown
- 1984-04-25 DK DK207184A patent/DK207184A/da not_active Application Discontinuation
- 1984-04-25 DE DE8484302772T patent/DE3478985D1/de not_active Expired
- 1984-04-25 EP EP84302772A patent/EP0127313B1/en not_active Expired
- 1984-04-26 AU AU27272/84A patent/AU562972B2/en not_active Ceased
- 1984-04-26 PT PT78490A patent/PT78490B/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU562972B2 (en) | 1987-06-25 |
| NO841567L (no) | 1984-10-29 |
| DK207184A (da) | 1984-10-27 |
| GR79912B (en, 2012) | 1984-10-31 |
| BR8401899A (pt) | 1984-12-04 |
| ES8605139A1 (es) | 1986-03-16 |
| DE3478985D1 (en) | 1989-08-24 |
| IL71635A (en) | 1988-12-30 |
| NZ207927A (en) | 1987-09-30 |
| HU191749B (en) | 1987-04-28 |
| CA1236700A (en) | 1988-05-17 |
| PH23110A (en) | 1989-04-19 |
| PT78490A (en) | 1984-05-01 |
| EP0127313B1 (en) | 1989-07-19 |
| HUT39061A (en) | 1986-08-28 |
| ES531843A0 (es) | 1986-03-16 |
| AU2727284A (en) | 1984-11-01 |
| EP0127313A1 (en) | 1984-12-05 |
| DK207184D0 (da) | 1984-04-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM3A | Annulment or lapse |
Free format text: LAPSE DUE TO NON-PAYMENT OF FEES Effective date: 19920817 |