HU191749B - Method for producing haploide seeds at angiosperms with creating haploides by the way of bringing on apomixis - Google Patents
Method for producing haploide seeds at angiosperms with creating haploides by the way of bringing on apomixis Download PDFInfo
- Publication number
- HU191749B HU191749B HU841595A HU159584A HU191749B HU 191749 B HU191749 B HU 191749B HU 841595 A HU841595 A HU 841595A HU 159584 A HU159584 A HU 159584A HU 191749 B HU191749 B HU 191749B
- Authority
- HU
- Hungary
- Prior art keywords
- alkyl
- hydrogen
- phenyl
- oxo
- apomixic
- Prior art date
Links
- 241000218922 Magnoliophyta Species 0.000 title claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 241000196324 Embryophyta Species 0.000 claims abstract description 62
- 238000000034 method Methods 0.000 claims abstract description 62
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 53
- 230000008569 process Effects 0.000 claims abstract description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims description 84
- 239000001257 hydrogen Substances 0.000 claims description 84
- 125000000217 alkyl group Chemical group 0.000 claims description 73
- 150000001875 compounds Chemical class 0.000 claims description 44
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 42
- -1 4-oxo-thionicotinate compounds Chemical class 0.000 claims description 38
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 31
- 229910052736 halogen Inorganic materials 0.000 claims description 28
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- 150000003839 salts Chemical class 0.000 claims description 24
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 229910052760 oxygen Inorganic materials 0.000 claims description 18
- 239000001301 oxygen Substances 0.000 claims description 18
- 229910052708 sodium Inorganic materials 0.000 claims description 18
- 239000011734 sodium Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 244000098338 Triticum aestivum Species 0.000 claims description 16
- 235000021307 Triticum Nutrition 0.000 claims description 15
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 12
- 239000011591 potassium Substances 0.000 claims description 12
- 229910052700 potassium Inorganic materials 0.000 claims description 12
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 11
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 11
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- 239000000126 substance Substances 0.000 claims description 9
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-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 description 2
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- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims description 2
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
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- MGIUUAHJVPPFEV-ABXDCCGRSA-N magainin ii Chemical compound C([C@H](NC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(O)=O)C1=CC=CC=C1 MGIUUAHJVPPFEV-ABXDCCGRSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 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
- 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
- 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
- ZYTYOUNYLKOKAR-UHFFFAOYSA-N morpholine;pyrrolidine Chemical compound C1CCNC1.C1COCCN1 ZYTYOUNYLKOKAR-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 238000003541 multi-stage reaction Methods 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000006911 nucleation 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
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 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
- TXIBRVZDJXKLGE-UHFFFAOYSA-M potassium;5-(carboxymethyl)-1-(3,4-dichlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C(Cl)=C1 TXIBRVZDJXKLGE-UHFFFAOYSA-M 0.000 description 1
- RFKWRQQVNQSAJK-UHFFFAOYSA-M potassium;5-(carboxymethyl)-6-ethyl-1-(4-iodophenyl)-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(I)C=C1 RFKWRQQVNQSAJK-UHFFFAOYSA-M 0.000 description 1
- SJVXIDLZFULOKO-UHFFFAOYSA-M potassium;5-acetyl-1-(4-bromophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Br)C=C1 SJVXIDLZFULOKO-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
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- IEPZHOPFBLVNFY-UHFFFAOYSA-N prop-1-enyl 1-(4-chlorophenyl)-6-methyl-4-oxopyridazine-3-carboxylate Chemical compound CC1=CC(=O)C(C(=O)OC=CC)=NN1C1=CC=C(Cl)C=C1 IEPZHOPFBLVNFY-UHFFFAOYSA-N 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 150000008318 pyrimidones Chemical class 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003445 sucroses Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- 150000007970 thio esters Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229950003937 tolonium Drugs 0.000 description 1
- HNONEKILPDHFOL-UHFFFAOYSA-M tolonium chloride Chemical compound [Cl-].C1=C(C)C(N)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 HNONEKILPDHFOL-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000008736 traumatic injury Effects 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 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
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 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
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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 |
|---|---|
| HUT39061A HUT39061A (en) | 1986-08-28 |
| HU191749B true HU191749B (en) | 1987-04-28 |
Family
ID=27049511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU841595A HU191749B (en) | 1983-04-26 | 1984-04-25 | Method for producing haploide seeds at angiosperms with creating haploides by the way of bringing on apomixis |
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 |
| PT78490B (en) | 1987-02-16 |
| IL71635A (en) | 1988-12-30 |
| NZ207927A (en) | 1987-09-30 |
| 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 |
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| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |