ZA200605258B - Synthetic compounds useful as nodulation agents of leguminous plants and preparation processes thereof - Google Patents
Synthetic compounds useful as nodulation agents of leguminous plants and preparation processes thereof Download PDFInfo
- Publication number
- ZA200605258B ZA200605258B ZA200605258A ZA200605258A ZA200605258B ZA 200605258 B ZA200605258 B ZA 200605258B ZA 200605258 A ZA200605258 A ZA 200605258A ZA 200605258 A ZA200605258 A ZA 200605258A ZA 200605258 B ZA200605258 B ZA 200605258B
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- ZA
- South Africa
- Prior art keywords
- alkyl
- represent
- nhc
- fucosyl
- chosen
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 100
- 230000024121 nodulation Effects 0.000 title claims description 9
- 238000002360 preparation method Methods 0.000 title description 4
- 125000001424 substituent group Chemical group 0.000 claims description 129
- 229910052799 carbon Inorganic materials 0.000 claims description 93
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 90
- 229910052739 hydrogen Inorganic materials 0.000 claims description 88
- 125000002446 fucosyl group Chemical group C1([C@@H](O)[C@H](O)[C@H](O)[C@@H](O1)C)* 0.000 claims description 60
- -1 methylifucosyl Chemical group 0.000 claims description 49
- 229910052757 nitrogen Inorganic materials 0.000 claims description 45
- 229910052760 oxygen Inorganic materials 0.000 claims description 45
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 44
- 125000005842 heteroatom Chemical group 0.000 claims description 44
- 239000001301 oxygen Substances 0.000 claims description 44
- 229920006395 saturated elastomer Polymers 0.000 claims description 44
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 43
- 229910052717 sulfur Inorganic materials 0.000 claims description 43
- 239000011593 sulfur Substances 0.000 claims description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 34
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 34
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 27
- 241000196324 Embryophyta Species 0.000 claims description 20
- 125000004429 atom Chemical group 0.000 claims description 20
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 20
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 125000000089 arabinosyl group Chemical group C1([C@@H](O)[C@H](O)[C@H](O)CO1)* 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 17
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 15
- 239000011734 sodium Substances 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 229910006069 SO3H Inorganic materials 0.000 claims description 13
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 13
- 239000004215 Carbon black (E152) Substances 0.000 claims description 12
- 125000000732 arylene group Chemical group 0.000 claims description 12
- 125000005549 heteroarylene group Chemical group 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 12
- 150000002430 hydrocarbons Chemical class 0.000 claims description 12
- 125000004957 naphthylene group Chemical group 0.000 claims description 11
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims description 10
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 9
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 9
- 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 9
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 9
- 150000001204 N-oxides Chemical class 0.000 claims description 9
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 9
- 229910052744 lithium Inorganic materials 0.000 claims description 9
- 229910052751 metal Chemical class 0.000 claims description 9
- 239000002184 metal Chemical class 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 230000003287 optical effect Effects 0.000 claims description 9
- 229910052700 potassium Inorganic materials 0.000 claims description 9
- 239000011591 potassium Substances 0.000 claims description 9
- 229910052708 sodium Inorganic materials 0.000 claims description 9
- 150000003457 sulfones Chemical class 0.000 claims description 9
- 150000003462 sulfoxides Chemical class 0.000 claims description 9
- 235000021374 legumes Nutrition 0.000 claims description 8
- 150000005621 tetraalkylammonium salts Chemical class 0.000 claims description 8
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 claims description 6
- 229910052752 metalloid Chemical class 0.000 claims description 6
- 150000002738 metalloids Chemical class 0.000 claims description 6
- 244000068988 Glycine max Species 0.000 claims description 3
- 235000010469 Glycine max Nutrition 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 230000008635 plant growth Effects 0.000 claims description 3
- 235000003276 Apios tuberosa Nutrition 0.000 claims description 2
- 244000105624 Arachis hypogaea Species 0.000 claims description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 claims description 2
- 235000010744 Arachis villosulicarpa Nutrition 0.000 claims description 2
- 102100028717 Cytosolic 5'-nucleotidase 3A Human genes 0.000 claims description 2
- 241000219745 Lupinus Species 0.000 claims description 2
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
- 240000004713 Pisum sativum Species 0.000 claims description 2
- 235000010582 Pisum sativum Nutrition 0.000 claims description 2
- 241000219793 Trifolium Species 0.000 claims description 2
- 240000006677 Vicia faba Species 0.000 claims description 2
- 235000002096 Vicia faba var. equina Nutrition 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- GOWMBYUZXIZENX-CAUSLRQDSA-N 1-[(2r,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-(hexadecylamino)pyrimidin-2-one Chemical compound O=C1N=C(NCCCCCCCCCCCCCCCC)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 GOWMBYUZXIZENX-CAUSLRQDSA-N 0.000 claims 10
- 229920000728 polyester Polymers 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 3
- 101100141379 Bacillus subtilis rizA gene Proteins 0.000 claims 1
- 101000961332 Homo sapiens Interferon-inducible GTPase 5 Proteins 0.000 claims 1
- 102100039393 Interferon-inducible GTPase 5 Human genes 0.000 claims 1
- 240000004658 Medicago sativa Species 0.000 claims 1
- 101100113485 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) chs-3 gene Proteins 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 230000000638 stimulation Effects 0.000 claims 1
- 239000003284 nod factor Substances 0.000 description 10
- 241000219823 Medicago Species 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 150000002632 lipids Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000009418 agronomic effect Effects 0.000 description 3
- 244000038559 crop plants Species 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000001850 reproductive effect Effects 0.000 description 3
- 235000000346 sugar Nutrition 0.000 description 3
- 230000031068 symbiosis, encompassing mutualism through parasitism Effects 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 241000219873 Vicia Species 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 150000002482 oligosaccharides Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- GRFOHUBBUMAJMM-UHFFFAOYSA-N 3-(2-aminoquinolin-3-yl)-n-cyclohexyl-n-methylpropanamide Chemical compound C=1C2=CC=CC=C2N=C(N)C=1CCC(=O)N(C)C1CCCCC1 GRFOHUBBUMAJMM-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 241000218922 Magnoliophyta Species 0.000 description 1
- 108010064851 Plant Proteins Proteins 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000933336 Ziziphus rignonii Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229930003935 flavonoid Natural products 0.000 description 1
- 150000002215 flavonoids Chemical class 0.000 description 1
- 235000017173 flavonoids Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000010353 genetic engineering Methods 0.000 description 1
- MSWZFWKMSRAUBD-IVMDWMLBSA-N glucosamine group Chemical group OC1[C@H](N)[C@@H](O)[C@H](O)[C@H](O1)CO MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000003324 growth hormone secretagogue Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 239000000618 nitrogen fertilizer Substances 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 235000021251 pulses Nutrition 0.000 description 1
- 238000010187 selection method Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
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- 150000008163 sugars Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 241001478887 unidentified soil bacteria Species 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Fertilizers (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Steroid Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0315543A FR2864538B1 (fr) | 2003-12-30 | 2003-12-30 | Composes synthetiques utiles comme facteurs de nodulation des plantes legumineuses et procedes de preparation de tels composes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200605258B true ZA200605258B (en) | 2007-04-25 |
Family
ID=34639685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200605258A ZA200605258B (en) | 2003-12-30 | 2006-06-26 | Synthetic compounds useful as nodulation agents of leguminous plants and preparation processes thereof |
Country Status (25)
| Country | Link |
|---|---|
| US (3) | US7619076B2 (https=) |
| EP (1) | EP1701967B1 (https=) |
| JP (1) | JP5031376B2 (https=) |
| KR (1) | KR101127785B1 (https=) |
| CN (1) | CN100549020C (https=) |
| AP (1) | AP2328A (https=) |
| AR (2) | AR047174A1 (https=) |
| AT (1) | ATE504593T1 (https=) |
| AU (1) | AU2004309089B2 (https=) |
| BR (1) | BRPI0417892B1 (https=) |
| CA (1) | CA2540074C (https=) |
| DE (1) | DE602004032175D1 (https=) |
| EA (1) | EA009557B1 (https=) |
| ES (1) | ES2364556T3 (https=) |
| FR (1) | FR2864538B1 (https=) |
| IL (1) | IL175658A (https=) |
| IN (1) | IN2006DE01668A (https=) |
| MA (1) | MA28296A1 (https=) |
| MX (1) | MX258070B (https=) |
| NZ (1) | NZ546188A (https=) |
| OA (1) | OA13354A (https=) |
| PL (1) | PL1701967T3 (https=) |
| PT (1) | PT1701967E (https=) |
| WO (1) | WO2005063784A1 (https=) |
| ZA (1) | ZA200605258B (https=) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2644172A1 (en) | 2006-04-07 | 2007-10-18 | E.I. Du Pont De Nemours And Company | Processes for chemical synthesis of lipochitooligosaccharides |
| TWI421030B (zh) * | 2006-12-12 | 2014-01-01 | Bayer Cropscience Ag | 包括用作豆科植物生結瘤劑（ｎｏｄｕｌａｔｉｏｎ ａｇｅｎｔ）之合成化合物及殺真菌劑化合物之農藥組合物 |
| TWI462698B (zh) * | 2006-12-12 | 2014-12-01 | Bayer Cropscience Ag | 包括作為豆科植物生結瘤劑（ｎｏｄｕｌａｔｉｏｎ ａｇｅｎｔ）之合成化合物及殺昆蟲劑化合物之農藥組合物 |
| US8357631B2 (en) | 2007-01-09 | 2013-01-22 | Novozymes Bioag, Inc. | Lipo-chitooligosaccharide combination compositions for enhanced plant growth and yield |
| WO2009049747A2 (en) * | 2007-10-16 | 2009-04-23 | Merck Patent Gmbh | Lipo-chitooligosaccharide and flavonoid combination for enhanced plant growth and yield |
| WO2010049751A1 (en) | 2008-10-29 | 2010-05-06 | Institut National De La Recherche Agronomique | Lipochitooligosaccharides stimulating arbuscular mycorrhizal symbiosis |
| WO2010125065A2 (en) * | 2009-04-28 | 2010-11-04 | Bayer Cropscience Ag | Compositions comprising a strigolactone compound and a chito-oligosaccharide compound for enhanced plant growth and yield |
| EP2683239A1 (en) * | 2011-03-10 | 2014-01-15 | Bayer Intellectual Property GmbH | Use of lipochito-oligosaccharide compounds for safeguarding seed safety of treated seeds |
| WO2012135704A1 (en) | 2011-03-31 | 2012-10-04 | Novozymes Biologicials, Inc | Competitive and effective bradyrhizobium japonicum strains |
| AR090026A1 (es) | 2011-09-08 | 2014-10-15 | Novozymes Bioag As | Metodos y composiciones para tratamiento de semillas |
| ES2970761T3 (es) | 2011-09-14 | 2024-05-30 | Novozymes Bioag As | Uso de lipoquitooligosacáridos y/o quitooligosacáridos en combinación con microorganismos solubilizadores de fosfato para potenciar el crecimiento de las plantas |
| RU2564844C1 (ru) | 2011-09-23 | 2015-10-10 | Новозимс Биоаг А/С | Хитоолигосахариды и способы их применения для усиления роста растений |
| UA123664C2 (uk) | 2011-09-23 | 2021-05-12 | Новозаймс Біоаг А/С | Комбінації ліпохітоолігосахаридів і способи для застосування при стимулюванні росту рослин |
| CA2849899A1 (en) | 2011-09-23 | 2013-03-28 | Novozymes Bioag A/S | Chitooligosaccharides and methods for use in enhancing soybean growth |
| AU2012312006B2 (en) | 2011-09-23 | 2015-10-29 | Novozymes Bioag A/S | Chitooligosaccharides and methods for use in enhancing corn growth |
| RU2646138C1 (ru) | 2011-12-16 | 2018-03-01 | Новозимс Биоаг А/С | Способ обработки семени растения |
| WO2013107785A1 (en) | 2012-01-21 | 2013-07-25 | Bayer Intellectual Property Gmbh | Use of host defense inducers for controlling bacterial harmful organisms in useful plants |
| WO2013139949A1 (en) | 2012-03-23 | 2013-09-26 | Bayer Intellectual Property Gmbh | Compositions comprising a strigolactame compound for enhanced plant growth and yield |
| AR091104A1 (es) | 2012-05-22 | 2015-01-14 | Bayer Cropscience Ag | Combinaciones de compuestos activos que comprenden un derivado lipo-quitooligosacarido y un compuesto nematicida, insecticida o fungicida |
| FR2991682A1 (fr) * | 2012-06-12 | 2013-12-13 | Centre Nat Rech Scient | Procedes de preparation de lipochito-oligosaccharides et de leurs precurseurs |
| FR2994793A1 (fr) | 2012-08-30 | 2014-03-07 | Agronomique Inst Nat Rech | Utilisation d'un recepteur kinase a motifs lysm pour ameliorer la reponse des plantes aux lipochitooligosaccharides. |
| WO2014049546A2 (en) | 2012-09-27 | 2014-04-03 | Institut National De La Recherche Agronomique | Compositions and methods for enhancing plant growth and development |
| US9365464B2 (en) | 2012-11-16 | 2016-06-14 | Novozymes Bioag A/S | Microbial strains, compositions, and methods for increasing available phosphate for plants |
| CA2904328A1 (en) * | 2013-03-06 | 2014-09-12 | E. I. Du Pont De Nemours And Company | Synthetic lipochitooligosaccharide analogs for enhancing plant performance |
| US20160024108A1 (en) | 2013-03-12 | 2016-01-28 | Bayer Cropscience Aktiengesellschaft | Use of dithiine-tetracarboximides for controlling bacterial harmful organisms in useful plants |
| WO2014160827A1 (en) | 2013-03-28 | 2014-10-02 | Novozymes Bioag A/S | Compositions and methods for enhancing microbial stability |
| WO2015048627A1 (en) | 2013-09-30 | 2015-04-02 | Bayer Cropscience Lp, A Delaware Limited Partnership | Streptomyces microflavus strains and methods of their use for the treatment and prevention of citrus greening disease |
| UA119331C2 (uk) | 2013-11-08 | 2019-06-10 | Новозімес Біоаґ А/С | Композиції та способи для обробки від шкідників |
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| FR2660658A1 (fr) * | 1990-04-06 | 1991-10-11 | Centre Nat Rech Scient | Substances de structure oligosaccharidique propres a jouer le role de signaux symbiotiques plantes-specifiques, leurs procedes de production et leurs applications. |
| US5175149A (en) * | 1991-10-04 | 1992-12-29 | The University Of Tennessee Research Corporation | Pentasaccharide phytohormones and methods for their use |
| FR2692896B1 (fr) * | 1992-06-29 | 1994-09-09 | Institut Rech Agronomique | Signaux de nodulation de rhizobiaceae à large spectre d'hôte. |
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