WO1996006529A1 - Plant growth promoter - Google Patents
Plant growth promoter Download PDFInfo
- Publication number
- WO1996006529A1 WO1996006529A1 PCT/JP1995/001693 JP9501693W WO9606529A1 WO 1996006529 A1 WO1996006529 A1 WO 1996006529A1 JP 9501693 W JP9501693 W JP 9501693W WO 9606529 A1 WO9606529 A1 WO 9606529A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- plant growth
- growth promoter
- group
- jasmonic acid
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/02—Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
-
- 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
- A01N43/22—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 rings with more than six members
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/06—Unsaturated carboxylic acids or thio analogues thereof; Derivatives thereof
-
- 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
- A01N49/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group, wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group, wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof
Definitions
- the present invention relates to a plant growth promoter, and more particularly, to plant growth on root crops, potatoes, cereals, fruits and vegetables, beans, leafy vegetables, fruit trees, woody plants, flowers, special crops, etc. For accelerators.
- bioactive substances from plant tissue fragments and studied their effects on the living environment of plants (germination, growth, flowering, fruit set, and aging) to promote crop growth and increase production. Attempts have been made to measure.
- bioactive substances having the action of brass on the growth and development of plants, and at present there are very few substances that can exert the growth promoting action in actual open-field cultivation. is there.
- An object of the present invention is to provide a plant growth promoter having a high plant growth promoting action.
- equation (1) equation (1)
- Ri represents a pentyl group or a pentenyl group
- R 2 represents a hydrogen atom or an alkyl group.
- a plant growth promoting agent containing brassinosteroid represented by the following formula as an active ingredient.
- Ri in the above formula (1) is a ventil group or a bentenyl group, and the bentenyl group is preferably a 2-pentenyl group.
- R 2 is a hydrogen atom or an alkynole group, preferably an alkyl group.
- the number of carbon atoms in the alkyl group is usually 1 to 10, preferably 2 to 6, and more preferably 3 to 4.
- alkyl group examples include a methyl group, an ethyl group, an n-bromo group, an isobromo group, an n-butyl group, an isobutyl group, a sec-butyl group, a t-butyl group, an n-pentyl group, and an isopentyl group.
- Such jasmonic acids can be produced according to a conventional method.
- dihydrodiasmonic acids in which Ri is a ventilyl group and R2 is an alkyl group having 1 to 10 carbon atoms are obtained by Michael addition of 2-bentylcyclopentene-11one and an alkyl ester of malonic acid. After that, it can be obtained by decarboxylation.
- the brassinosteride represented by the formula (2) is a compound of ⁇ and can be produced according to a conventional method. For example, add (22E, 24S) -24S-ethyl-5 ⁇ -cholester 2,22-gen-16-one, ⁇ -methylmorpholine- ⁇ -oxide and acetone, and a catalytic amount of osmium tetroxide to oxidize.
- reaction is carried out to obtain 2 ⁇ , 3 ⁇ -dihydroxy-24S-ethyl-5 ⁇ -cholest-1 22-en-6-one, which is then reacted with brobionic anhydride or propionyl chloride to give 2 ⁇ , 3 Synthesis of ⁇ -dibu-pionyoxy 24 S-ethyl-5- "cholest-1 22-en-6-one, followed by reaction with an organic peracid such as m-chloroperbenzoic acid, (22R, 23R, 24 S ) -2 ⁇ , 3—Jib mouth pionyloxy-1,22,23—Epoxy B—Homo 7—Oxa-1 5 ⁇ —Stigmastan 1—6-one can be produced 0
- composition ratio of jasmonic acids and brassinosteroids in the plant growth ( ⁇ ! Agent) of the present invention cannot be specified unconditionally depending on the target crop, the purpose of use and the time of application, etc.
- the strength of brassinosteroids: weight of jasmonic acids The ratio is usually 1: 0.1 L: 1, 0 0, 0 0 0, preferably 1: 1; L: 1 0 0, 0 0 0, more preferably 1:: L 0-1: 1 0, 0 0 0 is there.
- the plant growth promoter of the present invention may be sprayed on the drug substance itself, or may be mixed with a carrier or, if necessary, other adjuvants, prepared and sprayed.
- the formulation is not particularly limited, and a conventionally known formulation is applied. Examples include emulsions, suspensions, powders, wettable powders, aqueous solvents, granules, bases, aerosols and the like.
- the plant growth inhibitor of the present invention may contain, if necessary, auxiliary agents such as commonly used carriers, emulsifiers, dispersants, spreading agents, wetting agents, fixing agents, and disintegrating agents. Can be.
- auxiliary agents such as commonly used carriers, emulsifiers, dispersants, spreading agents, wetting agents, fixing agents, and disintegrating agents. Can be.
- a solid carrier or a liquid carrier is used as the carrier.
- the solid carrier preferably used in the present invention include, for example, talc, bentonite, clay, clay, diatomaceous earth, white carbon, gay anhydride, synthetic gay acid calcium, vermiculite, gay sand, mica, pumice, Inorganic substances such as gypsum, calcium carbonate, calcium hydroxide, magnesium, slaked lime, phosphorus lime, zeolite, ammonium sulfate; soybean flour, tobacco flour, walnut flour, flour, wood flour, starch, crystal cell mouth, etc.
- the liquid carrier suitably used in the present invention includes, for example, paraffinic or naphthenic hydrocarbons such as kerosene, mineral oil, spindle oil, and white oil; benzene, toluene, xylene, ethylbenzene, cumene, methylnaphthalene.
- Aromatic hydrocarbons such as carbon tetrachloride, carbon form, trichloroethylene, monochlorobenzene and o-chlorotoluene; ethers such as dioxane and tetrahydrofuran; acetone, methyl ethyl ketone, di Sobutyl ketone, cyclohexanone, acetophenone, isofolone, etc.
- Ketones such as ethyl acetate, amyl acetate, ethylene glycol acetate, diethylene glycol acetate, dibutyl maleate and getyl succinate; methanol, ethanol, isopropanol, butanol, n-hexanol, ethylene Alcohols such as glycol, propylene glycol, and ethylene glycol; ether alcohols such as ethylene glycol phenyl ether and diethylene glycol butyl ether; polar solvents such as dimethylformamide and dimethyl sulfoxide; and water.
- Surfactants are usually used as emulsifiers or dispersants.
- a nonionic, cationic, anionic or zwitterionic surfactant can be used.
- a nonionic, Z or anionic surfactant is suitably used.
- Suitable nonionic surfactants include, for example, higher alcohols such as lauryl alcohol, stearyl alcohol, and oleyl alcohol polymerized with ethylene oxide; and alkylphenols such as isooctyl phenol and nonyl phenol.
- ethylene naphthol such as butyl naphthol and octyl naphthol polymerized with ethylene oxide
- Suitable anionic surfactants include, for example, alkyl sulfates such as sodium parasulfate and oleyl alcohol sulfate; sodium octyl sulfosuccinate; Alkyl sulfonates such as sodium methylhexenesulfonate; aryl sulfonates such as sodium isobromovirnaphthalenesulfonate, sodium methylenebisnaphthalenesulfonate, sodium ligninsulfonate and sodium dodecylbenzenesulfonate; Examples include phosphates such as sodium tripolyphosphate.
- the content of jasmonic acids and brassinosteroids in the plant length of the plant of the present invention cannot be specified unconditionally depending on the type of plant, the use form, the method of use, the time of use, etc.
- the liquid carrier When used in combination as a solution, emulsion, suspension, etc., the content (weight Z volume) of jasmonic acids in these solutions is usually 0.01 to 500 ppm, preferably 0 to 500 ppm. It is adjusted to be from 0.05 to 300 ppm, more preferably from 0.1 to 200 ppm, and the content (weight Z volume) of brassinosteroid in these liquids is usually 0.0000000:
- the concentration is adjusted to a concentration ranging from! To I ppm, preferably from 0.0001 to 0.1 ppm, and more preferably from 0.001 to 0.01 ppm. When the concentration of each component is within the above range, a growth promoting effect is particularly effectively exhibited.
- the content of jasmonic acids in the total weight is usually in the range of 0.001 to 90% by weight, preferably 0.01 to 50% by weight.
- the content of brassinosteroid in it is usually in the range of 0.001 to 90% by weight, preferably 0.01 to 50% by weight.
- the preferred method of applying the plant length ⁇ 3 ⁇ 4! Agent of the present invention varies depending on the target plant, the purpose, and the like. Examples thereof include immersion treatment of seeds and seeds, seed foliage spraying, soil watering, Foliar application, inflorescence application, fruit application, injection treatment, etc. are adopted, and these can be applied in combination or once to several times.
- the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples.
- Example 1 growth promoting effect by seed treatment of wheat
- PDJ n-bromodihydrosimonate
- 22R, 23R, 24S 2 ⁇
- 3 ⁇ -Jib mouth pionyloxy 22, 23-Epoxy 1-Homo 7-Oxa 5 ⁇ -Stigmastan 1-6-one (hereinafter referred to as BL) was prepared as a test solution so as to have the concentration shown in Table 1, and wheat was added thereto.
- BL volume ratio
- Example 2 growth promoting effect of twenty radish on plant application
- a solution was prepared and mixed and diluted to the aqueous solution concentration shown in Table 2 to prepare a test solution.
- Twenty days radish (cultivar: Akamarcomet) was cultivated conventionally in an open-field field, and at the beginning of root enlargement, the above test solution was sprayed at 10 liters per cultivated area.
- Sixteen days after spraying, 15 well-growing individuals were harvested from each plot, and the weight of leaves and roots was measured to calculate the value (%) in comparison with the untreated plot.
- Table 2 shows the results. From Table 2, a synergistic effect between PD J and BL was observed.
- Table 2 shows the results. From Table 2, a synergistic effect between PD J and BL was observed.
- Table 3 shows the results. Table 3 shows a synergistic effect between PDJ and BL.
- Example 2 In the same manner as in Example 2, a test solution containing both compounds alone or in a mixture was prepared so as to have the concentrations shown in Table 4, and a tomato (cultivar: Momotarou) conventionally cultivated in a greenhouse in winter was used.
- a tomato cultivar: Momotarou
- the fourth fruit cluster In the early stage of the third fruit cluster, the fourth fruit cluster is in the early stage of flowering at the early stage of flower blossoming, the first time, the second time 20 days later, and the further 20 days later
- Example 2 A single or mixed test solution of both compounds was prepared in the same manner as in Example 2 so that the concentrations shown in Table 5 were obtained, and bottom-cultivated in a greenhouse by conventional methods.
- 2 Om 1 trees were sprayed on the tree with an average length of 30 to 40 cm and 150 to 200 leaves.
- Table 5 shows the results. Table 5 shows that the combination treatment of PD J and BL has a high effect of preventing ⁇
- Seeds (variety: Nipponbare) were immersed in 15 pieces of low-temperature water for 1 day, and then immersed for 24 hours in an aqueous drug solution prepared to the concentration shown in Table 6 according to the same method as in Example 2. The seeds were then soaked in water only for 3 hours, then seeded, seeded in 7 cm diameter pots, and grown in a 15,000 Lux artificial climate chamber at low temperatures of 20 to 21 ° C. When 1/4 (25%) of the individuals in the untreated plot reached the 3 leaf stage, the growth status of each plot was investigated and the untreated contrast value (%) was calculated. The results are shown in Table 6. Table 6
- Example 7 In the same manner as in Example 1, a test solution containing both compounds alone or in a mixture was prepared so as to have the concentrations shown in Table 7, and seeds (corn: honey ban) were added to this solution. (Tam, soybean: Mag bean) was instantaneously soaked and immediately air-dried. This was sown under field conditions during conventional cultivation. The live weight was examined 25 days after sowing, and the value () in comparison with the untreated group was calculated. Table 7 shows that the mixing treatment effect of both agents is high. Table 7
- Example 8 Yield improvement effect by spraying rice seedlings
- test solutions having the concentrations described in Table 9 were prepared.
- Table 9
- the plant growth promoter of the present invention has a growth promoting effect on a wide range of plants including root crops, potatoes, cereals, fruits and vegetables, leafy vegetables, fruit trees, woody plants, flowers and special crops. Demonstrate. Specific examples of applicable plants include root vegetables such as radish, carrot, onion, beet, turnip, and burdock; potatoes such as potato, sweet potato, taro, and sorghum; rice, barley, wheat, oat, millet, Cereals such as leeks, corn, buckwheat, corn and corn; Fruits and vegetables such as cucumber, eggplant, veman, kabochiya, watermelon, shirouri, makuwauri, melon, okra, strawberry, tomato; Legumes such as Chinese cabbage, lanterns, green onions, Hanayasai, parsley, mitsuba, celery, shiyungiku, spinach, lettuce, rapeseed, mizuna; fruit trees such as grape, pear,
- the site where the promoting effect of the plant growth promoter of the present invention is expressed varies depending on the type of plant, and includes, for example, rice, stem, root, tuber, rhizome, fruit, flower bud, and the like. It has the effect of promoting growth and increasing length and weight on leaves, stems, roots, tubers, rhizomes and fruits. It also has the effect of promoting differentiation of flower buds, increasing the rate of germination and increasing the number of flowers. It also has the effects of increasing fruit set, increasing fruit weight, increasing sugar content, increasing chromaticity, etc. for fruits.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Insects & Arthropods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
Claims
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/793,335 US5814581A (en) | 1994-08-26 | 1995-08-25 | Plant growth promoter comprising jasmonate and brassinolide |
| RU97104474A RU2145165C1 (ru) | 1994-08-26 | 1995-08-25 | Стимулятор роста растений |
| KR1019970701145A KR970705339A (ko) | 1994-08-26 | 1995-08-25 | 식물성장촉진제(plant growth promoter) |
| EP95929230A EP0777965A4 (en) | 1994-08-26 | 1995-08-25 | PROMOTER OF PLANT GROWTH |
| AU32654/95A AU3265495A (en) | 1994-08-26 | 1995-08-25 | Plant growth promoter |
| BR9508636A BR9508636A (pt) | 1994-08-26 | 1995-08-25 | Promotor do crescimento de plantas |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6/225674 | 1994-08-26 | ||
| JP22567494 | 1994-08-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1996006529A1 true WO1996006529A1 (en) | 1996-03-07 |
Family
ID=16833009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP1995/001693 Ceased WO1996006529A1 (en) | 1994-08-26 | 1995-08-25 | Plant growth promoter |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5814581A (ja) |
| EP (1) | EP0777965A4 (ja) |
| KR (1) | KR970705339A (ja) |
| CN (1) | CN1168619A (ja) |
| AU (1) | AU3265495A (ja) |
| BR (1) | BR9508636A (ja) |
| CA (1) | CA2198481A1 (ja) |
| PL (1) | PL318809A1 (ja) |
| RU (1) | RU2145165C1 (ja) |
| WO (1) | WO1996006529A1 (ja) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU742322B2 (en) * | 1999-10-08 | 2001-12-20 | National Agricultural Research Organization | A method for preventing the release of gramineous plant pollens |
| RU2471348C1 (ru) * | 2011-09-01 | 2013-01-10 | Михаил Аркадьевич Ершов | Стимулятор для предпосевной обработки семян зерновых культур |
| RU2485778C2 (ru) * | 2011-09-01 | 2013-06-27 | Михаил Аркадьевич Ершов | Способ получения стимулятора зерновых культур |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6239073B1 (en) | 1999-03-30 | 2001-05-29 | Exelixis Plant Sciences, Inc. | Brassinosteroid analogs useful as plant growth regulators |
| CA2274873A1 (en) * | 1999-07-06 | 2001-01-06 | Satinder Gidda | Methods and compositions for modulating flowering |
| US20060051868A1 (en) * | 2001-02-22 | 2006-03-09 | Pullman Gerald S | Methods for increasing conifer somatic embryo initiation, capture, and multiplication |
| RU2212135C2 (ru) * | 2001-10-15 | 2003-09-20 | Всероссийский научно-исследовательский институт биологической защиты растений | Способ обработки растений и используемая в нём композиция для защиты растений |
| RU2212136C2 (ru) * | 2001-10-15 | 2003-09-20 | Всероссийский научно-исследовательский институт биологической защиты растений | Способ обработки растений и используемая в нём композиция для защиты растений |
| RU2212137C2 (ru) * | 2001-10-15 | 2003-09-20 | Всероссийский научно-исследовательский институт биологической защиты растений | Способ обработки растений и используемая в нём композиция для защиты растений |
| CA2414487A1 (en) * | 2003-01-13 | 2004-07-13 | Florisys Inc. | Methods and genetic sequences for producing male sterile plants, and plants genetically modified to alter anther development |
| RU2282961C2 (ru) * | 2004-04-13 | 2006-09-10 | Государственное учреждение "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством" (НИТИГ) | Состав для протравливания семян |
| GB0409011D0 (en) | 2004-04-23 | 2004-05-26 | Biofutures Pi Ltd | Chemical compounds and use thereof in agriculture |
| GB0520726D0 (en) * | 2005-10-12 | 2005-11-23 | Plant Impact Plc | Agricultural composition |
| GB0521993D0 (en) * | 2005-10-28 | 2005-12-07 | Plant Impact Plc | Agricultural composition |
| EA013321B1 (ru) * | 2006-08-02 | 2010-04-30 | Государственное Научное Учреждение "Институт Биоорганической Химии Национальной Академии Наук Беларуси" | Биогербицидная композиция и способ ее применения |
| US20090082453A1 (en) * | 2007-09-25 | 2009-03-26 | New Biology, Inc. | Exogenous Methyl Dihydrojasmonate for Prevention and Control of Biotic Attack in Plants |
| WO2009067404A2 (en) * | 2007-11-19 | 2009-05-28 | New Biology, Inc. | Methods for improving flowering characteristics using methyl dihydrojasmonate |
| US8013226B2 (en) * | 2008-05-06 | 2011-09-06 | New Biology, Inc. | Methods for reducing leaf senescence using methyl dihydrojasmonate |
| US8563839B2 (en) * | 2008-05-06 | 2013-10-22 | New Biology, Inc. | Methods of reducing leaf senescence using methyl dihydrojasmonate |
| RU2370957C1 (ru) * | 2008-05-22 | 2009-10-27 | Сергей Ананьевич Тюрин | Препарат "биос" - стимулятор роста и развития растений |
| RU2409949C1 (ru) * | 2009-08-13 | 2011-01-27 | Валерий Федорович Швец | Способ повышения продуктивности растениеводческих и плодоовощных культур и увеличения срока хранения урожая |
| WO2014037202A2 (en) * | 2012-09-10 | 2014-03-13 | Syngenta Participations Ag | Pesticidal mixtures |
| RU2543276C2 (ru) * | 2013-04-30 | 2015-02-27 | Государственное научное учреждение Татарский научно-исследовательский институт агрохимии и почвоведения Российской академии сельскохозяйственных наук (ГНУ Татарский НИИАХП Россельхозакадемии) | Наноструктурная водно-цеолитная суспензия в качестве средства для предпосевной обработки семян гречихи |
| WO2015109061A2 (en) * | 2014-01-15 | 2015-07-23 | New Biology, Inc. | Methods for improving germination and stress tolerance characteristics with jasmonates |
| RU2630298C1 (ru) * | 2016-04-22 | 2017-09-06 | Андрей Владимирович Ковзелев | Способ получения стимулятора роста растений |
| CN106234365B (zh) * | 2016-07-13 | 2018-08-03 | 四川国光农化股份有限公司 | 一种植物生长调节组合物、制剂及其应用 |
| CN113973823A (zh) * | 2020-07-27 | 2022-01-28 | 郑州尼采生物科技有限公司 | 一种二氢茉莉酸丙酯可溶液及其制备方法 |
| CN114081033A (zh) * | 2020-08-24 | 2022-02-25 | 郑州尼采生物科技有限公司 | 一种农药制剂及其制备方法 |
| CN113170789B (zh) * | 2021-04-26 | 2023-04-28 | 郑州尼采生物科技有限公司 | 与高盐分溶液复配的二氢茉莉酸丙酯剂型及其制备方法 |
| CN115886001B (zh) * | 2023-01-04 | 2024-06-25 | 宁夏农林科学院枸杞科学研究所 | 一种枸杞子留树脱叶制干剂制备方法和应用 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD215928A1 (de) * | 1983-05-31 | 1984-11-28 | Adw Ddr | Mittel zur beeinflussung von wachstums-, entwicklungs- und stoffwechselprozessen in pflanzen |
| DD263914A1 (de) * | 1987-07-13 | 1989-01-18 | Akad Wissenschaften Ddr | Mittel zur beeinflussung von wachstums-, entwicklungs- und stoffwechselprozessen bei rispengetreide |
| SU1741704A1 (ru) * | 1990-04-09 | 1992-06-23 | Институт биоорганической химии АН БССР | Стимул тор роста картофел |
| DE69429336T2 (de) * | 1993-02-26 | 2002-08-22 | Zeon Corp., Tokio | Zusammensetzung von Pflanzenwachstums-Beschleuniger |
| EP0702027B1 (en) * | 1993-06-01 | 1999-09-08 | TAMA BIOCHEMICAL Co., Ltd. | Brassinosteroid derivatives and plant growth regulator containing the same |
-
1995
- 1995-08-25 WO PCT/JP1995/001693 patent/WO1996006529A1/ja not_active Ceased
- 1995-08-25 PL PL95318809A patent/PL318809A1/xx unknown
- 1995-08-25 AU AU32654/95A patent/AU3265495A/en not_active Abandoned
- 1995-08-25 BR BR9508636A patent/BR9508636A/pt not_active Application Discontinuation
- 1995-08-25 CN CN95195361A patent/CN1168619A/zh active Pending
- 1995-08-25 EP EP95929230A patent/EP0777965A4/en not_active Withdrawn
- 1995-08-25 KR KR1019970701145A patent/KR970705339A/ko not_active Withdrawn
- 1995-08-25 CA CA002198481A patent/CA2198481A1/en not_active Abandoned
- 1995-08-25 US US08/793,335 patent/US5814581A/en not_active Expired - Fee Related
- 1995-08-25 RU RU97104474A patent/RU2145165C1/ru active
Non-Patent Citations (1)
| Title |
|---|
| J. PLANT GROWTH REGUL., Vol. 13, No. 2, (1994), GROSS DIETER et al., "Novel Natural Substances Acting in Plant Growth Regulation", pages 93-114. * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU742322B2 (en) * | 1999-10-08 | 2001-12-20 | National Agricultural Research Organization | A method for preventing the release of gramineous plant pollens |
| US6651382B1 (en) | 1999-10-08 | 2003-11-25 | National Agricultural Research Organization | Method for preventing the release of gramineous plant pollens |
| RU2471348C1 (ru) * | 2011-09-01 | 2013-01-10 | Михаил Аркадьевич Ершов | Стимулятор для предпосевной обработки семян зерновых культур |
| RU2485778C2 (ru) * | 2011-09-01 | 2013-06-27 | Михаил Аркадьевич Ершов | Способ получения стимулятора зерновых культур |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2145165C1 (ru) | 2000-02-10 |
| PL318809A1 (en) | 1997-07-07 |
| EP0777965A4 (en) | 1997-12-10 |
| KR970705339A (ko) | 1997-10-09 |
| EP0777965A1 (en) | 1997-06-11 |
| AU3265495A (en) | 1996-03-22 |
| CA2198481A1 (en) | 1996-03-07 |
| US5814581A (en) | 1998-09-29 |
| BR9508636A (pt) | 1997-11-25 |
| CN1168619A (zh) | 1997-12-24 |
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