RU96115042A - NEW METHOD OF PLANT PROTECTION AGAINST FUNGAL INFECTION - Google Patents
NEW METHOD OF PLANT PROTECTION AGAINST FUNGAL INFECTIONInfo
- Publication number
- RU96115042A RU96115042A RU96115042/04A RU96115042A RU96115042A RU 96115042 A RU96115042 A RU 96115042A RU 96115042/04 A RU96115042/04 A RU 96115042/04A RU 96115042 A RU96115042 A RU 96115042A RU 96115042 A RU96115042 A RU 96115042A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- phenyl
- compound
- hydrogen
- means hydrogen
- Prior art date
Links
- 206010017533 Fungal infection Diseases 0.000 title claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 35
- 239000001257 hydrogen Substances 0.000 claims 35
- 125000000217 alkyl group Chemical group 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 25
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 18
- 150000002431 hydrogen Chemical class 0.000 claims 16
- 241000196324 Embryophyta Species 0.000 claims 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
- 240000001016 Solanum tuberosum Species 0.000 claims 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 6
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 240000008067 Cucumis sativus Species 0.000 claims 4
- 240000006394 Sorghum bicolor Species 0.000 claims 4
- 230000001939 inductive effect Effects 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 235000012015 potatoes Nutrition 0.000 claims 4
- 239000002689 soil Substances 0.000 claims 4
- 240000001498 Asparagus officinalis Species 0.000 claims 3
- 235000005340 Asparagus officinalis Nutrition 0.000 claims 3
- 240000007124 Brassica oleracea Species 0.000 claims 3
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 claims 3
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 claims 3
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 claims 3
- 240000003259 Brassica oleracea var. botrytis Species 0.000 claims 3
- 240000008664 Brassica oleracea var. gongylodes Species 0.000 claims 3
- 240000000613 Citrullus lanatus Species 0.000 claims 3
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 claims 3
- 235000009849 Cucumis sativus Nutrition 0.000 claims 3
- 240000006669 Helianthus annuus Species 0.000 claims 3
- 235000003222 Helianthus annuus Nutrition 0.000 claims 3
- 240000008962 Nicotiana tabacum Species 0.000 claims 3
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims 3
- 241000219094 Vitaceae Species 0.000 claims 3
- 241000209149 Zea Species 0.000 claims 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 3
- 235000005042 Zier Kohl Nutrition 0.000 claims 3
- 125000001589 carboacyl group Chemical group 0.000 claims 3
- 235000005822 corn Nutrition 0.000 claims 3
- 235000005824 corn Nutrition 0.000 claims 3
- 235000021021 grapes Nutrition 0.000 claims 3
- OQEBBZSWEGYTPG-GSVOUGTGSA-N (3R)-3-aminobutanoic acid Chemical compound C[C@@H](N)CC(O)=O OQEBBZSWEGYTPG-GSVOUGTGSA-N 0.000 claims 2
- QFRURJKLPJVRQY-UHFFFAOYSA-N 3-azaniumylpentanoate Chemical compound CCC(N)CC(O)=O QFRURJKLPJVRQY-UHFFFAOYSA-N 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 2
- 244000302526 Cucurbita pepo subsp pepo Species 0.000 claims 2
- 235000003954 Cucurbita pepo var melopepo Nutrition 0.000 claims 2
- 240000006962 Gossypium hirsutum Species 0.000 claims 2
- 235000008694 Humulus lupulus Nutrition 0.000 claims 2
- 240000006600 Humulus lupulus Species 0.000 claims 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims 2
- 240000007594 Oryza sativa Species 0.000 claims 2
- 235000007164 Oryza sativa Nutrition 0.000 claims 2
- 240000003768 Solanum lycopersicum Species 0.000 claims 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 230000002538 fungal Effects 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 235000019713 millet Nutrition 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 235000009566 rice Nutrition 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000011780 sodium chloride Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- OQEBBZSWEGYTPG-UHFFFAOYSA-N 3-aminobutanoic acid Chemical compound CC(N)CC(O)=O OQEBBZSWEGYTPG-UHFFFAOYSA-N 0.000 claims 1
- 240000002840 Allium cepa Species 0.000 claims 1
- 241000207199 Citrus Species 0.000 claims 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 claims 1
- QWCKQJZIFLGMSD-GSVOUGTGSA-N D-α-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- 241000223221 Fusarium oxysporum Species 0.000 claims 1
- QWCKQJZIFLGMSD-VKHMYHEASA-N L-α-aminobutyrate zwitterion Chemical compound CC[C@H](N)C(O)=O QWCKQJZIFLGMSD-VKHMYHEASA-N 0.000 claims 1
- 240000008415 Lactuca sativa Species 0.000 claims 1
- 235000003228 Lactuca sativa Nutrition 0.000 claims 1
- 240000008426 Persea americana Species 0.000 claims 1
- 241000233647 Phytophthora nicotianae var. parasitica Species 0.000 claims 1
- 241000208292 Solanaceae Species 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 235000020971 citrus fruits Nutrition 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
- 230000036039 immunity Effects 0.000 claims 1
- 235000021374 legumes Nutrition 0.000 claims 1
- 235000002732 oignon Nutrition 0.000 claims 1
- 230000001717 pathogenic Effects 0.000 claims 1
- 235000005426 persea americana Nutrition 0.000 claims 1
Claims (34)
где a) R1 и R2 каждый независимо означает водород, C1-C8 алкил, фенил и фенил-C1-C4алкил;
(b) R3 означает водород; C1-C23 алкил; карбокси-C1-C4алкил; фенил-C1-C4 алкил; где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; или C2-C23-алкоксикарбонил, C1-C4 алкил;
(c) R4 и R5 каждый независимо означает водород или C1-C8-алкил;
(d) R6 и R7 каждый независимо означает водород; C1-C8алкил; C2-C8-алканоил; фенил-C1-C4алкил, где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; C2-C8-алкоксикарбонил; CONR8, где R8 означает водород, C1-C8-алкил, фенил, фенил-C1-C4 алкил; фенил-C2-C4 алкилоксикарбонил;
(e) X означает O, S или N, и его соли; и культуру выбирают из группы зерновых, огурцов, арбуза, спаржевой капусты, цветной капусты, капусты кольраби, подсолнечника, картофеля, табака, винограда, хлопчатника, кабачка, кукурузы, сорго, просо американского, риса, салата латук, хмеля, авокадо, цитрусовых, бобовых и лука, в количестве, достаточном для индуцироваия механизма локального и системного иммунитета указанного культурного растения для подавления грибковой болезни.1. The method of protecting plants against fungal infections caused by pathogenic fungi by inducing the systemic resistance of the specified culture, characterized in that the specified culture or the place of its growth cause a composition containing an effective amount of the compounds of formula I:
where a) R 1 and R 2 each independently means hydrogen, C 1 -C 8 alkyl, phenyl and phenyl-C 1 -C 4 alkyl;
(b) R 3 is hydrogen; C 1 -C 23 alkyl; carboxy-C 1 -C 4 alkyl; phenyl-C 1 -C 4 alkyl; where the phenyl residue means unsubstituted or monohalogenated phenyl; or C 2 -C 23 -alkoxycarbonyl, C 1 -C 4 alkyl;
(c) R 4 and R 5 each independently means hydrogen or C 1 -C 8 alkyl;
(d) R 6 and R 7 each independently means hydrogen; C 1 -C 8 alkyl; C 2 -C 8 alkanoyl; phenyl-C 1 -C 4 alkyl, where the phenyl residue is unsubstituted or monohalo-substituted phenyl; C 2 -C 8 alkoxycarbonyl; CONR 8 , where R 8 means hydrogen, C 1 -C 8 -alkyl, phenyl, phenyl-C 1 -C 4 alkyl; phenyl-C 2 -C 4 alkyloxycarbonyl;
(e) X is O, S or N, and its salts; and the crop is selected from the group of cereals, cucumbers, watermelon, asparagus cabbage, cauliflower, kohlrabi cabbage, sunflower, potatoes, tobacco, grapes, cotton, zucchini, corn, sorghum, millet American, rice, lettuce, hops, avocado, citrus, legumes and onions, in an amount sufficient to induce the mechanism of local and systemic immunity of the specified cultivated plant to suppress the fungal disease.
где a) R1 и R2 каждый независимо означает водород, C1-C8 алкил, фенил, и фенил-C1-C4 алкил;
(b) R3 означает водород; C1-C23 алкил; карбокси-C1-C4 алкил; фенил-C1-C4 алкил, где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; или C2-C23-алкоксикарбонил, C1-C4 алкил;
(c) R4 и R5 каждый независимо означает водород или C1-C8 алкил;
(d) R6 и R7 каждый независимо означает водород; C1-C8-алкил; C2-C8-алканоил; фенил-C1 -C4 алкил, где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; C2-C8-алкоксикарбонил; CONR8, где R8 означает водород, C1-C6-алкил, фенил, фенил-C1-C4 алкил; фенил-C2-C4 алкоксикарбонил;
(e) X означает O, S или N, и его соли.15. A way to protect tomatoes from Fusarium oxysporum of Sp. Lycopersici by inducing the systemic resistance of said culture, characterized in that an effective amount of the compound of formula I is applied to said culture or the place of its growth:
where a) R 1 and R 2 each independently means hydrogen, C 1 -C 8 alkyl, phenyl, and phenyl-C 1 -C 4 alkyl;
(b) R 3 is hydrogen; C 1 -C 23 alkyl; carboxy-C 1 -C 4 alkyl; phenyl-C 1 -C 4 alkyl, where the phenyl residue is unsubstituted or monohalo-substituted phenyl; or C 2 -C 23 -alkoxycarbonyl, C 1 -C 4 alkyl;
(c) R 4 and R 5 each independently means hydrogen or C 1 -C 8 alkyl;
(d) R 6 and R 7 each independently means hydrogen; C 1 -C 8 alkyl; C 2 -C 8 alkanoyl; phenyl-C 1 -C 4 alkyl, where the phenyl residue is unsubstituted or monohalo-substituted phenyl; C 2 -C 8 alkoxycarbonyl; CONR 8 where R 8 means hydrogen, C 1 -C 6 -alkyl, phenyl, phenyl-C 1 -C 4 alkyl; phenyl C 2 -C 4 alkoxycarbonyl;
(e) X is O, S or N, and its salts.
где a) R1 и R2 каждый независимо означает водород, C1-C8 алкил, фенил, и фенил-C1-4 алкил;
(b) R3 означает водород; C1-C23 алкил; карбокси-C1-C4 алкил; фенил-C1-C4 алкил, где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; или C2-C23-алкоксикарбонил, C1-C4 алкил;
(c) R4 и R5 каждый независимо означает водород или C1-C8 алкил;
(d) R6 b R7 каждый независимо означает водород; C1-C8 алкил; C2-C8-алканоил; фенил-C1-C4 алкил, бензоил, где фенильный остаток означает незамещенный или моногалоидзамещенный фенил; C2 -C8 алкоксикарбонил; CONR8 , где R8 означает водород, C1-C8-алкил, фенил, фенил-C1-C4 алкил; фенил-C2-C4 алкоксикарбонил.29. A method of protecting a cultivated plant from gray rot by inducing the systemic resistance of said culture, characterized in that a composition containing an effective amount of a compound of formula I is applied to a given culture or a place of its growth:
wherein a) R 1 and R 2 are each independently hydrogen, C 1 -C 8 alkyl, phenyl, and phenyl-C 1 - 4 alkyl;
(b) R 3 is hydrogen; C 1 -C 23 alkyl; carboxy-C 1 -C 4 alkyl; phenyl-C 1 -C 4 alkyl, where the phenyl residue is unsubstituted or monohalo-substituted phenyl; or C 2 -C 23 -alkoxycarbonyl, C 1 -C 4 alkyl;
(c) R 4 and R 5 each independently means hydrogen or C 1 -C 8 alkyl;
(d) R 6 b R 7 each independently is hydrogen; C 1 -C 8 alkyl; C 2 -C 8 alkanoyl; phenyl-C 1 -C 4 alkyl, benzoyl, where the phenyl residue is unsubstituted or monohalo-substituted phenyl; C 2 -C 8 alkoxycarbonyl; CONR 8 , where R 8 means hydrogen, C 1 -C 8 -alkyl, phenyl, phenyl-C 1 -C 4 alkyl; phenyl-C 2 -C 4 alkoxycarbonyl.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL107992 | 1993-12-12 | ||
IL10799293A IL107992A0 (en) | 1993-12-12 | 1993-12-12 | Crop improvement |
IL109474 | 1994-04-28 | ||
IL10947494A IL109474A0 (en) | 1994-04-28 | 1994-04-28 | Crop improvement |
IL111824 | 1994-11-30 | ||
IL11182494A IL111824A0 (en) | 1994-11-30 | 1994-11-30 | A novel method for to protect plants from fungal infection |
PCT/US1994/014108 WO1995015684A1 (en) | 1993-12-12 | 1994-12-09 | A novel method to protect plants from fungal infection |
Publications (2)
Publication Number | Publication Date |
---|---|
RU96115042A true RU96115042A (en) | 1998-10-20 |
RU2141760C1 RU2141760C1 (en) | 1999-11-27 |
Family
ID=27271632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU96115042A RU2141760C1 (en) | 1993-12-12 | 1994-12-09 | Method of protecting plants against fungal infection (versions) |
Country Status (10)
Country | Link |
---|---|
US (2) | US5830919A (en) |
EP (1) | EP0732874A4 (en) |
JP (1) | JPH09506369A (en) |
CN (1) | CN1134212C (en) |
AU (1) | AU700579B2 (en) |
BR (1) | BR9408197A (en) |
CA (1) | CA2178829A1 (en) |
EG (1) | EG20402A (en) |
RU (1) | RU2141760C1 (en) |
WO (1) | WO1995015684A1 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR9408197A (en) * | 1993-12-12 | 1997-08-26 | Agrogene Ltd | Method to protect plants against fungal diseases |
US5739140A (en) * | 1995-11-03 | 1998-04-14 | Monsanto Company | Selected novel aryl acrylics |
US6495572B1 (en) * | 1997-04-04 | 2002-12-17 | Agrogene Ltd. | Synergistic mixtures of an amino acid |
US6414019B1 (en) | 1997-04-16 | 2002-07-02 | Agrogene Ltd. | Synergistic mixtures of selected amino acids |
US6083877A (en) * | 1998-03-10 | 2000-07-04 | Auxein Corporation | Methods for regulating plant growth |
WO2003000039A2 (en) * | 2001-06-22 | 2003-01-03 | University Of Chicago | Regulation of plant fertility by modulation of gaba levels in flowers |
NI200300043A (en) | 2002-03-28 | 2003-11-05 | Warner Lambert Co | AMINO ACIDS WITH AFFINITY FOR THE PROTEIN a2DELTA. |
US6743752B2 (en) | 2003-03-28 | 2004-06-01 | Northern Quinoa Corporation | Method of protecting plants from bacterial diseases |
ITMI20031020A1 (en) | 2003-05-21 | 2004-11-22 | Isagro Spa | COPPER SALTS OF ORGANIC ACIDS AND USE AS FUNGICIDES. |
MXPA06003396A (en) | 2003-09-25 | 2006-06-08 | Warner Lambert Co | PRODRUGS OF AMINO ACIDS WITH AFFINITY FOR THE alpha2?- PROTEIN. |
FR2863168A1 (en) * | 2003-12-04 | 2005-06-10 | Centre Nat Rech Scient | Antibacterial agents comprising gamma--butyrolactone degradation pathway inducers, e.g. succinate semialdehyde, useful in human or veterinary medicine, plant or foodstuff protection or disinfection |
US20100261694A1 (en) * | 2009-04-07 | 2010-10-14 | Eric Lam | Chemical chaperones and methods of use thereof for inhibiting proliferation of the phytopathogenic fungus Fusarium ssp. |
KR20200074252A (en) | 2012-05-17 | 2020-06-24 | 제넨테크, 인크. | Amorphous form of an akt inhibiting pyrimidinyl - cyclopentane compound, compositions and methods thereof |
CN104487430B (en) | 2012-05-17 | 2016-08-24 | 阵列生物制药公司 | For the method manufacturing hydroxylated cyclopenta pyrimidine compound |
CA2873661C (en) | 2012-05-17 | 2020-07-21 | Genentech, Inc. | Process of making hydroxylated cyclopentapyrimidine compounds and salts thereof |
ES2582557T3 (en) | 2012-05-17 | 2016-09-13 | Array Biopharma, Inc. | Process for the preparation of hydroxylated cyclopentylpyrimidine compounds |
WO2013173779A1 (en) | 2012-05-17 | 2013-11-21 | Genentech, Inc. | Process for making amino acid compounds |
CN110036855B (en) * | 2019-05-23 | 2022-02-01 | 申琳 | Method for regulating high yield and high quality of sweet potatoes |
CN112300017B (en) * | 2019-08-01 | 2023-06-09 | 浙江九洲药业股份有限公司 | Racemization preparation method of chiral beta-amino acid and derivative thereof |
CN113785842A (en) * | 2021-10-20 | 2021-12-14 | 海南大学 | Pesticide composition for preventing and treating plant fungal diseases and preparation method thereof |
CN114885945A (en) * | 2022-03-30 | 2022-08-12 | 云南农业大学 | Method for preventing and treating black shank by inducing tobacco |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL251479A (en) * | 1959-05-13 | |||
DE1567221A1 (en) * | 1965-06-01 | 1970-04-16 | Berlin Chemie Veb | Systemic fungicides |
US3899585A (en) * | 1972-01-20 | 1975-08-12 | Rikagaku Kenkyusho | Fungicidal method for protecting a plant |
US3991208A (en) * | 1973-12-28 | 1976-11-09 | Millmaster Onyx Corporation | Amphoteric surface-active agents |
GB2106389B (en) * | 1981-07-16 | 1985-07-17 | Nat Res Dev | The inhibition of growth in fungi |
US5096700A (en) * | 1990-09-28 | 1992-03-17 | The Procter & Gamble Company | Halogenated aminohexanoates and aminobutyrates antimicrobial agents |
BR9408197A (en) * | 1993-12-12 | 1997-08-26 | Agrogene Ltd | Method to protect plants against fungal diseases |
-
1994
- 1994-12-09 BR BR9408197A patent/BR9408197A/en not_active IP Right Cessation
- 1994-12-09 JP JP7516339A patent/JPH09506369A/en not_active Ceased
- 1994-12-09 AU AU15119/95A patent/AU700579B2/en not_active Ceased
- 1994-12-09 EP EP95906610A patent/EP0732874A4/en not_active Withdrawn
- 1994-12-09 RU RU96115042A patent/RU2141760C1/en not_active IP Right Cessation
- 1994-12-09 CN CNB941949281A patent/CN1134212C/en not_active Expired - Fee Related
- 1994-12-09 WO PCT/US1994/014108 patent/WO1995015684A1/en not_active Application Discontinuation
- 1994-12-09 CA CA002178829A patent/CA2178829A1/en not_active Abandoned
- 1994-12-11 EG EG77994A patent/EG20402A/en active
-
1996
- 1996-06-05 US US08/658,636 patent/US5830919A/en not_active Expired - Fee Related
-
1998
- 1998-10-29 US US09/181,747 patent/US6075051A/en not_active Expired - Fee Related
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU96115042A (en) | NEW METHOD OF PLANT PROTECTION AGAINST FUNGAL INFECTION | |
US5830919A (en) | Method to protect plants from fungal infection | |
SU824877A3 (en) | Fungicidic agent | |
AU600032B2 (en) | Process for protecting plants against diseases | |
Larsson et al. | Disease progression and yield losses from root diseases caused by soilborne pathogens of spinach. | |
MD950364A (en) | Process for weed control, process for selective monocotyledenous weed control in the presence of cereal crops, 4-(2,6-disubstituted-phenoxy) coumarin derivatives, process for preparation thereof, herbicidal composition | |
RU2004115620A (en) | FUNGICID COMPOSITION BASED ON THE EXTREME ONE OF ONE DERIVATIVE OF PYRIDYLMETHYLBENZAMIDE AND ON THE EXTREME ONE OF ONE DERIVATIVE OF DITIOCARBAMATE | |
Stephenson et al. | Structure-activity relationships for antidotes to thiocarbamate herbicides in corn | |
KR850000338B1 (en) | Process for the acylated naphthylamines | |
CA1073922A (en) | Microbicidal acylated thiopropionyl anilines | |
Rahman et al. | Selective action of trifluralin for control of green foxtail in wheat | |
CS219929B2 (en) | Means for destruction or/and profylaxy of infections brought about by fytopathogennous microorganisms and method of making the active substances | |
SU1322967A3 (en) | Method of fighting unwanted plants | |
Ogawa et al. | Isourea and triazinone derivatives as related to their ability to stimulate rice seedling growth | |
US3862325A (en) | Method of combating plant fungi | |
BR8306966A (en) | GUANIDINE COMPOUNDS, PROCESS TO INCREASE THE YIELD OF CROP CULTURES FROM BURYED STEMS, PROCESS TO INDUCE A RESPONSE LIKE CYTOKIN, AND PROCESS FOR THE PREPARATION OF A COMPOUND | |
AU595269B2 (en) | Plant growth promotion | |
KR102013571B1 (en) | Composition for controlling nematodes comprising N,N-dimethyl decanamide as effective component and uses thereof | |
Burrage et al. | Common rootrot and plant development following treatments of wheat seed with aldrin, gamma BHC, and heptachlor, with and without mercury fungicides | |
Srivastava et al. | Morpho-Phystological Response of Garden Pea to Sowing Dates. Ii—Growth Analysis | |
Das et al. | Effect of growth substances and nitrogen on the growth, yield and quality of pumpkin (Cucurbita moschata Duchesne) | |
Hait et al. | Protection of wheat seedlings from Helminthosporium infection by seed treatment with chemicals | |
US3657449A (en) | Control of virus diseases of plants with carboxamido oxathins | |
US3284287A (en) | Inhibiting growth of fungi and bacteria | |
KR880011164A (en) | 23-deoxy-27-halo (chloro or bromo) derivatives of LL-F28249 compounds, methods of use thereof and compositions comprising the derivatives |