SU328538A1 - - Google Patents
Info
- Publication number
- SU328538A1 SU328538A1 SU1399055A SU1399055A SU328538A1 SU 328538 A1 SU328538 A1 SU 328538A1 SU 1399055 A SU1399055 A SU 1399055A SU 1399055 A SU1399055 A SU 1399055A SU 328538 A1 SU328538 A1 SU 328538A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- infection
- oxygen
- plants
- fungicide
- pots
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 description 9
- 208000015181 infectious disease Diseases 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000000417 fungicide Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 230000000855 fungicidal effect Effects 0.000 description 5
- 125000001841 imino group Chemical group [H]N=* 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 240000007594 Oryza sativa Species 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- -1 2,5-dichlorophenyl Chemical group 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- HIIMRUPQOKCXFO-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-1,3-thiazolidine-2,4-dione Chemical compound ClC1=CC(Cl)=CC(N2C(SCC2=O)=O)=C1 HIIMRUPQOKCXFO-UHFFFAOYSA-N 0.000 description 1
- 235000000832 Ayote Nutrition 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000228437 Cochliobolus Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 235000009854 Cucurbita moschata Nutrition 0.000 description 1
- 240000001980 Cucurbita pepo Species 0.000 description 1
- 235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 1
- 241000289659 Erinaceidae Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 241001617088 Thanatephorus sasakii Species 0.000 description 1
- 229940053194 antiepileptics oxazolidine derivative Drugs 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 150000002917 oxazolidines Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU328538A1 true SU328538A1 (cs) |
Family
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