DD133885B1 - Mittel zur bekaempfung von phytopathogenen bakterien und pilzen - Google Patents

Mittel zur bekaempfung von phytopathogenen bakterien und pilzen Download PDF

Info

Publication number: DD133885B1
Authority: DD; German Democratic Republic
Prior art keywords: fungicide; control; hydrogen; item; agents
Prior art date: 1978-01-04

Application number

DD20308878A

Other languages

German (de)

English (en)

Other versions

DD133885A1 (de

Inventor

Hans Lehmann

Manfred Gross

Alfred Jumar

Paul Held

Annerose Rehnig

Gerda Tschampel

Original Assignee

Hans Lehmann

Manfred Gross

Alfred Jumar

Paul Held

Annerose Rehnig

Gerda Tschampel

Priority date (The priority date 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 date listed.)

1978-01-04

Filing date

1978-01-04

Publication date

1981-02-25

1978-01-04 Application filed by Hans Lehmann, Manfred Gross, Alfred Jumar, Paul Held, Annerose Rehnig, Gerda Tschampel filed Critical Hans Lehmann

1978-01-04 Priority to DD20308878A priority Critical patent/DD133885B1/de

1978-12-06 Priority to CS808278A priority patent/CS217403B1/cs

1978-12-08 Priority to DE19782853040 priority patent/DE2853040A1/de

1979-01-03 Priority to FR7900072A priority patent/FR2413879A1/fr

1979-01-03 Priority to GB7900125A priority patent/GB2016273B/en

1979-01-04 Priority to NL7900046A priority patent/NL7900046A/xx

1979-01-31 Publication of DD133885A1 publication Critical patent/DD133885A1/xx

1981-02-25 Publication of DD133885B1 publication Critical patent/DD133885B1/de

Links

241000894006 Bacteria Species 0.000 title claims description 5
230000003032 phytopathogenic effect Effects 0.000 title claims 2
239000000417 fungicide Substances 0.000 claims description 14
230000000855 fungicidal effect Effects 0.000 claims description 12
239000004480 active ingredient Substances 0.000 claims description 9
-1 aromatic carboxylic acids Chemical class 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
239000000203 mixture Substances 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
241000233866 Fungi Species 0.000 claims description 4
239000012990 dithiocarbamate Substances 0.000 claims description 4
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
150000003931 anilides Chemical class 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
239000013543 active substance Substances 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
229940051881 anilide analgesics and antipyretics Drugs 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
150000004659 dithiocarbamates Chemical class 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
125000005543 phthalimide group Chemical class 0.000 claims description 2
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims description 2
239000004606 Fillers/Extenders Substances 0.000 claims 1
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
238000012272 crop production Methods 0.000 claims 1
239000003085 diluting agent Substances 0.000 claims 1
230000035515 penetration Effects 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
238000003860 storage Methods 0.000 description 13
230000000844 anti-bacterial effect Effects 0.000 description 11
239000003242 anti bacterial agent Substances 0.000 description 6
229940088710 antibiotic agent Drugs 0.000 description 6
239000003814 drug Substances 0.000 description 6
230000000694 effects Effects 0.000 description 6
208000035143 Bacterial infection Diseases 0.000 description 5
241000196324 Embryophyta Species 0.000 description 5
244000061456 Solanum tuberosum Species 0.000 description 5
235000002595 Solanum tuberosum Nutrition 0.000 description 5
230000001580 bacterial effect Effects 0.000 description 5
239000003899 bactericide agent Substances 0.000 description 4
238000003306 harvesting Methods 0.000 description 4
229960005091 chloramphenicol Drugs 0.000 description 3
WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 3
238000009472 formulation Methods 0.000 description 3
235000012015 potatoes Nutrition 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000005507 spraying Methods 0.000 description 3
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 3
AHAJEGBFJIEDIS-UHFFFAOYSA-N 1-bromo-3,3,3-trichloro-1-nitropropan-1-ol Chemical compound [O-][N+](=O)C(Br)(O)CC(Cl)(Cl)Cl AHAJEGBFJIEDIS-UHFFFAOYSA-N 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
244000291564 Allium cepa Species 0.000 description 2
235000002732 Allium cepa var. cepa Nutrition 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
208000031888 Mycoses Diseases 0.000 description 2
239000008272 agar Substances 0.000 description 2
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YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 2
230000007812 deficiency Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
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239000000463 material Substances 0.000 description 2
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230000017066 negative regulation of growth Effects 0.000 description 2
UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004308 thiabendazole Substances 0.000 description 2
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238000011282 treatment Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
VKLPUUWTAMOCAW-UHFFFAOYSA-N 1-(2-nitro-3-piperidin-1-ylpropyl)piperidine Chemical compound [N+](=O)([O-])C(CN1CCCCC1)CN1CCCCC1 VKLPUUWTAMOCAW-UHFFFAOYSA-N 0.000 description 1
PHFWIVUXNVZTGK-UHFFFAOYSA-N 1-bromo-1-nitroethanol Chemical compound CC(O)(Br)[N+]([O-])=O PHFWIVUXNVZTGK-UHFFFAOYSA-N 0.000 description 1
IGRHQNITNJZXKA-UHFFFAOYSA-N 1-bromo-1-nitropropan-1-ol Chemical class CCC(O)(Br)[N+]([O-])=O IGRHQNITNJZXKA-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
UPTVJAJPBGIRLZ-UHFFFAOYSA-N 2-(trichloromethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 UPTVJAJPBGIRLZ-UHFFFAOYSA-N 0.000 description 1
OGGHUMVMTWCANK-UHFFFAOYSA-N 2-bromo-2-nitroethanol Chemical compound OCC(Br)[N+]([O-])=O OGGHUMVMTWCANK-UHFFFAOYSA-N 0.000 description 1
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
JMKSQPHJYIHKQU-UHFFFAOYSA-N 6-methyl-2,3-dihydro-1,4-oxathiine-5-carboxylic acid Chemical compound CC1=C(C(O)=O)SCCO1 JMKSQPHJYIHKQU-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
240000007087 Apium graveolens Species 0.000 description 1
235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 1
235000010591 Appio Nutrition 0.000 description 1
241000235349 Ascomycota Species 0.000 description 1
241000221198 Basidiomycota Species 0.000 description 1
244000178937 Brassica oleracea var. capitata Species 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
244000000626 Daucus carota Species 0.000 description 1
235000002767 Daucus carota Nutrition 0.000 description 1
241000588694 Erwinia amylovora Species 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
MZNCVTCEYXDDIS-UHFFFAOYSA-N Mebenil Chemical compound CC1=CC=CC=C1C(=O)NC1=CC=CC=C1 MZNCVTCEYXDDIS-UHFFFAOYSA-N 0.000 description 1
229930193140 Neomycin Natural products 0.000 description 1
206010034133 Pathogen resistance Diseases 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
239000004098 Tetracycline Substances 0.000 description 1
239000005843 Thiram Substances 0.000 description 1
241001668516 Xanthomonas citri subsp. malvacearum Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
KIPLYOUQVMMOHB-MXWBXKMOSA-L [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O Chemical compound [Ca++].CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O.CN(C)[C@H]1[C@@H]2[C@@H](O)[C@H]3C(=C([O-])[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c1c(O)cccc1[C@@]3(C)O KIPLYOUQVMMOHB-MXWBXKMOSA-L 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000000843 anti-fungal effect Effects 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
244000052616 bacterial pathogen Species 0.000 description 1
230000003385 bacteriostatic effect Effects 0.000 description 1
RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
150000001556 benzimidazoles Chemical class 0.000 description 1
MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000013365 dairy product Nutrition 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000010410 dusting Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000009920 food preservation Methods 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
230000001408 fungistatic effect Effects 0.000 description 1
150000003977 halocarboxylic acids Chemical class 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
229940107698 malachite green Drugs 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
238000005555 metalworking Methods 0.000 description 1
229960004927 neomycin Drugs 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
244000052769 pathogen Species 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
229960005322 streptomycin Drugs 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
229940063650 terramycin Drugs 0.000 description 1
238000012360 testing method Methods 0.000 description 1
229960002180 tetracycline Drugs 0.000 description 1
229930101283 tetracycline Natural products 0.000 description 1
235000019364 tetracycline Nutrition 0.000 description 1
150000003522 tetracyclines Chemical class 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/26—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups and being further substituted by halogen atoms
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/13—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups
- C07C205/14—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms
- C07C205/15—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by hydroxy groups having nitro groups and hydroxy groups bound to acyclic carbon atoms of a saturated carbon skeleton

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Air Conditioning Control Device (AREA)

DD20308878A 1978-01-04 1978-01-04 Mittel zur bekaempfung von phytopathogenen bakterien und pilzen DD133885B1 (de)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
DD20308878A DD133885B1 (de)	1978-01-04	1978-01-04	Mittel zur bekaempfung von phytopathogenen bakterien und pilzen
CS808278A CS217403B1 (en)	1978-01-04	1978-12-06	Composition against phytopathogeneous bacteria
DE19782853040 DE2853040A1 (de)	1978-01-04	1978-12-08	Mittel zur bekaempfung von phytopathogenen bakterien und pilzen
FR7900072A FR2413879A1 (fr)	1978-01-04	1979-01-03	Agent pour lutter contre les bacteries et champignons phytopathogenes a base de nitroalcanols
GB7900125A GB2016273B (en)	1978-01-04	1979-01-03	Compositions for controlling phytopathogenic bacteria and fungi in agriculture and horticulture
NL7900046A NL7900046A (nl)	1978-01-04	1979-01-04	Middel ter bestrijding van fytopathogene bacterieen en schimmels.

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD20308878A DD133885B1 (de)	1978-01-04	1978-01-04	Mittel zur bekaempfung von phytopathogenen bakterien und pilzen

Publications (2)

Publication Number	Publication Date
DD133885A1 DD133885A1 (de)	1979-01-31
DD133885B1 true DD133885B1 (de)	1981-02-25

Family

ID=5511164

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD20308878A DD133885B1 (de)	1978-01-04	1978-01-04	Mittel zur bekaempfung von phytopathogenen bakterien und pilzen

Country Status (6)

Country	Link
CS (1)	CS217403B1 (cs)
DD (1)	DD133885B1 (cs)
DE (1)	DE2853040A1 (cs)
FR (1)	FR2413879A1 (cs)
GB (1)	GB2016273B (cs)
NL (1)	NL7900046A (cs)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0231488A1 (de) *	1985-12-23	1987-08-12	Bayer Ag	Mittel zur Beizung von Pflanzkartoffeln
DE3622976A1 (de) *	1986-07-09	1988-01-21	Bayer Ag	Fluor enthaltende dimethylolnitromethane, verfahren zu ihrer herstellung sowie ihre verwendung
EP0291561A1 (de) *	1987-05-19	1988-11-23	Bayer Ag	Mittel zur Beizung von Kartoffeln, die für Ernährungszwecke bestimmt sind
GB8830266D0 (en) *	1988-12-24	1989-02-22	Laporte Industries Ltd	Absorbent material
CN102282155B (zh)	2008-12-02	2017-06-09	日本波涛生命科学公司	磷原子修饰的核酸的合成方法
RU2612521C2 (ru)	2009-07-06	2017-03-09	Онтории, Инк.	Новые пролекарства нуклеиновых кислот и способы их применения
ES2586683T3 (es) *	2009-09-16	2016-10-18	Wave Life Sciences Japan, Inc.	Grupo protector novedoso para sintetizar ARN y derivados del mismo
JP5868324B2 (ja)	2010-09-24	2016-02-24	株式会社Wave Life Sciences Japan	不斉補助基
CN103796657B (zh)	2011-07-19	2017-07-11	波涛生命科学有限公司	合成官能化核酸的方法
PL2872485T3 (pl)	2012-07-13	2021-05-31	Wave Life Sciences Ltd.	Asymetryczna grupa pomocnicza
CA2879066C (en)	2012-07-13	2019-08-13	Shin Nippon Biomedical Laboratories, Ltd.	Chiral nucleic acid adjuvant
KR102213609B1 (ko)	2012-07-13	2021-02-08	웨이브 라이프 사이언시스 리미티드	키랄 제어
US10322173B2 (en)	2014-01-15	2019-06-18	Shin Nippon Biomedical Laboratories, Ltd.	Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent
JPWO2015108048A1 (ja)	2014-01-15	2017-03-23	株式会社新日本科学	抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤
JPWO2015108047A1 (ja)	2014-01-15	2017-03-23	株式会社新日本科学	免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤
BR112016016400A2 (pt)	2014-01-16	2017-10-03	Wave Life Sciences Ltd	Composições de oligonucleotídeos quiralmente controlados, seu uso, sua composição farmacêutica, e métodos

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FR922380A (fr) *	1945-02-15	1947-06-06	Geigy Ag J R	Produits antiparasitaires
US3415936A (en) *	1963-11-26	1968-12-10	Phillips Petroleum Co	Bactericide for brine injection
GB1145496A (en) *	1965-06-29	1969-03-12	Thomson Res Associates Ltd	Control of fungal disease in trees
GB1193954A (en) *	1966-08-12	1970-06-03	Boots Pure Drug Co Ltd	Control of Micro-Organisms
US3546346A (en) *	1969-03-24	1970-12-08	Morton Int Inc	Systemic plant and seed fungicide comprising 1,1,1 - trichloro - 2 - hydroxy-3-nitropropane
DE2054887A1 (en) *	1970-11-07	1972-05-10	Badische Anilin- & Soda-Fabrik Ag, 6700 Ludwigshafen	Antifungal bromonitroalkanols - for plant protection

1978
- 1978-01-04 DD DD20308878A patent/DD133885B1/de not_active IP Right Cessation
- 1978-12-06 CS CS808278A patent/CS217403B1/cs unknown
- 1978-12-08 DE DE19782853040 patent/DE2853040A1/de not_active Ceased
1979
- 1979-01-03 FR FR7900072A patent/FR2413879A1/fr active Pending
- 1979-01-03 GB GB7900125A patent/GB2016273B/en not_active Expired
- 1979-01-04 NL NL7900046A patent/NL7900046A/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
GB2016273B (en)	1982-06-30
DE2853040A1 (de)	1979-07-12
DD133885A1 (de)	1979-01-31
GB2016273A (en)	1979-09-26
NL7900046A (nl)	1979-07-06
CS217403B1 (en)	1983-01-28
FR2413879A1 (fr)	1979-08-03

Legal Events

Date	Code	Title	Description
1995-08-17	UW	Conversion of economic patent into exclusive patent
1995-12-21	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
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DD141898A1 (de)	1980-05-28	Mittel zur bekaempfung von phytopathogenen bakterien und pilzen
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