HU190080B - Fungicide preparations of synergetic effect - Google Patents
Fungicide preparations of synergetic effect Download PDFInfo
- Publication number
- HU190080B HU190080B HU831059A HU105983A HU190080B HU 190080 B HU190080 B HU 190080B HU 831059 A HU831059 A HU 831059A HU 105983 A HU105983 A HU 105983A HU 190080 B HU190080 B HU 190080B
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- HU
- Hungary
- Prior art keywords
- formula
- phenyl
- dinitro
- deep
- dncb
- Prior art date
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- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 15
- 230000002195 synergetic effect Effects 0.000 title claims abstract description 9
- 239000000417 fungicide Substances 0.000 title description 19
- 238000002360 preparation method Methods 0.000 title description 8
- 239000000203 mixture Substances 0.000 claims abstract description 41
- 239000004480 active ingredient Substances 0.000 claims abstract description 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 19
- -1 phenyl-phenoxy group Chemical group 0.000 claims abstract description 19
- PCTFIHOVQYYAMH-UHFFFAOYSA-N 3,5-dinitro-4-chlorobenzoic acid Chemical class OC(=O)C1=CC([N+]([O-])=O)=C(Cl)C([N+]([O-])=O)=C1 PCTFIHOVQYYAMH-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- HZGCZRCZOMANHK-UHFFFAOYSA-N pyrimidin-2-ylmethanol Chemical class OCC1=NC=CC=N1 HZGCZRCZOMANHK-UHFFFAOYSA-N 0.000 claims abstract description 3
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- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 3
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- 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
- 235000021028 berry Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 210000005056 cell body Anatomy 0.000 description 1
- 239000010630 cinnamon oil Substances 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000012272 crop production Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- XLIDPNGFCHXNGX-UHFFFAOYSA-N dialuminum;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Si+4] XLIDPNGFCHXNGX-UHFFFAOYSA-N 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 229950004394 ditiocarb Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 230000009422 growth inhibiting effect Effects 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 230000000869 mutational effect Effects 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000007918 pathogenicity Effects 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- OVQGLFMHMWJIBD-UHFFFAOYSA-N propan-2-yl 4-chloro-3,5-dinitrobenzoate Chemical compound CC(C)OC(=O)C1=CC([N+]([O-])=O)=C(Cl)C([N+]([O-])=O)=C1 OVQGLFMHMWJIBD-UHFFFAOYSA-N 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- JYQUHIFYBATCCY-UHFFFAOYSA-N quinalphos Chemical compound C1=CC=CC2=NC(OP(=S)(OCC)OCC)=CN=C21 JYQUHIFYBATCCY-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Chemical class 0.000 description 1
- 229920005989 resin Chemical class 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000006152 selective media Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000011869 shoot development Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- XMUSXQUBKOIUQO-UHFFFAOYSA-J vondocarb Chemical compound [Mn+2].[Zn+2].[S-]C(=S)NCCNC([S-])=S.[S-]C(=S)NCCNC([S-])=S.C1=CC=C2NC(NC(=O)OC)=NC2=C1 XMUSXQUBKOIUQO-UHFFFAOYSA-J 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (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)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (23)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU831059A HU190080B (en) | 1983-03-29 | 1983-03-29 | Fungicide preparations of synergetic effect |
| ZA84839A ZA84839B (en) | 1983-03-29 | 1984-02-03 | Fungicide composition with a synergistic action |
| CH701/84A CH659762A5 (de) | 1983-03-29 | 1984-02-14 | Synergistische fungizide. |
| GB08406179A GB2137094B (en) | 1983-03-29 | 1984-03-09 | Fungicide composition |
| DE3410566A DE3410566A1 (de) | 1983-03-29 | 1984-03-22 | Synergistische fungizide |
| DD84261279A DD216375A5 (de) | 1983-03-29 | 1984-03-27 | Synergistische fungizide mittel |
| IT83339/84A IT1181170B (it) | 1983-03-29 | 1984-03-27 | Composizioni fungicide con azione sinergica |
| PL24688984A PL246889A1 (en) | 1983-03-29 | 1984-03-27 | Fungicide of synergic action |
| FR8404752A FR2543404A1 (fr) | 1983-03-29 | 1984-03-27 | Composition fongicide contenant un derive d'acide 3,5-dinitro-4-chlorobenzoique, a action synergique |
| JP59060519A JPS59205303A (ja) | 1983-03-29 | 1984-03-28 | 殺菌剤組成物 |
| GR74242A GR81466B (enrdf_load_stackoverflow) | 1983-03-29 | 1984-03-28 | |
| CS842303A CS241543B2 (en) | 1983-03-29 | 1984-03-28 | Fungicide |
| BR8401441A BR8401441A (pt) | 1983-03-29 | 1984-03-28 | Composicoes fungicidas sinergicamente ativas e processo para sua preparacao |
| RO84114097A RO88657A (ro) | 1983-03-29 | 1984-03-28 | Compozitie fungicida cu actiune sinergica |
| RO119345A RO92291B (ro) | 1983-03-29 | 1984-03-28 | Compozitie fungicida cu actiune sinergica |
| AU26256/84A AU563166B2 (en) | 1983-03-29 | 1984-03-28 | Synergistic fungicide |
| RO119347A RO92292B (ro) | 1983-03-29 | 1984-03-29 | Compozitie fungicida cu actiune sinergica |
| RO119346A RO92290B (ro) | 1983-03-29 | 1984-03-29 | Compozitie fungicida cu actiune sinergica |
| ES531101A ES8602349A1 (es) | 1983-03-29 | 1984-03-29 | Procedimiento para preparar composiciones fungicidas a base de derivados de acido clorobenzoico |
| CS848732A CS244843B2 (cs) | 1983-03-29 | 1984-11-15 | Synergicky působte! fungícidnf prostředek |
| CS848733A CS247090B2 (cs) | 1983-03-29 | 1984-11-15 | Synergicky půsabící fungicidní prostředek |
| CS848731A CS244842B2 (cs) | 1983-03-29 | 1984-11-15 | Synergicky působící fungicidnf prostředek |
| ES545094A ES545094A0 (es) | 1983-03-29 | 1985-07-11 | Procedimiento para preparar composiciones fungicidas a base de derivados de acido clorobenzoico |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU831059A HU190080B (en) | 1983-03-29 | 1983-03-29 | Fungicide preparations of synergetic effect |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HUT34869A HUT34869A (en) | 1985-05-28 |
| HU190080B true HU190080B (en) | 1986-08-28 |
Family
ID=10952673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU831059A HU190080B (en) | 1983-03-29 | 1983-03-29 | Fungicide preparations of synergetic effect |
Country Status (16)
-
1983
- 1983-03-29 HU HU831059A patent/HU190080B/hu unknown
-
1984
- 1984-02-03 ZA ZA84839A patent/ZA84839B/xx unknown
- 1984-02-14 CH CH701/84A patent/CH659762A5/de not_active IP Right Cessation
- 1984-03-09 GB GB08406179A patent/GB2137094B/en not_active Expired
- 1984-03-22 DE DE3410566A patent/DE3410566A1/de not_active Withdrawn
- 1984-03-27 PL PL24688984A patent/PL246889A1/xx unknown
- 1984-03-27 FR FR8404752A patent/FR2543404A1/fr not_active Withdrawn
- 1984-03-27 IT IT83339/84A patent/IT1181170B/it active
- 1984-03-27 DD DD84261279A patent/DD216375A5/de unknown
- 1984-03-28 RO RO119345A patent/RO92291B/ro unknown
- 1984-03-28 RO RO84114097A patent/RO88657A/ro unknown
- 1984-03-28 JP JP59060519A patent/JPS59205303A/ja active Pending
- 1984-03-28 AU AU26256/84A patent/AU563166B2/en not_active Ceased
- 1984-03-28 BR BR8401441A patent/BR8401441A/pt unknown
- 1984-03-28 CS CS842303A patent/CS241543B2/cs unknown
- 1984-03-28 GR GR74242A patent/GR81466B/el unknown
- 1984-03-29 RO RO119347A patent/RO92292B/ro unknown
- 1984-03-29 RO RO119346A patent/RO92290B/ro unknown
- 1984-03-29 ES ES531101A patent/ES8602349A1/es not_active Expired
-
1985
- 1985-07-11 ES ES545094A patent/ES545094A0/es active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| CS241543B2 (en) | 1986-03-13 |
| ES531101A0 (es) | 1985-12-01 |
| ES8603745A1 (es) | 1986-01-01 |
| RO92291B (ro) | 1987-12-01 |
| GR81466B (enrdf_load_stackoverflow) | 1984-12-11 |
| DE3410566A1 (de) | 1984-10-04 |
| HUT34869A (en) | 1985-05-28 |
| JPS59205303A (ja) | 1984-11-20 |
| IT1181170B (it) | 1987-09-23 |
| FR2543404A1 (fr) | 1984-10-05 |
| AU563166B2 (en) | 1987-07-02 |
| GB2137094B (en) | 1986-06-25 |
| RO88657A (ro) | 1986-02-28 |
| CH659762A5 (de) | 1987-02-27 |
| ZA84839B (en) | 1984-09-26 |
| GB2137094A (en) | 1984-10-03 |
| AU2625684A (en) | 1984-10-04 |
| BR8401441A (pt) | 1984-11-06 |
| CS230384A2 (en) | 1985-07-16 |
| IT8483339A0 (it) | 1984-03-27 |
| DD216375A5 (de) | 1984-12-12 |
| PL246889A1 (en) | 1985-02-13 |
| RO92292B (ro) | 1987-12-01 |
| RO92292A (ro) | 1987-11-30 |
| RO92290B (ro) | 1987-12-01 |
| GB8406179D0 (en) | 1984-04-11 |
| ES8602349A1 (es) | 1985-12-01 |
| RO92290A (ro) | 1987-11-30 |
| ES545094A0 (es) | 1986-01-01 |
| RO92291A (ro) | 1987-11-30 |
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