DD156562A5 - Fungizide mittel - Google Patents
Fungizide mittel Download PDFInfo
- Publication number
- DD156562A5 DD156562A5 DD80227898A DD22789880A DD156562A5 DD 156562 A5 DD156562 A5 DD 156562A5 DD 80227898 A DD80227898 A DD 80227898A DD 22789880 A DD22789880 A DD 22789880A DD 156562 A5 DD156562 A5 DD 156562A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- dione
- pyrrolidine
- sulfonyl
- cyclohexyl
- phenyl
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 17
- 239000004480 active ingredient Substances 0.000 claims abstract description 11
- -1 nitro, hydroxy, carboxy, sulfo Chemical group 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 150000002367 halogens Chemical class 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- 150000003839 salts Chemical class 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 3
- 239000000203 mixture Substances 0.000 claims description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 239000003380 propellant Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- YEUSKMIQJAFXJZ-UHFFFAOYSA-N 3-cyclohexylsulfonyl-1-(3-nitrophenyl)pyrrolidine-2,5-dione Chemical compound [O-][N+](=O)C1=CC=CC(N2C(C(CC2=O)S(=O)(=O)C2CCCCC2)=O)=C1 YEUSKMIQJAFXJZ-UHFFFAOYSA-N 0.000 claims description 2
- WVOFTOZDSKVFSA-UHFFFAOYSA-N 3-cyclohexylsulfonyl-1-(4-methylphenyl)pyrrolidine-2,5-dione Chemical compound C1=CC(C)=CC=C1N1C(=O)C(S(=O)(=O)C2CCCCC2)CC1=O WVOFTOZDSKVFSA-UHFFFAOYSA-N 0.000 claims description 2
- 229920000715 Mucilage Polymers 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 2
- CGHHKCYQBCFICS-UHFFFAOYSA-N 1-(2-chlorophenyl)-3-cyclohexylsulfonylpyrrolidine-2,5-dione Chemical compound ClC1=CC=CC=C1N1C(=O)C(S(=O)(=O)C2CCCCC2)CC1=O CGHHKCYQBCFICS-UHFFFAOYSA-N 0.000 claims 1
- WFZNBGHXOYVLEK-UHFFFAOYSA-N 3-cyclohexylsulfonyl-1-(4-methoxyphenyl)pyrrolidine-2,5-dione Chemical compound C1=CC(OC)=CC=C1N1C(=O)C(S(=O)(=O)C2CCCCC2)CC1=O WFZNBGHXOYVLEK-UHFFFAOYSA-N 0.000 claims 1
- ROPDHOFDWRERBT-UHFFFAOYSA-N 3-cyclopentylsulfonyl-1-(4-methylphenyl)pyrrolidine-2,5-dione Chemical compound C1=CC(C)=CC=C1N1C(=O)C(S(=O)(=O)C2CCCC2)CC1=O ROPDHOFDWRERBT-UHFFFAOYSA-N 0.000 claims 1
- AZRRZGIBBLWSSQ-UHFFFAOYSA-N 4-ethyl-7-phenyl-3,5-diazabicyclo[2.2.2]octane-2,6-dione Chemical compound N1C(=O)C2C(=O)NC1(CC)CC2C1=CC=CC=C1 AZRRZGIBBLWSSQ-UHFFFAOYSA-N 0.000 claims 1
- SSZQOLAZJVCLNT-UHFFFAOYSA-N 5-(3-cyclohexylsulfonyl-2,5-dioxopyrrolidin-1-yl)-2-methylbenzoic acid Chemical compound C1=C(C(O)=O)C(C)=CC=C1N1C(=O)C(S(=O)(=O)C2CCCCC2)CC1=O SSZQOLAZJVCLNT-UHFFFAOYSA-N 0.000 claims 1
- 239000011149 active material Substances 0.000 claims 1
- 239000012764 mineral filler Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
- 208000002193 Pain Diseases 0.000 abstract 1
- 239000000700 radioactive tracer Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 description 10
- 230000002401 inhibitory effect Effects 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 244000005700 microbiome Species 0.000 description 6
- 230000000855 fungicidal effect Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000443 aerosol Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 230000000845 anti-microbial effect Effects 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000002674 ointment Substances 0.000 description 3
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241001337994 Cryptococcus <scale insect> Species 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 241000228143 Penicillium Species 0.000 description 2
- 241001507673 Penicillium digitatum Species 0.000 description 2
- 241000235645 Pichia kudriavzevii Species 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- 235000010633 broth Nutrition 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000008298 dragée Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- DGOUCROQMVJTNG-UHFFFAOYSA-N 1-hexylsulfonylpyrrolidine Chemical compound CCCCCCS(=O)(=O)N1CCCC1 DGOUCROQMVJTNG-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- LGOZKWNMOGHQIY-UHFFFAOYSA-N 3-sulfonylpyrrolidine-2,5-dione Chemical compound O=C1CC(=S(=O)=O)C(=O)N1 LGOZKWNMOGHQIY-UHFFFAOYSA-N 0.000 description 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 description 1
- 241001273451 Ascochyta pisi Species 0.000 description 1
- 241000228197 Aspergillus flavus Species 0.000 description 1
- 241001225321 Aspergillus fumigatus Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000222122 Candida albicans Species 0.000 description 1
- 241000222173 Candida parapsilosis Species 0.000 description 1
- 241000222178 Candida tropicalis Species 0.000 description 1
- 241001480036 Epidermophyton floccosum Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000223194 Fusarium culmorum Species 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241000233732 Fusarium verticillioides Species 0.000 description 1
- 241001661539 Kregervanrija fluxuum Species 0.000 description 1
- 241000235048 Meyerozyma guilliermondii Species 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 241000893976 Nannizzia gypsea Species 0.000 description 1
- 241000233622 Phytophthora infestans Species 0.000 description 1
- 241000235062 Pichia membranifaciens Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 1
- 241001085826 Sporotrichum Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000228448 Taphrina deformans Species 0.000 description 1
- 241001045770 Trichophyton mentagrophytes Species 0.000 description 1
- 241000223229 Trichophyton rubrum Species 0.000 description 1
- 241000222050 Vanrija humicola Species 0.000 description 1
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
- 241001123668 Verticillium dahliae Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940091771 aspergillus fumigatus Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 229940095731 candida albicans Drugs 0.000 description 1
- 229940055022 candida parapsilosis Drugs 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000007765 cera alba Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229940075614 colloidal silicon dioxide Drugs 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000002366 lipolytic effect Effects 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 125000001209 o-nitrophenyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])[N+]([O-])=O 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000563 toxic property Toxicity 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/416—2,5-Pyrrolidine-diones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU79CI1951A HU178455B (en) | 1979-07-17 | 1979-07-17 | Process for producing new 1-substituted-3-cycloalkyl-sulfonyl-pyrrolidine-2,5-dione derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD156562A5 true DD156562A5 (de) | 1982-09-08 |
Family
ID=10994755
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80222669A DD152126A5 (de) | 1979-07-17 | 1980-07-16 | Verfahren zur herstellung von neuen 1-substituierten-3-cycloalkyl-sulfonyl-pyrrolidin-2,5-dion-derivaten |
| DD80227899A DD156572A5 (de) | 1979-07-17 | 1980-07-16 | Verfahren zur herstellung von fungiziden pharmazeutischen praeparaten |
| DD80227898A DD156562A5 (de) | 1979-07-17 | 1980-07-16 | Fungizide mittel |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80222669A DD152126A5 (de) | 1979-07-17 | 1980-07-16 | Verfahren zur herstellung von neuen 1-substituierten-3-cycloalkyl-sulfonyl-pyrrolidin-2,5-dion-derivaten |
| DD80227899A DD156572A5 (de) | 1979-07-17 | 1980-07-16 | Verfahren zur herstellung von fungiziden pharmazeutischen praeparaten |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4364958A (no) |
| JP (1) | JPS5639067A (no) |
| AT (1) | AT374177B (no) |
| AU (1) | AU535388B2 (no) |
| BE (1) | BE884353A (no) |
| CA (1) | CA1135707A (no) |
| CH (1) | CH651296A5 (no) |
| CS (1) | CS226015B2 (no) |
| DD (3) | DD152126A5 (no) |
| DE (1) | DE3026755A1 (no) |
| DK (1) | DK159418C (no) |
| ES (1) | ES8106141A1 (no) |
| FI (1) | FI74948C (no) |
| FR (1) | FR2461700A1 (no) |
| GB (1) | GB2054589B (no) |
| GR (1) | GR69590B (no) |
| HU (1) | HU178455B (no) |
| IL (1) | IL60612A (no) |
| IN (1) | IN151488B (no) |
| IT (1) | IT1141606B (no) |
| LU (1) | LU82636A1 (no) |
| NL (1) | NL8004093A (no) |
| NO (1) | NO154493C (no) |
| PL (4) | PL127256B1 (no) |
| SE (1) | SE450831B (no) |
| SU (5) | SU1007555A3 (no) |
| YU (1) | YU41935B (no) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3637507A1 (de) * | 1986-11-04 | 1988-05-05 | Bayer Ag | Neues verfahren zur herstellung von teilweise neuen 3-sulfenylmaleinimiden und ihre verwendung |
| DE3719764A1 (de) * | 1987-06-13 | 1988-12-22 | Bayer Ag | Ionenaustauscherharze beladen mit chinoloncarbonsaeurederivaten, ihre herstellung und verwendung |
| AU9318498A (en) * | 1997-09-18 | 1999-04-05 | Pierce Chemical Company | Sulfo-n-hydroxy succinimide and method of preparation |
| US5892057A (en) | 1997-09-18 | 1999-04-06 | Pierce Chemical Company | Preparation of sulfo-N-hydroxysuccinimide salts |
| EP1132379A4 (en) | 1998-09-21 | 2005-02-16 | Takeda Pharmaceutical | THIOL DERIVATIVES, METHOD FOR THEIR PREPARATION AND THEIR USE |
| HU226421B1 (en) * | 1998-11-09 | 2008-12-29 | Sanofi Aventis | Process for racemizing optically active 2-(2-chlorophenyl)-2-(2-(2-thienyl)-ethylamino)-acetamides |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538114A (en) * | 1966-08-12 | 1970-11-03 | Basf Ag | N-(substituted-phenyl)-succinimides |
| GB1319772A (en) * | 1969-06-18 | 1973-06-06 | Geistlich Soehne Ag | Succinimides |
| CA950916A (en) * | 1970-09-04 | 1974-07-09 | Shigehiro Ooba | N-phenylsuccinimide derivatives |
| US3804856A (en) * | 1970-09-04 | 1974-04-16 | Sumitomo Chemical Co | N-phenylsuccinimides |
| JPS4833025A (no) * | 1971-08-28 | 1973-05-07 | ||
| JPS5412904B2 (no) * | 1973-05-18 | 1979-05-26 |
-
1979
- 1979-07-17 HU HU79CI1951A patent/HU178455B/hu not_active IP Right Cessation
-
1980
- 1980-07-15 DE DE19803026755 patent/DE3026755A1/de active Granted
- 1980-07-16 DK DK307580A patent/DK159418C/da not_active IP Right Cessation
- 1980-07-16 CH CH5466/80A patent/CH651296A5/de not_active IP Right Cessation
- 1980-07-16 LU LU82636A patent/LU82636A1/de unknown
- 1980-07-16 FR FR8015678A patent/FR2461700A1/fr active Granted
- 1980-07-16 PL PL1980231601A patent/PL127256B1/pl unknown
- 1980-07-16 NL NL8004093A patent/NL8004093A/nl not_active Application Discontinuation
- 1980-07-16 YU YU1830/80A patent/YU41935B/xx unknown
- 1980-07-16 DD DD80222669A patent/DD152126A5/de not_active IP Right Cessation
- 1980-07-16 PL PL1980225695A patent/PL127097B1/pl unknown
- 1980-07-16 AT AT0368480A patent/AT374177B/de not_active IP Right Cessation
- 1980-07-16 PL PL1980231600A patent/PL127257B1/pl unknown
- 1980-07-16 PL PL1980231602A patent/PL127255B1/pl unknown
- 1980-07-16 IL IL60612A patent/IL60612A/xx unknown
- 1980-07-16 SE SE8005208A patent/SE450831B/sv not_active IP Right Cessation
- 1980-07-16 GR GR62474A patent/GR69590B/el unknown
- 1980-07-16 GB GB8023219A patent/GB2054589B/en not_active Expired
- 1980-07-16 US US06/169,439 patent/US4364958A/en not_active Expired - Lifetime
- 1980-07-16 DD DD80227899A patent/DD156572A5/de not_active IP Right Cessation
- 1980-07-16 IN IN814/CAL/80A patent/IN151488B/en unknown
- 1980-07-16 CS CS805047A patent/CS226015B2/cs unknown
- 1980-07-16 DD DD80227898A patent/DD156562A5/de not_active IP Right Cessation
- 1980-07-16 NO NO802134A patent/NO154493C/no unknown
- 1980-07-16 SU SU802953400A patent/SU1007555A3/ru active
- 1980-07-16 SU SU802950855A patent/SU1373704A1/ru active
- 1980-07-17 BE BE0/201435A patent/BE884353A/fr not_active IP Right Cessation
- 1980-07-17 ES ES494310A patent/ES8106141A1/es not_active Expired
- 1980-07-17 CA CA000356425A patent/CA1135707A/en not_active Expired
- 1980-07-17 IT IT68139/80A patent/IT1141606B/it active
- 1980-07-17 AU AU60480/80A patent/AU535388B2/en not_active Ceased
- 1980-07-17 FI FI802268A patent/FI74948C/fi not_active IP Right Cessation
- 1980-07-17 JP JP9813780A patent/JPS5639067A/ja active Granted
-
1981
- 1981-08-12 SU SU813317073A patent/SU1156594A3/ru active
- 1981-08-12 SU SU813322502A patent/SU1165231A3/ru active
- 1981-08-12 SU SU813315400A patent/SU1192616A3/ru active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2037610C3 (no) | ||
| CA2153681C (en) | Topical ketoconazole compositions | |
| US20070259839A1 (en) | Triterpene quaternary salts as biologically active surfactants | |
| DD156562A5 (de) | Fungizide mittel | |
| EP0004898B1 (de) | Feste stabile pharmazeutische Zusammensetzung auf Basis von einem 1,3-Diester des 17-alpha-Ethinyl-7-alpha-methyl-1,3,5(10)-östratrien-1,3,17-beta-triols | |
| EP0036153B1 (de) | 1,1-Diphenyl-2-(1,2,4-triazol-1-yl)-äthan-1-ole als Antimykotika | |
| DE2053080C3 (de) | N-substituierte Imidazole und ihre Verwendung als Arzneimittel | |
| AT375921B (de) | Verfahren zur herstellung von neuen 1-substituierten-3-cycloalkylsulfonyl-pyrrolidi -2,5-dion-derivaten sowie von deren salzen | |
| EP0043548B1 (de) | Salz aus Furosemid oder Piretanid als Säurekomponente und Penbutolol als Basenkomponente sowie Arzneimittel, das beide Komponenten enthält | |
| AT375920B (de) | Verfahren zur herstellung von neuen 1-substituierten-3-cycloalkylsulfonyl-pyrrolidi -2,5-dion-derivaten sowie von deren salzen | |
| AT375922B (de) | Verfahren zur herstellung von neuen 1-substituierten-3-cycloalkylsulfonyl-pyrrolidi -2,5-dion-derivaten sowie von deren salzen | |
| US4305953A (en) | Synergistic fungicidal compositions | |
| GB2208598A (en) | Antimicrobial preparations for external use | |
| EP0156508B1 (en) | Antifungal aerosol solution | |
| US3072525A (en) | Fungicidal composition comprising a salicylate and a pyrazole | |
| EP0087105B1 (de) | Fungizid wirksame Benzhydrolderivate | |
| DE2044621B2 (de) | 33-D^phenyl-3-imidazol-l-yl-propine, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Arzneimittel | |
| DE2050072C3 (de) | Aluminium-tri-3-acetyl-18 betaglycyrrthetinat, Verfahren zu seiner Herstellung und dieses enthaltende pharmazeutische Zubereitungen | |
| DE2715775A1 (de) | Neue d-homosteroide | |
| DE1212777B (de) | Fungitoxische Mittel | |
| DE1911710B2 (de) | Neue Ester der a-Hydroperoxy- bis (p-chlor-oder brom-phenyl) essigsäure, Verfahren zu deren Herstellung und ihre Verwendung in Akariziden | |
| DE2104017A1 (de) | Bakterizid und fungizid wirkende, 1-Hydroxy 2 pyndinthion-zinn (IV) salz enthaltende Arzneipraparate | |
| DE2322394A1 (de) | As-triazino eckige klammer auf 5,6-c eckige klammer zu chinolin beziehungsweise dessen derivate und ihre salze sowie ihre verwendung und verfahren zur herstellung derselben | |
| DE2204416A1 (de) | Benzimidazole | |
| CS226050B2 (cs) | Způsob výroby derivátů 3-cykloalkylsulfonytpyrrolidin-2,5-dionu, substituovaného v poloze 1 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |