PH27027A - Composition for controlling parasites in productive livestock - Google Patents
Composition for controlling parasites in productive livestock Download PDFInfo
- Publication number
- PH27027A PH27027A PH36667A PH36667A PH27027A PH 27027 A PH27027 A PH 27027A PH 36667 A PH36667 A PH 36667A PH 36667 A PH36667 A PH 36667A PH 27027 A PH27027 A PH 27027A
- Authority
- PH
- Philippines
- Prior art keywords
- group
- subst
- tuted
- sting
- halogen
- Prior art date
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- 244000045947 parasite Species 0.000 title abstract description 11
- 244000144972 livestock Species 0.000 title abstract description 4
- 239000000203 mixture Substances 0.000 title description 38
- -1 hydroxy, benzyloxy Chemical group 0.000 claims abstract description 116
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- 229910052736 halogen Inorganic materials 0.000 claims abstract description 67
- 150000002367 halogens Chemical class 0.000 claims abstract description 62
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 61
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 57
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 55
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 49
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 49
- 125000001424 substituent group Chemical group 0.000 claims abstract description 49
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 42
- 239000001257 hydrogen Substances 0.000 claims abstract description 34
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- 241000607479 Yersinia pestis Species 0.000 claims abstract description 8
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- 238000001640 fractional crystallisation Methods 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 239000003120 macrolide antibiotic agent Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 235000012439 matzos Nutrition 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical class COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical class O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 1
- BWCRYQGQPDBOAU-WZBVPYLGSA-N milbemycin D Chemical compound C1C[C@H](C)[C@@H](C(C)C)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 BWCRYQGQPDBOAU-WZBVPYLGSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 230000001459 mortal effect Effects 0.000 description 1
- LHMUZCNPQGLQPE-UHFFFAOYSA-N n-pyrrolidin-1-ylpyridin-4-amine Chemical compound C1CCCN1NC1=CC=NC=C1 LHMUZCNPQGLQPE-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000006146 oximation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 229930004008 p-menthane Natural products 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 206010033675 panniculitis Diseases 0.000 description 1
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- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical class [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
- 125000006187 phenyl benzyl group Chemical group 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
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- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- 101150069548 ppan gene Proteins 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 102220102088 rs878853592 Human genes 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 210000004304 subcutaneous tissue Anatomy 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 150000008334 thiadiazines Chemical class 0.000 description 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 description 1
- 235000019157 thiamine Nutrition 0.000 description 1
- 229960003495 thiamine Drugs 0.000 description 1
- 239000011721 thiamine Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/22—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/01—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing oxygen
-
- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Molecular Biology (AREA)
- Veterinary Medicine (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH111787 | 1987-03-24 | ||
CH487887 | 1987-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
PH27027A true PH27027A (en) | 1993-02-01 |
Family
ID=25686704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH36667A PH27027A (en) | 1987-03-24 | 1988-03-21 | Composition for controlling parasites in productive livestock |
Country Status (18)
Country | Link |
---|---|
US (2) | US4871719A (fr) |
EP (1) | EP0284563B1 (fr) |
JP (1) | JP2683583B2 (fr) |
KR (1) | KR960004533B1 (fr) |
AT (1) | ATE107307T1 (fr) |
AU (1) | AU614509B2 (fr) |
CA (1) | CA1300609C (fr) |
DE (1) | DE3850160D1 (fr) |
DK (1) | DK167682B1 (fr) |
ES (1) | ES2054862T3 (fr) |
FI (1) | FI92831C (fr) |
HU (1) | HUT46322A (fr) |
IE (1) | IE63143B1 (fr) |
IL (1) | IL85810A (fr) |
NZ (1) | NZ223970A (fr) |
PH (1) | PH27027A (fr) |
PT (1) | PT87033B (fr) |
ZW (1) | ZW2788A1 (fr) |
Families Citing this family (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4906619A (en) * | 1988-07-22 | 1990-03-06 | Merck & Co., Inc. | Alkyl avermectin derivatives |
NZ232422A (en) * | 1989-02-16 | 1992-11-25 | Merck & Co Inc | 13-ketal milbemycin derivatives and parasiticides |
US6001822A (en) * | 1989-04-11 | 1999-12-14 | Pfizer Inc. | Antiparasitic formulations |
US6514951B1 (en) | 1989-12-15 | 2003-02-04 | American Cyanamid Company | Pour-on formulations effective for the control of internal and external parasites of homothermic animals |
JP3804072B2 (ja) * | 1991-08-07 | 2006-08-02 | 日産化学工業株式会社 | 水性懸濁状農薬製剤 |
NZ334028A (en) * | 1996-08-05 | 2000-11-24 | Bayer Ag | 1-heterocyclic substituted 2- and 2,5-substituted phenylketoenol derivatives |
KR970014851A (ko) * | 1997-01-03 | 1997-04-28 | 김동규 | 음식물 쓰레기의 건조발효방법 및 그 건조발효장치 |
BR9815352A (pt) * | 1997-12-03 | 2000-10-17 | Merck & Co Inc | "formulação injetável de longa ação, e, processos para a prevenção ou tratamento de infestação parasìtica em um hospedeiro em necessidade dele, para tratamento ou prevenção de infestação por insetos por um perìodo prolongado de tempo em um hospedeiro em necessidade dele, para promover crescimento em animais, e para tratar inflamação, dor ou febre por um perìodo estendido de tempo em um hospedeiro em necessidade. " |
ES2359973T3 (es) * | 1998-03-19 | 2011-05-30 | MERCK SHARP & DOHME CORP. | Composiciones poliméricas líquidas para la liberación controlada de sustancias bioactivas. |
US7229447B1 (en) | 1998-08-25 | 2007-06-12 | Advanced Photodynamics Technologies, Inc. | Photodynamic therapy utilizing a solution of photosensitizing compound and surfactant |
US6787342B2 (en) | 2000-02-16 | 2004-09-07 | Merial Limited | Paste formulations |
CA2401624C (fr) | 2000-02-26 | 2011-08-16 | Merrill A. Biel | Eradication photodynamique d'organisme acellulaire et cellulaire, a l'aide d'un materiau photosensible et d'un tensioactif |
US7001889B2 (en) * | 2002-06-21 | 2006-02-21 | Merial Limited | Anthelmintic oral homogeneous veterinary pastes |
US20060205681A1 (en) * | 2002-06-21 | 2006-09-14 | Maryam Moaddeb | Homogenous paste formulations |
US20040077703A1 (en) * | 2002-10-02 | 2004-04-22 | Soll Mark D. | Nodulisporic acid derivative spot-on formulations for combating parasites |
US7531186B2 (en) | 2003-12-17 | 2009-05-12 | Merial Limited | Topical formulations comprising 1-N-arylpyrazole derivatives and amitraz |
US8362086B2 (en) | 2005-08-19 | 2013-01-29 | Merial Limited | Long acting injectable formulations |
US20080027011A1 (en) * | 2005-12-20 | 2008-01-31 | Hassan Nached | Homogeneous paste and gel formulations |
NZ573758A (en) | 2006-07-05 | 2012-01-12 | Aventis Agriculture | 1-Phenyl-3-cyano-pyrazole derivatives and pesticidal formulations containing them |
EP2155699B9 (fr) | 2007-05-15 | 2016-09-14 | Merial, Inc. | Composés d'aryloazol-2-yl-cyanoéthylamino, leur procédé de fabrication et leur procédé d'utilisation |
NZ585499A (en) | 2007-11-26 | 2011-12-22 | Merial Ltd | Solvent systems for pour-on formulations for combating parasites |
NZ590141A (en) * | 2008-06-24 | 2012-05-25 | Merial Ltd | Anthelminthic formulations including castor oil and another vegetable oil |
MX2011005011A (es) | 2008-11-14 | 2011-07-29 | Merial Ltd | Compuestos de arilazol-2-il-cianoetilamino enantiomericamente enriquecidos, metodo de elaboracion y de uso de los mismos. |
US9173728B2 (en) | 2008-11-19 | 2015-11-03 | Merial Inc. | Multi-cavity container having offset indentures for dispensing fluids |
JP5755143B2 (ja) * | 2008-11-19 | 2015-07-29 | メリアル リミテッド | アリールピラゾールおよび/またはホルムアミジンを含む組成物、それらの方法ならびに使用 |
NZ593184A (en) | 2008-12-04 | 2012-11-30 | Merial Ltd | Dimeric avermectin and milbemycin derivatives |
AU2010278948B2 (en) | 2009-07-30 | 2015-04-23 | Boehringer Ingelheim Animal Health USA Inc. | Insecticidal 4-Amino-thieno(2,3-d)-pyrimidine compounds and methods of their use |
ES2546100T3 (es) | 2009-12-04 | 2015-09-18 | Merial, Inc. | Compuestos pesticidas bis-organosulfurados |
EA021522B9 (ru) | 2009-12-17 | 2016-08-31 | Мериал Лимитед | Противопаразитарные дигидроазоловые соединения и содержащие их композиции |
WO2011075592A1 (fr) | 2009-12-17 | 2011-06-23 | Merial Limited | Compositions contenant des composés de lactone macrocyclique et des spiro-dioxépino-indoles |
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-
1988
- 1988-03-16 US US07/168,766 patent/US4871719A/en not_active Expired - Fee Related
- 1988-03-18 ES ES88810175T patent/ES2054862T3/es not_active Expired - Lifetime
- 1988-03-18 AT AT88810175T patent/ATE107307T1/de not_active IP Right Cessation
- 1988-03-18 EP EP88810175A patent/EP0284563B1/fr not_active Expired - Lifetime
- 1988-03-18 DE DE3850160T patent/DE3850160D1/de not_active Expired - Fee Related
- 1988-03-21 PH PH36667A patent/PH27027A/en unknown
- 1988-03-21 FI FI881328A patent/FI92831C/fi not_active IP Right Cessation
- 1988-03-22 NZ NZ223970A patent/NZ223970A/xx unknown
- 1988-03-22 PT PT87033A patent/PT87033B/pt active IP Right Grant
- 1988-03-22 CA CA000562065A patent/CA1300609C/fr not_active Expired - Lifetime
- 1988-03-22 ZW ZW27/88A patent/ZW2788A1/xx unknown
- 1988-03-22 IL IL85810A patent/IL85810A/xx not_active IP Right Cessation
- 1988-03-23 DK DK157188A patent/DK167682B1/da not_active IP Right Cessation
- 1988-03-23 AU AU13502/88A patent/AU614509B2/en not_active Ceased
- 1988-03-23 IE IE87188A patent/IE63143B1/en not_active IP Right Cessation
- 1988-03-23 HU HU881498A patent/HUT46322A/hu unknown
- 1988-03-23 JP JP63069204A patent/JP2683583B2/ja not_active Expired - Lifetime
- 1988-03-24 KR KR88003168A patent/KR960004533B1/ko not_active IP Right Cessation
-
1989
- 1989-07-13 US US07/380,844 patent/US4973711A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ATE107307T1 (de) | 1994-07-15 |
DE3850160D1 (de) | 1994-07-21 |
CA1300609C (fr) | 1992-05-12 |
PT87033A (pt) | 1988-04-01 |
FI92831B (fi) | 1994-09-30 |
DK167682B1 (da) | 1993-12-06 |
EP0284563A3 (en) | 1989-10-25 |
ES2054862T3 (es) | 1994-08-16 |
ZW2788A1 (en) | 1988-11-16 |
DK157188A (da) | 1988-09-25 |
KR880011169A (ko) | 1988-10-27 |
FI881328A (fi) | 1988-09-25 |
IE63143B1 (en) | 1995-03-22 |
FI92831C (fi) | 1995-01-10 |
US4871719A (en) | 1989-10-03 |
JPS63255286A (ja) | 1988-10-21 |
EP0284563B1 (fr) | 1994-06-15 |
PT87033B (pt) | 1992-06-30 |
NZ223970A (en) | 1990-05-28 |
DK157188D0 (da) | 1988-03-23 |
AU614509B2 (en) | 1991-09-05 |
AU1350288A (en) | 1988-09-22 |
HUT46322A (en) | 1988-10-28 |
JP2683583B2 (ja) | 1997-12-03 |
US4973711A (en) | 1990-11-27 |
IE880871L (en) | 1988-09-24 |
IL85810A0 (en) | 1988-09-30 |
KR960004533B1 (en) | 1996-04-06 |
FI881328A0 (fi) | 1988-03-21 |
IL85810A (en) | 1992-06-21 |
EP0284563A2 (fr) | 1988-09-28 |
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