DK167136B1 - Fremgangsmaade til foroegelse af fedtindholdet i colostrum eller maelk hos maelkegivende soeer - Google Patents

Fremgangsmaade til foroegelse af fedtindholdet i colostrum eller maelk hos maelkegivende soeer Download PDF

Info

Publication number: DK167136B1
Authority: DK; Denmark
Prior art keywords: hydrogen; approx; hydroxy; day; compound
Prior art date: 1985-11-27

Application number

DK562086A

Other languages

Danish (da)

English (en)

Other versions

DK562086A (da

DK562086D0 (da

Inventor

David Bennett Anderson

Edward Lee Veenhuizen

Original Assignee

Lilly Co Eli

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.)

1985-11-27

Filing date

1986-11-24

Publication date

1993-09-06

1986-11-24 Application filed by Lilly Co Eli filed Critical Lilly Co Eli

1986-11-24 Publication of DK562086D0 publication Critical patent/DK562086D0/da

1987-05-28 Publication of DK562086A publication Critical patent/DK562086A/da

1993-09-06 Application granted granted Critical

1993-09-06 Publication of DK167136B1 publication Critical patent/DK167136B1/da

Links

235000013336 milk Nutrition 0.000 title claims abstract description 14
210000004080 milk Anatomy 0.000 title claims abstract description 14
239000008267 milk Substances 0.000 title claims abstract description 14
238000000034 method Methods 0.000 title claims description 21
235000021277 colostrum Nutrition 0.000 title claims description 8
210000003022 colostrum Anatomy 0.000 title claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
239000001257 hydrogen Substances 0.000 claims abstract description 30
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 14
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 10
150000002431 hydrogen Chemical group 0.000 claims abstract description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 8
150000003839 salts Chemical class 0.000 claims abstract description 8
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 7
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 5
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 4
-1 hydroxy, methoxy Chemical group 0.000 claims abstract description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 58
239000003814 drug Substances 0.000 claims description 3
229940079593 drug Drugs 0.000 claims description 2
YJQZYXCXBBCEAQ-UHFFFAOYSA-N ractopamine Chemical compound C=1C=C(O)C=CC=1C(O)CNC(C)CCC1=CC=C(O)C=C1 YJQZYXCXBBCEAQ-UHFFFAOYSA-N 0.000 claims description 2
YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 abstract description 4
239000002253 acid Substances 0.000 abstract description 2
ULSIYEODSMZIPX-UHFFFAOYSA-N phenylethanolamine Chemical compound NCC(O)C1=CC=CC=C1 ULSIYEODSMZIPX-UHFFFAOYSA-N 0.000 abstract 1
229950006768 phenylethanolamine Drugs 0.000 abstract 1
241001465754 Metazoa Species 0.000 description 23
239000003925 fat Substances 0.000 description 7
238000011282 treatment Methods 0.000 description 7
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
235000021243 milk fat Nutrition 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000000203 mixture Substances 0.000 description 5
238000007920 subcutaneous administration Methods 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
241000282887 Suidae Species 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000008280 blood Substances 0.000 description 3
210000004369 blood Anatomy 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
235000021588 free fatty acids Nutrition 0.000 description 3
238000002347 injection Methods 0.000 description 3
239000007924 injection Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
235000005911 diet Nutrition 0.000 description 2
230000037213 diet Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
235000020997 lean meat Nutrition 0.000 description 2
125000003884 phenylalkyl group Chemical group 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000010254 subcutaneous injection Methods 0.000 description 2
239000007929 subcutaneous injection Substances 0.000 description 2
230000004083 survival effect Effects 0.000 description 2
ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 description 1
WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 1
RXHRQYABEKOWNT-UHFFFAOYSA-N 2-[4-(4-fluorophenyl)butan-2-ylamino]-1-phenylethanol Chemical compound C=1C=CC=CC=1C(O)CNC(C)CCC1=CC=C(F)C=C1 RXHRQYABEKOWNT-UHFFFAOYSA-N 0.000 description 1
BWGRYTOAZRVKQF-UHFFFAOYSA-N 2-[4-(4-nitrophenyl)butan-2-ylamino]-1-phenylethanol Chemical compound C=1C=CC=CC=1C(O)CNC(C)CCC1=CC=C([N+]([O-])=O)C=C1 BWGRYTOAZRVKQF-UHFFFAOYSA-N 0.000 description 1
QRFCIBCKFBRQQR-UHFFFAOYSA-N 2-[[4-(4-fluorophenyl)-2-methylbutan-2-yl]amino]-1-phenylethanol Chemical compound C=1C=CC=CC=1C(O)CNC(C)(C)CCC1=CC=C(F)C=C1 QRFCIBCKFBRQQR-UHFFFAOYSA-N 0.000 description 1
BUXRLJCGHZZYNE-UHFFFAOYSA-N 2-amino-5-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzonitrile Chemical compound CC(C)NCC(O)C1=CC=C(N)C(C#N)=C1 BUXRLJCGHZZYNE-UHFFFAOYSA-N 0.000 description 1
UPPASVLPIIHXCA-UHFFFAOYSA-N 2-amino-5-[2-(ethylamino)-1-hydroxyethyl]benzonitrile Chemical compound CCNCC(O)C1=CC=C(N)C(C#N)=C1 UPPASVLPIIHXCA-UHFFFAOYSA-N 0.000 description 1
YKKQAXQGZIBJFS-UHFFFAOYSA-N 2-amino-5-[2-(tert-butylamino)-1-hydroxyethyl]benzonitrile Chemical compound CC(C)(C)NCC(O)C1=CC=C(N)C(C#N)=C1 YKKQAXQGZIBJFS-UHFFFAOYSA-N 0.000 description 1
SNHUXKRSXFKHBQ-UHFFFAOYSA-N 3-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzonitrile Chemical compound CC(C)NCC(O)C1=CC=CC(C#N)=C1 SNHUXKRSXFKHBQ-UHFFFAOYSA-N 0.000 description 1
ACRSTTREFKXCSS-UHFFFAOYSA-N 4-[1-hydroxy-2-[(2-methyl-4-phenylbutan-2-yl)amino]ethyl]phenol Chemical compound C=1C=C(O)C=CC=1C(O)CNC(C)(C)CCC1=CC=CC=C1 ACRSTTREFKXCSS-UHFFFAOYSA-N 0.000 description 1
SQGSWPDYJPKLHU-UHFFFAOYSA-N 4-[3-[(2-hydroxy-2-phenylethyl)amino]butyl]benzamide Chemical compound C=1C=CC=CC=1C(O)CNC(C)CCC1=CC=C(C(N)=O)C=C1 SQGSWPDYJPKLHU-UHFFFAOYSA-N 0.000 description 1
GYXKVYVRPDGCNC-UHFFFAOYSA-N 4-[3-[[2-hydroxy-2-(4-hydroxyphenyl)ethyl]amino]-3-methylbutyl]phenol Chemical compound C=1C=C(O)C=CC=1C(O)CNC(C)(C)CCC1=CC=C(O)C=C1 GYXKVYVRPDGCNC-UHFFFAOYSA-N 0.000 description 1
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 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
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
235000019750 Crude protein Nutrition 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
229920002527 Glycogen Polymers 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical class CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
208000008589 Obesity Diseases 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
XNOPRXBHLZRZKH-UHFFFAOYSA-N Oxytocin Natural products N1C(=O)C(N)CSSCC(C(=O)N2C(CCC2)C(=O)NC(CC(C)C)C(=O)NCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C(C(C)CC)NC(=O)C1CC1=CC=C(O)C=C1 XNOPRXBHLZRZKH-UHFFFAOYSA-N 0.000 description 1
101800000989 Oxytocin Proteins 0.000 description 1
102100031951 Oxytocin-neurophysin 1 Human genes 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000700159 Rattus Species 0.000 description 1
235000019764 Soybean Meal Nutrition 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
238000003556 assay Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
239000004927 clay Substances 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000008021 deposition Effects 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
239000003651 drinking water Substances 0.000 description 1
235000020188 drinking water Nutrition 0.000 description 1
239000000428 dust Substances 0.000 description 1
150000004675 formic acid derivatives Chemical class 0.000 description 1
229940096919 glycogen Drugs 0.000 description 1
210000004209 hair Anatomy 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000010903 husk Substances 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
239000007972 injectable composition Substances 0.000 description 1
238000010255 intramuscular injection Methods 0.000 description 1
239000007927 intramuscular injection Substances 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
150000003893 lactate salts Chemical class 0.000 description 1
230000006651 lactation Effects 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
210000005075 mammary gland Anatomy 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
150000005830 nonesterified fatty acids Chemical class 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
235000020824 obesity Nutrition 0.000 description 1
XNOPRXBHLZRZKH-DSZYJQQASA-N oxytocin Chemical compound C([C@H]1C(=O)N[C@H](C(N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@H](N)C(=O)N1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC(C)C)C(=O)NCC(N)=O)=O)[C@@H](C)CC)C1=CC=C(O)C=C1 XNOPRXBHLZRZKH-DSZYJQQASA-N 0.000 description 1
229960001723 oxytocin Drugs 0.000 description 1
239000008177 pharmaceutical agent Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
NIXKBAZVOQAHGC-UHFFFAOYSA-N phenylmethanesulfonic acid Chemical class OS(=O)(=O)CC1=CC=CC=C1 NIXKBAZVOQAHGC-UHFFFAOYSA-N 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
238000002464 physical blending Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000006308 propyl amino group Chemical group 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000004455 soybean meal Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002459 sustained effect Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000032258 transport Effects 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000005303 weighing Methods 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/111—Aromatic compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/14—Drugs for genital or sexual disorders; Contraceptives for lactation disorders, e.g. galactorrhoea

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Polymers & Plastics (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Zoology (AREA)
Animal Husbandry (AREA)
Pregnancy & Childbirth (AREA)
Bioinformatics & Cheminformatics (AREA)
Endocrinology (AREA)
Reproductive Health (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Organic Chemistry (AREA)
Gynecology & Obstetrics (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Dairy Products (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Feed For Specific Animals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Fodder In General (AREA)
Fats And Perfumes (AREA)
Edible Oils And Fats (AREA)
Coloring Foods And Improving Nutritive Qualities (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

DK562086A 1985-11-27 1986-11-24 Fremgangsmaade til foroegelse af fedtindholdet i colostrum eller maelk hos maelkegivende soeer DK167136B1 (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US80254185A	1985-11-27	1985-11-27
US80254185		1985-11-27

Publications (3)

Publication Number	Publication Date
DK562086D0 DK562086D0 (da)	1986-11-24
DK562086A DK562086A (da)	1987-05-28
DK167136B1 true DK167136B1 (da)	1993-09-06

Family

ID=25183984

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK562086A DK167136B1 (da)	1985-11-27	1986-11-24	Fremgangsmaade til foroegelse af fedtindholdet i colostrum eller maelk hos maelkegivende soeer

Country Status (18)

Country	Link
US (1)	US4904662A (fr)
EP (1)	EP0225165B1 (fr)
JP (1)	JPH06104037B2 (fr)
CN (1)	CN1021630C (fr)
AT (1)	ATE79726T1 (fr)
AU (1)	AU591730B2 (fr)
CA (1)	CA1298785C (fr)
DE (1)	DE3686559T2 (fr)
DK (1)	DK167136B1 (fr)
ES (1)	ES2033685T3 (fr)
GR (1)	GR3005962T3 (fr)
HU (1)	HU203031B (fr)
IE (1)	IE58461B1 (fr)
IL (1)	IL80748A (fr)
NZ (1)	NZ218398A (fr)
PH (1)	PH23714A (fr)
RU (1)	RU1802689C (fr)
ZA (1)	ZA868891B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5216029A (en) *	1991-11-26	1993-06-01	Eli Lilly And Company	Fish production
US5308870A (en) *	1992-12-21	1994-05-03	Eli Lilly And Company	Ractopamine for pre-and peripubertal female bovidae
US8519008B2 (en)	2003-01-22	2013-08-27	Purina Animal Nutrition Llc	Method and composition for improving the health of young monogastric mammals
US7165508B2 (en) *	2004-04-21	2007-01-23	Bryant Robert E	Hog farrowing system for use in a cold environment and method of use
FR2874156B1 (fr) *	2004-08-13	2007-04-06	Univ Rennes 1 Etablissement Pu	Complement alimentaire pour animaux d'elevage et procede de mise en oeuvre de celui-ci
JP6886411B2 (ja) *	2016-01-29	2021-06-16	サトーホールディングス株式会社	スタッカ、および、スタッカの制御方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3994974A (en) *	1972-02-05	1976-11-30	Yamanouchi Pharmaceutical Co., Ltd.	α-Aminomethylbenzyl alcohol derivatives
US4391826A (en) *	1978-07-03	1983-07-05	Eli Lilly And Company	Phenethanolamines, compositions containing the same, and method for effecting weight control
JPS5710864A (en) *	1980-06-23	1982-01-20	Sharp Corp	Cash register
US4407819A (en) *	1980-08-25	1983-10-04	American Cyanamid Company	Phenylethanolamine derivatives and acid addition salts thereof for the depression of fat deposition in warm blooded animals
US4432995A (en) *	1980-12-22	1984-02-21	American Cyanamid Company	5-[2-(Ethylamino)-1-hydroxylethyl] anthranilonitrile and the use thereof in meat producing animals
EP0117647B1 (fr) *	1983-01-31	1988-08-17	Eli Lilly And Company	Phénéthanol-amines
ES8800842A1 (es) *	1985-03-01	1987-12-01	Beecham Group Plc	Un procedimiento para preparar una formulacion veterinariamente aceptable de ariletanolaminas promotora del crecimiento.
US4614746A (en) *	1985-03-21	1986-09-30	American Cyanamid Company	5-fluorobenzonitrile derivatives for increasing the lean meat to fat ratio and/or enhancing the growth rate of warm-blooded animals
AU592557B2 (en) *	1985-04-16	1990-01-18	F. Hoffmann-La Roche Ag	Phenethanolamine derivatives

1986
- 1986-11-24 IL IL80748A patent/IL80748A/xx not_active IP Right Cessation
- 1986-11-24 ZA ZA868891A patent/ZA868891B/xx unknown
- 1986-11-24 CA CA000523611A patent/CA1298785C/fr not_active Expired - Lifetime
- 1986-11-24 DK DK562086A patent/DK167136B1/da not_active IP Right Cessation
- 1986-11-25 RU SU864028596A patent/RU1802689C/ru active
- 1986-11-25 NZ NZ218398A patent/NZ218398A/xx unknown
- 1986-11-26 AU AU65723/86A patent/AU591730B2/en not_active Expired
- 1986-11-26 HU HU864903A patent/HU203031B/hu not_active IP Right Cessation
- 1986-11-26 AT AT86309206T patent/ATE79726T1/de not_active IP Right Cessation
- 1986-11-26 IE IE311786A patent/IE58461B1/en not_active IP Right Cessation
- 1986-11-26 DE DE8686309206T patent/DE3686559T2/de not_active Expired - Fee Related
- 1986-11-26 EP EP86309206A patent/EP0225165B1/fr not_active Expired - Lifetime
- 1986-11-26 ES ES198686309206T patent/ES2033685T3/es not_active Expired - Lifetime
- 1986-11-27 JP JP61284101A patent/JPH06104037B2/ja not_active Expired - Fee Related
- 1986-11-27 PH PH34530A patent/PH23714A/en unknown
- 1986-11-27 CN CN86108047A patent/CN1021630C/zh not_active Expired - Lifetime
1987
- 1987-03-23 US US07/029,024 patent/US4904662A/en not_active Expired - Lifetime
1992
- 1992-10-12 GR GR920402285T patent/GR3005962T3/el unknown

Also Published As

Publication number	Publication date
IE863117L (en)	1987-05-27
IL80748A (en)	1990-11-29
DK562086A (da)	1987-05-28
HU203031B (en)	1991-05-28
NZ218398A (en)	1989-04-26
ES2033685T3 (es)	1993-04-01
IL80748A0 (en)	1987-02-27
RU1802689C (ru)	1993-03-15
AU6572386A (en)	1987-06-04
US4904662A (en)	1990-02-27
HUT41621A (en)	1987-05-28
JPH06104037B2 (ja)	1994-12-21
CN1021630C (zh)	1993-07-21
PH23714A (en)	1989-09-27
ZA868891B (en)	1988-07-27
DE3686559T2 (de)	1993-03-18
JPS62130650A (ja)	1987-06-12
CA1298785C (fr)	1992-04-14
IE58461B1 (en)	1993-09-22
ATE79726T1 (de)	1992-09-15
EP0225165B1 (fr)	1992-08-26
EP0225165A3 (en)	1989-05-10
DK562086D0 (da)	1986-11-24
AU591730B2 (en)	1989-12-14
CN86108047A (zh)	1987-07-08
DE3686559D1 (de)	1992-10-01
GR3005962T3 (fr)	1993-06-07
EP0225165A2 (fr)	1987-06-10

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