FI65259C - Foerfarande foer framstaellning av omaettade derivat av 7-acylamido-3-cefem-4-karboxylsyra - Google Patents
Foerfarande foer framstaellning av omaettade derivat av 7-acylamido-3-cefem-4-karboxylsyra Download PDFInfo
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- FI65259C FI65259C FI772411A FI772411A FI65259C FI 65259 C FI65259 C FI 65259C FI 772411 A FI772411 A FI 772411A FI 772411 A FI772411 A FI 772411A FI 65259 C FI65259 C FI 65259C
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- methyl
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- 238000000034 method Methods 0.000 title claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 115
- 150000003839 salts Chemical class 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 21
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
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- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229940124587 cephalosporin Drugs 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 206010008323 cervicitis Diseases 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 201000001352 cholecystitis Diseases 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 201000003146 cystitis Diseases 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical group C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 208000019258 ear infection Diseases 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- MXZBXCKWSHEHAP-UHFFFAOYSA-N ethanethioyl chloride Chemical compound CC(Cl)=S MXZBXCKWSHEHAP-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 206010022000 influenza Diseases 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229960004393 lidocaine hydrochloride Drugs 0.000 description 1
- YECIFGHRMFEPJK-UHFFFAOYSA-N lidocaine hydrochloride monohydrate Chemical compound O.[Cl-].CC[NH+](CC)CC(=O)NC1=C(C)C=CC=C1C YECIFGHRMFEPJK-UHFFFAOYSA-N 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052751 metal Chemical class 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- ACTNHJDHMQSOGL-UHFFFAOYSA-N n',n'-dibenzylethane-1,2-diamine Chemical compound C=1C=CC=CC=1CN(CCN)CC1=CC=CC=C1 ACTNHJDHMQSOGL-UHFFFAOYSA-N 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000011356 non-aqueous organic solvent Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N ortho-diethylbenzene Natural products CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 1
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 206010034674 peritonitis Diseases 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 208000008423 pleurisy Diseases 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 229940007042 proteus vulgaris Drugs 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 208000013223 septicemia Diseases 0.000 description 1
- 201000009890 sinusitis Diseases 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- VYPDUQYOLCLEGS-UHFFFAOYSA-M sodium;2-ethylhexanoate Chemical compound [Na+].CCCCC(CC)C([O-])=O VYPDUQYOLCLEGS-UHFFFAOYSA-M 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- MHMUCYJKZUZMNJ-OWOJBTEDSA-N trans-3-chloroacrylic acid Chemical compound OC(=O)\C=C\Cl MHMUCYJKZUZMNJ-OWOJBTEDSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 210000001635 urinary tract Anatomy 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
- C07D501/28—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by an aliphatic carboxylic acid, which is substituted by hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D501/14—Compounds having a nitrogen atom directly attached in position 7
- C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
- C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
- C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
- C07D501/36—Methylene radicals, substituted by sulfur atoms
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)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2017377 | 1977-02-11 | ||
| IT20173/77A IT1075277B (it) | 1977-02-11 | 1977-02-11 | Derivati insaturi e epossidici dell'acio 7-acilamido-3-cefem-4-carbossilico e procedimento per la loro preparazione |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI772411A FI772411A (fi) | 1978-08-12 |
| FI65259B FI65259B (fi) | 1983-12-30 |
| FI65259C true FI65259C (fi) | 1984-04-10 |
Family
ID=11164407
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI772411A FI65259C (fi) | 1977-02-11 | 1977-08-10 | Foerfarande foer framstaellning av omaettade derivat av 7-acylamido-3-cefem-4-karboxylsyra |
| FI780437A FI780437A (fi) | 1977-02-11 | 1978-02-10 | Foerfarande foer framstaellning av heteromonocykliska och heterobicykliska derivat av omaettad 7-acylamido-3-kefem-karboxyl-syra |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI780437A FI780437A (fi) | 1977-02-11 | 1978-02-10 | Foerfarande foer framstaellning av heteromonocykliska och heterobicykliska derivat av omaettad 7-acylamido-3-kefem-karboxyl-syra |
Country Status (29)
| Country | Link |
|---|---|
| US (3) | US4154830A (nl) |
| JP (2) | JPS5398991A (nl) |
| AT (2) | AT355206B (nl) |
| AU (2) | AU512934B2 (nl) |
| BE (2) | BE858433A (nl) |
| CA (2) | CA1103237A (nl) |
| CH (3) | CH632513A5 (nl) |
| CS (3) | CS196381B2 (nl) |
| CY (1) | CY1234A (nl) |
| DE (2) | DE2736471A1 (nl) |
| DK (2) | DK155944C (nl) |
| FI (2) | FI65259C (nl) |
| FR (3) | FR2380285A1 (nl) |
| GB (4) | GB1582295A (nl) |
| GR (2) | GR71901B (nl) |
| HK (1) | HK55284A (nl) |
| HU (2) | HU177596B (nl) |
| IL (3) | IL52708A0 (nl) |
| IT (1) | IT1075277B (nl) |
| MY (1) | MY8500446A (nl) |
| NL (2) | NL7708943A (nl) |
| NO (4) | NO152654C (nl) |
| NZ (2) | NZ184889A (nl) |
| PH (1) | PH16946A (nl) |
| SE (4) | SE7709002L (nl) |
| SG (1) | SG9484G (nl) |
| SU (4) | SU845788A3 (nl) |
| YU (1) | YU40307B (nl) |
| ZA (2) | ZA774835B (nl) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1075277B (it) * | 1977-02-11 | 1985-04-22 | Erba Carlo Spa | Derivati insaturi e epossidici dell'acio 7-acilamido-3-cefem-4-carbossilico e procedimento per la loro preparazione |
| JPS5593413A (en) * | 1979-01-11 | 1980-07-15 | Osaka Gas Co Ltd | Lining method for inner surface of pipe |
| US4331666A (en) * | 1979-05-11 | 1982-05-25 | Farmitalia Carlo Erba S.P.A. | 3-[(8-Carboxy-6-tetrazolo[1,5-b]pyridazinyl)-thiomethyl]-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-3-cephem-4-carboxylic acid |
| US4420477A (en) * | 1979-11-30 | 1983-12-13 | Fujisawa Pharmaceutical Co., Ltd. | Cephem compounds |
| US4405617A (en) * | 1980-02-11 | 1983-09-20 | Fujisawa Pharmaceutical Co., Ltd. | 3-(Propynyltetrazol)thiomethyl-3-cephems |
| GB2076803B (en) * | 1980-05-16 | 1984-02-08 | Erba Farmitalia | Substituted 7-(a-oxy-imino-acetamido)-cephalosporins and process for their preparation |
| GB2186875A (en) * | 1983-10-31 | 1987-08-26 | Fujisawa Pharmaceutical Co | New cephem compounds and processes for preparation thereof |
| DE3689762T2 (de) * | 1985-12-13 | 1994-08-18 | Takeda Chemical Industries Ltd | Antibakterielle Verbindungen, ihre Herstellung und Verwendung. |
| JPH0544294Y2 (nl) * | 1986-06-10 | 1993-11-10 | ||
| EP0594583A1 (en) * | 1990-01-12 | 1994-05-04 | The Dow Chemical Company | Composition and use of substituted 3-thio-2-propynenitriles as an industrial antimicrobial |
| US5126349A (en) * | 1990-01-12 | 1992-06-30 | The Dow Chemical Company | Composition and use of substituted 3-thio-2-propynenitriles as an industrial antimicrobial |
| US5198445A (en) * | 1990-01-12 | 1993-03-30 | The Dow Chemical Company | Composition and use of substituted 3-thio-2-propynenitriles as industrial antimicrobials |
| US5157051A (en) * | 1992-03-05 | 1992-10-20 | The Dow Chemical Company | Composition and use of 3-thiocyano-2-halo-2-propenenitriles as antimicrobial agents |
| US5155119A (en) * | 1992-03-05 | 1992-10-13 | The Dow Chemical Company | 3-(2-pyridinylthio)-N-oxide, 2-halo-2-propenenitrile compounds useful as antimicrobials |
| US5206227A (en) * | 1992-06-02 | 1993-04-27 | The Dow Chemical Company | Composition and use of phosphonic acid, (2-halo-2-cyanoethenyl)-dialkyl esters as antimicrobials |
| JP3115455B2 (ja) * | 1992-12-18 | 2000-12-04 | 明治製菓株式会社 | 新規セファロスポリン誘導体 |
| SE9802974D0 (sv) * | 1998-09-03 | 1998-09-03 | Astra Ab | New crystalline forms |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1478055A (en) * | 1973-07-27 | 1977-06-29 | Erba Carlo Spa | Cephalosporin compounds |
| IT1075277B (it) * | 1977-02-11 | 1985-04-22 | Erba Carlo Spa | Derivati insaturi e epossidici dell'acio 7-acilamido-3-cefem-4-carbossilico e procedimento per la loro preparazione |
| US3883520A (en) * | 1973-08-17 | 1975-05-13 | Smithkline Corp | Substituted mercaptoacetamidocephalosporins |
| AU1303576A (en) * | 1975-04-21 | 1977-10-20 | Erba Carlo Spa | Cephalosporins |
| ZA767084B (en) * | 1975-12-16 | 1977-10-26 | Erba Carlo Spa | Thiadiazolyl derivatives of 7-acylamido 3-cephem-4-carboxylic acid and process for their preparation |
| US4057631A (en) * | 1976-09-02 | 1977-11-08 | Smithkline Corporation | 7-(α-Substituted phenylacetamido)-3-(1-carboxymethylthioethyltetrazolyl-5-thiomethyl)-3-cephem-4-carboxylic acids |
| US4079134A (en) * | 1976-09-24 | 1978-03-14 | Smithkline Corporation | 7-Acylamino-3-(5-sulfomethyl-1,3,4-thiadiazol-2-ylthiomethyl)-3-cephem-4-carboxylic acids |
-
1977
- 1977-02-11 IT IT20173/77A patent/IT1075277B/it active
- 1977-08-08 US US05/822,638 patent/US4154830A/en not_active Expired - Lifetime
- 1977-08-08 DK DK353577A patent/DK155944C/da not_active IP Right Cessation
- 1977-08-08 NO NO772779A patent/NO152654C/no unknown
- 1977-08-09 CY CY1234A patent/CY1234A/xx unknown
- 1977-08-09 GB GB33418/77A patent/GB1582295A/en not_active Expired
- 1977-08-09 GB GB43324/79A patent/GB1590610A/en not_active Expired
- 1977-08-09 SE SE7709002A patent/SE7709002L/xx not_active Application Discontinuation
- 1977-08-10 NZ NZ184889A patent/NZ184889A/xx unknown
- 1977-08-10 ZA ZA00774835A patent/ZA774835B/xx unknown
- 1977-08-10 CA CA284,460A patent/CA1103237A/en not_active Expired
- 1977-08-10 HU HU77EA176A patent/HU177596B/hu not_active IP Right Cessation
- 1977-08-10 FI FI772411A patent/FI65259C/fi not_active IP Right Cessation
- 1977-08-11 CH CH984577A patent/CH632513A5/de not_active IP Right Cessation
- 1977-08-11 AT AT585677A patent/AT355206B/de not_active IP Right Cessation
- 1977-08-11 CS CS775327A patent/CS196381B2/cs unknown
- 1977-08-11 GR GR54135A patent/GR71901B/el unknown
- 1977-08-12 DE DE19772736471 patent/DE2736471A1/de active Granted
- 1977-08-12 FR FR7724952A patent/FR2380285A1/fr active Granted
- 1977-08-12 IL IL52708A patent/IL52708A0/xx not_active IP Right Cessation
- 1977-08-12 AU AU27865/77A patent/AU512934B2/en not_active Expired
- 1977-08-12 NL NL7708943A patent/NL7708943A/nl not_active Application Discontinuation
- 1977-08-13 JP JP9742077A patent/JPS5398991A/ja active Granted
- 1977-08-22 SU SU772516753A patent/SU845788A3/ru active
- 1977-09-06 YU YU2109/77A patent/YU40307B/xx unknown
- 1977-09-06 BE BE180695A patent/BE858433A/xx not_active IP Right Cessation
-
1978
- 1978-01-09 NO NO780074A patent/NO780074L/no unknown
- 1978-01-10 DK DK11578A patent/DK11578A/da not_active Application Discontinuation
- 1978-01-11 GB GB4691/80A patent/GB1597262A/en not_active Expired
- 1978-01-11 ZA ZA00780181A patent/ZA78181B/xx unknown
- 1978-01-11 GB GB1121/78A patent/GB1597261A/en not_active Expired
- 1978-01-11 US US05/868,665 patent/US4172892A/en not_active Expired - Lifetime
- 1978-01-11 SE SE7800292A patent/SE7800292L/xx unknown
- 1978-01-12 HU HU78EA182A patent/HU178918B/hu unknown
- 1978-01-13 NL NL7800443A patent/NL7800443A/nl not_active Application Discontinuation
- 1978-01-16 AU AU32476/78A patent/AU513444B2/en not_active Expired
- 1978-01-16 DE DE19782801644 patent/DE2801644A1/de not_active Withdrawn
- 1978-01-17 IL IL53830A patent/IL53830A/xx unknown
- 1978-01-17 CS CS78331A patent/CS199713B2/cs unknown
- 1978-01-17 AT AT32778A patent/AT356270B/de not_active IP Right Cessation
- 1978-01-17 CS CS788042A patent/CS199714B2/cs unknown
- 1978-01-17 NZ NZ186236A patent/NZ186236A/xx unknown
- 1978-01-19 GR GR55208A patent/GR72589B/el unknown
- 1978-01-20 PH PH20693A patent/PH16946A/en unknown
- 1978-01-24 FR FR7801928A patent/FR2384783A1/fr active Granted
- 1978-01-26 JP JP676978A patent/JPS53121788A/ja active Pending
- 1978-02-03 BE BE184877A patent/BE863625A/xx not_active IP Right Cessation
- 1978-02-10 CH CH153278A patent/CH636359A5/de not_active IP Right Cessation
- 1978-02-10 SU SU782578100A patent/SU856388A3/ru active
- 1978-02-10 CA CA296,689A patent/CA1108603A/en not_active Expired
- 1978-02-10 FI FI780437A patent/FI780437A/fi not_active Application Discontinuation
- 1978-07-28 SU SU782640405A patent/SU753361A3/ru active
-
1979
- 1979-04-26 SU SU792759905A patent/SU904524A3/ru active
- 1979-12-14 NO NO794101A patent/NO794101L/no unknown
-
1980
- 1980-01-08 SE SE8000110A patent/SE446536B/sv not_active IP Right Cessation
- 1980-01-24 CH CH58280A patent/CH634330A5/de not_active IP Right Cessation
- 1980-01-31 NO NO800239A patent/NO800239L/no unknown
- 1980-03-05 IL IL59527A patent/IL59527A0/xx unknown
- 1980-03-07 FR FR8005220A patent/FR2445834A1/fr active Granted
- 1980-04-18 SE SE8002904A patent/SE8002904L/sv not_active Application Discontinuation
-
1981
- 1981-08-21 US US06/295,074 patent/US4388314A/en not_active Expired - Fee Related
-
1984
- 1984-02-06 SG SG94/84A patent/SG9484G/en unknown
- 1984-07-19 HK HK552/84A patent/HK55284A/xx unknown
-
1985
- 1985-12-30 MY MY446/85A patent/MY8500446A/xx unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
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| MM | Patent lapsed |
Owner name: FARMITALIA CARLO ERBA S.R.L |