CA1077848A - Anti-viral composition containing phosphonoformic acid - Google Patents
Anti-viral composition containing phosphonoformic acidInfo
- Publication number
- CA1077848A CA1077848A CA281,863A CA281863A CA1077848A CA 1077848 A CA1077848 A CA 1077848A CA 281863 A CA281863 A CA 281863A CA 1077848 A CA1077848 A CA 1077848A
- Authority
- CA
- Canada
- Prior art keywords
- acid
- phosphonoformic acid
- salt
- phosphonoformic
- virus
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
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- 239000000203 mixture Substances 0.000 title description 19
- 230000000840 anti-viral effect Effects 0.000 title description 4
- 150000003839 salts Chemical class 0.000 claims abstract description 35
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- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 11
- -1 phosphonoformic acid monocyclohexyl-ammonium salt Chemical compound 0.000 claims description 9
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- DFHAXXVZCFXGOQ-UHFFFAOYSA-K trisodium phosphonoformate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)P([O-])([O-])=O DFHAXXVZCFXGOQ-UHFFFAOYSA-K 0.000 claims description 3
- IRMYJSKYCFRVAR-UHFFFAOYSA-L P(=O)(O)(O)C(=O)[O-].[Na+].[Na+].P(=O)(O)(O)C(=O)[O-] Chemical compound P(=O)(O)(O)C(=O)[O-].[Na+].[Na+].P(=O)(O)(O)C(=O)[O-] IRMYJSKYCFRVAR-UHFFFAOYSA-L 0.000 claims 1
- 230000009385 viral infection Effects 0.000 abstract description 6
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- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
- BDWCBOUQHJMMPD-UHFFFAOYSA-K [O-]C(P([O-])(O)=O)=O.[O-]C(P(O)(O)=O)=O.[Na+].[Na+].[Na+] Chemical compound [O-]C(P([O-])(O)=O)=O.[O-]C(P(O)(O)=O)=O.[Na+].[Na+].[Na+] BDWCBOUQHJMMPD-UHFFFAOYSA-K 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- TTWYZDPBDWHJOR-IDIVVRGQSA-L adenosine triphosphate disodium Chemical compound [Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O TTWYZDPBDWHJOR-IDIVVRGQSA-L 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 235000010385 ascorbyl palmitate Nutrition 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 230000003915 cell function Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229940081734 cellulose acetate phthalate Drugs 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 210000004087 cornea Anatomy 0.000 description 1
- 150000003946 cyclohexylamines Chemical class 0.000 description 1
- PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 1
- NHVNXKFIZYSCEB-XLPZGREQSA-N dTTP Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)C1 NHVNXKFIZYSCEB-XLPZGREQSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000312 effect on influenza Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229960003971 influenza vaccine Drugs 0.000 description 1
- 229940079322 interferon Drugs 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000007923 nasal drop Substances 0.000 description 1
- 229940100662 nasal drops Drugs 0.000 description 1
- 229940097496 nasal spray Drugs 0.000 description 1
- 239000007922 nasal spray Substances 0.000 description 1
- 230000002276 neurotropic effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000013421 nuclear magnetic resonance imaging Methods 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000003833 nucleoside derivatives Chemical class 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229940093430 polyethylene glycol 1500 Drugs 0.000 description 1
- 229940057838 polyethylene glycol 4000 Drugs 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000006190 sub-lingual tablet Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000002511 suppository base Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 125000002264 triphosphate group Chemical class [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 150000003751 zinc Chemical class 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
- A61K31/66—Phosphorus compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3886—Acids containing the structure -C(=X)-P(=X)(XH)2 or NC-P(=X)(XH)2, (X = O, S, Se)
- C07F9/3891—Acids containing the structure -C(=X)-P(=X)(XH)2, (X = O, S, Se)
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biochemistry (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7607496A SE7607496L (sv) | 1976-07-01 | 1976-07-01 | Sett for bekempning av virusinfektioner |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1077848A true CA1077848A (en) | 1980-05-20 |
Family
ID=20328354
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA281,863A Expired CA1077848A (en) | 1976-07-01 | 1977-06-30 | Anti-viral composition containing phosphonoformic acid |
Country Status (22)
| Country | Link |
|---|---|
| US (4) | US4215113A (enExample) |
| JP (1) | JPS536428A (enExample) |
| AT (1) | AT369014B (enExample) |
| AU (1) | AU510809B2 (enExample) |
| BE (1) | BE856355A (enExample) |
| BG (1) | BG60834B2 (enExample) |
| CA (1) | CA1077848A (enExample) |
| CH (1) | CH641471A5 (enExample) |
| DE (1) | DE2728685C2 (enExample) |
| DK (1) | DK288877A (enExample) |
| FI (1) | FI772030A7 (enExample) |
| FR (1) | FR2356424A1 (enExample) |
| GB (1) | GB1585615A (enExample) |
| HK (1) | HK28984A (enExample) |
| IE (1) | IE45753B1 (enExample) |
| LU (2) | LU77666A1 (enExample) |
| MX (1) | MX9203635A (enExample) |
| MY (1) | MY8500125A (enExample) |
| NL (2) | NL180068C (enExample) |
| NO (1) | NO772299L (enExample) |
| SE (1) | SE7607496L (enExample) |
| SG (1) | SG80383G (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK564378A (da) * | 1977-12-22 | 1979-06-23 | Astra Laekemedel Ab | Fremgangsmaade til fremstilling af amidderivater til bekaempelse af virusinfektioner |
| CA1140049A (en) * | 1977-12-22 | 1983-01-25 | Dke J.E. Helgstran | Pharmaceutical preparations from derivatives of hydroxycarbonylphosphonic acid |
| DE2926799A1 (de) * | 1979-07-03 | 1981-01-15 | Bayer Ag | Phosphonoameisensaeurehydrazide, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE2941384A1 (de) * | 1979-10-12 | 1981-04-23 | Bayer Ag, 5090 Leverkusen | Phosphono-hydroxy-essigsaeure, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel |
| DE3127237A1 (de) * | 1981-07-10 | 1983-01-20 | Hoechst Ag, 6000 Frankfurt | Magenvertraegliche arzneiformen von xanthinderivaten und verfahren zu ihrer herstellung |
| US4902678A (en) * | 1982-02-12 | 1990-02-20 | Syntex (U.S.A.) Inc. | Anti-viral compositions |
| WO1983002723A1 (en) * | 1982-02-12 | 1983-08-18 | Smith, Kendall, O. | Anti-viral compositions |
| JPH0761814B2 (ja) * | 1984-09-10 | 1995-07-05 | 三菱化学株式会社 | 搬送装置 |
| JPS6194925A (ja) * | 1984-10-12 | 1986-05-13 | Mitsubishi Chem Ind Ltd | 搬送用装置 |
| JPS61217434A (ja) * | 1985-03-20 | 1986-09-27 | Mitsubishi Chem Ind Ltd | 搬送用装置 |
| GB8501374D0 (en) * | 1985-01-18 | 1985-02-20 | Wellcome Found | Treatment of aids |
| US4590064A (en) * | 1985-03-11 | 1986-05-20 | Colgate-Palmolive Company | Anticalculus oral composition |
| US4880619A (en) * | 1985-03-11 | 1989-11-14 | Colgate-Palmolive Company | Anticalculus oral composition |
| GB8512330D0 (en) * | 1985-05-15 | 1985-06-19 | Wellcome Found | Antiviral compounds |
| US4806532A (en) * | 1985-10-08 | 1989-02-21 | Mayo Foundation For Medical Education And Research | Inhibition of epithelial phosphate transport |
| WO1987002246A1 (en) * | 1985-10-21 | 1987-04-23 | William Sergio | Method for reducing the risk or probability of infection from the aids virus (htlv-iii/lav/arv) |
| US6492352B1 (en) * | 1985-10-31 | 2002-12-10 | Astra Lakemedel Aktiebolag | Method for the control and treatment of acquired immunodeficiency syndrome (AIDS) |
| US5194654A (en) * | 1989-11-22 | 1993-03-16 | Vical, Inc. | Lipid derivatives of phosphonoacids for liposomal incorporation and method of use |
| US5463092A (en) * | 1989-11-22 | 1995-10-31 | Vestar, Inc. | Lipid derivatives of phosphonacids for liposomal incorporation and method of use |
| US6110901A (en) * | 1990-07-03 | 2000-08-29 | American Cyanamid Company | Method for treating RNA viral infections by using RNA chain terminators |
| SE9403861D0 (sv) * | 1994-11-09 | 1994-11-09 | Astra Ab | Novel medicinal use |
| US5696277A (en) * | 1994-11-15 | 1997-12-09 | Karl Y. Hostetler | Antiviral prodrugs |
| EP0831842A4 (en) * | 1995-06-06 | 1998-08-19 | Univ Southern California | METHOD AND MEANS FOR INHIBITING PROPAGATION OF THE CYTOMEGALOVIRUS |
| US7517858B1 (en) | 1995-06-07 | 2009-04-14 | The Regents Of The University Of California | Prodrugs of pharmaceuticals with improved bioavailability |
| RU2116790C1 (ru) * | 1997-07-02 | 1998-08-10 | Закрытое акционерное общество "Рефарм" | Наружное противоинфекционное средство "рефарм" |
| RU2124881C1 (ru) * | 1997-11-26 | 1999-01-20 | Матковская Татьяна Александровна | Наружное лечебно-косметическое средство |
| FI980216A0 (fi) * | 1998-01-30 | 1998-01-30 | Bene Pharma Oy | Medicin foer behandling av vaorfor |
| US20040002079A1 (en) * | 1998-02-11 | 2004-01-01 | Gunn Robert B. | Sodium-phosphate cotransporter in lithium therapy for the treatment of mental illness |
| DE19940748A1 (de) * | 1999-08-27 | 2001-03-01 | Hugo Seinfeld | Arzneimittel enthaltend xenogene Oligo- oder/und Polyribonukleotide |
| US7455833B2 (en) * | 2002-07-15 | 2008-11-25 | Board Of Regents, The University Of Texas System | Methods and compositions for treating viral infections using antibodies and immunoconjugates to aminophospholipids |
| US7906115B2 (en) | 2002-07-15 | 2011-03-15 | Thorpe Philip E | Combinations kits and methods for treating viral infections using antibodies and immunoconjugates to aminophospholipids |
| US7790159B2 (en) * | 2002-07-15 | 2010-09-07 | Board Of Regents, The University Of Texas System | Methods, combinations and kits for treating viral infections using immunoconjugates and antibodies to aminophospholipids |
| US20040131622A1 (en) * | 2002-07-15 | 2004-07-08 | Board Of Regents | Combinations and kits for treating viral infections using immunoconjugates to aminophospholipids |
| US7611704B2 (en) * | 2002-07-15 | 2009-11-03 | Board Of Regents, The University Of Texas System | Compositions and methods for treating viral infections using antibodies and immunoconjugates to aminophospholipids |
| US7132452B2 (en) * | 2003-03-10 | 2006-11-07 | Fang-Yu Lee | Topical formulation having effects on alleviating pain/inflammation caused by herpes virus infection |
| JP2006520374A (ja) * | 2003-03-14 | 2006-09-07 | エピスタム リミテッド | 非ウィルス性上皮損傷の治療および／または予防 |
| US7424812B2 (en) | 2003-05-16 | 2008-09-16 | Stanton Concepts Inc. | Multiple function lock |
| US20090214676A1 (en) * | 2005-04-30 | 2009-08-27 | Tissuetech, Inc. | Method for treating ocular demodex |
| US20080045482A1 (en) * | 2006-01-27 | 2008-02-21 | Adventrx Pharmaceuticals, Inc. | Compositions and methods for the treatment of viral infections |
| US8128968B2 (en) * | 2007-08-29 | 2012-03-06 | Tissuetech, Inc. | Compositions and methods for treating Demodex infestations |
| WO2009114153A1 (en) | 2008-03-12 | 2009-09-17 | Nektar Therapeutics | Oligomer-foscarnet conjugates |
| ES2578902B1 (es) * | 2014-12-29 | 2017-07-07 | Agencia Pública Empresarial Sanitaria Costa Del Sol | Uso de análogos del ión pirofosfato para el tratamiento de la infección por VPH |
| WO2022153334A1 (en) * | 2021-01-15 | 2022-07-21 | Jubilant Generics Ltd | Transmucosal dosage forms of foscarnet |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3767795A (en) * | 1971-02-25 | 1973-10-23 | Abbott Lab | Method for combating certain virus infection |
| US3836650A (en) * | 1971-02-25 | 1974-09-17 | Abbott Lab | Method for combating marek's disease in poultry |
| DE2360797C2 (de) * | 1973-12-06 | 1985-05-23 | Henkel KGaA, 4000 Düsseldorf | Pharmazeutische Präparate |
-
1976
- 1976-07-01 SE SE7607496A patent/SE7607496L/xx unknown
-
1977
- 1977-06-20 US US05/807,783 patent/US4215113A/en not_active Expired - Lifetime
- 1977-06-25 DE DE2728685A patent/DE2728685C2/de not_active Expired
- 1977-06-27 AU AU26505/77A patent/AU510809B2/en not_active Expired
- 1977-06-27 IE IE1311/77A patent/IE45753B1/en not_active IP Right Cessation
- 1977-06-29 FI FI772030A patent/FI772030A7/fi not_active Application Discontinuation
- 1977-06-29 NL NLAANVRAGE7707235,A patent/NL180068C/xx not_active IP Right Cessation
- 1977-06-29 NO NO772299A patent/NO772299L/no unknown
- 1977-06-29 DK DK288877A patent/DK288877A/da not_active Application Discontinuation
- 1977-06-30 LU LU77666A patent/LU77666A1/xx unknown
- 1977-06-30 FR FR7720100A patent/FR2356424A1/fr active Granted
- 1977-06-30 CA CA281,863A patent/CA1077848A/en not_active Expired
- 1977-06-30 CH CH808577A patent/CH641471A5/de not_active IP Right Cessation
- 1977-06-30 AT AT0465477A patent/AT369014B/de active Protection Beyond IP Right Term
- 1977-06-30 GB GB27464/77A patent/GB1585615A/en not_active Expired
- 1977-07-01 BE BE178982A patent/BE856355A/xx not_active IP Right Cessation
- 1977-07-01 JP JP7797777A patent/JPS536428A/ja active Granted
-
1978
- 1978-12-21 US US05/971,931 patent/US4339445A/en not_active Expired - Lifetime
-
1982
- 1982-08-02 US US06/404,295 patent/US4665062A/en not_active Expired - Lifetime
-
1983
- 1983-12-20 SG SG803/83A patent/SG80383G/en unknown
-
1984
- 1984-03-29 HK HK289/84A patent/HK28984A/xx unknown
-
1985
- 1985-10-31 US US06/793,575 patent/US4771041A/en not_active Expired - Fee Related
- 1985-12-30 MY MY125/85A patent/MY8500125A/xx unknown
-
1992
- 1992-06-26 MX MX9203635A patent/MX9203635A/es unknown
-
1993
- 1993-06-10 NL NL930053C patent/NL930053I2/nl unknown
- 1993-06-16 LU LU88310C patent/LU88310I2/fr unknown
-
1994
- 1994-02-18 BG BG098492A patent/BG60834B2/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AT369014B (de) | 1982-11-25 |
| LU88310I2 (fr) | 1994-05-04 |
| AU2650577A (en) | 1979-01-04 |
| US4215113A (en) | 1980-07-29 |
| FR2356424B1 (enExample) | 1980-04-18 |
| SG80383G (en) | 1984-08-03 |
| NL7707235A (nl) | 1978-01-03 |
| JPS562046B2 (enExample) | 1981-01-17 |
| NO772299L (no) | 1978-04-25 |
| LU77666A1 (enExample) | 1977-10-07 |
| FR2356424A1 (fr) | 1978-01-27 |
| MY8500125A (en) | 1985-12-31 |
| DE2728685C2 (de) | 1982-09-16 |
| BG60834B2 (bg) | 1996-04-30 |
| NL930053I1 (nl) | 1993-09-01 |
| MX9203635A (es) | 1992-09-01 |
| AU510809B2 (en) | 1980-07-17 |
| BE856355A (fr) | 1978-01-02 |
| GB1585615A (en) | 1981-03-11 |
| FI772030A7 (enExample) | 1978-01-02 |
| IE45753B1 (en) | 1982-11-17 |
| HK28984A (en) | 1984-04-06 |
| IE45753L (en) | 1978-01-01 |
| NL930053I2 (nl) | 1994-01-03 |
| DE2728685A1 (de) | 1978-01-12 |
| DK288877A (da) | 1978-01-02 |
| US4771041A (en) | 1988-09-13 |
| ATA465477A (de) | 1982-04-15 |
| NL180068B (nl) | 1986-08-01 |
| US4339445A (en) | 1982-07-13 |
| CH641471A5 (de) | 1984-02-29 |
| US4665062A (en) | 1987-05-12 |
| JPS536428A (en) | 1978-01-20 |
| NL180068C (nl) | 1987-01-02 |
| SE7607496L (sv) | 1978-01-02 |
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