FI65438C - Foerfarande foer framstaellning av farmakologiskt aktiva estrar av fosfonomyrsyra - Google Patents
Foerfarande foer framstaellning av farmakologiskt aktiva estrar av fosfonomyrsyra Download PDFInfo
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- FI65438C FI65438C FI783931A FI783931A FI65438C FI 65438 C FI65438 C FI 65438C FI 783931 A FI783931 A FI 783931A FI 783931 A FI783931 A FI 783931A FI 65438 C FI65438 C FI 65438C
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- Finland
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- phenyl
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- vis
- formula
- acid
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- -1 formic acid ester Chemical class 0.000 claims description 209
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 158
- 150000001875 compounds Chemical class 0.000 claims description 123
- 238000000034 method Methods 0.000 claims description 73
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- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 239000001257 hydrogen Substances 0.000 claims description 43
- 150000003839 salts Chemical class 0.000 claims description 41
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 34
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- 238000006243 chemical reaction Methods 0.000 claims description 31
- 239000002253 acid Substances 0.000 claims description 29
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- 125000004185 ester group Chemical group 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 19
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 150000002148 esters Chemical class 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 16
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- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
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- RZJCVIRWTUPMPT-UHFFFAOYSA-L disodium;(4-methoxyphenyl) phosphonatoformate Chemical compound [Na+].[Na+].COC1=CC=C(OC(=O)P([O-])([O-])=O)C=C1 RZJCVIRWTUPMPT-UHFFFAOYSA-L 0.000 description 1
- DOWINSUKNDQWRF-UHFFFAOYSA-L disodium;(4-methylphenyl) phosphonatoformate Chemical compound [Na+].[Na+].CC1=CC=C(OC(=O)P([O-])([O-])=O)C=C1 DOWINSUKNDQWRF-UHFFFAOYSA-L 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
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- 239000003937 drug carrier Substances 0.000 description 1
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- 238000005886 esterification reaction Methods 0.000 description 1
- 229940011871 estrogen Drugs 0.000 description 1
- 239000000262 estrogen Substances 0.000 description 1
- DWMKQFTYSGRBKU-UHFFFAOYSA-N ethoxy-dihydroxy-bis(4-methylphenyl)-lambda5-phosphane Chemical compound C=1C=C(C)C=CC=1P(O)(O)(OCC)C1=CC=C(C)C=C1 DWMKQFTYSGRBKU-UHFFFAOYSA-N 0.000 description 1
- BSUDARYZVWJOBI-UHFFFAOYSA-N ethyl dimethoxyphosphorylformate Chemical compound CCOC(=O)P(=O)(OC)OC BSUDARYZVWJOBI-UHFFFAOYSA-N 0.000 description 1
- MSXLZDIUXZWZDO-UHFFFAOYSA-N ethyl diphenoxyphosphorylformate Chemical compound C=1C=CC=CC=1OP(=O)(C(=O)OCC)OC1=CC=CC=C1 MSXLZDIUXZWZDO-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003889 eye drop Substances 0.000 description 1
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- 239000003925 fat Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 210000004211 gastric acid Anatomy 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
- 238000011331 genomic analysis Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical class [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 210000001144 hymen Anatomy 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 210000000088 lip Anatomy 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 210000004698 lymphocyte Anatomy 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 210000005075 mammary gland Anatomy 0.000 description 1
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- 150000002736 metal compounds Chemical class 0.000 description 1
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
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- 229940100662 nasal drops Drugs 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 210000001331 nose Anatomy 0.000 description 1
- 239000003865 nucleic acid synthesis inhibitor Substances 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical compound [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- QWTKOKXIYQZOTL-UHFFFAOYSA-N phenoxycarbonylphosphonic acid Chemical compound OP(O)(=O)C(=O)OC1=CC=CC=C1 QWTKOKXIYQZOTL-UHFFFAOYSA-N 0.000 description 1
- UFUOXRRWKKRSOH-UHFFFAOYSA-N phenyl [ethoxy-(4-methoxyphenoxy)phosphoryl]formate Chemical compound C=1C=CC=CC=1OC(=O)P(=O)(OCC)OC1=CC=C(OC)C=C1 UFUOXRRWKKRSOH-UHFFFAOYSA-N 0.000 description 1
- IORAAQDUDVGXSM-UHFFFAOYSA-N phenyl bis(4-methylphenoxy)phosphorylformate Chemical compound C1=CC(C)=CC=C1OP(=O)(C(=O)OC=1C=CC=CC=1)OC1=CC=C(C)C=C1 IORAAQDUDVGXSM-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- 125000005496 phosphonium group Chemical group 0.000 description 1
- 125000005499 phosphonyl group Chemical group 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 238000002962 plaque-reduction assay Methods 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- LGHBCOPAKMBMKP-UHFFFAOYSA-N propane-1,2,3-triol;propan-2-ol Chemical compound CC(C)O.OCC(O)CO LGHBCOPAKMBMKP-UHFFFAOYSA-N 0.000 description 1
- KDIBIPDUGGBUDB-UHFFFAOYSA-N propane-1,2,3-triol;propan-2-ol;hydrate Chemical compound O.CC(C)O.OCC(O)CO KDIBIPDUGGBUDB-UHFFFAOYSA-N 0.000 description 1
- 210000002307 prostate Anatomy 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 201000008261 skin carcinoma Diseases 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- CMHAUVUWBLYSRC-UHFFFAOYSA-M sodium;(4-methoxyphenoxy)-phenoxycarbonylphosphinate Chemical compound [Na+].C1=CC(OC)=CC=C1OP([O-])(=O)C(=O)OC1=CC=CC=C1 CMHAUVUWBLYSRC-UHFFFAOYSA-M 0.000 description 1
- BRJQWFPYPBXHOB-UHFFFAOYSA-M sodium;(4-methylphenoxy)-phenoxycarbonylphosphinate Chemical compound [Na+].C1=CC(C)=CC=C1OP([O-])(=O)C(=O)OC1=CC=CC=C1 BRJQWFPYPBXHOB-UHFFFAOYSA-M 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 230000002311 subsequent effect Effects 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
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- 230000014723 transformation of host cell by virus Effects 0.000 description 1
- 230000014599 transmission of virus Effects 0.000 description 1
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- 210000001635 urinary tract Anatomy 0.000 description 1
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Classifications
-
- 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)
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- 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)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4062—Esters of acids containing the structure -C(=X)-P(=X)(XR)2 or NC-P(=X)(XR)2, (X = O, S, Se)
- C07F9/4065—Esters of acids containing the structure -C(=X)-P(=X)(XR)2, (X = O, S, Se)
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5358377 | 1977-12-22 | ||
| GB5358177 | 1977-12-22 | ||
| GB5358277 | 1977-12-22 | ||
| GB5358277 | 1977-12-22 | ||
| GB5358077 | 1977-12-22 | ||
| GB5358377 | 1977-12-22 | ||
| GB5358077 | 1977-12-22 | ||
| GB5358177 | 1977-12-22 | ||
| GB7828548 | 1978-07-03 | ||
| GB7828552 | 1978-07-03 | ||
| GB7828555 | 1978-07-03 | ||
| GB7828552 | 1978-07-03 | ||
| GB7828548 | 1978-07-03 | ||
| GB7828555 | 1978-07-03 | ||
| GB7828553 | 1978-07-03 | ||
| GB7828553 | 1978-07-03 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI783931A7 FI783931A7 (fi) | 1979-06-23 |
| FI65438B FI65438B (fi) | 1984-01-31 |
| FI65438C true FI65438C (fi) | 1984-05-10 |
Family
ID=27571200
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI783931A FI65438C (fi) | 1977-12-22 | 1978-12-20 | Foerfarande foer framstaellning av farmakologiskt aktiva estrar av fosfonomyrsyra |
| FI783932A FI68626C (fi) | 1977-12-22 | 1978-12-20 | Foerfarande foer framstaellning av nya terapeutiskt aktiva hydroxikarbonylfosfonsyraderivat |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI783932A FI68626C (fi) | 1977-12-22 | 1978-12-20 | Foerfarande foer framstaellning av nya terapeutiskt aktiva hydroxikarbonylfosfonsyraderivat |
Country Status (14)
| Country | Link |
|---|---|
| US (4) | US4386081A (https=) |
| EP (2) | EP0003275B1 (https=) |
| JP (2) | JPS54109951A (https=) |
| AT (1) | AT369017B (https=) |
| AU (1) | AU530031B2 (https=) |
| CA (2) | CA1144937A (https=) |
| DE (2) | DE2861729D1 (https=) |
| DK (2) | DK148632C (https=) |
| FI (2) | FI65438C (https=) |
| HK (1) | HK33584A (https=) |
| IE (1) | IE48011B1 (https=) |
| MY (1) | MY8500058A (https=) |
| NO (2) | NO156611C (https=) |
| SG (1) | SG82383G (https=) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CA1144937A (en) * | 1977-12-22 | 1983-04-19 | Dke J.E. Helgstrand | Aromatic derivatives, pharmaceutical compositions and methods for combatting virus infections |
| GB8501374D0 (en) * | 1985-01-18 | 1985-02-20 | Wellcome Found | Treatment of aids |
| US4806532A (en) * | 1985-10-08 | 1989-02-21 | Mayo Foundation For Medical Education And Research | Inhibition of epithelial phosphate transport |
| US6492352B1 (en) * | 1985-10-31 | 2002-12-10 | Astra Lakemedel Aktiebolag | Method for the control and treatment of acquired immunodeficiency syndrome (AIDS) |
| US5025003A (en) * | 1989-09-18 | 1991-06-18 | E. R. Squibb & Sons, Inc. | Isoprenoid phosphinylformic acid squalene synthetase inhibitors |
| US5166386A (en) * | 1989-09-18 | 1992-11-24 | E. R. Squibb & Sons, Inc. | Process of making isoprenoid phosphinylformic acid squalene synthetase inhibitors |
| US5463092A (en) * | 1989-11-22 | 1995-10-31 | Vestar, Inc. | Lipid derivatives of phosphonacids for liposomal incorporation and method of use |
| US5132414A (en) * | 1990-05-10 | 1992-07-21 | Dana-Farber Cancer Institute, Inc. | Dideoxynucleoside-5'-phosphonoformic acid compounds |
| US5696277A (en) * | 1994-11-15 | 1997-12-09 | Karl Y. Hostetler | Antiviral prodrugs |
| US7517858B1 (en) | 1995-06-07 | 2009-04-14 | The Regents Of The University Of California | Prodrugs of pharmaceuticals with improved bioavailability |
| US6096730A (en) * | 1997-07-24 | 2000-08-01 | University Of Kentucky Research Foundation | Phosphonated agents and their antiangiogenic and antitumorigenic use |
| US5869469A (en) * | 1997-08-18 | 1999-02-09 | Queen's University At Kingston | Phosphonocarboxylate compounds for treating amyloidosis |
| NZ550116A (en) * | 1997-08-18 | 2008-03-28 | Neurochem Int Ltd | Phosphono-carboxylate compounds for treating amyloidosis |
| US20020022657A1 (en) * | 1998-02-11 | 2002-02-21 | Francine Gervais | Methods for modulating neuronal cell death |
| US20040002079A1 (en) * | 1998-02-11 | 2004-01-01 | Gunn Robert B. | Sodium-phosphate cotransporter in lithium therapy for the treatment of mental illness |
| WO1999040909A1 (en) * | 1998-02-11 | 1999-08-19 | Neurochem, Inc. | Method for modulating macrophage activation |
| US6329356B1 (en) | 1998-04-10 | 2001-12-11 | Neurochem, Inc. | Phosphono-carboxylate compounds for treating amyloidosis |
| US6310073B1 (en) | 1998-07-28 | 2001-10-30 | Queen's University At Kingston | Methods and compositions to treat glycosaminoglycan-associated molecular interactions |
| CA2369997C (en) * | 1999-04-28 | 2009-11-17 | Queen's University At Kingston | Compositions and methods for treating amyloidosis |
| US6562836B1 (en) | 1999-05-24 | 2003-05-13 | Queen's University Of Kingston | Methods and compounds for inhibiting amyloid deposits |
| IL150374A0 (en) | 1999-12-23 | 2002-12-01 | Neurochem Inc | Compounds and methods for modulating cerebral amyloid angiopathy |
| ATE337309T1 (de) * | 2002-04-01 | 2006-09-15 | Pfizer | Pyranon- und pyrandioninhibitoren der rna- abhängigen rna-polymerase des hepatitis-c-virus |
| DOP2003000641A (es) * | 2002-05-10 | 2003-11-15 | Pfizer | Inhibidores de las arn polimerasa dependiente de arn del virus de las hepatitis c y composiciones y tratamiento que los usan |
| US7148226B2 (en) * | 2003-02-21 | 2006-12-12 | Agouron Pharmaceuticals, Inc. | Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same |
| US20040214178A1 (en) * | 2003-04-24 | 2004-10-28 | Agouron Pharmaceuticals, Inc. | Reporter-selectable Hepatitis C virus replicon |
| US20070010573A1 (en) | 2003-06-23 | 2007-01-11 | Xianqi Kong | Methods and compositions for treating amyloid-related diseases |
| US7414076B2 (en) | 2003-06-23 | 2008-08-19 | Neurochem (International) Limited | Methods and compositions for treating amyloid-related diseases |
| US7244764B2 (en) | 2003-06-23 | 2007-07-17 | Neurochem (International) Limited | Methods and compositions for treating amyloid-related diseases |
| UA88909C2 (ru) * | 2004-08-18 | 2009-12-10 | Пфайзер Инк. | Ингибиторы рнк-зависимой рнк-полимеразы вируса гепатита с, фармацевтическая композиция на их основе и их применение |
| ITMI20041822A1 (it) * | 2004-09-24 | 2004-12-24 | Pharmaproducts Uk Ltd | "agente terapeutico utile per il trattamento di neoplasie plasmacellulari" |
| US20060167057A1 (en) * | 2004-11-16 | 2006-07-27 | Xianqi Kong | Compounds for the treatment of CNS and amyloid associated diseases |
| WO2006085149A2 (en) | 2004-12-22 | 2006-08-17 | Neurochem (International) Limited | Methods and compositions for treating amyloid-related diseases |
| EP1968561B8 (en) * | 2005-12-22 | 2010-10-20 | Kiacta Sàrl | Treatment of diabetic nephropathy |
| PT2089417E (pt) | 2006-10-12 | 2015-04-14 | Bhi Ltd Partnership | Métodos, compostos, composições e veículos para administrar o ácido 3-amino-1-propanossulfónico |
| WO2008078176A1 (en) * | 2006-12-22 | 2008-07-03 | Bellus Health (International) Limited | Methods, compounds, and compositions for treating metabolic disorders and diabetes |
| US20080293648A1 (en) * | 2007-01-05 | 2008-11-27 | Saha Pharmaceuticals, Inc. | Compositions and Methods for Cancer Treatment |
| DE102012103717A1 (de) * | 2012-04-27 | 2013-11-14 | Westfälische Wilhelms-Universität Münster | Arzneimittel zur Behandlung von Tumorerkrankungen |
| WO2015093091A1 (ja) * | 2013-12-19 | 2015-06-25 | 宇部興産株式会社 | 非水電解液、それを用いた蓄電デバイス、及びそれに用いられるホスホノぎ酸化合物 |
| 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 |
| CN109400645A (zh) * | 2017-08-18 | 2019-03-01 | 四川海思科制药有限公司 | 一种磷酸衍生物及制备方法和用途 |
| WO2025106974A1 (en) * | 2023-11-17 | 2025-05-22 | The Board Of Trustees Of The Leland Stanford Junior University | Prodrug moieties and compounds comprising the same |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155597A (en) * | 1961-06-23 | 1964-11-03 | Monsanto Co | Extractive separation process |
| CH513590A (de) | 1968-05-24 | 1971-10-15 | Du Pont | Carbamoylphosphonat enthaltender Pflanzenwachstumsregler |
| US3997544A (en) * | 1968-05-24 | 1976-12-14 | E. I. Du Pont De Nemours And Company | Plant growth regulant carbamoylphosphonates |
| US3846512A (en) * | 1968-05-24 | 1974-11-05 | Du Pont | Carbamoylphosphonates |
| US3533995A (en) * | 1968-08-27 | 1970-10-13 | Fmc Corp | Heat stabilization of polyester resin with alkyl dialkoxyphosphinyl formate |
| GB1317768A (en) | 1969-08-14 | 1973-05-23 | Du Pont | Plant growth regulants |
| US3849102A (en) * | 1969-08-14 | 1974-11-19 | Du Pont | Plant growth regulant method |
| US3767795A (en) * | 1971-02-25 | 1973-10-23 | Abbott Lab | Method for combating certain virus infection |
| HU171255B (hu) | 1973-07-23 | 1977-12-28 | Du Pont | Kompozicii dlja regulirovki rosta rastenijj |
| US3943201A (en) * | 1973-07-23 | 1976-03-09 | E. I. Du Pont De Nemours And Comapny | Alkoxy carboxycarbonylphosphonic acid esters |
| US4017297A (en) * | 1975-08-29 | 1977-04-12 | E. I. Du Pont De Nemours And Company | Phosphonates for the control of bindweed |
| US4092412A (en) * | 1976-04-30 | 1978-05-30 | Abbott Laboratories | Treatment of herpes simplex infections |
| CA1069526A (en) * | 1976-04-30 | 1980-01-08 | Thomas R. Herrin | Phosphorus esters of phosphonoacetic acid |
| US4052439A (en) * | 1976-04-30 | 1977-10-04 | Abbott Laboratories | Carboxylic esters of phosphonoacetic acid |
| SE7607496L (sv) * | 1976-07-01 | 1978-01-02 | Astra Laekemedel Ab | Sett for bekempning av virusinfektioner |
| CA1144937A (en) * | 1977-12-22 | 1983-04-19 | Dke J.E. Helgstrand | Aromatic derivatives, pharmaceutical compositions and methods for combatting virus infections |
-
1978
- 1978-12-06 CA CA000317520A patent/CA1144937A/en not_active Expired
- 1978-12-06 CA CA000317487A patent/CA1140049A/en not_active Expired
- 1978-12-15 DK DK564278A patent/DK148632C/da not_active IP Right Cessation
- 1978-12-15 DK DK564178A patent/DK148631C/da not_active IP Right Cessation
- 1978-12-18 IE IE2493/78A patent/IE48011B1/en not_active IP Right Cessation
- 1978-12-19 DE DE7878850028T patent/DE2861729D1/de not_active Expired
- 1978-12-19 DE DE7878850027T patent/DE2861045D1/de not_active Expired
- 1978-12-19 AU AU42682/78A patent/AU530031B2/en not_active Expired
- 1978-12-19 EP EP78850027A patent/EP0003275B1/en not_active Expired
- 1978-12-19 EP EP78850028A patent/EP0003007B1/en not_active Expired
- 1978-12-20 FI FI783931A patent/FI65438C/fi not_active IP Right Cessation
- 1978-12-20 FI FI783932A patent/FI68626C/fi not_active IP Right Cessation
- 1978-12-21 NO NO784331A patent/NO156611C/no unknown
- 1978-12-21 NO NO784330A patent/NO154751C/no unknown
- 1978-12-22 AT AT0921778A patent/AT369017B/de not_active IP Right Cessation
- 1978-12-22 JP JP15839878A patent/JPS54109951A/ja active Granted
- 1978-12-22 JP JP15839978A patent/JPS54106431A/ja active Granted
-
1979
- 1979-11-13 US US06/093,167 patent/US4386081A/en not_active Expired - Lifetime
- 1979-11-13 US US06/093,166 patent/US4372894A/en not_active Expired - Lifetime
-
1982
- 1982-09-10 US US06/416,632 patent/US4536400A/en not_active Expired - Lifetime
- 1982-12-17 US US06/450,656 patent/US4591583A/en not_active Expired - Fee Related
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1983
- 1983-12-23 SG SG823/83A patent/SG82383G/en unknown
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1984
- 1984-04-18 HK HK335/84A patent/HK33584A/en not_active IP Right Cessation
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1985
- 1985-12-30 MY MY58/85A patent/MY8500058A/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: ASTRA LAEKEMEDEL AKTIEBOLAG |