FI111161B - Menetelmä kemoherkistävinä aineina käyttökelpoisten 10,11-metanodibentsosuberaanijohdannaisten valmistamiseksi - Google Patents
Menetelmä kemoherkistävinä aineina käyttökelpoisten 10,11-metanodibentsosuberaanijohdannaisten valmistamiseksi Download PDFInfo
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- FI111161B FI111161B FI954979A FI954979A FI111161B FI 111161 B FI111161 B FI 111161B FI 954979 A FI954979 A FI 954979A FI 954979 A FI954979 A FI 954979A FI 111161 B FI111161 B FI 111161B
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- compound
- compounds
- pharmaceutically acceptable
- acid
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 208000037965 uterine sarcoma Diseases 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- CXBGOBGJHGGWIE-IYJDUVQVSA-N vindoline Chemical compound CN([C@H]1[C@](O)([C@@H]2OC(C)=O)C(=O)OC)C3=CC(OC)=CC=C3[C@]11CCN3CC=C[C@]2(CC)[C@@H]13 CXBGOBGJHGGWIE-IYJDUVQVSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Tropical Medicine & Parasitology (AREA)
- Addiction (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Pyridine Compounds (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4906593 | 1993-04-19 | ||
| US08/049,065 US5643909A (en) | 1993-04-19 | 1993-04-19 | 10,11-Methanodibenzosuberane derivatives |
| US9404215 | 1994-04-13 | ||
| PCT/US1994/004215 WO1994024107A1 (fr) | 1993-04-19 | 1994-04-13 | Derives de 10,11-methanodibenzosuberane utilises comme agents de chimiosensibilisation |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI954979A7 FI954979A7 (fi) | 1995-10-18 |
| FI954979A0 FI954979A0 (fi) | 1995-10-18 |
| FI111161B true FI111161B (fi) | 2003-06-13 |
Family
ID=21957890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI954979A FI111161B (fi) | 1993-04-19 | 1995-10-18 | Menetelmä kemoherkistävinä aineina käyttökelpoisten 10,11-metanodibentsosuberaanijohdannaisten valmistamiseksi |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US5643909A (fr) |
| EP (2) | EP0695293B1 (fr) |
| JP (1) | JP3020607B2 (fr) |
| KR (1) | KR100248591B1 (fr) |
| CN (2) | CN1045204C (fr) |
| AT (1) | ATE172194T1 (fr) |
| AU (1) | AU678470B2 (fr) |
| BR (1) | BR9405965A (fr) |
| CA (1) | CA2160881C (fr) |
| CZ (1) | CZ287273B6 (fr) |
| DE (1) | DE69413958T2 (fr) |
| DK (1) | DK0695293T3 (fr) |
| ES (1) | ES2121603T3 (fr) |
| FI (1) | FI111161B (fr) |
| HU (2) | HU227824B1 (fr) |
| NO (1) | NO313284B1 (fr) |
| NZ (1) | NZ265547A (fr) |
| PL (1) | PL183375B1 (fr) |
| RU (1) | RU2167154C2 (fr) |
| UA (1) | UA42720C2 (fr) |
| WO (1) | WO1994024107A1 (fr) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5643909A (en) * | 1993-04-19 | 1997-07-01 | Syntex (U.S.A.) Inc. | 10,11-Methanodibenzosuberane derivatives |
| US5661152A (en) * | 1993-10-15 | 1997-08-26 | Schering Corporation | Tricyclic sulfonamide compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US6365588B1 (en) | 1993-10-15 | 2002-04-02 | Schering Corporation | Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US6075025A (en) | 1993-10-15 | 2000-06-13 | Schering Corporation | Tricyclic carbamate compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US5721236A (en) * | 1993-10-15 | 1998-02-24 | Schering Corporation | Tricyclic carbamate compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US5719148A (en) * | 1993-10-15 | 1998-02-17 | Schering Corporation | Tricyclic amide and urea compounds useful for inhibition of g-protein function and for treatment of proliferative diseases |
| US5567592A (en) * | 1994-02-02 | 1996-10-22 | Regents Of The University Of California | Screening method for the identification of bioenhancers through the inhibition of P-glycoprotein transport in the gut of a mammal |
| EP0777472A2 (fr) | 1994-08-31 | 1997-06-11 | Eli Lilly And Company | Procedes d'identification et de traitement de tumeurs resistantes |
| US5684013A (en) * | 1995-03-24 | 1997-11-04 | Schering Corporation | Tricyclic compounds useful for inhibition of g-protein function and for treatment of proliferative diseases |
| US5700806A (en) * | 1995-03-24 | 1997-12-23 | Schering Corporation | Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US5801175A (en) | 1995-04-07 | 1998-09-01 | Schering Corporation | Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US5891872A (en) * | 1995-04-07 | 1999-04-06 | Schering Corporation | Tricyclic compounds |
| US5712280A (en) * | 1995-04-07 | 1998-01-27 | Schering Corporation | Tricyclic compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| US5874442A (en) * | 1995-12-22 | 1999-02-23 | Schering-Plough Corporation | Tricyclic amides useful for inhibition of G-protein function and for treatment of proliferative disease |
| ES2151277T3 (es) * | 1996-05-22 | 2000-12-16 | Protarga Inc | Composiciones que comprenden conjugados de acido cis-docosahexaenoico y taxotere. |
| US5795909A (en) | 1996-05-22 | 1998-08-18 | Neuromedica, Inc. | DHA-pharmaceutical agent conjugates of taxanes |
| US5919815A (en) * | 1996-05-22 | 1999-07-06 | Neuromedica, Inc. | Taxane compounds and compositions |
| AU3486297A (en) * | 1996-06-17 | 1998-01-07 | Eli Lilly And Company | Drug resistance and multidrug resistance modulators |
| IL130055A0 (en) * | 1996-11-22 | 2000-02-29 | Lilly Co Eli | Drug resistance and multidrug resistance modulators |
| US6268500B1 (en) | 1997-01-31 | 2001-07-31 | Eli Lilly And Company | Separation of 5-nitroquinoline and 8-nitroquinoline |
| US5776939A (en) * | 1997-06-12 | 1998-07-07 | Eli Lilly And Company | Drug resistance and multidrug resistance modulators |
| US6635281B2 (en) | 1998-12-23 | 2003-10-21 | Alza Corporation | Gastric retaining oral liquid dosage form |
| US6342249B1 (en) | 1998-12-23 | 2002-01-29 | Alza Corporation | Controlled release liquid active agent formulation dosage forms |
| US7235583B1 (en) | 1999-03-09 | 2007-06-26 | Luitpold Pharmaceuticals, Inc., | Fatty acid-anticancer conjugates and uses thereof |
| CA2373484C (fr) | 1999-05-19 | 2009-01-20 | Noboru Kaneko | Utilisation de derives 1,4-benzothiazepine en tant que medicaments contre la tolerance cancerostatique |
| TWI267511B (en) | 1999-06-03 | 2006-12-01 | Lilly Co Eli | Process for preparing 10,11-methanobenzosuberane derivatives |
| DE60014386T2 (de) | 1999-06-03 | 2005-10-13 | Eli Lilly And Co., Indianapolis | Verfahren zur herstellung von 10,11methanodibenzosuberanderivaten |
| WO2001010387A2 (fr) * | 1999-08-09 | 2001-02-15 | Vanderbilt University | Utilisation de modulateurs de p-glycoproteine dans un traitement antiviral |
| US6426342B2 (en) * | 1999-08-16 | 2002-07-30 | Revaax Pharmaceuticals, Llc | Use of β-lactamase inhibitors as neuroprotectants |
| ATE518540T1 (de) * | 1999-08-16 | 2011-08-15 | Revaax Pharmaceuticals Llc | Beta-lactam verbindung enthaltende neurotherapeutische zusammensetzung |
| WO2002005818A2 (fr) * | 2000-07-18 | 2002-01-24 | Eli Lilly And Company | Methode d'utilisation de modulateurs de la resistance multiple aux medicaments |
| US7342016B2 (en) | 2000-08-30 | 2008-03-11 | Schering Corporation | Farnesyl protein transferase inhibitors as antitumor agents |
| US6376514B1 (en) | 2000-10-17 | 2002-04-23 | The Procter & Gamble Co. | Substituted six-membered heterocyclic compounds useful for treating multidrug resistance and compositions and methods thereof |
| US6693099B2 (en) | 2000-10-17 | 2004-02-17 | The Procter & Gamble Company | Substituted piperazine compounds optionally containing a quinolyl moiety for treating multidrug resistance |
| DE60202944T2 (de) * | 2001-04-25 | 2006-03-23 | Eli Lilly And Co., Indianapolis | Neue salze und kristalline formen von (2r)-anti-5-3-(4-(10,11-difluoromethanodibenzosuber-5-yl)piperazin-1-yl)-2-hydroxypropoxy quinolin |
| US20050232995A1 (en) | 2002-07-29 | 2005-10-20 | Yam Nyomi V | Methods and dosage forms for controlled delivery of paliperidone and risperidone |
| US20050208132A1 (en) * | 2002-07-29 | 2005-09-22 | Gayatri Sathyan | Methods and dosage forms for reducing side effects of benzisozazole derivatives |
| US20050152967A1 (en) * | 2003-03-28 | 2005-07-14 | Pfab, Lp | Dynamic variable release |
| AU2004291081A1 (en) * | 2003-11-14 | 2005-06-02 | Alza Corporation | Controlled release of topirimate in liquid dosage forms |
| WO2006023286A2 (fr) * | 2004-08-19 | 2006-03-02 | Alza Corporation | Formes posologiques renfermant une formulation d'agent actif nanoparticulaire a liberation retardee et procedes |
| KR20080005429A (ko) * | 2005-04-19 | 2008-01-11 | 알자 코포레이션 | 트라마돌 및 가바펜틴을 포함하는 물질의 배합물 |
| US20070010486A1 (en) * | 2005-07-06 | 2007-01-11 | Jeff Schwegman | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070009531A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of patients with cancer using a calicheamicin-antibody conjugate in combination with zosuquidar |
| US20070009535A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism |
| US20070010478A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Zosuquidar, daunorubicin, and cytarabine for the treatment of cancer |
| US20070009534A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism |
| AU2006269498A1 (en) * | 2005-07-06 | 2007-01-18 | Edgar, Mark | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070009533A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism |
| US20070010487A1 (en) * | 2005-07-06 | 2007-01-11 | Jeff Schwegman | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070010485A1 (en) * | 2005-07-06 | 2007-01-11 | Jeff Schwegman | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| AR055099A1 (es) * | 2005-07-28 | 2007-08-08 | Alza Corp | Formulaciones liquidas para la administracion controlada de derivados de bencisoxazol |
| EP1933811A2 (fr) * | 2005-09-30 | 2008-06-25 | Alza Corporation | Formes posologiques a liberation regulee a bandelettes renfermant des preparations d'agents actifs nanoparticulaires |
| PL116330U1 (en) * | 2005-10-31 | 2007-04-02 | Alza Corp | Method for the reduction of alcohol provoked rapid increase in the released dose of the orally administered opioide with prolonged liberation |
| TW200908957A (en) * | 2007-06-15 | 2009-03-01 | Xenoport Inc | Use of prodrugs of GABA analogs, antispasticity agents, and prodrugs of GABAB receptor agonists for treating spasticity |
| CN102413814A (zh) * | 2009-04-29 | 2012-04-11 | 瑞恩药品公司 | 用于神经保护和治疗神经变性病症的克拉维酸类物质制剂 |
| US9617230B2 (en) | 2014-12-22 | 2017-04-11 | Farmington Pharma Development | Creatine prodrugs, compositions and methods of use thereof |
| US11240349B2 (en) | 2014-12-31 | 2022-02-01 | Ebay Inc. | Multimodal content recognition and contextual advertising and content delivery |
| US11332438B2 (en) | 2017-12-01 | 2022-05-17 | Ultragenyx Pharmaceutical Inc. | Creatine prodrugs, compositions and methods of use thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3133925A (en) * | 1960-12-22 | 1964-05-19 | Searle & Co | Ether derivatives of n-benzhydryl-n'-dihydroxypropylpiperazines and homopiperazines |
| GB1317034A (en) * | 1970-11-06 | 1973-05-16 | Pfizer Ltd | 1-2-hydroxy-3-phenoxy- or -phenylthiopropyl-piperazine derivatives |
| IT1037099B (it) * | 1975-01-24 | 1979-11-10 | Erba Carlo Spa | N derivati tricilici dell azetidina |
| US4015003A (en) * | 1975-09-26 | 1977-03-29 | E. I. Du Pont De Nemours And Company | Antidepressant 1,1a,6,10b-tetrahydrodibenzo[a,e]-cyclopropa-[c]-cyclohepten-6-substituted oximes |
| JPS5278882A (en) * | 1975-12-24 | 1977-07-02 | Sumitomo Chem Co Ltd | Synthesis of novel morpholine derivatives |
| JPS5278881A (en) * | 1975-12-24 | 1977-07-02 | Sumitomo Chem Co Ltd | Synthesis of novel morpholine derivativs |
| JPS5278884A (en) * | 1975-12-25 | 1977-07-02 | Sumitomo Chem Co Ltd | Synthesis of novel morpholine derivatives |
| JPS52105184A (en) * | 1976-02-26 | 1977-09-03 | Sumitomo Chem Co Ltd | Novel morpholine derivatives |
| GB2163150B (en) * | 1984-07-19 | 1988-05-25 | Sandoz Ltd | 3-aminopropoxyaryl derivatives |
| JPS6147466A (ja) * | 1984-08-10 | 1986-03-07 | Dainippon Pharmaceut Co Ltd | アミン誘導体 |
| DE3600390A1 (de) * | 1986-01-09 | 1987-07-16 | Hoechst Ag | Diarylalkyl-substituierte alkylamine, verfahren zu ihrer herstellung, ihre verwendung sowie sie enthaltende arzneimittel |
| JPH0278884A (ja) * | 1987-11-06 | 1990-03-19 | Sanyo Electric Co Ltd | 断熱箱体の内箱 |
| JPH0278881A (ja) * | 1988-09-13 | 1990-03-19 | Waaku:Kk | 真空冷却装置 |
| JPH0278882A (ja) * | 1988-09-14 | 1990-03-19 | Toshiba Corp | 冷蔵庫 |
| CA1340821C (fr) * | 1988-10-06 | 1999-11-16 | Nobuyuki Fukazawa | Composes heterocycliques, ainsi que des adjuvants de produits anti-cancereux les comprenant |
| JPH02105184A (ja) * | 1988-10-14 | 1990-04-17 | Canon Inc | 現像装置 |
| JP2781073B2 (ja) * | 1991-02-16 | 1998-07-30 | 三井化学株式会社 | 新規キノリン誘導体及びそれを有効成分として含有する制癌剤効果増強剤 |
| JPH0525168A (ja) * | 1991-07-15 | 1993-02-02 | Kyorin Pharmaceut Co Ltd | 癌細胞に対する感受性増強剤及びその製造方法 |
| CA2074061A1 (fr) * | 1991-08-26 | 1993-02-27 | Ivo Monkovic | Benzamides, agents d'inversion de la resistance multiple aux anti-cancereux |
| JP3076672B2 (ja) * | 1992-06-18 | 2000-08-14 | 三井化学株式会社 | キノリン誘導体のフマル酸塩 |
| US5643909A (en) * | 1993-04-19 | 1997-07-01 | Syntex (U.S.A.) Inc. | 10,11-Methanodibenzosuberane derivatives |
-
1993
- 1993-04-19 US US08/049,065 patent/US5643909A/en not_active Expired - Lifetime
-
1994
- 1994-04-13 KR KR1019950704552A patent/KR100248591B1/ko not_active Expired - Lifetime
- 1994-04-13 NZ NZ265547A patent/NZ265547A/en not_active IP Right Cessation
- 1994-04-13 DK DK94914200T patent/DK0695293T3/da active
- 1994-04-13 EP EP94914200A patent/EP0695293B1/fr not_active Expired - Lifetime
- 1994-04-13 DE DE69413958T patent/DE69413958T2/de not_active Expired - Lifetime
- 1994-04-13 HU HU9503004A patent/HU227824B1/hu unknown
- 1994-04-13 RU RU95120598/04A patent/RU2167154C2/ru active
- 1994-04-13 PL PL94311164A patent/PL183375B1/pl unknown
- 1994-04-13 CZ CZ19952724A patent/CZ287273B6/cs not_active IP Right Cessation
- 1994-04-13 WO PCT/US1994/004215 patent/WO1994024107A1/fr not_active Ceased
- 1994-04-13 CN CN94191807A patent/CN1045204C/zh not_active Expired - Lifetime
- 1994-04-13 EP EP98100510A patent/EP0866063A1/fr not_active Ceased
- 1994-04-13 AU AU66362/94A patent/AU678470B2/en not_active Expired
- 1994-04-13 BR BR9405965A patent/BR9405965A/pt not_active Application Discontinuation
- 1994-04-13 JP JP6523504A patent/JP3020607B2/ja not_active Expired - Lifetime
- 1994-04-13 AT AT94914200T patent/ATE172194T1/de active
- 1994-04-13 UA UA95114910A patent/UA42720C2/uk unknown
- 1994-04-13 ES ES94914200T patent/ES2121603T3/es not_active Expired - Lifetime
- 1994-04-13 CA CA002160881A patent/CA2160881C/fr not_active Expired - Lifetime
-
1995
- 1995-05-08 US US08/435,070 patent/US5654304A/en not_active Expired - Lifetime
- 1995-05-08 US US08/436,992 patent/US5889007A/en not_active Expired - Lifetime
- 1995-06-20 HU HU95P/P00274P patent/HU211682A9/hu unknown
- 1995-10-18 FI FI954979A patent/FI111161B/fi not_active IP Right Cessation
- 1995-10-18 NO NO19954161A patent/NO313284B1/no not_active IP Right Cessation
-
1997
- 1997-02-03 US US08/792,746 patent/US5874434A/en not_active Expired - Lifetime
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1999
- 1999-01-25 US US09/236,525 patent/US6087365A/en not_active Expired - Fee Related
- 1999-04-22 CN CN99105238A patent/CN1119149C/zh not_active Expired - Lifetime
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| Date | Code | Title | Description |
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| MA | Patent expired |