ES2121603T3 - Derivados de 10,11-metanodibenzosuberano usados como agentes quimiosensibilizantes. - Google Patents
Derivados de 10,11-metanodibenzosuberano usados como agentes quimiosensibilizantes.Info
- Publication number
- ES2121603T3 ES2121603T3 ES94914200T ES94914200T ES2121603T3 ES 2121603 T3 ES2121603 T3 ES 2121603T3 ES 94914200 T ES94914200 T ES 94914200T ES 94914200 T ES94914200 T ES 94914200T ES 2121603 T3 ES2121603 T3 ES 2121603T3
- Authority
- ES
- Spain
- Prior art keywords
- sub
- sup
- methanodibenzosuberano
- derivatives
- chr
- 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 - Lifetime
Links
Classifications
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- 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
-
- 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)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Addiction (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Neurosurgery (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)
Abstract
LOS DERIVADOS DE 10,11-METANODIBENZOSUBERANO, A SABER, LOS COMPUESTOS DE LA FORMULA (I), EN LA QUE A ES -CH{SUB,2}CH{SUB,2}-, CH{SUB,2}-CHR{SUP,A}-CH{SUB,2}- O -CH{SUB,2}CHR{SUP,A}-CHR{SUP,B}-CH{SUB,2}-, DONDE UNO DE ENTRE R{SUP,A} O R{SUP,B} ES H, OH, O ACILOXI INFERIOR, Y EL OTRO ES HIDROGENO; R{SUP,1} ES H, F, CL O BR; R{SUP,2} ES H, F, CL O BR; Y R{SUP,3} ES HETEROARILO O FENILO OPCIONALMENTE SUSTITUIDO POR F, CL, BR, CF{SUB,3}, CN, NO{SUB,2} U OCHF{SUB,2}; Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS, SON AGENTES QUIMIOSENSIBILIZADORES UTILES, EJ., PARA UNA QUIMIOTERAPIA CONTRA EL CANCER, EN PARTICULAR PARA EL TRATAMIENTO DE UNA RESISTENCIA A MULTIPLES FARMACOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/049,065 US5643909A (en) | 1993-04-19 | 1993-04-19 | 10,11-Methanodibenzosuberane derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2121603T3 true ES2121603T3 (es) | 1998-12-01 |
Family
ID=21957890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES94914200T Expired - Lifetime ES2121603T3 (es) | 1993-04-19 | 1994-04-13 | Derivados de 10,11-metanodibenzosuberano usados como agentes quimiosensibilizantes. |
Country Status (21)
| Country | Link |
|---|---|
| US (5) | US5643909A (es) |
| EP (2) | EP0866063A1 (es) |
| JP (1) | JP3020607B2 (es) |
| KR (1) | KR100248591B1 (es) |
| CN (2) | CN1045204C (es) |
| AT (1) | ATE172194T1 (es) |
| AU (1) | AU678470B2 (es) |
| BR (1) | BR9405965A (es) |
| CA (1) | CA2160881C (es) |
| CZ (1) | CZ287273B6 (es) |
| DE (1) | DE69413958T2 (es) |
| DK (1) | DK0695293T3 (es) |
| ES (1) | ES2121603T3 (es) |
| FI (1) | FI111161B (es) |
| HU (2) | HU227824B1 (es) |
| NO (1) | NO313284B1 (es) |
| NZ (1) | NZ265547A (es) |
| PL (1) | PL183375B1 (es) |
| RU (1) | RU2167154C2 (es) |
| UA (1) | UA42720C2 (es) |
| WO (1) | WO1994024107A1 (es) |
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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| JPH10505348A (ja) | 1994-08-31 | 1998-05-26 | イーライ・リリー・アンド・カンパニー | 耐性腫瘍の同定および治療方法 |
| 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 |
| 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 |
| US5891872A (en) * | 1995-04-07 | 1999-04-06 | Schering Corporation | Tricyclic compounds |
| 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 |
| US5795909A (en) * | 1996-05-22 | 1998-08-18 | Neuromedica, Inc. | DHA-pharmaceutical agent conjugates of taxanes |
| JP4172726B2 (ja) * | 1996-05-22 | 2008-10-29 | ルイトポルド・ファーマシューティカルズ・インコーポレーテッド | シス―ドコサヘキサエン酸とドセタキセルとの共有複合体を含有する製剤 |
| US5919815A (en) * | 1996-05-22 | 1999-07-06 | Neuromedica, Inc. | Taxane compounds and compositions |
| CA2258556A1 (en) * | 1996-06-17 | 1997-12-24 | Julian Stanley Kroin | Drug resistance and multidrug resistance modulators |
| EP0844244A1 (en) * | 1996-11-22 | 1998-05-27 | Eli Lilly And Company | 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 |
| DE60021075T2 (de) | 1999-05-19 | 2006-05-24 | Noboru Kaneko | Verwendung von 1,4-benzothiazepinderivaten als arzneimittel zur überwindung einer resistenz gegenüber einem arzneimittel gegen krebs |
| TWI267511B (en) | 1999-06-03 | 2006-12-01 | Lilly Co Eli | Process for preparing 10,11-methanobenzosuberane derivatives |
| EP1198462B1 (en) | 1999-06-03 | 2004-09-29 | Eli Lilly And Company | Process for preparing a 10,11-methanodibenzosuberane derivative |
| WO2001010387A2 (en) * | 1999-08-09 | 2001-02-15 | Vanderbilt University | Antiviral therapy use of p-glycoprotein modulators |
| US6610681B1 (en) * | 1999-08-16 | 2003-08-26 | Revaax Pharmaceuticals, Llc | Neurotherapeutic clavulanate composition and method |
| US6426342B2 (en) * | 1999-08-16 | 2002-07-30 | Revaax Pharmaceuticals, Llc | Use of β-lactamase inhibitors as neuroprotectants |
| WO2002005818A2 (en) * | 2000-07-18 | 2002-01-24 | Eli Lilly And Company | Novel method of use of multidrug resistance modulators |
| 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 |
| WO2002087581A1 (en) * | 2001-04-25 | 2002-11-07 | Eli Lilly And Company | Novel salt and crystalline forms of (2r)-anti-5-{3-[4-(10,11-difluoromethanodibenzosuber-5-yl)piperazin-1-yl]-2-hydroxypropoxy}quinoline |
| US20050208132A1 (en) * | 2002-07-29 | 2005-09-22 | Gayatri Sathyan | Methods and dosage forms for reducing side effects of benzisozazole derivatives |
| US20050232995A1 (en) | 2002-07-29 | 2005-10-20 | Yam Nyomi V | Methods and dosage forms for controlled delivery of paliperidone and risperidone |
| US20050152967A1 (en) * | 2003-03-28 | 2005-07-14 | Pfab, Lp | Dynamic variable release |
| JP2007511519A (ja) * | 2003-11-14 | 2007-05-10 | アルザ・コーポレーシヨン | 液状投薬形態物におけるトピラメートの制御放出 |
| EP1791520A2 (en) * | 2004-08-19 | 2007-06-06 | Alza Corporation | Controlled release nanoparticle active agent formulation dosage forms and methods |
| CA2605180A1 (en) * | 2005-04-19 | 2006-10-26 | Alza Corporation | Controlled delivery dosage form of tramadol and gabapentin |
| 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 |
| US20070009531A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of patients with cancer using a calicheamicin-antibody conjugate in combination with zosuquidar |
| US20070009533A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism |
| CA2630087A1 (en) * | 2005-07-06 | 2007-01-18 | Kanisa Pharmaceuticals, Inc. | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070010487A1 (en) * | 2005-07-06 | 2007-01-11 | Jeff Schwegman | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070010486A1 (en) * | 2005-07-06 | 2007-01-11 | Jeff Schwegman | Chemotherapeutic formulations of zosuquidar trihydrochloride and modified cyclodextrins |
| US20070009535A1 (en) * | 2005-07-06 | 2007-01-11 | Branimir Sikic | Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism |
| 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 |
| WO2007041079A2 (en) * | 2005-09-30 | 2007-04-12 | Alza Corporation | Banded controlled release nanoparticle active agent formulation dosage forms and methods |
| 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 |
| WO2008157408A2 (en) * | 2007-06-15 | 2008-12-24 | Xenoport, Inc. | Use of prodrugs of gaba analogs, antispasticity agents, and prodrugs of gaba b receptor agonists for treating spasticity |
| MX2011011459A (es) * | 2009-04-29 | 2011-11-18 | Rexahn Pharmaceuticals Inc | Formulacion de clavulanato para neuroproteccion y tratamiento de trastornos neurodegenerativos. |
| 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 |
| IL274701B2 (en) | 2017-12-01 | 2024-07-01 | Ultragenyx Pharmaceutical Inc | Promote drugs, compositions and methods of their use |
Family Cites Families (21)
| 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 |
| JPS5278881A (en) * | 1975-12-24 | 1977-07-02 | Sumitomo Chem Co Ltd | Synthesis of novel morpholine derivativs |
| JPS5278882A (en) * | 1975-12-24 | 1977-07-02 | Sumitomo Chem Co Ltd | Synthesis of novel morpholine derivatives |
| 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 (en) * | 1988-10-06 | 1999-11-16 | Nobuyuki Fukazawa | Heterocyclic compounds and anticancer-drug reinforcing agents containing them as effective components |
| 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 (en) * | 1991-08-26 | 1993-02-27 | Ivo Monkovic | Benzamide multidrug resistance reversing agents |
| 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 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 JP JP6523504A patent/JP3020607B2/ja not_active Expired - Lifetime
- 1994-04-13 CA CA002160881A patent/CA2160881C/en not_active Expired - Lifetime
- 1994-04-13 CN CN94191807A patent/CN1045204C/zh not_active Expired - Lifetime
- 1994-04-13 NZ NZ265547A patent/NZ265547A/en not_active IP Right Cessation
- 1994-04-13 EP EP98100510A patent/EP0866063A1/en not_active Ceased
- 1994-04-13 AU AU66362/94A patent/AU678470B2/en not_active Expired
- 1994-04-13 CZ CZ19952724A patent/CZ287273B6/cs not_active IP Right Cessation
- 1994-04-13 DK DK94914200T patent/DK0695293T3/da active
- 1994-04-13 EP EP94914200A patent/EP0695293B1/en not_active Expired - Lifetime
- 1994-04-13 WO PCT/US1994/004215 patent/WO1994024107A1/en not_active Ceased
- 1994-04-13 ES ES94914200T patent/ES2121603T3/es not_active Expired - Lifetime
- 1994-04-13 BR BR9405965A patent/BR9405965A/pt not_active Application Discontinuation
- 1994-04-13 DE DE69413958T patent/DE69413958T2/de not_active Expired - Lifetime
- 1994-04-13 AT AT94914200T patent/ATE172194T1/de active
- 1994-04-13 UA UA95114910A patent/UA42720C2/uk unknown
-
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
-
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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