[go: up one dir, main page]

UA42720C2 - Похідні 10, 11 - метандибензосуберану, хемосенсибілізуюча композиція, спосіб подолання резистентності до протипухлинних ліків та спосіб лікування пухлинних захворювань - Google Patents

Похідні 10, 11 - метандибензосуберану, хемосенсибілізуюча композиція, спосіб подолання резистентності до протипухлинних ліків та спосіб лікування пухлинних захворювань

Info

Publication number
UA42720C2
UA42720C2 UA95114910A UA95114910A UA42720C2 UA 42720 C2 UA42720 C2 UA 42720C2 UA 95114910 A UA95114910 A UA 95114910A UA 95114910 A UA95114910 A UA 95114910A UA 42720 C2 UA42720 C2 UA 42720C2
Authority
UA
Ukraine
Prior art keywords
treating
chemosensitizing
multidrug resistance
composition
methanodibenzosuberane
Prior art date
Application number
UA95114910A
Other languages
English (en)
Russian (ru)
Inventor
Юрг Роланд Пфістер
Юрг Роланд Пфистер
Доріс Лінн Слейт
Дорис Линн Слейт
Original Assignee
Сінтекс (Ю.Ес.Ей.) Інк
Синтекс (Ю.ЭС.ЭЙ.) Инк
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Сінтекс (Ю.Ес.Ей.) Інк, Синтекс (Ю.ЭС.ЭЙ.) Инк filed Critical Сінтекс (Ю.Ес.Ей.) Інк
Publication of UA42720C2 publication Critical patent/UA42720C2/uk

Links

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
    • 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)

Abstract

Похідні 10,11-метандибензосуберану формули I де А означає -CH2-CH2-, -CH 2-CHRаCH2-, де Rа означає Н, ОН або нижчий ацилокси, або -CH2-CHRa-CHRb-CH2-, де один з Ra або Rb означає Н, ОН або нижчий ацилокси, а інший означає Н, R1 означає Н, F, Cl або Вr, R2 означає Н, F, Cl або Вr, і R3 означає гетероарил, що складається із двох конденсованих кілець, які містять від 1 до 3 гетероатомов, вибраних з N, О або S, або їх фармацевтично прийнятні солі, використовувані як хемосенсибілізуючі речовини, наприклад, для лікування раку й для запобігання резистентності до багатьох лікарських препаратів.
UA95114910A 1993-04-19 1994-04-13 Похідні 10, 11 - метандибензосуберану, хемосенсибілізуюча композиція, спосіб подолання резистентності до протипухлинних ліків та спосіб лікування пухлинних захворювань UA42720C2 (uk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/049,065 US5643909A (en) 1993-04-19 1993-04-19 10,11-Methanodibenzosuberane derivatives
PCT/US1994/004215 WO1994024107A1 (en) 1993-04-19 1994-04-13 10,11-methanodibenzosuberane derivatives used as chemosensitizing agents

Publications (1)

Publication Number Publication Date
UA42720C2 true UA42720C2 (uk) 2001-11-15

Family

ID=21957890

Family Applications (1)

Application Number Title Priority Date Filing Date
UA95114910A UA42720C2 (uk) 1993-04-19 1994-04-13 Похідні 10, 11 - метандибензосуберану, хемосенсибілізуюча композиція, спосіб подолання резистентності до протипухлинних ліків та спосіб лікування пухлинних захворювань

Country Status (21)

Country Link
US (5) US5643909A (uk)
EP (2) EP0866063A1 (uk)
JP (1) JP3020607B2 (uk)
KR (1) KR100248591B1 (uk)
CN (2) CN1045204C (uk)
AT (1) ATE172194T1 (uk)
AU (1) AU678470B2 (uk)
BR (1) BR9405965A (uk)
CA (1) CA2160881C (uk)
CZ (1) CZ287273B6 (uk)
DE (1) DE69413958T2 (uk)
DK (1) DK0695293T3 (uk)
ES (1) ES2121603T3 (uk)
FI (1) FI111161B (uk)
HU (2) HU227824B1 (uk)
NO (1) NO313284B1 (uk)
NZ (1) NZ265547A (uk)
PL (1) PL183375B1 (uk)
RU (1) RU2167154C2 (uk)
UA (1) UA42720C2 (uk)
WO (1) WO1994024107A1 (uk)

Families Citing this family (58)

* Cited by examiner, † Cited by third party
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
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
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
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
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
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
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
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
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
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
US5919815A (en) * 1996-05-22 1999-07-06 Neuromedica, Inc. Taxane compounds and compositions
US5795909A (en) 1996-05-22 1998-08-18 Neuromedica, Inc. DHA-pharmaceutical agent conjugates of taxanes
EP0914116B1 (en) * 1996-05-22 2000-10-11 Protarga Inc. Compositions comprising conjugates of cis-docosahexaenoic acid and taxotere
JP2000512997A (ja) 1996-06-17 2000-10-03 イーライ・リリー・アンド・カンパニー 薬物耐性および多薬物耐性調節物質
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
US6342249B1 (en) 1998-12-23 2002-01-29 Alza Corporation Controlled release liquid active agent formulation dosage forms
US6635281B2 (en) 1998-12-23 2003-10-21 Alza Corporation Gastric retaining oral liquid dosage form
US7235583B1 (en) 1999-03-09 2007-06-26 Luitpold Pharmaceuticals, Inc., Fatty acid-anticancer conjugates and uses thereof
CA2373484C (en) 1999-05-19 2009-01-20 Noboru Kaneko Use of 1,4-benzothiazepine derivatives as drugs for overcoming resistance to anticancer drugs
CA2375283A1 (en) * 1999-06-03 2000-12-14 Eli Lilly And Company Process for preparing a 10,11-methanodibenzosuberane derivative
TWI267511B (en) 1999-06-03 2006-12-01 Lilly Co Eli Process for preparing 10,11-methanobenzosuberane derivatives
CA2378984A1 (en) * 1999-08-09 2001-02-15 Richard B. Kim Antiviral therapy use of p-glycoprotein modulators
US6426342B2 (en) * 1999-08-16 2002-07-30 Revaax Pharmaceuticals, Llc Use of β-lactamase inhibitors as neuroprotectants
NZ517663A (en) 1999-08-16 2006-02-24 Revaax Pharmaceuticals Llc Neurotherapeutic clavulanate composition and method
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
PT1387683E (pt) * 2001-04-25 2005-06-30 Lilly Co Eli Novos sais e formas cristalinas de (2r) -anti-5{3-[4-(10,11-difluorometanodibenzosuber-5-il]-2-hidroxipropoxi}quinolina
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
WO2005048981A1 (en) * 2003-11-14 2005-06-02 Alza Corporation Controlled release of topirimate in liquid dosage forms
EP1791520A2 (en) * 2004-08-19 2007-06-06 Alza Corporation Controlled release nanoparticle active agent formulation dosage forms and methods
CN101232868A (zh) * 2005-04-19 2008-07-30 阿尔扎公司 曲马多和加巴喷丁的控释递药剂型
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
US20070009533A1 (en) * 2005-07-06 2007-01-11 Branimir Sikic Treatment of cancer patients exhibiting activation of the P-glycoprotein efflux pump mechanism
US20070009534A1 (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
AU2006269498A1 (en) * 2005-07-06 2007-01-18 Edgar, Mark 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
US20070009532A1 (en) * 2005-07-06 2007-01-11 Branimir Sikic Treatment of patients with cancer using a calicheamicin-antibody conjugate in combination with zosuquidar
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
US20090041806A1 (en) * 2007-06-15 2009-02-12 Xenoport, Inc. Use of prodrugs of gaba analogs, antispasticity agents, and prodrugs of gaba b 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
AU2018375199B2 (en) 2017-12-01 2023-03-30 Ultragenyx Pharmaceutical Inc. Creatine prodrugs, compositions and methods of use thereof

Family Cites Families (21)

* Cited by examiner, † Cited by third party
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 (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

Also Published As

Publication number Publication date
US5643909A (en) 1997-07-01
HK1011981A1 (en) 1999-07-23
EP0695293B1 (en) 1998-10-14
FI954979A7 (fi) 1995-10-18
HU227824B1 (en) 2012-03-28
EP0695293A1 (en) 1996-02-07
PL183375B1 (pl) 2002-06-28
NO954161D0 (no) 1995-10-18
CN1235826A (zh) 1999-11-24
KR100248591B1 (ko) 2000-04-01
US5654304A (en) 1997-08-05
RU2167154C2 (ru) 2001-05-20
FI111161B (fi) 2003-06-13
BR9405965A (pt) 1996-01-30
US6087365A (en) 2000-07-11
EP0866063A1 (en) 1998-09-23
CA2160881C (en) 2000-12-12
PL311164A1 (en) 1996-02-05
DE69413958T2 (de) 1999-03-11
CN1045204C (zh) 1999-09-22
CA2160881A1 (en) 1994-10-27
NO954161L (no) 1995-12-05
CN1119149C (zh) 2003-08-27
WO1994024107A1 (en) 1994-10-27
HU9503004D0 (en) 1995-12-28
CZ287273B6 (en) 2000-10-11
ES2121603T3 (es) 1998-12-01
HU211682A9 (en) 1995-12-28
US5889007A (en) 1999-03-30
AU6636294A (en) 1994-11-08
CZ272495A3 (en) 1996-04-17
FI954979A0 (fi) 1995-10-18
JPH08509223A (ja) 1996-10-01
CN1121346A (zh) 1996-04-24
DE69413958D1 (de) 1998-11-19
AU678470B2 (en) 1997-05-29
ATE172194T1 (de) 1998-10-15
NO313284B1 (no) 2002-09-09
HUT73180A (en) 1996-06-28
JP3020607B2 (ja) 2000-03-15
NZ265547A (en) 1997-03-24
US5874434A (en) 1999-02-23
DK0695293T3 (da) 1999-06-23

Similar Documents

Publication Publication Date Title
UA42720C2 (uk) Похідні 10, 11 - метандибензосуберану, хемосенсибілізуюча композиція, спосіб подолання резистентності до протипухлинних ліків та спосіб лікування пухлинних захворювань
DE3564941D1 (en) Dihydropyridazinones
EP0525472A3 (en) Methylen-oxindole derivatives and process for their preparation
BG103417A (en) Condensed pyrimidine bicyclic derivatives
WO2002009715A3 (en) Use of an arylaldehyde 5-oxo-1, 2, 4-triazine hydrazide for the treatment of cancer
BG103207A (en) Esters of the arylcycloalkanecarboxylic acids, their application, pharmaceutical compositions and their preparation
PL313078A1 (en) Novel bis-naphtalimides for use in treating carcinoma
GR3031114T3 (en) Use of a pregnane derivatives for the treatment of tumours.
BG103271A (en) Derivatives of n-(benzothiazol-2-yl) piperidine-1-ethaneamines, method for their preparation and application as therapeutical means
IE894175L (en) N-pyridinyl-9h-carbazol-9-amines, a process for their¹preparation and their use as medicaments
DE3379255D1 (en) Pyridyl alkyl nitrate compound, process for preparation thereof and pharmaceutical composition comprising the same
MX9601163A (es) Nuevos compuestos derivados de cromeno.
PL318539A1 (en) Inhibition of biosynthesis
ES2101644A1 (es) Nuevo compuesto derivado del cromeno
TW288015B (en) New chromene derivatives
ES8102144A2 (es) Procedimiento para la preparacion de derivados de la isoqui-noleina