JPH11510141A5 - - Google Patents

Info

Publication number
JPH11510141A5
JPH11510141A5 JP1997506890A JP50689097A JPH11510141A5 JP H11510141 A5 JPH11510141 A5 JP H11510141A5 JP 1997506890 A JP1997506890 A JP 1997506890A JP 50689097 A JP50689097 A JP 50689097A JP H11510141 A5 JPH11510141 A5 JP H11510141A5
Authority
JP
Japan
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.)
Granted
Application number
JP1997506890A
Other languages
English (en)
Japanese (ja)
Other versions
JPH11510141A (ja
JP4422796B2 (ja
Filing date
Publication date
Priority claimed from US08/505,439 external-priority patent/US5728707A/en
Application filed filed Critical
Priority claimed from PCT/US1996/011957 external-priority patent/WO1997003668A1/en
Publication of JPH11510141A publication Critical patent/JPH11510141A/ja
Publication of JPH11510141A5 publication Critical patent/JPH11510141A5/ja
Application granted granted Critical
Publication of JP4422796B2 publication Critical patent/JP4422796B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP50689097A 1995-07-21 1996-07-18 アミノイミダゾールカルボキサミドおよび５−アミノ、または置換アミノ１，２，３−トリアゾールの塩による癌の治療および阻止 Expired - Fee Related JP4422796B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US08/505,439 US5728707A (en) 1995-07-21 1995-07-21 Treatment and prevention of primary and metastatic neoplasms with salts of aminoimidazole carboxamide
US08/505,439 1995-07-21
US08/684,297 US5861406A (en) 1995-07-21 1996-07-18 Treatment and prevention of neoplasms with salts of aminoimidazole carboxamide and 5-amino or substituted amino 1,2,3-triazoles
US08/684,297 1996-07-18
PCT/US1996/011957 WO1997003668A1 (en) 1995-07-21 1996-07-18 Treatment and prevention of neoplasms with salts of aminoimidazole carboxamide and 5-amino or substituted amino 1,2,3-triazoles

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2008027656A Division JP4842286B2 (ja) 1995-07-21 2008-02-07 アミノイミダゾールカルボキサミドの塩による腫瘍の治療および阻止

Publications (3)

Publication Number Publication Date
JPH11510141A JPH11510141A (ja) 1999-09-07
JPH11510141A5 true JPH11510141A5 (2) 2004-08-26
JP4422796B2 JP4422796B2 (ja) 2010-02-24

Family

ID=27055145

Family Applications (2)

Application Number Title Priority Date Filing Date
JP50689097A Expired - Fee Related JP4422796B2 (ja) 1995-07-21 1996-07-18 アミノイミダゾールカルボキサミドおよび５−アミノ、または置換アミノ１，２，３−トリアゾールの塩による癌の治療および阻止
JP2008027656A Expired - Fee Related JP4842286B2 (ja) 1995-07-21 2008-02-07 アミノイミダゾールカルボキサミドの塩による腫瘍の治療および阻止

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2008027656A Expired - Fee Related JP4842286B2 (ja) 1995-07-21 2008-02-07 アミノイミダゾールカルボキサミドの塩による腫瘍の治療および阻止

Country Status (10)

Country Link
US (2) US5912346A (2)
EP (1) EP0840608B1 (2)
JP (2) JP4422796B2 (2)
CN (1) CN1318029C (2)
AT (1) ATE278399T1 (2)
AU (1) AU725035B2 (2)
CA (2) CA2227205C (2)
DE (1) DE69633566T2 (2)
IL (1) IL122782A (2)
WO (1) WO1997003668A1 (2)

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US6184227B1 (en) * 1995-07-21 2001-02-06 Savvipharm Inc. Salts of aminoimidazole carboxamide useful in the prevention and treatment of liver diseases
US20040072889A1 (en) * 1997-04-21 2004-04-15 Pharmacia Corporation Method of using a COX-2 inhibitor and an alkylating-type antineoplastic agent as a combination therapy in the treatment of neoplasia
DE69924004T2 (de) * 1998-12-22 2006-02-09 United States Of America Represented By The Secretary, Department Of Health & Human Services Verabreichungssystem für wasserunlösliche arzneistoffe
US20040122011A1 (en) * 1998-12-23 2004-06-24 Pharmacia Corporation Method of using a COX-2 inhibitor and a TACE inhibitors as a combination therapy
AU2001271341A1 (en) * 2000-06-20 2002-01-02 Arthur L. Herbst COX-2 inhibitors and the prevention of the side effects of radiation therapy
EP1353693B1 (en) 2001-01-16 2005-03-16 Glaxo Group Limited Pharmaceutical combination containing a 4-quinazolineamine and paclitaxel, carboplatin or vinorelbine for the treatment of cancer
KR100686537B1 (ko) * 2001-12-28 2007-02-27 씨제이 주식회사 사이클로옥시게나제-2 의 저해제로서 선택성이 뛰어난디아릴 1,2,4-트리아졸 유도체
US20030220374A1 (en) * 2002-01-14 2003-11-27 Pharmacia Corporation Compositions and methods of treatment involving peroxisome proliferator-activated receptor-gamma agonists and cyclooxygenase-2 selective inhibitors
US20030212138A1 (en) * 2002-01-14 2003-11-13 Pharmacia Corporation Combinations of peroxisome proliferator-activated receptor-alpha agonists and cyclooxygenase-2 selective inhibitors and therapeutic uses therefor
US20040147581A1 (en) * 2002-11-18 2004-07-29 Pharmacia Corporation Method of using a Cox-2 inhibitor and a 5-HT1A receptor modulator as a combination therapy
DE60332387D1 (de) 2002-12-13 2010-06-10 Warner Lambert Co Alpha-2-delta-ligand zur behandlung vonsymptomen der unteren harnwege
US20040220155A1 (en) * 2003-03-28 2004-11-04 Pharmacia Corporation Method of providing a steroid-sparing benefit with a cyclooxygenase-2 inhibitor and compositions therewith
WO2005009342A2 (en) * 2003-07-16 2005-02-03 Pharmacia Corporation Method for the treatment or prevention of dermatological disorders with a cyclooxygenase-2 inhibitor alone and in combination with a dermatological treatment agent and compositions therewith
US20050119262A1 (en) * 2003-08-21 2005-06-02 Pharmacia Corporation Method for preventing or treating an optic neuropathy with a cox-2 inhibitor and an intraocular pressure reducing agent
US20050107350A1 (en) * 2003-08-22 2005-05-19 Pharmacia Corporation Method for the treatment or prevention of bone disorders with a cyclooxygenase-2 inhibitor alone and in combination with a bone disorder treatment agent and compositions therewith
US20050187278A1 (en) * 2003-08-28 2005-08-25 Pharmacia Corporation Treatment or prevention of vascular disorders with Cox-2 inhibitors in combination with cyclic AMP-specific phosphodiesterase inhibitors
WO2005023189A2 (en) * 2003-09-03 2005-03-17 Pharmacia Corporation Method of cox-2 selective inhibitor and nitric oxide-donating agent
JP2007518788A (ja) 2004-01-22 2007-07-12 ファイザー・インク バソプレッシンのアンタゴニスト活性を阻害するトリアゾール誘導体
US7276050B2 (en) * 2004-03-02 2007-10-02 Alan Franklin Trans-scleral drug delivery method and apparatus
CA2563963A1 (en) * 2004-04-28 2005-11-10 Pfizer Inc. 3-heterocyclyl-4-phenyl-triazole derivatives as inhibitors of the vasopressin v1a receptor
KR100615277B1 (ko) 2004-08-18 2006-08-25 엠텍비젼 주식회사 이미지 센서에서의 렌즈 셰이딩 현상 보정 방법 및 장치
US7601834B2 (en) * 2005-02-22 2009-10-13 Savvipharm Inc Compositions and methods of reducing side effects and toxicity of methotrexate when given as orotate derivatives
US8034823B2 (en) * 2005-02-22 2011-10-11 Savvipharm Inc Method of increasing drug oral bioavailability and compositions of less toxic orotate salts
US7470672B2 (en) * 2006-07-31 2008-12-30 Savvipharm Inc. Compositions and methods of reducing tissue levels of drugs when given as orotate derivatives
US7750018B2 (en) * 2006-12-06 2010-07-06 Tactical Therapeutics, Inc Use of carboxiamidotriazole (CAI) orotate in macular degeneration
ATE511860T1 (de) 2006-12-22 2011-06-15 Recordati Ireland Ltd Kombinationstherapie für erkrankungen der unteren harnwege mit 2 liganden und nsar
US8146798B2 (en) 2008-11-07 2012-04-03 Advanced Custom Engineered Systems & Equipment Co. Method and apparatus for monitoring waste removal and administration
RU2405833C2 (ru) * 2008-12-26 2010-12-10 Федеральное государственное унитарное предприятие "Государственный научно-исследовательский институт генетики и селекции промышленных микроорганизмов" (ФГУП ГосНИИгенетика) Способ микробиологического синтеза пуринового нуклеозида 5'-аминоимидазол-4-карбоксамидрибозида (аикар) и штамм бактерий bacillus subtilis - продуцент аикар
CA2772075C (en) * 2009-09-04 2017-02-28 Rashida A. Karmali Novel compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazole orotate formulations
US8912223B2 (en) 2009-09-04 2014-12-16 Tactical Therapeutics Inc Compositions and processes for preparing 5-amino or substituted amino 1,2,3-triazoles and triazoles orotate formulations
ATE536870T1 (de) 2009-09-25 2011-12-15 Iasomai Aktiebolag N-acetyl-l-cystein zur behandlung von endometriose
US9089570B2 (en) * 2010-09-03 2015-07-28 Tactical Therapeutics Inc Compositions for treating cancers having acquired resitance to prior chemotherapeutic and targeted drugs using carboxyamidotriazole orotate
CN102586187A (zh) * 2012-02-23 2012-07-18 深圳市中美康士生物科技有限公司 一种中性粒细胞体外保存方法及培养基
US10378059B2 (en) * 2013-08-02 2019-08-13 Tactical Therapeutics, Inc. Methods and molecular pharmacodynamic biomarkers for multiple signaling pathways in response to carboxyamidotriazole orotate
JP6619758B2 (ja) 2014-07-03 2019-12-11 ボード・オブ・リージエンツ，ザ・ユニバーシテイ・オブ・テキサス・システム 疾患を処置するためのｇｌｓ１阻害薬
ES2794868T3 (es) 2015-06-30 2020-11-19 Univ Texas Inhibidores de GLS1 para el tratamiento de enfermedades
MX384732B (es) 2015-12-22 2025-03-14 Univ Texas Formas de sales y polimorfos de (r)-1-(4-(6-(2-(4-(3,3-difluorociclobutoxi)-6-metilpiridin-2-il)acetamido)piridazin-3-il)-2-fluorobutil)-n-metil-1h-1,2,3-triazol-4-carboxamida.
CN109906082A (zh) 2016-09-07 2019-06-18 塔夫茨大学信托人 使用免疫dash抑制剂和pge2拮抗剂的组合治疗
RU2020112558A (ru) 2017-10-18 2021-11-18 Боард Оф Регентс, Зе Юниверсити Оф Тексас Систем Терапия на основе ингибитора глутаминазы
CN116854644B (zh) * 2023-07-06 2025-10-21 浙江大学 5-氨基-1-烷基-1h-1,2,3-三氮唑-4-甲酰胺类化合物及其制备和应用

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DE1210865B (de) * 1962-03-05 1966-02-17 Fujisawa Pharmaceutical Co Verfahren zur Herstellung des 2, 6-dioxo-tetrahydropyrimidin-4-carbonsauren Salzes des 4-Amino-5-imidazolcarbonsaeureamids
DE1227190B (de) * 1962-08-02 1966-10-20 Fujisawa Pharmaceutical Co Verfahren zur Herstellung von haltbaren und injizierbaren Loesungen der Salze des 4-Amino-5-imidazolcarboxamids mit organischen Saeuren
US3997518A (en) * 1970-12-09 1976-12-14 Beecham Group Limited 2-Alkyl-4-carboxyalkyl-5-(3,3'-dimethyltriazeno)-imidazoles
JPS5283750A (en) * 1976-01-01 1977-07-12 Ajinomoto Co Inc Crystals of 5-amino-4-imidazol-carboxyamide
RO70184A2 (ro) * 1976-12-30 1981-08-30 Institutul Oncologic,Ro Procedeu de preparare a clorhidratului de 4(5)-amino-5(4)imidazol carboxamida
HUT36464A (en) * 1983-05-24 1985-09-30 Newport Pharmaceuticals Process for producing erythro-4-amino-3-/2-hydroxy-3-alkyl/-imidazol-5-carboxamide
HU190597B (en) * 1983-07-11 1986-09-29 Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu Process for preparing synrtgetic pharmaceutical compositions
US4590201A (en) * 1984-02-02 1986-05-20 Merck & Co., Inc. 5-amino or substituted amino 1,2,3-triazoles
US4752611A (en) * 1985-11-29 1988-06-21 Merck & Co., Inc. Anticoccidial 1,2,3-trazole compounds
US4847257A (en) * 1987-08-20 1989-07-11 Merck & Co., Inc. 5-Amino or substituted amino 1,2,3,-triazoles useful as antiproliferative agents
US4923885A (en) * 1988-08-19 1990-05-08 Merck & Co., Inc. 5-amino-1-(4-naphthoylbenzyl)-1,2,3-triazole-4-carboxamides and analogs as antiproliferative agents
US5359078A (en) * 1989-05-19 1994-10-25 The United States Of America As Represented By The Department Of Health And Human Services Signal transduction inhibitor compounds
US5132315A (en) * 1989-05-19 1992-07-21 The United States Of America As Represented By The Department Of Health And Human Services Therapeutic application of an anti-invasive compound
US5498620A (en) * 1989-05-19 1996-03-12 The United States Of America As Represented By The Department Of Health And Human Services Signal transduction inhibitor 1,2,3-triazolo compounds
US5728707A (en) * 1995-07-21 1998-03-17 Constantia Gruppe Treatment and prevention of primary and metastatic neoplasms with salts of aminoimidazole carboxamide

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