JP2004509061A5 - - Google Patents

Download PDF

Info

Publication number
JP2004509061A5
JP2004509061A5 JP2001559475A JP2001559475A JP2004509061A5 JP 2004509061 A5 JP2004509061 A5 JP 2004509061A5 JP 2001559475 A JP2001559475 A JP 2001559475A JP 2001559475 A JP2001559475 A JP 2001559475A JP 2004509061 A5 JP2004509061 A5 JP 2004509061A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
pharmaceutically acceptable
hepatitis
virus
use according
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.)
Granted
Application number
JP2001559475A
Other languages
English (en)
Japanese (ja)
Other versions
JP4975930B2 (ja
JP2004509061A (ja
Filing date
Publication date
Priority claimed from US09/595,365 external-priority patent/US6455508B1/en
Application filed filed Critical
Publication of JP2004509061A publication Critical patent/JP2004509061A/ja
Publication of JP2004509061A5 publication Critical patent/JP2004509061A5/ja
Application granted granted Critical
Publication of JP4975930B2 publication Critical patent/JP4975930B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2001559475A 2000-02-15 2001-02-15 カルボキサミジンで修飾した単環式塩基を有するヌクレオシドアナログ Expired - Fee Related JP4975930B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US18267600P 2000-02-15 2000-02-15
US60/182,676 2000-02-15
US09/595,365 2000-06-16
US09/595,365 US6455508B1 (en) 2000-02-15 2000-10-05 Methods for treating diseases with tirazole and pyrrolo-pyrimidine ribofuranosyl nucleosides
PCT/US2001/040148 WO2001060379A1 (en) 2000-02-15 2001-02-15 Nucleoside analogs with carboxamidine modified monocyclic base

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2009018382A Division JP5253204B2 (ja) 2000-02-15 2009-01-29 カルボキサミジンで修飾した単環式塩基を有するヌクレオシドアナログ

Publications (3)

Publication Number Publication Date
JP2004509061A JP2004509061A (ja) 2004-03-25
JP2004509061A5 true JP2004509061A5 (enExample) 2006-01-05
JP4975930B2 JP4975930B2 (ja) 2012-07-11

Family

ID=26878297

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2001559475A Expired - Fee Related JP4975930B2 (ja) 2000-02-15 2001-02-15 カルボキサミジンで修飾した単環式塩基を有するヌクレオシドアナログ
JP2001559477A Pending JP2004510691A (ja) 2000-02-15 2001-02-15 カルボキサミジンで修飾した二環式塩基を有するヌクレオシドアナログ
JP2009018382A Expired - Fee Related JP5253204B2 (ja) 2000-02-15 2009-01-29 カルボキサミジンで修飾した単環式塩基を有するヌクレオシドアナログ

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2001559477A Pending JP2004510691A (ja) 2000-02-15 2001-02-15 カルボキサミジンで修飾した二環式塩基を有するヌクレオシドアナログ
JP2009018382A Expired - Fee Related JP5253204B2 (ja) 2000-02-15 2009-01-29 カルボキサミジンで修飾した単環式塩基を有するヌクレオシドアナログ

Country Status (28)

Country Link
US (1) US6455508B1 (enExample)
EP (3) EP1278528A4 (enExample)
JP (3) JP4975930B2 (enExample)
KR (2) KR100811927B1 (enExample)
CN (2) CN1420779A (enExample)
AT (1) ATE377422T1 (enExample)
AU (2) AU3845001A (enExample)
BR (2) BR0108401A (enExample)
CA (2) CA2395854A1 (enExample)
CY (1) CY1107103T1 (enExample)
CZ (2) CZ20022799A3 (enExample)
DE (1) DE60131250T8 (enExample)
DK (1) DK1257281T3 (enExample)
ES (2) ES2295148T3 (enExample)
HR (2) HRP20020583A2 (enExample)
HU (2) HUP0300912A2 (enExample)
IL (3) IL150990A0 (enExample)
MX (2) MXPA02007931A (enExample)
NO (2) NO20023852L (enExample)
NZ (2) NZ521390A (enExample)
PL (2) PL200140B1 (enExample)
PT (1) PT1257281E (enExample)
RS (1) RS20090086A (enExample)
RU (2) RU2002120483A (enExample)
SI (2) SI21077A (enExample)
SK (2) SK287765B6 (enExample)
WO (2) WO2001060379A1 (enExample)
YU (1) YU61502A (enExample)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6831069B2 (en) * 1999-08-27 2004-12-14 Ribapharm Inc. Pyrrolo[2,3-d]pyrimidine nucleoside analogs
US7056895B2 (en) * 2000-02-15 2006-06-06 Valeant Pharmaceuticals International Tirazole nucleoside analogs and methods for using same
US7638496B2 (en) * 2000-02-15 2009-12-29 Valeant Pharmaceuticals North America Nucleoside analogs with carboxamidine modified monocyclic base
MY164523A (en) * 2000-05-23 2017-12-29 Univ Degli Studi Cagliari Methods and compositions for treating hepatitis c virus
IL153020A0 (en) 2000-05-26 2003-06-24 Idenix Cayman Ltd Methods and compositions for treating flaviviruses and pestiviruses
DZ3487A1 (fr) 2001-01-22 2002-07-25 Merck Sharp & Dohme Derives de nucleoside comme inhibiteurs de l'arn polymerase virale d'arn-dependant
WO2003037908A1 (en) * 2001-10-31 2003-05-08 Ribapharm Inc. Antiviral combination therapy and compositions
KR20050035194A (ko) 2002-06-28 2005-04-15 이데닉스 (케이만) 리미티드 플라비비리다에 감염 치료용 2'-c-메틸-3'-o-l-발린에스테르 리보푸라노실 사이티딘
CN101172993A (zh) 2002-06-28 2008-05-07 埃迪尼克斯(开曼)有限公司 用于治疗黄病毒感染的2′-c-甲基-3′-o-l-缬氨酸酯核糖呋喃基胞苷
US7608600B2 (en) 2002-06-28 2009-10-27 Idenix Pharmaceuticals, Inc. Modified 2′ and 3′-nucleoside prodrugs for treating Flaviviridae infections
ES2624353T3 (es) 2002-11-15 2017-07-13 Idenix Pharmaceuticals Llc 2'-Metil nucleósidos en combinación con interferón y mutación de Flaviviridae
AU2003300901A1 (en) 2002-12-12 2004-06-30 Idenix (Cayman) Limited Process for the production of 2'-branched nucleosides
JP2006524227A (ja) * 2003-03-28 2006-10-26 ファーマセット,インク. フラビウイルス科ウイルス感染の治療のための化合物
US20040202636A1 (en) * 2003-04-11 2004-10-14 Kaczvinsky Joseph Robert Personal care composition containing an antidandruff component and a nonionic surfactant
US20040197292A1 (en) * 2003-04-04 2004-10-07 The Procter & Gamble Company Personal care composition containing an antidandruff component and a nonionic surfactant
US20040197287A1 (en) * 2003-04-04 2004-10-07 The Procter & Gamble Company Personal care composition containing an antidandruff component and a nonionic surfactant
US20050009848A1 (en) * 2003-07-10 2005-01-13 Icn Pharmaceuticals Switzerland Ltd. Use of antivirals against inflammatory bowel diseases
US6930093B2 (en) * 2003-07-10 2005-08-16 Valeant Research & Development Use of ribofuranose derivatives against inflammatory bowel diseases
WO2005018330A1 (en) * 2003-08-18 2005-03-03 Pharmasset, Inc. Dosing regimen for flaviviridae therapy
US20050095218A1 (en) * 2003-10-29 2005-05-05 The Procter & Gamble Company Personal care composition containing a detersive surfactant, an antidandruff component, and ketoamide surfactants
US20050182252A1 (en) 2004-02-13 2005-08-18 Reddy K. R. Novel 2'-C-methyl nucleoside derivatives
JP5055564B2 (ja) 2004-06-15 2012-10-24 メルク・シャープ・エンド・ドーム・コーポレイション Rna依存性rnaウイルスポリメラーゼの阻害剤としてのc−プリンヌクレオシド類似体
JP4516863B2 (ja) * 2005-03-11 2010-08-04 株式会社ケンウッド 音声合成装置、音声合成方法及びプログラム
AU2006242475B2 (en) 2005-05-02 2011-07-07 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
AR057456A1 (es) 2005-07-20 2007-12-05 Merck & Co Inc Inhibidores de la proteasa ns3 del vhc
US8278322B2 (en) 2005-08-01 2012-10-02 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
EP1976382B1 (en) 2005-12-23 2013-04-24 IDENIX Pharmaceuticals, Inc. Process for preparing a synthetic intermediate for preparation of branched nucleosides
CA2633715C (en) * 2005-12-28 2016-06-14 Gordon A. Jamieson Translational dysfunction based therapeutics
US8497292B2 (en) 2005-12-28 2013-07-30 Translational Therapeutics, Inc. Translational dysfunction based therapeutics
GB0609492D0 (en) 2006-05-15 2006-06-21 Angeletti P Ist Richerche Bio Therapeutic agents
GB0612423D0 (en) 2006-06-23 2006-08-02 Angeletti P Ist Richerche Bio Therapeutic agents
WO2008005542A2 (en) * 2006-07-07 2008-01-10 Gilead Sciences, Inc., Antiviral phosphinate compounds
US8138164B2 (en) 2006-10-24 2012-03-20 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
WO2008051477A2 (en) 2006-10-24 2008-05-02 Merck & Co., Inc. Hcv ns3 protease inhibitors
US8309540B2 (en) 2006-10-24 2012-11-13 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
JP5268927B2 (ja) 2006-10-27 2013-08-21 メルク・シャープ・アンド・ドーム・コーポレーション Hcvns3プロテアーゼ阻害剤
US8377874B2 (en) 2006-10-27 2013-02-19 Merck Sharp & Dohme Corp. HCV NS3 protease inhibitors
GB0625349D0 (en) 2006-12-20 2007-01-31 Angeletti P Ist Richerche Bio Therapeutic compounds
GB0625345D0 (en) 2006-12-20 2007-01-31 Angeletti P Ist Richerche Bio Therapeutic compounds
CA2672250C (en) 2006-12-20 2013-04-30 Ian Stansfield Antiviral indoles
CN101754970B (zh) 2007-07-17 2013-07-10 P.安杰莱蒂分子生物学研究所 用于治疗丙型肝炎的大环吲哚衍生物
US8927569B2 (en) 2007-07-19 2015-01-06 Merck Sharp & Dohme Corp. Macrocyclic compounds as antiviral agents
JP2011518882A (ja) 2008-04-28 2011-06-30 メルク・シャープ・エンド・ドーム・コーポレイション Hcvns3プロテアーゼ阻害剤
PE20110212A1 (es) 2008-07-22 2011-04-10 Merck Sharp & Dohme (1aR, 5S, 8S, 10R, 22aR)-5-TERT-BUTIL-N-{(1R, 2S)-1-{[(CICLOPROPILSULFONIL) AMINO] CARBONIL}-2-VINILCICLOPROPIL}-14-METOXI-3,6-DIOXO-1, 1a, 3, 4, 5, 6, 9, 10, 18, 19, 20, 21, 22, 22a-TETRADECAHIDRO-8H-7, 10-METANOCICLOPROPA[18, 19] [1, 10, 3, 6] DIOXADIAZACICLONONADECINO[11, 12-b] QUINOXALIN-8-CARBOXAMIDA COMO INHIBIDOR DE LA PROTEASA HCV NS3
WO2010082050A1 (en) 2009-01-16 2010-07-22 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Macrocyclic and 7-aminoalkyl-substituted benzoxazocines for treatment of hepatitis c infections
GB0900914D0 (en) 2009-01-20 2009-03-04 Angeletti P Ist Richerche Bio Antiviral agents
WO2011014487A1 (en) 2009-07-30 2011-02-03 Merck Sharp & Dohme Corp. Hepatitis c virus ns3 protease inhibitors
EP2780026B1 (en) 2011-11-15 2019-10-23 Merck Sharp & Dohme Corp. Hcv ns3 protease inhibitors
US20140356325A1 (en) 2012-01-12 2014-12-04 Ligand Pharmaceuticals Incorporated Novel 2'-c-methyl nucleoside derivative compounds
CN102978264B (zh) * 2012-11-14 2014-12-10 广东肇庆星湖生物科技股份有限公司 一种他立韦林的制备方法
WO2014121418A1 (en) 2013-02-07 2014-08-14 Merck Sharp & Dohme Corp. Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c
WO2014121417A1 (en) 2013-02-07 2014-08-14 Merck Sharp & Dohme Corp. Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c
EP3105238A4 (en) 2014-02-13 2017-11-08 Ligand Pharmaceuticals, Inc. Prodrug compounds and their uses
JP2017520545A (ja) 2014-07-02 2017-07-27 リガンド・ファーマシューティカルズ・インコーポレイテッド プロドラッグ化合物およびそれらの使用
EP3331895B1 (en) 2015-08-06 2020-07-29 Chimerix, Inc. Pyrrolopyrimidine nucleosides and analogs thereof useful as antiviral agents
ES3011607T3 (en) 2017-09-21 2025-04-07 Chimerix Inc Morphic forms of 4-amino-7-(3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-methyl-7h-pyrrolo(2,3-d)pyrimidine-5-carboxamide and uses thereof
JP2021509907A (ja) 2018-01-09 2021-04-08 リガンド・ファーマシューティカルズ・インコーポレイテッド アセタール化合物およびその治療的使用

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3991078A (en) 1971-06-01 1976-11-09 Icn Pharmaceuticals, Inc. N-substituted 1,2,4-triazoles
USRE29835E (en) 1971-06-01 1978-11-14 Icn Pharmaceuticals 1,2,4-Triazole nucleosides
US3798209A (en) 1971-06-01 1974-03-19 Icn Pharmaceuticals 1,2,4-triazole nucleosides
US3984396A (en) 1971-06-01 1976-10-05 Icn Pharmaceuticals, Inc. 1-(β,-D-ribofuranosyl)-1,2,4-triazole acid esters
US3962211A (en) * 1975-01-13 1976-06-08 The University Of Utah 7-substituted nucleoside compounds
US4093624A (en) 1977-01-31 1978-06-06 Icn Pharmaceuticals, Inc. 1,2,4-Thiadiazolidine-3,5-dione
SU1124559A1 (ru) * 1983-06-08 1986-07-07 Институт молекулярной биологии АН СССР 1-(2-Оксиэтоксиметил)-1,2,4-триазол-5-карбоксамид,обладающий активностью противвируса герпеса
JPS6426593A (en) 1987-07-21 1989-01-27 Asahi Glass Co Ltd Nucleoside derivative
US4892865A (en) * 1987-12-01 1990-01-09 The Regents Of The University Of Michigan Pyrrolo[2,3-d]pyrimidine nucleosides as antiviral agents
US5405837A (en) * 1993-05-18 1995-04-11 Indiana University Foundation Method for the treatment of neoplastic disease utilizing tiazofurin and ribavirin
SK283342B6 (sk) * 1996-01-23 2003-06-03 Icn Pharmaceuticals Použitie ribavirínu na prípravu farmaceutického prostriedku
US5767097A (en) * 1996-01-23 1998-06-16 Icn Pharmaceuticals, Inc. Specific modulation of Th1/Th2 cytokine expression by ribavirin in activated T-lymphocytes
CZ120699A3 (cs) * 1996-10-16 1999-09-15 Icn Pharmaceuticals, Inc. Monocyklická L-nukleosidová analoga a jejich využití
HUP0301875A2 (hu) * 1999-08-27 2003-09-29 Icn Pharmaceuticals, Inc. Pirrolo[2,3-d]pirimidinnukleozid-származékok

Similar Documents

Publication Publication Date Title
JP2004509061A5 (enExample)
RU2002120922A (ru) Нуклеозидные аналоги с карбоксамидин-модифицированным моноциклическим основанием
JP2003526662A5 (enExample)
JP2004504406A5 (enExample)
JP2003526673A5 (enExample)
WO2003063771A3 (en) N4-acylcytosine nucleosides for treatment of viral iinfections
JP2021100937A5 (enExample)
JP2008514732A5 (enExample)
JP2003501474A5 (enExample)
JP2008511633A5 (enExample)
JP2002543144A5 (enExample)
RU95117097A (ru) ПРИМЕНЕНИЕ ДИДЕЗОКСИ-АНАЛОГОВ НУКЛЕОЗИДОВ ДЛЯ ЛЕЧЕНИЯ ВИРУСНЫХ ИНФЕКЦИЙ, СПОСОБ ЛЕЧЕНИЯ ВИРУСНЫХ ИНФЕКЦИЙ, β -Z-5-ФТОР-2',3'-ДИДЕЗОКСИЦИТОЗИН И ЕГО ФАРМАЦЕВТИЧЕСКИ ПРИЕМЛЕМЫЕ ПРОИЗВОДНЫЕ
JP2003503449A5 (enExample)
JP2002527522A5 (enExample)
JPWO2021050956A5 (enExample)
JP2003514025A5 (enExample)
JP2008521934A5 (enExample)
RU2002112248A (ru) Лечение вирусных инфекций с использованием левовирина
JPWO2019200005A5 (enExample)
CA2368352A1 (en) Method for treating neurodegeneration
JP2003512421A5 (enExample)
JP2004529158A5 (enExample)
JP2005509615A5 (enExample)
JP2007516296A5 (enExample)
JP2018131439A5 (enExample)