PE20130307A1 - Formas cristalinas de un derivado de 2-tiazolil-4-quinolinil-oxi, un potente inhibidor de hcv - Google Patents

Formas cristalinas de un derivado de 2-tiazolil-4-quinolinil-oxi, un potente inhibidor de hcv

Info

Publication number
PE20130307A1
PE20130307A1 PE2012002419A PE2012002419A PE20130307A1 PE 20130307 A1 PE20130307 A1 PE 20130307A1 PE 2012002419 A PE2012002419 A PE 2012002419A PE 2012002419 A PE2012002419 A PE 2012002419A PE 20130307 A1 PE20130307 A1 PE 20130307A1
Authority
PE
Peru
Prior art keywords
quinolinyl
derivative
thiazolil
oxi
powerful
Prior art date
Application number
PE2012002419A
Other languages
English (en)
Inventor
Thilo Berkenbusch
Carl Alan Bussaca
Burkhard Jaeger
Richard J Varsolona
Original Assignee
Boehringer Ingelheim Int
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41268627&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20130307(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of PE20130307A1 publication Critical patent/PE20130307A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • A61P31/12—Antivirals
    • 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
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A UNA SAL DE SODIO CRISTALINA DE UN DERIVADO DE 2-TIAZOLIL-4-QUINOLINIL-OXI DE FORMULA (1) QUE TIENE UN PATRON DE DIFRACCION DE RAYOS X EN POLVO QUE COMPRENDE PICOS A 5,4; 6,5; 8,7; 10,1; 11,9; 13,0; 18,2; 20,2 Y 24,7 GRADOS 2THETA CUANDO SE MIDE USANDO RADIACION CuKa. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA SERINA PROTEASA NS3 DEL VIRUS DE LA HEPATITIS C SIENDO UTILES EN EL TRATAMIENTO DE INFECCIONES CAUSADAS POR EL VIRUS DE LA HEPATITIS C
PE2012002419A 2008-09-16 2009-09-14 Formas cristalinas de un derivado de 2-tiazolil-4-quinolinil-oxi, un potente inhibidor de hcv PE20130307A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9729108P 2008-09-16 2008-09-16
US15082609P 2009-03-09 2009-03-09

Publications (1)

Publication Number Publication Date
PE20130307A1 true PE20130307A1 (es) 2013-03-22

Family

ID=41268627

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2011000636A PE20110388A1 (es) 2008-09-16 2009-09-14 Formas cristalinas de un derivado de peptido como inhibidores de hcv
PE2012002419A PE20130307A1 (es) 2008-09-16 2009-09-14 Formas cristalinas de un derivado de 2-tiazolil-4-quinolinil-oxi, un potente inhibidor de hcv

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PE2011000636A PE20110388A1 (es) 2008-09-16 2009-09-14 Formas cristalinas de un derivado de peptido como inhibidores de hcv

Country Status (34)

Country Link
US (2) US8232293B2 (es)
EP (2) EP2687526A1 (es)
JP (2) JP5520301B2 (es)
KR (1) KR101653550B1 (es)
CN (1) CN102159571B (es)
AR (1) AR073298A1 (es)
AU (1) AU2009293494B2 (es)
BR (1) BRPI0918513A2 (es)
CA (1) CA2737055C (es)
CL (1) CL2011000558A1 (es)
CO (1) CO6351741A2 (es)
CY (1) CY1115253T1 (es)
DK (1) DK2331538T3 (es)
EA (1) EA018603B1 (es)
EC (1) ECSP11010878A (es)
ES (1) ES2474992T3 (es)
HK (1) HK1156624A1 (es)
HR (1) HRP20140666T1 (es)
IL (1) IL210345A (es)
MA (1) MA32633B1 (es)
ME (1) ME01831B (es)
MX (1) MX2011002828A (es)
MY (1) MY153093A (es)
NZ (2) NZ591013A (es)
PE (2) PE20110388A1 (es)
PL (1) PL2331538T3 (es)
PT (1) PT2331538E (es)
RS (1) RS53292B (es)
SG (1) SG189740A1 (es)
SI (1) SI2331538T1 (es)
TW (1) TWI471323B (es)
UY (1) UY32119A (es)
WO (1) WO2010033444A1 (es)
ZA (1) ZA201100096B (es)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UY32099A (es) 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
PE20110388A1 (es) 2008-09-16 2011-07-01 Boehringer Ingelheim Int Formas cristalinas de un derivado de peptido como inhibidores de hcv
NZ591030A (en) 2008-09-17 2012-10-26 Boehringer Ingelheim Int Combination of hcv ns3 protease inhibitor with interferon and ribavirin
US9522068B2 (en) * 2009-03-13 2016-12-20 The University Of Toledo Minimally invasive collapsible cage
JP2012520891A (ja) * 2009-03-19 2012-09-10 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング スルホニルキノリンの製造方法
JP5647673B2 (ja) 2009-05-05 2015-01-07 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ブロモ置換キノリンの調製方法
CA2767692C (en) 2009-07-07 2017-03-07 Boehringer Ingelheim International Gmbh Pharmaceutical composition for a hepatitis c viral protease inhibitor
KR20120106942A (ko) 2009-10-30 2012-09-27 베링거 인겔하임 인터내셔날 게엠베하 Ｂｉ２０１３３５, 인터페론 알파 및 리바비린을 포함하는 ｈｃｖ 병용 치료요법을 위한 투여 용법
US8530497B2 (en) 2010-03-11 2013-09-10 Boehringer Ingelheim International Gmbh Crystalline salts of a potent HCV inhibitor
KR20130116245A (ko) * 2010-09-30 2013-10-23 베링거 인겔하임 인터내셔날 게엠베하 Ｈｃｖ 감염 치료용 병용 요법
MX2013007677A (es) 2010-12-30 2013-07-30 Abbvie Inc Inhibidores macrociclicos de serina proteasa de hepatitis.
AU2011352145A1 (en) 2010-12-30 2013-07-18 Abbvie Inc. Phenanthridine macrocyclic hepatitis C serine protease inhibitors
US10201584B1 (en) 2011-05-17 2019-02-12 Abbvie Inc. Compositions and methods for treating HCV
US8466159B2 (en) 2011-10-21 2013-06-18 Abbvie Inc. Methods for treating HCV
US8492386B2 (en) 2011-10-21 2013-07-23 Abbvie Inc. Methods for treating HCV
EA201490836A1 (ru) 2011-10-21 2014-11-28 Эббви Инк. Комбинационное лечение (например, с abt-072 или abt-333) с помощью daa для применения при лечении hcv
GB2515941A (en) 2011-10-21 2015-01-07 Abbvie Inc Methods for treating HCV comprising at least two direct acting antiviral agent, ribavirin but not interferon
KR20140109433A (ko) 2012-01-12 2014-09-15 베링거 인겔하임 인터내셔날 게엠베하 강력한 hcv 억제제의 안정화된 약제학적 제형
WO2013137869A1 (en) 2012-03-14 2013-09-19 Boehringer Ingelheim International Gmbh Combination therapy for treating hcv infection in an hcv-hiv coinfected patient population
WO2013147749A1 (en) 2012-03-27 2013-10-03 Boehringer Ingelheim International Gmbh Oral combination therapy for treating hcv infection in specific patient subgenotype populations
WO2013147750A1 (en) 2012-03-27 2013-10-03 Boehringer Ingelheim International Gmbh Oral combination therapy for treating hcv infection in specific patient sub-population
JP2015512900A (ja) 2012-03-28 2015-04-30 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 特別な患者の遺伝子亜型分集団のｈｃｖ感染症を治療するための併用療法
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
WO2014138374A1 (en) 2013-03-08 2014-09-12 Boehringer Ingelheim International Gmbh Oral combination therapy for treating hcv infection in specific patient sub-population
JP6511432B2 (ja) 2013-03-15 2019-05-15 ギリアード サイエンシーズ， インコーポレイテッド Ｃ型肝炎ウイルスの大環状二環式阻害剤
US9732076B2 (en) * 2013-03-15 2017-08-15 Boehringer Ingelheim International Gmbh Solid oral dosage formulation of HCV inhibitor in the amorphous state
EP3089757A1 (en) 2014-01-03 2016-11-09 AbbVie Inc. Solid antiviral dosage forms
CN109689063A (zh) 2016-04-28 2019-04-26 埃默里大学 含有炔烃的核苷酸和核苷治疗组合物及其相关用途
WO2022107182A1 (en) * 2020-11-18 2022-05-27 University Of Petra A composition of fentanyl and fatty acids, and a method of preparation thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE398448T1 (de) 1993-09-28 2008-07-15 Scherer Gmbh R P Herstellung von weichgelatinekapseln
AR022061A1 (es) 1998-08-10 2002-09-04 Boehringer Ingelheim Ca Ltd Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos.
US6323180B1 (en) 1998-08-10 2001-11-27 Boehringer Ingelheim (Canada) Ltd Hepatitis C inhibitor tri-peptides
US6608027B1 (en) 1999-04-06 2003-08-19 Boehringer Ingelheim (Canada) Ltd Macrocyclic peptides active against the hepatitis C virus
UA74546C2 (en) 1999-04-06 2006-01-16 Boehringer Ingelheim Ca Ltd Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition
CZ20022332A3 (cs) * 2000-01-07 2003-01-15 Transform Pharmaceuticals, Inc. Sestava vzorků
UY28240A1 (es) * 2003-03-27 2004-11-08 Boehringer Ingelheim Pharma Fases cristalinas de un potente inhibidor de la hcv
PT1654261E (pt) 2003-05-21 2008-01-18 Boehringer Ingelheim Int Compostos inibidores da hepatite c
JP5156374B2 (ja) 2004-05-25 2013-03-06 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 非環式ｈｃｖプロテアーゼインヒビターの調製方法
PE20110388A1 (es) 2008-09-16 2011-07-01 Boehringer Ingelheim Int Formas cristalinas de un derivado de peptido como inhibidores de hcv
US8530497B2 (en) 2010-03-11 2013-09-10 Boehringer Ingelheim International Gmbh Crystalline salts of a potent HCV inhibitor

Also Published As

Publication number Publication date
PE20110388A1 (es) 2011-07-01
CA2737055C (en) 2016-08-30
US8362035B2 (en) 2013-01-29
US8232293B2 (en) 2012-07-31
EP2687526A1 (en) 2014-01-22
CA2737055A1 (en) 2010-03-25
HRP20140666T1 (hr) 2014-10-10
PL2331538T3 (pl) 2014-09-30
US20120270775A1 (en) 2012-10-25
JP2014062116A (ja) 2014-04-10
MA32633B1 (fr) 2011-09-01
CN102159571A (zh) 2011-08-17
NZ591013A (en) 2012-09-28
EP2331538A1 (en) 2011-06-15
CO6351741A2 (es) 2011-12-20
CY1115253T1 (el) 2017-01-04
MX2011002828A (es) 2011-04-05
DK2331538T3 (da) 2014-06-02
CN102159571B (zh) 2014-10-01
CL2011000558A1 (es) 2011-07-15
ES2474992T3 (es) 2014-07-10
UY32119A (es) 2010-04-30
RS53292B (en) 2014-08-29
ME01831B (me) 2014-12-20
KR20110059841A (ko) 2011-06-07
PT2331538E (pt) 2014-05-12
WO2010033444A8 (en) 2010-06-17
MY153093A (en) 2014-12-31
ZA201100096B (en) 2011-09-28
EP2331538B1 (en) 2014-04-16
TW201024292A (en) 2010-07-01
KR101653550B1 (ko) 2016-09-02
US20100093792A1 (en) 2010-04-15
IL210345A0 (en) 2011-03-31
WO2010033444A1 (en) 2010-03-25
SG189740A1 (en) 2013-05-31
TWI471323B (zh) 2015-02-01
HK1156624A1 (en) 2012-06-15
JP2012502910A (ja) 2012-02-02
BRPI0918513A2 (pt) 2015-12-01
EA018603B1 (ru) 2013-09-30
AR073298A1 (es) 2010-10-28
AU2009293494B2 (en) 2014-04-24
EA201100482A1 (ru) 2011-10-31
SI2331538T1 (sl) 2014-06-30
IL210345A (en) 2015-06-30
JP5520301B2 (ja) 2014-06-11
AU2009293494A1 (en) 2010-03-25
NZ602163A (en) 2013-06-28
ECSP11010878A (es) 2011-07-29

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