BG107165A - Кристални фармацевтични форми - Google Patents

Кристални фармацевтични форми Download PDF

Info

Publication number
BG107165A
BG107165A BG107165A BG10716502A BG107165A BG 107165 A BG107165 A BG 107165A BG 107165 A BG107165 A BG 107165A BG 10716502 A BG10716502 A BG 10716502A BG 107165 A BG107165 A BG 107165A
Authority
BG
Bulgaria
Prior art keywords
lopinavir
type
crystalline form
crystalline
solvated
Prior art date
Application number
BG107165A
Other languages
Bulgarian (bg)
English (en)
Inventor
Daniel Dickman
Sanjay Chemburkar
James Fort
Rodger Henry
David Lechuga-Ballesteros
Yuping Niu
William Porter
Original Assignee
Abbott Laboratories
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=27065762&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BG107165(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US09/793,536 external-priority patent/US6608198B2/en
Application filed by Abbott Laboratories filed Critical Abbott Laboratories
Publication of BG107165A publication Critical patent/BG107165A/bg

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/10Oxygen or sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • AIDS & HIV (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
BG107165A 2000-03-30 2002-10-03 Кристални фармацевтични форми BG107165A (bg)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US53825700A 2000-03-30 2000-03-30
US09/793,536 US6608198B2 (en) 2000-03-30 2001-02-27 Crystalline pharmaceutical
PCT/US2001/009112 WO2001074787A2 (en) 2000-03-30 2001-03-21 Crystalline pharmaceutical

Publications (1)

Publication Number Publication Date
BG107165A true BG107165A (bg) 2003-07-31

Family

ID=27065762

Family Applications (1)

Application Number Title Priority Date Filing Date
BG107165A BG107165A (bg) 2000-03-30 2002-10-03 Кристални фармацевтични форми

Country Status (22)

Country Link
EP (1) EP1268442A2 (ko)
JP (1) JP2003529592A (ko)
KR (1) KR100773258B1 (ko)
CN (2) CN1330639C (ko)
AR (2) AR033360A1 (ko)
AU (3) AU2001250920B2 (ko)
BG (1) BG107165A (ko)
BR (1) BR0109433A (ko)
CA (1) CA2403635A1 (ko)
CZ (1) CZ20023529A3 (ko)
HU (1) HUP0302675A3 (ko)
IL (1) IL151551A0 (ko)
MX (1) MXPA02009559A (ko)
MY (1) MY128296A (ko)
NO (1) NO325005B1 (ko)
NZ (1) NZ521183A (ko)
PE (1) PE20011232A1 (ko)
PL (1) PL359727A1 (ko)
SA (2) SA06270303B1 (ko)
SK (1) SK14832002A3 (ko)
TW (1) TWI284640B (ko)
WO (1) WO2001074787A2 (ko)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6608198B2 (en) 2000-03-30 2003-08-19 Abbott Laboratories Crystalline pharmaceutical
US8025899B2 (en) 2003-08-28 2011-09-27 Abbott Laboratories Solid pharmaceutical dosage form
WO2010089753A2 (en) * 2009-02-06 2010-08-12 Hetero Research Foundation Novel polymorphs of lopinavir
WO2011025849A1 (en) * 2009-08-27 2011-03-03 Merck Sharp & Dohme Corp. Processes for preparing protease inhibitors of hepatitis c virus
CN112830899A (zh) * 2021-01-18 2021-05-25 合肥华方医药科技有限公司 一种洛匹那韦新晶型及其制备方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5914332A (en) * 1995-12-13 1999-06-22 Abbott Laboratories Retroviral protease inhibiting compounds
WO1998057648A1 (en) * 1997-06-16 1998-12-23 Vertex Pharmaceuticals Incorporated Methods of increasing the bioavailability of stable crystal polymorphs of a compound

Also Published As

Publication number Publication date
JP2003529592A (ja) 2003-10-07
SA06270303B1 (ar) 2009-08-02
TWI284640B (en) 2007-08-01
HUP0302675A2 (hu) 2003-12-29
KR100773258B1 (ko) 2007-11-05
KR20030011807A (ko) 2003-02-11
WO2001074787A2 (en) 2001-10-11
NO20024679D0 (no) 2002-09-30
AU5092001A (en) 2001-10-15
NZ521183A (en) 2004-03-26
AU2001250920B2 (en) 2006-06-29
CN101066952A (zh) 2007-11-07
PL359727A1 (en) 2004-09-06
WO2001074787A3 (en) 2002-02-07
NO325005B1 (no) 2008-01-14
AU2006222711A1 (en) 2006-10-19
BR0109433A (pt) 2004-08-10
AR049560A2 (es) 2006-08-16
SK14832002A3 (sk) 2003-02-04
PE20011232A1 (es) 2001-12-08
MY128296A (en) 2007-01-31
AR033360A1 (es) 2003-12-17
CN1330639C (zh) 2007-08-08
HUP0302675A3 (en) 2004-03-29
CA2403635A1 (en) 2001-10-11
IL151551A0 (en) 2003-04-10
EP1268442A2 (en) 2003-01-02
MXPA02009559A (es) 2003-05-21
SA01220270B1 (ar) 2006-11-14
NO20024679L (no) 2002-09-30
CN1422259A (zh) 2003-06-04
CZ20023529A3 (cs) 2003-02-12

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