FI944217L - Substituoidut pipekoliinihappojohdannaiset HIV-proteaasin estäjinä - Google Patents

Substituoidut pipekoliinihappojohdannaiset HIV-proteaasin estäjinä Download PDF

Info

Publication number
FI944217L
FI944217L FI944217A FI944217A FI944217L FI 944217 L FI944217 L FI 944217L FI 944217 A FI944217 A FI 944217A FI 944217 A FI944217 A FI 944217A FI 944217 L FI944217 L FI 944217L
Authority
FI
Finland
Prior art keywords
acid derivatives
protease inhibitors
hiv protease
pipecolic acid
substituted pipecolic
Prior art date
Application number
FI944217A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI944217A7 (fi
FI944217A0 (fi
Inventor
Paul Cates Anderson
Francois Soucy
Christiane Yoakim
Pierre Lavallee
Pierre Louis Beaulieu
Original Assignee
Bio Mega Boehringer Ingelheim
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 Bio Mega Boehringer Ingelheim filed Critical Bio Mega Boehringer Ingelheim
Publication of FI944217L publication Critical patent/FI944217L/fi
Publication of FI944217A7 publication Critical patent/FI944217A7/fi
Publication of FI944217A0 publication Critical patent/FI944217A0/fi

Links

Classifications

    • 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
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Virology (AREA)
  • Immunology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • AIDS & HIV (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
FI944217A 1992-03-13 1993-03-12 Substituoidut pipekoliinihappojohdannaiset HIV-proteaasin estäjinä FI944217A0 (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85071692A 1992-03-13 1992-03-13
PCT/CA1993/000096 WO1993018003A1 (en) 1992-03-13 1993-03-12 Substitued pipecolinic acid derivatives as hiv protease inhibitors

Publications (3)

Publication Number Publication Date
FI944217L true FI944217L (fi) 1994-09-13
FI944217A7 FI944217A7 (fi) 1994-09-13
FI944217A0 FI944217A0 (fi) 1994-09-13

Family

ID=25308925

Family Applications (1)

Application Number Title Priority Date Filing Date
FI944217A FI944217A0 (fi) 1992-03-13 1993-03-12 Substituoidut pipekoliinihappojohdannaiset HIV-proteaasin estäjinä

Country Status (25)

Country Link
US (1) US5807870A (de)
EP (1) EP0560268B1 (de)
JP (1) JP3258422B2 (de)
KR (1) KR950700253A (de)
AP (1) AP393A (de)
AT (1) ATE116640T1 (de)
AU (1) AU670582B2 (de)
CA (1) CA2131185C (de)
CZ (1) CZ285589B6 (de)
DE (1) DE69300043T2 (de)
DK (1) DK0560268T3 (de)
ES (1) ES2066623T3 (de)
FI (1) FI944217A0 (de)
GR (1) GR3015622T3 (de)
HU (2) HUT70617A (de)
IL (1) IL105035A (de)
NO (1) NO302570B1 (de)
NZ (1) NZ251267A (de)
OA (1) OA10092A (de)
PH (1) PH30734A (de)
PL (1) PL176362B1 (de)
RU (1) RU2140911C1 (de)
SK (1) SK280161B6 (de)
WO (1) WO1993018003A1 (de)
ZA (1) ZA931776B (de)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5888992A (en) 1992-03-11 1999-03-30 Narhex Limited Polar substituted hydrocarbons
US6071895A (en) 1992-03-11 2000-06-06 Narhex Limited Polar-substituted hydrocarbons
JPH07504654A (ja) 1992-03-11 1995-05-25 ナルヘックス リミテッド オキソ及びヒドロキシ置換炭化水素のアミン誘導体
ATE253050T1 (de) 1992-03-11 2003-11-15 Narhex Ltd Aminderivate von oxo- und hydroxy- substituierten kohlenwasserstoffen
US5559256A (en) * 1992-07-20 1996-09-24 E. R. Squibb & Sons, Inc. Aminediol protease inhibitors
EP0656887B1 (de) 1992-08-25 1998-10-28 G.D. Searle & Co. Hydroxyethylaminosulfonamide verwendbar als inhibitoren retroviraler proteasen
US5846993A (en) * 1992-12-22 1998-12-08 Agouron Pharmaceuticals, Inc. HIV protease inhibitors
US5484926A (en) * 1993-10-07 1996-01-16 Agouron Pharmaceuticals, Inc. HIV protease inhibitors
EP0610745A3 (en) * 1993-02-09 1994-09-28 Miles Inc Novel aminomethylene derivatives as immunosuppressants.
IL110898A0 (en) * 1993-09-10 1994-11-28 Narhex Australia Pty Ltd Polar-substituted hydrocarbons
US5527829A (en) * 1994-05-23 1996-06-18 Agouron Pharmaceuticals, Inc. HIV protease inhibitors
CA2137406C (en) * 1994-12-06 2005-09-13 Pierre Louis Beaulieu Process for key intermediates for hiv protease inhibitors
US6037157A (en) 1995-06-29 2000-03-14 Abbott Laboratories Method for improving pharmacokinetics
US5914332A (en) 1995-12-13 1999-06-22 Abbott Laboratories Retroviral protease inhibiting compounds
US5883252A (en) * 1996-01-26 1999-03-16 Vertex Pharmaceuticals Incorporated Aspartyl protease inhibitors
US5705647A (en) * 1996-09-05 1998-01-06 Agouron Pharmaceuticals, Inc. Intermediates for making HIV-protease inhibitors
US5962725A (en) 1996-09-05 1999-10-05 Agouron Pharmaceuticals, Inc. Intermediate compounds useful for making HIV protease inhibitors such as nelfinavir
US5925759A (en) 1996-09-05 1999-07-20 Agouron Pharmaceuticals, Inc. Methods of making HIV-protease inhibitors and intermediates for making HIV-protease inhibitors
US6232333B1 (en) 1996-11-21 2001-05-15 Abbott Laboratories Pharmaceutical composition
US6001851A (en) * 1997-03-13 1999-12-14 Agouron Pharmaceuticals, Inc. HIV protease inhibitors
US6084107A (en) * 1997-09-05 2000-07-04 Agouron Pharmaceuticals, Inc. Intermediates for making HIV-protease inhibitors
US6251906B1 (en) 1998-05-15 2001-06-26 Abbott Laboratories Retroviral protease inhibiting compounds
CA2395987C (en) 2000-01-19 2009-12-22 Abbott Laboratories Improved pharmaceutical formulations
ES2275675T3 (es) * 2000-03-23 2007-06-16 Elan Pharmaceuticals, Inc. Compuestos y metodos para tratar la enfermedad de alzheimer.
US6992081B2 (en) 2000-03-23 2006-01-31 Elan Pharmaceuticals, Inc. Compounds to treat Alzheimer's disease
EP1666452A2 (de) 2000-06-30 2006-06-07 Elan Pharmaceuticals, Inc. Verbindungen zur Behandlung der Alzheimerischen Krankheit
US20030096864A1 (en) * 2000-06-30 2003-05-22 Fang Lawrence Y. Compounds to treat alzheimer's disease
PE20020276A1 (es) 2000-06-30 2002-04-06 Elan Pharm Inc COMPUESTOS DE AMINA SUSTITUIDA COMO INHIBIDORES DE ß-SECRETASA PARA EL TRATAMIENTO DE ALZHEIMER
US6846813B2 (en) * 2000-06-30 2005-01-25 Pharmacia & Upjohn Company Compounds to treat alzheimer's disease
CN1217920C (zh) * 2000-06-30 2005-09-07 艾兰制药公司 治疗早老性痴呆的化合物
EP1401452A1 (de) * 2001-06-27 2004-03-31 Elan Pharmaceuticals, Inc. Beta-hydroxyamin-derivate zur behandlung von alzheimer krankheit
US20070213407A1 (en) * 2001-06-29 2007-09-13 Elan Pharmaceuticals And Pharmacia & Upjohn Company Llc Compounds to treat Alzheimer's disease
WO2004103360A1 (ja) 2003-05-22 2004-12-02 Lead Chemical Co.,Ltd. 抗ウイルス作用を有する化合物および配合剤
BRPI0510746A (pt) 2004-06-10 2007-11-20 Univ Michigan State sìntese de caprolactama a partir de lisina
US8106090B2 (en) * 2005-07-20 2012-01-31 Eli Lilly And Company 1-amino linked compounds
US8283466B2 (en) * 2007-02-20 2012-10-09 Board Of Trustees Of Michigan State University Catalytic deamination for caprolactam production
KR101518079B1 (ko) 2007-03-12 2015-05-06 넥타르 테라퓨틱스 올리고머-프로테아제 억제제 컨주게이트
EP2262538B1 (de) 2008-03-12 2014-12-10 Nektar Therapeutics Oligomer-aminosäure konjugate
KR20110046487A (ko) * 2008-07-24 2011-05-04 드라스 코포레이션 사이클릭 아미드 모노머들의 형성 방법, 그 유도체 및 형성 방법
US20120108501A1 (en) 2009-06-12 2012-05-03 Nektar Therapeutics Protease Inhibitors

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3789347D1 (de) * 1986-10-14 1994-04-21 Banyu Pharma Co Ltd 5-Substituierte Amino-4-hydroxy-pentansäure-Derivate und deren Verwendung.
CA1340588C (en) * 1988-06-13 1999-06-08 Balraj Krishan Handa Amino acid derivatives
JPH07106992B2 (ja) * 1988-06-13 1995-11-15 三菱石油株式会社 2,6―ジメチルナフタレンの分離方法
EP0361341A3 (de) * 1988-09-28 1991-07-03 Miles Inc. Therapeutika für AIDS auf der Basis von HIV-Protease-Inhibitoren
GB8927913D0 (en) * 1989-12-11 1990-02-14 Hoffmann La Roche Amino acid derivatives
GB8927915D0 (en) * 1989-12-11 1990-02-14 Hoffmann La Roche Novel alcohols
CA2060844A1 (en) * 1991-02-08 1992-08-09 Yabe Yuichiro Beta-amino-alpha-hydroxycarboxylic acids and their use
MY110227A (en) * 1991-08-12 1998-03-31 Ciba Geigy Ag 1-acylpiperindine compounds.
ZA931777B (en) * 1992-03-13 1993-09-23 Bio Mega Boehringer Ingelheim Substituted pyrrolidine derivatives as HIV protease inhibitors.
IL110255A (en) * 1993-07-16 1998-12-06 Merck & Co Inc Formation and resolution of 2-tert-butylcarboxamido-piperazine
US5480887A (en) * 1994-02-02 1996-01-02 Eli Lilly And Company Protease inhibitors
GB2292146A (en) * 1994-08-11 1996-02-14 Merck & Co Inc HIV protease inhibitors useful for the treatment of AIDS

Also Published As

Publication number Publication date
AU3880893A (en) 1993-10-05
CZ223294A3 (en) 1995-11-15
IL105035A (en) 1997-07-13
GR3015622T3 (en) 1995-06-30
ATE116640T1 (de) 1995-01-15
SK280161B6 (sk) 1999-09-10
NZ251267A (en) 1996-09-25
ES2066623T3 (es) 1995-03-01
CA2131185C (en) 1997-05-27
RU2140911C1 (ru) 1999-11-10
SK109094A3 (en) 1995-05-10
AP9300495A0 (en) 1993-04-30
RU94040841A (ru) 1996-07-20
HU9402613D0 (en) 1994-11-28
PL176362B1 (pl) 1999-05-31
WO1993018003A1 (en) 1993-09-16
DE69300043D1 (de) 1995-02-16
HU211854A9 (en) 1995-12-28
PH30734A (en) 1997-10-17
JP3258422B2 (ja) 2002-02-18
DE69300043T2 (de) 1995-05-24
AP393A (en) 1995-08-07
ZA931776B (en) 1993-09-24
KR950700253A (ko) 1995-01-16
IL105035A0 (en) 1993-07-08
CZ285589B6 (cs) 1999-09-15
JPH0673004A (ja) 1994-03-15
US5807870A (en) 1998-09-15
OA10092A (en) 1996-12-18
CA2131185A1 (en) 1993-09-16
FI944217A7 (fi) 1994-09-13
FI944217A0 (fi) 1994-09-13
EP0560268B1 (de) 1995-01-04
NO302570B1 (no) 1998-03-23
NO943383D0 (no) 1994-09-12
NO943383L (no) 1994-09-12
AU670582B2 (en) 1996-07-25
DK0560268T3 (da) 1995-06-12
HUT70617A (en) 1995-10-30
EP0560268A1 (de) 1993-09-15

Similar Documents

Publication Publication Date Title
FI944217A7 (fi) Substituoidut pipekoliinihappojohdannaiset HIV-proteaasin estäjinä
FI20012317L (fi) Retrovirusproteaasi-inhibiittoreina käyttökelpoisia hydroksietyyliaminosulfoniamideja
FI950651L (fi) Retrovirusproteaasi-inhibiittoreina käyttökelpoisia sulfonyylialkanoyyliaminohydroksietyyliaminosulfoniamideja
DE69434214D1 (de) HIV protease inhibitoren
NO932620D0 (no) Amindiol-proteaseinhibitorer
FI954404A7 (fi) Fenoksifenyylietikkahappojohdannaiset
FI943948L (fi) Heterosykliset hiilihappojohdannaiset
FI950841L (fi) Retrovirusproteaasi-inhibiittoreina käyttökelpoisia N-(alkanoyyliamino-2-hydroksipropyyli)-sulfoniamideja
FI940659A7 (fi) Heterosyklisesti substituoituja fenyylisykloheksaanikarboksyylihappojohdannaisia
FI933424A7 (fi) Peptidyyli-4-amino-2,2-difluori-3-okso-1,6-heksaanidinihappojohdannaiset tulehdusta vastustavina aineina
FI962488L (fi) HIV:n proteaasin inhibiittoreita
FI941712L (fi) Heterosykliset iminobismetyleenibisfosfonihappojohdannaiset
DE59402621D1 (de) Fluor-trifluormethylbenzoesäure-Derivate
FI941064A7 (fi) Asyylioksiheksaanihappojohdannaiset
FI953106A7 (fi) Difuoripentapeptidijohdannaiset anti-inflammatorisina aineina
FI940133L (fi) Uudet nikotiinihappojohdannaiset
FI893162A7 (fi) 19-hydroksylaasin inhibiittoreina käyttökelpoisia 19-fluori- tai syano- 21-hydroksiprogesteronin johdannaisia
NO950212D0 (no) Indolinyl-N-hydroksyurinstoff- og -N-hydroksamsyrederivater som lipoksygenase-inhibitorer
NO920023D0 (no) Hiv-proteaseinhibitorer
DE69302425D1 (de) Quadratsäurederivate

Legal Events

Date Code Title Description
GB Transfer or assigment of application

Owner name: BOEHRINGER INGELHEIM (CANADA) LTD.