[go: up one dir, main page]

AR004663A1 - Un compuesto inhibidor de proteasa aspartilo, una composicion farmaceutica que lo comprende y metodos para inhibir la actividad de proteasa aspartilo,para adherir reversiblemente proteasa aspartilo y para evitar o tratar infecciones vih con dicho compuesto. - Google Patents

Un compuesto inhibidor de proteasa aspartilo, una composicion farmaceutica que lo comprende y metodos para inhibir la actividad de proteasa aspartilo,para adherir reversiblemente proteasa aspartilo y para evitar o tratar infecciones vih con dicho compuesto.

Info

Publication number
AR004663A1
AR004663A1 ARP960102210A AR10221096A AR004663A1 AR 004663 A1 AR004663 A1 AR 004663A1 AR P960102210 A ARP960102210 A AR P960102210A AR 10221096 A AR10221096 A AR 10221096A AR 004663 A1 AR004663 A1 AR 004663A1
Authority
AR
Argentina
Prior art keywords
aspartile
protease
compound
methods
understands
Prior art date
Application number
ARP960102210A
Other languages
English (en)
Original Assignee
Vertex Pharma
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 Vertex Pharma filed Critical Vertex Pharma
Publication of AR004663A1 publication Critical patent/AR004663A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/18Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings 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
    • C07D307/20Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings 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
    • C07D309/10Oxygen atoms
    • C07D309/12Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/18Radicals substituted by singly bound oxygen or sulfur atoms
    • C07D317/24Radicals substituted by singly bound oxygen or sulfur atoms esterified
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/32Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
    • C07D317/34Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/32Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
    • C07D317/34Oxygen atoms
    • C07D317/36Alkylene carbonates; Substituted alkylene carbonates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/041,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/061,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (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)
  • Virology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Furan Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

Una clase de sulfonamidas inhibidoras de proteasa aspartilo las cuales tienen la fórmula (I) donde A, R, D, D y E son tal como se definen en lamemoria descriptiva. Los compuestos y las composiciones farmacéuticas que los comprenden sonparticu larmente apropiados para inhibir la actividad de laproteasa VIH-1 y VIH-2 y por consiguiente, pueden usarse ventajosamente como agentes anti-virales contra los virus VIH-1 y VIH-2. Esta invención se refieretambién a métodos para inhibirla activid ad de proteasa aspartilo VIH usando los compuestos de esta invención.
ARP960102210A 1995-04-19 1996-04-17 Un compuesto inhibidor de proteasa aspartilo, una composicion farmaceutica que lo comprende y metodos para inhibir la actividad de proteasa aspartilo,para adherir reversiblemente proteasa aspartilo y para evitar o tratar infecciones vih con dicho compuesto. AR004663A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/424,810 US5691372A (en) 1995-04-19 1995-04-19 Oxygenated-Heterocycle containing sulfonamide inhibitors of aspartyl protease

Publications (1)

Publication Number Publication Date
AR004663A1 true AR004663A1 (es) 1999-03-10

Family

ID=23683966

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960102210A AR004663A1 (es) 1995-04-19 1996-04-17 Un compuesto inhibidor de proteasa aspartilo, una composicion farmaceutica que lo comprende y metodos para inhibir la actividad de proteasa aspartilo,para adherir reversiblemente proteasa aspartilo y para evitar o tratar infecciones vih con dicho compuesto.

Country Status (34)

Country Link
US (2) US5691372A (es)
EP (3) EP1136479B1 (es)
JP (1) JP4240532B2 (es)
KR (1) KR100485237B1 (es)
CN (1) CN1110491C (es)
AP (2) AP9600827A0 (es)
AR (1) AR004663A1 (es)
AT (3) ATE479674T1 (es)
AU (1) AU712913B2 (es)
BG (1) BG102041A (es)
BR (1) BR9608033A (es)
CA (1) CA2217745C (es)
CO (1) CO4700433A1 (es)
CZ (1) CZ329497A3 (es)
DE (3) DE69635679T2 (es)
DK (1) DK0833826T3 (es)
EA (1) EA000906B1 (es)
EE (1) EE9700254A (es)
ES (3) ES2256117T3 (es)
GE (1) GEP20001915B (es)
HU (1) HUP9801948A3 (es)
IL (1) IL117962A0 (es)
IS (1) IS4575A (es)
MY (1) MY115797A (es)
NO (1) NO974744D0 (es)
NZ (1) NZ307342A (es)
PE (1) PE43697A1 (es)
PL (1) PL322904A1 (es)
PT (1) PT833826E (es)
SK (1) SK143097A3 (es)
TR (1) TR199701194T1 (es)
TW (1) TW404945B (es)
WO (1) WO1996033187A1 (es)
ZA (1) ZA962891B (es)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040122000A1 (en) 1981-01-07 2004-06-24 Vertex Pharmaceuticals Incorporated. Inhibitors of aspartyl protease
DK0656887T3 (da) 1992-08-25 1999-07-05 Searle & Co Hydroxyethylaminosulfonamider til anvendelse som inhibitorer af retrovirale proteaser
US7141609B2 (en) 1992-08-25 2006-11-28 G.D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US5942253A (en) 1995-10-12 1999-08-24 Immunex Corporation Prolonged release of GM-CSF
EA002593B1 (ru) 1996-12-31 2002-06-27 Гилфорд Фармасьютикалз Инк. N-связанные сульфонамиды гетероциклических тиоэфиров
US5874449A (en) * 1996-12-31 1999-02-23 Gpi Nil Holdings, Inc. N-linked sulfonamides of heterocyclic thioesters
CA2289654A1 (en) * 1997-05-17 1998-11-26 Glaxo Group Limited Antiviral combinations containing the carbocyclic nucleoside 1592u89
US20010049381A1 (en) 1997-06-04 2001-12-06 Gpl Nil Holdings, Inc., Pyrrolidine derivative hair growth compositions and uses
US5945441A (en) 1997-06-04 1999-08-31 Gpi Nil Holdings, Inc. Pyrrolidine carboxylate hair revitalizing agents
US6576231B2 (en) * 1997-09-12 2003-06-10 Schering Ag Methods for treating HIV-Infected Patients by the Administration of GM-CSF and a protease inhibitor
BR9814484A (pt) * 1997-12-24 2000-10-10 Vertex Pharma "pró-drogas de inibidores de aspartil protease"
US6436989B1 (en) 1997-12-24 2002-08-20 Vertex Pharmaceuticals, Incorporated Prodrugs of aspartyl protease inhibitors
NZ508855A (en) * 1998-06-19 2003-10-31 Vertex Pharma Sulfonamide inhibitors of HIV aspartyl protease
PT1088098E (pt) * 1998-06-23 2011-05-25 Univ Illinois Medicamento para tratar mam?feros infectados com hiv
US6339101B1 (en) 1998-08-14 2002-01-15 Gpi Nil Holdings, Inc. N-linked sulfonamides of N-heterocyclic carboxylic acids or isosteres for vision and memory disorders
US6399648B1 (en) 1998-08-14 2002-06-04 Gpi Nil Holdings, Inc. N-oxides of heterocyclic ester, amide, thioester, or ketone for vision and memory disorders
US6376517B1 (en) 1998-08-14 2002-04-23 Gpi Nil Holdings, Inc. Pipecolic acid derivatives for vision and memory disorders
US6218423B1 (en) 1998-08-14 2001-04-17 Gpi Nil Holdings, Inc. Pyrrolidine derivatives for vision and memory disorders
US7338976B1 (en) 1998-08-14 2008-03-04 Gpi Nil Holdings, Inc. Heterocyclic esters or amides for vision and memory disorders
US6395758B1 (en) 1998-08-14 2002-05-28 Gpi Nil Holdings, Inc. Small molecule carbamates or ureas for vision and memory disorders
US6337340B1 (en) 1998-08-14 2002-01-08 Gpi Nil Holdings, Inc. Carboxylic acids and isosteres of heterocyclic ring compounds having multiple heteroatoms for vision and memory disorders
US6462072B1 (en) 1998-09-21 2002-10-08 Gpi Nil Holdings, Inc. Cyclic ester or amide derivatives
TNSN00027A1 (fr) 1999-02-12 2005-11-10 Vertex Pharma Inhibiteurs de l'aspartyle protease
DK1159278T3 (da) * 1999-02-12 2006-04-10 Vertex Pharma Inhibitorer af aspartylprotease
AR031520A1 (es) * 1999-06-11 2003-09-24 Vertex Pharma Un compuesto inhibidor de aspartilo proteasa, una composicion que lo comprende y un metodo para tratar un paciente con dicha composicion
CZ300031B6 (cs) * 1999-10-06 2009-01-14 Tibotec Pharmaceuticals Ltd. Hexahydrofuro[2,3-b]furan-3-yl-N-{3-[(1,3-benzodioxol-5-ylsulfonyl) (isobutyl)amino]-1-benzyl-2-hydroxypropyl}karbamát a farmaceutický prípravek s jeho obsahem
EE200200564A (et) 2000-03-30 2004-06-15 Bristol-Myers Squibb Company Stavudiini sisaldavad toimeainet aeglustatult vabastavad graanulid
BR0208796A (pt) * 2001-04-09 2004-03-09 Tibotec Pharm Ltd Inibidores 2-(amino substituìdo)-benzoxazol sulfonamida hiv protease de amplo espectro
AU2003202914A1 (en) * 2002-01-07 2003-07-24 Sequoia Pharmaceuticals Broad spectrum inhibitors
US7157489B2 (en) * 2002-03-12 2007-01-02 The Board Of Trustees Of The University Of Illinois HIV protease inhibitors
US7160493B2 (en) * 2002-10-11 2007-01-09 Semplastics, Llc Retaining ring for use on a carrier of a polishing apparatus
DOP2003000765A (es) * 2002-11-27 2004-05-31 Elan Fharmaceuticals Inc Ureas substituidas y carbamatos utiles para el tratamiento de la enfermedad de alzheimer (substituted ureas and carbamates useful in the treatment of alzheimer`s disease
US20050131042A1 (en) * 2003-12-11 2005-06-16 Flentge Charles A. HIV protease inhibiting compounds
US7763609B2 (en) * 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
US20080194554A1 (en) * 2005-03-11 2008-08-14 Mclean Ed W Hiv Protease Inhibitors
JP2007202679A (ja) * 2006-01-31 2007-08-16 Juki Corp ミシンの糸調子装置
JP2007202833A (ja) * 2006-02-02 2007-08-16 Juki Corp ミシンの糸調子装置
US9808527B2 (en) 2006-11-21 2017-11-07 Purdue Research Foundation Methods and compositions for treating HIV infections
US20110046199A1 (en) 2008-01-17 2011-02-24 Purdue Research Foundation Small molecule inhibitors of hiv proteases
US8791135B2 (en) 2008-07-01 2014-07-29 Purdue Research Foundation Nonpeptide HIV-1 protease inhibitors
WO2010006050A1 (en) 2008-07-09 2010-01-14 Purdue Research Foundation Hiv protease inhibitors and methods for using
CN105272991B (zh) * 2014-06-26 2017-11-07 成都中医药大学 一种化合物晶型
US11090030B2 (en) 2016-11-10 2021-08-17 Leltek Inc. Ultrasound apparatus and ultrasound emission method

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3743722A (en) * 1971-07-14 1973-07-03 Abbott Lab Anti-coagulant isolation
FR2459235A1 (fr) * 1979-06-14 1981-01-09 Sanofi Sa Nouveaux derives de sulfonyl-aniline, leur procede de preparation et leur application therapeutique
JPS5946252A (ja) * 1982-09-09 1984-03-15 Dainippon Ink & Chem Inc 含フツ素アミノカルボキシレ−トおよびその製法
JPS5948449A (ja) * 1982-09-13 1984-03-19 Dainippon Ink & Chem Inc 直鎖状含フツ素アニオン化合物およびその製造方法
JPS6171830A (ja) * 1984-09-17 1986-04-12 Dainippon Ink & Chem Inc 界面活性剤組成物
US4616088A (en) * 1984-10-29 1986-10-07 E. R. Squibb & Sons, Inc. Amino acid ester and amide renin inhibitor
US4629724A (en) * 1984-12-03 1986-12-16 E. R. Squibb & Sons, Inc. Amino acid ester and amide renin inhibitors
DE3635907A1 (de) * 1986-10-22 1988-04-28 Merck Patent Gmbh Hydroxy-aminosaeurederivate
NL8800100A (nl) * 1987-01-21 1988-08-16 Sandoz Ag Nieuwe peptidederivaten en werkwijzen voor het bereiden en toepassen van deze derivaten.
CA1340588C (en) * 1988-06-13 1999-06-08 Balraj Krishan Handa Amino acid derivatives
IL91780A (en) * 1988-10-04 1995-08-31 Abbott Lab History of the amine of the xenon-preventing xanine acid, the process for their preparation and the pharmaceutical preparations containing them
WO1990007330A1 (en) * 1989-01-06 1990-07-12 The Regents Of The University Of California Selection method for specific useful pharmaceutical compounds
US5151438A (en) * 1989-05-23 1992-09-29 Abbott Laboratories Retroviral protease inhibiting compounds
US5354866A (en) * 1989-05-23 1994-10-11 Abbott Laboratories Retroviral protease inhibiting compounds
IE902295A1 (en) * 1989-07-07 1991-01-16 Abbott Lab Amino acid analog cck antagonists
GB8927913D0 (en) * 1989-12-11 1990-02-14 Hoffmann La Roche Amino acid derivatives
JPH07502970A (ja) * 1990-06-01 1995-03-30 ザ・デュポン・メルク・ファーマシュウティカル・カンパニー 1,4―ジアミノ―2,3―ジヒドロキシブタン類
TW225540B (es) * 1990-06-28 1994-06-21 Shionogi & Co
EP0558673B1 (en) * 1990-11-19 1996-04-17 Monsanto Company Retroviral protease inhibitors
ATE196759T1 (de) * 1990-11-19 2000-10-15 Monsanto Co Inhibitoren retroviraler proteasen
DK0813867T3 (da) * 1990-11-19 2005-10-03 Monsanto Co Retrovirale proteaseinhibitorer
DE69126987T2 (de) * 1990-11-19 1998-03-05 Monsanto Co Retrovirale protease-inhibitoren
IE913840A1 (en) * 1990-11-20 1992-05-20 Abbott Lab Retroviral protease inhibiting compounds
ATE163926T1 (de) * 1991-11-08 1998-03-15 Merck & Co Inc Hiv-protease-inhibitoren verwendbar in der aids- behandlung
ATE141265T1 (de) * 1992-05-20 1996-08-15 Searle & Co Verfahren zur herstellung von intermediaten in der synthese von retroviralen protease inhibitoren
WO1993023379A1 (en) * 1992-05-21 1993-11-25 Monsanto Company Retroviral protease inhibitors
EP0656886B1 (en) * 1992-08-25 1997-06-25 G.D. Searle & Co. N-(alkanoylamino-2-hydroxypropyl)-sulfonamides useful as retroviral protease inhibitors
KR100296462B1 (ko) * 1992-08-25 2001-10-24 죤 에이치. 뷰센 레트로바이러스프로테아제억제제로서유용한술포닐알칸오일아미노히드록시에틸아미노술폰아미드
DK0656887T3 (da) * 1992-08-25 1999-07-05 Searle & Co Hydroxyethylaminosulfonamider til anvendelse som inhibitorer af retrovirale proteaser
IS2334B (is) * 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl próteasi hemjari af nýjum flokki súlfonamíða
US5723490A (en) * 1992-09-08 1998-03-03 Vertex Pharmaceuticals Incorporated THF-containing sulfonamide inhibitors of aspartyl protease
CA2142997A1 (en) * 1992-10-30 1994-05-11 Michael L. Vazquez Hydroxyethylamino sulfamic acid derivatives useful as retroviral protease inhibitors
DK0666843T3 (da) * 1992-10-30 2000-03-20 Searle & Co Sulfonylalkanoylaminohydroxyethylaminosulfaminsyrer, der kan anvendes som inhibitorer af retrovirale proteaser
WO1994018192A1 (en) * 1993-02-12 1994-08-18 Merck & Co., Inc. Piperazine derivatives as hiv protease inhibitors
TW281669B (es) * 1993-02-17 1996-07-21 Chugai Pharmaceutical Co Ltd
ATE174587T1 (de) * 1993-08-24 1999-01-15 Searle & Co Hydroxyaminosulfonamide verwendbar als inhibitoren retroviraler proteasen
UA49803C2 (uk) * 1994-06-03 2002-10-15 Дж.Д. Сьорль Енд Ко Спосіб лікування ретровірусних інфекцій

Also Published As

Publication number Publication date
CN1184474A (zh) 1998-06-10
TR199701194T1 (xx) 1998-03-21
KR19990007823A (ko) 1999-01-25
NZ307342A (en) 1999-04-29
HUP9801948A2 (hu) 1999-09-28
GEP20001915B (en) 2000-01-05
EP0833826B1 (en) 2002-01-23
DE69638252D1 (de) 2010-10-14
HUP9801948A3 (en) 2002-04-29
EP0833826A1 (en) 1998-04-08
EA199700330A1 (ru) 1998-04-30
PL322904A1 (en) 1998-03-02
AP9600827A0 (en) 1997-10-17
US5990155A (en) 1999-11-23
NO974744L (no) 1997-10-14
EP1637528B1 (en) 2010-09-01
BG102041A (en) 1998-09-30
JPH11504628A (ja) 1999-04-27
HK1092791A1 (en) 2007-02-16
ES2171670T3 (es) 2002-09-16
CA2217745C (en) 2011-07-05
CO4700433A1 (es) 1998-12-29
PT833826E (pt) 2002-06-28
AU5665596A (en) 1996-11-07
BR9608033A (pt) 1999-01-12
TW404945B (en) 2000-09-11
AP9701104A0 (en) 1997-10-31
ATE212344T1 (de) 2002-02-15
AP862A (en) 2000-08-04
ES2256117T3 (es) 2006-07-16
DE69635679D1 (de) 2006-02-02
CA2217745A1 (en) 1996-10-24
ES2351970T3 (es) 2011-02-14
US5691372A (en) 1997-11-25
WO1996033187A1 (en) 1996-10-24
IL117962A0 (en) 1996-08-04
JP4240532B2 (ja) 2009-03-18
EP1136479B1 (en) 2005-12-28
EE9700254A (et) 1998-04-15
ATE479674T1 (de) 2010-09-15
ZA962891B (en) 1996-10-15
DE69635679T2 (de) 2006-08-31
DE69618779D1 (de) 2002-03-14
IS4575A (is) 1997-10-02
PE43697A1 (es) 1997-10-11
SK143097A3 (en) 1998-03-04
AU712913B2 (en) 1999-11-18
KR100485237B1 (ko) 2005-09-30
CZ329497A3 (cs) 1998-03-18
MY115797A (en) 2003-09-30
EA000906B1 (ru) 2000-06-26
CN1110491C (zh) 2003-06-04
NO974744D0 (no) 1997-10-14
DK0833826T3 (da) 2002-05-06
HK1009811A1 (en) 1999-06-11
ATE314360T1 (de) 2006-01-15
EP1637528A1 (en) 2006-03-22
EP1136479A1 (en) 2001-09-26
DE69618779T2 (de) 2002-08-29

Similar Documents

Publication Publication Date Title
AR004663A1 (es) Un compuesto inhibidor de proteasa aspartilo, una composicion farmaceutica que lo comprende y metodos para inhibir la actividad de proteasa aspartilo,para adherir reversiblemente proteasa aspartilo y para evitar o tratar infecciones vih con dicho compuesto.
ES2131589T3 (es) Sulfonamidas inhibidoras de aspartil-proteasa del vih.
AR031520A1 (es) Un compuesto inhibidor de aspartilo proteasa, una composicion que lo comprende y un metodo para tratar un paciente con dicha composicion
MX9307821A (es) Nueva clase de inhibidores de proteasa aspartilo.
MX9603909A (es) Derivados de sulfonamida como inhibidores de proteasa aspartilo.
EA199700331A1 (ru) Тгф-содержащие сульфонамидные ингибиторы аспартил-протеазы
CY1110690T1 (el) Ενωσεις 4-οξοκινολινης και χρησιμοποιηση αυτων ως αναστολεις της ενσωματασης του hiv
EA199700222A1 (ru) Сульфонилалканоиламиногидроксиэтиламиносульфонамид в качестве ингибиторов ретровирусной протеазы
DK0813543T3 (da) Bis-aminosyrehydroxyethylaminsulfonamider som inhibitorer af retrovirale proteaser
NO974147D0 (no) Heterocykelkarbonyl aminosyre hydroksyetylamino sulfonamid retroviral protease
ATE311391T1 (de) Aspartyl-protease-inhibitoren
AR009935A1 (es) Un compuesto efectivo para inhibir aspartilproteasa, composiciones que lo incorporan y metodos para prevenir o tratar infecciones con hiv
DE60104530D1 (de) Diphenyl ketoaldehyde-derivate mit wirkung gegen hiv
MX9708057A (es) Sulfonamidas que contienen thf inhibidoras de la aspartilproteasa.
MX9708055A (es) Inhibidores de aspartil proteasa consistentes en sulfonamida que contiene heterociclo oxigenado.
MY135869A (en) Inhibitors of aspartyl protease