PE20020610A1 - Compuestos hidroxietilamina tripeptidos mimeticos como inhibidores de la aspartil proteasa de vih - Google Patents

Compuestos hidroxietilamina tripeptidos mimeticos como inhibidores de la aspartil proteasa de vih

Info

Publication number
PE20020610A1
PE20020610A1 PE2001001170A PE2001001170A PE20020610A1 PE 20020610 A1 PE20020610 A1 PE 20020610A1 PE 2001001170 A PE2001001170 A PE 2001001170A PE 2001001170 A PE2001001170 A PE 2001001170A PE 20020610 A1 PE20020610 A1 PE 20020610A1
Authority
PE
Peru
Prior art keywords
alkyl
aspartile
tripeptide
mimetic
hiv
Prior art date
Application number
PE2001001170A
Other languages
English (en)
Inventor
Joseph Armstrong Martin
Sally Redshaw
Steven Swallow
Gareth John Thomas
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20020610A1 publication Critical patent/PE20020610A1/es

Links

Classifications

    • 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
    • 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
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
    • C07D217/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links

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)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • AIDS & HIV (AREA)
  • Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A COMPUESTOS HIDROXIETILAMINA TRIPEPTIDOS MIMETICOS DE FORMULA I DONDE R1 ES H, OH, NHR2 DONDE R2 ES H, ALQUILO, ALQUENILO, ALQUINILO, ARILALQUILO, HETEROCICLILALQUILO, CICLOALQUIL ALQUIL CARBONILO, ENTRE OTROS; R3 Y R4 SON ALQUILO O JUNTO AL CARBONO AL QUE ESTAN UNIDOS FORMAN UN CARBOCICLO; R5 ES ALQUIL, ARIL ALQUILO HETEROCICLIL ALQUILO; R4 Y R5 JUNTO A C Y S AL QUE ESTAN UNIDOS FORMAN UN HETEROCICLO; R6 ES ALQUILO, ARIL ALQUILO, HETEROCICLIL ALQUILO, ENTRE OTROS; R13 ES UN ESTER INORGANICO U ORGANICO; R15 ES ARILO. SON COMPUESTOS PREFERIDOS 2-[3(S)-[[N-BENZOIL-3-(METANOSULFONIL)-L-VALIL]-AMINO]-2(R)-HIDROXI-4-FENILBUTIL]-N-BENCIL-1,2,3,4,4a(S),5,6,7,8,8a(S)-DECAHIDRO-3(S)-ISOQUINOLINA-CARBOXAMIDA, N-TERC-BUTIL-2-[3(S)-[[N-[(9-FLUORFENI)-METOXI-CARBONIL]-3-(METANO-SULFONIL)-L-VALIL]-AMINO]-2(R)-HIDROXI-4-FENILBUTIL]-1,2,3,4,4a(S),5,6,7,8,8a(S)-DECAHIDRO-3(S)-ISOQUINOLINA-CARBOXAMIDA. LOS COMPUESTOS MENCIONADOS SON INHIBIDORES DE LA ASPARTIL PROTEASA DE VIH.
PE2001001170A 2000-11-22 2001-11-22 Compuestos hidroxietilamina tripeptidos mimeticos como inhibidores de la aspartil proteasa de vih PE20020610A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0028483.6A GB0028483D0 (en) 2000-11-22 2000-11-22 Hydroxyethylamine HIV protease inhibitors

Publications (1)

Publication Number Publication Date
PE20020610A1 true PE20020610A1 (es) 2002-07-13

Family

ID=9903670

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2001001170A PE20020610A1 (es) 2000-11-22 2001-11-22 Compuestos hidroxietilamina tripeptidos mimeticos como inhibidores de la aspartil proteasa de vih

Country Status (27)

Country Link
US (1) US6472404B1 (es)
EP (1) EP1339692A1 (es)
JP (1) JP2004520283A (es)
KR (1) KR20030060953A (es)
CN (1) CN1476436A (es)
AR (1) AR031763A1 (es)
AU (2) AU2954602A (es)
BG (1) BG107839A (es)
BR (1) BR0115566A (es)
CA (1) CA2428459A1 (es)
CZ (1) CZ20031667A3 (es)
EC (1) ECSP034618A (es)
GB (1) GB0028483D0 (es)
GT (1) GT200100233A (es)
HU (1) HUP0303007A2 (es)
IL (1) IL155573A0 (es)
MA (1) MA26966A1 (es)
MX (1) MXPA03004534A (es)
NO (1) NO20032290D0 (es)
NZ (1) NZ525550A (es)
PA (1) PA8533401A1 (es)
PE (1) PE20020610A1 (es)
PL (1) PL366704A1 (es)
RU (1) RU2265016C2 (es)
SK (1) SK7602003A3 (es)
UY (1) UY27033A1 (es)
WO (1) WO2002042277A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101014572B (zh) * 2004-09-15 2011-07-06 盐野义制药株式会社 具有hiv整合酶抑制活性的氨基甲酰基吡啶酮衍生物
UA87884C2 (uk) * 2004-12-03 2009-08-25 Мерк Энд Ко., Инк. Безводна кристалічна калієва сіль інгібітора віл-інтегрази
MY161992A (en) * 2008-03-26 2017-05-31 Daiichi Sankyo Co Ltd Novel tetrahydroisoquinoline derivative

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8927913D0 (en) 1989-12-11 1990-02-14 Hoffmann La Roche Amino acid derivatives
MX9308016A (es) * 1992-12-22 1994-08-31 Lilly Co Eli Compuestos inhibidores de la proteasa del virus de la inmunodeficiencia humana, procedimiento para su preparacion y formulacion farmaceutica que los contiene.

Also Published As

Publication number Publication date
NO20032290L (no) 2003-05-21
BG107839A (bg) 2004-06-30
NO20032290D0 (no) 2003-05-21
RU2003117468A (ru) 2005-01-27
BR0115566A (pt) 2003-09-30
MXPA03004534A (es) 2003-09-10
RU2265016C2 (ru) 2005-11-27
GT200100233A (es) 2002-07-04
EP1339692A1 (en) 2003-09-03
AR031763A1 (es) 2003-10-01
CZ20031667A3 (cs) 2004-01-14
PA8533401A1 (es) 2002-10-31
WO2002042277A1 (en) 2002-05-30
CA2428459A1 (en) 2002-05-30
SK7602003A3 (en) 2004-01-08
GB0028483D0 (en) 2001-01-10
HUP0303007A2 (hu) 2003-12-29
MA26966A1 (fr) 2004-12-20
KR20030060953A (ko) 2003-07-16
AU2954602A (en) 2002-06-03
ECSP034618A (es) 2003-06-25
JP2004520283A (ja) 2004-07-08
CN1476436A (zh) 2004-02-18
PL366704A1 (en) 2005-02-07
US6472404B1 (en) 2002-10-29
NZ525550A (en) 2004-11-26
IL155573A0 (en) 2003-11-23
AU2002229546B2 (en) 2006-05-04
UY27033A1 (es) 2002-06-20

Similar Documents

Publication Publication Date Title
EA200100755A1 (ru) 4-оксо-1,4-дигидро-3-хинолинкарбоксамиды как антивирусные агенты
ECSP034660A (es) Derivados del novedoso carbamato de quinuclidina y las composiciones medicinales que los contienen
EA200200708A1 (ru) Производные бензазола и их применение в качестве модуляторов jnk
LU91196I2 (fr) Picoxystrobin et ses dérivlés pharmaceutiquement acceptables(ACANTO).
CO4940458A1 (es) Novedosos inhibidores de urea n-sustituida de transferasa de proteina farnesilo
ATE270103T1 (de) Aminophenoxyessigsäure derivate als neuroschützende mittel
EA200100970A1 (ru) Аминопроизводные как ингибиторы протеазы
CO5650168A2 (es) Nuevos peptidos como inhibidores de la proteasa serina ns3 del virus de la hepatitis c
PE20020566A1 (es) DERIVADOS DE FENILACETAMIDO-PIRAZOLES COMO INHIBIDORES DE LA cdk/CICLINA QUINASA
CO5160347A1 (es) Derivados de acido carbamico
AR039226A2 (es) Compuestos utiles como intermediarios de preparacion y procedimientos
EA200201071A1 (ru) Циклопентилзамещенные производные глутарамида в качестве ингибиторов нейтральной эндопептидазы
ES2133504T3 (es) Derivados peptidicos del acido boronico con una actividad inhibidora de proteasa, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen.
CO4940477A1 (es) Inhibidores de proteasa
CO4950553A1 (es) Compuestos de 7-tetrahidroisoquinolinas y procedimiento para su preparacion
CO4950567A1 (es) Inhibidores de proteasas dores de proteasas.
EA200300044A1 (ru) Новые замещенные фталиды, способ их получения и содержащие их фармацевтические композиции
ES553058A0 (es) Procedimiento de preparacion de aminoacidos opticamente activos.
EA200100297A1 (ru) Моногидрат гидробромида элетриптана
PE20020610A1 (es) Compuestos hidroxietilamina tripeptidos mimeticos como inhibidores de la aspartil proteasa de vih
PT97766A (pt) Processo depreparacao de derivados de isocromano e de composicoes farmaceuticas que os contem
AR024219A1 (es) COMPUESTOS DE QUINOLONAS 2-(NH- U O-SUSTITUIDAS) UTILES COMO INHIBIDORES DE LA METIONIL t-RNA SINTETASA (MRS) COMPOSICIONES FARMACEUTICAS FORMULADAS CONDICHOS COMPUESTOS; PROCEDIMIENTO PARA SU PREPARACION Y USO DE DICHOS COMPUESTOS PARA PREPARAR MEDICAMENTOS PARA EL TRATAMIENTO DE INFECCIONES BACTER
ES2183434T3 (es) Derivados de cromano sustituidos con carboxilo utiles como agonistas de adrenoreceptores.
MX9302165A (es) Derivados de benzoxazinona y benzothiazinona y composiciones farmaceuticas que los comprende
AR027454A1 (es) Derivados de beta-alanina, utiles como antagonistas de receptores, las composiciones farmaceuticas que las contienen y el uso de los mismos para lapreparacion de medicamentos

Legal Events

Date Code Title Description
FA Abandonment or withdrawal