[go: up one dir, main page]

AR028958A1 - INHIBIDORES DE TRANSCRIPTASA INVERSA NO NUCLEoSIDOS - Google Patents

INHIBIDORES DE TRANSCRIPTASA INVERSA NO NUCLEoSIDOS

Info

Publication number
AR028958A1
AR028958A1 ARP010102870A ARP010102870A AR028958A1 AR 028958 A1 AR028958 A1 AR 028958A1 AR P010102870 A ARP010102870 A AR P010102870A AR P010102870 A ARP010102870 A AR P010102870A AR 028958 A1 AR028958 A1 AR 028958A1
Authority
AR
Argentina
Prior art keywords
nucleosidos
formula
group
inhibitors
inverse
Prior art date
Application number
ARP010102870A
Other languages
English (en)
Inventor
Bruno Simoneau
Original Assignee
Boehringer Ingelheim Ca Ltd
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 Boehringer Ingelheim Ca Ltd filed Critical Boehringer Ingelheim Ca Ltd
Publication of AR028958A1 publication Critical patent/AR028958A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-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
    • 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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
  • Steroid Compounds (AREA)

Abstract

Se proporcionan compuestos de la formula general (1) en donde R2 se selecciona del grupo que consiste en H, F, Cl, alquilo (C1-4), cicloalquilo (C3-4) y CF3; R4 es H o Me; R5 es H, Me o Et, con la condicion de que R4 y R5 no sean ambos Me y si R4 es Me, entonces R5 no puede ser Et; R11 es Et, ciclopropilo, propilo, isopropilo o isobutilo; y Q se selecciona del grupo de formula (2) y sus sales farmacéuticamente aceptables, como inhibidores de la transcriptasa inversa de VIHH, cepas de tipo salvaje,y varias cepas mutantes. Una composicion farmacéutica que contiene al compuesto de formula (1)
ARP010102870A 2000-06-16 2001-06-15 INHIBIDORES DE TRANSCRIPTASA INVERSA NO NUCLEoSIDOS AR028958A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US21232900P 2000-06-16 2000-06-16
US25663800P 2000-12-18 2000-12-18

Publications (1)

Publication Number Publication Date
AR028958A1 true AR028958A1 (es) 2003-05-28

Family

ID=26907019

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP010102870A AR028958A1 (es) 2000-06-16 2001-06-15 INHIBIDORES DE TRANSCRIPTASA INVERSA NO NUCLEoSIDOS

Country Status (35)

Country Link
US (1) US6420359B1 (es)
EP (1) EP1294720B1 (es)
JP (1) JP3923894B2 (es)
KR (1) KR20030017540A (es)
CN (1) CN1178939C (es)
AR (1) AR028958A1 (es)
AT (1) ATE322492T1 (es)
AU (2) AU7037001A (es)
BG (1) BG107348A (es)
BR (1) BR0102377A (es)
CA (1) CA2411766C (es)
CZ (1) CZ20024114A3 (es)
DE (1) DE60118560T2 (es)
DK (1) DK1294720T3 (es)
EA (1) EA005598B1 (es)
EE (1) EE200200690A (es)
ES (1) ES2261433T3 (es)
HR (1) HRP20021003A2 (es)
HU (1) HUP0301105A2 (es)
IL (1) IL152819A0 (es)
MX (1) MXPA02012205A (es)
MY (1) MY130375A (es)
NO (1) NO323830B1 (es)
NZ (1) NZ523549A (es)
PE (1) PE20020083A1 (es)
PL (1) PL360370A1 (es)
PT (1) PT1294720E (es)
SA (1) SA01220202B1 (es)
SK (1) SK17722002A3 (es)
TW (1) TWI270547B (es)
UA (1) UA74834C2 (es)
UY (1) UY26767A1 (es)
WO (1) WO2001096338A1 (es)
YU (1) YU94202A (es)
ZA (1) ZA200209807B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6716836B2 (en) 2001-03-22 2004-04-06 Boehringer Ingelheim (Canada) Ltd. Non-nucleoside reverse transcriptase inhibitors
US6673791B2 (en) * 2001-07-30 2004-01-06 Boehringer Ingelheim (Canada) Ltd. Non-nucleoside reverse transcriptase inhibitors
US6706706B2 (en) * 2002-03-27 2004-03-16 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
US6806265B2 (en) * 2002-05-16 2004-10-19 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
US6759533B2 (en) * 2002-06-28 2004-07-06 Boehringer Ingelheim Pharmaceuticals, Inc. Process and intermediates for making non-nucleoside HIV-1 reverse transcriptase inhibitors
US7642277B2 (en) 2002-12-04 2010-01-05 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
KR20050085681A (ko) * 2002-12-16 2005-08-29 베링거 인겔하임 인터내셔날 게엠베하 프로테아제 억제제와 같은 사이토크롬 p450의 억제제와함께 비-뉴클레오시드 역전사효소 억제제(nnrti)를함유하는 배합물의 용도
WO2004087140A1 (en) * 2003-03-27 2004-10-14 Boehringer Ingelheim International Gmbh Antiviral combination of a dipyridodiazepinone and a further antiretroviral compound
US7309700B2 (en) * 2004-04-02 2007-12-18 Boehringer Ingelheim International Gmbh Crystalline forms of 5,11-dihydro-11-ethyl-5-methyl-8-{2-{(1-oxido-4-quinolinyl)oxy}ethyl}-6H-dipyrido[3,2-b:2′,3′-e] [1,4]diazepin-6-one
US20060025480A1 (en) 2004-08-02 2006-02-02 Boehringer Ingelheim International Gmbh Benzoic acid derivatives as non nucleoside reverse transcriptase inhibitors
US7151174B2 (en) 2004-11-05 2006-12-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Process for making a non-nucleoside HIV-1 reverse transcriptase inhibitor
WO2007067844A1 (en) * 2005-12-05 2007-06-14 Boehringer Ingelheim International Gmbh Process for making 5,11-dihydro-11-ethyl-5-methyl-8-{2-{(1-oxido-4-quinolinyl)oxy}ethyl}-6h-di pyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
EP2085390A1 (en) 2008-01-31 2009-08-05 Institut National De La Sante Et De La Recherche Medicale (Inserm) Labelled analogues of halobenzamides as multimodal radiopharmaceuticals and their precursors
JP5643290B2 (ja) * 2009-04-09 2014-12-17 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 Hiv複製の阻害薬

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5366972A (en) * 1989-04-20 1994-11-22 Boehringer Ingelheim Pharmaceuticals, Inc. 5,11-dihydro-6H-dipyrido(3,2-B:2',3'-E)(1,4)diazepines and their use in the prevention or treatment of HIV infection
US5705499A (en) * 1995-10-06 1998-01-06 Boehringer Ingelheim Pharmaceuticals, Inc. 8-arylalkyl- and 8-arylheteroalkyl-5,11-dihydro-6H-dipyrido 3,2-B:2',3'-e! 1!diazepines and their use in the treatment of HIV-1 infection

Also Published As

Publication number Publication date
CZ20024114A3 (cs) 2003-04-16
US20020028807A1 (en) 2002-03-07
PT1294720E (pt) 2006-06-30
EE200200690A (et) 2004-06-15
IL152819A0 (en) 2003-06-24
HUP0301105A2 (hu) 2003-08-28
HRP20021003A2 (en) 2005-02-28
UY26767A1 (es) 2002-01-31
KR20030017540A (ko) 2003-03-03
AU2001270370B2 (en) 2006-08-03
CN1178939C (zh) 2004-12-08
NO20025844D0 (no) 2002-12-05
JP2004502787A (ja) 2004-01-29
NO20025844L (no) 2002-12-05
YU94202A (sh) 2005-11-28
BG107348A (bg) 2004-06-30
ATE322492T1 (de) 2006-04-15
AU7037001A (en) 2001-12-24
SK17722002A3 (sk) 2003-06-03
MXPA02012205A (es) 2003-09-10
DK1294720T3 (da) 2006-07-31
CA2411766A1 (en) 2001-12-20
EA005598B1 (ru) 2005-04-28
EP1294720A1 (en) 2003-03-26
SA01220202B1 (ar) 2006-09-05
EA200201255A1 (ru) 2003-06-26
JP3923894B2 (ja) 2007-06-06
CA2411766C (en) 2006-05-23
MY130375A (en) 2007-06-29
PE20020083A1 (es) 2002-02-28
EP1294720B1 (en) 2006-04-05
CN1436189A (zh) 2003-08-13
US6420359B1 (en) 2002-07-16
HK1057558A1 (en) 2004-04-08
UA74834C2 (en) 2006-02-15
DE60118560D1 (de) 2006-05-18
WO2001096338A1 (en) 2001-12-20
PL360370A1 (en) 2004-09-06
BR0102377A (pt) 2002-02-19
TWI270547B (en) 2007-01-11
ES2261433T3 (es) 2006-11-16
ZA200209807B (en) 2003-10-16
NO323830B1 (no) 2007-07-09
DE60118560T2 (de) 2006-09-28
NZ523549A (en) 2004-08-27

Similar Documents

Publication Publication Date Title
AR028958A1 (es) INHIBIDORES DE TRANSCRIPTASA INVERSA NO NUCLEoSIDOS
PE20021056A1 (es) Derivados de pirazol
ATE244241T1 (de) Hemmung der menschlichen telomerase durch g- quadruplex interaktionverbindung
MY152153A (en) Macrocylic inhibitors of hepatitis c virus
CA2295063A1 (en) Indole compounds as anti-inflammatory/analgesic agents
CO5611139A2 (es) Pirimidinas aril sustituidas y el uso de las mismas
ES2422383T3 (es) Activadores de urea glucoquinasa
AR077416A2 (es) Compuesto polimorfo estable de flibanserina , procedimiento industrial para su preparacion y uso del mismo para preparar medicamentos
AR060545A1 (es) Compuestos de benzoaxol y benzotiazol 6-0- sustituidos y metodos de inhibicion de la senalizacion de csf-1r. composiciones farmaceuticas
NO166129C (no) Analogifremgangsmaate for fremstilling av terapeutisk aktive tetrahydro-9h-pyrido (3,4-b)indoler.
ES8600211A1 (es) Un procedimiento para la preparacion de nuevos derivados arilfenilicos
DE60306539D1 (de) Nicht-nukleosidische inhibitoren der reverse transkriptase
CL2024001620A1 (es) Inhibidores del sarcómero cardíaco
DE60121587D1 (de) Zyklische gmp-spezifische phosphodiesteraseinhibitoren
CA2450868A1 (en) Non-nucleoside reverse transcriptase inhibitors
AR044175A1 (es) Compuestos de cefemo
AP2004003143A0 (en) Fungicidal triazolopyrimidines, methods for producing the same, use thereof for combating harmful fungi and agents containing said substances.
ID30435A (id) Proses-proses untuk menyiapkan perantara-perantara pestisidal
AR053345A1 (es) Compuesto de 1,2,4 triazolo-5-ona como inhibidores de la transcriptasa inversa
CO5180536A1 (es) Inhibidores de proteasas catepsina
AR023528A1 (es) Derivados de ciclobuten-3,4-diona, su preparacion y su aplicacion en terapeutica
WO2002018350A1 (en) Grk inhibitor
DE3860667D1 (de) 1-aminomethyl-3-aryl-4-cyano-pyrrole.
TW330203B (en) 1-Cycloalkenyltetrazolinones
AR048631A1 (es) Derivados de dialcoxi-imidazopiridinas, composiciones farmaceuticas que los contienen y usos,

Legal Events

Date Code Title Description
FB Suspension of granting procedure