ECSP045432A - Inhibidores de la transcriptasa inversa no nucleosidos - Google Patents

Inhibidores de la transcriptasa inversa no nucleosidos

Info

Publication number
ECSP045432A
ECSP045432A EC2004005432A ECSP045432A ECSP045432A EC SP045432 A ECSP045432 A EC SP045432A EC 2004005432 A EC2004005432 A EC 2004005432A EC SP045432 A ECSP045432 A EC SP045432A EC SP045432 A ECSP045432 A EC SP045432A
Authority
EC
Ecuador
Prior art keywords
alkyl
group
aryl
heterocycle
ring
Prior art date
Application number
EC2004005432A
Other languages
English (en)
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 filed Critical
Publication of ECSP045432A publication Critical patent/ECSP045432A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/12—Heterocyclic 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
    • C07D471/14—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • AIDS & HIV (AREA)
  • Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Compuestos representados por la fórmula I; en dondeR2 se selecciona del grupo que consiste en H, alquilo (C1-4), halo, haloalquilo, OH, alcoxi (C1-6), NH(alquilo C1-4) o N(alquilo C1-4)2; R4 es H o Me; R5 es H o Me; R11 es H, alquilo (C1-4), cicloalquilo (C3-4) y alquil (C1-4)-cicloalquilo (C3-4);A es una cadena de conexión de alquilo (C1-3); B es O S; n es 0 ó 1; en donde, cuando n es 0:el anillo C es arilo de 6 ó 10 miembros o un heterociclo de 5 ó 6 miembros con 1 a 4 heteroátomos seleccionados del grupo que consiste en O, N y S, estando dicho arilo y dicho heterociclo opcionalmente sustituidos;y E es CONR12R13; CONHNR14R15; NR16COR17; NR18SO2alquilo (C1-6); SO2NR19R20 o SO2R21; o cuando n es 1: el anillo C es como se define anteriormente yE es un enlace sencillo o un grupo de conexión; y el anillo D es un arilo de 6 ó 10 miembros o un heterociclo de 5 ó 6 miembros con 1 a 4 heteroátomos seleccionados del grupo que consiste en O, N y S, estando dicho arilo y dicho heterociclo opcionalmente sustituidos con 1 a 5 sustituyentes; o una sal o un profármaco se proporcionan como inhibidores de transcriptasa inversa de VIH.
EC2004005432A 2002-05-16 2004-11-16 Inhibidores de la transcriptasa inversa no nucleosidos ECSP045432A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US38088602P 2002-05-16 2002-05-16

Publications (1)

Publication Number Publication Date
ECSP045432A true ECSP045432A (es) 2005-01-03

Family

ID=29550032

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2004005432A ECSP045432A (es) 2002-05-16 2004-11-16 Inhibidores de la transcriptasa inversa no nucleosidos

Country Status (28)

Country Link
US (1) US6806265B2 (es)
EP (1) EP1506195B1 (es)
JP (1) JP4230448B2 (es)
KR (1) KR20050008716A (es)
CN (1) CN1318421C (es)
AR (1) AR040027A1 (es)
AT (1) ATE412653T1 (es)
AU (1) AU2003229186A1 (es)
BR (1) BR0310033A (es)
CA (1) CA2485916C (es)
DE (1) DE60324418D1 (es)
EA (1) EA009178B1 (es)
EC (1) ECSP045432A (es)
ES (1) ES2315492T3 (es)
HR (1) HRP20041065A2 (es)
IL (1) IL163753A0 (es)
MX (1) MXPA04010409A (es)
MY (1) MY134646A (es)
NO (1) NO20044104L (es)
NZ (1) NZ536736A (es)
PE (1) PE20040365A1 (es)
PL (1) PL371663A1 (es)
RS (1) RS98004A (es)
TW (1) TW200404071A (es)
UA (1) UA79285C2 (es)
UY (1) UY27809A1 (es)
WO (1) WO2003097644A2 (es)
ZA (1) ZA200406912B (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0302094D0 (en) 2003-01-29 2003-02-26 Pharmagene Lab Ltd EP4 receptor antagonists
EP1610797A1 (en) * 2003-03-27 2006-01-04 Boehringer Ingelheim International GmbH Antiviral combination of nevirapine and a further antiretroviral compound
US7348338B2 (en) 2003-07-17 2008-03-25 Plexxikon, Inc. PPAR active compounds
BRPI0412684A (pt) * 2003-07-17 2006-10-03 Plexxinko Inc compostos ppar-ativos
GB0324269D0 (en) 2003-10-16 2003-11-19 Pharmagene Lab Ltd EP4 receptor antagonists
DE102004051277A1 (de) * 2004-10-21 2006-04-27 Merck Patent Gmbh Heterocyclische Carbonylverbindungen
EP1819673A2 (en) * 2004-11-30 2007-08-22 Plexxikon, Inc. Indole derivatives for use as ppar active compounds
CA2621406A1 (en) * 2005-09-07 2007-03-15 Plexxikon, Inc. Pparactive compounds
CA2621474A1 (en) * 2005-09-07 2007-03-15 Plexxikon, Inc. 1,3-disubstituted indole derivatives for use as ppar modulators
CA2621275A1 (en) * 2005-09-07 2007-03-15 Plexxikon, Inc. 1 , 4 and 1 , 5-disubstituted indole derivatives for use as ppar active compounds
WO2008051197A2 (en) 2005-09-20 2008-05-02 Mayo Foundation For Medical Education And Research Small-molecule botulinum toxin inhibitors
PE20090159A1 (es) * 2007-03-08 2009-02-21 Plexxikon Inc COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs
CA2968464A1 (en) 2014-11-25 2016-06-02 Bayer Pharma Aktiengesellschaft Substituted pyridobenzodiazepinone-derivatives and use thereof
KR20200030584A (ko) 2017-07-21 2020-03-20 앤타바이오 에스에이에스 화합물
CR20200464A (es) 2018-03-08 2021-04-14 Incyte Corp Compuestos diólicos de aminopirazina como inhibidores de pi3k-y
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
CA3229569A1 (en) * 2021-08-20 2023-02-23 Enanta Pharmaceuticals, Inc. 17-beta-hydroxysteroid dehydrogenase type 13 inhibitors and methods of use thereof

Family Cites Families (5)

* 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
TWI270547B (en) 2000-06-16 2007-01-11 Boehringer Ingelheim Ca Ltd Non-nucleoside reverse transcriptase inhibitors
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

Also Published As

Publication number Publication date
UA79285C2 (en) 2007-06-11
US6806265B2 (en) 2004-10-19
TW200404071A (en) 2004-03-16
CA2485916C (en) 2009-12-08
CN1653066A (zh) 2005-08-10
NO20044104L (no) 2004-12-01
EA009178B1 (ru) 2007-12-28
HRP20041065A2 (en) 2005-04-30
JP2005526851A (ja) 2005-09-08
PL371663A1 (en) 2005-06-27
HK1080849A1 (en) 2006-05-04
CN1318421C (zh) 2007-05-30
EP1506195B1 (en) 2008-10-29
MY134646A (en) 2007-12-31
PE20040365A1 (es) 2004-07-22
BR0310033A (pt) 2005-02-15
NZ536736A (en) 2006-11-30
UY27809A1 (es) 2003-12-31
US20040006071A1 (en) 2004-01-08
ES2315492T3 (es) 2009-04-01
AU2003229186A1 (en) 2003-12-02
RS98004A (sr) 2006-12-15
ATE412653T1 (de) 2008-11-15
JP4230448B2 (ja) 2009-02-25
CA2485916A1 (en) 2003-11-27
MXPA04010409A (es) 2005-02-17
EP1506195A2 (en) 2005-02-16
WO2003097644A3 (en) 2004-02-05
KR20050008716A (ko) 2005-01-21
DE60324418D1 (de) 2008-12-11
ZA200406912B (en) 2006-06-28
IL163753A0 (en) 2005-12-18
EA200401482A1 (ru) 2005-06-30
AR040027A1 (es) 2005-03-09
WO2003097644A2 (en) 2003-11-27

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