PE20090067A1 - Inhibidores no nucleosidos de transcriptasa inversa - Google Patents

Inhibidores no nucleosidos de transcriptasa inversa

Info

Publication number
PE20090067A1
PE20090067A1 PE2008000552A PE2008000552A PE20090067A1 PE 20090067 A1 PE20090067 A1 PE 20090067A1 PE 2008000552 A PE2008000552 A PE 2008000552A PE 2008000552 A PE2008000552 A PE 2008000552A PE 20090067 A1 PE20090067 A1 PE 20090067A1
Authority
PE
Peru
Prior art keywords
alkyl
reverse transcriptase
inhibitors
nucleosid
ch2oc
Prior art date
Application number
PE2008000552A
Other languages
English (en)
Inventor
Zachary Kevin Sweeney
Michael Welch
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 PE20090067A1 publication Critical patent/PE20090067A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/12—Oxygen or sulfur atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Obesity (AREA)
  • Virology (AREA)
  • Hematology (AREA)
  • Molecular Biology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

SE REFIERE A COMPUESTOS DE FORMULA I, EN LA QUE X ES CH2 O NH; Y ES CH2 U O; R1 ES H O ALQUILO(C1-C6); R2 ES C(=O)Ar U OAr; R3 Y R4 SON H, HALOGENO, ALQUILO(C1-C6), ALCOXI(C1-C6) O CICLOALQUILO(C3-C5); R5 ES CH2OH, CH2OC(=O)(CH2)nC(=O)OH, CH2OC(=O)-ALQUILO(C1-C6), ENTRE OTROS; n ES DE 2 A 5; Ar ES FENILO SUSTITUIDO POR 1-3 GRUPOS ELEGIDOS DE HALOGENO, CIANO, CICLOALQUILO(C3-C5), ENTRE OTROS. SON SELECCIONADOS 3-YODOMETIL-5-METANOSULFONIL-4-METIL-4H-[1,2,4]TRIAZOL, 3-[6-BROMO-2-FLUOR-3-(4-METIL-5-OXO-4,5-DIHIDRO-1H-[1,2,4]TRIAZOL-3-ILMETOXI)-FENOXI]-5-DIFLUORMETIL-BENZONITRILO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y COMPOSICION FARMACEUTICA. DICHOS COMPÙESTOS SON INHIBIDORES DE TRANSCRIPTASA INVERSA, UTILES EN EL TRATAMIENTO DE VIH-1, SIDA Y/O ARC
PE2008000552A 2007-03-29 2008-03-27 Inhibidores no nucleosidos de transcriptasa inversa PE20090067A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US92063507P 2007-03-29 2007-03-29

Publications (1)

Publication Number Publication Date
PE20090067A1 true PE20090067A1 (es) 2009-01-26

Family

ID=39591446

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000552A PE20090067A1 (es) 2007-03-29 2008-03-27 Inhibidores no nucleosidos de transcriptasa inversa

Country Status (15)

Country Link
US (1) US7906540B2 (es)
EP (1) EP2142520A1 (es)
JP (1) JP2010522706A (es)
KR (1) KR20090127178A (es)
CN (1) CN101657433A (es)
AR (1) AR067271A1 (es)
AU (1) AU2008233929A1 (es)
BR (1) BRPI0809617A2 (es)
CA (1) CA2682637A1 (es)
CL (1) CL2008000862A1 (es)
IL (1) IL200748A0 (es)
MX (1) MX2009009920A (es)
PE (1) PE20090067A1 (es)
TW (1) TW200901985A (es)
WO (1) WO2008119662A1 (es)

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TWI490214B (zh) 2008-05-30 2015-07-01 艾德克 上野股份有限公司 苯或噻吩衍生物及該等作為ｖａｐ－１抑制劑之用途
WO2013056003A2 (en) * 2011-10-12 2013-04-18 Yale University Catechol diethers as potent anti-hiv agents
WO2013134562A1 (en) 2012-03-09 2013-09-12 Inception 2, Inc. Triazolone compounds and uses thereof
CA2872213A1 (en) 2012-06-13 2013-12-19 F. Hoffmann-La Roche Ag New diazaspirocycloalkane and azaspirocycloalkane
UA116547C2 (uk) 2012-09-25 2018-04-10 Ф. Хоффманн-Ля Рош Аг Біциклічні похідні
EP2935228B9 (en) 2012-12-20 2017-12-06 Inception 2, Inc. Triazolone compounds and uses thereof
AR095079A1 (es) 2013-03-12 2015-09-16 Hoffmann La Roche Derivados de octahidro-pirrolo[3,4-c]-pirrol y piridina-fenilo
CA2921420A1 (en) 2013-09-06 2015-03-12 Inception 2, Inc. Triazolone compounds and uses thereof
CN105764905B (zh) 2013-11-26 2019-06-07 豪夫迈·罗氏有限公司 新的八氢-环丁二烯并[1，2-c；3，4-c’]二吡咯-2基
CA2935612A1 (en) 2014-03-26 2015-10-01 F. Hoffmann-La Roche Ag Condensed [1,4]diazepine compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors
HUE046820T2 (hu) 2014-03-26 2020-03-30 Hoffmann La Roche Biciklusos vegyületek autotaxin (ATX) és lizofoszfatidsav (LPA) termelésgátlókként
MA41898A (fr) 2015-04-10 2018-02-13 Hoffmann La Roche Dérivés de quinazolinone bicyclique
CR20180058A (es) 2015-09-04 2018-02-26 Hoffmann La Roche Nuevos derivados de fenoximetilo
CN107614505B (zh) 2015-09-24 2021-05-07 豪夫迈·罗氏有限公司 作为双重atx/ca抑制剂的新型二环化合物
EP3353178B1 (en) 2015-09-24 2021-07-14 F. Hoffmann-La Roche AG Bicyclic compounds as dual atx/ca inhibitors
CA2991615A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag Bicyclic compounds as atx inhibitors
JP6846414B2 (ja) 2015-09-24 2021-03-24 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ Ａｔｘ阻害剤としての二環式化合物
CN110382484B (zh) 2017-03-16 2022-12-06 豪夫迈·罗氏有限公司 新的作为atx抑制剂的二环化合物
KR20190129924A (ko) 2017-03-16 2019-11-20 에프. 호프만-라 로슈 아게 이중 오토탁신(atx)/탄산 무수화효소(ca) 억제제로서 유용한 헤테로환형 화합물
KR20190110736A (ko) * 2018-03-21 2019-10-01 주식회사유한양행 신규의 트라이아졸론 유도체 또는 이의 염 및 이를 포함하는 약학 조성물
KR20190110740A (ko) * 2018-03-21 2019-10-01 주식회사유한양행 신규의 아릴 또는 헤테로아릴 트라이아졸론 유도체 또는 이의 염 및 이를 포함하는 약학 조성물
TW202039486A (zh) 2018-12-14 2020-11-01 南韓商柳韓洋行股份有限公司 ***并吡啶-3-酮化物或其鹽及包含彼之醫藥組合物
CR20210308A (es) * 2018-12-14 2021-08-30 Yuhan Corp 3,3- difluoroalilaminas o sales de las mismas y composiciones farmacéuticas que los comprenden
CN111440147B (zh) * 2020-05-19 2023-03-07 苏州卫生职业技术学院 N-(2-甲基-5-氨基苯基)-4-(3-吡啶基)-2-嘧啶胺的合成方法
GB2598624A (en) * 2020-09-07 2022-03-09 Lorico Aurelio Use of triazole analogues for inhibition of a tripartite VOR protein complex in multicellular organisms
CN112220771B (zh) * 2020-11-10 2023-03-31 成都大学 扎西他滨渗透泵型控释片及其制备方法

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Also Published As

Publication number Publication date
IL200748A0 (en) 2010-05-17
TW200901985A (en) 2009-01-16
JP2010522706A (ja) 2010-07-08
MX2009009920A (es) 2009-10-19
US20080249151A1 (en) 2008-10-09
KR20090127178A (ko) 2009-12-09
CL2008000862A1 (es) 2008-11-14
CA2682637A1 (en) 2008-10-09
CN101657433A (zh) 2010-02-24
BRPI0809617A2 (pt) 2014-09-16
WO2008119662A1 (en) 2008-10-09
AU2008233929A1 (en) 2008-10-09
US7906540B2 (en) 2011-03-15
AR067271A1 (es) 2009-10-07
EP2142520A1 (en) 2010-01-13

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