MX2009012704A - Inhibidores de transcriptasa inversa de no nucleosidos. - Google Patents

Inhibidores de transcriptasa inversa de no nucleosidos.

Info

Publication number
MX2009012704A
MX2009012704A MX2009012704A MX2009012704A MX2009012704A MX 2009012704 A MX2009012704 A MX 2009012704A MX 2009012704 A MX2009012704 A MX 2009012704A MX 2009012704 A MX2009012704 A MX 2009012704A MX 2009012704 A MX2009012704 A MX 2009012704A
Authority
MX
Mexico
Prior art keywords
reverse transcriptase
treatment
transcriptase inhibitors
nucleoside reverse
hiv
Prior art date
Application number
MX2009012704A
Other languages
English (en)
Inventor
Jeffrey Wu
Zachary Kevin Sweeney
Joshua Kennedy-Smith
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39712538&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX2009012704(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2009012704A publication Critical patent/MX2009012704A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/20Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D239/22Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • A61K31/4174Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • C07D233/76Two oxygen atoms, e.g. hydantoin with substituted hydrocarbon radicals attached to the third ring carbon atom
    • C07D233/78Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/553Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms with halogen atoms or nitro radicals directly attached to ring carbon atoms, e.g. fluorouracil

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • General Chemical & Material Sciences (AREA)
  • AIDS & HIV (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente invención se refiere a compuestos de Fórmula (I), en donde R1, X1, X2 y A, son como se definen en la presente, o sales de los mismos farmacéuticamente aceptables, inhiben la transcriptasa inversa del VIH-1 y proporcionan un medio para la prevención y tratamiento de infecciones por VIH-1 y el tratamiento de SIDA y/o ARC. La presente invención también se refiere a composiciones que contienen compuestos de fórmula (I), útiles para la prevención y tratamiento de infecciones por VIH-1 y el tratamiento de SIDA y/o ARC.
MX2009012704A 2007-05-30 2008-05-20 Inhibidores de transcriptasa inversa de no nucleosidos. MX2009012704A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US93225107P 2007-05-30 2007-05-30
PCT/EP2008/056165 WO2008145562A1 (en) 2007-05-30 2008-05-20 Non-nucleoside reverse transcriptase inhibitors

Publications (1)

Publication Number Publication Date
MX2009012704A true MX2009012704A (es) 2009-12-08

Family

ID=39712538

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009012704A MX2009012704A (es) 2007-05-30 2008-05-20 Inhibidores de transcriptasa inversa de no nucleosidos.

Country Status (17)

Country Link
US (1) US8026362B2 (es)
EP (1) EP2155692B1 (es)
JP (1) JP5167350B2 (es)
KR (1) KR101542629B1 (es)
CN (1) CN101679294B (es)
AR (1) AR066743A1 (es)
AU (1) AU2008257771B2 (es)
BR (1) BRPI0811645A2 (es)
CA (1) CA2687747C (es)
CL (1) CL2008001537A1 (es)
EA (1) EA016386B1 (es)
ES (1) ES2542153T3 (es)
IL (1) IL202143A (es)
MX (1) MX2009012704A (es)
PE (1) PE20090296A1 (es)
TW (1) TWI425946B (es)
WO (1) WO2008145562A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CL2008001631A1 (es) * 2007-06-06 2009-01-02 Smithkline Beecham Corp Compuestos derivados de heterociclos sustituidos, con la presencia de un grupo fenoxi, inhibidores de transcriptasa inversa; composicion farmaceutica; y uso en el tratamiento de infecciones virales por vih.
DE102008030091B4 (de) * 2008-06-25 2011-03-03 Resprotect Gmbh Uracilderivate und deren Verwendung
WO2019224754A1 (en) * 2018-05-23 2019-11-28 Mor Research Applications Ltd. Toll-like receptor 4 (tlr4) inhibitors and use thereof

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4110470A (en) * 1965-10-07 1978-08-29 Horst Kummer Pharmaceutical composition comprising d,l-α-methyl-thyroxine ethyl ester and the salts thereof and the control of cholesterol and triglyceride blood level therewith
US4949314A (en) 1966-08-16 1990-08-14 The United States Of America As Represented By The Secretary Of The Navy Method and means for increasing echo-ranging-search rate
GB1601310A (en) * 1978-05-23 1981-10-28 Lilly Industries Ltd Aryl hydantoins
US4518584A (en) 1983-04-15 1985-05-21 Cetus Corporation Human recombinant interleukin-2 muteins
GB8327880D0 (en) 1983-10-18 1983-11-16 Ajinomoto Kk Saccharomyces cerevisiae
US4569790A (en) 1984-03-28 1986-02-11 Cetus Corporation Process for recovering microbially produced interleukin-2 and purified recombinant interleukin-2 compositions
US4530787A (en) 1984-03-28 1985-07-23 Cetus Corporation Controlled oxidation of microbially produced cysteine-containing proteins
US4604377A (en) 1984-03-28 1986-08-05 Cetus Corporation Pharmaceutical compositions of microbially produced interleukin-2
IL76360A0 (en) 1984-09-26 1986-01-31 Takeda Chemical Industries Ltd Mutual separation of proteins
US4752585A (en) 1985-12-17 1988-06-21 Cetus Corporation Oxidation-resistant muteins
US4748234A (en) 1985-06-26 1988-05-31 Cetus Corporation Process for recovering refractile bodies containing heterologous proteins from microbial hosts
AU622926B2 (en) 1988-09-09 1992-04-30 Nippon Kayaku Kabushiki Kaisha Pyrimidine or purine cyclobutane derivatives
US5925643A (en) 1990-12-05 1999-07-20 Emory University Enantiomerically pure β-D-dioxolane-nucleosides
US5489697A (en) 1994-08-03 1996-02-06 Medichem Research, Inc. Method for the preparation of (+)-calanolide A and intermediates thereof
IL117574A0 (en) 1995-04-03 1996-07-23 Bristol Myers Squibb Co Processes for the preparation of cyclobutanone derivatives
US7166730B2 (en) 2000-01-27 2007-01-23 Fine Tech Laboratories, Ltd Process for the preparation of prostaglandin derivatives
JO3429B1 (ar) 2001-08-13 2019-10-20 Janssen Pharmaceutica Nv مشتقات برميدينات مثبطة فيروس الايدز
TW200505441A (en) 2003-03-24 2005-02-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitorsⅠ
BRPI0408704A (pt) * 2003-03-24 2006-03-07 Hoffmann La Roche benzil-piridazinonas como inibidores de transcriptase reversa
JP4107658B2 (ja) 2003-07-23 2008-06-25 インターナショナル・ビジネス・マシーンズ・コーポレーション 分類因子検出装置、分類因子検出方法、プログラム、及び記録媒体
EP1721165B1 (en) 2004-02-27 2010-03-03 Institut Curie New proliferation markers in clinical practice and their use for cancer prognosis or diagnosis
JP4627315B2 (ja) 2004-03-23 2011-02-09 エフ.ホフマン−ラ ロシュ アーゲー 非ヌクレオシド逆転写酵素阻害剤としてのベンジルピリダジノン誘導体
WO2005100323A1 (en) 2004-04-15 2005-10-27 F. Hoffmann-La Roche Ag Process for preparing pyridazinone compounds
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US7625949B2 (en) 2004-04-23 2009-12-01 Roche Palo Alto Llc Methods for treating retroviral infections
CA2471006A1 (en) * 2004-06-23 2005-12-23 Bayer Inc. Silica reinforced elastomer compounds prepared with dry liquid modifiers
EP1773790B1 (en) 2004-07-27 2012-08-15 F.Hoffmann-La Roche Ag Benzyltriazolone compounds as non-nucleoside reverse transcriptase inhibitors
WO2006026356A2 (en) 2004-08-25 2006-03-09 Ardea Biosciences, Inc. S-TRIAZOLYL α-MERCAPTOACETANILDES AS INHIBITORS OF HIV REVERSE TRANSCRIPTASE
ATE479693T1 (de) 2004-09-17 2010-09-15 Idenix Pharmaceuticals Inc Phosphoindole als hiv-inhibitoren
EP1797062B8 (en) 2004-09-30 2011-05-25 Boehringer Ingelheim International GmbH Alkynyl based dervatives of benzophenone as non-nucleoside reverse transcriptase inhibitors
JP4423166B2 (ja) 2004-10-29 2010-03-03 富士通株式会社 電子部品の超音波実装方法および超音波実装装置
WO2006067587A2 (en) 2004-12-22 2006-06-29 Pfizer Limited Nonnucleoside inhibitors of hiv-1 reverse transcriptase
EP1863777A1 (en) 2005-03-24 2007-12-12 F.Hoffmann-La Roche Ag 1,2,4 -triazole-5-one compounds as heterocyclic reverse transcriptase inhibitors
US20060225874A1 (en) 2005-04-11 2006-10-12 Shives Gary D Sandwiched thermal article
AR057455A1 (es) 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
WO2007039463A1 (en) 2005-09-30 2007-04-12 F. Hoffmann-La Roche Ag Nnrt inhibitors
RU2008119412A (ru) 2005-10-19 2009-11-27 Ф.Хоффманн-Ля Рош Аг (Ch) N-фенил-фенилацетамидные ненуклеозидные ингибиторы обратной транскриптазы
CN101291905A (zh) 2005-10-19 2008-10-22 弗·哈夫曼-拉罗切有限公司 苯乙酰胺nnrt抑制剂
KR20100039348A (ko) * 2007-06-22 2010-04-15 에프. 호프만-라 로슈 아게 비-뉴클레오사이드 역 전사효소 억제제로서 우레아 및 카바메이트 유도체

Also Published As

Publication number Publication date
CN101679294B (zh) 2012-08-08
IL202143A (en) 2014-06-30
CA2687747A1 (en) 2008-12-04
KR101542629B1 (ko) 2015-08-06
CL2008001537A1 (es) 2008-12-05
US8026362B2 (en) 2011-09-27
WO2008145562A1 (en) 2008-12-04
JP2010528083A (ja) 2010-08-19
EP2155692A1 (en) 2010-02-24
JP5167350B2 (ja) 2013-03-21
KR20100028584A (ko) 2010-03-12
ES2542153T3 (es) 2015-07-31
CN101679294A (zh) 2010-03-24
PE20090296A1 (es) 2009-03-27
TW200911260A (en) 2009-03-16
BRPI0811645A2 (pt) 2014-11-11
IL202143A0 (en) 2010-06-16
AU2008257771A1 (en) 2008-12-04
EA016386B1 (ru) 2012-04-30
TWI425946B (zh) 2014-02-11
US20090076045A1 (en) 2009-03-19
EA200901599A1 (ru) 2010-06-30
AR066743A1 (es) 2009-09-09
EP2155692B1 (en) 2015-06-17
CA2687747C (en) 2015-11-17
AU2008257771B2 (en) 2015-02-19

Similar Documents

Publication Publication Date Title
MX2009009920A (es) Inhibidores no nucleosidos de transcriptasa inversa.
MX2010006397A (es) Compuestos heterociclicos antivirales.
GEP20115320B (en) Non-nucleoside reverse transcriptase inhibitors
PH12017501429A1 (en) Derivatives of betulin
JOP20210301A1 (ar) بيرولات ثلاثية الحلقة مكثفة كمُعدِّلات مضاد تريبسين ألفا-1
MX2009005881A (es) Derivados de 2-(piperidin-4-il)-4-fenoxi o fenilamino-pirimidina como inhibidores de la transcriptasa inversa no nucleosida.
MX2009012168A (es) Derivados de pirrolopiridina y su uso como inhibidores de la enzima que escinde la proteina precursora de amiloide por el sitio beta.
TN2015000121A1 (en) Gdf-8 inhibitors
TW200603783A (en) Non-nucleoside reverse transcriptase inhibitors
UA95955C2 (ru) Ингибиторы обратной транскриптазы вич
UA105911C2 (uk) Сульфонамідні похідні
MX2011013771A (es) Derivados de imidazolidin-2-ona 1,3-disustituida como inhibidores de cyp17.
GEP20156368B (en) Non-nucleoside reverse transcriptase inhibitors
GEP20186838B (en) 5-phenoxy-3h-pyrimidin-4-one derivatives and their usage as hiv reverse transcriptase inhibitors
MY147390A (en) Substituted isoindoles as bace inhibitors and their use
WO2009146555A8 (en) Hiv integrase inhibitors from pyridoxine
MX2012010918A (es) Analogos para el tratamiento o prevencion de infecciones por flavivirus.
MX2009012847A (es) Analogos dipeptidicos como inhibidores de factores de coagulacion.
MX2009013804A (es) Inhibidores novedosos de transcriptasa inversa de vih.
PH12019501198A1 (en) Tetracyclic heterocycle compounds useful as hiv integrase inhibitors
JO3067B1 (ar) بيرميدينات بيرازولو امينو كمثبطات ل fak
MX2012006805A (es) Indolil-piperidinil bencilaminas como inhibidores de beta-triptasa.
MX2020011317A (es) Compuestos heterociclicos triciclicos utiles como inhibidores de la integrasa de vih.
TW200716571A (en) Heterocyclic reverse transcriptase inhibitors
MX2009010932A (es) Inhibidores no nucleosidos de transcriptasa inversa.

Legal Events

Date Code Title Description
FG Grant or registration