IL222030A - Non-Nuclusid Reverse Transcriptase Inhibitors - Google Patents

Non-Nuclusid Reverse Transcriptase Inhibitors

Info

Publication number
IL222030A
IL222030A IL222030A IL22203012A IL222030A IL 222030 A IL222030 A IL 222030A IL 222030 A IL222030 A IL 222030A IL 22203012 A IL22203012 A IL 22203012A IL 222030 A IL222030 A IL 222030A
Authority
IL
Israel
Prior art keywords
reverse transcriptase
transcriptase inhibitors
nucleoside reverse
nucleoside
inhibitors
Prior art date
Application number
IL222030A
Other languages
English (en)
Hebrew (he)
Original Assignee
Merck Canada Inc
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=44710363&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IL222030(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Canada Inc filed Critical Merck Canada Inc
Publication of IL222030A publication Critical patent/IL222030A/en

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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • AIDS & HIV (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
IL222030A 2010-03-30 2012-09-20 Non-Nuclusid Reverse Transcriptase Inhibitors IL222030A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US31882410P 2010-03-30 2010-03-30
US32157310P 2010-04-07 2010-04-07
PCT/CA2011/000320 WO2011120133A1 (en) 2010-03-30 2011-03-28 Non-nucleoside reverse transcriptase inhibitors

Publications (1)

Publication Number Publication Date
IL222030A true IL222030A (en) 2014-07-31

Family

ID=44710363

Family Applications (2)

Application Number Title Priority Date Filing Date
IL222030A IL222030A (en) 2010-03-30 2012-09-20 Non-Nuclusid Reverse Transcriptase Inhibitors
IL233334A IL233334A (en) 2010-03-30 2014-06-23 Compounds 3– (optionally converted aromatic hydrochloride and elliptic hydrocarbyl) –1 - [(5-oxo-5,4-dihydro-1h – 4,2,1-triazole-3-ram) methyl] -pyridine-2– (1h) - On, the pharmacy composition containing and using them

Family Applications After (1)

Application Number Title Priority Date Filing Date
IL233334A IL233334A (en) 2010-03-30 2014-06-23 Compounds 3– (optionally converted aromatic hydrochloride and elliptic hydrocarbyl) –1 - [(5-oxo-5,4-dihydro-1h – 4,2,1-triazole-3-ram) methyl] -pyridine-2– (1h) - On, the pharmacy composition containing and using them

Country Status (44)

Country Link
US (2) US8486975B2 (enExample)
EP (2) EP2924034B1 (enExample)
JP (2) JP5281718B2 (enExample)
KR (1) KR101421861B1 (enExample)
CN (1) CN102971308B (enExample)
AR (1) AR080859A1 (enExample)
AU (1) AU2011235568B2 (enExample)
BR (1) BR112012024691B1 (enExample)
CA (1) CA2794377C (enExample)
CL (1) CL2012002744A1 (enExample)
CO (1) CO6630126A2 (enExample)
CR (1) CR20120503A (enExample)
CY (3) CY1118774T1 (enExample)
DK (2) DK2924034T3 (enExample)
DO (1) DOP2012000256A (enExample)
EA (1) EA024804B1 (enExample)
EC (1) ECSP12012201A (enExample)
ES (2) ES2609636T3 (enExample)
FI (1) FIC20190021I1 (enExample)
GE (1) GEP20156368B (enExample)
HN (1) HN2012002039A (enExample)
HR (2) HRP20150427T1 (enExample)
HU (4) HUE025336T2 (enExample)
IL (2) IL222030A (enExample)
LT (3) LT2924034T (enExample)
LU (2) LUC00114I2 (enExample)
MA (1) MA34170B1 (enExample)
ME (2) ME02181B (enExample)
MX (1) MX2012011379A (enExample)
MY (1) MY163979A (enExample)
NI (1) NI201200146A (enExample)
NL (1) NL300980I2 (enExample)
NO (2) NO2019018I1 (enExample)
NZ (1) NZ602670A (enExample)
PE (1) PE20130158A1 (enExample)
PH (1) PH12012501923A1 (enExample)
PL (2) PL2552902T3 (enExample)
PT (2) PT2924034T (enExample)
RS (2) RS55505B1 (enExample)
SG (1) SG184347A1 (enExample)
SI (2) SI2924034T1 (enExample)
TN (1) TN2012000455A1 (enExample)
TW (1) TWI458719B (enExample)
WO (1) WO2011120133A1 (enExample)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA34170B1 (fr) * 2010-03-30 2013-04-03 Merck Canada Inc Inhibiteurs de transcriptase inverse non nucléosidiques
WO2012048113A2 (en) 2010-10-07 2012-04-12 The General Hospital Corporation Biomarkers of cancer
CN109384765A (zh) * 2012-09-26 2019-02-26 默沙东公司 逆转录酶抑制剂的晶型
JO3470B1 (ar) * 2012-10-08 2020-07-05 Merck Sharp & Dohme مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv
EP2928472B1 (en) * 2012-12-05 2018-05-02 Merck Sharp & Dohme Corp. Process for making reverse transcriptase inhibitors
BR112016011605A8 (pt) * 2013-11-22 2023-04-25 Merck Sharp & Dohme Composição de um inibidor de transcriptase reversa não nucleosídeo
ES2977643T3 (es) * 2013-12-04 2024-08-28 Merck Sharp & Dohme Llc Proceso para fabricar inhibidores de la transcriptasa inversa
CN106456639B (zh) * 2014-04-01 2019-05-10 默沙东公司 Hiv逆转录酶抑制剂的前药
US10301624B2 (en) 2014-06-25 2019-05-28 The General Hospital Corporation Targeting human satellite II (HSATII)
HUE056978T2 (hu) 2015-12-02 2022-04-28 Merck Sharp & Dohme Doravirint, tenofovir-dizoproxil-fumarátot és lamivudint tartalmazó gyógyszerészeti kompozíciók
US11077050B2 (en) 2017-03-24 2021-08-03 Merck Sharp & Dohme Corp. Formulation for parenteral administration
BR112019021918A2 (pt) 2017-04-18 2020-05-26 Cipla Limited Terapia de combinação para uso no tratamento de infecções retroviriais
EP3749330A4 (en) 2018-02-06 2021-11-17 The General Hospital Corporation REPEATED PATTERN RNA USED AS BIOMARKERS OF TUMOR IMMUNE RESPONSE
EP3823632B1 (en) * 2018-07-17 2025-10-29 Merck Sharp & Dohme LLC Efda in combination with doravirine for use in treating f227c mutated hiv infections
CN113423695A (zh) 2018-12-18 2021-09-21 默沙东公司 作为针对hiv感染细胞的选择性细胞毒剂的嘧啶酮衍生物
CN110801455B (zh) * 2019-11-12 2020-06-02 河北医科大学第二医院 用于治疗mrsa的药物组合物及其应用
CN114163309B (zh) * 2021-12-27 2023-04-25 甘肃皓天医药科技有限责任公司 一种多拉韦林中间体的制备方法
CN114349690B (zh) * 2022-02-15 2023-04-25 甘肃皓天医药科技有限责任公司 一种多拉韦林中间体合成方法
CN116903590A (zh) * 2023-06-06 2023-10-20 延边大学 一种含杂环结构的吡啶酮类化合物及其制备方法和用途
CN120157613A (zh) * 2023-12-15 2025-06-17 山东诚创蓝海医药科技有限公司 多拉韦林中间体及其应用和合成方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9904045D0 (sv) 1999-11-09 1999-11-09 Astra Ab Compounds
TW200423930A (en) 2003-02-18 2004-11-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitors
MXPA05010081A (es) 2003-03-24 2005-11-23 Hoffmann La Roche Bencil-piridazinonas como inhibidores de transcriptasa inversa.
TW200505441A (en) * 2003-03-24 2005-02-16 Hoffmann La Roche Non-nucleoside reverse transcriptase inhibitorsⅠ
AU2005235692B2 (en) 2004-04-23 2011-11-10 F. Hoffmann-La Roche Ag Non-nucleoside reverse transcriptase inhibitors
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
EP1831157A2 (en) 2004-12-22 2007-09-12 Pfizer Limited Nonnucleoside inhibitors of hiv-1 reverse transcriptase
AR057455A1 (es) 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
ES2320042T3 (es) 2005-10-19 2009-05-18 F. Hoffmann-La Roche Ag Inhibidores de transcriptasa reversa con nucleosidos de n-fenil fenilacetamida.
JP2009515826A (ja) 2005-10-19 2009-04-16 エフ.ホフマン−ラ ロシュ アーゲー フェニル−アセトアミドnnrt阻害剤
TW200831085A (en) 2006-12-13 2008-08-01 Merck & Co Inc Non-nucleoside reverse transcriptase inhibitors
RU2010125220A (ru) 2007-11-20 2011-12-27 Мерк Шарп Энд Домэ Корп. (Us) Ненуклеозидные ингибиторы обратной транскриптазы
MA34170B1 (fr) * 2010-03-30 2013-04-03 Merck Canada Inc Inhibiteurs de transcriptase inverse non nucléosidiques

Also Published As

Publication number Publication date
LTPA2019506I1 (lt) 2019-04-25
TN2012000455A1 (en) 2014-01-30
SI2924034T1 (sl) 2017-05-31
DK2552902T3 (en) 2015-06-15
JP2013209405A (ja) 2013-10-10
ME02181B (me) 2015-10-20
LTPA2019507I1 (lt) 2019-04-25
HN2012002039A (es) 2015-08-24
HK1209121A1 (en) 2016-03-24
LUC00114I2 (enExample) 2020-07-10
MY163979A (en) 2017-11-15
ECSP12012201A (es) 2012-10-30
EA024804B1 (ru) 2016-10-31
HUS1900021I1 (hu) 2019-05-28
EA201290976A1 (ru) 2013-03-29
HUS1900022I1 (hu) 2019-05-28
MX2012011379A (es) 2012-11-30
CA2794377A1 (en) 2011-10-06
ES2536295T3 (es) 2015-05-22
LUC00113I9 (enExample) 2024-06-07
AU2011235568B2 (en) 2013-09-12
IL233334A0 (en) 2014-09-01
KR20120128703A (ko) 2012-11-27
CY2019026I2 (el) 2020-05-29
CY2019025I2 (el) 2019-11-27
CR20120503A (es) 2013-01-09
NO2019018I1 (no) 2019-04-24
EP2924034A1 (en) 2015-09-30
MA34170B1 (fr) 2013-04-03
CN102971308A (zh) 2013-03-13
TW201139409A (en) 2011-11-16
RS55505B1 (sr) 2017-05-31
NO2019019I1 (no) 2019-04-24
LUC00113I2 (enExample) 2024-05-22
NL300980I2 (nl) 2021-06-17
PT2552902E (pt) 2015-06-02
PT2924034T (pt) 2017-01-06
LTC2924034I2 (lt) 2020-10-12
CY1118774T1 (el) 2017-07-12
GEP20156368B (en) 2015-09-25
IL233334A (en) 2015-09-24
HRP20150427T1 (hr) 2015-07-03
HUE031785T2 (en) 2017-08-28
US8486975B2 (en) 2013-07-16
EP2552902A1 (en) 2013-02-06
CO6630126A2 (es) 2013-03-01
ME02570B (me) 2017-06-20
LTC2552902I2 (lt) 2019-12-10
RS54017B1 (sr) 2015-10-30
EP2552902B1 (en) 2015-03-11
JP5886790B2 (ja) 2016-03-16
DK2924034T3 (en) 2017-02-06
PL2552902T3 (pl) 2015-10-30
HRP20161680T1 (hr) 2017-01-27
SI2552902T1 (sl) 2015-10-30
LUC00114I1 (enExample) 2019-04-17
BR112012024691A2 (pt) 2019-07-02
CA2794377C (en) 2015-06-16
CN102971308B (zh) 2015-02-04
PH12012501923A1 (en) 2013-02-04
US20130296382A1 (en) 2013-11-07
NI201200146A (es) 2013-03-18
CY2019026I1 (el) 2020-05-29
NL300980I1 (nl) 2019-04-24
PE20130158A1 (es) 2013-02-28
JP5281718B2 (ja) 2013-09-04
AU2011235568A1 (en) 2012-11-01
EP2552902A4 (en) 2013-09-04
US20110245296A1 (en) 2011-10-06
FIC20190021I1 (fi) 2019-04-17
SG184347A1 (en) 2012-11-29
LT2924034T (lt) 2016-12-27
BR112012024691B1 (pt) 2020-11-17
HK1175471A1 (en) 2013-07-05
CL2012002744A1 (es) 2012-12-14
NZ602670A (en) 2014-09-26
DOP2012000256A (es) 2012-12-15
PL2924034T3 (pl) 2017-07-31
EP2924034B1 (en) 2016-11-02
AR080859A1 (es) 2012-05-16
ES2609636T3 (es) 2017-04-21
CY2019025I1 (el) 2019-11-27
WO2011120133A1 (en) 2011-10-06
HUE025336T2 (en) 2016-03-29
KR101421861B1 (ko) 2014-07-22
TWI458719B (zh) 2014-11-01
JP2013510800A (ja) 2013-03-28

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Legal Events

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EXTF Application for patent extension filed

Filing date: 20200729

KB Patent renewed