PL3125894T3 - Proleki inhibitorów odwrotnej transkryptazy hiv - Google Patents

Proleki inhibitorów odwrotnej transkryptazy hiv

Info

Publication number
PL3125894T3
PL3125894T3 PL15774282T PL15774282T PL3125894T3 PL 3125894 T3 PL3125894 T3 PL 3125894T3 PL 15774282 T PL15774282 T PL 15774282T PL 15774282 T PL15774282 T PL 15774282T PL 3125894 T3 PL3125894 T3 PL 3125894T3
Authority
PL
Poland
Prior art keywords
prodrugs
reverse transcriptase
transcriptase inhibitors
hiv reverse
hiv
Prior art date
Application number
PL15774282T
Other languages
English (en)
Inventor
Christopher S. Burgey
Jeffrey F. Fritzen
Jaume Balsells
Mehul Patel
Original Assignee
Merck Sharp & Dohme Corp.
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 Merck Sharp & Dohme Corp. filed Critical Merck Sharp & Dohme Corp.
Publication of PL3125894T3 publication Critical patent/PL3125894T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6558Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/662Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
    • 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
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
    • C07D237/22Nitrogen and 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
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biochemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
PL15774282T 2014-04-01 2015-03-27 Proleki inhibitorów odwrotnej transkryptazy hiv PL3125894T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201461973689P 2014-04-01 2014-04-01
PCT/US2015/022868 WO2015153304A1 (en) 2014-04-01 2015-03-27 Prodrugs of hiv reverse transcriptase inhibitors
EP15774282.6A EP3125894B1 (en) 2014-04-01 2015-03-27 Prodrugs of hiv reverse transcriptase inhibitors

Publications (1)

Publication Number Publication Date
PL3125894T3 true PL3125894T3 (pl) 2021-02-08

Family

ID=54241131

Family Applications (1)

Application Number Title Priority Date Filing Date
PL15774282T PL3125894T3 (pl) 2014-04-01 2015-03-27 Proleki inhibitorów odwrotnej transkryptazy hiv

Country Status (21)

Country Link
US (1) US10004740B2 (pl)
EP (2) EP3125894B1 (pl)
JP (1) JP6342011B2 (pl)
KR (1) KR102440843B1 (pl)
CN (1) CN106456639B (pl)
AU (1) AU2015241247B2 (pl)
BR (1) BR112016022722B8 (pl)
CA (1) CA2944187C (pl)
CY (1) CY1123582T1 (pl)
DK (1) DK3125894T3 (pl)
ES (1) ES2828951T3 (pl)
HR (1) HRP20201780T1 (pl)
HU (1) HUE051848T2 (pl)
LT (1) LT3125894T (pl)
MX (1) MX2016012915A (pl)
PL (1) PL3125894T3 (pl)
PT (1) PT3125894T (pl)
RS (1) RS61016B1 (pl)
RU (1) RU2693622C2 (pl)
SI (1) SI3125894T1 (pl)
WO (1) WO2015153304A1 (pl)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3470B1 (ar) 2012-10-08 2020-07-05 Merck Sharp & Dohme مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv
CA2944187C (en) 2014-04-01 2018-06-19 Merck Sharp & Dohme Corp. Prodrugs of hiv reverse transcriptase inhibitors
CN106008362B (zh) * 2016-05-24 2018-08-10 杰达维(上海)医药科技发展有限公司 一种嘧啶衍生物的制备方法
AU2018390284A1 (en) 2017-12-22 2020-06-11 Sumitomo Chemical Company, Limited Heterocyclic compound and harmful arthropod controlling agent containing same
AU2019402998B2 (en) * 2018-12-18 2022-12-15 Merck Sharp & Dohme Llc Pyrimidone derivatives as selective cytotoxic agents against HIV infected cells
WO2020171129A1 (ja) 2019-02-20 2020-08-27 住友化学株式会社 エーテル化合物及びそれを含有する有害節足動物防除組成物
KR20220011673A (ko) * 2019-05-22 2022-01-28 머크 샤프 앤드 돔 코포레이션 Hiv 감염된 세포에 대한 선택적 세포독성제로서의 피리디논 유도체
US20230167082A1 (en) * 2019-07-16 2023-06-01 Bristol-Myers Squibb Company Prodrugs in the modulation of interleukin
WO2022208370A1 (en) 2021-03-31 2022-10-06 Pi Industries Ltd. Fused heterocyclic compounds and their use as pest control agents

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5665720A (en) 1992-08-07 1997-09-09 Merck & Co., Inc. Benzoxazinones as inhibitors of HIV reverse transcriptase
IT1305313B1 (it) * 1998-07-17 2001-05-04 Colla Paolo 3,4 - diidro- 6- benzil-4-oxopirimidine sostituite e relativo processodi produzione e impiego nella terapia delle infezioni da hiv-1.
SE9904045D0 (sv) 1999-11-09 1999-11-09 Astra Ab Compounds
US20070021449A1 (en) 2003-02-07 2007-01-25 Jan Heeres Pyrimidine derivatives for the prevention of hiv infection
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
US7790734B2 (en) 2003-09-08 2010-09-07 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
US7288942B2 (en) * 2003-10-02 2007-10-30 Naoyuki Sato Plasma potential measuring method and apparatus, and plasma potential measuring probe
KR20060124701A (ko) 2004-01-12 2006-12-05 길리애드 사이언시즈, 인코포레이티드 피리미딜 포스포네이트 항바이러스성 화합물 및 그의 사용방법
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
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
ES2333802T3 (es) 2004-04-23 2010-03-01 F. Hoffmann-La Roche Ag Inhibidores no nucleicos de transcriptasa inversa.
US20090264425A1 (en) 2004-12-22 2009-10-22 Pfizer Limited Chemical compounds
AR057455A1 (es) 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
AU2006303368B2 (en) 2005-10-19 2011-05-26 F. Hoffmann-La Roche Ag Non-Nucleoside Reverse Transcriptase Inhibitors
CA2625039A1 (en) 2005-10-19 2007-04-26 F. Hoffmann-La Roche Ag N-phenyl phenylacetamide non-nucleoside reverse transcriptase inihibitors
CA2670404A1 (en) 2006-11-24 2008-05-29 Takeda Pharmaceutical Company Limited Heteromonocyclic compound and use thereof
US7803940B2 (en) 2006-11-24 2010-09-28 Takeda Pharmaceutical Company Limited Heteromonocyclic compound or a salt thereof having strong antihypertensive action, insulin sensitizing activity and the like production thereof and use thereof for prophylaxis or treatment of cardiovascular diseases, metabolic diseases and/or central nervous system diseases
TW200831085A (en) 2006-12-13 2008-08-01 Merck & Co Inc Non-nucleoside reverse transcriptase inhibitors
US8404253B2 (en) 2006-12-28 2013-03-26 Newport Laboratories, Inc. Modified live (JMSO strain) Haemophilus parasuis vaccine
DE102007032507A1 (de) * 2007-07-12 2009-04-02 Merck Patent Gmbh Pyridazinonderivate
RU2010125220A (ru) * 2007-11-20 2011-12-27 Мерк Шарп Энд Домэ Корп. (Us) Ненуклеозидные ингибиторы обратной транскриптазы
JP5564435B2 (ja) 2008-01-08 2014-07-30 メルク・シャープ・アンド・ドーム・コーポレーション N−置換ヒドロキシピリミジノンカルボキサミドの製造方法
DK2924034T3 (en) 2010-03-30 2017-02-06 Merck Canada Inc PHARMACEUTICAL COMPOSITION CONTAINING A NON-NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR
EP2558093A4 (en) 2010-04-08 2013-10-02 Merck Sharp & Dohme PRODRUGS OF HIV INVERTER TRANSCRIPTASE INHIBITOR
JO3470B1 (ar) 2012-10-08 2020-07-05 Merck Sharp & Dohme مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv
CA2944187C (en) 2014-04-01 2018-06-19 Merck Sharp & Dohme Corp. Prodrugs of hiv reverse transcriptase inhibitors

Also Published As

Publication number Publication date
SI3125894T1 (sl) 2020-12-31
CA2944187A1 (en) 2015-10-08
CA2944187C (en) 2018-06-19
US10004740B2 (en) 2018-06-26
JP6342011B2 (ja) 2018-06-13
EP3785714A1 (en) 2021-03-03
DK3125894T3 (da) 2020-11-16
CY1123582T1 (el) 2022-03-24
CN106456639B (zh) 2019-05-10
EP3125894A4 (en) 2017-12-13
MX2016012915A (es) 2016-12-07
WO2015153304A1 (en) 2015-10-08
BR112016022722A2 (pt) 2017-10-31
KR102440843B1 (ko) 2022-09-29
LT3125894T (lt) 2020-12-10
AU2015241247B2 (en) 2017-09-14
EP3125894A1 (en) 2017-02-08
HRP20201780T1 (hr) 2021-06-25
RU2016142611A3 (pl) 2018-12-26
HUE051848T2 (hu) 2021-03-29
US20170173015A1 (en) 2017-06-22
EP3125894B1 (en) 2020-09-09
JP2017512802A (ja) 2017-05-25
RU2016142611A (ru) 2018-05-03
AU2015241247A1 (en) 2016-10-06
RS61016B1 (sr) 2020-12-31
KR20160133000A (ko) 2016-11-21
ES2828951T3 (es) 2021-05-28
CN106456639A (zh) 2017-02-22
RU2693622C2 (ru) 2019-07-03
BR112016022722B1 (pt) 2023-03-07
PT3125894T (pt) 2020-11-05
BR112016022722B8 (pt) 2023-11-21

Similar Documents

Publication Publication Date Title
IL287113A (en) smyd inhibitors
IL247923A0 (en) 4-substituted nucleotide derivatives as HIV reverse transcriptase inhibitors
IL251584A0 (en) Dihydropyrrolopyridines ror-gamma inhibitors
IL246902A0 (en) Dihydropyrrolopyridine ror–gamma inhibitors
ZA201604272B (en) Inhibitors of glutaminase
IL248895A0 (en) Phosphatidylinositol 3-kinase inhibitors
PT3125894T (pt) Profármacos de inibidores da transcriptase reversa do vih
EP3494971C0 (en) SALTS OF ERK INHIBITORS
GB201521059D0 (en) Inhibitors of metallo-beta-lactamases
LT3226888T (lt) Selektyvaus il-6-trans-signalinio inhibitoriaus skyrimas
GB201402169D0 (en) Viral inhibitors
GB201407822D0 (en) Use of a composition
GB201401005D0 (en) Inhibitor
HUP1500506A2 (en) Salts of palbociclib
GB201417347D0 (en) Prodrugs of delanzomib
GB201417348D0 (en) Prodrugs of lxazomib
TH1501005447A (th) สารยับยั้ง ido
GB201417192D0 (en) Deposition of graphene
GB201418154D0 (en) Inhibitors