ES2394952T3 - Derivados de axapéptido como inhibidores de la proteasa VIH - Google Patents

Derivados de axapéptido como inhibidores de la proteasa VIH Download PDF

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Publication number
ES2394952T3
ES2394952T3 ES11155667T ES11155667T ES2394952T3 ES 2394952 T3 ES2394952 T3 ES 2394952T3 ES 11155667 T ES11155667 T ES 11155667T ES 11155667 T ES11155667 T ES 11155667T ES 2394952 T3 ES2394952 T3 ES 2394952T3
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ES
Spain
Prior art keywords
compound
pharmaceutically acceptable
composition
acceptable salt
efavirenz
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
ES11155667T
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English (en)
Spanish (es)
Inventor
Roger D Tung
Scott L Harbeson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Concert Pharmaceuticals Inc
Original Assignee
Concert Pharmaceuticals 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
Application filed by Concert Pharmaceuticals Inc filed Critical Concert Pharmaceuticals Inc
Application granted granted Critical
Publication of ES2394952T3 publication Critical patent/ES2394952T3/es
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
    • C07D213/42Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
    • 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
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring 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
    • C07F9/553Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/576Six-membered rings
    • C07F9/58Pyridine rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Biochemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Pyridine Compounds (AREA)
ES11155667T 2007-06-12 2008-06-12 Derivados de axapéptido como inhibidores de la proteasa VIH Active ES2394952T3 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US93420107P 2007-06-12 2007-06-12
US934201P 2007-06-12
US6762708P 2008-02-29 2008-02-29
US67627P 2008-02-29

Publications (1)

Publication Number Publication Date
ES2394952T3 true ES2394952T3 (es) 2013-02-07

Family

ID=39730784

Family Applications (3)

Application Number Title Priority Date Filing Date
ES11155667T Active ES2394952T3 (es) 2007-06-12 2008-06-12 Derivados de axapéptido como inhibidores de la proteasa VIH
ES08252023T Active ES2356334T3 (es) 2007-06-12 2008-06-12 Derivados de azapéptidos como inhibidores de la proteasa vih.
ES09075359T Active ES2395137T3 (es) 2007-06-12 2008-06-12 Derivados de azapéptidos como inhibidores de la proteasa VIH

Family Applications After (2)

Application Number Title Priority Date Filing Date
ES08252023T Active ES2356334T3 (es) 2007-06-12 2008-06-12 Derivados de azapéptidos como inhibidores de la proteasa vih.
ES09075359T Active ES2395137T3 (es) 2007-06-12 2008-06-12 Derivados de azapéptidos como inhibidores de la proteasa VIH

Country Status (25)

Country Link
US (4) US20090036357A1 (cg-RX-API-DMAC10.html)
EP (3) EP2322509B1 (cg-RX-API-DMAC10.html)
JP (1) JP2010529196A (cg-RX-API-DMAC10.html)
KR (2) KR101185899B1 (cg-RX-API-DMAC10.html)
CN (2) CN101711237B (cg-RX-API-DMAC10.html)
AR (1) AR066972A1 (cg-RX-API-DMAC10.html)
AT (2) ATE536343T1 (cg-RX-API-DMAC10.html)
AU (1) AU2008267048C1 (cg-RX-API-DMAC10.html)
BR (2) BRPI0813911A2 (cg-RX-API-DMAC10.html)
CA (1) CA2692028C (cg-RX-API-DMAC10.html)
CO (1) CO6241121A2 (cg-RX-API-DMAC10.html)
CY (1) CY1109766T1 (cg-RX-API-DMAC10.html)
DE (1) DE602008000255D1 (cg-RX-API-DMAC10.html)
DK (1) DK2003120T3 (cg-RX-API-DMAC10.html)
ES (3) ES2394952T3 (cg-RX-API-DMAC10.html)
HR (1) HRP20100065T1 (cg-RX-API-DMAC10.html)
MX (1) MX2009013565A (cg-RX-API-DMAC10.html)
PL (1) PL2003120T3 (cg-RX-API-DMAC10.html)
PT (1) PT2003120E (cg-RX-API-DMAC10.html)
RS (1) RS51226B (cg-RX-API-DMAC10.html)
RU (2) RU2448958C2 (cg-RX-API-DMAC10.html)
SI (1) SI2003120T1 (cg-RX-API-DMAC10.html)
TW (1) TW200908970A (cg-RX-API-DMAC10.html)
WO (1) WO2008156632A1 (cg-RX-API-DMAC10.html)
ZA (1) ZA200909079B (cg-RX-API-DMAC10.html)

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WO2010041241A2 (en) * 2008-10-06 2010-04-15 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Hiv-1 integrase derived peptides and compositions
WO2010132663A1 (en) * 2009-05-13 2010-11-18 Concert Pharmaceticals, Inc. Pegylated azapeptide derivatives as hiv protease inhibitors
WO2010135424A1 (en) * 2009-05-19 2010-11-25 Glaxosmithkline Llc Chemical compounds
MY163383A (en) 2009-12-21 2017-09-15 Janssen Sciences Ireland Uc Degradable removable implant for the sustained release of an active compound
WO2011080562A1 (en) 2009-12-29 2011-07-07 Hetero Research Foundation Novel aza-peptides containing 2,2-disubstituted cyclobutyl and/or substituted alkoxy benzyl derivatives as antivirals
SMT201900179T1 (it) 2011-06-20 2019-05-10 H Lundbeck As 1–piperazino–3–fenil indani deuterati per il trattamento della schizofrenia
CN106543073A (zh) * 2015-09-17 2017-03-29 宁波杰尔盛化工有限公司 2-[4-(2-吡啶基)苄基]-肼羧酸叔丁酯的制备方法
DK3383397T3 (da) * 2015-12-02 2021-11-08 Merck Sharp & Dohme Farmaceutiske sammensætninger indeholdende doravirin, tenofovirdisoproxilfumarat og lamivudin
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WO2019025250A1 (en) 2017-08-04 2019-02-07 Basf Se SUBSTITUTED TRIFLUOROMETHYLOXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI
KR102739325B1 (ko) 2017-09-27 2024-12-09 인사이트 코포레이션 Tam 억제제로서 유용한 피롤로트리아진 유도체의 염
ES3031110T3 (en) * 2018-06-29 2025-07-04 Incyte Corp Formulations of an axl/mer inhibitor
TWI766172B (zh) 2018-07-30 2022-06-01 美商基利科學股份有限公司 抗hiv化合物
AU2021230385A1 (en) 2020-03-06 2022-09-22 Incyte Corporation Combination therapy comprising AXL/MER and PD-1/PD-L1 inhibitors
JP2023522210A (ja) * 2020-04-16 2023-05-29 ザ メディカル カレッジ オブ ウィスコンシン インク 気道逆流の治療のためのhivプロテアーゼ阻害剤のエアロゾル化製剤
CN115385983A (zh) * 2022-01-11 2022-11-25 嘉兴安谛康生物科技有限公司 氮杂双环类化合物及其制备方法、药物组合物和用途
US20250051375A1 (en) 2023-05-31 2025-02-13 Gilead Sciences, Inc. Anti-hiv compounds
CN116987024A (zh) * 2023-08-01 2023-11-03 浙江荣耀生物科技股份有限公司 一种阿扎那韦中间体的制备方法

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Also Published As

Publication number Publication date
EP2003120B9 (en) 2010-06-02
SI2003120T1 (sl) 2010-03-31
BRPI0813911A2 (pt) 2012-02-22
CN102424668A (zh) 2012-04-25
ATE447554T1 (de) 2009-11-15
KR20100020033A (ko) 2010-02-19
ES2395137T3 (es) 2013-02-08
ZA200909079B (en) 2011-05-25
ES2356334T3 (es) 2011-04-07
EP2116532B1 (en) 2011-12-07
EP2003120A1 (en) 2008-12-17
CA2692028A1 (en) 2008-12-24
US20130041156A1 (en) 2013-02-14
CN101711237A (zh) 2010-05-19
RU2010100821A (ru) 2011-07-20
TW200908970A (en) 2009-03-01
WO2008156632A1 (en) 2008-12-24
DE602008000255D1 (de) 2009-12-17
US8158805B2 (en) 2012-04-17
CO6241121A2 (es) 2011-01-20
CY1109766T1 (el) 2014-09-10
KR20120029480A (ko) 2012-03-26
PL2003120T3 (pl) 2010-04-30
MX2009013565A (es) 2010-06-02
DK2003120T3 (da) 2010-03-15
AR066972A1 (es) 2009-09-23
BRPI0823520A2 (pt) 2013-12-17
KR101185899B1 (ko) 2012-09-27
AU2008267048B2 (en) 2012-05-31
US8258309B2 (en) 2012-09-04
HK1136576A1 (en) 2010-07-02
CN101711237B (zh) 2013-08-07
RS51226B (sr) 2010-12-31
RU2012101881A (ru) 2013-07-27
HK1127345A1 (en) 2009-09-25
AU2008267048A1 (en) 2008-12-24
EP2116532A1 (en) 2009-11-11
HRP20100065T1 (hr) 2010-03-31
RU2448958C2 (ru) 2012-04-27
EP2322509B1 (en) 2012-08-22
US20120165288A1 (en) 2012-06-28
PT2003120E (pt) 2010-02-11
US20110009355A1 (en) 2011-01-13
US20090036357A1 (en) 2009-02-05
JP2010529196A (ja) 2010-08-26
CA2692028C (en) 2013-06-04
EP2003120B1 (en) 2009-11-04
AU2008267048C1 (en) 2013-01-17
EP2322509A1 (en) 2011-05-18
ATE536343T1 (de) 2011-12-15

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