EA200701654A1 - Дикетокислоты с каркасом из нуклеинового основания в качестве ингибиторов анти-вич репликации, направленных на вич-интегразу - Google Patents

Дикетокислоты с каркасом из нуклеинового основания в качестве ингибиторов анти-вич репликации, направленных на вич-интегразу

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Publication number
EA200701654A1
EA200701654A1 EA200701654A EA200701654A EA200701654A1 EA 200701654 A1 EA200701654 A1 EA 200701654A1 EA 200701654 A EA200701654 A EA 200701654A EA 200701654 A EA200701654 A EA 200701654A EA 200701654 A1 EA200701654 A1 EA 200701654A1
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EA
Eurasian Patent Office
Prior art keywords
hiv
inhibitors
aids
compounds
pharmaceutically acceptable
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Application number
EA200701654A
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English (en)
Inventor
Васу Наир
Гуочен Чи
Винод Р. Учил
Original Assignee
Юниверсити Оф Джорджия Рисерч Фаундейшн, Инк.
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Application filed by Юниверсити Оф Джорджия Рисерч Фаундейшн, Инк. filed Critical Юниверсити Оф Джорджия Рисерч Фаундейшн, Инк.
Publication of EA200701654A1 publication Critical patent/EA200701654A1/ru

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/28Oxygen atom
    • C07D473/30Oxygen atom attached in position 6, e.g. hypoxanthine
    • 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
    • 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • 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
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6509Six-membered rings
    • C07F9/6512Six-membered rings having the nitrogen atoms in positions 1 and 3
    • 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
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C07F9/65616Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs

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

Abstract

Приводится описание нового класса дикетокислот, сконструированных на клеточных каркасах нуклеинового основания, предназначенный для применения в качестве ингибиторов репликации ВИЧ путем ингибирования ВИЧ-интегразы. Указанные соединения являются пригодными для профилактики или лечения ВИЧ-инфекции и для лечения СПИДа и СПИД-ассоциированного комплекса либо в виде соединений, либо в виде фармацевтически приемлемых солей с фармацевтически приемлемыми носителями, применяемые отдельно или в сочетании с противовирусными препаратами, иммуномодуляторами, антибиотиками, вакцинами и иными терапевтическими средствами. Также приведено описание способов лечения СПИДа и СПИД-ассоциированного комплекса и способы лечения и профилактики ВИЧ-инфекции. Соединения в соответствии с настоящим изобретением включают соединения формулы I и определяются следующим образом: формула (I), включающая их таутомеры, региоизомеры, геометрические изомеры и оптические изомеры в тех случаях, где это применимо, а также их фармацевтически приемлемые соли, в которых клеточный каркас нуклеиновой кислоты и R группы определены во всех других отношениях в настоящем описании изобретения.
EA200701654A 2005-01-31 2006-01-18 Дикетокислоты с каркасом из нуклеинового основания в качестве ингибиторов анти-вич репликации, направленных на вич-интегразу EA200701654A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11/047,229 US7250421B2 (en) 2005-01-31 2005-01-31 Diketo acids with nucleobase scaffolds: anti-HIV replication inhibitors targeted at HIV integrase
PCT/US2006/001692 WO2006083553A2 (en) 2005-01-31 2006-01-18 Diketo acids with nucleobase scaffolds: anti-hiv replication inhibitors targeted at hiv integrase

Publications (1)

Publication Number Publication Date
EA200701654A1 true EA200701654A1 (ru) 2008-02-28

Family

ID=36757398

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200701654A EA200701654A1 (ru) 2005-01-31 2006-01-18 Дикетокислоты с каркасом из нуклеинового основания в качестве ингибиторов анти-вич репликации, направленных на вич-интегразу

Country Status (12)

Country Link
US (2) US7250421B2 (ru)
EP (1) EP1848697A4 (ru)
JP (1) JP2008528584A (ru)
KR (1) KR20070112121A (ru)
CN (1) CN101151254A (ru)
AU (1) AU2006211548A1 (ru)
CA (1) CA2596368A1 (ru)
EA (1) EA200701654A1 (ru)
IL (1) IL184926A0 (ru)
MX (1) MX2007009234A (ru)
WO (1) WO2006083553A2 (ru)
ZA (1) ZA200706306B (ru)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7888375B2 (en) 2006-07-19 2011-02-15 The University Of Georgia Research Foundation, Inc Pyridinone diketo acids: inhibitors of HIV replication
NZ573793A (en) * 2006-07-24 2012-01-12 Korea Res Inst Chem Tech Hiv reverse transcriptase inhibitors
BRPI0813269A2 (pt) * 2007-06-29 2014-12-30 Korean Res Inst Of Chemical Technology Inibidores de hiv transcriptase reversa
US8354421B2 (en) * 2007-06-29 2013-01-15 Korea Research Insitute Of Chemical Technology HIV reverse transcriptase inhibitors
WO2009085797A1 (en) * 2007-12-21 2009-07-09 Gilead Sciences, Inc. Processes for preparing hiv reverse transcriptase inhibitors
EP2254582B1 (en) 2008-01-25 2016-01-20 Chimerix, Inc. Methods of treating viral infections
EP2509949B1 (en) * 2009-12-07 2014-04-23 University Of Georgia Research Foundation, Inc. Pyridinone hydroxycyclopentyl carboxamides: hiv integrase inhibitors with therapeutic applications
US9006218B2 (en) 2010-02-12 2015-04-14 Chimerix Inc. Nucleoside phosphonate salts
CN104185420B (zh) 2011-11-30 2017-06-09 埃默里大学 用于治疗或预防逆转录病毒和其它病毒感染的抗病毒jak抑制剂
US9650360B2 (en) 2012-03-31 2017-05-16 University Of Georgia Research Foundation, Inc. Anti-mycobacterial drugs against tuberculosis
WO2015130947A1 (en) * 2014-02-26 2015-09-03 Howard University Benzende sulfonamide derivatives as hiv integrase inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9816358D0 (en) * 1998-07-27 1998-09-23 Angeletti P Ist Richerche Bio Enzyme inhibitors
WO2000006529A1 (en) 1998-07-27 2000-02-10 Istituto Di Ricerche Di Biologia Molecolare P Angeletti S.P.A. Diketoacid-derivatives as inhibitors of polymerases
AP2001002169A0 (en) * 1998-12-25 2001-06-30 Shionogi & Co Aromatic heterocycle compounds having hiv intergrase inhibiting activities
CN1239472C (zh) * 2000-06-16 2006-02-01 布里斯托尔-迈尔斯斯奎布公司 Hiv整合酶抑制剂
AU2002337765A1 (en) * 2001-09-26 2003-04-07 Bristol-Myers Squibb Company Compounds useful for treating hepatitus c virus
US20050026902A1 (en) 2003-01-31 2005-02-03 Timothy Maziasz Methods and compositions for the treatment or prevention of human immunodeficiency virus and related conditions using cyclooxygenase-2 selective inhibitors and antiviral agents

Also Published As

Publication number Publication date
IL184926A0 (en) 2007-12-03
US7569573B2 (en) 2009-08-04
WO2006083553A2 (en) 2006-08-10
KR20070112121A (ko) 2007-11-22
EP1848697A2 (en) 2007-10-31
ZA200706306B (en) 2008-10-29
JP2008528584A (ja) 2008-07-31
EP1848697A4 (en) 2011-06-15
WO2006083553A3 (en) 2007-04-19
MX2007009234A (es) 2007-10-08
US20070259823A1 (en) 2007-11-08
AU2006211548A1 (en) 2006-08-10
US20060172973A1 (en) 2006-08-03
US7250421B2 (en) 2007-07-31
CN101151254A (zh) 2008-03-26
CA2596368A1 (en) 2006-08-10

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