BG99149A - Нови хиназолини-инхибитори на нiv реверсивна транскриптаза - Google Patents

Нови хиназолини-инхибитори на нiv реверсивна транскриптаза

Info

Publication number
BG99149A
BG99149A BG99149A BG9914994A BG99149A BG 99149 A BG99149 A BG 99149A BG 99149 A BG99149 A BG 99149A BG 9914994 A BG9914994 A BG 9914994A BG 99149 A BG99149 A BG 99149A
Authority
BG
Bulgaria
Prior art keywords
treatment
reserve
inhibitors
niv
prevention
Prior art date
Application number
BG99149A
Other languages
English (en)
Inventor
Terry Lyle
Thomas Tucker
Catherine Wiscount
Original Assignee
Merck & Co. 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 Merck & Co. Inc. filed Critical Merck & Co. Inc.
Publication of BG99149A publication Critical patent/BG99149A/bg

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
    • C07D239/80—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/06—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Communicable Diseases (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Изобретението се отнася до съединения, които иматхиназолин-2-он-ядро, заместено на 4-позиция с алкинил или алкенил. Те намират приложение за инхибиране на нiv обратната транскриптаза, включително нанейните резистентни варианти, за предотвратяване или за лечение на инфекции, предизвикани от нiv, и за лечение на спин, под формата на съединения или на фармацевтично приемливи соли, или на съставки за фармацевтични състави самостоятелно и в комбинация с други антивирусни средства, имуностимулатори,антибиотици или ваксини. Изобретението се отнася също до методи за лечение на спин и за предотвратяване или лечение на предизвиквани от нiv инфекции.
BG99149A 1992-05-07 1994-10-31 Нови хиназолини-инхибитори на нiv реверсивна транскриптаза BG99149A (bg)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US88011992A 1992-05-07 1992-05-07
US99116492A 1992-12-16 1992-12-16
PCT/US1993/003975 WO1993022292A1 (en) 1992-05-07 1993-04-28 New quinazolines as inhibitors of hiv reverse transcriptase

Publications (1)

Publication Number Publication Date
BG99149A true BG99149A (bg) 1995-06-30

Family

ID=27128564

Family Applications (1)

Application Number Title Priority Date Filing Date
BG99149A BG99149A (bg) 1992-05-07 1994-10-31 Нови хиназолини-инхибитори на нiv реверсивна транскриптаза

Country Status (15)

Country Link
EP (2) EP0639184A1 (bg)
JP (1) JPH0813805B2 (bg)
KR (1) KR950701322A (bg)
CN (1) CN1085550A (bg)
AU (2) AU4220493A (bg)
BG (1) BG99149A (bg)
CA (1) CA2095194A1 (bg)
CZ (1) CZ272494A3 (bg)
FI (1) FI945199A (bg)
HR (1) HRP930857A2 (bg)
HU (1) HUT71401A (bg)
IL (1) IL105551A0 (bg)
MX (1) MX9302681A (bg)
SI (1) SI9300244A (bg)
WO (1) WO1993022292A1 (bg)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2281297A (en) * 1993-08-27 1995-03-01 Merck & Co Inc Quinazoline compounds
US5434152A (en) * 1993-11-08 1995-07-18 Merck & Co., Inc. Asymmetric synthesis of (S)-(-)-6-chloro-4- cyclopropyl-3,4-dihydro-4-[(2-pyridyl)ethynyl]-2(1H)-quinazolinone
HRP980143A2 (en) * 1997-04-09 1999-02-28 Soo Sung Ko 4,4-disubstituted-3,4-dihydro-2 (1h)-quinazolinones useful as hiv reverse transcriptase inhibitors
US6124302A (en) * 1997-04-09 2000-09-26 Dupont Pharmaceuticals 4,4-disubstituted-3,4-dihydro-2(1H)-quinazolinones useful as HIV reverse transcriptase inhibitors
EP1091939A1 (en) * 1998-06-30 2001-04-18 Du Pont Pharmaceuticals Company Substituted quinolin-2(1h)-ones useful as hiv reverse transcriptase inhibitors
AU5588400A (en) 1999-05-26 2000-12-18 Du Pont Pharmaceuticals Company 1,4-benzodiazepin-2-ones useful as hiv reverse transcriptase inhibitors
CA2377629A1 (en) * 2000-04-25 2001-11-08 Hae-Young Bae Biphenyl butyric acid derivative as a matrix metalloproteinase inhibitor
US7119111B2 (en) 2002-05-29 2006-10-10 Amgen, Inc. 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use
WO2009044788A1 (ja) * 2007-10-05 2009-04-09 Banyu Pharmaceutical Co., Ltd. ベンゾオキサジノン誘導体
CN101544630B (zh) * 2009-05-13 2013-03-13 中国科学院广州生物医药与健康研究院 羟基化茚地那韦的制备方法
EP3317278B1 (en) 2015-07-01 2021-04-14 Crinetics Pharmaceuticals, Inc. Somatostatin modulators and uses thereof
JOP20180009A1 (ar) 2017-02-06 2019-01-30 Gilead Sciences Inc مركبات مثبط فيروس hiv
US11028068B2 (en) 2017-07-25 2021-06-08 Crinetics Pharmaceuticals, Inc. Somatostatin modulators and uses thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL147140B (nl) * 1968-11-26 1975-09-15 Farmaceutici Italia Werkwijze voor het bereiden van geneesmiddelen met een remmende werking op het centrale zenuwstelsel.
IL102764A0 (en) * 1991-08-16 1993-01-31 Merck & Co Inc Quinazoline derivatives,and pharmaceutical compositions containing them

Also Published As

Publication number Publication date
CN1085550A (zh) 1994-04-20
FI945199A0 (fi) 1994-11-04
AU3841393A (en) 1993-11-11
CA2095194A1 (en) 1993-11-08
CZ272494A3 (en) 1995-10-18
JPH069578A (ja) 1994-01-18
SI9300244A (sl) 1993-12-31
WO1993022292A1 (en) 1993-11-11
EP0569083A1 (en) 1993-11-10
HUT71401A (en) 1995-11-28
MX9302681A (es) 1994-05-31
IL105551A0 (en) 1993-08-18
FI945199A (fi) 1994-11-04
HRP930857A2 (en) 1995-06-30
AU4220493A (en) 1993-11-29
EP0639184A1 (en) 1995-02-22
KR950701322A (ko) 1995-03-23
JPH0813805B2 (ja) 1996-02-14

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