NO20033857L - Benzofenoner som inhibitorer av revers transkriptase - Google Patents

Benzofenoner som inhibitorer av revers transkriptase

Info

Publication number
NO20033857L
NO20033857L NO20033857A NO20033857A NO20033857L NO 20033857 L NO20033857 L NO 20033857L NO 20033857 A NO20033857 A NO 20033857A NO 20033857 A NO20033857 A NO 20033857A NO 20033857 L NO20033857 L NO 20033857L
Authority
NO
Norway
Prior art keywords
benzophenones
inhibitors
reverse transcriptase
transcriptase
reverse
Prior art date
Application number
NO20033857A
Other languages
English (en)
Norwegian (no)
Other versions
NO20033857D0 (no
Inventor
Joseph Howing Chan
Original Assignee
Smithkline Beecham 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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of NO20033857D0 publication Critical patent/NO20033857D0/no
Publication of NO20033857L publication Critical patent/NO20033857L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/145Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/15Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
    • C07C311/46Y being a hydrogen or a carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/51Y being a hydrogen or a carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/52Y being a hetero atom
    • C07C311/53X and Y not being nitrogen atoms, e.g. N-sulfonylcarbamic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D207/16Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
  • Medicinal Preparation (AREA)
NO20033857A 2001-03-02 2003-09-01 Benzofenoner som inhibitorer av revers transkriptase NO20033857L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US27295301P 2001-03-02 2001-03-02
PCT/US2002/006037 WO2002070470A2 (fr) 2001-03-02 2002-02-28 Benzophenones en tant qu'inhibiteurs de la transcriptase inverse

Publications (2)

Publication Number Publication Date
NO20033857D0 NO20033857D0 (no) 2003-09-01
NO20033857L true NO20033857L (no) 2003-10-27

Family

ID=23041935

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20033857A NO20033857L (no) 2001-03-02 2003-09-01 Benzofenoner som inhibitorer av revers transkriptase

Country Status (18)

Country Link
US (2) US6995283B2 (fr)
EP (1) EP1363877A2 (fr)
JP (1) JP2004525914A (fr)
KR (1) KR100638954B1 (fr)
CN (1) CN1494528A (fr)
AR (2) AR035436A1 (fr)
AU (1) AU2002254056C1 (fr)
BR (1) BR0207752A (fr)
CA (1) CA2439820A1 (fr)
CZ (1) CZ20032366A3 (fr)
HU (1) HUP0303326A2 (fr)
IL (1) IL157348A0 (fr)
MX (1) MXPA03007883A (fr)
NO (1) NO20033857L (fr)
NZ (1) NZ527864A (fr)
PL (1) PL364658A1 (fr)
WO (1) WO2002070470A2 (fr)
ZA (1) ZA200306549B (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8101629B2 (en) 2001-08-13 2012-01-24 Janssen Pharmaceutica N.V. Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile
US7638522B2 (en) 2001-08-13 2009-12-29 Janssen Pharmaceutica N.V. Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino] benzonitrile
JO3429B1 (ar) 2001-08-13 2019-10-20 Janssen Pharmaceutica Nv مشتقات برميدينات مثبطة فيروس الايدز
AR039540A1 (es) * 2002-05-13 2005-02-23 Tibotec Pharm Ltd Compuestos microbicidas con contenido de pirimidina o triazina
JP4822707B2 (ja) 2002-08-09 2011-11-24 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 4−[[4−[[4−(2−シアノエテニル)−2,6−ジメチルフェニル]アミノ]−2−ピリミジニル]アミノ]ベンゾニトリルの製造方法
CA2496565C (fr) 2002-08-23 2013-04-02 Ribapharm Inc. Inhibiteurs non nucleosidiques de transcriptases inverses
US7642277B2 (en) 2002-12-04 2010-01-05 Boehringer Ingelheim International Gmbh Non-nucleoside reverse transcriptase inhibitors
US20070021449A1 (en) * 2003-02-07 2007-01-25 Jan Heeres Pyrimidine derivatives for the prevention of hiv infection
JP2006521402A (ja) 2003-03-27 2006-09-21 スミスクライン ビーチャム コーポレーション 逆転写酵素阻害剤を調製するための方法
WO2005026114A1 (fr) * 2003-09-17 2005-03-24 Pfizer Inc. Inhibiteurs de la protease du vih, compositions les contenant et leurs utilisations pharmaceutiques
EP1740550A1 (fr) * 2004-04-14 2007-01-10 Pfizer Limited Composes d'imidazole a liaison souphre pour le traitement du vih
US20060025480A1 (en) * 2004-08-02 2006-02-02 Boehringer Ingelheim International Gmbh Benzoic acid derivatives as non nucleoside reverse transcriptase inhibitors
WO2007050087A1 (fr) 2004-08-25 2007-05-03 Ardea Biosciences, Inc. Acides N[S(4-aryltriazol-3-yl)α-mercaptoacétyl]-p-aminobenzoïques EN TANT QU'INHIBITEURS DE TRANSCRIPTASE INVERSE DE VIH
ME01512B (me) 2004-08-25 2014-04-20 Ardea Biosciences Inc S-triazolil alfa-merkaptoacetanilida kao inhibitori HIV reversne transkriptaze
CA2577144C (fr) * 2004-09-30 2011-06-21 Boehringer Ingelheim International Gmbh Derives de benzophenone a base d'alkynyle utilises comme inhibiteurs de transcriptase inverse de non nucleoside
WO2006067587A2 (fr) * 2004-12-22 2006-06-29 Pfizer Limited Composes chimiques
US20060280791A1 (en) * 2005-04-08 2006-12-14 Ju Tzuchi R Pharmaceutical formulations
AR057455A1 (es) * 2005-07-22 2007-12-05 Merck & Co Inc Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica
WO2007121415A2 (fr) * 2006-04-17 2007-10-25 Smithkline Beecham Corporation Composés chimiques
WO2007121416A2 (fr) * 2006-04-17 2007-10-25 Smithkline Beecham Corporation Composés chimiques
AR060492A1 (es) * 2006-04-17 2008-06-18 Smithkline Beecham Corp Compuestos quimicos
EP2044037A2 (fr) * 2006-07-24 2009-04-08 Gilead Sciences, Inc. Inhibiteurs inédits de la transcriptase inverse du vih
CN101407476B (zh) 2007-10-12 2012-07-18 中国人民解放军军事医学科学院毒物药物研究所 作为非核苷类hiv逆转录酶抑制剂的间二芳烃-多取代苯胺类化合物、其制备方法及用途
SI2217577T1 (sl) 2007-11-27 2014-11-28 Ardea Biosciences, Inc. Nove spojine in sestavki ter metode uporabe
CN101450911B (zh) * 2007-11-30 2012-02-29 山东轩竹医药科技有限公司 被金刚烷取代的苯甲酸衍生物
CN102219717A (zh) * 2011-04-20 2011-10-19 复旦大学 N-苯基芳基甲酰胺衍生物及其制备方法和用途
CN102206177A (zh) * 2011-04-20 2011-10-05 复旦大学 1-萘基苯甲酮衍生物及其制备方法和用途
CN102212022A (zh) * 2011-04-20 2011-10-12 复旦大学 二苯甲醇衍生物及其制备方法和用途
CN110015963A (zh) * 2019-04-12 2019-07-16 上海优合生物科技有限公司 一种2-氯-6-甲基苯胺的制备方法
US11116737B1 (en) 2020-04-10 2021-09-14 University Of Georgia Research Foundation, Inc. Methods of using probenecid for treatment of coronavirus infections

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03198050A (ja) * 1989-12-27 1991-08-29 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料

Also Published As

Publication number Publication date
AR043367A2 (es) 2005-07-27
CA2439820A1 (fr) 2002-09-12
CZ20032366A3 (en) 2004-04-14
NZ527864A (en) 2004-05-28
PL364658A1 (en) 2004-12-13
HUP0303326A2 (hu) 2004-01-28
AU2002254056C1 (en) 2006-04-13
US20040122064A1 (en) 2004-06-24
AU2002254056B2 (en) 2005-09-29
KR20030086283A (ko) 2003-11-07
WO2002070470A3 (fr) 2003-03-06
EP1363877A2 (fr) 2003-11-26
AR035436A1 (es) 2004-05-26
NO20033857D0 (no) 2003-09-01
IL157348A0 (en) 2004-02-19
US6995283B2 (en) 2006-02-07
MXPA03007883A (es) 2003-12-04
BR0207752A (pt) 2004-03-23
JP2004525914A (ja) 2004-08-26
CN1494528A (zh) 2004-05-05
US20060009651A1 (en) 2006-01-12
WO2002070470A2 (fr) 2002-09-12
ZA200306549B (en) 2004-11-22
KR100638954B1 (ko) 2006-10-25

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