WO1999062520A1 - Inhibiteurs de vih integrase - Google Patents

Inhibiteurs de vih integrase Download PDF

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Publication number
WO1999062520A1
WO1999062520A1 PCT/US1999/012093 US9912093W WO9962520A1 WO 1999062520 A1 WO1999062520 A1 WO 1999062520A1 US 9912093 W US9912093 W US 9912093W WO 9962520 A1 WO9962520 A1 WO 9962520A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
phenyl
substituted
benzyl
hydroxy
Prior art date
Application number
PCT/US1999/012093
Other languages
English (en)
Inventor
Steven D. Young
Melissa Egbertson
Linda S. Payne
John S. Wai
Thorsten E. Fisher
James P. Guare, Jr.
Mark W. Embrey
Lee Tran
Linghang Zhuang
Joseph P. Vacca
Marie Langford
Jeffrey Melamed
David L. Clark
Julio C. Medina
Juan Jaen
Original Assignee
Merck & Co., Inc.
Tularik, 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
Priority claimed from GBGB9815175.6A external-priority patent/GB9815175D0/en
Application filed by Merck & Co., Inc., Tularik, Inc. filed Critical Merck & Co., Inc.
Priority to JP2000551776A priority Critical patent/JP2002516863A/ja
Priority to CA002333707A priority patent/CA2333707A1/fr
Priority to EP99926094A priority patent/EP1082121A4/fr
Priority to AU42254/99A priority patent/AU4225499A/en
Publication of WO1999062520A1 publication Critical patent/WO1999062520A1/fr

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    • 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
    • C07D213/60Heterocyclic 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 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/60Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/40Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/42Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton with carboxyl groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by saturated carbon chains
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/57Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C233/63Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
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    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/58Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/60Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring with carbon atoms of carboxamide groups and singly-bound oxygen atoms, bound in ortho-position to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/01Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/32Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
    • C07C255/41Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by carboxyl groups, other than cyano groups
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/16Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
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    • C07C271/26Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
    • C07C271/28Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/50Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
    • C07C323/62Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
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    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
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    • C07C59/40Unsaturated compounds
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    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/73Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
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    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
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    • C07D241/12Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D253/08Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 condensed with carbocyclic rings or ring systems
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    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
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    • 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
    • C07D295/08Heterocyclic 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 singly bound oxygen or sulfur atoms
    • C07D295/084Heterocyclic 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 singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088Heterocyclic 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 singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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    • 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
    • C07D295/155Heterocyclic 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 separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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    • 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
    • C07D295/16Heterocyclic 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 acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic 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 acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/192Radicals derived from carboxylic acids from aromatic carboxylic acids
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    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
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    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

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  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Cette invention a trait à certains dérivés d'acide dioxo-butyrique à 6 chaînons, aromatique et hétéro-aromatique, agissant en tant qu'inhibiteurs de VIH intégrase et de la réplication du VIH. Ces composés sont utilisés dans le cadre de la prévention et du traitement des infections par le VIH et du sida, que ce soit sous forme de composés, de sels acceptables du point de vue pharmaceutique ou d'ingrédients de composition pharmaceutique, seuls ou associés à d'autres antiviraux, immunorégulateurs, antibiotiques ou vaccins. L'invention concerne également des méthodes de traitement du sida ainsi que des méthodes de prévention et de traitement des infections par VIH.
PCT/US1999/012093 1998-06-03 1999-06-01 Inhibiteurs de vih integrase WO1999062520A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2000551776A JP2002516863A (ja) 1998-06-03 1999-06-01 Hivインテグラーゼ阻害薬
CA002333707A CA2333707A1 (fr) 1998-06-03 1999-06-01 Inhibiteurs de vih integrase
EP99926094A EP1082121A4 (fr) 1998-06-03 1999-06-01 Inhibiteurs de vih integrase
AU42254/99A AU4225499A (en) 1998-06-03 1999-06-01 Hiv integrase inhibitors

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US8782098P 1998-06-03 1998-06-03
US60/087,820 1998-06-03
GBGB9815175.6A GB9815175D0 (en) 1998-07-13 1998-07-13 HIV integrase inhibitors
GB9815175.6 1998-07-13

Publications (1)

Publication Number Publication Date
WO1999062520A1 true WO1999062520A1 (fr) 1999-12-09

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/012093 WO1999062520A1 (fr) 1998-06-03 1999-06-01 Inhibiteurs de vih integrase

Country Status (4)

Country Link
EP (1) EP1082121A4 (fr)
AU (1) AU4225499A (fr)
CA (1) CA2333707A1 (fr)
WO (1) WO1999062520A1 (fr)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000039086A1 (fr) * 1998-12-25 2000-07-06 Shionogi & Co., Ltd. Composes heterocycliques aromatiques possedant des activites inhibitrices de l'integrase du vih
WO2001096283A2 (fr) * 2000-06-16 2001-12-20 Bristol-Myers Squibb Company Inhibiteurs d'integrase du vih
US6333323B1 (en) 1998-03-26 2001-12-25 Shionogi & Co., Ltd. Indole derivatives with antiviral activity
WO2002090336A1 (fr) * 2001-05-09 2002-11-14 Bayer Cropscience Ag Arylcetones substituees
US6492423B1 (en) 1998-07-27 2002-12-10 Istituto Di Ricerche Di Biologia Molecolare Pangeletti Spa Diketoacid-derivatives as inhibitors of polymerases
WO2003016266A1 (fr) * 2001-08-16 2003-02-27 Japan Tobacco Inc. Composes $g(b)-cetoamides et leur utilisation medicinale
WO2003035076A1 (fr) * 2001-10-26 2003-05-01 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Inhibiteurs de l'integrase du vih a base de dihydroxypyrimidine carboxamide
EP1463741A2 (fr) * 2001-12-07 2004-10-06 The Government of the United States of America, as represented by the Secretary of the Department of Health and Human Services Composes destines a traiter l'infection au vih et le sida
US6858602B2 (en) 2001-06-12 2005-02-22 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
WO2005087759A1 (fr) 2004-03-10 2005-09-22 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Quinolin-4-ones utilises comme inhibiteurs de l'integrase retrovirale pour le traitement du vih, du sida et du syndrome apparente au sida (arc)
US7169780B2 (en) 2001-10-26 2007-01-30 Istitute Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
US7253180B2 (en) 2002-10-16 2007-08-07 Gilead Sciences, Inc. Pre-organized tricyclic integrase inhibitor compounds
US7323460B2 (en) 2002-03-15 2008-01-29 Merck & Co., Inc. N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as HIV integrase inhibitors
WO2008010953A3 (fr) * 2006-07-19 2008-05-08 Univ Georgia Res Found Dicétoacides de pyridinone : inhibiteurs de la réplication du vih dans une thérapie combinée
US7462721B2 (en) 2003-09-19 2008-12-09 Gilead Sciences, Inc. Aza-quinolinol phosphonate integrase inhibitor compounds
EP2033952A1 (fr) 2001-03-01 2009-03-11 Shionogi&Co., Ltd. Composés d'hétéroaryle contenant de l'azote exerçant un effet inhibiteur sur l'intégrase du VIH
EP2045242A1 (fr) 2002-08-13 2009-04-08 Shionogi&Co., Ltd. Composants hétérocycliques disposant d'une activité inhibitoire contre l'intégrase du HIV
WO2009094190A2 (fr) 2008-01-25 2009-07-30 Chimerix, Inc. Méthodes de traitement d’infections virales
WO2010047774A2 (fr) * 2008-10-20 2010-04-29 The Texas A & M University System Inhibiteurs de la mycobacterium tuberculosis malate synthase, procédés de marquage et utilisations de ceux-ci
US20110184028A1 (en) * 2010-01-22 2011-07-28 Brent Richard Stranix Derivatives of pyridoxine for inhibiting hiv integrase
US8008287B2 (en) 2006-05-16 2011-08-30 Gilead Sciences, Inc. Integrase inhibitors
EP2522670A1 (fr) 2004-04-07 2012-11-14 Takeda Pharmaceutical Company Limited Antagonistes hétérocycliques des récépteurs du CRF
CN103420894A (zh) * 2012-05-22 2013-12-04 中国科学院上海药物研究所 丁-2-烯-1,4-二酮类化合物及其制备方法和用途
US8703801B2 (en) 2009-12-07 2014-04-22 University Of Georgia Research Foundation, Inc. Pyridinone hydroxycyclopentyl carboxamides: HIV integrase inhibitors with therapeutic applications
EP3042894A1 (fr) 2001-08-10 2016-07-13 Shionogi & Co., Ltd. Agent antiviral
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EP3216789A1 (fr) 2010-02-12 2017-09-13 Chimerix, Inc. Procédés de traitement d'une infection virale

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US6716605B2 (en) 1998-03-26 2004-04-06 Shionogi & Co., Ltd. Indole derivatives having an antiviral activity
US6506787B2 (en) 1998-03-26 2003-01-14 Shionogi & Co., Ltd. Indole derivatives having an antiviral activity
US6492423B1 (en) 1998-07-27 2002-12-10 Istituto Di Ricerche Di Biologia Molecolare Pangeletti Spa Diketoacid-derivatives as inhibitors of polymerases
US6620841B1 (en) 1998-12-25 2003-09-16 Shionogi & Co., Ltd. Aromatic heterocycle compounds having HIV integrase inhibiting activities
WO2000039086A1 (fr) * 1998-12-25 2000-07-06 Shionogi & Co., Ltd. Composes heterocycliques aromatiques possedant des activites inhibitrices de l'integrase du vih
US7098201B2 (en) 1998-12-25 2006-08-29 Shionogi & Co., Ltd. Heteroaromatic derivatives having an inhibitory activity against HIV integrase
US6645956B1 (en) 1998-12-25 2003-11-11 Shionogi & Co., Ltd. Heteroaromatic derivatives having an inhibitory activity against HIV integrase
WO2001096283A3 (fr) * 2000-06-16 2002-05-02 Bristol Myers Squibb Co Inhibiteurs d'integrase du vih
WO2001098248A3 (fr) * 2000-06-16 2003-07-10 Bristol Myers Squibb Co Inhibiteurs d'integrase du vih
WO2001098248A2 (fr) * 2000-06-16 2001-12-27 Bristol-Myers Squibb Company Inhibiteurs d'integrase du vih
WO2001096283A2 (fr) * 2000-06-16 2001-12-20 Bristol-Myers Squibb Company Inhibiteurs d'integrase du vih
EP2033952A1 (fr) 2001-03-01 2009-03-11 Shionogi&Co., Ltd. Composés d'hétéroaryle contenant de l'azote exerçant un effet inhibiteur sur l'intégrase du VIH
US7456133B2 (en) 2001-05-09 2008-11-25 Bayer Cropscience Ag Substituted arylketones
WO2002090336A1 (fr) * 2001-05-09 2002-11-14 Bayer Cropscience Ag Arylcetones substituees
US7112554B2 (en) 2001-05-09 2006-09-26 Bayer Cropscience Ag Substituted arylketones
US7012071B2 (en) * 2001-06-12 2006-03-14 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US7101910B2 (en) 2001-06-12 2006-09-05 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US6946491B2 (en) 2001-06-12 2005-09-20 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US7329782B2 (en) 2001-06-12 2008-02-12 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US7863475B2 (en) 2001-06-12 2011-01-04 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US7041659B2 (en) 2001-06-12 2006-05-09 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US7045541B2 (en) 2001-06-12 2006-05-16 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
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US6916848B2 (en) 2001-06-12 2005-07-12 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US8604083B2 (en) 2001-06-12 2013-12-10 Wellstat Therapeutics Corporation Method for the treatment of metabolic disorders
US6858602B2 (en) 2001-06-12 2005-02-22 Wellstat Therapeutics Corporation Compounds for the treatment of metabolic disorders
US8487000B2 (en) 2001-06-12 2013-07-16 Wellstat Therapertics Corporation Compound for the treatment of metabolic disorders
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US8552062B2 (en) 2001-06-12 2013-10-08 Wellstat Therapeutics Corporation Methods for the treatment of metabolic disorders such as diabetes
EP3042894A1 (fr) 2001-08-10 2016-07-13 Shionogi & Co., Ltd. Agent antiviral
US9572813B2 (en) 2001-08-10 2017-02-21 Shionogi & Co., Ltd. Antiviral agent
WO2003016266A1 (fr) * 2001-08-16 2003-02-27 Japan Tobacco Inc. Composes $g(b)-cetoamides et leur utilisation medicinale
WO2003035076A1 (fr) * 2001-10-26 2003-05-01 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Inhibiteurs de l'integrase du vih a base de dihydroxypyrimidine carboxamide
US7435734B2 (en) 2001-10-26 2008-10-14 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
US7459452B2 (en) 2001-10-26 2008-12-02 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Dihydroxypyrimidine carboxamide inhibitors of HIV integrase
US7232819B2 (en) 2001-10-26 2007-06-19 Istituto Di Ricerche Di Biologia P. Angeletti S.P.A. Dihydroxypyrimidine carboxamide inhibitors of HIV integrase
US7217713B2 (en) 2001-10-26 2007-05-15 Istituto Di Richerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
US7169780B2 (en) 2001-10-26 2007-01-30 Istitute Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
US7820660B2 (en) 2001-10-26 2010-10-26 Instituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. N-substituted hydroxypyrimidinone carboxamide inhibitors of HIV integrase
EP1463741A2 (fr) * 2001-12-07 2004-10-06 The Government of the United States of America, as represented by the Secretary of the Department of Health and Human Services Composes destines a traiter l'infection au vih et le sida
EP1463741A4 (fr) * 2001-12-07 2006-07-05 Us Gov Health & Human Serv Composes destines a traiter l'infection au vih et le sida
US7323460B2 (en) 2002-03-15 2008-01-29 Merck & Co., Inc. N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as HIV integrase inhibitors
EP2045242A1 (fr) 2002-08-13 2009-04-08 Shionogi&Co., Ltd. Composants hétérocycliques disposant d'une activité inhibitoire contre l'intégrase du HIV
US7253180B2 (en) 2002-10-16 2007-08-07 Gilead Sciences, Inc. Pre-organized tricyclic integrase inhibitor compounds
US7462721B2 (en) 2003-09-19 2008-12-09 Gilead Sciences, Inc. Aza-quinolinol phosphonate integrase inhibitor compounds
US7776883B2 (en) 2004-03-10 2010-08-17 The United States Of America As Represented By The Department Of Health And Human Services Quinolin-4-ones as inhibitors of retroviral integrase for the treatment of HIV, AIDS and AIDS related complex (ARC)
WO2005087759A1 (fr) 2004-03-10 2005-09-22 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Quinolin-4-ones utilises comme inhibiteurs de l'integrase retrovirale pour le traitement du vih, du sida et du syndrome apparente au sida (arc)
EP2522670A1 (fr) 2004-04-07 2012-11-14 Takeda Pharmaceutical Company Limited Antagonistes hétérocycliques des récépteurs du CRF
US8008287B2 (en) 2006-05-16 2011-08-30 Gilead Sciences, Inc. Integrase inhibitors
US7888375B2 (en) 2006-07-19 2011-02-15 The University Of Georgia Research Foundation, Inc Pyridinone diketo acids: inhibitors of HIV replication
WO2008010953A3 (fr) * 2006-07-19 2008-05-08 Univ Georgia Res Found Dicétoacides de pyridinone : inhibiteurs de la réplication du vih dans une thérapie combinée
EP3085377A1 (fr) 2008-01-25 2016-10-26 Chimerix, Inc. Méthodes de traitement d'infections virales
WO2009094190A2 (fr) 2008-01-25 2009-07-30 Chimerix, Inc. Méthodes de traitement d’infections virales
WO2010047774A2 (fr) * 2008-10-20 2010-04-29 The Texas A & M University System Inhibiteurs de la mycobacterium tuberculosis malate synthase, procédés de marquage et utilisations de ceux-ci
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US8664255B2 (en) 2008-10-20 2014-03-04 The Texas A&M University System Inhibitors of mycobacterium tuberculosis malate synthase, methods of making and uses thereof
US8703801B2 (en) 2009-12-07 2014-04-22 University Of Georgia Research Foundation, Inc. Pyridinone hydroxycyclopentyl carboxamides: HIV integrase inhibitors with therapeutic applications
US8664248B2 (en) 2010-01-22 2014-03-04 Taimed Biologics, Inc. Derivatives of pyridoxine for inhibiting HIV integrase
US8283366B2 (en) * 2010-01-22 2012-10-09 Ambrilia Biopharma, Inc. Derivatives of pyridoxine for inhibiting HIV integrase
US20110184028A1 (en) * 2010-01-22 2011-07-28 Brent Richard Stranix Derivatives of pyridoxine for inhibiting hiv integrase
EP3216789A1 (fr) 2010-02-12 2017-09-13 Chimerix, Inc. Procédés de traitement d'une infection virale
CN103420894A (zh) * 2012-05-22 2013-12-04 中国科学院上海药物研究所 丁-2-烯-1,4-二酮类化合物及其制备方法和用途
CN106905244A (zh) * 2017-02-27 2017-06-30 武汉工程大学 二芳基嘧啶‑二酮酸类杂合型hiv‑1抑制剂及其制备方法

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