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Results 1 - 20 of 206  for All Library Resources

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Refined by: Journal Title: Journal Of Medicinal Chemistry remove
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1
α-Ketoamides as Broad-Spectrum Inhibitors of Coronavirus and Enterovirus Replication: Structure-Based Design, Synthesis, and Activity Assessment
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α-Ketoamides as Broad-Spectrum Inhibitors of Coronavirus and Enterovirus Replication: Structure-Based Design, Synthesis, and Activity Assessment

Journal of Medicinal Chemistry, 2020-05, Vol.63 (9) [Peer Reviewed Journal]

2020. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://www.acs.org/content/acs/en/terms.html ;DOI: 10.1021/acs.jmedchem.9b01828

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2
Antiviral Activity of Glycyrrhizic Acid Derivatives against SARS−Coronavirus
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Antiviral Activity of Glycyrrhizic Acid Derivatives against SARS−Coronavirus

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.1256-1259 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0493008 ;PMID: 15715493

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3
6-(1-Benzyl-1H-pyrrol-2-yl)-2,4-dioxo-5-hexenoic acids as dual inhibitors of recombinant HIV-1 integrase and ribonuclease H, synthesized by a parallel synthesis approach
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6-(1-Benzyl-1H-pyrrol-2-yl)-2,4-dioxo-5-hexenoic acids as dual inhibitors of recombinant HIV-1 integrase and ribonuclease H, synthesized by a parallel synthesis approach

Journal of medicinal chemistry, 2013-11, Vol.56 (21), p.8588-98 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm401040b ;PMID: 24124919

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4
Design, Synthesis, and Antiviral Activity of 2‘-Deoxy-2‘-fluoro-2‘-C-methylcytidine, a Potent Inhibitor of Hepatitis C Virus Replication
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Design, Synthesis, and Antiviral Activity of 2‘-Deoxy-2‘-fluoro-2‘-C-methylcytidine, a Potent Inhibitor of Hepatitis C Virus Replication

Journal of medicinal chemistry, 2005-08, Vol.48 (17), p.5504-5508 [Peer Reviewed Journal]

Copyright © 2005 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0502788 ;PMID: 16107149 ;CODEN: JMCMAR

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5
Lipid-Conjugated Oligonucleotides via “Click Chemistry” Efficiently Inhibit Hepatitis C Virus Translation
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Lipid-Conjugated Oligonucleotides via “Click Chemistry” Efficiently Inhibit Hepatitis C Virus Translation

Journal of medicinal chemistry, 2008-08, Vol.51 (15), p.4374-4376 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm800518u ;PMID: 18605715 ;CODEN: JMCMAR

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6
Ring Expanded Nucleoside Analogues Inhibit RNA Helicase and Intracellular Human Immunodeficiency Virus Type 1 Replication
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Ring Expanded Nucleoside Analogues Inhibit RNA Helicase and Intracellular Human Immunodeficiency Virus Type 1 Replication

Journal of medicinal chemistry, 2008-08, Vol.51 (16), p.5043-5051 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm800332m ;PMID: 18680273 ;CODEN: JMCMAR

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7
Synthesis, Crystal Structure, Structure−Activity Relationships, and Antiviral Activity of a Potent SARS Coronavirus 3CL Protease Inhibitor
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Synthesis, Crystal Structure, Structure−Activity Relationships, and Antiviral Activity of a Potent SARS Coronavirus 3CL Protease Inhibitor

Journal of medicinal chemistry, 2006-08, Vol.49 (16), p.4971-4980 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0603926 ;PMID: 16884309 ;CODEN: JMCMAR

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8
Identification of Compounds with Anti-West Nile Virus Activity
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Identification of Compounds with Anti-West Nile Virus Activity

Journal of medicinal chemistry, 2006-03, Vol.49 (6), p.2127-2137 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm051229y ;PMID: 16539402 ;CODEN: JMCMAR

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9
A Copper(I)-Catalyzed 1,2,3-Triazole Azide−Alkyne Click Compound Is a Potent Inhibitor of a Multidrug-Resistant HIV-1 Protease Variant
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A Copper(I)-Catalyzed 1,2,3-Triazole Azide−Alkyne Click Compound Is a Potent Inhibitor of a Multidrug-Resistant HIV-1 Protease Variant

Journal of medicinal chemistry, 2008-10, Vol.51 (20), p.6263-6270 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2009 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm800149m ;PMID: 18823110 ;CODEN: JMCMAR

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10
Quantitative Structure−Activity Relationship Studies of [(Biphenyloxy)propyl]isoxazole Derivatives. Inhibitors of Human Rhinovirus 2 Replication
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Quantitative Structure−Activity Relationship Studies of [(Biphenyloxy)propyl]isoxazole Derivatives. Inhibitors of Human Rhinovirus 2 Replication

Journal of medicinal chemistry, 2007-08, Vol.50 (17), p.4205-4213 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0704806 ;PMID: 17665898 ;CODEN: JMCMAR

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11
Design and Synthesis of Human Immunodeficiency Virus Entry Inhibitors: Sulfonamide as an Isostere for the α-Ketoamide Group
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Design and Synthesis of Human Immunodeficiency Virus Entry Inhibitors: Sulfonamide as an Isostere for the α-Ketoamide Group

Journal of medicinal chemistry, 2007-12, Vol.50 (26), p.6535-6544 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm070650e ;PMID: 18052117 ;CODEN: JMCMAR

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12
First Example of Phosphoramidate Approach Applied to a 4‘-Substituted Purine Nucleoside (4‘-Azidoadenosine):  Conversion of an Inactive Nucleoside to a Submicromolar Compound versus Hepatitis C Virus
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First Example of Phosphoramidate Approach Applied to a 4‘-Substituted Purine Nucleoside (4‘-Azidoadenosine):  Conversion of an Inactive Nucleoside to a Submicromolar Compound versus Hepatitis C Virus

Journal of medicinal chemistry, 2007-11, Vol.50 (22), p.5463-5470 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm070362i ;PMID: 17914786 ;CODEN: JMCMAR

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13
Discovery and Synthesis of HIV Integrase Inhibitors:  Development of Potent and Orally Bioavailable N-Methyl Pyrimidones
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Discovery and Synthesis of HIV Integrase Inhibitors:  Development of Potent and Orally Bioavailable N-Methyl Pyrimidones

Journal of medicinal chemistry, 2007-10, Vol.50 (20), p.4953-4975 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0704705 ;PMID: 17824681 ;CODEN: JMCMAR

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14
4-Aryl-2,4-dioxobutanoic Acid Inhibitors of HIV-1 Integrase and Viral Replication in Cells
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4-Aryl-2,4-dioxobutanoic Acid Inhibitors of HIV-1 Integrase and Viral Replication in Cells

Journal of medicinal chemistry, 2000-12, Vol.43 (26), p.4923-4926 [Peer Reviewed Journal]

Copyright © 2000 American Chemical Society ;2001 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm000176b ;PMID: 11150161 ;CODEN: JMCMAR

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15
Structure Activity of 3-Aryl-1,3-diketo-Containing Compounds as HIV-1 Integrase Inhibitors
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Structure Activity of 3-Aryl-1,3-diketo-Containing Compounds as HIV-1 Integrase Inhibitors

Journal of medicinal chemistry, 2002-07, Vol.45 (15), p.3184-3194 [Peer Reviewed Journal]

Copyright © 2002 American Chemical Society ;2002 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm020037p ;PMID: 12109903 ;CODEN: JMCMAR

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16
2-(2-Thienyl)-5,6-dihydroxy-4-carboxypyrimidines as Inhibitors of the Hepatitis C Virus NS5B Polymerase:  Discovery, SAR, Modeling, and Mutagenesis
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2-(2-Thienyl)-5,6-dihydroxy-4-carboxypyrimidines as Inhibitors of the Hepatitis C Virus NS5B Polymerase:  Discovery, SAR, Modeling, and Mutagenesis

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1693-1705 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm051064t ;PMID: 16509585

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17
Design, Synthesis, and Biological Evaluation of the Combinatorial Library with a New Spirodiketopiperazine Scaffold. Discovery of Novel Potent and Selective Low-Molecular-Weight CCR5 Antagonists
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Design, Synthesis, and Biological Evaluation of the Combinatorial Library with a New Spirodiketopiperazine Scaffold. Discovery of Novel Potent and Selective Low-Molecular-Weight CCR5 Antagonists

Journal of medicinal chemistry, 2006-07, Vol.49 (14), p.4140-4152 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm060051s ;PMID: 16821774 ;CODEN: JMCMAR

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18
Inhibition of Clinically Relevant Mutant Variants of HIV-1 by Quinazolinone Non-Nucleoside Reverse Transcriptase Inhibitors
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Inhibition of Clinically Relevant Mutant Variants of HIV-1 by Quinazolinone Non-Nucleoside Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 2000-05, Vol.43 (10), p.2019-2030 [Peer Reviewed Journal]

Copyright © 2000 American Chemical Society ;2000 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm990580e ;PMID: 10821714 ;CODEN: JMCMAR

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19
Synthesis and Anti-BVDV Activity of Acridones As New Potential Antiviral Agents
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Synthesis and Anti-BVDV Activity of Acridones As New Potential Antiviral Agents

Journal of medicinal chemistry, 2006-04, Vol.49 (8), p.2621-2627 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2006 INIST-CNRS ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm051250z ;PMID: 16610805 ;CODEN: JMCMAR

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20
Nonpeptide Inhibitors of Measles Virus Entry
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Nonpeptide Inhibitors of Measles Virus Entry

Journal of medicinal chemistry, 2006-08, Vol.49 (17), p.5080-5092 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;ISSN: 0022-2623 ;EISSN: 1520-4804 ;DOI: 10.1021/jm0602559 ;PMID: 16913698

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Results 1 - 20 of 206  for All Library Resources

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