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Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor

Identifieur interne : 004408 ( Main/Exploration ); précédent : 004407; suivant : 004409

Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor

Auteurs : Syaulan Yang [Taïwan] ; Shu-Jen Chen [Taïwan] ; Min-Feng Hsu [Taïwan] ; Jen-Dar Wu [Taïwan] ; Chien-Te K. Tseng [États-Unis] ; Yu-Fan Liu [Taïwan] ; Hua-Chien Chen [Taïwan] ; Chun-Wei Kuo [Taïwan] ; Chi-Shen Wu [Taïwan] ; Li-Wen Chang [Taïwan] ; Wen-Chang Chen [Taïwan] ; Shao-Ying Liao [Taïwan] ; Teng-Yuan Chang [Taïwan] ; Hsin-Hui Hung [Taïwan] ; Hui-Lin Shr [Taïwan] ; Cheng-Yuan Liu [Taïwan] ; Yu-An Huang [Taïwan] ; Ling-Yin Chang [Taïwan] ; Jen-Chi Hsu [Taïwan] ; Clarence J. Peters [États-Unis] ; Andrew H.-J. Wang [Taïwan] ; Ming-Chu Hsu [Taïwan]

Source :

RBID : Pascal:06-0539611

Descripteurs français

English descriptors

Abstract

A potent SARS coronavirus (CoV) 3CL protease inhibitor (TG-0205221, Ki = 53 nM) has been developed. TG-0205221 showed remarkable activity against SARS CoV and human coronavirus (HCoV) 229E replications by reducing the viral titer by 4.7 log (at 5 μM) for SARS CoV and 5.2 log (at 1.25 μM) for HCoV 229E. The crystal structure of TG-0205221 (resolution = 1.93 Å) has revealed a unique binding mode comprising a covalent bond, hydrogen bonds, and numerous hydrophobic interactions. Structural comparisons between TG-0205221 and a natural peptide substrate were also discussed. This information may be applied toward the design of other 3CL protease inhibitors.


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<title xml:lang="en" level="a">Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor</title>
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<name sortKey="Yang, Syaulan" sort="Yang, Syaulan" uniqKey="Yang S" first="Syaulan" last="Yang">Syaulan Yang</name>
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<name sortKey="Hsu, Min Feng" sort="Hsu, Min Feng" uniqKey="Hsu M" first="Min-Feng" last="Hsu">Min-Feng Hsu</name>
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<name sortKey="Wu, Jen Dar" sort="Wu, Jen Dar" uniqKey="Wu J" first="Jen-Dar" last="Wu">Jen-Dar Wu</name>
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<name sortKey="Hsu, Jen Chi" sort="Hsu, Jen Chi" uniqKey="Hsu J" first="Jen-Chi" last="Hsu">Jen-Chi Hsu</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>TaiGen Biotechnology Co</s1>
<s2>Taipei 114</s2>
<s3>TWN</s3>
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</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>TaiGen Biotechnology Co</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Peters, Clarence J" sort="Peters, Clarence J" uniqKey="Peters C" first="Clarence J." last="Peters">Clarence J. Peters</name>
<affiliation wicri:level="1">
<inist:fA14 i1="05">
<s1>Department of Microbiology and Immunology, University of Texas Medical Branch</s1>
<s2>Galveston, Texas 77555</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
<sZ>20 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<wicri:noRegion>Galveston, Texas 77555</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Wang, Andrew H J" sort="Wang, Andrew H J" uniqKey="Wang A" first="Andrew H.-J." last="Wang">Andrew H.-J. Wang</name>
<affiliation wicri:level="1">
<inist:fA14 i1="02">
<s1>Institute of Biochemical Sciences, National Taiwan University</s1>
<s2>Taipei 106</s2>
<s3>TWN</s3>
<sZ>3 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>Taipei 106</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<inist:fA14 i1="03">
<s1>Institute of Biological Chemistry, Academia Sinica</s1>
<s2>Taipei 115</s2>
<s3>TWN</s3>
<sZ>3 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>Taipei 115</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<inist:fA14 i1="04">
<s1>Core Facility for Protein X-ray Crystallography, Academia Sinica</s1>
<s2>Taipei 115</s2>
<s3>TWN</s3>
<sZ>3 aut.</sZ>
<sZ>15 aut.</sZ>
<sZ>21 aut.</sZ>
</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>Taipei 115</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Hsu, Ming Chu" sort="Hsu, Ming Chu" uniqKey="Hsu M" first="Ming-Chu" last="Hsu">Ming-Chu Hsu</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>TaiGen Biotechnology Co</s1>
<s2>Taipei 114</s2>
<s3>TWN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
<sZ>12 aut.</sZ>
<sZ>13 aut.</sZ>
<sZ>14 aut.</sZ>
<sZ>16 aut.</sZ>
<sZ>17 aut.</sZ>
<sZ>18 aut.</sZ>
<sZ>19 aut.</sZ>
<sZ>22 aut.</sZ>
</inist:fA14>
<country>Taïwan</country>
<wicri:noRegion>TaiGen Biotechnology Co</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Journal of medicinal chemistry : (Print)</title>
<title level="j" type="abbreviated">J. med. chem. : (Print)</title>
<idno type="ISSN">0022-2623</idno>
<imprint>
<date when="2006">2006</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<title level="j" type="main">Journal of medicinal chemistry : (Print)</title>
<title level="j" type="abbreviated">J. med. chem. : (Print)</title>
<idno type="ISSN">0022-2623</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Aminoaldehyde</term>
<term>Animals</term>
<term>Antiviral</term>
<term>Antiviral Agents (chemical synthesis)</term>
<term>Antiviral Agents (chemistry)</term>
<term>Antiviral Agents (pharmacology)</term>
<term>Biological fluid</term>
<term>Blood</term>
<term>Blood plasma</term>
<term>Carbamates (chemical synthesis)</term>
<term>Carbamates (chemistry)</term>
<term>Carbamates (pharmacology)</term>
<term>Carboxamide</term>
<term>Cell Line</term>
<term>Chemical synthesis</term>
<term>Chlorocebus aethiops</term>
<term>Coronavirus 229E, Human (drug effects)</term>
<term>Crystalline structure</term>
<term>Crystallography, X-Ray</term>
<term>Cysteine Endopeptidases (chemistry)</term>
<term>Dipeptides (chemical synthesis)</term>
<term>Dipeptides (chemistry)</term>
<term>Dipeptides (pharmacology)</term>
<term>Drug Stability</term>
<term>Enzyme inhibitor</term>
<term>Five membered ring</term>
<term>Humans</term>
<term>Hydrogen Bonding</term>
<term>Hydrolysis resistance</term>
<term>Hydrophobic and Hydrophilic Interactions</term>
<term>In vitro</term>
<term>Inhibitor enzyme complex</term>
<term>Lactam</term>
<term>Mice</term>
<term>Modeling</term>
<term>Models, Molecular</term>
<term>Molecular Structure</term>
<term>Molecular model</term>
<term>Molecular structure</term>
<term>Nitrogen heterocycle</term>
<term>Peptidases</term>
<term>Peptide synthesis</term>
<term>Peptides</term>
<term>Protease inhibitor</term>
<term>Rats</term>
<term>SARS Virus (drug effects)</term>
<term>Severe acute respiratory syndrome virus</term>
<term>Structure activity relation</term>
<term>Structure-Activity Relationship</term>
<term>Tripeptide</term>
<term>Viral Proteins (antagonists & inhibitors)</term>
<term>Viral Proteins (chemistry)</term>
<term>Virus Replication (drug effects)</term>
<term>X ray diffraction</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Antiviraux ()</term>
<term>Antiviraux (pharmacologie)</term>
<term>Antiviraux (synthèse chimique)</term>
<term>Carbamates ()</term>
<term>Carbamates (pharmacologie)</term>
<term>Carbamates (synthèse chimique)</term>
<term>Coronavirus humain 229E ()</term>
<term>Cristallographie aux rayons X</term>
<term>Cysteine endopeptidases ()</term>
<term>Dipeptides ()</term>
<term>Dipeptides (pharmacologie)</term>
<term>Dipeptides (synthèse chimique)</term>
<term>Humains</term>
<term>Interactions hydrophobes et hydrophiles</term>
<term>Liaison hydrogène</term>
<term>Lignée cellulaire</term>
<term>Modèles moléculaires</term>
<term>Protéines virales ()</term>
<term>Protéines virales (antagonistes et inhibiteurs)</term>
<term>Rats</term>
<term>Relation structure-activité</term>
<term>Réplication virale ()</term>
<term>Souris</term>
<term>Stabilité de médicament</term>
<term>Structure moléculaire</term>
<term>Virus du SRAS ()</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="antagonists & inhibitors" xml:lang="en">
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en">
<term>Antiviral Agents</term>
<term>Carbamates</term>
<term>Dipeptides</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Antiviral Agents</term>
<term>Carbamates</term>
<term>Cysteine Endopeptidases</term>
<term>Dipeptides</term>
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Antiviral Agents</term>
<term>Carbamates</term>
<term>Dipeptides</term>
</keywords>
<keywords scheme="MESH" qualifier="antagonistes et inhibiteurs" xml:lang="fr">
<term>Protéines virales</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Coronavirus 229E, Human</term>
<term>SARS Virus</term>
<term>Virus Replication</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Antiviraux</term>
<term>Carbamates</term>
<term>Dipeptides</term>
</keywords>
<keywords scheme="MESH" qualifier="synthèse chimique" xml:lang="fr">
<term>Antiviraux</term>
<term>Carbamates</term>
<term>Dipeptides</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>Crystallography, X-Ray</term>
<term>Drug Stability</term>
<term>Humans</term>
<term>Hydrogen Bonding</term>
<term>Hydrophobic and Hydrophilic Interactions</term>
<term>Mice</term>
<term>Models, Molecular</term>
<term>Molecular Structure</term>
<term>Rats</term>
<term>Structure-Activity Relationship</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Animaux</term>
<term>Antiviraux</term>
<term>Carbamates</term>
<term>Coronavirus humain 229E</term>
<term>Cristallographie aux rayons X</term>
<term>Cysteine endopeptidases</term>
<term>Dipeptides</term>
<term>Humains</term>
<term>Interactions hydrophobes et hydrophiles</term>
<term>Liaison hydrogène</term>
<term>Lignée cellulaire</term>
<term>Modèles moléculaires</term>
<term>Protéines virales</term>
<term>Rats</term>
<term>Relation structure-activité</term>
<term>Réplication virale</term>
<term>Souris</term>
<term>Stabilité de médicament</term>
<term>Structure moléculaire</term>
<term>Synthèse chimique</term>
<term>Structure cristalline</term>
<term>Relation structure activité</term>
<term>Antiviral</term>
<term>Synthèse peptidique</term>
<term>Virus du SRAS</term>
<term>Virus syndrome respiratoire aigu sévère</term>
<term>Inhibiteur protease</term>
<term>Résistance hydrolyse</term>
<term>Plasma sanguin</term>
<term>Tripeptide</term>
<term>Aminoaldéhyde</term>
<term>Hétérocycle azote</term>
<term>Cycle 5 chaînons</term>
<term>Lactame</term>
<term>Modèle moléculaire</term>
<term>Complexe enzyme inhibiteur</term>
<term>Carboxamide</term>
<term>In vitro</term>
<term>Peptidases</term>
<term>Inhibiteur enzyme</term>
<term>Diffraction RX</term>
<term>Structure moléculaire</term>
<term>Liquide biologique</term>
<term>Sang</term>
<term>Peptide</term>
<term>Modélisation</term>
<term>Cyclohexylalanamide([N-benzyloxycarbonyl-3-O-t-butyl-thréonyl]-N-[1-forrmyl-2-(2-oxopyrrolidin-3-yl)éthyl])</term>
<term>TG 0205221</term>
<term>Pyrrolidin-2-one dérivé</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">A potent SARS coronavirus (CoV) 3CL protease inhibitor (TG-0205221, K
<sub>i</sub>
= 53 nM) has been developed. TG-0205221 showed remarkable activity against SARS CoV and human coronavirus (HCoV) 229E replications by reducing the viral titer by 4.7 log (at 5 μM) for SARS CoV and 5.2 log (at 1.25 μM) for HCoV 229E. The crystal structure of TG-0205221 (resolution = 1.93 Å) has revealed a unique binding mode comprising a covalent bond, hydrogen bonds, and numerous hydrophobic interactions. Structural comparisons between TG-0205221 and a natural peptide substrate were also discussed. This information may be applied toward the design of other 3CL protease inhibitors.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Taïwan</li>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="Taïwan">
<noRegion>
<name sortKey="Yang, Syaulan" sort="Yang, Syaulan" uniqKey="Yang S" first="Syaulan" last="Yang">Syaulan Yang</name>
</noRegion>
<name sortKey="Chang, Li Wen" sort="Chang, Li Wen" uniqKey="Chang L" first="Li-Wen" last="Chang">Li-Wen Chang</name>
<name sortKey="Chang, Ling Yin" sort="Chang, Ling Yin" uniqKey="Chang L" first="Ling-Yin" last="Chang">Ling-Yin Chang</name>
<name sortKey="Chang, Teng Yuan" sort="Chang, Teng Yuan" uniqKey="Chang T" first="Teng-Yuan" last="Chang">Teng-Yuan Chang</name>
<name sortKey="Chen, Hua Chien" sort="Chen, Hua Chien" uniqKey="Chen H" first="Hua-Chien" last="Chen">Hua-Chien Chen</name>
<name sortKey="Chen, Shu Jen" sort="Chen, Shu Jen" uniqKey="Chen S" first="Shu-Jen" last="Chen">Shu-Jen Chen</name>
<name sortKey="Chen, Wen Chang" sort="Chen, Wen Chang" uniqKey="Chen W" first="Wen-Chang" last="Chen">Wen-Chang Chen</name>
<name sortKey="Hsu, Jen Chi" sort="Hsu, Jen Chi" uniqKey="Hsu J" first="Jen-Chi" last="Hsu">Jen-Chi Hsu</name>
<name sortKey="Hsu, Min Feng" sort="Hsu, Min Feng" uniqKey="Hsu M" first="Min-Feng" last="Hsu">Min-Feng Hsu</name>
<name sortKey="Hsu, Min Feng" sort="Hsu, Min Feng" uniqKey="Hsu M" first="Min-Feng" last="Hsu">Min-Feng Hsu</name>
<name sortKey="Hsu, Min Feng" sort="Hsu, Min Feng" uniqKey="Hsu M" first="Min-Feng" last="Hsu">Min-Feng Hsu</name>
<name sortKey="Hsu, Ming Chu" sort="Hsu, Ming Chu" uniqKey="Hsu M" first="Ming-Chu" last="Hsu">Ming-Chu Hsu</name>
<name sortKey="Huang, Yu An" sort="Huang, Yu An" uniqKey="Huang Y" first="Yu-An" last="Huang">Yu-An Huang</name>
<name sortKey="Hung, Hsin Hui" sort="Hung, Hsin Hui" uniqKey="Hung H" first="Hsin-Hui" last="Hung">Hsin-Hui Hung</name>
<name sortKey="Kuo, Chun Wei" sort="Kuo, Chun Wei" uniqKey="Kuo C" first="Chun-Wei" last="Kuo">Chun-Wei Kuo</name>
<name sortKey="Liao, Shao Ying" sort="Liao, Shao Ying" uniqKey="Liao S" first="Shao-Ying" last="Liao">Shao-Ying Liao</name>
<name sortKey="Liu, Cheng Yuan" sort="Liu, Cheng Yuan" uniqKey="Liu C" first="Cheng-Yuan" last="Liu">Cheng-Yuan Liu</name>
<name sortKey="Liu, Yu Fan" sort="Liu, Yu Fan" uniqKey="Liu Y" first="Yu-Fan" last="Liu">Yu-Fan Liu</name>
<name sortKey="Shr, Hui Lin" sort="Shr, Hui Lin" uniqKey="Shr H" first="Hui-Lin" last="Shr">Hui-Lin Shr</name>
<name sortKey="Shr, Hui Lin" sort="Shr, Hui Lin" uniqKey="Shr H" first="Hui-Lin" last="Shr">Hui-Lin Shr</name>
<name sortKey="Wang, Andrew H J" sort="Wang, Andrew H J" uniqKey="Wang A" first="Andrew H.-J." last="Wang">Andrew H.-J. Wang</name>
<name sortKey="Wang, Andrew H J" sort="Wang, Andrew H J" uniqKey="Wang A" first="Andrew H.-J." last="Wang">Andrew H.-J. Wang</name>
<name sortKey="Wang, Andrew H J" sort="Wang, Andrew H J" uniqKey="Wang A" first="Andrew H.-J." last="Wang">Andrew H.-J. Wang</name>
<name sortKey="Wu, Chi Shen" sort="Wu, Chi Shen" uniqKey="Wu C" first="Chi-Shen" last="Wu">Chi-Shen Wu</name>
<name sortKey="Wu, Jen Dar" sort="Wu, Jen Dar" uniqKey="Wu J" first="Jen-Dar" last="Wu">Jen-Dar Wu</name>
</country>
<country name="États-Unis">
<noRegion>
<name sortKey="Tseng, Chien Te K" sort="Tseng, Chien Te K" uniqKey="Tseng C" first="Chien-Te K." last="Tseng">Chien-Te K. Tseng</name>
</noRegion>
<name sortKey="Peters, Clarence J" sort="Peters, Clarence J" uniqKey="Peters C" first="Clarence J." last="Peters">Clarence J. Peters</name>
</country>
</tree>
</affiliations>
</record>

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