EMD-50324
Coxsackievirus A9 bound with compound 17 (CL301)
EMD-50324
Single-particle2.53 Å
Deposition: 16/05/2024Map released: 02/10/2024
Last modified: 23/10/2024
Sample Organism:
Human coxsackievirus A9 (strain Griggs)
Sample: Human coxsackievirus A9 (strain Griggs)
Fitted models: 9fcz (Avg. Q-score: 0.573)
Raw data: EMPIAR-12396
Deposition Authors: Plavec Z, Butcher SJ
,
Mitchell C ,
Buckner C
Sample: Human coxsackievirus A9 (strain Griggs)
Fitted models: 9fcz (Avg. Q-score: 0.573)
Raw data: EMPIAR-12396
Deposition Authors: Plavec Z, Butcher SJ
,
Mitchell C ,
Buckner C
SAR Analysis of Novel Coxsackie virus A9 Capsid Binders.
Tammaro C,
Plavec Z,
Myllymaki L ,
Mitchell C ,
Consalvi S,
Biava M,
Ciogli A ,
Domanska A ,
Leppilampi V,
Buckner C,
Manetto S,
Scio P,
Coluccia A ,
Laajala M ,
Dondio GM ,
Bigogno C,
Marjomaki V ,
Butcher SJ ,
Poce G
(2024) J Med Chem , 67 , 17144 - 17161
,
Mitchell C ,
Consalvi S,
Biava M,
Ciogli A ,
Domanska A ,
Leppilampi V,
Buckner C,
Manetto S,
Scio P,
Coluccia A ,
Laajala M ,
Dondio GM ,
Bigogno C,
Marjomaki V ,
Butcher SJ ,
Poce G
(2024) J Med Chem , 67 , 17144 - 17161
Abstract:
Enterovirus infections are common in humans, yet there are no approved antiviral treatments. In this study we concentrated on inhibition of one of the Enterovirus B (EV-B), namely Coxsackievirus A9 (CVA9), using a combination of medicinal chemistry, virus inhibition assays, structure determination from cryogenic electron microscopy and molecular modeling, to determine the structure activity relationships for a promising class of novel N-phenylbenzylamines. Of the new 29 compounds synthesized, 10 had half maximal effective concentration (EC50) values between 0.64-10.46 μM, and of these, 7 had 50% cytotoxicity concentration (CC50) values higher than 200 μM. In addition, this new series of compounds showed promising physicochemical properties and act through capsid stabilization, preventing capsid expansion and subsequent release of the genome.
Enterovirus infections are common in humans, yet there are no approved antiviral treatments. In this study we concentrated on inhibition of one of the Enterovirus B (EV-B), namely Coxsackievirus A9 (CVA9), using a combination of medicinal chemistry, virus inhibition assays, structure determination from cryogenic electron microscopy and molecular modeling, to determine the structure activity relationships for a promising class of novel N-phenylbenzylamines. Of the new 29 compounds synthesized, 10 had half maximal effective concentration (EC50) values between 0.64-10.46 μM, and of these, 7 had 50% cytotoxicity concentration (CC50) values higher than 200 μM. In addition, this new series of compounds showed promising physicochemical properties and act through capsid stabilization, preventing capsid expansion and subsequent release of the genome.