Chemical Information | |
Antiviral agent ID | DrugRepV_5659 | |
Antiviral agent name | Bortezomib | |
IUPAC Name | [(1R)-3-methyl-1-[[(2S)-3-phenyl-2-(pyrazine-2-carbonylamino)propanoyl]amino]butyl]boronic acid | |
SMILES (canonical) | B(C(CC(C)C)NC(=O)C(CC1=CC=CC=C1)NC(=O)C2=NC=CN=C2)(O)O | |
SMILES (isomeric) | B([C@H](CC(C)C)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)C2=NC=CN=C2)(O)O | |
Molecular Formula | C19H25BN4O4 | |
Molecular Weight (g/mol) | 384.24 | |
InChl | InChI=1S/C19H25BN4O4/c1-13(2)10-17(20(27)28)24-18(25)15(11-14-6-4-3-5-7-14)23-19(26)16-12-21-8-9-22-16/h3-9,12-13,15,17,27-28H,10-11H2,1-2H3,(H,23,26)(H,24,25)/t15-,17-/m0/s1 | |
Common Name | Bortezomib | |
Synonyms | [(1R)-3-methyl-1-({(2S)-3-phenyl-2-[(pyrazin-2-ylcarbonyl)amino]propanoyl}amino)butyl]boronic acid | N-[(1R)-1-(DIHYDROXYBORYL)-3-methylbutyl]-N-(pyrazin-2-ylcarbonyl)-L-phenylalaninamide | N-[(1R)-1-(DIHYDROXYBORYL)-3-METHYLBUTYL]-N-(PYRAZIN-2-YLCARBONYL)-L-PHENYLALANINAMIDE | |
Structural Information | |
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Clinical Information | |
Category | Antineoplastic and Immunomodulating Agents
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Primary Indication (Clinical trial phases) | Approved
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Biological Information | |
Primary Indication (Disease Category) | Non Infectious Disease
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Primary Indication (Disease) | Multiple Myeloma
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Secondary Indication | Dengue virus (DENV) 1 EDEN3300 | |
Secondary Indication (Approaches) | Experimental | |
Secondary Indication (Methods) | In-vitro | |
Secondary Indication (Model system) [cell lines/ animal models] | THP-1 + ADE
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Secondary Indication (Mode of viral infection) | Opsonization
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Secondary Indication (Viral titer) | 10 MOI
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Secondary Indication (Mode of drug delivery) | Culture
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Secondary Indication (Time of drug delivery) | Pre infection
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Secondary Indication (Duration of drug delivery) | 48 hours
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Secondary Indication (Drug concentration) | 4.2 nM
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Secondary Indication (Cell based assay) | Plaque assay
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Secondary Indication (Change) | Decrease
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Secondary Indication (Type of Inhibition) | IC50 [ 50 % ] | |
Reference | Choy MM, Zhang SL, Costa VV, Tan HC, Horrevorts S, Ooi EE..Proteasome Inhibition Suppresses Dengue Virus Egress in Antibody Dependent Infection..PLoS Negl Trop Dis. 2015 Nov 13;9(11):e0004058. doi: 10.1371/journal.pntd.0004058. eCollection 2015 PMID:26565697
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Comment | Proteasome inhibitor, bortezomib, is able to inhibit DENV titers at low nanomolar drug concentrations for different strains of all four serotypes of DENV in primary monocytes. Furthermore, bortezomib treatment of DENV-infected mice inhibited the spread of DENV in the spleen as well as the overall pathological changes. The findings suggest that preventing DENV egress through proteasome inhibition could be a suitable therapeutic strategy against dengue
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