Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_1905



Chemical Information
Antiviral agent IDDrugRepV_1905
Antiviral agent namePHA-690509
IUPAC Name(2S)-2-(4-acetamidophenyl)-N-(5-propan-2-yl-1,3-thiazol-2-yl)propanamide PubChem
SMILES (canonical)CC(C)C1=CN=C(S1)NC(=O)C(C)C2=CC=C(C=C2)NC(=O)C PubChem
SMILES (isomeric)C[C@@H](C1=CC=C(C=C1)NC(=O)C)C(=O)NC2=NC=C(S2)C(C)C PubChem
Molecular FormulaC17H21N3O2S PubChem
Molecular Weight (g/mol)331.434 PubChem
InChlInChI=1S/C17H21N3O2S/c1-10(2)15-9-18-17(23-15)20-16(22)11(3)13-5-7-14(8-6-13)19-12(4)21/h5-11H,1-4H3,(H,19,21)(H,18,20,22)/t11-/m0/s1 PubChem
SynonymsPHA-690509 | (2S)-2-[4-(Acetylamino)phenyl]-N-(5-isopropyl-1,3-thiazol-2-yl)propanamide
Structural Information
  
Clinical Information
Biological Information
Primary Indication (Disease Category) Non Infectious Disease
Primary Indication (Disease)Cancer
Secondary Indication Zika virus (ZIKV) NA PRVABC-59 (2015 Puerto Rican strain)World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Model system) [cell lines/ animal models]SNB-19 glioblastoma
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)1 MOI
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Time of drug delivery) Pre infection (1 hour)
Secondary Indication (Duration of drug delivery)24 hours
Secondary Indication (Drug concentration)92 μM
Secondary Indication (Cell based assay)Western blot
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) Protein Expression [ Decrease Band intensity ]
ReferenceXu M, Lee EM, Wen Z, Cheng Y, Huang WK, Qian X, Tcw J, Kouznetsova J, Ogden SC, Hammack C, Jacob F,.Identification of small-molecule inhibitors of Zika virus infection and induced neural cell death via a drug repurposing screen.Nat Med. 2016 Oct;22(10):1101-1107. doi: 10.1038/nm.4184. Epub 2016 Aug 29. PMID:27571349 PubMed
CommentThe identified compounds that either inhibit ZIKV infection or suppress infection-induced caspase-3 activity in different neural cells