Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_5861



Chemical Information
Antiviral agent IDDrugRepV_5861
Antiviral agent nameFluoxetine Drug Bank
IUPAC NameN-methyl-3-phenyl-3-[4-(trifluoromethyl)phenoxy]propan-1-amine PubChem
SMILES (canonical)CNCCC(C1=CC=CC=C1)OC2=CC=C(C=C2)C(F)(F)F PubChem
Molecular FormulaC17H18F3NO PubChem
Molecular Weight (g/mol)309.332 PubChem
InChlInChI=1S/C17H18F3NO/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20/h2-10,16,21H,11-12H2,1H3 PubChem
Common NameFluoxetine Drug Bank
Synonyms(+-)-N-Methyl-3-phenyl-3-((alpha,alpha,alpha-trifluoro-P-tolyl)oxy)propylamine | (+-)-N-Methyl-gamma-(4-(trifluoromethyl)phenoxy)benzenepropanamine | Fluoxetin | Fluoxetina | Fluoxétine | Fluoxetinum
Structural Information
  
Clinical Information
CategoryNervous System
Primary Indication (Clinical trial phases)Approved, Vet approved Drug Bank
Biological Information
Primary Indication (Disease Category) Non Infectious Disease
Primary Indication (Disease)Major depressive disorder | Bulimia nervosa | Obsessive-compulsive disorder | Premenstrual dysphoric disorder | Panic disorder with or without agoraphobia
Primary Indication (Drug target/Mode of Action) Intercellular adhesion molecule 4
Secondary Indication Dengue virus (DENV) 2 NAWorld Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)In-vitro
Secondary Indication (Model system) [cell lines/ animal models]Huh-7
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)3 MOI
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Time of drug delivery) Post infection
Secondary Indication (Duration of drug delivery)24 hours
Secondary Indication (Drug concentration)0.38 μM
Secondary Indication (Cell based assay)Plaque assay
Secondary Indication (Change)Decrease
Secondary Indication (Type of Inhibition) IC50 [ 50 % ]
ReferenceMedigeshi GR, Kumar R, Dhamija E, Agrawal T, Kar M..N-Desmethylclozapine, Fluoxetine, and Salmeterol Inhibit Postentry Stages of the Dengue Virus Life C.Antimicrob Agents Chemother. 2016 Oct 21;60(11):6709-6718. doi: 10.1128/AAC.01367-16. Print 2016 Nov PMID:27572397 PubMed
CommentInhibition of DENV occurs at a postentry stage, most probably at the initiation of viral RNA replication and due to the modulation of the endolysosomal pathway and induction of autophagy.