Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_2111



Chemical Information
Antiviral agent IDDrugRepV_2111
Antiviral agent nameNITD008
IUPAC Name(2R,3R,4R,5R)-2-(4-aminopyrrolo[2,3-d]pyrimidin-7-yl)-3-ethynyl-5-(hydroxymethyl)oxolane-3,4-diol PubChem
SMILES (canonical)C#CC1(C(C(OC1N2C=CC3=C2N=CN=C3N)CO)O)O PubChem
SMILES (isomeric)C#C[C@]1([C@@H]([C@H](O[C@H]1N2C=CC3=C2N=CN=C3N)CO)O)O PubChem
Molecular FormulaC13H14N4O4 PubChem
Molecular Weight (g/mol)290.279 PubChem
InChlInChI=1S/C13H14N4O4/c1-2-13(20)9(19)8(5-18)21-12(13)17-4-3-7-10(14)15-6-16-11(7)17/h1,3-4,6,8-9,12,18-20H,5H2,(H2,14,15,16)/t8-,9-,12-,13-/m1/s1 PubChem
Synonyms7-Deaza-2'-C-ethynyladenosine | 7-(2-C-Ethynyl-?-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
Structural Information
  
Clinical Information
CategoryAntiviral
Biological Information
Secondary Indication Zika virus (ZIKV) NA GZ01/2016World Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)in-vivo
Secondary Indication (Model system) [cell lines/ animal models]AG129
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)100000 PFU
Secondary Indication (Mode of drug delivery) Intraperitoneal
Secondary Indication (Time of drug delivery) After infection
Secondary Indication (Duration of drug delivery)3 days
Secondary Indication (Drug concentration)50 mg/kg/day
Secondary Indication (Cell based assay)Survival assay
Secondary Indication (Change)Increase
Secondary Indication (Type of Inhibition) Percentage survival [ NA NA ]
Secondary Indication (Survival rate)50
ReferenceDeng YQ, Zhang NN, Li CF, Tian M, Hao JN, Xie XP, Shi PY, Qin CF..Adenosine Analog NITD008 Is a Potent Inhibitor of Zika Virus..Open Forum Infect Dis. 2016 Aug 30;3(4):ofw175. eCollection 2016 Oct. PMID:27747251 PubMed
CommentNITD008 is potent inhibitor of ZIKV and can be used as reference inhibitor for future ZIKV antiviral drug screen and discovery.