Chemical Information | |
Antiviral agent ID | DrugRepV_2111 | |
Antiviral agent name | NITD008 | |
IUPAC Name | (2R,3R,4R,5R)-2-(4-aminopyrrolo[2,3-d]pyrimidin-7-yl)-3-ethynyl-5-(hydroxymethyl)oxolane-3,4-diol | |
SMILES (canonical) | C#CC1(C(C(OC1N2C=CC3=C2N=CN=C3N)CO)O)O | |
SMILES (isomeric) | C#C[C@]1([C@@H]([C@H](O[C@H]1N2C=CC3=C2N=CN=C3N)CO)O)O | |
Molecular Formula | C13H14N4O4 | |
Molecular Weight (g/mol) | 290.279 | |
InChl | InChI=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 | |
Synonyms | 7-Deaza-2'-C-ethynyladenosine | 7-(2-C-Ethynyl-?-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine | |
Structural Information | |
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Clinical Information | |
Category | Antiviral
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Biological Information | |
Secondary Indication | Zika virus (ZIKV) NA GZ01/2016 | |
Secondary Indication (Approaches) | Experimental | |
Secondary Indication (Methods) | in-vivo | |
Secondary Indication (Model system) [cell lines/ animal models] | AG129
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Secondary Indication (Mode of viral infection) | Adsorption
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Secondary Indication (Viral titer) | 100000 PFU
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Secondary Indication (Mode of drug delivery) | Intraperitoneal
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Secondary Indication (Time of drug delivery) | After infection
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Secondary Indication (Duration of drug delivery) | 3 days
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Secondary Indication (Drug concentration) | 50 mg/kg/day
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Secondary Indication (Cell based assay) | Survival assay
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Secondary Indication (Change) | Increase
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Secondary Indication (Type of Inhibition) | Percentage survival [ NA NA ] | |
Secondary Indication (Survival rate) | 50 | |
Reference | Deng 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
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Comment | NITD008 is potent inhibitor of ZIKV and can be used as reference inhibitor for future ZIKV antiviral drug screen and discovery.
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