| Chemical Information | |
| Antiviral agent ID | DrugRepV_2167 | |
| Antiviral agent name | Diclofenac Diethylamine |  |
| IUPAC Name | 2-[2-(2,6-dichloroanilino)phenyl]acetic acid;N-ethylethanamine |  |
| SMILES (canonical) | CCNCC.C1=CC=C(C(=C1)CC(=O)O)NC2=C(C=CC=C2Cl)Cl | |
| Molecular Formula | C18H22Cl2N2O2 | |
| Molecular Weight (g/mol) | 369.286 | |
| InChl | InChI=1S/C14H11Cl2NO2.C4H11N/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19;1-3-5-4-2/h1-7,17H,8H2,(H,18,19);5H,3-4H2,1-2H3 | |
| Common Name | Diclofenac | |
| Synonyms | [2-(2,6-dichloroanilino)phenyl]acetic acid | 2-((2,6-dichlorophenyl)amino)benzeneacetic acid | Diclofenac Acid | Diclofenaco | Diclofenacum | |
| Structural Information | |
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| Clinical Information | |
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Category | Dermatologicals; Musculo-Skeletal System and Sensory Organ
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Primary Indication (Clinical trial phases) | Approved
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| Biological Information | |
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Primary Indication (Disease Category) | Non Infectious Disease
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Primary Indication (Disease) | Osteoarthritis and rheumatoid arthritis
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Secondary Indication | Chikungunya virus (CHIKV) NA vAc-CHIKV 26S-Rhir-E |   |
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Secondary Indication (Approaches) | Experimental | |
| Secondary Indication (Methods) | in-vitro | |
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Secondary Indication (Model system) [cell lines/ animal models] | Sf21
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Secondary Indication (Mode of viral infection) | Adsorption
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Secondary Indication (Viral titer) | 2 MOI
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Secondary Indication (Mode of drug delivery) | Culture
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Secondary Indication (Drug concentration) | 100 μM
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Secondary Indication (Cell based assay) | Fusion index-Fluorescent Intensities
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Secondary Indication (Change) | No significant decrease
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Secondary Indication (Type of Inhibition) | Percentage inhibition [ 40.6760631 % ] | |
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Reference | Wang YM, Lu JW, Lin CC, Chin YF, Wu TY, Lin LI, Lai ZZ, Kuo SC, Ho YJ..Antiviral activities of niclosamide and nitazoxanide against chikungunya virus entry and transmissio.Antiviral Res. 2016 Nov;135:81-90. doi: 10.1016/j.antiviral.2016.10.003. Epub 2016 Oct 11. PMID:27742486
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Comment | Niclosamide and nitazoxanide were able to inhibit CHIKV entry and transmission, which might provide a basis for the development of novel human drug therapies against CHIKV and other alphavirus infections.
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