Chemical, Structural, Clinical and Biological details of Antiviral agents ID: DrugRepV_2368



Chemical Information
Antiviral agent IDDrugRepV_2368
Antiviral agent nameAmpicillin Sodium Drug Bank
IUPAC Namesodium;(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate PubChem
SMILES (canonical)CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)[O-])C.[Na+] PubChem
SMILES (isomeric)CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)[O-])C.[Na+] PubChem
Molecular FormulaC16H18N3NaO4S PubChem
Molecular Weight (g/mol)371.387 PubChem
InChlInChI=1S/C16H19N3O4S.Na/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1 PubChem
Common NameAmpicillin Drug Bank
Synonyms(2S,6R)-6-{[(2R)-2-amino-2-phenylethanoyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid | 6-(D-(2-amino-2-phenylacetamido))-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid | ABPC | Aminobenzylpenicillin | Ampicilina | Ampicillin | Ampicillin (anhydrous) | Ampicillin Acid | Ampicillin Anhydrous | Ampicillin, anhydrous | Ampicilline | Ampicillinum | Anhydrous ampicillin | AP | D-(−)-6-(α-aminophenylacetamido)penicillanic acid | D-(−)-ampi
Structural Information
  
Clinical Information
CategoryAntiinfectives For Systemic Use
Primary Indication (Clinical trial phases)Approved Drug Bank
Biological Information
Primary Indication (Disease Category) Infectious Disease
Primary Indication (Disease)Bacterial infections
Secondary Indication Chikungunya virus (CHIKV) NA vAc-CHIKV 26S-Rhir-EWorld Health OrganisationCDC
Secondary Indication (Approaches)Experimental
Secondary Indication (Methods)in-vitro
Secondary Indication (Model system) [cell lines/ animal models]Sf21
Secondary Indication (Mode of viral infection)Adsorption
Secondary Indication (Viral titer)2 MOI
Secondary Indication (Mode of drug delivery) Culture
Secondary Indication (Drug concentration)100 μM
Secondary Indication (Cell based assay)Fusion index-Fluorescent Intensities
Secondary Indication (Change)No significant decrease
Secondary Indication (Type of Inhibition) Percentage inhibition [ 2.75763916 % ]
ReferenceWang 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 PubMed
CommentNiclosamide 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.