Repositioning Candidate Details

Candidate ID: R0422
Source ID: DB01140
Source Type: approved; vet_approved; withdrawn
Compound Type: small molecule
Compound Name: Cefadroxil
Synonyms: CDX; Cefadroxil; Cefadroxil anhydrous; Cephadroxil; D-Cefadroxil
Molecular Formula: C16H17N3O5S
SMILES: [H][C@]12SCC(C)=C(N1C(=O)[C@H]2NC(=O)[C@H](N)C1=CC=C(O)C=C1)C(O)=O
Structure:
DrugBank Description: Long-acting, broad-spectrum, water-soluble, cephalexin derivative.
CAS Number: 50370-12-2
Molecular Weight: 363.388
DrugBank Indication: For the treatment of the following infections (skin, UTI, ENT) caused by; <i>S. pneumoniae, H. influenzae, staphylococci, S. pyogenes</i> (group A beta-hemolytic streptococci), <i>E. coli, P. mirabilis, Klebsiella</i> sp, coagulase-negative staphylococci and <i>Streptococcus pyogenes</i>
DrugBank Pharmacology: Cefadroxil, a first-generation cephalosporin antibiotic, is used to treat urinary tract infections, skin and skin structure infections, pharyngitis, and tonsillitis.
DrugBank MoA: Like all beta-lactam antibiotics, cefadroxil binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that cefadroxil interferes with an autolysin inhibitor.
Targets: Penicillin-binding protein 3 inhibitor; Penicillin-binding protein 1A inhibitor; Penicillin-binding protein 1b inhibitor; Penicillin-binding protein 2B inhibitor
Inclusion Criteria: Indication associated