Structure-activity relationships of new cyanothiophene inhibitors of the essential peptidoglycan biosynthesis enzyme MurF.
Eur J Med Chem
; 66: 32-45, 2013 Aug.
Article
em En
| MEDLINE
| ID: mdl-23786712
ABSTRACT
Peptidoglycan is an essential component of the bacterial cell wall, and enzymes involved in its biosynthesis represent validated targets for antibacterial drug discovery. MurF catalyzes the final intracellular peptidoglycan biosynthesis step the addition of D-Ala-D-Ala to the nucleotide precursor UDP-MurNAc-L-Ala-γ-D-Glu-meso-DAP (or L-Lys). As MurF has no human counterpart, it represents an attractive target for the development of new antibacterial drugs. Using recently published cyanothiophene inhibitors of MurF from Streptococcus pneumoniae as a starting point, we designed and synthesized a series of structurally related derivatives and investigated their inhibition of MurF enzymes from different bacterial species. Systematic structural modifications of the parent compounds resulted in a series of nanomolar inhibitors of MurF from S. pneumoniae and micromolar inhibitors of MurF from Escherichia coli and Staphylococcus aureus. Some of the inhibitors also show antibacterial activity against S. pneumoniae R6. These findings, together with two new co-crystal structures, represent an excellent starting point for further optimization toward effective novel antibacterials.
Palavras-chave
2,6-diaminopimelic acid; Antibacterial agents; Crystal structures; DAP; GlcNAc; MurC; MurD; MurE; MurF; MurF inhibitors; MurNAc; N-acetyl glucosamine; N-acetyl muramic acid; UDP; UDP-N-acetylmuramate:l-Ala ligase; UDP-N-acetylmuramoyl-l-Ala-d-Glu-l-Lys; UDP-N-acetylmuramoyl-l-Ala-d-Glu:meso-DAP ligase or l-Lys; UDP-N-acetylmuramoyl-l-Ala-γ-d-Glu-meso-DAP; UDP-N-acetylmuramoyl-l-Ala-γ-d-Glu-meso-DAP (or l-Lys):d-Ala-d-Ala ligase; UDP-N-acetylmuramoyl-l-Ala:d-Glu ligase; UMtri-l-Lys; UMtri-mDAP; uridine 5'-diphosphate
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Peptídeo Sintases
/
Tiofenos
/
Peptidoglicano
Tipo de estudo:
Prognostic_studies
Idioma:
En
Revista:
Eur J Med Chem
Ano de publicação:
2013
Tipo de documento:
Article
País de afiliação:
Eslovênia