Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.3.1.9 extracted from

  • Deraeve, C.; Dorobantu, I.M.; Rebbah, F.; Le Quemener, F.; Constant, P.; Quemard, A.; Bernardes-Genisson, V.; Bernadou, J.; Pratviel, G.
    Chemical synthesis, biological evaluation and structure-activity relationship analysis of azaisoindolinones, a novel class of direct enoyl-ACP reductase inhibitors as potential antimycobacterial agents (2011), Bioorg. Med. Chem., 19, 6225-6232.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
(RS)-1-hydroxy-1-[3-(octadecyloxy)-phenyl]-1,2-dihydro-3H-pyrrolo[3,4-c]pyridin-3-one 28% inhibition at 0.03 mM, IC50 for growth of Mycobacterium tuberculosis is 0.012 mM Mycobacterium tuberculosis
(RS)-1-[3-(dodecylsulfanyl)phenyl]-1-hydroxy-1,2-dihydro-3H-pyrrolo[3,4-c]pyridin-3-one 15% inhibition at 0.03 mM, IC50 for growth of Mycobacterium tuberculosis is 0.0065 mM Mycobacterium tuberculosis
triclosan 37% inhibition at 0.03 mM Mycobacterium tuberculosis

Organism

Organism UniProt Comment Textmining
Mycobacterium tuberculosis
-
-
-

Synonyms

Synonyms Comment Organism
InhA
-
Mycobacterium tuberculosis