Compound ID | 3551
Synonym(s): Indolcarboxamide analogue
Class: Mycobacterial cell wall synthesis inhibitor
Details of activity: | Active against Mycobacterium tuberculosis including multidrug-resistant strains; mycobacterial cell wall synthesis inhibitor (mycolic acid transporter inhibitor [MmpL3 inhibitor]) |
Description: | Synthetic compound; indolcarboxamide analogue; shows efficacy in treating chronic and acute Mycobacterium tuberculosis infection in mouse models; shows synergistic effect with antituberculosis drugs |
Institute where first reported: | Novartis Institute for Tropical Diseases, Singapore |
Year first mentioned: | 2013 |
Highest developmental phase: | Preclinical |
Development status: | Experimental |
Chemical structure(s): | |
Canonical SMILES: | CC1(C)CCC(CC1)NC(=O)C2=CC3=C(C=C(C=C3F)F)N2 |
Isomeric SMILES: | CC1(CCC(CC1)NC(=O)C2=CC3=C(N2)C=C(C=C3F)F)C |
InChI: | InChI=1S/C17H20F2N2O/c1-17(2)5-3-11(4-6-17)20-16(22)15-9-12-13(19)7-10(18)8-14(12)21-15/h7-9,11,21H,3-6H2,1-2H3,(H,20,22) |
InChI Key: | UATYSFRIVIHVKL-UHFFFAOYSA-N |
External links: | |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/72711190 |
Main Source: | https://journals.asm.org/doi/full/10.1128/aac.02399-16?rfr_dat=cr_pub++0pubmed&url_ver=Z39.88-2003&rfr_id=ori%3Arid%3Acrossref.org |