Compound ID | 2168
Synonym(s): GSK286
Class: Substituted 4-aryloxypiperidine
Details of activity: | Active against Mycobacterium tuberculosis; ongoing studies to evaluate mode of action but potential cholesterol-dependent mode of action |
Propensity to select resistant mutants: | Yes |
Description: | Synthetic novel small-molecule |
Institute where first reported: | GlaxoSmithKline |
Year first mentioned: | 2022 |
Highest developmental phase: | Phase 1 (NCT04472897) |
Development status: | Active (as of 2023) |
Chemical structure(s): | |
Canonical SMILES: | CC1=CC=CC(=C1C)OC2CCN(CC2)CC3=CC(=O)NC(=O)N3 |
Isomeric SMILES: | CC1=C(C(=CC=C1)OC2CCN(CC2)CC3=CC(=O)NC(=O)N3)C |
InChI: | InChI=1S/C18H23N3O3/c1-12-4-3-5-16(13(12)2)24-15-6-8-21(9-7-15)11-14-10-17(22)20-18(23)19-14/h3-5,10,15H,6-9,11H2,1-2H3,(H2,19,20,22,23) |
InChI Key: | AZOFJHATIPDIER-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/45833762 |
External links: | |
Guide to Pharmacology: | GSK2556286 |
Main Source: | https://journals.asm.org/doi/10.1128/aac.00132-22 |