Compound ID | 2182
Synonym(s): Pyrifazimine
Class: Riminophenazine
Details of activity: | Active against Mycobacterium sp. |
Description: | Synthetic compound derived from optimization of riminophenazine analogues |
Institute where first reported: | Institute of Materia Medica of the Chinese Academy of Medical Sciences |
Year first mentioned: | 2012 |
Highest developmental phase: | Phase 2 (NCT04670120) |
Development status: | Active (as of 2023) |
Chemical structure(s): | |
Canonical SMILES: | COC1CCC(CC1)N=C2C=C3C(=NC4=C(C=CC=C4)N3C5=CC=C(C=C5)OC(F)(F)F)C=C2NC6=CC=CN=C6OC |
Isomeric SMILES: | COC1CCC(CC1)N=C2C=C3C(=NC4=CC=CC=C4N3C5=CC=C(C=C5)OC(F)(F)F)C=C2NC6=C(N=CC=C6)OC |
InChI: | InChI=1S/C32H30F3N5O3/c1-41-22-13-9-20(10-14-22)37-27-19-30-28(18-26(27)39-25-7-5-17-36-31(25)42-2)38-24-6-3-4-8-29(24)40(30)21-11-15-23(16-12-21)43-32(33,34)35/h3-8,11-12,15-20,22,39H,9-10,13-14H2,1-2H3 |
InChI Key: | GUSGYHIQYWRCQO-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/53377576 |
External links: | |
Guide to Pharmacology: | TBI-166 |
Main Source: | https://journals.asm.org/doi/10.1128/aac.00658-22 |
Citation: | https://journals.asm.org/doi/10.1128/AAC.00699-11 |
Patent: | WO2012003190A1 |