| Literature DB >> 25828928 |
Priyanka Singh1, Sudipta Kumar Manna1, Amit Kumar Jana1, Tiash Saha1, Pankaj Mishra1, Saurav Bera1, Maloy Kumar Parai1, Srinivas Lavanya Kumar M1, Sankalan Mondal1, Priyanka Trivedi2, Vinita Chaturvedi2, Shyam Singh2, Sudhir Sinha3, Gautam Panda4.
Abstract
Triarylmethanes (TRAMs) and thiophene containing trisubstituted methanes (TRSMs) have been reported by us, having potential against Mycobacterium tuberculosis and Mycobacterium fortuitum strains, respectively. Further, extension through synthesis and biological evaluation of novel TRSMs resulted into an identified lead 36 (S006-830) [(diisopropyl-(2-{4-[(4-methoxy-phenyl)- thiophen-2-yl-methyl]-phenoxy}-ethyl)-amine)] with MIC: 1.33 mg/L, non-toxic against Vero C-1008 cell line with selectivity index >10, ex vivo efficacy equivalent to first line TB drugs-isoniazid (INH), rifampicin (RFM) and pyrazinamide (PZA) in the mouse and human macrophages, and lung CFU count of 2.2 × 10(7) (approximately 15 fold lesser than untreated mice, 31 × 10(7)) with efficacies comparable to ethambutol (EMB) (1.27 × 10(7)) and PZA (1.9 × 10(7)). Further, S006-830 also showed potent bactericidal activity against multi-drug resistant and single-drug resistant clinical isolates of M. tuberculosis.Entities:
Keywords: Antimycobacterial agents; Mycobacterium tuberculosis H37R(V); Trisubstituted methanes
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Year: 2015 PMID: 25828928 DOI: 10.1016/j.ejmech.2015.03.036
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514