Recommanded Product: 2,6-Difluorobenzoic acid. In 2021 MED CHEM RES published article about MYCOBACTERIUM-TUBERCULOSIS; CRYSTAL-STRUCTURE; DRUG; INHIBITORS; DPRE1; MODEL; MACOZINONE; INSIGHT; DESIGN; AURUM in [Madikizela, Balungile; Eckhardt, Tamira; Richter, Adrian; Lins, Anika; Lehmann, Christoph; Imming, Peter; Seidel, Ruediger W.] Martin Luther Univ Halle Wittenberg, Inst Pharm, Wolfgang Langenbeck Str 4, D-06120 Halle, Saale, Germany; [Madikizela, Balungile] Univ Pretoria, Dept Paraclin Sci, Phytomed Programme, Private Bag X04, ZA-0110 Onderstepoort, South Africa; [Goddard, Richard] Max Planck Inst Kohlenforsch, Kaiser Wilhelm Pl 1, D-45470 Mulheim, Germany; [Richter, Adrian] Univ British Columbia, Dept Med, Vancouver, BC V6T 1Z3, Canada; [Richter, Adrian] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada in 2021, Cited 57. The Name is 2,6-Difluorobenzoic acid. Through research, I have a further understanding and discovery of 385-00-2.
8-Nitro-1,3-benzothiazin-4-ones (BTZs), with BTZ043 and PBTZ169 as the most advanced compounds, represent a new class of potent antitubercular agents, which irreversibly inhibit decaprenylphosphoryl-beta-d-ribose-2 ‘-epimerase (DprE1), an enzyme crucial for cell wall synthesis in the pathogen Mycobacterium tuberculosis. Synthesis, structural characterization and in vitro testing against Mycobacterium aurum DSM 43999 and M. tuberculosis H(37)Rv of halogenated 2-(4-ethoxycarbonylpiperazin-1-yl)-1,3-benzothiazin-4-ones lacking a nitro group are reported. X-ray crystallography reveals that the structure of the BTZ scaffold can significantly deviate from planarity. In contrast to recent reports, the results of the present study indicate that further investigation of halogenated non-nitro BTZs for antitubercular activity is less than a promising approach.
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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com