Maddirala, Amarendar Reddy’s team published research in Journal of Medicinal Chemistry in 2019 | CAS: 1214323-39-3

2-Bromo-3-(trifluoromethyl)phenol(cas: 1214323-39-3) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.Related Products of 1214323-39-3

Maddirala, Amarendar Reddy; Klein, Roger; Pinkner, Jerome S.; Kalas, Vasilios; Hultgren, Scott J.; Janetka, James W. published an article on January 24 ,2019. The article was titled 《Biphenyl Gal and GalNAc FmlH Lectin Antagonists of Uropathogenic E. coli (UPEC): Optimization through Iterative Rational Drug Design》, and you may find the article in Journal of Medicinal Chemistry.Related Products of 1214323-39-3 The information in the text is summarized as follows:

The F9/Yde/Fml pilus, tipped with the FmlH adhesin, has been shown to provide uropathogenic Escherichia coli (UPEC) a fitness advantage in urinary tract infections (UTIs). Here, the authors used X-ray structure guided design to optimize our previously described ortho-biphenyl Gal and GalNAc FmlH antagonists by replacing the carboxylate with a sulfonamide. Other groups which can accept H-bonds were also tolerated. The authors pursued further modifications to the biphenyl aglycon resulting in significantly improved activity. Two of the most potent compounds (IC50 = 0.051 μM) and (IC50 = 0.034 μM), exhibited excellent metabolic stability in mouse plasma and liver microsomes but showed only limited oral bioavailability (<1%) in rats. Another compound also showed a good pharmacokinetic (PK) profile in mice after IP dosing with compound exposure above the IC50 for 6 h. These new FmlH antagonists represent new antivirulence drugs for UTIs. In addition to this study using 2-Bromo-3-(trifluoromethyl)phenol, there are many other studies that have used 2-Bromo-3-(trifluoromethyl)phenol(cas: 1214323-39-3Related Products of 1214323-39-3) was used in this study.

2-Bromo-3-(trifluoromethyl)phenol(cas: 1214323-39-3) belongs to organobromine compounds.The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides.Related Products of 1214323-39-3

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary