Published January 1, 2021
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Taurultams incorporating arylsulfonamide: First in vitro inhibition studies of alpha-, beta- and gamma-class Carbonic Anhydrases from Vibrio cholerae and Burkholderia pseudomallei
Creators
- 1. Ege Univ, Fac Pharm, Dept Pharmaceut Chem, TR-35100 Izmir, Turkey
- 2. Univ Firenze, NEUROFARBA Dept, Sez Sci Farmaceut & Nutraceut, Via Ugo Schiff 6, I-50019 Florence, Italy
- 3. CNR, Ist Biosci & Biorisorse, Via Pietro Castellino 111, I-80131 Naples, Italy
Description
A new series of taurultambenzenesulfonamides 1-17 were prepared and considered for their inhibitory activity in vitro against the Carbonic Anhydrases from Vibrio cholerae (VchCA-alpha, VchCA-beta and VchCA-gamma) and Burkholderia pseudomallei (BpsCA-beta and BpsCA-gamma). Among the compounds tested, derivatives 4, 5, 7, 10, 12, and 16 resulted in highly effective VchCA alpha inhibitors (K-I values spanning within the 6.1-9.6 nM range) and endowed with excellent Selectivity Indexes (SIs; K-I VchCA-alpha/K-I hCA II) all comprised between 0.04 and 0.09. Potent in vitro inhibitors for the BpsCA-gamma were also identified (K(I)s of 18.9-19.5 nM). The results here reported may represent the blueprint for the future development of a new generation of CA-based antibiotics integrated with free of resistance mechanisms of action adopted from known drugs. (C) 2021 Elsevier Masson SAS. All rights reserved.
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