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Research Article

A novel proton transfer salt of 2-amino-6-sulfamoylbenzothiazole and its metal complexes: the evaluation of their inhibition effects on human cytosolic carbonic anhydrases

, , , , , & show all
Pages 231-239 | Received 27 May 2016, Accepted 20 Sep 2016, Published online: 19 Jan 2017

Figures & data

Figure 1. Syntheses of all compounds (a for SMABT and b for 1 and c for 2–4 and d for 5).

Figure 1. Syntheses of all compounds (a for SMABT and b for 1 and c for 2–4 and d for 5).

Table 1. Crystal data and structure refinement details for compounds 2–4.

Figure 2. An ORTEP drawing of asymmetric unit of 2 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Figure 2. An ORTEP drawing of asymmetric unit of 2 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Figure 3. An ORTEP drawing of asymmetric unit of 3 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Figure 3. An ORTEP drawing of asymmetric unit of 3 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Figure 4. An ORTEP drawing of asymmetric unit of 4 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Figure 4. An ORTEP drawing of asymmetric unit of 4 with the atom-numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

Table 2. Selected bond distances [Å] and angles [°] of compounds 2–4.

Table 3. Hydrogen bonds for compounds 2–4 (Å, °).

Table 4. 1H-NMR and 13C-NMR chemical shifts (ppm) with coupling constants and assignments for compound 1.

Table 5. The inhibition data and Ki values of hCA I and hCA II isozymes for hydratase and esterase activity.

Supplemental material

IENZ_1267058_Supplementary_Material.pdf

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