ts-SA is a potent carbonic anhydrase (CA) inhibitor that demonstrates inhibitory activity against seven human CA homologues. It effectively binds to the Zn(II) ion in the enzyme's active site in its deprotonated form, with its organic structure extending into the enzyme cavity, facilitating interactions with amino acid residues and water molecules. With low nanomolar inhibitory activity, ts-SA serves as a multi-target CA inhibitor, making it valuable for research applications in enzymatic regulation and metabolic studies.
ts-SA is a potent carbonic anhydrase (CA) inhibitor that demonstrates inhibitory activity against seven human CA homologues. It effectively binds to the Zn(II) ion in the enzyme's active site in its deprotonated form, with its organic structure extending into the enzyme cavity, facilitating interactions with amino acid residues and water molecules. With low nanomolar inhibitory activity, ts-SA serves as a multi-target CA inhibitor, making it valuable for research applications in enzymatic regulation and metabolic studies.
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