Abstract
Background: Carbonic anhydrase IX (CAIX) is an attractive target for anticancer therapy because it is selectively overexpressed in tumor cells. Various CAs' inhibitors (sulfonamides/sulfaumates and coumarins) are reported as promising anti-cancer agents, showed appreciable affinity and selectivity. Novel chemical scaffolds with improved pharmacological properties are essential for the development of safe and potent CAIX inhibitors.
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CITATION STYLE
Asimul Islam, K. K. (2014). Receptor Chemoprint Derived Pharmacophore Model for Development of CAIX Inhibitors. Journal of Carcinogenesis & Mutagenesis, s8(01). https://doi.org/10.4172/2157-2518.s8-003
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