MDR-652 is a targeted agonist of the transient receptor potential vanilloid 1 (TRPV1) channel. This compound displays high specificity with binding affinities (Kis) of 11.4 nM for human TRPV1 and 23.8 nM for rat TRPV1. The effective concentrations (EC50s) are 5.05 nM and 93 nM for hTRPV1 and rTRPV1, respectively. MDR-652 demonstrates significant potential as a topical analgesic, making it a valuable tool in pain research and therapeutic applications.
MDR-652 is a targeted agonist of the transient receptor potential vanilloid 1 (TRPV1) channel. This compound displays high specificity with binding affinities (Kis) of 11.4 nM for human TRPV1 and 23.8 nM for rat TRPV1. The effective concentrations (EC50s) are 5.05 nM and 93 nM for hTRPV1 and rTRPV1, respectively. MDR-652 demonstrates significant potential as a topical analgesic, making it a valuable tool in pain research and therapeutic applications.
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