Description
A URAT1 inhibitor (IC50 = 0.025 µM for the human transporter); selective for human URAT1 over rat URAT1 (IC50 = 41 µM), as well as human OAT1 and OAT4 (IC50s = 4.6 and 5.9 µM, respectively)
Formal name: 2-[[3-(4-cyano-1-naphthalenyl)-4-pyridinyl]thio]-2-methyl-propanoic acid
Synonyms:
Molecular weight: 348.4
CAS: 1352792-74-5
Purity: ≥98%
Formulation: A crystalline solid