1397274-71-3Relevant academic research and scientific papers
Synthesis and structure-activity relationship of (1-halo-2-naphthyl) carbamate-based inhibitors of KIAA1363 (NCEH1/AADACL1)
Shreder, Kevin R.,Lin, Emme C.K.,Wu, Jiangyue,Cajica, Julia,Amantea, Christopher M.,Hu, Yi,Okerberg, Eric,Brown, Heidi E.,Pham, Lan M.,Chung, De Michael,Fraser, Allister S.,McGee, Ethel,Rosenblum, Jonathan S.,Kozarich, John W.
, p. 5748 - 5751 (2012)
KIAA1363 is a serine hydrolase whose activity has been shown to be positively associated with tumor cell invasiveness. Thus, inhibitors of KIAA1363 represent a novel targeted therapy approach towards cancer. AX11890 ((1-bromo-2-naphthyl) N,N-dimethylcarbamate) was identified as a KIAA1363 inhibitor with an IC50 value of 1.2 μM and was shown using ESI-MS to carbamylate the catalytic residue Ser191. SAR studies explored both substitution of the 1-bromo group and derivatization of the 6-position. Activity-based protein profiling demonstrated AX13057 inhibited tumor-localized KIAA1363 in SK-OV-3 xenograft-bearing mice.
