LY56110 is an orally active aromatase inhibitor. LY56110 inhibits P-450-dependent p-nitroanisole O-demethylation and ethylmorphine N-demethylation in hepatic microsomes isolated from rat, with the IC50 of 2.5 and 11 µM, respectively. LY56110 can be used for neurological disorder study[1][2].
Molecular Weight:
315.20
CAS Number:
[26766-37-0]
Formula:
C17H12Cl2N2
Target:
Cytochrome P450,Monoamine Oxidase
Application Notes:
MCE Product type: Reference compound
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