2. Metabolic Enzyme/Protease Neuronal Signaling
  3. Monoamine Oxidase Cytochrome P450
  4. LY56110

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 μΜ, respectively. LY56110 can be used for neurological disorder study.

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LY56110 Chemical Structure

LY56110 Chemical Structure

CAS No. : 26766-37-0

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LY56110 Related Antibodies

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Description

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 μΜ, respectively. LY56110 can be used for neurological disorder study[1][2].

Molecular Weight

315.20

Formula

C17H12Cl2N2
CAS No.
SMILES

ClC1=CC=C(C=C1)C(C2=CC=C(C=C2)Cl)C3=CN=CN=C3
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
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LY56110 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

LY5611026766-37-0LY 56110LY-56110Monoamine OxidaseCytochrome P450MAOCYPsAromataseP450Inhibitorinhibitorinhibit

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