1031063-36-1

(E/Z)-DMU2105 Chemical Structure
1031063-36-1

Chemical Structure

(E/Z)-DMU2105

  • CAS No.: 1031063-36-1
  • Formula:C18H13NO
  • Molecular Weight:259.30

IUPAC Name: (E)-3-(naphthalen-2-yl)-1-(pyridin-3-yl)prop-2-en-1-one

InChIKey: VWBDGXJRQZDLRV-CSKARUKUSA-N

SMILES: O=C(C1=CC=CN=C1)/C=C/C2=CC=C3C=CC=CC3=C2

Biological Activity: (E/Z)-DMU2105 (Compound 7k) is a potent and highly selective CYP1B1 inhibitor. (E/Z)-DMU2105 inhibits human CYP1B1 enzyme bound to yeast-derived microsomes with an IC50 value of 10 nM. (E/Z)-DMU2105 also potently inhibits CYP1B1 expressed within ‘live’ recombinant yeast and human HEK293 kidney cells with an IC50 value of 63.65 nM. (E/Z)-DMU2105 can be used for the research of cancer, glaucoma, ischemia and obesity[1].

Cat. No. Product Name Purity Description Pricing
HY-101284A
(E/Z)-DMU2105 (E/Z)-DMU2105 (Compound 7k) is a potent and highly selective CYP1B1 inhibitor. (E/Z)-DMU2105 inhibits human CYP1B1 enzyme bound to yeast-derived microsomes with an IC50 value of 10 nM. (E/Z)-DMU2105 also potently inhibits CYP1B1 expressed within ‘live’ recombinant yeast and human HEK293 kidney cells with an IC50 value of 63.65 nM. (E/Z)-DMU2105 can be used for the research of cancer, glaucoma, ischemia and obesity.
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