126463-64-7

Dihydroeponemycin Chemical Structure
126463-64-7

Chemical Structure

Dihydroeponemycin

  • CAS No.: 126463-64-7
  • Formula:C20H36N2O6
  • Molecular Weight:400.51

IUPAC Name: N-((S)-3-hydroxy-1-(((S)-1-((R)-2-(hydroxymethyl)oxiran-2-yl)-4-methyl-1-oxopentan-2-yl)amino)-1-oxopropan-2-yl)-6-methylheptanamide

InChIKey: IUDBVFIQSSOIDB-TWOQFEAHSA-N

SMILES: CC(C)CCCCC(N[C@@H](CO)C(N[C@@H](CC(C)C)C([C@]1(CO1)CO)=O)=O)=O

Biological Activity: Dihydroeponemycin, an analogue of the antitumor and antiangiogenic natural product eponemycin, selectively targets the 20S proteasome. Dihydroeponemycin covalently modifies a subset of catalytic proteasomal subunits, binding preferentially to the IFN-gamma-inducible subunits LMP2 and LMP7. Dihydroeponemycin-mediated proteasome inhibition induces a spindle-like cellular morphological change and apoptosis[1].

Cat. No. Product Name Purity Description Pricing
HY-108553
Dihydroeponemycin Dihydroeponemycin, an analogue of the antitumor and antiangiogenic natural product eponemycin, selectively targets the 20S proteasome. Dihydroeponemycin covalently modifies a subset of catalytic proteasomal subunits, binding preferentially to the IFN-gamma-inducible subunits LMP2 and LMP7. Dihydroeponemycin-mediated proteasome inhibition induces a spindle-like cellular morphological change and apoptosis.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References