197506-04-0

MEN-91507 Chemical Structure
197506-04-0

Chemical Structure

MEN-91507

  • CAS No.: 197506-04-0
  • Formula:C28H23FN4O3
  • Molecular Weight:482.51

IUPAC Name: (E)-8-(4-(4-(4-fluorophenyl)butoxy)styryl)-2-(1H-tetrazol-5-yl)-4H-chromen-4-one

InChIKey: PYUGFOWNYMLROI-KPKJPENVSA-N

SMILES: O=C1C=C(C2=NN=NN2)OC3=C(/C=C/C4=CC=C(OCCCCC5=CC=C(F)C=C5)C=C4)C=CC=C13

Biological Activity: MEN-91507 is an orally activecysteinyl leukotriene receptor 1 (CysLTR1) receptor antagonist. MEN-91507 behaves as insurmountable antagonist of Leukotriene D4 (HY-113456)-induced calcium transients, with a pKb of 10.25. MEN-91507 can inhibit Leukotriene D4-induced bronchoconstriction and microvascular leakage in guinea-pigs. MEN-91507 can be used for the researches of inflammation, immunology[1].

Cat. No. Product Name Purity Description Pricing
HY-19395
MEN-91507 MEN-91507 is an orally activecysteinyl leukotriene receptor 1 (CysLTR1) receptor antagonist. MEN-91507 behaves as insurmountable antagonist of Leukotriene D4 (HY-113456)-induced calcium transients, with a pKb of 10.25. MEN-91507 can inhibit Leukotriene D4-induced bronchoconstriction and microvascular leakage in guinea-pigs. MEN-91507 can be used for the researches of inflammation, immunology.
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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