Apararenone

Source: Wikipedia, the free encyclopedia.
Apararenone
Antimineralocorticoid
Identifiers
  • N-[4-(4-fluorophenyl)-2,2-dimethyl-3-oxo-1,4-benzoxazin-7-yl]methanesulfonamide
JSmol)
  • CC1(C(=O)N(C2=C(O1)C=C(C=C2)NS(=O)(=O)C)C3=CC=C(C=C3)F)C
  • InChI=1S/C17H17FN2O4S/c1-17(2)16(21)20(13-7-4-11(18)5-8-13)14-9-6-12(10-15(14)24-17)19-25(3,22)23/h4-10,19H,1-3H3
  • Key:AZNHWXAFPBYFGH-UHFFFAOYSA-N

Apararenone (

non-alcoholic steatohepatitis.[1][2][3] It was also previously being developed for the treatment of hypertension, but development was discontinued for this indication.[1] Apararenone acts as a highly selective antagonist of the mineralocorticoid receptor (Ki < 50 nM), the receptor for aldosterone.[1][2][3] As of 2017, it is in phase II clinical trials.[1]

See also

References

  1. ^ a b c d "Apararenone - Mitsubishi Tanabe Pharma - AdisInsight".
  2. ^
    PMID 26939027
    .
  3. ^ .

External links