ML-SA1

Source: Wikipedia, the free encyclopedia.
ML-SA1
Identifiers
  • 2-[2-oxo-2-(2,2,4-trimethyl-3,4-dihydroquinolin-1-yl)ethyl]isoindole-1,3-dione
JSmol)
  • CC1CC(N(C2=CC=CC=C12)C(=O)CN3C(=O)C4=CC=CC=C4C3=O)(C)C
  • InChI=1S/C22H22N2O3/c1-14-12-22(2,3)24(18-11-7-6-8-15(14)18)19(25)13-23-20(26)16-9-4-5-10-17(16)21(23)27/h4-11,14H,12-13H2,1-3H3
  • Key:KDDHBJICVBONAX-UHFFFAOYSA-N

ML-SA1 is a chemical compound which acts as an "agonist" (i.e. channel opener) of the

Niemann-Pick's disease type C,[1][2][3][4] as well as other conditions such as stroke and Alzheimer's disease.[5][6]

References

This page is based on the copyrighted Wikipedia article: ML-SA1. Articles is available under the CC BY-SA 3.0 license; additional terms may apply.Privacy Policy