Romidepsin-d7 (FK 228-d7) is deuterium labeled Romidepsin. Romidepsin (FK 228) is a Histone deacetylase (HDAC) inhibitor with anti-tumor activities. Romidepsin (FK 228) inhibits HDAC1, HDAC2, HDAC4, and HDAC6 with IC50s of 36 nM, 47 nM, 510 nM and 1.4 µM, respectively[1]. Romidepsin (FK 228) is produced by Chromobacterium violaceum, induces cell G2/M phase arrest and apoptosis[2].
Molecular Weight:
547.74
Formula:
C24H29D7N4O6S2
Target:
Apoptosis,HDAC,Isotope-Labeled Compounds
Application Notes:
MCE Product type: Isotope-Labeled Compounds
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