Romidepsin
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Romidepsin
Description :
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].Product Name Alternative :
FK 228; FR 901228; NSC 630176UNSPSC :
12352005Hazard Statement :
H302, H315, H319, H335Target :
Apoptosis; HDACType :
Reference compoundRelated Pathways :
Apoptosis; Cell Cycle/DNA Damage; EpigeneticsApplications :
Cancer-programmed cell deathField of Research :
CancerAssay Protocol :
https://www.medchemexpress.com/Romidepsin.htmlPurity :
99.98Solubility :
DMSO : ≥ 100 mg/mLSmiles :
C/C=C(NC([C@@H](CSSCC/C=C/[C@@H](O1)CC2=O)NC([C@@H](C(C)C)N2)=O)=O)/C(N[C@@H](C(C)C)C1=O)=OMolecular Formula :
C24H36N4O6S2Molecular Weight :
540.70Precautions :
H302, H315, H319, H335References & Citations :
[1]Furumai R, et al. FK228 (depsipeptide) as a natural prodrug that inhibits class I histone deacetylases. Cancer Res. 2002 Sep 1;62 (17) :4916-21.|[2]Sun WJ, et al. Romidepsin induces G2/M phase arrest via Erk/cdc25C/cdc2/cyclinB pathway and apoptosis induction through JNK/c-Jun/caspase3 pathway in hepatocellular carcinoma cells. Biochem Pharmacol. 2017 Mar 1;127:90-100.Shipping Conditions :
Blue IceStorage Conditions :
-20°C, 3 years (Powder)Scientific Category :
Reference compound1Clinical Information :
LaunchedIsoform :
HDAC1; HDAC2; HDAC4; HDAC6CAS Number :
[128517-07-7]

