Romidepsin

CAT:
804-HY-15149-01
Size:
1 mg

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 - image 1

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 630176
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Apoptosis; HDAC
  • Type :

    Reference compound
  • Related Pathways :

    Apoptosis; Cell Cycle/DNA Damage; Epigenetics
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/Romidepsin.html
  • Purity :

    99.98
  • Solubility :

    DMSO : ≥ 100 mg/mL
  • Smiles :

    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)=O
  • Molecular Formula :

    C24H36N4O6S2
  • Molecular Weight :

    540.70
  • Precautions :

    H302, H315, H319, H335
  • References & 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 Ice
  • Storage Conditions :

    -20°C, 3 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • Isoform :

    HDAC1; HDAC2; HDAC4; HDAC6
  • CAS Number :

    [128517-07-7]

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