I-BET 151 dihydrochloride

Catalog # Availability Size / Price Qty
4650/10
4650/50
I-BET 151 dihydrochloride | CAS No. 1883545-47-8 | Bromodomain Inhibitors
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Description: BET bromodomain inhibitor; also promotes differentiation of hiPSCs into megakaryocytes

Chemical Name: 7-(3,5-Dimethyl-4-isoxazolyl)-1,3-dihydroxy-8-methoxy-1-[(1R)-1-(2-pyridinyl)ethyl]-2H-imidazo[4,5-c]quinolin-2-one dihydrochloride

Purity: ≥98%

Product Details
Citations (7)
Reviews

Biological Activity

I-BET 151 dihydrochloride is a BET bromodomain inhibitor; blocks recruitment of BET to chromatin. Induces apoptosis and G0/G1 cell cycle arrest in MLL-fusion leukemic cell lines in vitro (IC50 values are 15, 26, 120 and 192 nM for NOMO1, MV4;11, MOLM13 and RS4;11 cell lines respectively); reduces BCL2 expression in NOMO1 cells. Improves survival in two rodent models of MLL-fusion leukemia in vivo. Enhances differentiation of human iPSC into megakaryocytes. Also enhances fibroblast reprogramming to hiPSCs at low concentration.

For more information about how I-BET 151 dihydrochloride may be used, see our protocol: Transdifferentiating Fibroblasts into Neurons.

External Portal Information

Chemicalprobes.org is a portal that offers independent guidance on the selection and/or application of small molecules for research. The use of I-BET 151 is reviewed on the chemical probes website.

Technical Data

M.Wt:
488.37
Formula:
C23H21N5O3.2HCl
Solubility:
Soluble to 100 mM in DMSO and to 100 mM in ethanol and to 100 mM in water
Purity:
≥98%
Storage:
Store at -20°C
CAS No:
1883545-47-8

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Additional Information

Licensing Caveats:
Sold for research purposes under agreement from GlaxoSmithKline

Background References

  1. Epigenetically-driven anatomical diversity of synovial fibroblasts guides joint-specific fibroblast functions
    M Frank-Bert, M Trenkmann, K Klein, E Karouzakis, H Rehrauer, A Bratus, C Kolling, M Armaka, A Filer, BA Michel, RE Gay, CD Buckley, G Kollias, S Gay, C Ospelt
    Nat Commun, 2017;8(0):14852.
  2. Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia.
    Dawson et al.
    Nature, 2011;478:529
  3. Scalable generation of universal platelets from human induced pluripotent stem cells.
    Feng et al.
    Stem Cell Reports, 2014;3:817
  4. Reprogramming by de-bookmarking the somatic transcriptional program through targeting of BET bromodomains.
    Shao et al.
    Cell Rep., 2016;16:3138

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