Ro 5-3335

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4694/10
Ro 5-3335 | CAS No. 30195-30-3 | Additional Transcription Factor Compounds
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Description: Core binding factor inhibitor; attenuates hematopoiesis
Alternative Names: CBFβ-Runx1 inhibitor II

Chemical Name: 7-Chloro-1,3-dihydro-5-(1H-pyrrol-2-yl)-2H-1,4-benzodiazepin-2-one

Purity: ≥98%

Product Details
Citations (2)
Reviews

Biological Activity

Ro 5-3335 is a core binding factor (CBF) inhibitor; preferentially kills human leukemia cell lines with CBF fusion proteins (IC50 = 1.1 μM). Represses RUNX1/CBFβ-dependent transactivation in reporter assays and inhibits transcriptional regulation by RUNX1 and CBFβ. Reduces leukemia burden in a mouse model. Attenuates RUNX1-dependent hematopoiesis in zebrafish embryos. Also a Tat antagonist; inhibits HIV-1 replication in vitro.

Technical Data

M.Wt:
259.69
Formula:
C13H10ClN3O
Solubility:
Soluble to 100 mM in DMSO
Purity:
≥98%
Storage:
Store at +4°C
CAS No:
30195-30-3

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.

Background References

  1. The human immunodeficiency virus type 1 Tat antagonist, Ro 5-3335, predominantly inhibits transcription initiation from the viral promoter.
    Cupelli et al.
    J.Virol., 1995;69:2640
  2. Identification of benzodiazepine Ro5-3335 as an inhibitor of CBF leukemia through quantitative high throughput screen against RUNX1-CBF� interaction.
    Cunningham et al.
    Proc.Natl.Acad.Sci.USA, 2012;109:14592
  3. RUNX1/AML1: a central player in hematopoiesis.
    Okuda et al.
    Int. J. Hematol., 2001;74:252
  4. A transcriptional landscape of 28 porcine tissues obtained by super deepSAGE sequencing
    T Huang, M Yang, K Dong, M Xu, J Liu, Z Chen, S Zhu, W Chen, J Yin, K Jin, Y Deng, Z Guan, X Huang, J Yang, R Han, M Yao
    BMC Genomics, 2020;21(1):229.

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Citations for Ro 5-3335

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2 Citations: Showing 1 - 2

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