JQ1

CAS No. 1268524-70-4

JQ1 ( JQ-1;(+)-JQ-1 )

Catalog No. M11126 CAS No. 1268524-70-4

(+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    JQ1
  • Note
    Research use only, not for human use.
  • Brief Description
    (+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively.
  • Description
    (+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively; induces rapid expression of keratin in treated NMC 797 cells, displaces the BRD4 fusion oncoprotein from chromatin, prompting squamous differentiation and specific antiproliferative effects in BRD4-dependent cell lines and patient-derived xenograft models.
  • Synonyms
    JQ-1;(+)-JQ-1
  • Pathway
    Chromatin/Epigenetic
  • Target
    Bromodomain
  • Recptor
    BRD4(1);BRD4(2)
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1268524-70-4
  • Formula Weight
    456.99
  • Molecular Formula
    C23H25ClN4O2S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 45 mg/mL
  • SMILES
    O=C(OC(C)(C)C)C[C@H]1C2=NN=C(C)N2C3=C(C(C)=C(C)S3)C(C4=CC=C(Cl)C=C4)=N1
  • Chemical Name
    6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-trimethyl-, 1,1-dimethylethyl ester, (6S)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Filippakopoulos P, et al. Nature. 2010 Dec 23;468(7327):1067-73.
2. Matzuk MM, et al. Cell. 2012 Aug 17;150(4):673-84.
3. Peirs S, et al. Leukemia. 2017 Oct;31(10):2037-2047.
4. Tgel L, et al. Mol Cancer Ther. 2016 Jun;15(6):1217-26.
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  • JQ1

    (+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively.