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YUKA1

Axon 2674
CAS:  708991-09-7
Purity:  99%
  • Soluble in DMSO
  • MF:  C13H16N4O2S
  • MW:  292.36

Description

YUKA1 is a potent, cell-permeable, and selective inhibitor of the histone demethylase KDM5A (IC50 = 2.66 µM). Mechanistically, it blocks KDM5A activity to increase cellular levels of trimethylated histone H3 lysine 4 (H3K4me3), which restores active gene transcription. In oncology research, YUKA1 effectively suppresses cell proliferation and blocks the emergence of drug-tolerant persister (DTP) cells in lung and breast cancers, overcoming resistance to targeted therapies.

Key Features

  • Specifically targets the KDM5A histone demethylase enzyme
  • IC50: 2.66 µM
  • Cell permeable: Readily enters intact cells to modify nuclear chromatin.
  • Epigenetic Protection: Prevents demethylation to maintain active H3K4me3 marks.

Applications

  • KDM5A and histone demethylase research
  • H3K4 methylation and chromatin regulation
  • Epigenetic mechanisms of drug resistance
  • Breast and cervical cancer cell studies

More Information

Parent CAS No. 708991-09-7
Chemical Name 4-(2-(Allyloxy)-3-methoxybenzylamino)-4H-1,2,4-triazole-3-thiol
SMILES C1(OC)C(OCC=C)=C(CNN2C=NN=C2S)C=CC=1
MFCD N.A.
InChi InChI=1S/C13H16N4O2S/c1-3-7-19-12-10(5-4-6-11(12)18-2)8-15-17-9-14-16-13(17)20/h3-6,9,15H,1,7-8H2,2H3,(H,16,20)
InChiKey NHJCZZWENDYDEP-UHFFFAOYSA-N
CID 2215170
Short Description KDM5A inhibitor

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