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PTC 209

Axon 2420
CAS:  315704-66-6
Purity:  99%
  • Soluble in DMSO
  • MF:  C17H13Br2N5OS
  • MW:  495.19

Description

PTC 209 is a small-molecule inhibitor of BMI-1, a core regulator of Polycomb repressive complex 1 (PRC1) and cancer stem-cell self-renewal. It suppresses BMI-1 reporter activity and reduces tumor-initiating cell phenotypes in colorectal cancer models.

BMI-1 supports chromatin repression, stemness, proliferation and therapy resistance in several tumor types. PTC 209 is useful for studying PRC1 biology, cancer stem-cell maintenance and pharmacological modulation of self-renewal pathways.

Key Features

  • BMI-1/PRC1 pathway inhibitor
  • Reported IC50: 0.5 µM in a BMI-1 UTR luciferase reporter assay
  • Suppresses self-renewal regulator BMI-1 expression
  • Reduces colorectal cancer xenograft and tumor-initiating cell phenotypes in reported studies

Applications

  • Cancer stem-cell biology
  • Polycomb repressive complex research
  • Colorectal cancer pharmacology models
  • Stemness and self-renewal pathway assays

More Information

Parent CAS No. 315704-66-6
Chemical Name N-(2,6-dibromo-4-methoxyphenyl)-4-(2-methylimidazo[1,2-a]pyrimidin-3-yl)thiazol-2-amine
SMILES S1C=C(C2N3C(=NC=2C)N=CC=C3)N=C1NC1=C(Br)C=C(OC)C=C1Br
MFCD N.A.
InChi InChI=1S/C17H13Br2N5OS/c1-9-15(24-5-3-4-20-16(24)21-9)13-8-26-17(22-13)23-14-11(18)6-10(25-2)7-12(14)19/h3-8H,1-2H3,(H,22,23)
InChiKey XVOOCQSWCCRVDY-UHFFFAOYSA-N
CID 1117196
Short Description BMI-1 inhibitor

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