Chemical Structure : UR214-9
Catalog No.: PC-27131Not For Human Use, Lab Use Only.
UR214-9 is a forchlorfenuron (FCF) analog and inhibitor of septin oligomeric assembly via preventing incorporation of SEPT2/7/9, into canonical hetero-octamers, decreases viability and proliferation in both ovarian and endometrial cancer cell lines, selectively suppress HER2 expression.
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UR214-9 is a forchlorfenuron (FCF) analog and inhibitor of septin oligomeric assembly via preventing incorporation of SEPT2/7/9, into canonical hetero-octamers, decreases viability and proliferation in both ovarian and endometrial cancer cell lines, selectively suppress HER2 expression.
UR214-9 decreases the expression of human epididymis protein 4 (HE4) in ECC-1 and HCH-1 cells.
UR214-9 (33 uM) selectively inhibits HER2 expression in both ECC-1 and HCH-1 cells, but not EGFR also suppress HER2 expression.
UR214-9 disrupts the incorporation of SEPT2, SEPT7, and SEPT9 into canonical septin hetero-octamers. causes defects in cytokinesis, altered cell migration, viability, and remodels septin-actin architectures, ultimately impairing tumor cell growth.
| M.Wt | 368.11 | |
| Formula | C13H7Cl2F4N3O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Kim KK, et al. Sci Rep. 2020 Feb 24;10(1):3241.
2. Khazan N, et al. bioRxiv [Preprint]. 2026 Jun 9:2026.06.09.731048.

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