Chemical Structure : YTHDC1 PROTAC XY-2
Catalog No.: PC-27441Not For Human Use, Lab Use Only.
YTHDC1 PROTAC XY-2 is a selective, efficient PROTAC degrader of N6-Methyladenosine (m6A) reader YTHDC1 with DC50 of 11.42 nM in MOLM13 and 13.59 nM in Kasumi-1 cells respectively.
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YTHDC1 PROTAC XY-2 is a selective, efficient PROTAC degrader of N6-Methyladenosine (m6A) reader YTHDC1 with DC50 of 11.42 nM in MOLM13 and 13.59 nM in Kasumi-1 cells respectively.
XY-2 does not cause appreciable changes in the protein levels of YTHDC2 or YTHDF2.
XY-2 induces potent degradation of YTHDC1 at nanomolar concentrations in multiple AML cell lines.
XY-2 promotes celebron- and proteasome-dependent degradation of YTHDC1, without altering YTHDC1 mRNA expression.
XY-2 markedly suppressed proliferation, colony formation, migration and invasion, while inducing robust apoptosis in AML cells.
XY-2 exhibits potent antiproliferative activity in chronic myeloid leukemia K562 cells with IC50 of 125.2 nM.
XY-2 (2.5 or 5 mg/kg, intraperitoneally, once daily) exerts significant antitumor activity in AML xenograft tumor models.
| M.Wt | 658.12 | |
| Formula | C32H32ClN9O5 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zhongpao Xie, et al. Development of the First YTHDC1 Degrader with Improved Antileukemia Activity. JACS Au. 2026 Jun 10;6(7):3778-3789.

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