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XRK3F2

Catalog No. T13360   CAS 2375193-43-2

XRK3F2 is an inhibitor of the p62-ZZ domain, blunts MM-induced Runx2 suppression in vitro, and induces new bone formation and remodeling in the presence of tumor in vivo.

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XRK3F2 Chemical Structure
XRK3F2, CAS 2375193-43-2
Pack Size Availability Price/USD Quantity
1 mg In stock $ 34.00
5 mg In stock $ 79.00
10 mg In stock $ 122.00
25 mg In stock $ 236.00
50 mg In stock $ 372.00
100 mg In stock $ 559.00
1 mL * 10 mM (in DMSO) In stock $ 89.00
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Purity: 98.91%
Purity: 98.75%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description XRK3F2 is an inhibitor of the p62-ZZ domain, blunts MM-induced Runx2 suppression in vitro, and induces new bone formation and remodeling in the presence of tumor in vivo.
In vitro XRK3F2 inhibits p62-ZZ domain signaling and rescues Myeloma-induced Gfi1-driven epigenetic repression of the Runx2 gene in pre-osteoblasts to overcome differentiation suppression. XRK3F2 prevents MM-induced upregulation of Gfi1 and repression of the Runx2 gene when present in MM-preOB co-cultures. p62-ZZ-domain blocking by XRK3F2 prevents MM conditioned media and TNF plus IL7-mediated Gfi1 mRNA upregulation and the concomitant Runx2 repression. XRK3F2 decreased MM-induced GFI1 occupancy at the Runx2-P1 promoter and prevented recruitment of HDAC1, thus preserving the transcriptionally permissive chromatin mark H3K9ac on Runx2 and allowing osteogenic differentiation[1].
Molecular Weight 435.89
Formula C23H24ClF2NO3
CAS No. 2375193-43-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 135.0 mg/mL (309.7 mM), Sonication is recommended.

H2O: 0.8 mg/mL (1.9 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Adamik J, et al. XRK3F2 Inhibition of p62-ZZ Domain Signaling Rescues Myeloma-Induced GFI1-Driven Epigenetic Repression of the Runx2 Gene in Pre-osteoblasts to Overcome Differentiation Suppression. Front Endocrinol (Lausanne). 2018 Jun 29;9:344.

TargetMolCitations

1. Xu Y, Zhu C, Zhu C, et al.SQSTM1/p62 promotes the progression of gastric cancer through epithelial-mesenchymal transition.Heliyon.2024

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library Inhibitor Library Bioactive Compounds Library Max Autophagy Compound Library Bioactive Compound Library

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Keywords

XRK3F2 2375193-43-2 Autophagy XRK-3F2 inhibitor inhibit

 

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