10058-F4

Based on 16 reference(s) in Google Scholar 9 10 16

Axon 2222

CAS [403811-55-2]

MF C12H11NOS2
MW 249.35

Purity: 99%
Soluble in 0.1N NaOH(aq) and DMSO

10058-F4

Description

Small-molecule c-Myc inhibitor that induces cell-cycle arrest at G0/G1 phase in a dose-dependent manner. 10058-F4 targets c-Myc-Max, to disrupt the heterodimer and/or to prevent its formation, and abrogates various c-Myc–dependent functions, and induces myeloid differentiation of human acute myeloid leukemia.

M.J. Huang et al. A small-molecule c-Myc inhibitor, 10058-F4, induces cell-cycle arrest, apoptosis, and myeloid differentiation of human acute myeloid leukemia. Exp. Hematol. 2006, 34, 1480-1489.

H. Wang et al. Improved low molecular weight Myc-Max inhibitors. Mol. Cancer Ther. 2007, 6, 2399-2408.

Apoptosis Cell Cycle Regulation Cell Signaling & Oncology c-MYC Transcription Factors TF class 1.3.2 Stem Cell Differentiator

c-Myc inhibitor inducing cell-cycle arrest at G0/G1 phase

Chemical name

5-(4-ethylbenzylidene)-2-thioxothiazolidin-4-one

Parent CAS No.

[403811-55-2]

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