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SH5-07 Chemical Structure

SH5-07

Data Sheet For research use only. Not for human use.
Cat. No. :BCP19924CAS No. :1456632-41-9Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 1456632-41-9 Cat. No. BCP19924
Name SH5-07
Synonyms SH-5-07; SH 5-07;
SMILES
Chemical Name
Formula C29H28F5N3O5S M. Wt 625.61
Purity 98% Storage Store at 4-8°C
Description In Vitro: SH5-07 is a hydroxamic acid analog of BP-1-102. SH5-07 dose-dependently inhibits Stat3 activity with an IC50 of 3.9±0.6 μM in in vitro assay. It preferentially inhibits Stat3:Stat3 DNA-binding activity, ahead of inhibiting Stat1:Stat3 activity, with minimal effects on Stat1:Stat1 activity. SH5-07 binds Stat3, disrupts Stat3 association with growth factor receptor, and thereby inhibits Stat3 phosphorylation. It induces antitumor cell effects against malignant cells harboring constitutively-active Stat3. SH5-07 inhibits the expression of known Stat3-regulated genes. Bcl-2, Bcl-xL, c-Myc, Survivin, Cyclin D1 and Mcl-1 expression is reduced in response to 24 h, 5 μM SH5-07 treatment. In Vivo: Tail vein injection or oral gavage delivery of SH5-07 or SH4-54 inhibits growth of 90-150 mm3 established subcutaneous mouse xenografts of human glioma (U251MG) and breast (MDA-MB-231) tumors that harbor aberrantly-active Stat3, associated with decreased c-Myc, Mcl-1 and Cyclin D1 expression
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