3 Results for "

SI-109

" in MedChemExpress (MCE) Product Catalog:
Products (3)

3 Results for "SI-109" in MCE Product Catalog:

9
9 Cited Publications
Cat. No.: HY-129602
CAS No.: 2429877-44-9
Purity:  99.73%
Target:  

PROTACs STAT Apoptosis

Research Areas:  

Cancer

SD-36 is a potent and efficacious STAT3 PROTAC degrader (Kd=~50 nM), and demonstrates high selectivity over other STAT members. SD-36 also effectively degrades mutated STAT3 proteins in cells and suppresses the transcriptional activity of STAT3 (IC50=10 nM). SD-36 exerts robust anti-tumor activity, and achieves complete and long-lasting tumor regression in mouse tumor models. SD-36 is composed of the STAT3 inhibitor SI-109, a linker, and an analog of Cereblon ligand Lenalidomide for E3 ubiquitin ligase . SD-36 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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2
2 Cited Publications
Cat. No.: HY-129603
CAS No.: 2429877-30-3
Purity:  98.96%
Research Areas:  

Cancer

SI-109 is a potent STAT3 SH2 domain inhibitor (Ki=9 nM) with antitumor activity. SI-109 effectively inhibits the transcriptional activity of STAT3 (IC50=3 μM). SI-109 and an analog of CRBN ligand lenalidomide have been used to design PROTAC STAT3 degrader SD-36 .
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Cat. No.: HY-131559
CAS No.: 2429878-64-6
Research Areas:  

Cancer

N-Deacetyl-SI-109-(OEt)2 (Compound 11) is a STAT3 ligand. N-Deacetyl-SI-109-(OEt)2 serves as a Ligand for target protein for the synthesis of STAT3 PROTAC degraders, such as SD-36 (HY-129602). N-Deacetyl-SI-109-(OEt)2 is applicable for cancer research .
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