S3I-201 (NSC 74859)

Catalog No. A10817

S3I-201(NSC 74859)是Stat3的新型抑制剂,可在体外抑制Stat3,Stat3复合物的形成以及Stat3-DNA结合活性(IC50 = 86±33 ?M)和Stat3依赖性转录活性。
  • Bae WJ, .et al. PTPRD-inactivation-induced CXCL8 promotes angiogenesis and metastasis in gastric cancer and is inhibited. J Exp Clin Cancer Res, 2019, 38:484 PMID: 31805999
  • Nishimura K, .et al. Effect of erythropoietin production induced by hypoxia on autophagy in HepG2 cells, Biochem Biophys Res Commun, 2018, Jan 1;495(1):1317-1321 PMID: 29191652
  • Ethan L. Morgan, .et al. STAT3 activation by E6 is essential for the differentiation-dependent HPV18 life cycle, PLoS Pathog, 2018, Apr; 14(4): e1006975 PMID: 29630659
  • Soleimani AH, .et al. Micellar nano-carriers for the delivery of STAT3 dimerization inhibitors to melanoma, Drug Deliv Transl Res, 2017, Aug;7(4):571-581 PMID: 28290050
Catalog Num A10817
M. Wt 365.4
Formula C16H15NO7S
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 501919-59-1
Synonyms S3I201, NSC74859 , NSC-74859
SMILES CC1=CC=C(C=C1)S(=O)(=O)OCC(=O)NC2=CC(=C(C=C2)C(=O)O)O
S3I-201(NSC 74859)是Stat3的新型抑制剂,可在体外抑制Stat3,Stat3复合物的形成以及Stat3-DNA结合活性(IC50 = 86±33 ?M)和Stat3依赖性转录活性。
Targets
STAT3 (Cell-free assay)
86 μM
In vitro (25°C) DMSO 66 mg/mL (180.64 mM)
Water Insoluble
Ethanol Insoluble
In vivo 5% DMSO+corn oil 2 mg/mL
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 27.37 mL 136.84 mL 273.67 mL
0.5 mM 5.47 mL 27.37 mL 54.73 mL
1 mM 2.74 mL 13.68 mL 27.37 mL
5 mM 0.55 mL 2.74 mL 5.47 mL

*The above data is based on the productmolecular weight 365.4 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.