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SH-4-54

SH-4-54 Suppliers list
Company Name: Chengdu Celes Technology Co., Ltd  Gold
Tel: 19982073091
Email: 2538834896@qq.com
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Company Name: Dalian Meilun Biotech Co., Ltd.  
Tel: 0411-62910999 13889544652
Email: sales@meilune.com
Company Name: Haoyuan Chemexpress Co., Ltd.  
Tel: 021-58950125
Email: info@chemexpress.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com

SH-4-54 manufacturers

  • SH-4-54
  • SH-4-54 pictures
  • $43.00
  • 2026-06-02
  • CAS:1456632-40-8
  • Purity: 98.00%
  • Supply Ability: 10g
  • SH-4-54
  • SH-4-54 pictures
  • $200.00
  • 2023-06-26
  • CAS:1456632-40-8
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 1000kg/Months
SH-4-54 Basic information
Product Name:SH-4-54
Synonyms:4-[[(4-cyclohexylphenyl)methyl][2-[methyl[(2,3,4,5,6-pentafluorophenyl)sulfonyl]amino]acetyl]amino]-Benzoic Acid SH-4-54;SH-4-54;4-[[(4-cyclohexylphenyl)methyl][2-[methyl[(2,3,4,5,6-pentafluorophenyl)sulfonyl]amino]acetyl]amino]-benzoic acid;Benzoic acid, 4-[[(4-cyclohexylphenyl)methyl][2-[methyl[(2,3,4,5,6-pentafluorophenyl)sulfonyl]amino]acetyl]amino]-;CS-1773;SH-4-54 USP/EP/BP;SH 4 54,Inhibitor,SH454,inhibit,STAT;SH-4-54, 10 mM in DMSO
CAS:1456632-40-8
MF:C29H27F5N2O5S
MW:610.59
EINECS:
Product Categories:Inhibitors;API
Mol File:1456632-40-8.mol
SH-4-54 Structure
SH-4-54 Chemical Properties
Boiling point 717.2±70.0 °C(Predicted)
density 1.431±0.06 g/cm3(Predicted)
storage temp. Desiccate at -20°C
solubility DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 20 mg/ml
form A crystalline solid
pka4.29±0.10(Predicted)
color White to off-white
InChIKeyVFPYGNNOSJWBHF-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC=C(N(CC2=CC=C(C3CCCCC3)C=C2)C(CN(C)S(C2=C(F)C(F)=C(F)C(F)=C2F)(=O)=O)=O)C=C1
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
SH-4-54 Usage And Synthesis
DescriptionSH-4-54 is an inhibitor of signal transducer and activator of transcription 3 (STAT3; IC50 = 4.7 μM for STAT3 homodimer DNA binding activity). It selectively inhibits STAT3 homodimer over STAT1 and STAT5 homodimer and STAT3:STAT1 heterodimer DNA binding in EGF-stimulated NIH3T3/hEGFR nuclear extracts containing activated STAT1, STAT3, and STAT5 and decreases STAT3 iNOS, Survivin, and Bcl-2 promoter occupancy in MDA-MB-231 cells. SH-4-54 inhibits growth of glioma, breast, and prostate cancer cell lines that express constitutively active STAT3 (IC50s = 1-7.4, 3.8-4.5, and 5.3-5.8 μM, respectively). In vivo, SH-4-54 (3 mg/kg per day) inhibits tumor growth in the U251MG glioma and MDA-MB-231 breast cancer mouse xenograft models.
Uses4-[[(4-Cyclohexylphenyl)methyl][2-[methyl[(2,3,4,5,6-pentafluorophenyl)sulfonyl]amino]acetyl]amino]benzoic Acid acts as a STAT 3 and STAT5 inhibitor. STAT 3 is unusually active in glioblastoma and plays a crucial role in tumor growth
in vivo

SH-4-54 exhibits blood-brain barrier permeability potently controls glioma tumor growth, and inhibits pSTAT3 in vivo. SH-4-54 demonstrates the power of STAT3 inhibitors for the treatment of BTSCs and validates the therapeutic efficacy of a STAT3 inhibitor for GBM clinical application.SH-4-54 decreases pSTAT3 expression in tumor cells of treated mice. SH-4-54 appears to decrease proliferation and increase apoptosis of treated tumors[1].

IC 50STAT3: 300 nM (Kd); STAT5: 464 nM (Kd)
References[1] PEIBIN YUE. Hydroxamic Acid and Benzoic Acid-Based STAT3 Inhibitors Suppress Human Glioma and Breast Cancer Phenotypes In Vitro and In Vivo.[J]. Cancer research, 2016, 76 3: 652-663. DOI: 10.1158/0008-5472.can-14-3558
SH-4-54 Preparation Products And Raw materials
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