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Stattic

Stattic Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:Stattic
CAS:19983-44-9
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: factory@coreychem.com
Products Intro: Product Name:Stattic
CAS:19983-44-9
Purity:97%-99.9% Package:1ASSAYS;1USD
Company Name: Shanghai Safer Pharmaceutical Technology Co., Ltd.
Tel: 021-31761238
Email: sales@saferph.com
Products Intro: Product Name:1,1-Dioxide-6-nitro-benzo[b]thiophene
CAS:19983-44-9
Purity:0.98 Package:1g,25g,100g,1kg Remarks:For research purposes only
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Stattic
CAS:19983-44-9
Purity:99.76% Package:5mg;30USD|10mg;47USD|25mg;77USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shanghai Gubang New Materail Technology Co. LTD
Tel: 21-51317962 +8618721305404
Email: 16728589@qq.com
Products Intro: CAS:19983-44-9
Package:1 g 2 g, 5 g, 10 g, 1000 g, 25 kg

Stattic manufacturers

  • Stattic
  • Stattic pictures
  • $30.00 / 5mg
  • 2026-04-13
  • CAS:19983-44-9
  • Min. Order:
  • Purity: 98.54%
  • Supply Ability: 10g
  • Stattic
  • Stattic pictures
  • $1.00 / 1ASSAYS
  • 2019-12-23
  • CAS:19983-44-9
  • Min. Order: 1ASSAYS
  • Purity: 97%-99.9%
  • Supply Ability: 100kg
Stattic Basic information
Background
Product Name:Stattic
Synonyms:BUTTPARK 97\04-73;6-NITRO-1H-1LAMBDA6-BENZO[B]THIOPHENE-1,1-DIONE;AKOS 1001;6-Nitro-1-benzothiophene 1,1-dioxide;1,1-DIOXO-6-NITROBENZO(B)THIOPHENE;6-Nitrobenzo[b]thiophene-1,1-dioxide, Stat three inhibitory compound;Stattic;6-Nitrobenzo[b]thiophene1,1-dioxide
CAS:19983-44-9
MF:C8H5NO4S
MW:211.19
EINECS:
Product Categories:Inhibitors;JAK;STAT;JAK/STAT
Mol File:19983-44-9.mol
Stattic Structure
Stattic Chemical Properties
Melting point 187-188 °C
Boiling point 461.1±45.0 °C(Predicted)
density 1.621±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO: >20mg/mL
form powder
color white to beige
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
InChIInChI=1S/C8H5NO4S/c10-9(11)7-2-1-6-3-4-14(12,13)8(6)5-7/h1-5H
InChIKeyZRRGOUHITGRLBA-UHFFFAOYSA-N
SMILESC12=CC([N+]([O-])=O)=CC=C1C=CS2(=O)=O
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38-22
Safety Statements 26-36/37/39
WGK Germany 3
Hazard Note Irritant
HS Code 2934999090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
Stattic Usage And Synthesis
DescriptionStattic (19983-44-9) is a STAT3 inhibitor that inhibits binding of tyrosine-phosphorylated peptides to STAT3 SH2 domain and inhibiting STAT3 activation, dimerization and nuclear translocation.1 Displays selectivity over STAT1, STAT5, c-Myc/Max, Jun/Jun and Lck. Induces apoptosis in STAT3-dependent cancer cell lines. Alkyates four cysteine residues on STAT3.2 Exhibits potent antitumor activity.3 Protects against angiotensin II-induced vascular dysfunction and hypertension.4Stattic is an extremely useful tool to probe involvement of STAT3 in cellular signaling.
UsesStattic is a Stat3 inhibitor which exhibited potent anti-tumor and induced chemo- and radio-sensitivity in nasopharyngeal carcinoma.
UsesStattic was used to study Stat3-mediated cell signaling in human lung carcinoma cells.5
DefinitionChEBI: Stattic is a member of the class of 1-benzothiophenes that is 1-benzothiophene-1,1-dioxide substituted at position 6 by a nitro group. Used as a radiosensitising agent for esophageal squamous cell carcinoma. It has a role as an antineoplastic agent, a STAT3 inhibitor and a radiosensitizing agent. It is a member of 1-benzothiophenes, a C-nitro compound and a sulfone.
Biological ActivitySmall molecule inhibitor of STAT3. Inhibits binding of tyrosine-phosphorylated peptide motifs to STAT3 SH2 domain and inhibits STAT3 activation, dimerization and nuclear translocation. Displays selectivity over STAT1, STAT5, c-Myc/Max, Jun/Jun and Lck. Induces apoptosis in STAT3-dependent cancer cell lines.
Biochem/physiol ActionsStattic (Stat3 three inhibitory compound) alters the SH2 domain of Stat3 and indirectly inhibits with phosphopeptide binding. It is readily transported across the cell membrane compared to other phosphopeptides.2 Stattic induces increased formation of ROS and negatively affects the cardiomyocyte mitochondrial function,3 and sensitizes nasopharyngeal carcinoma cells to chemoradiotherapy.4
Synthesis
THIANAPHTHENE-1,1-DIOXIDE

825-44-5

Stattic

19983-44-9

General procedure for the synthesis of 6-nitrobenzo[b]thiophene 1,1-dioxide from benzo[b]thiophene 1,1-dioxide: with reference to Example 118, nitric acid (10 mL) was slowly added dropwise to sulfuric acid (10 mL) at 0° C. The temperature was kept constant and the reaction mixture was stirred for 10 minutes. Subsequently, benzo[b]thiophene 1,1-dioxide (3.99 g) was slowly added to the above mixed acid solution at 0°C, and stirring was continued at the same temperature for 30 minutes. After completion of the reaction, the reaction mixture was slowly poured into ice water and extracted with ethyl acetate. The organic phases were combined and washed twice sequentially with water, saturated aqueous sodium bicarbonate solution and saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The resulting residue was recrystallized by ethyl acetate-hexane mixed solvent to give light yellow solid 6-nitrobenzo[b]thiophene 1,1-dioxide (yield 4.26 g, 84% yield). The product was characterized by 1H-NMR (CDCl3): δ 7.00 (1H, d, J = 6.9 Hz), 7.33 (1H, dd, J = 1.2,6.9 Hz), 7.58 (1H, d, J = 8.4 Hz), 8.47 (1H, dd, J = 1.8,8.4 Hz), 8.55-8.57 (1H, m).

storage+4°C
BackgroundStattic is a nonpeptidic selective Stat3 inhibitor. This small molecule prevents the binding of tyrosine-phosphorylated peptide motifs to the Stat3 SH2 domain, inhibiting Stat3 activation, dimerization, and nuclear translocation with an IC50 value of 5.1 μM. Stattic blocks IL-6-induced Stat3 activation, reducing cell viability in tumor cells. Treatment with 10 μM induces apoptosis in Stat3-dependent cancer cell lines MDA-MB-231 and MDA-MB-435S.
References[1] JOCHEN SCHUST. Stattic: a small-molecule inhibitor of STAT3 activation and dimerization.[J]. Chemistry & biology, 2006, 13 11: 1235-1242. DOI:10.1016/j.chembiol.2006.09.018
[2] SIBYLLE HEIDELBERGER . Investigation of the protein alkylation sites of the STAT3:STAT3 inhibitor Stattic by mass spectrometry[J]. Bioorganic & Medicinal Chemistry Letters, 2013, 23 16: Pages 4719-4722. DOI:10.1016/j.bmcl.2013.05.066
[3] YUNBAO PAN. Stat3 inhibitor Stattic exhibits potent antitumor activity and induces chemo- and radio-sensitivity in nasopharyngeal carcinoma.[J]. PLoS ONE, 2013: e54565. DOI:10.1371/journal.pone.0054565
[4] ANDREW W JOHNSON. Small-molecule inhibitors of signal transducer and activator of transcription 3 protect against angiotensin II-induced vascular dysfunction and hypertension.[J]. Hypertension, 2013, 61 2: 437-442. DOI:10.1161/hypertensionaha.111.00299
Stattic Preparation Products And Raw materials
Raw materialsTHIANAPHTHENE-1,1-DIOXIDE
Preparation Products2,3-dihydro-1-benzothiophen-6-amine
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