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PTP CD45 Inhibitor

Base Information
  • Chemical Name:PTP CD45 Inhibitor
  • CAS No.:345630-40-2
  • Molecular Formula:C19H17NO3
  • Molecular Weight:307.34
  • Hs Code.:
  • European Community (EC) Number:803-514-0
  • Nikkaji Number:J1.562.949E
  • Pharos Ligand ID:51VD7DT93JXB
  • ChEMBL ID:CHEMBL51314
  • Mol file:345630-40-2.mol
PTP CD45 Inhibitor

Synonyms:SF1670

Suppliers and Price of PTP CD45 Inhibitor
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • SF1670
  • 50mg
  • $ 550.00
  • Tocris
  • SF1670 ≥98%(HPLC)
  • 50
  • $ 668.00
  • Tocris
  • SF1670 ≥98%(HPLC)
  • 10
  • $ 159.00
  • Sigma-Aldrich
  • SF1670 ≥98% (HPLC)
  • 5mg
  • $ 204.00
  • Sigma-Aldrich
  • PTP CD45 Inhibitor
  • 5mg
  • $ 200.00
  • Sigma-Aldrich
  • SF1670 ≥98% (HPLC)
  • 25mg
  • $ 817.00
  • DC Chemicals
  • SF1670 >98%
  • 250 mg
  • $ 900.00
  • CSNpharm
  • SF1670
  • 1mg
  • $ 51.00
  • CSNpharm
  • SF1670
  • 10mg
  • $ 133.00
  • CSNpharm
  • SF1670
  • 100mg
  • $ 898.00
Total 15 raw suppliers
Chemical Property of PTP CD45 Inhibitor
Chemical Property:
  • Boiling Point:554.1±29.0 °C(Predicted) 
  • PKA:14.31±0.20(Predicted) 
  • PSA:66.73000 
  • Density:1.271±0.06 g/cm3(Predicted) 
  • LogP:4.36670 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: soluble10mg/mL, clear 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:307.12084340
  • Heavy Atom Count:23
  • Complexity:519
Purity/Quality:

99%, *data from raw suppliers

SF1670 *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C(=O)C2=O
  • Uses SF1670 is used in the methods and compositions for treating tumor or cancer by administering to a subject a PTEN inhibitor and chemotherapeutic agents, immume dysregulation in patients with PTEN harmartoma tumor syndrome and analysis of FOXP3 regulatory T cells. SF1670 has been used:To study the effect of microRNA-30a on PTEN (phosphatase and tensin homologue deleted on chromosome 10 ) expression regulation.To study the formation of autophagosomes, induced by EGF (Epidermal growth factor) - dependent PTEN expression.To study the role of PTEN in the regulation of autophagy induction in human normal endometrial stromal cells.
Refernces

Design and synthesis of phosphotyrosine mimetics

10.1016/S0960-894X(03)00253-1

The research focuses on the design and synthesis of phosphotyrosine mimetics, which are of significant interest as potential therapeutic agents and research tools for selectively inhibiting protein tyrosine phosphatases (PTPases). These enzymes play a crucial role in regulating tyrosine phosphorylation and cellular function, and their inhibition could have therapeutic potential for diseases such as diabetes, cancer, and osteoporosis. The study involved the synthesis of phenylalanine derivatives, designed to mimic phosphorylated tyrosine or to act as irreversible active site inhibitors of PTPases. Key chemicals used in the synthesis process included Fmoc-l-Tyr-(3-NO2)-OH, CDI, MeOH, SnCl2, phosgene, TsCl, pyridine, SO2Cl2, and various other reagents and solvents. The synthesized compounds were then incorporated into a combinatorial library and screened for their ability to inhibit four phosphatases, showing moderate potency and selectivity, with the type 2d phosphotyrosine mimetic exhibiting the best activity. However, further analysis of enzymatic inhibition was not possible due to the termination of operations at Molecumetics.

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