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Technology Process of Triciribine phosphate

Triciribine phosphate

Base Information
  • Chemical Name:Triciribine phosphate
  • CAS No.:61966-08-3
  • Molecular Formula:C13H17N6O7P
  • Molecular Weight:400.29
  • Hs Code.:
  • UNII:5L5GE3DV88
  • DSSTox Substance ID:DTXSID30210993
  • Nikkaji Number:J69.483E
  • Wikidata:Q27262513
  • NCI Thesaurus Code:C1262
  • Metabolomics Workbench ID:154996
  • ChEMBL ID:CHEMBL462018
  • Mol file:61966-08-3.mol
Triciribine phosphate

Synonyms:1,4,5,6,8-pentaazaacenaphthylene-3-amino-1,5-dihydro-5-methyl-1-beta-D-ribofuranosyl 5'-phosphate ester;NSC 280594;NSC-280594;TCN-monophosphate;TCN-P;TCNP;triciribine phosphate

Suppliers and Price of Triciribine phosphate
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
  • Usbiological
  • Tricyclic nucleoside phosphate
  • 5mg
  • $ 460.00
  • TRC
  • Triciribinephosphate
  • 25mg
  • $ 920.00
  • TRC
  • Triciribinephosphate
  • 10mg
  • $ 395.00
  • Biosynth Carbosynth
  • Tricyclic nucleoside phosphate
  • 10 mg
  • $ 395.00
  • Biosynth Carbosynth
  • Tricyclic nucleoside phosphate
  • 5 mg
  • $ 250.00
Total 21 raw suppliers
Chemical Property of Triciribine phosphate
Chemical Property:
  • Vapor Pressure:2.1E-29mmHg at 25°C 
  • Refractive Index:1.924 
  • Boiling Point:832.8 °C at 760 mmHg 
  • Flash Point:457.4 °C 
  • PSA：200.81000 
  • Density:2.23 g/cm3 
  • LogP:-0.79010 
  • XLogP3:-3.3
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:4
  • Exact Mass:400.08963390
  • Heavy Atom Count:27
  • Complexity:663
Purity/Quality:

97% *data from raw suppliers

Tricyclic nucleoside phosphate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C2=NC=NC3=C2C(=CN3C4C(C(C(O4)COP(=O)(O)O)O)O)C(=N1)N
  • Isomeric SMILES:CN1C2=NC=NC3=C2C(=CN3[C@H]4[C@@H]([C@@H]([C@H](O4)COP(=O)(O)O)O)O)C(=N1)N
  • Recent ClinicalTrials:PTX-200, Paclitaxel, Doxorubicin Hydrochloride, and Cyclophosphamide in Treating Patients With Stage IIB-IV Breast Cancer
  • Uses Triciribine phosphate is an Akt activation inhibitor that inhibits Akt phosphorylation by binding to the pleckstrin homology (PH) domain of the Akt and blocking its recruitment to the plasma membrane.
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