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Enzastaurin

Base Information Edit
  • Chemical Name:Enzastaurin
  • CAS No.:170364-57-5
  • Molecular Formula:C32H29N5O2
  • Molecular Weight:515.615
  • Hs Code.:29339900
  • European Community (EC) Number:806-090-5
  • UNII:UC96G28EQF
  • DSSTox Substance ID:DTXSID5044029
  • Nikkaji Number:J1.692.444J
  • Wikipedia:Enzastaurin
  • Wikidata:Q5381479
  • NCI Thesaurus Code:C77392
  • Pharos Ligand ID:LSYLPJPK7GJ2
  • Metabolomics Workbench ID:149805
  • ChEMBL ID:CHEMBL300138
  • Mol file:170364-57-5.mol
Enzastaurin

Synonyms:enzastaurin;LY317615.HCl

Suppliers and Price of Enzastaurin
Supply Marketing:Edit
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
  • Enzastaurin
  • 50mg
  • $ 825.00
  • Tocris
  • Enzastaurin ≥98%(HPLC)
  • 50
  • $ 609.00
  • Tocris
  • Enzastaurin ≥98%(HPLC)
  • 10
  • $ 145.00
  • Sigma-Aldrich
  • Enzastaurin ≥98% (HPLC)
  • 25mg
  • $ 404.00
  • Sigma-Aldrich
  • Enzastaurin ≥98% (HPLC)
  • 5mg
  • $ 106.00
  • Matrix Scientific
  • 3-(1-Methyl-1H-indol-3-yl)-4-(1-(1-(pyridin-2-ylmethyl)-piperidin-4-yl)-1H-indol-3-yl)-1H-pyrrole-2,5-dione 95+%
  • 1g
  • $ 2268.00
  • Matrix Scientific
  • 3-(1-Methyl-1H-indol-3-yl)-4-(1-(1-(pyridin-2-ylmethyl)-piperidin-4-yl)-1H-indol-3-yl)-1H-pyrrole-2,5-dione 95+%
  • 250mg
  • $ 1021.00
  • DC Chemicals
  • Enzastaurin(LY317615) >98%
  • 250 mg
  • $ 600.00
  • CSNpharm
  • Enzastaurin
  • 5mg
  • $ 43.00
  • CSNpharm
  • Enzastaurin
  • 10mg
  • $ 60.00
Total 61 raw suppliers
Chemical Property of Enzastaurin Edit
Chemical Property:
  • Vapor Pressure:1.87E-23mmHg at 25°C 
  • Melting Point:249-261℃ 
  • Refractive Index:1.722 
  • Boiling Point:767.2 °C at 760 mmHg 
  • PKA:7.88±0.60(Predicted) 
  • Flash Point:417.8 °C 
  • PSA:72.16000 
  • Density:1.34 g/cm3 
  • LogP:5.19900 
  • Storage Temp.:?20°C 
  • Solubility.:DMSO: soluble10mg/mL, clear (warmed) 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:515.23212518
  • Heavy Atom Count:39
  • Complexity:974
Purity/Quality:

98% *data from raw suppliers

Enzastaurin *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C=C(C2=CC=CC=C21)C3=C(C(=O)NC3=O)C4=CN(C5=CC=CC=C54)C6CCN(CC6)CC7=CC=CC=N7
  • Recent ClinicalTrials:Investigate Efficacy, Safety, and Pharmacokinetics of Enzastaurin for the Prevention of Arterial Events in Patients With Vascular Ehlers-Danlos Syndrome.
  • Recent EU Clinical Trials:A multicenter, randomized, double-blind, placebo-controlled study of enzastaurin for the prevention of arterial events in patients with vascular Ehlers-Danlos Syndrome (vEDS) confirmed with COL3A1 mutations, followed by an open label extension (OLE)
  • Description Enzastaurin (170364-57-5) is a potent and selective PKCβ inhibitor.? IC50 = 6, 39, 83 and 110 nM, for PKCβ, PKCα, PKCγ and PKCε respectively.1 Induces apoptosis in multiple myeloma cell lines via inhibition of the AKT signaling pathway.2 Induces mitotic missegregation and preferential cytotoxicity in colorectal cancer cells with chromosomal instability.3 Attenuates amphetamine-stimulated dopamine efflux.4 Inhibits blood-brain barrier leakiness in a mouse model.5
  • Uses PKCβ-selective inhibitor, suppresses angiogenesis. Enzastaurin has been used in splicing analysis to study its effects on splicing of a mutated exon.
Technology Process of Enzastaurin

There total 27 articles about Enzastaurin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1002/jlcr.1497
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