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3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione

Base Information Edit
  • Chemical Name:3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione
  • CAS No.:133053-19-7
  • Molecular Formula:C26H26N4O3
  • Molecular Weight:442.517
  • Hs Code.:2933998090
  • European Community (EC) Number:634-328-6
  • DSSTox Substance ID:DTXSID60274402
  • Nikkaji Number:J636.732A
  • Wikidata:Q27077833
  • Pharos Ligand ID:NUFRBFSSS7HQ
  • ChEMBL ID:CHEMBL261491
  • Mol file:133053-19-7.mol
3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione

Synonyms:2-(1-(3-dimethylaminopropyl)-5-methoxyindol-3-yl)-3-(1H-indol-3-yl)maleimide;G?6983;Go 6983;Go-6983;Go6983

Suppliers and Price of 3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione
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
  • Go6983
  • 10mg
  • $ 120.00
  • TRC
  • Go6983
  • 50mg
  • $ 375.00
  • Sigma-Aldrich
  • G 6983 ≥97%
  • 1mg
  • $ 186.00
  • Sigma-Aldrich
  • G? 6983 ≥97%
  • 500 μg
  • $ 109.00
  • Sigma-Aldrich
  • G? 6983
  • 500ug
  • $ 105.00
  • Sigma-Aldrich
  • G 6983 ≥97%
  • 500ug
  • $ 105.00
  • Sigma-Aldrich
  • G? 6983 - CAS 133053-19-7 - Calbiochem A potent, cell-permeable, reversible, and ATP-competitive inhibitor of protein kinase C (PKC) that inhibits several PKC isozymes.
  • 500 μg
  • $ 129.50
  • DC Chemicals
  • Go6983 >98%
  • 1 g
  • $ 2100.00
  • DC Chemicals
  • Go6983 >98%
  • 250 mg
  • $ 950.00
  • CSNpharm
  • Go6983
  • 5mg
  • $ 82.00
Total 25 raw suppliers
Chemical Property of 3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione Edit
Chemical Property:
  • Vapor Pressure:5.97E-20mmHg at 25°C 
  • Boiling Point:709°C at 760 mmHg 
  • PKA:8.02±0.60(Predicted) 
  • Flash Point:382.6°C 
  • PSA:79.36000 
  • Density:1.31g/cm3 
  • LogP:3.97890 
  • Storage Temp.:−20°C 
  • Solubility.:DMSO: 20 mg/mL, clear, red 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:442.20049070
  • Heavy Atom Count:33
  • Complexity:796
Purity/Quality:

98%,99%, *data from raw suppliers

Go6983 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(C)CCCN1C=C(C2=C1C=CC(=C2)OC)C3=C(C(=O)NC3=O)C4=CNC5=CC=CC=C54
  • Description Go-6983 (133053-19-7) potent and pan-specific, ATP-competitive protein kinase C inhibitor. PKC isotype IC50s= 7, 7, 6, 10 and 60 nM for PKC α, β, γ, δ, ζ respectively.1 Suppresses stress induced HSP27 disassociation.2 Maintains rat embryonic stem cell pluripotency.3 Attenuates myocardial ischemia/reperfusion injury.4
  • Uses Go 6983, is a protein kinase C (PKC) inhibitor.Potent PKC Inhibitor GO6983 has been used as a protein kinase C (PKC) inhibitor to study its effects on the nuclear import. It has also been used as a supplement in Fc medium to culture mouse embryonic stem (mES) cells on mitomycin C treated mouse embryonic fibroblasts (MEFs).
Technology Process of 3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione

There total 5 articles about 3-[1-[3-(Dimethylamino)propyl]-5-methoxy-1H-indol-3-yl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione 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:
In N,N-dimethyl-formamide; at 80 ℃; for 13h; Heating / reflux;
Guidance literature:
Multi-step reaction with 3 steps
1.1: potassium tert-butylate / tetrahydrofuran / 12.17 h / 0 - 20 °C
1.2: 1 h
2.1: triethylamine / N,N-dimethyl-formamide / 6.22 h / 0 - 20 °C
3.1: N,N-dimethyl-formamide / 13 h / 80 °C / Heating / reflux
With potassium tert-butylate; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 6.22 h / 0 - 20 °C
2: N,N-dimethyl-formamide / 13 h / 80 °C / Heating / reflux
With triethylamine; In N,N-dimethyl-formamide;
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