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6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole

Base Information
  • Chemical Name:6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole
  • CAS No.:163239-22-3
  • Molecular Formula:C15H11FN2
  • Molecular Weight:238.264
  • Hs Code.:
  • European Community (EC) Number:803-131-9
  • DSSTox Substance ID:DTXSID401226445
  • Nikkaji Number:J650.689E
  • Wikidata:Q27225279
  • Pharos Ligand ID:WG8JA9YXXVTV
  • ChEMBL ID:CHEMBL355606
  • Mol file:163239-22-3.mol
6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole

Synonyms:6-fluoro-3-(2-(3-pyridyl)vinyl)-1H-indole;680C91;LM10;TDO inhibitor LM-10;TDO inhibitor LM10

Suppliers and Price of 6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole
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
  • 680C91
  • 5mg
  • $ 389.00
  • TRC
  • 6-Fluoro-3-[(1E)-2-(3-pyridinyl)ethenyl]-1H-indole
  • 2.5mg
  • $ 220.00
  • Sigma-Aldrich
  • 680C91 ≥98% (HPLC)
  • 5mg
  • $ 92.10
  • Sigma-Aldrich
  • 680C91 ≥98% (HPLC)
  • 25mg
  • $ 370.00
  • ApexBio Technology
  • 680C91
  • 10mg
  • $ 308.00
  • ApexBio Technology
  • 680C91
  • 50mg
  • $ 1329.00
  • American Custom Chemicals Corporation
  • 6-FLUORO-3-[(1E)-2-(3-PYRIDINYL)ETHENYL]-1H-INDOLE 95.00%
  • 50MG
  • $ 1269.35
  • American Custom Chemicals Corporation
  • 6-FLUORO-3-[(1E)-2-(3-PYRIDINYL)ETHENYL]-1H-INDOLE 95.00%
  • 10MG
  • $ 744.98
Total 8 raw suppliers
Chemical Property of 6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole
Chemical Property:
  • Boiling Point:431.2±35.0 °C(Predicted) 
  • PKA:15.92±0.30(Predicted) 
  • PSA:28.68000 
  • Density:1.305±0.06 g/cm3(Predicted) 
  • LogP:3.87240 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: ≥10mg/mL 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:238.09062652
  • Heavy Atom Count:18
  • Complexity:305
Purity/Quality:

99%, *data from raw suppliers

680C91 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 41 
  • Safety Statements: 26-39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CN=C1)C=CC2=CNC3=C2C=CC(=C3)F
  • Isomeric SMILES:C1=CC(=CN=C1)/C=C/C2=CNC3=C2C=CC(=C3)F
  • Description 680C91 (163239-22-3) is a potent and selective inhibitor of tryptophan 2,3-dioxygenase (TDO) Ki=42 nM).1,2?Displays no activity against indoleamine 2,3-dioxygenase, MAO-A and B and does not effect serotonin uptake. Elevates CSF tryptophan by up to 260% and CSF serotonin by 170% of basal.2?TDO inhibition by 680C91 in glioma cells blocked the release of kynurenine (Cat.# 10-2666), an endogenous tumor promoting AHR ligand.4
  • Uses 680C91 has been used:as a tryptophan 2,3 dioxygenase (TDO) inhibitor to study its effects on the pigmentation in Doryteuthis pealeii embryosas a TDO inhibitor to study its effects on esophageal squamous cell carcinoma in xenograft tumor assayas a tryptophan 2,3 dioxygenase 2 (TDO2) inhibitor to study its effects on toxic fragment formation in human embryonic kidney cells
Technology Process of 6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole

There total 5 articles about 6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole 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:
3-pyridineacetic acid hydrochloride; With triethylamine; In 1,4-dioxane; at 20 ℃; for 0.166667h; Inert atmosphere;
6-fluoro-1H-indole-3-carbaldehyde; With piperidine; In 1,4-dioxane; for 18h; Inert atmosphere; Reflux;
DOI:10.1021/jm2006782
Guidance literature:
Multi-step reaction with 4 steps
1: dimethylformamide
2: Raney Ni, H2NNH2 / methanol
3: 1) POCl3, 2) NaOH
4: piperidine / Heating
With piperidine; sodium hydroxide; nickel; hydrazine; trichlorophosphate; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/0960-894X(96)00124-2
Guidance literature:
Multi-step reaction with 3 steps
1: Raney Ni, H2NNH2 / methanol
2: 1) POCl3, 2) NaOH
3: piperidine / Heating
With piperidine; sodium hydroxide; nickel; hydrazine; trichlorophosphate; In methanol;
DOI:10.1016/0960-894X(96)00124-2
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