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6-((Naphthalen-1-ylmethyl)thio)-7H-purine

Base Information
  • Chemical Name:6-((Naphthalen-1-ylmethyl)thio)-7H-purine
  • CAS No.:313984-77-9
  • Molecular Formula:C16H12N4S
  • Molecular Weight:292.4
  • Hs Code.:
  • ChEMBL ID:CHEMBL1382868
  • Mol file:313984-77-9.mol
6-((Naphthalen-1-ylmethyl)thio)-7H-purine

Synonyms:6-((1-naphthylmethyl)sulfanyl)-9H-purine;NMMP compound

Suppliers and Price of 6-((Naphthalen-1-ylmethyl)thio)-7H-purine
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
  • PU 02
  • 10mg
  • $ 403.00
  • Tocris
  • PU02 ≥97%(HPLC)
  • 50
  • $ 397.00
  • Tocris
  • PU02 ≥97%(HPLC)
  • 10
  • $ 95.00
  • CSNpharm
  • PU-02
  • 50mg
  • $ 280.00
  • Crysdot
  • 6-((Naphthalen-1-ylmethyl)thio)-7H-purine 97%
  • 5g
  • $ 2230.00
  • Crysdot
  • 6-((Naphthalen-1-ylmethyl)thio)-7H-purine 97%
  • 1g
  • $ 845.00
  • ChemScene
  • PU02 99.29%
  • 10mg
  • $ 85.00
  • ChemScene
  • PU02 99.29%
  • 50mg
  • $ 300.00
  • Chemenu
  • 6-((Naphthalen-1-ylmethyl)thio)-7H-purine 97%
  • 5g
  • $ 2085.00
  • Chemenu
  • 6-((Naphthalen-1-ylmethyl)thio)-7H-purine 97%
  • 1g
  • $ 790.00
Total 5 raw suppliers
Chemical Property of 6-((Naphthalen-1-ylmethyl)thio)-7H-purine
Chemical Property:
  • Storage Temp.:2-8°C 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:292.07826757
  • Heavy Atom Count:21
  • Complexity:353
Purity/Quality:

97% *data from raw suppliers

PU 02 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2CSC3=NC=NC4=C3NC=N4
  • Description PU 02 is an antagonist of the serotonin (5-HT) receptor subtype 5-HT3 with IC50 values ranging from 0.36 to 1.3 μM for human 5-HT3A, 5-HT3AB, 5-HT3AC, and 5-HT3AE in a FLIPR membrane potential assay using HEK293 cells expressing human recombinant receptors. It is selective for 5-HT3 over other Cys-loop containing receptors with IC50 values >100 μM for mouse, rat, and human nicotinic (nACh), human GABAA, and human glycine (Gly) receptors. PU 02 inhibits currents induced by 5-HT in COS-7 cells expressing human 5-HT3A (IC50 = 0.49 μM). PU 02 also reduces growth of HepG2 cells in a dose-dependent manner via induction of cell cycle arrest at the G2/M phase and apoptosis.
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