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SB-218078

Base Information Edit
  • Chemical Name:SB-218078
  • CAS No.:135897-06-2
  • Deprecated CAS:154624-50-7
  • Molecular Formula:C24H15N3O3
  • Molecular Weight:393.401
  • Hs Code.:
  • UNII:S6U3J3UP11
  • DSSTox Substance ID:DTXSID10392024
  • Nikkaji Number:J1.250.690B
  • Wikidata:Q27088703
  • Pharos Ligand ID:DU8HFVWYGMDM
  • ChEMBL ID:CHEMBL304428
  • Mol file:135897-06-2.mol
SB-218078

Synonyms:SB 218078;SB-218078

Suppliers and Price of SB-218078
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
  • SB218078
  • 2.5mg
  • $ 160.00
  • Sigma-Aldrich
  • SB 218078 - CAS 135897-06-2 - Calbiochem
  • 1mg
  • $ 181.00
  • DC Chemicals
  • SB218078 >98%
  • 1 g
  • $ 1700.00
  • DC Chemicals
  • SB218078 >98%
  • 250 mg
  • $ 850.00
  • CSNpharm
  • SB218078
  • 1mg
  • $ 140.00
  • CSNpharm
  • SB218078
  • 5mg
  • $ 353.00
  • ChemScene
  • SB-218078 ≥98.0%
  • 5mg
  • $ 380.00
  • ChemScene
  • SB-218078 ≥98.0%
  • 1mg
  • $ 150.00
  • Cayman Chemical
  • SB 218078 ≥98%
  • 1mg
  • $ 115.00
  • ApexBio Technology
  • SB218078
  • 1mg
  • $ 160.00
Total 5 raw suppliers
Chemical Property of SB-218078 Edit
Chemical Property:
  • PSA:69.02000 
  • Density:1.8g/cm3 
  • LogP:4.36310 
  • Storage Temp.:Store at RT 
  • Solubility.:≤5mg/ml in DMSO;5mg/ml in dimethyl formamide 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:393.11134135
  • Heavy Atom Count:30
  • Complexity:754
Purity/Quality:

98% *data from raw suppliers

SB218078 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N(C1O2)C7=C53)C(=O)NC6=O
  • Description SB 218078 is an inhibitor of checkpoint kinase 1 (Chk1) that blocks phosphorylation of cdc25 with an IC50 value of 15 nM. It less potently inhibits cdc2 and PKC (IC50s = 250 and 1,000 nM, respectively) and causes 85% inhibition of PKD1 at 1 μM. SB 218078 releases G2 cell cycle arrest induced by γ-irradiation or the topoisomerase I inhibitor topotecan . In this way, SB 218078 enhances the cytotoxicity of DNA-damaging compounds.
  • Uses SB 218078 is a selective inhibitor of Chk1.
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