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Search term: 5167 (Found by CSID)

ChemSpider 2D Image | Suramin sodium | C51H34N6Na6O23S6

Suramin sodium

  • Molecular FormulaC51H34N6Na6O23S6
  • Average mass1429.171 Da
  • Monoisotopic mass1427.938599 Da
  • ChemSpider ID5167
  • Charge - Charge


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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

Suramin sodium [BAN] [INN]
1,3,5-Naphthalenetrisulfonic acid, 8,8'-[carbonylbis[imino-3,1-phenylenecarbonylimino(4-methyl-3,1-phenylene)carbonylimino]]bis-, sodium salt (1:6) [ACD/Index Name]
129-46-4 [RN]
204-949-3 [EINECS]
309f
8,8'-{Carbonylbis[imino-3,1-phénylènecarbonylimino(4-méthyl-3,1-phénylène)carbonylimino]}di(1,3,5-naphtalènetrisulfonate) de hexasodium [French] [ACD/IUPAC Name]
Hexanatrium-8,8'-{carbonylbis[imino-3,1-phenylencarbonylimino(4-methyl-3,1-phenylen)carbonylimino]}di(1,3,5-naphthalintrisulfonat) [German] [ACD/IUPAC Name]
Hexasodium 8,8'-{carbonylbis[imino-3,1-phenylenecarbonylimino(4-methyl-3,1-phenylene)carbonylimino]}di(1,3,5-naphthalenetrisulfonate) [ACD/IUPAC Name]
Hexasodium 8-[(4-methyl-3-{[3-({[3-({2-methyl-5-[(4,6,8-trisulfonato-1-naphthyl)carbamoyl]phenyl}carbamoyl)phenyl]carbamoyl}amino)benzoyl]amino}benzoyl)amino]naphthalene-1,3,5-trisulfonate
hexasodium 8-[(4-methyl-3-{[3-({[3-({2-methyl-5-[(4,6,8-trisulfonatonaphthalen-1-yl)carbamoyl]phenyl}carbamoyl)phenyl]carbamoyl}amino)benzoyl]amino}benzoyl)amino]naphthalene-1,3,5-trisulfonate
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

GCI-1003 [DBID]
BAY 205 [DBID]
Bayer 205 [DBID] [Trade name]
CI-1003 [DBID]
D00808 [DBID]
EU-0101182 [DBID]
Lopac-S-149 [DBID]
NCGC00016201-01 [DBID]
NF-060 [DBID] [NF]
NSC 34936 [DBID]
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  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Target Organs:

      P2 Receptor inhibitor TargetMol T2160
    • Bio Activity:

      Ion Channels Tocris Bioscience 1472
      Ligand-gated Ion Channels Tocris Bioscience 1472
      Neuroscience TargetMol T2160
      Non-selective P2 antagonist Tocris Bioscience 1472
      Non-selective P2 purinergic antagonist. Also blocks calmodulin binding to recognition sites and G protein coupling to G protein-coupled receptors. Increases open probability of ryanodine receptor (RyR ) channels. Anticancer and antiviral agent. Tocris Bioscience 1472
      Non-selective P2 purinergic antagonist. Also blocks calmodulin binding to recognition sites and G protein coupling to G protein-coupled receptors. Increases open probability of ryanodine receptor (RyR) channels. Anticancer and antiviral agent. Tocris Bioscience 1472
      P2X Receptors Tocris Bioscience 1472
      P2Y Receptor TargetMol T2160

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site






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