39628-94-9

p-Nitrobenzyl mesylate Chemical Structure
39628-94-9

Chemical Structure

p-Nitrobenzyl mesylate

Synonym(s): 4-Nitrobenzyl mesylate; para-Nitrobenzyl mesylate; PNBM

  • CAS. Nr.: 39628-94-9
  • Formula:C8H9NO5S
  • Molecular Weight:231.23

IUPAC Name: 4-nitrobenzyl methanesulfonate

InChIKey: QZIYKAFPHRTIAI-UHFFFAOYSA-N

SMILES: CS(OCC1=CC=C(C=C1)[N+]([O-])=O)(=O)=O

Biological Activity: p-Nitrobenzyl mesylate (4-Nitrobenzyl mesylate) is an alkylating reagent. p-Nitrobenzyl mesylate alkylates thiophosphorylated serine, threonine, tyrosine residues and cysteine thiols, without modifying hydroxyl, amino or carboxylic acid functional groups. p-Nitrobenzyl mesylate generates thiophosphate epitopes on thiophosphorylated substrate proteins for recognition by thiophosphate-specific antibodies. p-Nitrobenzyl mesylate facilitates the identification and purification of kinase substrates. p-Nitrobenzyl mesylate is applicable to studies related to cerebral ischemia-reperfusion injury[1][2][3].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-118380
p-Nitrobenzyl mesylate 98.78% p-Nitrobenzyl mesylate (4-Nitrobenzyl mesylate) is an alkylating reagent. p-Nitrobenzyl mesylate alkylates thiophosphorylated serine, threonine, tyrosine residues and cysteine thiols, without modifying hydroxyl, amino or carboxylic acid functional groups. p-Nitrobenzyl mesylate generates thiophosphate epitopes on thiophosphorylated substrate proteins for recognition by thiophosphate-specific antibodies. p-Nitrobenzyl mesylate facilitates the identification and purification of kinase substrates. p-Nitrobenzyl mesylate is applicable to studies related to cerebral ischemia-reperfusion injury.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References