Harman Patil (Editor)

Spermine

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3DMet
  
B01325

Formula
  
C10H26N4

Melting point
  
29 °C

Appearance
  
Colourless crystals

Molar mass
  
202.34 g/mol

Density
  
937 kg/m³

Boiling point
  
130 °C

Spermine Spermidine and spermine synthesis Polyamines nonprotein amino

Related compounds
  
Spermidine, Putrescine, Cadaverine, Diethylenetriamine

Spermine is a polyamine involved in cellular metabolism found in all eukaryotic cells. The precursor for synthesis of spermine is the amino acid ornithine. It is found in a wide variety of organisms and tissues and is an essential growth factor in some bacteria. It is found as a polycation at physiological pH. Spermine is associated with nucleic acids and is thought to stabilize helical structure, particularly in viruses.

Spermine wwwsigmaaldrichcomcontentdamsigmaaldrichstr

Crystals of spermine phosphate were first described in 1678, in human semen, by Antonie van Leeuwenhoek. The name spermin was first used by the German chemists Ladenburg and Abel in 1888, and the correct structure of spermine was not finally established until 1926, simultaneously in England (by Dudley, Rosenheim, and Starling) and Germany (by Wrede et al.). Spermine is the chemical primarily responsible for the characteristic odor of semen.

Spermine FileSperminesvg Wikimedia Commons

Derivative

Spermine bmse000117 Spermine at BMRB

A derivative of spermine, N1, N12-bis(ethyl)spermine (also known as BESm) was investigated in the late 1980s along with similar polyamine analogues for its potential as a cancer therapy.

Spermine spermine C10H26N4 PubChem

Spermine spermine Ligand page IUPHARBPS Guide to PHARMACOLOGY

Spermine Spermine biosynthesis

Spermine Regioselective binding of spermine NN12bismethylspermine and N

References

Spermine Wikipedia