Chemical Name:N,N'-Bis(3-aminopropyl)-1,4-butanediamine tetrahydrochloride
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Polyamine which produces a variety of modulatory effects on the NMDA receptor channel, acting through a specific site on the complex which can cause both agonist and antagonist effects.
Technical Data
M. Wt
348.19
Formula
C10H26N4.4HCl
Storage
Desiccate at +4°C
CAS Number
306-67-2
PubChem ID
9384
InChI Key
XLDKUDAXZWHPFH-UHFFFAOYSA-N
Smiles
NCCCNCCCCNCCCN.Cl.Cl.Cl.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solubility
Soluble to 100 mM in water
Preparing Stock Solutions
The following data is based on the product molecular weight 348.19. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
2.87 mL
14.36 mL
28.72 mL
5 mM
0.57 mL
2.87 mL
5.74 mL
10 mM
0.29 mL
1.44 mL
2.87 mL
50 mM
0.06 mL
0.29 mL
0.57 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
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References
References are publications that support the products' biological activity.
Benveniste and Mayer
(1993) Multiple effects of spermine on N-methyl-D-aspartic acid receptor responses of rat cultured hippocampal neurones. J.Physiol. 464 131 PMID: 8229795
Doyle and Shaw
(1998) Investigation of the actions and antagonist activity of some polyamine analogues in vivo. Br.J.Pharmacol. 124 386 PMID: 9641557
Johnson
(1996) Modulation of channel function by polyamines. TiPS 17 22 PMID: 8789355
Muniret al (1993) Polyamines modulate the neurotoxic effects of NMDA in vivo. Brain Res. 616 163 PMID: 8358608