Spermidine

Spermidine

Identifiers
CAS Number	124-20-9 Y
3D model (Jmol)	Interactive image
3DMet	B01214
Beilstein Reference	1698591
ChEBI	CHEBI:16610 N
ChEMBL	ChEMBL19612 N
ChemSpider	1071 N
DrugBank	DB03566 Y
ECHA InfoCard	100.004.264
EC Number	204-689-0
Gmelin Reference	454510
IUPHAR/BPS	2390
KEGG	C00315 N
MeSH	Spermidine
PubChem	1102
RTECS number	EJ7000000
UN number	2735
InChI InChI=1S/C7H19N3/c8-4-1-2-6-10-7-3-5-9/h10H,1-9H2 N Key: ATHGHQPFGPMSJY-UHFFFAOYSA-N N
SMILES NCCCCNCCCN
Properties
Chemical formula	C7H19N3
Molar mass	145.25 g·mol−1
Appearance	Colourless liquid
Odor	Ichtyal, ammoniacal
Density	925 mg mL−1
Melting point	22 to 25 °C (72 to 77 °F; 295 to 298 K)
Solubility in water	145 g L−1 (at 20 °C)
log P	−0.504
UV-vis (λmax)	260 nm
Absorbance	0.1
Refractive index (nD)	1.479
Hazards
GHS pictograms
GHS signal word	DANGER
GHS hazard statements	H314
GHS precautionary statements	P280, P305+351+338, P310
EU classification (DSD)	C
R-phrases	R34
S-phrases	S26, S36/37/39
Flash point	112 °C (234 °F; 385 K)
Related compounds
Related amines	Dipropylamine Methyl-n-amylnitrosamine Norspermidine Dibutylamine Iproheptine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Spermidine is a polyamine compound (C
7H
19N
3) found in ribosomes and living tissues, and having various metabolic functions within organisms. It was originally isolated from semen.^[1]

Function

Polyamines, such as spermidine, are polycationic aliphatic amines and are multifunctional. They serve vital roles in cell survival.

Spermidine synthase (SPDS) catalyzes the formation of spermidine from putrescine. Spermidine is a precursor to further polyamines, such as spermine and its structural isomer thermospermine.

Spermidine synchronizes an array of biological processes (such as Ca2+, Na+, K+ -ATPase) thus maintaining membrane potential and controlling intracellular pH and volume. Spermidine regulates biological processes, such as Ca2+ influx by glutamatergic N-methyl-d-aspartate receptor (NMDA receptor), which has been associated with nitric oxide synthase (NOS) and cGMP/PKG pathway activation and a decrease of Na+,K+-ATPase activity in cerebral cortex synaptosomes.

Spermidine is a longevity agent in mammals due to various mechanisms of action, which are just beginning to be understood. Autophagy is the main mechanism at the molecular level, but evidence has been found for other mechanisms, including inflammation reduction, lipid metabolism, and regulation of cell growth, proliferation and death.^[2]

Spermidine is known to regulate plant growth, assisting the in vitro process of transcribing RNA, and inhibition of NOS. Also, spermidine is a precursor to other polyamines, such as spermine and thermospermine, some of which contribute to tolerance against drought and salinity in plants.

Spermidine has been tested and discovered to encourage hair shaft elongation and lengthen hair growth. Spermidine has also been found to “upregulate expression of the epithelial stem cell-associated keratins K15 and K19, and dose-dependently modulated K15 promoter activity in situ and the colony forming efficiency, proliferation and K15 expression of isolated human K15-GFP+ cells in vitro.”

Biosynthesis of spermidine and spermine from putrescine. Ado = 5'-adenosyl.

Biochemical actions

Spermidine's known actions include:

• Inhibits neuronal nitric oxide synthase (nNOS)^[3]
• Binds and precipitates DNA^[4]
• Polyamine plant growth regulator^{[5][6][7][8][9][10][11]}

Sources

Good dietary sources of spermidine are aged cheese, mushrooms, soy products, legumes, corn, and whole grains.^[12]

Note - spermidine content varies by source and age. See ref for details.

In grains, the endosperm contains most of the spermidine. One of the best known grain dietary sources is wheat germ, containing as much as 243 mg/kg.^[13]

Uses

• Spermidine can be used in electroporation while transferring the DNA into the cell under the electrical impulse. May be used for purification of DNA-binding proteins.
• Spermidine is also used, along with calcium chloride, for precipitating DNA onto microprojectiles for bombardment with a gene gun.^[14]
• Spermidine has also been reported to protect the heart from aging and prolong the lifespan of mice, while in humans it was correlated with lower blood pressure.^[15] It also was found to reduce the amount of aging in yeast, flies, worms, and human immune cells by inducing autophagy.^[16] Recently Tirupathi Pichiah et al., suggested that spermidine may be helpful for treating type 2 diabetes.^[17]
• Spermidine is commonly used for in vitro molecular biology reactions, particularly, in vitro transcription by Phage RNA polymerases, in vitro transcription by human RNA polymerase II (in vitro transcription by human RNA polymerase II, and in vitro translation.
• Spermidine increases specificity and reproducibility of Taq-mediated PCR by neutralizing and stabilizing the negative charge on DNA phosphate backbone.
• Spermidine is a polycationic reagent that aids in enzyme digestion by forcing apart DNA molecules.

See also

• Norspermidine
• Spermine
• Putrescine

References

External links

• Safety Data Sheet