Substance

ID:182517

Names and Identifiers
IUPAC Traditional name
spermine
IUPAC name
(3-aminopropyl)({4-[(3-aminopropyl)amino]butyl})amine
Synonyms
精素肌胺肝胺精胺N,N′-双(3-氨基丙基)-1,4-丁二胺Spermine
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Safety Information
GHS Signal Word
Danger
GHS Hazard statements
H314
Packing Group
2
GHS Pictograms
GHS05
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
RID/ADR
UN 3259 8/PG 2
Safety Statements
26-36/37/39-45
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements
P280-P305+P351+P338-P310
Risk Statements
34
Storage Temperature
2-8°C
RTECS
EJ7175000
Hazard Class
8
UN Number
3259
German water hazard class
3
European Hazard Symbols
Corrosive Corrosive (C)
Physical Property
Apperance
amorphous semi-solid
Boiling Point
150 °C/5 mmHg(lit.)
Flash Point
230 °F
110 °C
Solubility
H2O: soluble50 mg/mL
Melting Point
28-30(lit.)
Pharmacology Properties
Gene Information
human ... GRIN2B(2904)rat ... Grin2a(24409)
Product Information
Purity
≥96%
Suitability
suitable for cell culture
Molecule Details
Biochem/physiol Actions
Spermine together with putrescine and spermidine compose a family of polyamines (polycations) that are required for the growth and survival of the vast majority of living cells. Polyamines interact with negatively charged molecules such as proteoglycans, glycated proteins and nucleic acids (DNA and RNA). Biogenic polyamines are found to modulate protein synthesis at different levels. This effect may be explained by the ability of polyamines to bind and influence the secondary structure of tRNA, mRNA, and rRNA. Spermine also helps stabilize nucleic acid helical structure and the conformation of glycated proteins such as the histones. Spermine and spermidine are components of various nucleic acid transfection protocols.Mixed NMDA glutamate receptor agonist/antagonist at the polyamine site. Neuroprotective effects have been observed at high concentrations (1 mM), while neurotoxicity is observed at lower concentrations. It enhances agonist effectiveness at the strychnine-insensitive glycine site. Plays a role in cellular proliferation and differentiation; inhibits neuronal nitric oxide synthase (nNOS).
多胺位点混合型 NMDA 谷氨酸受体激动剂/拮抗剂。在高浓度 (1mM) 下观察到神经保护作用,而在低浓度下则观察到神经毒性。它在番木鳖碱-不敏感性甘氨酸位点能够增强激动剂效应。在细胞增殖和分化中发挥作用;抑制神经元一氧化氮合成酶 (nNOS)。
Molecular Spectra
No Data Available
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References
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