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Spermine

Cat. No. M9387
Spermine Structure
Synonym:

Neuridine

Size Price Availability Quantity
100mg USD 40  USD40 In stock
500mg USD 80  USD80 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
  • Purity: >98%, for cell culture
  • COA
  • MSDS
Biological Activity

Spermine is a biogenic polyamine formed from spermidine and occurs in almost all tissues. It is essential for both neoplastic and normal tissue growth and is involved in the modulation of calcium-dependent immune processes. Spermine inhibits NOS1 (nNOS). Spermine binds to and activates NMDA and has been shown to potentiate NMDA-induced currents in a concentration-dependent manner. Spermine is a GluR inhibitor.

Chemical Information
Molecular Weight 202.34
Formula C10H26N4
CAS Number 71-44-3
Solubility (25°C) Water ≥ 50 mg/mL
Storage 2-8°C, dry, protect from light, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Md Mahadi Hasan, et al. Spermine: Its Emerging Role in Regulating Drought Stress Responses in Plants

[2] Melissa M Cadelis, et al. Spermine Derivatives of Indole-3-carboxylic Acid, Indole-3-acetic Acid and Indole-3-acrylic Acid as Gram-Negative Antibiotic Adjuvants

[3] Mozhgan Mohammadi, et al. Spermine as a possible endogenous allosteric activator of carboxypeptidase A: multispectroscopic and molecular simulation studies

[4] Silvia Grancara, et al. Bidirectional fluxes of spermine across the mitochondrial membrane

[5] R Amendola, et al. Spermine metabolism and anticancer therapy

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