Spermine-15N2

• Description:

  Spermine-15N2 (NSC 268508-15N2) is the 15N-labeled Spermine (HY-B1777) . Spermine is a natural antioxidant and anti-inflammatory agent. Spermine is known to inhibit some bacterial cultures, especially strains of Staphylococcus aureus. Spermine induces neurotoxicity in the striarum dose-dependently. Spermine can reversibly inhibits DNA synthetic response, mixed lymphocyte response and the induction of cytolytic lymphocyte response in primary cultures of murine spleen cells. Spermine tetrahydrochloride is a polyamine nitric oxide donor that can provide nitric oxide to platelets and inhibit platelet activation to a certain extent concentration-dependently. Spermine tetrahydrochloride occurs in mammalian tissues, plants, bacteria, ribosomes and bacteriophage. Spermine tetrahydrochloride inhibits primary human embryo lung fibroblasts in vitro[1][2][3][4][5][6].

• Product Name Alternative:

  NSC 268508-15N2; Neuridine-15N2

• UNSPSC:

  12352211

• Target:

  Bacterial; DNA/RNA Synthesis; Endogenous Metabolite; Isotope-Labeled Compounds; Reactive Oxygen Species (ROS)

• Related Pathways:

  Anti-infection; Cell Cycle/DNA Damage; Immunology/Inflammation; Metabolic Enzyme/Protease; NF-κB; Others

• Field of Research:

  Infection; Inflammation/Immunology; Neurological Disease

• Smiles:

  NCCC[15NH]CCCC[15NH]CCCN

• Molecular Formula:

  C10H26N2 15N2

• Molecular Weight:

  204.33

• References & Citations:

  [1]U. Bachrach & B. Reches, (1966) Enzymic assay for spermine and spermidine, Analytical Biochemistry, Volume 17, Issue 1, Volume 17, Issue 1, ISSN 0003-2697.|[2]Dawson, M., & Dryden, W. F. (1969) . The toxicity of spermine and spermidine to cells in culture. Biochemical pharmacology, 18 (6), 1307-1313. |[3]Byrd, W. J., et al., (1977) . Synthetic polyamines added to cultures containing bovine sera reversibly inhibit in vitro parameters of immunity. Nature, 267 (5612), 621–623. |[4]Løvaas, E., & Carlin, G. (1991) . Spermine: an anti-oxidant and anti-inflammatory agent. Free radical biology & medicine, 11 (5), 455-461.|[5]WANG Jing, et al., (2022) Preliminary Study on Spermine Tetrahydrochloride Inhibition of Platelet Activation[J]. JOURNAL OF CLINICAL TRANSFUSION AND LABORATORY MEDICINE, 2022, 24 (3) : 315-319.|[6]Otsuki, M., et al., (1995) . In vivo pharmacological study of spermine-induced neurotoxicity. Neuroscience letters, 196 (1-2), 81-84.

• Shipping Conditions:

  Room temperature

• Scientific Category:

  Isotope-Labeled Compounds

• Clinical Information:

  No Development Reported

• CAS Number:

  [93827-50-0]