Pentadecanoic acid (Standard)

• Description :

  α-Linolenic acid (Standard) is the analytical standard of α-Linolenic acid. This product is intended for research and analytical applications. α-Linolenic acid, isolated from Perilla frutescens, is an essential fatty acid that cannot be synthesized by humans. α-Linolenic acid can affect the process of thrombotic through the modulation of PI3K/Akt signaling. α-Linolenic acid possess the anti-arrhythmic properties and is related to cardiovascular disease and cancer[1].

• CAS Number :

  [1002-84-2]

• UNSPSC :

  12352211

• Hazard Statement :

  H315, H319, H335

• Target :

  Apoptosis; Caspase; Endogenous Metabolite; ERK; JAK; JNK; p38 MAPK; PPAR; Reference Standards; STAT

• Related Pathways :

  Apoptosis; Cell Cycle/DNA Damage; Epigenetics; JAK/STAT Signaling; MAPK/ERK Pathway; Metabolic Enzyme/Protease; Others; Protein Tyrosine Kinase/RTK; Stem Cell/Wnt; Vitamin D Related/Nuclear Receptor

• Applications :

  Metabolism-protein/nucleotide metabolism

• Field of Research :

  Cancer; Metabolic Disease

• Purity :

  99.92

• Smiles :

  O=C(CCCCCCCCCCCCCC)O

• Molecular Formula :

  C15H30O2

• Molecular Weight :

  242.40

• Precautions :

  H315, H319, H335

• References & Citations :

  [1]To N B, et al. Pentadecanoic acid, an odd-chain fatty acid, suppresses the stemness of MCF-7/SC human breast cancer stem-like cells through JAK2/STAT3 signaling[J]. Nutrients, 2020, 12 (6) : 1663.|[2]Wang J, et al. Pentadecanoic acid (C15: 0, PA) induces mild maternal glucose intolerance and promotes the growth of the offspring partly through up-regulating liver PPARα and MAPK signaling pathways[J]. Food & Function, 2024, 15 (23) : 11400-11414.

• Shipping Conditions :

  Blue Ice

• Storage Conditions :

  4°C, sealed storage, away from light and moisture

• Scientific Category :

  Reference Standards