Pentadecanoic acid (Standard)

CAT: 0804-HY-W004283R-01Size: 50 mgDry Ice: NoHazardous: No
CAT#:0804-HY-W004283R-01Size:50 mg
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AVAILABILITY: InStock
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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

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