3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol

3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol
Compound Structure:
Synonyms: Geranyllinalool;Geranyl linalool;1113-21-9;3,7,11,15-Tetramethyl-1,6,10,14-hexadecatetraen-3-ol;(E,E)-geranyllinalool;3,7,11,15-Tetramethylhexadeca-1,6,10,14-tetraen-3-ol;(6E,10E)-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-ol
Compound ID: NMPC-324
PubChem ID:

5365872

Molecular Formula: C20H34O
Canonical SMILES: CC(=CCCC(=CCCC(=CCCC(C)(C=C)O)C)C)C
InChIKey: IQDXAJNQKSIPGB-HQSZAHFGSA-N
About the compound:

Geranyllinalool is a diterpenoid compound with a structure derived from linalool, a common fragrance compound. Geranyllinalool is derived from linalool by substituting one of the terminal methyl hydrogens with a geranyl group. It exists in the 6E,10E-geometric isomer form. It belongs to the chemical class of diterpenoids, which are natural compounds made up of four isoprene units. Diterpenoids are known for their diverse biological activities and are often found in plants and some microorganisms. Like linalool, it contributes to fragrance and aroma. Its scent profile is likely influenced by the combination of linalool and geranyl components. It functions as an inhibitor of the enzyme serine C-palmitoyltransferase, which plays a role in lipid metabolism. Geranyllinalool's role as a fragrance compound suggests its use in perfumery and scented products. Its biological activities and potential enzymatic inhibitory effects make it an interesting compound for further research, particularly in the context of lipid metabolism and other physiological processes.

GHS Hazard Statements

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

H319 (31.81%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]

H335 (41.48%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]


Properties:
Source Species: Artocarpus altilis.
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