CAS 24034-73-9
:Geranylgeraniol
Description:
Geranylgeraniol is a naturally occurring acyclic terpene alcohol, classified as a sesquiterpene. It is characterized by its long carbon chain, consisting of 20 carbon atoms and multiple double bonds, which contribute to its hydrophobic nature. Geranylgeraniol is colorless to pale yellow in appearance and has a characteristic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic properties. This compound plays a significant role in various biological processes, including serving as a precursor for the synthesis of other important biomolecules, such as carotenoids and certain hormones. Additionally, geranylgeraniol has been studied for its potential therapeutic effects, including anti-inflammatory and anticancer properties. Its role in cellular signaling pathways, particularly in relation to the prenylation of proteins, highlights its importance in biochemistry. Overall, geranylgeraniol is a versatile compound with significant implications in both natural product chemistry and pharmacology.
Formula:C20H34O
InChI:InChI=1/C20H34O/c1-16(2)9-7-11-18(5)13-14-20(21)15-19(6)12-8-10-17(3)4/h9-10,13,15,20-21H,7-8,11-12,14H2,1-6H3/b18-13+,19-15+
InChI key:InChIKey=OJISWRZIEWCUBN-QIRCYJPOSA-N
SMILES:C(\CC/C=C(/CCC=C(C)C)\C)(=C/CC/C(=C/CO)/C)/C
Synonyms:- (2E,6E,10E)-3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraen-1-ol
- (2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ol
- (6E,10E)-2,6,11,15-tetramethylhexadeca-2,6,10,14-tetraen-8-ol
- (E,E,E)-Geranylgeraniol
- (E,E,E)-Geranylgeranyl alcohol
- 2,6,10,14-Hexadecatetraen-1-ol, 3,7,11,15-tetramethyl-, (2E,6E,10E)-
- 2,6,10,14-Hexadecatetraen-1-ol, 3,7,11,15-tetramethyl-, (E,E,E)-
- All-trans-Geranylgeraniol
- Geranylgeraniol
- Geranylgeranyl alcohol
- trans,trans,trans-Geranylgeraniol
- trans-Geranylgeraniol
- 3,7,11,15-TETRAMETHYL-2,6,10,14-HEXADECATRAEN-1-OL
- all-E-Geranylgeraniol
- ALL TRANS GERANYL GERANIOL
- Geranylgeraniol (mixture of isomers)
- ALL TRANS-3,7,11,15-TETRAMETHYL-2,6,10,14-HEXADECATETRAEN-1-OL
- Geranylgeraniol (Natural)
- 3,7,11,15-TETRAMETHYL-2,6,10,14-HEXADECATETRAEN-1-OL
- (2E,6E,10E)-3,7,11,15-Tetramethylhexadecane-2,6,10,14-tetrene-1-ol
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 10 products.
2E,6E,10E-Geranylgeraniol
CAS:Formula:C20H34OPurity:85%Color and Shape:LiquidMolecular weight:290.4834(2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-Tetraen-1-Ol
CAS:(2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-Tetraen-1-OlPurity:95%Molecular weight:290.48g/molGeranylgeraniol
CAS:Geranylgeraniol (FT0626663) is an isoprenoid found in fruits, vegetables, and grains, including rice.Formula:C20H34OPurity:99.17% - ≥98%Color and Shape:SolidMolecular weight:290.48Geranylgeraniol (Natural)
CAS:Controlled Product<p>Stability Light Sensistive, Temperature Sensitive<br>Applications Geranylgeraniol, a precursor to Geranylgeranylpyrophosphate (G367600), is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-adsorption, inhibition of osteoclast formation, and kinase activation in vitro.<br>References Aiuchi, T., et al.: J. Biochem., 124, 300 (1998), Fisher, J.E., et al.: Proc. Natl. Acad. Sci. U.S.A. 96, 133 (1999), Montero, M.T., et al.: J. Immunol., 173, 4936 (2004), Campia, I., et al.: Br. J. Pharmacol., 158, 1777 (2009),<br></p>Formula:C20H34OColor and Shape:NeatMolecular weight:290.48Geranylgeraniol
CAS:<p>Intermediate in the mevalonate pathway for biosynthesis of vitamins E and K</p>Formula:C20H34OPurity:Min. 85 Area-%Color and Shape:Clear LiquidMolecular weight:290.48 g/molGeranylgeraniol (Natural) ~85%
CAS:Controlled ProductFormula:C20H34OPurity:~85%Color and Shape:NeatMolecular weight:290.48Geranylgeraniol (Synthetic)
CAS:Controlled Product<p>Applications Geranylgeraniol is a precursor to Geranylgeranylpyrophosphate (G367600), is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-adsorption, inhibition of osteoclast formation, and kinase activation in vitro.<br>References Aiuchi, T., et al.: J. Biochem., 124, 300 (1998); Fisher, J.E., et al.: Proc. Natl. Acad. Sci. U.S.A. 96, 133 (1999); Montero, M.T., et al.: J. Immunol., 173, 4936 (2004); Campia, I., et al.: Br. J. Pharmacol., 158, 1777 (2009)<br></p>Formula:C20H34OColor and Shape:NeatMolecular weight:290.48






