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tocotrienol, delta

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tocotrienol, delta Basic information

Product Name:
tocotrienol, delta
Synonyms:
  • D-δ-Tocotrienol
  • (2R)-2β,8-Dimethyl-2-[(3E,7E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-3,4-dihydro-2H-1-benzopyran-6-ol
  • (R)-3,4-Dihydro-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]-2H-1-benzopyran-6-ol
  • 2H-1-Benzopyran-6-ol, 3,4-dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-, (R-(E,E))-
  • D-δ-Tocotrienol,(R-(E,E))-3,4-Dihydro-2,8-dimethyl-2-(4,8,12-trimethyl-3,7,11-tridecatrienyl)-2H-1-benzopyran-6-ol
  • D-delta- Tocotrienol
  • Deltadelta-tocotrienol
  • tocotrienol, delta
CAS:
25612-59-3
MF:
C27H40O2
MW:
396.61
EINECS:
1308068-626-2
Mol File:
25612-59-3.mol
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tocotrienol, delta Chemical Properties

Boiling point:
517.3±39.0 °C(Predicted)
Density 
0.968±0.06 g/cm3(Predicted)
storage temp. 
−20°C
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Liquid
pka
10.69±0.40(Predicted)
color 
Pale Yellow to Orange
biological source
rice
Stability:
Light Sensitive
LogP
9.840 (est)
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Safety Information

WGK Germany 
2
HS Code 
29061990
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tocotrienol, delta Usage And Synthesis

Uses

δ-Tocotrienol is a natural substance with vitamin E activity. It can work as an antioxidant. It inhibits the growth of human breast cancer cells.

Definition

ChEBI: A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2 and 8 and a farnesyl chain at position 2.

Biological Activity

D-δ-Tocotrienol suppresses ras sarcoma (Ras) protein levels. It elicits anti-proliferative functionality in melanoma cells by halting cell cycle and favoring apoptosis. δ-Tocotrienol is cytotoxic to human lung adenocarcinoma and glioblastoma cancer cells. δ-Tocotrienol possesses anti-inflammatory, antidiabetic and neuroprotective functionality. It is an effective hypocholesterolemic agent and an inhibitor of lipid peroxidation.', 'Tocotrienols are widely utilized for their strong antioxidant properties. The various isoforms of tocotrienols differ in their methyl substitution in the chromanol head. δ-tocotrienol, effectively blocks cleavage of SREBPs, ultimately decreasing the amount of cholesterol synthesized in the liver.

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