Taraxerol

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Names

[ CAS No. ]:
127-22-0

[ Name ]:
Taraxerol

[Synonym ]:
UNII-A32778O852
D-Friedoolean-14-en-3beta-ol
Isoolean-14-en-3b-ol
alnulin
(3S,4aR,6aR,8aR,12aR,12bS,14aR,14bR)-4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydro-3-picenol
3-Picenol, 1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-eicosahydro-4,4,6a,8a,11,11,12b,14b-octamethyl-, (3S,4aR,6aR,8aR,12aR,12bS,14aR,14bR)-
Skimmiol
D-friedoolean-14-en-3β-ol
Taraxerol
Tiliadin
(3S,4aR,6aR,6aS,8aR,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol
D-Friedoolean-14-en-3b-ol

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
490.7±44.0 °C at 760 mmHg

[ Melting Point ]:
282-285°

[ Molecular Formula ]:
C30H50O

[ Molecular Weight ]:
426.717

[ Flash Point ]:
217.7±20.7 °C

[ Exact Mass ]:
426.386169

[ PSA ]:
20.23000

[ LogP ]:
11.06

[ Vapour Pressure ]:
0.0±2.8 mmHg at 25°C

[ Index of Refraction ]:
1.539

[ Storage condition ]:
2-8℃

MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

Precursor & DownStream

Precursor

DownStream

  • 2,7-Dimethylnaphthalene
  • tetramethylbenzene
  • 1,2,5,6-Tetramethylnaphthalene
  • Naphthalene, 1,2,7-trimethyl-
  • 2,9-Dimethylpicene

Articles

A new taraxerol derivative from the roots of Microcos tomentosa.

Nat. Prod. Commun. 8(10) , 1371-2, (2013)

A new 3beta-O-vanilloyl-taraxerol, microcisin (1) and eight known compounds, 3beta-taraxerol acetate (2), 3beta-taraxerol (3), cholest-4-en-3-one (4), cholest-4-en-6beta-ol-3-one (5), beta-sitosterol ...

[Chemical constituents in the leave of Rhizophora stylosa L and their biological activities].

Yao Xue Xue Bao 43(9) , 974-8, (2008)

Ten compounds were isolated from the leaves of Rhizophora stylosa, one kind of mangrove plants distributed in the tropical and subtropical areas of the world. Their structures were identified as tarax...

Taraxerol inhibits LPS-induced inflammatory responses through suppression of TAK1 and Akt activation.

Int. Immunopharmacol. 15(2) , 316-24, (2013)

Taraxerol, a triterpenoid compound, has potent anti-inflammatory effects. However, the molecular mechanisms are not clear. In the study, taraxerol concentration dependently inhibited nitric-oxide synt...


More Articles


Related Compounds

  • Acetyl taraxerol
  • TARAXEROL,ACETATE
  • TARAXEROL,ACETATE
  • (3,4-Dihydroxy-5-methoxybenzoyl)taraxerol
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 3-Chloro-4-fluoro-5-methylphenylacetonitrile
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide