Taraxasterol Chemical Properties

Melting point:

221-222°

alpha 

D +96.3° (CHCl3)

Boiling point:

488.2±14.0 °C(Predicted)

Density 

1.00±0.1 g/cm3(Predicted)

solubility 

Ethanol : 5.5 mg/mL (12.89 mM; ultrasonic and warming and heat to 50°C)DMSO : 1 mg/mL (2.34 mM; ultrasonic and heat to 80°C)

form 

powder

pka

15.19±0.70(Predicted)

color 

White

InChIKey

XWMMEBCFHUKHEX-BUKJBVNQNA-N

SMILES

O[C@H]1CC[C@@]2([C@]3(CC[C@@]4([C@]5([C@@H](C(=C)CC[C@]5(C)CC[C@@]4(C)[C@]3(C)CC[C@@]2([H])C1(C)C)C)[H])[H])[H])C |&1:1,4,5,8,9,10,15,19,21,25,r|

Taraxasterol Usage And Synthesis

Chemical Properties

White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from bamboo leaves, inula flower, and dandelion.

Uses

4-Taraxasterol can be used to promote apoptosis in leukemic cells, as well as screening for antiviral activity against SARS-CoV-2 and related corona viruses.

Definition

ChEBI: A pentacyclic triterpenoid that is taraxastane with a beta-hydroxy group at position 3.

Taraxasterol(1059-14-9)Related Product Information

• dipotassium dihydrogen 15alpha-hydroxy-2beta-[[2-O-isovaleryl-3,4-di-O-sulphonato-beta-D-glucopyranosyl]oxy]kaur-16-ene-18,19-dioate
• Terrestrosin K
• taraxerol acetate
• (4aS,6aS,6aR,8aR,12aS,14aS,14bS)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4 a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one
• taraxerol
• Carboxyatractyloside
• Madecassoside
• Madecassic acid
• Pachymic acid
• Terrestrosin D
• taraxasteryl acetate
• Poricoic acid A(F)
• roburic acid
• ALLEOSIDE A
• LONICERAE JAPONICAE FLOS
• HOUTTUYNIAE HERBA
• Taraxasterol
• tercyclohexyl