taraxerol
taraxerol Basic information
- Product Name:
- taraxerol
- Synonyms:
-
- Alnulin
- D-Friedoolean-14-en-3β-ol
- Skimmiol
- Tiliadin
- (3β)-D-Friedoolean-14-en-3-ol
- (3β13α)-13-Methyl-27-norolean-14-en-3-ol
- 3β-Taraxerol
- Taraxero
- CAS:
- 127-22-0
- MF:
- C30H50O
- MW:
- 426.73
- Mol File:
- 127-22-0.mol
taraxerol Chemical Properties
- Melting point:
- 282-285°
- Boiling point:
- 490.7±44.0 °C(Predicted)
- Density
- 1.01±0.1 g/cm3(Predicted)
- storage temp.
- 4°C, protect from light
- solubility
- ≥ 40 mg/mL in DMSO
- pka
- 15.19±0.70(Predicted)
- form
- Solid
- color
- White
- Water Solubility
- insoluble in water
- Major Application
- food and beverages
- InChIKey
- GGGUGZHBAOMSFJ-GADYQYKKSA-N
- SMILES
- CC1(C)CC[C@]2(C)CC=C3[C@]4(C)CC[C@@]5([H])C(C)(C)[C@@H](O)CC[C@]5(C)[C@@]4([H])CC[C@@]3(C)[C@]2([H])C1
- LogP
- 11.060 (est)
taraxerol Usage And Synthesis
Chemical Properties
White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Aster tataricus, Bambusa chinensis, and Taraxacum officinale.
Uses
β-Taraxerol has potential application against novel coronavirus SARS-?CoV-?2, in silico approach to assess the inhibitory potential.
Definition
ChEBI: A pentacyclic triterpenoid that is oleanan-3-ol lacking the methyl group at position 14, with an alpha-methyl substituent at position 13 and a double bond between positions 14 and 15.
Synthesis
The use of efficient extraction method of dandelion root in dandelion racemosanol extraction and separation, including the following steps: (1) reflux method of dandelion root to 30% ~ 95% ethanol solution extraction 1 ~ 3 times, each time 1 ~ 3 hours, the extraction conditions preferably 75% of the ethanol solution extraction three times, each time 1 hour; (2) the combined extracts, concentrated under reduced pressure to the no-alcohol flavor, plus ethanol precipitation of polysaccharides, peptides, etc. (3) and then extracted with an equal volume of ethyl acetate or n-butanol for three times, the extract is concentrated to get the extract; (4) the extract is purified by silica gel column chromatography, reversed-phase column chromatography and other methods. Silica gel column chromatography: generally to petroleum ether - ethyl acetate or chloroform - methanol - water mixed solvent system gradient elution, reversed-phase silica gel column chromatography: commonly used C8 or C18, to gradient methanol and water gradient elution to get the compound dandelion Sai alcohol.
in vivo
Taraxerol (5 and 10mg/kg; i.p.) attenuates carrageenan induced paw edema. The effect of taraxerol at the dose of 5mg/kg is found to be significant (p<0.05) only after 4h of carrageenan treatment[2].
target
NO | PGE | TNF-α | IL Receptor | NF-kB | TGF-β/Smad | Akt
taraxerolSupplier
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taraxerol(127-22-0)Related Product Information
- Carboxyatractyloside
- Terrestrosin D
- taraxasteryl acetate
- Terrestrosin K
- dipotassium dihydrogen 15alpha-hydroxy-2beta-[[2-O-isovaleryl-3,4-di-O-sulphonato-beta-D-glucopyranosyl]oxy]kaur-16-ene-18,19-dioate
- roburic acid
- Taraxasterol
- (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
- Poricoic acid A(F)
- Madecassic acid
- Madecassoside
- ALLEOSIDE A
- Pachymic acid
- taraxerol acetate
- Dandelion extract