A-SPINASTEROL
A-SPINASTEROL Basic information
- Product Name:
- A-SPINASTEROL
- Synonyms:
-
- alpha-spinasterin
- spinasterol
- DELTA7-STIGMASTEROL
- (24R)-5α-Stigmasta-7,22-dien-3β-ol
- Hitdesterol
- (22E)-5α-Stigmasta-7,22-dien-3β-ol
- -amine D2
- HITODESTEROL
- CAS:
- 481-18-5
- MF:
- C29H48O
- MW:
- 412.69
- EINECS:
- 200-258-5
- Mol File:
- 481-18-5.mol
A-SPINASTEROL Chemical Properties
- Melting point:
- 168-169°
- alpha
- D25 -3.6° (c = 2.8 in chloroform)
- Boiling point:
- 500.0±44.0 °C(Predicted)
- Density
- 0.98±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- Chloroform (Slightly), Ethyl Acetate (Slightly, Heated), Methanol (Slightly, Heated)
- form
- Solid
- pka
- 15.10±0.70(Predicted)
- color
- White to Off-White
- biological source
- Aster scaber
- Stability:
- Light Sensitive
A-SPINASTEROL Usage And Synthesis
Uses
α-Spinasterol was identified as a novel transient receptor potential vanilloid 1 antagonist with antinociceptive properties.
Definition
ChEBI: Alpha-Spinasterol is a steroid. It derives from a hydride of a stigmastane.
Biological Activity
α-Spinasterol is a blood-brain barrier-permeable and orally active plant phytosterol with antioxidant, anticonvulsant (0.1-1 mg/kg i.p. in mice), antidepressant (1-2 mg/kg i.p. in mice) and anti-inflammatory (0.001-1 mg/kg, i.p. or 1-10 mg/kg, i.g. in mice) properties, as well as antinociceptive efficacy via dual actions against transient receptor potential vanilloid 1 (TrpV1; IC50/Emax = 1.4 μM/67% against 2 nM RTX for binding mouse spinal cord membranes; IC50/Emax = 40 μM/62% against 20 μM capsaicin-induced mouse spinal cord synaptosomes Ca2+ influx) and cyclooxygenases (IC50 = 16.17 μM/COX1 and 7.76μM/COX2). a-spinasterol can directly affect membrane structure and packing in a manner similar to cholesterol, both a-spinasterol and stitosterol are reported to lower plasma/liver cholesterol levels and increase fecal cholesterol excretion when supplemented in daily diet (1%) in mice in vivo.', 'α-Spinasterol is a constituent of argan oil. It regulates nuclear receptors expression and modulates mitochondrial function. It mimics natural cholesterol and its functionality. α-Spinastero lelicits cytoprotective and antiulcerogenic functionality. It has therapeutic potential towards diabetic nephropathy.
target
TRPV | HMG-CoA reductase
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A-SPINASTEROL(481-18-5)Related Product Information
- ALLEOSIDE A
- Bufa-20,22-dienolide, 3,5,14-trihydroxy-19-oxo-, (3beta,5beta)-
- poricoic acid A 3-methyl ester
- 22,25-Epoxy-2,3,14,20-tetrahydroxycholest-7-en-6-one
- Resibufogenin
- Bufotaline
- (3beta,25R)-14-Hydroxyspirost-5-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-2)-O-[beta-D-xylopyranosyl-(1-4)]-beta-D-glucopyranoside
- Bufalin
- Hydroxyecdysone
- beta-Sitosterol
- Stigmasterol
- A-SPINASTEROL
- 1 19-EICOSADIENE