Basic information Safety Supplier Related

(3beta,24S)-stigmast-5-en-3-ol

Basic information Safety Supplier Related

(3beta,24S)-stigmast-5-en-3-ol Basic information

Product Name:
(3beta,24S)-stigmast-5-en-3-ol
Synonyms:
  • (3beta,24S)-stigmast-5-en-3-ol
  • (3b,24S)-stigmast-5-en-3-ol
  • Clionasterol
  • gamma-sitosterol
  • (24S)-Stigmast-5-en-3β-ol
  • 22,23-Dihydroporiferasterol
  • beta-Dihydrofucosterol
  • Einecs 201-481-1
CAS:
83-47-6
MF:
C29H50O
MW:
414.71
EINECS:
201-481-1
Mol File:
83-47-6.mol
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(3beta,24S)-stigmast-5-en-3-ol Chemical Properties

Boiling point:
473.52°C (rough estimate)
Density 
0.9540 (rough estimate)
refractive index 
1.5000 (estimate)
Melting point:
147 °C
pka
15.03±0.70(Predicted)
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(3beta,24S)-stigmast-5-en-3-ol Usage And Synthesis

Uses

γ-Sitosterol is an inhibitor for c-Myc. γ-Sitosterol inhibits the proliferation of cancer cell MCF-7 and A549 with IC50 of 240.73 μg/mL and 696.6 μg/mL, arrests the cell cycle at G2/M phase, and induces apoptosis. γ-Sitosterol upregulates the expression of cell cycle regulators cyclin B/E[1].

Definition

ChEBI: Clionasterol is a member of the class of phytosterols that is poriferast-5-ene carrying a beta-hydroxy substituent at position 3. It has a role as a plant metabolite and a marine metabolite. It is a 3beta-sterol, a member of phytosterols and a 3beta-hydroxy-Delta(5)-steroid. It derives from a hydride of a poriferastane.

References

[1] Sundarraj S, et al., γ-Sitosterol from Acacia nilotica L. induces G2/M cell cycle arrest and apoptosis through c-Myc suppression in MCF-7 and A549 cells. J Ethnopharmacol. 2012 Jun 14;141(3):803-9. DOI:10.1016/j.jep.2012.03.014

(3beta,24S)-stigmast-5-en-3-ol Supplier

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