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β-Sitostenone

β-Sitostenone Suppliers list
Company Name: Stanford Chemicals Company  
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β-Sitostenone manufacturers

  • Sitostenone
  • Sitostenone pictures
  • $89.00
  • 2026-07-15
  • CAS:1058-61-3
  • Purity: 98.00%
  • Supply Ability: 10g
  • B-SITOSTENONE
  • B-SITOSTENONE pictures
  • 2025-12-24
  • CAS:1058-61-3
  • Min. Order: 1KG
  • Purity: 98.0%
  • Supply Ability: 10
β-Sitostenone Basic information
Product Name:β-Sitostenone
Synonyms:SITOSTENONE, BETA-;(24R)-24-Ethylcholest-4-en-3-one;3-Keto-β-cytostenol;3-Oxo-Δ4,5-sitosterone;4-Stigmasten-3-one;Nsc 49082;Stigmast-4-en-3-one (8ci)(9ci);SINOMENINE HYDROCHLORIDE (RG)
CAS:1058-61-3
MF:C29H48O
MW:412.69
EINECS:
Product Categories:Steroids
Mol File:1058-61-3.mol
β-Sitostenone Structure
β-Sitostenone Chemical Properties
Melting point 82 °C(Solv: methanol (67-56-1))
Boiling point 503.8±17.0 °C(Predicted)
density 0.97±0.1 g/cm3(Predicted)
solubility DMF: 0.33 mg/ml
Ethanol: Slightly soluble
form Solid
color White to off-white
LogP10.240 (est)
EPA Substance Registry SystemStigmast-4-en-3-one (1058-61-3)
Safety Information
MSDS Information
β-Sitostenone Usage And Synthesis
Usesβ-Sitostenone is a sterols that can be isolated from Cochlospermum vitifolium.β-Sitostenone inhibits tyrosinase activity, and has anti-melanogenic and anti-tumor activities[1][2][3].
DefinitionChEBI: Beta-sitostenone is a steroid and a C29-steroid. It has a role as a metabolite. It derives from a hydride of a stigmastane.
IC 50Human Endogenous Metabolite
References[1] Aguilar-Guadarrama AB, et al. Flavonoids, Sterols and Lignans from Cochlospermum vitifolium and Their Relationship with Its Liver Activity. Molecules. 2018 Aug 5;23(8):1952. DOI:10.3390/molecules23081952

[2] Chu CW, et al. Biofunctional Constituents from Michelia compressa var. lanyuensis with Anti-Melanogenic Properties. Molecules. 2015 Jul 3;20(7):12166-74. DOI:10.3390/molecules200712166

[3] Fan SQ, et al. Sarocladione, a unique 5,10:8,9-diseco-steroid from the deep-sea-derived fungus Sarocladium kiliense. Org Biomol Chem. 2019 Jun 18;17(24):5925-5928. DOI:10.1039/c9ob01159e
[4] SUPINYA TEWTRAKUL  Sanan S. Effects of compounds from Kaempferia parviflora on nitric oxide, prostaglandin E2 and tumor necrosis factor-alpha productions in RAW264.7 macrophage cells[J]. Journal of ethnopharmacology, 2008, 120 1: Pages 81-84. DOI: 10.1016/j.jep.2008.07.033

[5] KHINE SWE NYUNT. Isolation of antitrypanosomal compounds from Vitis repens, a medicinal plant of Myanmar.[J]. Natural Product Communications, 2012, 7 5: 609-610.


[6] De Souza, F.I., Zumiotti, A.V., and Da Silva, C.F. Neuregulins 1-α and 1-β on the regeneration the peripheral nerves[J]. Acta Ortop Bras.

[7] RUBY LISA ALEXANDER-LINDO  Muraleedharan G N  E Y St A Morrison. Hypoglycaemic effect of stigmast-4-en-3-one and its corresponding alcohol from the bark of Anacardium occidentale (cashew).[J]. Phytotherapy Research, 2004, 18 5: 403-407. DOI: 10.1002/ptr.1459
β-Sitostenone Preparation Products And Raw materials
Preparation Productsstigmast-4-ene-3,6-dione
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