Product name: Sitogluside

Synonym name: Beta-Sitosterol-D-glucoside;Daucosterol; Alexandrin; Daucosterin; Eleutheroside A
Catalogue No.: BP0524
Cas No.: 474-58-8
Formula: C₃₅H₆₀O₆
Mol Weight: 576.859
Botanical Source: many plants
Physical Description: Powder
Type of Compound: Steroids

Purity: 95%~99%
Analysis Method: HPLC-DAD or/and HPLC-ELSD
Identification Method: Mass, NMR
Packing: Brown vial or HDPE plastic bottle


The product can meet the large demand from grams to kilograms, and 90% of the products are in stock at kilogram level to meet the needs of food, cosmetics and health care products, please consult for details.

Inquire for bulk scale.

Descriptions:
Daucosterol can protect mice against disseminated candidiasis by the CD4+ Th1 immune response.[1]
Daucosterol has proliferation-enhancing activity for neural stem cells (NSCs), may be involved in IGF1-AKT pathway, and it as an efficient and inexpensive growth factor alternative that could be used in clinical medicine and research applications.[2]
Daucosterol exhibits moderate antibacterial activity against Bacillus subtilis and Staphylococcus aureus.[3]
Daucosterol can inhibit cancer cell proliferation by inducing autophagy through reactive oxygen species-dependent manner.[4]
Daucosterol has neuroprotective activity, could be potentially developed as a medicine for ischemic stroke treatment, can significantly reduce neuronal loss, as well as apoptotic rate and caspase-3 activity, increase the expression level of protein, diminish the down-regulation of p-AKT3 and p-GSK-3β4, thus activating the AKT5 signal pathway, diminish the down-regulation of the anti-apoptotic proteins Mcl-16 and Bcl-27, and decrease the expression level of the pro-apoptotic protein Bax8, thus raising the ratio of Bcl-2/Bax.[5]
Daucosterol has anti-cancer and apoptotic effects in human colon cancer cell line HCT-116, at different doses induces cell cycle arrest at sub-G1 phase of the cell cycle.[6]

References:
[1] Lee J H, Ju Y L, Ji H P, et al. Vaccine, 2007, 25(19):3834-40.
[2] Jiang L H, Yang N Y, Yuan X L, et al. J Steroid Biochem, 2014, 140(2):90-9.
[3] Sultana N, Afolayan A J. Nat Prod Res, 2007, 21(10):889-96.
[4] Zhao C, She T, Wang L, et al. Life Sci, 2015, 137:37-43.
[5] Jiang L H, Yuan X L, Yang N Y, et al. J Steroid Biochem 2015, 152:45-52.
[6] Wang G Q, Gu J F, Gao Y C, et al. Bangl J Pharmacol, 2016, 11(2).
[7] Hui-Ning L I, Liu H J, Xiao-Shuai F U, et al. 2013, 19(01):119-21.