Guggulsterone Z

Broad spectrum steroid receptor ligand. Antagonizes FXR and displays hypolipidemic activity CAS# 95975-55-6

Guggulsterone Z

Catalog No. BCN3793----Order now to get a substantial discount!

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Quality Control of Guggulsterone Z

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Chemical structure

Guggulsterone Z

3D structure

Chemical Properties of Guggulsterone Z

Cas No. 95975-55-6 SDF Download SDF
PubChem ID 13873622 Appearance Powder
Formula C21H28O2 M.Wt 312.5
Type of Compound Steroids Storage Desiccate at -20°C
Solubility DMSO : 20.83 mg/mL (66.67 mM; Need ultrasonic)
Chemical Name (17Z)-17-ethylidene-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthrene-3,16-dione
SMILES CC=C1C(=O)CC2C1(CCC3C2CCC4=CC(=O)CCC34C)C
Standard InChIKey WDXRGPWQVHZTQJ-AYSLTRBKSA-N
Standard InChI InChI=1S/C21H28O2/c1-4-16-19(23)12-18-15-6-5-13-11-14(22)7-9-20(13,2)17(15)8-10-21(16,18)3/h4,11,15,17-18H,5-10,12H2,1-3H3/b16-4+
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Guggulsterone Z

The herbs of Ailanthus grandis

Biological Activity of Guggulsterone Z

DescriptionGuggulsterone E&Z is a natural product from Ailanthus grandis, it did not show antimicrobial activity.
In vitro

Antimicrobial Activity of Guggulsterone E and Z[Reference: WebLink]

Int.J.Curr.Microbiol.App.Sci.,2016,5(10):20-6.

Guggulsterone is a main active compound of gum guggul, which has commonly used as ant-inflammatory, hepatoprotective, muscle relaxing, anti-arthritic, hypolipidemic, hypocholestrolemic and anti-obesity.
METHODS AND RESULTS:
In the present study, its antimicrobial activity of Guggulsterone E&Z against five microorganisms i.e. Escherichia coli (Wild), E. Cole (DH5α), Micrococcus luteus, Staphylococcus aureus and Bacillus subtilis were undertaken. Disc diffusion method was used for antimicrobial activity assessment of compound Guggulsterone E&Z . The discs were impregnated with 100 and 200 μg per disc and exposed to culture bed of five test organism i.e. E. coli (Wild), E. coli (DH5α), M. luteus, S. aureus and B. subtilis.
CONCLUSIONS:
After 24 hours of incubation at 37 °C, it was observed that the Guggulsterone E&Z did not show any inhibition zone against the all five test organisms.

Protocol of Guggulsterone Z

Structure Identification
Pharmacognosy Journal, 2013 , 5 (6) :259-264.

Development of HPTLC method for estimation of piperine, guggulsterone E and Z in polyherbal formulation[Reference: WebLink]

The different batches of formulation were prepared in laboratory by using authenticated raw material and were subjected to various physical and chemical evaluations. Then the prepared formulation and three commercial formulations were investigated for the qualitative and quantitative estimation of mentioned constituents.
METHODS AND RESULTS:
The methanolic extract of all formulations were quantified by using HPTLC studies. Linear regression data for the calibration curves of standards viz. piperine, guggulsterone E and Z showed a good linear relationship over a concentration range of 0.06–0.14 μg/spot, 2.5–17.5 μg/spot, 5–30 μg/spot respectively with the correlation coefficient of 0.99085, 0.99847, 0.9990 respectively and thus exhibits good linearity between concentration and area. The content of guggulsterone E (14.68 %w/w, 13.05 %w/w, 6.36 %w/w, 14.36 %w/w); guggulsterone Z (31.81 %w/w, 26.95 %w/w, 11.62 %w/w, 23.86 %w/w); and piperine (0.068 %w/w, 0.0150 %w/w, 0.321 %w/w, 0.0375 %w/w) were found in TF, TN, TM, TP prepared and three marketed formulation respectively.
CONCLUSIONS:
The proposed HPTLC method was found to be rapid, simple and linear for quantitative estimation of piperine, Guggulsterone E&Z in different formulations and extracts.

Guggulsterone Z Dilution Calculator

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Guggulsterone Z Molarity Calculator

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Preparing Stock Solutions of Guggulsterone Z

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.2 mL 16 mL 32 mL 64 mL 80 mL
5 mM 0.64 mL 3.2 mL 6.4 mL 12.8 mL 16 mL
10 mM 0.32 mL 1.6 mL 3.2 mL 6.4 mL 8 mL
50 mM 0.064 mL 0.32 mL 0.64 mL 1.28 mL 1.6 mL
100 mM 0.032 mL 0.16 mL 0.32 mL 0.64 mL 0.8 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Guggulsterone Z

Development of HPTLC method for estimation of piperine, guggulsterone E and Z in polyherbal formulation

Pharmacognosy Journal, 2013 , 5 (6) :259-264.

The different batches of formulation were prepared in laboratory by using authenticated raw material and were subjected to various physical and chemical evaluations. Then the prepared formulation and three commercial formulations were investigated for the qualitative and quantitative estimation of mentioned constituents. The methanolic extract of all formulations were quantified by using HPTLC studies. Linear regression data for the calibration curves of standards viz. piperine, guggulsterone E and Z showed a good linear relationship over a concentration range of 0.06–0.14 μg/spot, 2.5–17.5 μg/spot, 5–30 μg/spot respectively with the correlation coefficient of 0.99085, 0.99847, 0.9990 respectively and thus exhibits good linearity between concentration and area. The content of guggulsterone E (14.68 %w/w, 13.05 %w/w, 6.36 %w/w, 14.36 %w/w); Guggulsterone Z (31.81 %w/w, 26.95 %w/w, 11.62 %w/w, 23.86 %w/w); and piperine (0.068 %w/w, 0.0150 %w/w, 0.321 %w/w, 0.0375 %w/w) were found in TF, TN, TM, TP prepared and three marketed formulation respectively. Conclusion The proposed HPTLC method was found to be rapid, simple and linear for quantitative estimation of piperine, Guggulsterone E&Z in different formulations and extracts.

Description

Guggulsterone is a plant sterol derived from the gum resin of the tree Commiphora wightii. Guggulsterone inhibits the growth of a wide variety of tumor cells and induces apoptosis through down regulation of antiapoptotic gene products (IAP1, xIAP, Bfl-1/A1, Bcl-2, cFLIP and survivin), modulation of cell cycle proteins (cyclin D1 and c-Myc), activation of caspases and JNK, inhibition of Akt. Guggulsterone, a farnesoid X receptor (FXR) antagonist, decreases CDCA-induced FXR activation with IC50s of 17 and 15 μM for Z- and E-Guggulsterone, respectively.

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