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Ganoderic acid T-Q

CAS# 112430-66-7

Ganoderic acid T-Q

Catalog No. BCN3209----Order now to get a substantial discount!

Product Name & Size Price Stock
Ganoderic acid T-Q: 5mg $828 In Stock
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Quality Control of Ganoderic acid T-Q

Number of papers citing our products

Chemical structure

Ganoderic acid T-Q

3D structure

Chemical Properties of Ganoderic acid T-Q

Cas No. 112430-66-7 SDF Download SDF
PubChem ID 10436380 Appearance Powder
Formula C32H46O5 M.Wt 510.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (E,6R)-6-[(5R,10S,13R,14R,15S,17R)-15-acetyloxy-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid
SMILES CC(CCC=C(C)C(=O)O)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)OC(=O)C
Standard InChIKey JVABUELIHJXLKP-JBOPJBCTSA-N
Standard InChI InChI=1S/C32H46O5/c1-19(10-9-11-20(2)28(35)36)24-18-27(37-21(3)33)32(8)23-12-13-25-29(4,5)26(34)15-16-30(25,6)22(23)14-17-31(24,32)7/h11-12,14,19,24-25,27H,9-10,13,15-18H2,1-8H3,(H,35,36)/b20-11+/t19-,24-,25+,27+,30-,31-,32-/m1/s1
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 Ganoderic acid T-Q

The fruit body of Ganoderma lucidum

Biological Activity of Ganoderic acid T-Q

DescriptionGanoderic acid T-Q and TR are two inhibitors of H5N1 and H1N1 NAs.
TargetsH5N1 | H1N1
In vitro

Inhibition of neuraminidase by Ganoderma triterpenoids and implications for neuraminidase inhibitor design.[Reference: WebLink]

Scientific Reports, 2015, 5:13194.

Neuraminidase (NA) inhibitors are the dominant antiviral drugs for treating influenza in the clinic. Increasing prevalence of drug resistance makes the discovery of new NA inhibitors a high priority.
METHODS AND RESULTS:
Thirty-one triterpenoids from the medicinal mushroom Ganoderma lingzhi were analyzed in an in vitro NA inhibition assay, leading to the discovery of Ganoderic acid T-Q and TR as two inhibitors of H5N1 and H1N1 NAs. Structure-activity relationship studies revealed that the corresponding triterpenoid structure is a potential scaffold for the design of NA inhibitors. Using these triterpenoids as probes we found, through further in silico docking and interaction analysis, that interactions with the amino-acid residues Arg292 and/or Glu119 of NA are critical for the inhibition of H5N1 and H1N1.
CONCLUSIONS:
These findings should prove valuable for the design and development of NA inhibitors.

Protocol of Ganoderic acid T-Q

Structure Identification
Journal of Natural Medicines,2018, 72(3):734-744.

Changes in content of triterpenoids and polysaccharides in Ganoderma lingzhi at different growth stages.[Reference: WebLink]

Ganoderma lingzhi is a traditional medicinal mushroom, and its extract contains many bioactive compounds. Triterpenoids and polysaccharides are the primary bioactive components that contribute to its medicinal properties.
METHODS AND RESULTS:
In this study, we quantified 18 triterpenoids, total triterpenoid content and total polysaccharide content in the ethanol and water extracts of G. lingzhi at different growth stages. Triterpenoids were quantified by liquid chromatograph-tandem mass spectrometry in the multiple-reaction-monitoring mode. Total triterpenoid and total polysaccharide content were determined by colorimetric analysis. The results indicated that the fruit bodies at an early growth stage had a higher content of ganoderic acid A, C2, I and LM2, as well as of ganoderenic acid C and D, than those at a later growth stage. In contrast, ganoderic acid K, ganoderic acid TN and Ganoderic acid T-Q contents were higher in mature fruit bodies (maturation stage). The highest total triterpenoid and total polysaccharide contents were found in fruit bodies before maturity (stipe elongation stage or early stage of pileus formation).
CONCLUSIONS:
Our results provide information which will contribute to the establishment of an efficient cultivation system for G. lingzhi with a higher content of triterpenoids.

Ganoderic acid T-Q Dilution Calculator

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Ganoderic acid T-Q Molarity Calculator

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Preparing Stock Solutions of Ganoderic acid T-Q

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.9581 mL 9.7905 mL 19.581 mL 39.1619 mL 48.9524 mL
5 mM 0.3916 mL 1.9581 mL 3.9162 mL 7.8324 mL 9.7905 mL
10 mM 0.1958 mL 0.979 mL 1.9581 mL 3.9162 mL 4.8952 mL
50 mM 0.0392 mL 0.1958 mL 0.3916 mL 0.7832 mL 0.979 mL
100 mM 0.0196 mL 0.0979 mL 0.1958 mL 0.3916 mL 0.4895 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 Ganoderic acid T-Q

Tubulin polymerization-stimulating activity of Ganoderma triterpenoids.[Pubmed:28078535]

J Nat Med. 2017 Apr;71(2):457-462.

Tubulin polymerization is an important target for anticancer therapies. Even though the potential of Ganoderma triterpenoids against various cancer targets had been well documented, studies on their tubulin polymerization-stimulating activity are scarce. This study was conducted to evaluate the effect of Ganoderma triterpenoids on tubulin polymerization. A total of twenty-four compounds were investigated using an in vitro tubulin polymerization assay. Results showed that most of the studied triterpenoids exhibited microtuble-stabilizing activity to different degrees. Among the investigated compounds, Ganoderic acid T-Q, ganoderiol F, ganoderic acid S, ganodermanontriol and ganoderic acid TR were found to have the highest activities. A structure-activity relationship (SAR) analysis was performed. Extensive investigation of the SAR suggests the favorable structural features for the tubulin polymerization-stimulating activity of lanostane triterpenes. These findings would be helpful for further studies on the potential mechanisms of the anticancer activity of Ganoderma triterpenoids and give some indications on the design of tubulin-targeting anticancer agents.

Inhibition of neuraminidase by Ganoderma triterpenoids and implications for neuraminidase inhibitor design.[Pubmed:26307417]

Sci Rep. 2015 Aug 26;5:13194.

Neuraminidase (NA) inhibitors are the dominant antiviral drugs for treating influenza in the clinic. Increasing prevalence of drug resistance makes the discovery of new NA inhibitors a high priority. Thirty-one triterpenoids from the medicinal mushroom Ganoderma lingzhi were analyzed in an in vitro NA inhibition assay, leading to the discovery of Ganoderic acid T-Q and TR as two inhibitors of H5N1 and H1N1 NAs. Structure-activity relationship studies revealed that the corresponding triterpenoid structure is a potential scaffold for the design of NA inhibitors. Using these triterpenoids as probes we found, through further in silico docking and interaction analysis, that interactions with the amino-acid residues Arg292 and/or Glu119 of NA are critical for the inhibition of H5N1 and H1N1. These findings should prove valuable for the design and development of NA inhibitors.

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