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Zeorin
Zeorin
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Zeorin
Price:
CAS No.: 22570-53-2
Catalog No.: CFN98222
Molecular Formula: C30H52O2
Molecular Weight: 444.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The roots of Tripterygium regelii
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Zeorin shows strong inhibition activity against bacteria and fungi. It markedly exhibits inhibitory activity on histamine release from mast cell induced by DNP24-BSA, it shows potent inhibitory effect by 40% decrease of histamine release.
Targets: Calcium Channel | ATPase | Histamine Receptor | Antifection
In vitro:
Fungal Biol. 2011 Apr-May;115(4-5):401-5.
Chemical taxonomy of Torrubiella s. lat.: zeorin as a marker of Conoideocrella.[Pubmed: 21530922]
The insect pathogens in the genus Torrubiella s. lat. were recently divided into new genera based on molecular phylogenetic characters.
METHODS AND RESULTS:
Isolates collected at various locations in Thailand, were tested for their productivity of a hopane-type triterpene, Zeorin (6α,22-dihydroxyhopane), when cultured in potato dextrose broth under static conditions. Among the 49 strains of Torrubiella s. lat. species, Conoideocrella luteorostrata (ten strains) and C. tenuis (seven strains), all collected on scale insects (Hemiptera), produced Zeorin, whereas another six strains of Orbiocrella petchii (which was recently removed from Torrubiella) failed in the detection of this secondary metabolite. All other Torrubiella s. lat. (26 strains), collected on other insect hosts including leafhoppers (eight strains), Lepidoptera (one strain), and spiders (17 strains), produced no detectable Zeorin. Paecilomyces cinnamomeus (nine strains), the anamorph of C. luteorostrata, also produced Zeorin.
CONCLUSIONS:
These results correspond with the recent taxonomic reclassification based on multigene phylogeny.
African journal of microbiology research.2010 Apr; 4:885-890.
Antimicrobial activity of the lichen Lecanora frustulosa and Parmeliopsis hyperopta and their divaricatic acid and zeorin constituents.[Reference: WebLink]

METHODS AND RESULTS:
Antibacterial and antifungal activity of the acetone, methanol and aqueous extracts of the lichen Lecanora frustulosa and Parmeliopsis hyperopta and their divaricatic acid and Zeorin constituents has been screened in vitro against the following species of microorganisms: Bacillus mycoides, Bacillus subtilis, Staphylococcus aureus, Enterobacter cloaceae, Escerichia coli, Klebsiella pneumoniae, Aspergillus flavus, Aspergillus fumigatus, Botrytis cinerea, Candida albicans, Fusarium oxysporum, Mucor mucedo, Paecilomyces variotii, Penicillium purpurescens, Penicillium verrucosum and Trichoderma harsianum.Divaricatic acid and Zeorin also showed strong activity against bacteria and fungi.
Zeorin Description
Source: The roots of Tripterygium regelii
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2487 mL 11.2435 mL 22.4871 mL 44.9741 mL 56.2177 mL
5 mM 0.4497 mL 2.2487 mL 4.4974 mL 8.9948 mL 11.2435 mL
10 mM 0.2249 mL 1.1244 mL 2.2487 mL 4.4974 mL 5.6218 mL
50 mM 0.045 mL 0.2249 mL 0.4497 mL 0.8995 mL 1.1244 mL
100 mM 0.0225 mL 0.1124 mL 0.2249 mL 0.4497 mL 0.5622 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Cell Research:
Int. J. Pharm. Clin. Res.,2015; 7(6):420 -5.
Effects of zeorin and dustanin isolated from Aegle marmelos correa on histamine released from RBL-2H3 cells.[Reference: WebLink]
Two compounds have been isolated from the leaves and stem barks of Aegle marmelos Correa. They were Zeorin (6,22-dihydroxyhopane) and dustanin (15,22-dihydroxyhopane). A. marmelos has an indication as anti-inflammatory and anti-allergy.
METHODS AND RESULTS:
In the study, these compounds were evaluated for their inhibitory effect on histamine release from mast cell culture, rat basophilic leukemia (RBL-2H3) cell line, a tumor analog of mast cells. Histamine release from mast cell was induced by DNP24-BSA and thapsigargin, an immunologic and non-immunologic inducers respectively. The histamine release was determined by using HPLC with fluorometric detector. In the study, only Zeorin markedly exhibited inhibitory activity on histamine release from mast cell induced by DNP24-BSA. Zeorin showed potent inhibitory effect by 40% decrease of histamine release. However, dustanin did not alter the histamine release from mast cells induced by thapsigargin. Based on the results, the inhibitory effect of Zeorin is contributed by some mechanisms related to alteration on intracellular Ca2+ concentration. Molecular docking was conducted to examine possible mechanisms of Zeorin and dustanin on Sarcoplasmic Reticulum Ca2+-ATPase. Our results suggest that Zeorin does not blockade the sarcoplasmic reticulum Ca2+-ATPase.
CONCLUSIONS:
In conclusion, Zeorin isolated from A. marmelos inhibited the histamine release from mast cell by some mechanisms related to alteration on intracellular Ca2+ concentration however might be not related to blokage on sarcoplasmic reticulum Ca2+-ATPase.
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