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|Size /Price /Stock
||10 mM * 1 mL in DMSO / $368 / In-stock||Other Packaging
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More articles cited ChemFaces products.
Environ Toxicol.2019, 34(12):1354-1362Viruses.2021, 13(11):2118. Sci Rep.2018, 8(1):12970Planta Med.2019, 85(9-10):766-773Nutrients.2021, 13(8):2901.Int J Mol Sci.2021, 22(19):10220.Life Sci.2021, 286:120019. Plant Archives2020, 2(1),2929-2934
J Ginseng Res.2022, 46(1):104-114. BMC Complement Med Ther. ...2020...Enzyme and Microbial Technology...2022...Exp Parasitol.2018, 194:67-78J Chromatogr A.2017, 1518:46-58Cell Prolif.2021, 54(8):e13083.Biochem Biophys Res Commun....2020...LWT2020, 124:109163
Int J Mol Sci.2020, 21(8):2790.Plant Foods Hum Nutr....2021...Food Chem.2022, 373(Pt B):131364.J Sci Food Agric.2021, Aug 21.Phytomedicine.2020, 79, 153351Molecules.2018, 23(12):E3103J Nat Sc Biol Med2019, 10(2):149-156
Our products had been exported to the following research institutions and universities, And still growing.
Universidade do Porto (Portugal)Korea Food Research Institute(K... (Korea)Instituto de Investigaciones Ag... (Chile)Leibniz-Institut für Pflanzenb... (Germany)
Biotech R&D Institute (USA)Yale University (USA)University of East Anglia (United Kingdom)Uniwersytet Medyczny w ?odzi (Poland)
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Universidade Estadual Paulista2017, 11449Applied Biological Chemistry 2021, 64(75)J Formos Med Assoc.2020, S0929-6646(20)30425-3Molecules.2022, 27(2):451.Chung Shan Medical University2020, US20200323790A1Natural Product Communications2020, doi: 10.1177.Sci Rep.2019, 9(1):18080Plant Cell Physiol.2018, 59(1):128-141Industrial Crops and Products2017, 95:286-295Chem Pharm Bull (Tokyo).2017, 65(9):826-832
Related Screening Libraries
||Ganodermanondiol exhibits potent cytoprotective effects on t-BHP-induced hepatotoxicity in human liver-derived HepG2 cells, presumably through Nrf2-mediated antioxidant enzymes and AMPK.
It also can significantly inhibit the proliferation of leukemic cancer cells, and it could be one of the antileukemie active constituents of Ganoderma lucidum. Ganodermanondiol shows a strong anticomplement activity against the classical pathway (CP) of the complement system with IC(50) values of 41.7 microM. It shows significant anti-human immunodeficiency virus (anti-HIV)-1 protease activity with IC50 values of 20-90 microM. |
||Nrf2 | HIV | AMPK|
|Food Chem Toxicol. 2013 Mar;53:317-24. |
|Protective effect of ganodermanondiol isolated from the Lingzhi mushroom against tert-butyl hydroperoxide-induced hepatotoxicity through Nrf2-mediated antioxidant enzymes.[Pubmed: 23266269]|
|Ganodermanondiol, a biologically active compound, was isolated from the Lingzhi mushroom (Ganoderma lucidum). The present study examined the protective effects of Ganodermanondiol against tert-butyl hydroperoxide (t-BHP)-induced hepatotoxicity. |
METHODS AND RESULTS:
Ganodermanondiol protected human liver-derived HepG2 cells through nuclear factor-E2-related factor 2 (Nrf2) pathway-dependent heme oxygenase-1 expressions. Moreover, Ganodermanondiol increased cellular glutathione levels and the expression of the glutamine-cysteine ligase gene in a dose-dependent manner. Furthermore, Ganodermanondiol exposure enhanced the phosphorylation of adenosine monophosphate-activated protein kinase (AMPK) and its upstream kinase activators, LKB1 and Ca(2+)/calmodulin-dependent protein kinase-II (CaMKII).
This study indicates that Ganodermanondiol exhibits potent cytoprotective effects on t-BHP-induced hepatotoxicity in human liver-derived HepG2 cells, presumably through Nrf2-mediated antioxidant enzymes and AMPK.
|Planta Med. 2001 Dec;67(9):811-4. |
|Anticomplement activity of terpenoids from the spores of Ganoderma lucidum.[Pubmed: 11745016]|
|A new lanostane-type terpenoid, lucidenic acid SP1 (1), was isolated from a CHCl(3)-soluble fraction of Ganoderma lucidum spores together with four other known compounds (2 - 5). The structure of lucidenic acid SP1 was determined to be 3 beta,7 beta-dihydroxy-4,4,14 alpha-trimethyl-11,15-dioxo-5 alpha-chol-8-en-24-oic acid by spectroscopic means including 2D-NMR.|
METHODS AND RESULTS:
Twelve triterpenes (1-12) isolated from G. lucidum spores were investigated in vitro for their anticomplementary activity. Compounds 1 - 5 were inactive, whereas ganoderiol F (8), Ganodermanondiol (9) and ganodermanontriol (10) showed a strong anticomplement activity against the classical pathway (CP) of the complement system with IC(50) values of 4.8, 41.7, and 17.2 microM, respectively. The potency of these triterpene alcohols (8-10) in inhibiting CP activity was improved when the number of hydroxymethyl groups on the side chain moiety is increased. On the other hand, the ganoderic acids 1-7, which contain a carboxyl group in the side chain, and lucidumols A and B (11, 12) had little activity on this system.
|Int J Mol Sci . 2016 Oct 27;17(11):1798. |
|Effects of Ganodermanondiol, a New Melanogenesis Inhibitor from the Medicinal Mushroom Ganoderma lucidum[Pubmed: 27801787]|
Ganoderma lucidum, a species of the Basidiomycetes class, has been attracting international attention owing to its wide variety of biological activities and great potential as an ingredient in skin care cosmetics including "skin-whitening" products. However, there is little information available on its inhibitory effect against tyrosinase activity. Therefore, the objectives of this study were to investigate the chemical composition of G. lucidum and its inhibitory effects on melanogenesis. We isolated the active compound from G. lucidum using ethanol extraction and ethyl acetate fractionation. In addition, we assayed its inhibitory effects on tyrosinase activity and melanin biosynthesis in B16F10 melanoma cells. In this study, we identified a bioactive compound, Ganodermanondiol, which inhibits the activity and expression of cellular tyrosinase and the expression of tyrosinase-related protein-1 (TRP-1), TRP-2, and microphthalmia-associated transcription factor (MITF), thereby decreasing melanin production. Furthermore, Ganodermanondiol also affected the mitogen-activated protein kinase (MAPK) cascade and cyclic adenosine monophosphate (cAMP)-dependent signaling pathway, which are involved in the melanogenesis of B16F10 melanoma cells. The finding that Ganodermanondiol from G. lucidum exerts an inhibitory effect on tyrosinase will contribute to the use of this mushroom in the preparation of skin care products in the future.
Keywords: B16F10 melanoma cell; Ganoderma lucidum; Ganodermanondiol; microphthalmia-associated transcription factor; tyrosinase; tyrosinase-related proteins.|
||The fruit body of Ganoderma lucidum.
||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
||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: firstname.lastname@example.org
||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.
ChemFaces New Products and Compounds
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. doi: 10.1016/j.cell.2017.12.019.IF=36.216(2019)PMID: 29328914
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.IF=22.415(2019)PMID: 32004475
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.IF=14.548(2019)PMID: 29149595
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.IF=13.903(2019)PMID: 29553709
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.IF=13.297(2019)PMID: 28005066
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.IF=12.804(2019)PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
* 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.
|Chem Pharm Bull (Tokyo). 1998 Oct;46(10):1607-12. |
|Triterpenes from the spores of Ganoderma lucidum and their inhibitory activity against HIV-1 protease.[Pubmed: 9810695]|
|Two new lanostane-type triterpenes, lucidumol A and ganoderic acid beta, were isolated from the spores of Ganoderma (G.) lucidum, together with a new natural one and seven that were known. The structures of the new triterpenes were determined as (24S)-24,25-dihydroxylanost-8-ene-3,7-dione and 3 beta,7 beta-dihydroxy-11,15-dioxolanosta-8,24(E)-dien-26-oic acid, respectively, by chemical and spectroscopic means. |
METHODS AND RESULTS:
The quantitative analyses of 5 fruiting bodies, antlered form and spores of G. lucidum were performed by high performance liquid chromatography and demonstrated that ganoderic alcohol and acid contents were quite high in the spore. Of the compound isolated, ganoderic acid beta, (24S)-lanosta-7,9(11)-diene-3 beta,24,25-triol (called lucidumol B), Ganodermanondiol, ganodermanontriol and ganolucidic acid A showed significant anti-human immunodeficiency virus (anti-HIV)-1 protease activity with IC50 values of 20-90 microM.