ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
Citing Use of our Products
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* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
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
More articles cited ChemFaces products.
BMC Complement Altern Med.2014, 14:242Asian J Beauty Cosmetol...2016...Analytical sci. & Tech2016, 186-193Chem Biol Interact.2016, 258:59-68J Agric Food Chem.2016, 64(35):6783-90Nutrients.2017, 10(1)Acta horticulturae2017, 1158:257-268BMC Complement Altern Med....2017...
Cell Physiol Biochem....2017...Sci Rep.2017, 7:467-479Front Plant Sci.2017, 8:723Korean J. Medicinal Crop Sci....2018...J Sep Sci.2018, 41(7):1682-1690J Agric Food Chem.2018, 66(1):351-358The Japan Society for Analytical ...2018...Journal of Life Science2018, 917-922
Microb Pathog.2019, 131:128-134J Pharm Biomed Anal.2019, 164:119-127Molecules.2019, 24(21):E3834Saudi Pharm J.2019, 27(1):145-153J Sep Sci.2019, 42(21):3352-3362Comput Biol Chem.2019, 83:107096Biosci. Rep.2020, 10.1024
Our products had been exported to the following research institutions and universities, And still growing.
FORTH-IMBB (Greece)Charles Sturt University (Denmark)Korea Food Research Institute(K... (Korea)Universidad de Ciencias y Artes... (Mexico)
Weizmann Institute of Science (Israel)Istanbul University (Turkey)Charles University in Prague (Czech Republic)Michigan State University (USA)
Institute of Chinese Materia Me... (China)Max Rubner-Institut (MRI) (Germany)Stanford University (USA)
Related Screening Libraries
||Rediocide C exhibits antimycobacterial activity, with the MIC value of 3.84 uM; it also exhibits potent activity against D. pteronyssinus with respective LC50 values of 5.59 microg/cm2. |
|Chem Pharm Bull (Tokyo). 2005 Feb;53(2):241-3. |
|Acaricidal daphnane diterpenoids from Trigonostemon reidioides (KURZ) CRAIB roots.[Pubmed: 15684528]|
METHODS AND RESULTS:
A new daphnane diterpenoid, rediocide F (1), was isolated together with three known compounds, rediocides A (2), C (3) and E (4), from the hexane extract of Trigonostemon reidioides roots by bioassay-guided fractionation for acaricidal activity on Dermatophagoides pteronyssinus, Thai common house dust mite. The structure of rediocide F (1) was established as the demethyl analog of Rediocide C (3) on the basis of spectral analysis.
Compounds 1-4 exhibited potent activity against D. pteronyssinus with respective LC50 values of 2.53, 0.78, 5.59 and 0.92 microg/cm2.
Rediocide C Description
||The herbs of Trigonostemon reidioides (Kurz) Craib.
||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.
Recent 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.
|Tetrahedron , 2017,73( 12):1594–1601. |
|Terpenoids with potent antimycobacterial activity against Mycobacterium tuberculosis from Trigonostemon reidioides roots[Reference: WebLink]|
|Phytochemical investigation of Trigonostemon reidioides roots led to the isolation of fourteen compounds. These included six new diterpenoids, trigonoreidons A−F (1−6), together with eight known diterpenoids 7−14.
METHODS AND RESULTS:
The structures of the new compounds were elucidated by spectroscopic techniques and the absolute configuration at the asymmetric carbon was determined by the modified Mosher's method. The structure of trigonoreidon B (2) was confirmed by X-ray crystallographic analysis. The known compounds were identified by comparison of the spectroscopic and physical data with those of reported values. The isolated compounds were evaluated for antimycobacterial activity against Mycobacterium tuberculosis.
Among the compounds that exhibited antimycobacterial activity, the diterpenoids Rediocide C (12) and rediocide G (14) were the most active compounds, with the MIC value of 3.84 μM.