ChemFaces is a professional high-purity natural products manufacturer.
Product Intended Use
1. Reference standards
2. Pharmacological research
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Orders via your E-mail:
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Address: No. 83, CheCheng Rd., WETDZ, Wuhan, Hubei 430056, PRC
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1. Usually delivery time: Next day delivery by 9:00 a.m. Order now
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* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
More articles cited ChemFaces products.
J Chromatogr A. 2017 Oct 6;Mol Med Rep.2015 Sep 21J Ethnopharmacol. 2017 Jul 12;BMC Complement Altern Med.2017 Aug 3;Chemistr of plant2016021195
Sci Rep. 2017 Apr 11;The Korea Society of Pharmacognosy.2014Journal of Pharmaceutical Analysis2016 May 5; Evid Based Complement Alternat Med. 2017J Sep Sci.2018 Jan 23.
Tissue and Organ Culture (PCTOC)2016 Jun 28;Phytochemistry Letters2015 JuneGorana Nedin Rankovi?2017 Jan 15Fitoterapia. 2018 Jan;
Our products had been exported to the following research institutions and universities, And still growing.
Imperial College London (United Kingdom)University of Limpopo (South Africa)The Ohio State University (USA)Universitas Airlangga (Indonesia)
Uniwersytet Jagielloński w Krak... (Poland)University of Beira Interior (Portugal)Celltrion Chemical Research Inst... (Korea)Georgia Institute of Technology (USA)
Mahidol University (Thailand)National Research Council of Can... (Canada)Anna University (India)
Daphnicyclidin F Description
||The stems of Daphniphyllum humile and D.teijsmanni.
|Biological Activity or Inhibitors:
||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: email@example.com
||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.PMID: 29328914
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.PMID: 29149595
Scientific Reports 2017 Dec 11;7(1):17332.doi: 10.1038/s41598-017-17427-6.PMID: 29230013
Molecules. 2017 Oct 27;22(11). pii: E1829.doi: 10.3390/molecules22111829.PMID: 29077044
J Cell Biochem. 2018 Feb;119(2):2231-2239.doi: 10.1002/jcb.26385. PMID: 28857247
Phytomedicine. 2018 Feb 1;40:37-47. doi:10.1016/j.phymed.2017.12.030PMID: 29496173
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.
Daphnicyclidin F References Information
J Am Chem Soc. 2001 Nov 21;123(46):11402-8.
|Daphnicyclidins A-H, novel hexa- or pentacyclic alkaloids from two species of Daphniphyllum.[Pubmed: 11707117]|
|Eight highly modified Daphniphyllum alkaloids with unprecedented fused hexa- or pentacyclic skeletons, daphnicyclidin A,daphnicyclidin B, daphnicyclidin C, daphnicyclidin D, daphnicyclidin E, Daphnicyclidin F, daphnicyclidin G, daphnicyclidin H (1-8), have been isolated from the stems of Daphniphyllum humile and D.teijsmanni, and their structures were elucidated on the basis of spectroscopic data and chemical means. The stereochemistry was elucidated by combination of NOESY correlations, X-ray crystallographic data, and CD analyses.