4-O-Feruloylquinic acid | CAS:2613-86-7

4-O-Feruloylquinic acid

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More articles cited ChemFaces products.

J Basic Clin Physiol Pharmacol.2015 Aug 15

Journal of Medicinal Plant Research.2013 Nov 7

J Ethnopharmacol. 2017 Feb 2;

Food Chem. 2017 Apr 15;

Current Pharmaceutical AnalysisIssue 5, 2017

Sci Rep. 2017 Dec 11;

J Pharm Biomed Anal.2018 Mar 20;

Jou. of Agromedicine and Med. Sci.2018;

Molecules 2016, 21(6), 739;2016 Jun 14;21(6).

Sci Rep. 2017 Jun 12;

Molecules. 2017 Feb 8;

J Ethnopharmacol. 2017 Feb 23;

Am J Chin Med.2015 Jul 30:1-22.

Evid Based Complement Alternat Med. 2017:6360836.

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Our products had been exported to the following research institutions and universities, And still growing.

Medizinische Universit?t Wien (Austria)

Max-Planck-Insitut (Germany)

Lodz University of Technology (Poland)

University of Toulouse (France)

Chinese University of Hong Kong (China)

John Innes Centre (United Kingdom)

University of Illinois at Chicago (USA)

University of Hull (United Kingdom)

Stanford University (USA)

Imperial College London (United Kingdom)

Mendel University in Brno (Czech Republic)

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Description:

4-O-Feruloylquinic acid can be useful for the prevention of cardiovascular and other chronic diseases.

Targets:

H5N1

In vitro:

Phytochem Anal. 2007 May-Jun;18(3):213-8.

Isolation of chlorogenic acids and their derivatives from Stemona japonica by preparative HPLC and evaluation of their anti-AIV (H5N1) activity in vitro.[Pubmed: 17500364]

Two chlorogenic acids and five chlorogenic acid derivatives were simultaneously separated and purified from Stemona japonica by preparative high-performance liquid chromatography.
METHODS AND RESULTS:
Five of the collected compounds were over 95% pure while the other two compounds were over 90% pure. Their structures were elucidated as 3-O-feruloylquinic acid (1), 4-O-Feruloylquinic acid (2), methyl 3-O-feruloylquinate (3), methyl 5-O-caffeyolquinate (4), methyl 4-O-feruloylquinate (5), ethyl 3-O-feruloylquinate (6) and the new compound ethyl 4-O-feruloylquinate (7) by UV, NMR and ESI-MS. All compounds were obtained from Stemona species for the first time, however compounds 6 and 7 are believed to be artefacts from the ethanol extraction. The anti-AIV (H5N1) activities were evaluated by Neutral Red uptake assay.
CONCLUSIONS:
Compounds 3 and 4 exerted moderate inhibitory effect against AIV (H5N1) in vitro.

4-O-Feruloylquinic acid Description

Source:	The fruits of Coffea canephorra var. Robusta
Solvent:	DMSO, Pyridine, Methanol, Ethanol, 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.

Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

More...

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.2017.12.030

PMID: 29496173

CAS No.	2613-86-7	Price	$448 / 5mg
Catalog No.	CFN92392	Purity	>=98%
Molecular Weight	368.3	Type of Compound	Phenylpropanoids
Formula	C₁₇H₂₀O₉	Physical Description	Powder
Download	Manual COA MSDS	Similar structural	Comparison (Web)

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.7152 mL	13.5759 mL	27.1518 mL	54.3036 mL	67.8794 mL
5 mM	0.543 mL	2.7152 mL	5.4304 mL	10.8607 mL	13.5759 mL
10 mM	0.2715 mL	1.3576 mL	2.7152 mL	5.4304 mL	6.7879 mL
50 mM	0.0543 mL	0.2715 mL	0.543 mL	1.0861 mL	1.3576 mL
100 mM	0.0272 mL	0.1358 mL	0.2715 mL	0.543 mL	0.6788 mL

CFN99116	Chlorogenic acid	327-97-9	354.31	C₁₆H₁₈O₉
CFN92573	3-O-Caffeoylquinic acid methyl ester	123483-19-2	368.3	C₁₇H₂₀O₉
CFN92393	3-O-Feruloylquinic acid	1899-29-2	368.3	C₁₇H₂₀O₉
CFN92446	Methyl 3-O-feruloylquinate	154418-15-2	382.4	C₁₈H₂₂O₉
CFN92529	Cyclohexanecarboxylic acid	327161-03-5	354.3	C₁₆H₁₈O₉
CFN99117	Cryptochlorogenic acid	905-99-7	354.31	C₁₆H₁₈O₉
CFN92528	Methyl 4-caffeoylquinate	123372-74-7	368.3	C₁₇H₂₀O₉
CFN92392	4-O-Feruloylquinic acid	2613-86-7	368.3	C₁₇H₂₀O₉
CFN97472	Neochlorogenic acid	906-33-2	354.3	C₁₆H₁₈O₉
CFN95190	Neochlorogenic acid methyl ester	123410-65-1	368.3	C₁₇H₂₀O₉