CAS 195723-10-5 Methyl 4-O-feruloylquinate

Methyl 4-O-feruloylquinate - CAS 195723-10-5

Catalog number: 195723-10-5

Not Intended for Therapeutic Use. For research use only.

Molecular Formula:
Molecular Formula	C18H22O9
Molecular Weight:
Molecular Weight	382.36
COA:
COA	Inquire
Chemical Family:
Chemical Family	Other Natural Compounds
Description:
Description	Methyl 4-O-feruloylquinate is a natural compound found in several plants.

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Purity:
Purity	>95%
Appearance:
Appearance	Powder
Synonyms:
Synonyms	(1alpha,3R,4alpha,5R)-1,3,5-Trihydroxy-4-[[(2E)-3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propen-1-yl]oxy]cyclohexanecarboxylic acid methyl ester
MSDS:
MSDS	Inquire
Quality Standard:
Quality Standard	Enterprise Standard

Quantity:
Quantity	Milligrams-Grams
Density:
Density	1.4±0.1 g/cm3

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

Ge F;Ke C;Tang W;Yang X;Tang C;Qin G;Xu R;Li T;Chen X;Zuo J;Ye Y Phytochem Anal. 2007 May-Jun;18(3):213-8.

Two chlorogenic acids and five chlorogenic acid derivatives were simultaneously separated and purified from Stemona japonica by preparative high-performance liquid chromatography. 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. Compounds 3 and 4 exerted moderate inhibitory effect against AIV (H5N1) in vitro.

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