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Methyl caffeate acid

CAS# 3843-74-1

Methyl caffeate acid

2D Structure

Catalog No. BCN8712----Order now to get a substantial discount!

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3D structure

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Methyl caffeate acid

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Chemical Properties of Methyl caffeate acid

Cas No. 3843-74-1 SDF Download SDF
PubChem ID 689075 Appearance Powder
Formula C10H10O4 M.Wt 194.18
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (~{E})-3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES COC(=O)C=CC1=CC(=C(C=C1)O)O
Standard InChIKey OCNYGKNIVPVPPX-HWKANZROSA-N
Standard InChI InChI=1S/C10H10O4/c1-14-10(13)5-3-7-2-4-8(11)9(12)6-7/h2-6,11-12H,1H3/b5-3+
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of Methyl caffeate acid

DescriptionMethyl caffeate acid shows anti-complementary activity.
In vitro

Anti-complementary phenolic acids from Lonicera japonica.[Pubmed: 26080557]

Zhongguo Zhong Yao Za Zhi. 2015 Jan;40(2):269-74.

To study the anti-complementary phenolic acids from Lonicera japonica.
METHODS AND RESULTS:
The anti-complementary activity-directed isolation was carried out with the hemolysis test as guide. All isolation was evaluated for their in vitro anti-complementary activities. The structures were identified by various spectroscopic data including ESI-MS, 1H-NMR, 13C-NMR data. Fourteen compounds were isolated from the EtOAc fraction of L. japonica extracts, including 8 phenolic acids: 5-O-caffeoylquinic acid (1), chlorogenic (2), 4-O-caffeoylquinic acid (3), 3,5-di-O-caffeoylquinic acid (4), 4,5-di-O-caffeoylquinic acid (5), 3,4-di-O-caffeoylquinic acid (6), caffeic acid (7) and Methyl caffeate acid (8); 3 iridoids: secologanoside (9), sweroside (10) and secoxyloganin (11); and 3 flavonoids: luteolin (12), quercetin (13) and kaempferol (14). Compounds 1-9 and 11-14 showed anti-complementary activity in different extents and 3,5-di-O-caffeoylquinic acid (4) exhibited the most significant activity against the classical pathway.
CONCLUSIONS:
Compound 14 is obtained from this plant for the first time, phenolic acids are the main anti-complementary constituents of L. japonica and 3,5-di-O-caffeoylquinic acid(4) is a potential complement inhibitor with strong activity, which worthy to be studied further in the future.

Protocol of Methyl caffeate acid

Structure Identification
Chinese Traditional and Herbal Drugs, 2016.

Chemical constituents from aerial parts of Fagopyrum dibotrys.[Reference: WebLink]

To study the chemical constituents from the aerial parts of Fagopyrum dibotrys.
METHODS AND RESULTS:
The compounds were isolated and purified by means of chromatographic techniques and their structures were identified on the basis of spectral features. Fourteen known compounds were isolated in the methanol extract from the aerial parts of F. dibotrys and their structures were identified as benzoic acid (1), p-hydroxybenzoic acid (2), p-hydroxy benzaldehyde (3), 3,4-dihydroxy benzoic acid (4), succinic acid (5), caffeic acid (6), Methyl caffeate acid (7), luteolin (8), tricin (9), quercetin (10), afzelin A (11), 2α,3β,29-trihydroxyolean-12-en-28-oic acid (12), yarumic acid (13), and 3α-hydroxy-urs-12,15-dien (14).
CONCLUSIONS:
Compounds 2-3 and 6-9 are firstly obtained from the aerial parts of F. dibotrys. Compounds 11-14 are isolated from the genus of Fagopyrum Mill. for the first time.

Methyl caffeate acid Dilution Calculator

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Methyl caffeate acid Molarity Calculator

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Preparing Stock Solutions of Methyl caffeate acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.1499 mL 25.7493 mL 51.4986 mL 102.9972 mL 128.7465 mL
5 mM 1.03 mL 5.1499 mL 10.2997 mL 20.5994 mL 25.7493 mL
10 mM 0.515 mL 2.5749 mL 5.1499 mL 10.2997 mL 12.8747 mL
50 mM 0.103 mL 0.515 mL 1.03 mL 2.0599 mL 2.5749 mL
100 mM 0.0515 mL 0.2575 mL 0.515 mL 1.03 mL 1.2875 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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