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Glycosmisic acid

CAS# 443908-19-8

Glycosmisic acid

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Glycosmisic acid: 5mg $1277 In Stock
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Quality Control of Glycosmisic acid

Number of papers citing our products

Chemical structure

Glycosmisic acid

3D structure

Chemical Properties of Glycosmisic acid

Cas No. 443908-19-8 SDF Download SDF
PubChem ID 38356809 Appearance Powder
Formula C20H20O7 M.Wt 372.4
Type of Compound Lignans Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (E)-3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoic acid
SMILES COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC(=O)O
Standard InChIKey FHYQIQMSODIFCP-ZMOFONSMSA-N
Standard InChI InChI=1S/C20H20O7/c1-25-16-9-12(4-5-15(16)22)19-14(10-21)13-7-11(3-6-18(23)24)8-17(26-2)20(13)27-19/h3-9,14,19,21-22H,10H2,1-2H3,(H,23,24)/b6-3+/t14-,19+/m0/s1
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.

Source of Glycosmisic acid

The barks of Nauclea officinalis

Biological Activity of Glycosmisic acid

DescriptionGlycosmisic acid is a natural product from Nauclea officinalis.

Protocol of Glycosmisic acid

Structure Identification
Chinese Traditional & Herbal Drugs, 2010 , 41 (4) :509-514.

A new lignan from Gardenia jasminoides[Reference: WebLink]

To study the chemical constituents in 60% ethanol extract from the fruit of Gardenia jasminoides.
METHODS AND RESULTS:
The compounds were isolated by various chromatographic techniques and identified by spectroscopic methods. Twelve compounds were obtained and identified as gardenianan A (1), syringaresinol (2), pinoresinol (3), syringaresinol-4-O-β-D-glucopyranoside (4), lariciresinol (5), alangilignoside D (6), lyoniresinol (7), lyoniresinol-9-O-β-D-glucopyranoside (8), balanophonin (9), Glycosmisic acid (10), ficusal (11), and ceplignan (12).
CONCLUSIONS:
Compound 1 is a new compound named gardenianan A. Compounds 2 - 6 and 9 - 12 are reported for the first isolation from the plants of Gardenia Ellis.

Glycosmisic acid Dilution Calculator

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Glycosmisic acid Molarity Calculator

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Preparing Stock Solutions of Glycosmisic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.6853 mL 13.4264 mL 26.8528 mL 53.7057 mL 67.1321 mL
5 mM 0.5371 mL 2.6853 mL 5.3706 mL 10.7411 mL 13.4264 mL
10 mM 0.2685 mL 1.3426 mL 2.6853 mL 5.3706 mL 6.7132 mL
50 mM 0.0537 mL 0.2685 mL 0.5371 mL 1.0741 mL 1.3426 mL
100 mM 0.0269 mL 0.1343 mL 0.2685 mL 0.5371 mL 0.6713 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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References on Glycosmisic acid

[Studies on chemical constituents of Clerodendrum bungei].[Pubmed:29493148]

Zhongguo Zhong Yao Za Zhi. 2017 Dec;42(24):4788-4793.

Ten compounds were isolated from the 95% aqueous EtOH extract of Clerodendrum bungei by a combination of various chromatographic techniques including column chromatography over silica gel, Sephadex LH-20, MCI, ODS, and semi-preparative HPLC. Their structures were elucidated as 11,12,16S-trihydroxy-7-oxo-17(15-->16),18(4-->3)-diabeo-abieta-3,8,11,13-tetraen- 18-oic acid (1), 12S*,13R*-dihydroxy-9-oxo-octadeca-10(E)-enoic acid (2), clerodenoside A (3), trichotomoside (4), Glycosmisic acid (5), 4'-O-methylscutellarein (6), neroplomacrol (7), butylitaconic acid (8), hexylitaconic acid (9), p-hydroxybenzonic acid (10) by their physicochemical properties and spectroscopic data. Compounds 1 and 2 are new natural products, while compounds 7-10 were obtained from the genus Clerodendrum for the first time, and compounds 3, 5, 6 were isolated from this plant for the first time.

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