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Sophoracarpan A

CAS# 1674359-82-0

Sophoracarpan A

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Product Name & Size Price Stock
Sophoracarpan A: 5mg $828 In Stock
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Quality Control of Sophoracarpan A

Number of papers citing our products

Chemical structure

Sophoracarpan A

3D structure

Chemical Properties of Sophoracarpan A

Cas No. 1674359-82-0 SDF Download SDF
PubChem ID 131849416 Appearance Powder
Formula C17H16O5 M.Wt 300.31
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (6S,6aS,11aR)-6,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol
SMILES COC1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)OC
Standard InChIKey VDHFFCPQILOKFG-ULQDDVLXSA-N
Standard InChI InChI=1S/C17H16O5/c1-19-10-4-6-11-14(8-10)21-16-12-5-3-9(18)7-13(12)22-17(20-2)15(11)16/h3-8,15-18H,1-2H3/t15-,16-,17-/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 Sophoracarpan A

The aerial parts of Sophora tomentosa L.

Biological Activity of Sophoracarpan A

DescriptionSophoracarpan A is a natural product from Sophora tomentosa L.

Protocol of Sophoracarpan A

Structure Identification
Chemical & Pharmaceutical Bulletin, 1990, 38(10):2756-2759.

Chemical studies on Sophora tomentosa: the isolation of a new class of isoflavonoid.[Reference: WebLink]

Two new pterocarpans, Sophoracarpan A and Sophoracarpan B, were isolated from Sophora tomentosa L. (Leguminosae) in addition to three known isoflavonoids, wighteone (erythrinin B), sophoraisoflavanone A and l-maackiain.
METHODS AND RESULTS:
The structures of sophoracarpans A and B were elucidated as 6β, 9-dimethoxy-3-hydroxypterocarpan and 3-hydroxy-6β-methoxy-8, 9-methylenedioxypterocarpan, respectively, on the spectroscopic basis. The configurations at C-6, C-6a, and C-11a of both compounds were determined by a series of nuclear magnetic resonance irradiation experiments.
CONCLUSIONS:
The isoflavone wighteone, known as an antifungal phytoalexin in several genera of leguminous plants, was also found to occur in the genus Sophora.

Sophoracarpan A Dilution Calculator

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Sophoracarpan A Molarity Calculator

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Preparing Stock Solutions of Sophoracarpan A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.3299 mL 16.6495 mL 33.2989 mL 66.5978 mL 83.2473 mL
5 mM 0.666 mL 3.3299 mL 6.6598 mL 13.3196 mL 16.6495 mL
10 mM 0.333 mL 1.6649 mL 3.3299 mL 6.6598 mL 8.3247 mL
50 mM 0.0666 mL 0.333 mL 0.666 mL 1.332 mL 1.6649 mL
100 mM 0.0333 mL 0.1665 mL 0.333 mL 0.666 mL 0.8325 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 Sophoracarpan A

Unified total syntheses of (-)-medicarpin, (-)-sophoracarpan A, and (+/-)-kushecarpin A with some structural revisions.[Pubmed:25476784]

Angew Chem Int Ed Engl. 2015 Feb 2;54(6):1864-7.

The total syntheses of medicarpin, Sophoracarpan A, and kushecarpin A from a common intermediate are achieved by using ortho- and para-quinone methide chemistry. Additionally, the relative stereochemistry of Sophoracarpan A and B have been reassigned.

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