Angenomalin

CAS# 18199-64-9

Angenomalin

Catalog No. BCN8246----Order now to get a substantial discount!

Product Name & Size Price Stock
Angenomalin:5mg Please Inquire In Stock
Angenomalin:10mg Please Inquire In Stock
Angenomalin:20mg Please Inquire In Stock
Angenomalin:50mg Please Inquire In Stock

Quality Control of Angenomalin

Number of papers citing our products

Chemical structure

Angenomalin

3D structure

Chemical Properties of Angenomalin

Cas No. 18199-64-9 SDF Download SDF
PubChem ID 5318874 Appearance Powder
Formula C14H12O3 M.Wt 228.24
Type of Compound Coumarins Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one
SMILES CC(=C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3
Standard InChIKey WLRXMMDATRQQNQ-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H12O3/c1-8(2)12-7-10-11(16-12)5-3-9-4-6-13(15)17-14(9)10/h3-6,12H,1,7H2,2H3
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 Angenomalin

The roots of Angelica dahurica

Protocol of Angenomalin

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2010 May;35(9):1134-6.

O-methylnotopterol, a new natural product from the roots and rhizomes of Notopterygium incisum.[Pubmed: 20707067]

To study the chemical constituents of ethyl acetate-soluble fraction from methanolic extract of the roots and rhizomes of Notopterygium incisum .
METHODS AND RESULTS:
The chemical constituents were isolated and purified by various chromatographic methods, and their structures were identified by NMR and MS data analysis. Five compounds were obtained and identified as falcarindiol (1), 8-hydroxy-l-methoxy-( Z) -9-heptadecene-4, 6-diyn-3-one (2) Angenomalin (3), scopoletin (4), O-methylnotopterol (5).
CONCLUSIONS:
Compound 5 was a new natural product and compounds 2-4 were isolated from the roots and rhizomes of N. incisum for the first time.

Angenomalin Dilution Calculator

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Preparing Stock Solutions of Angenomalin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.3814 mL 21.9068 mL 43.8135 mL 87.6271 mL 109.5338 mL
5 mM 0.8763 mL 4.3814 mL 8.7627 mL 17.5254 mL 21.9068 mL
10 mM 0.4381 mL 2.1907 mL 4.3814 mL 8.7627 mL 10.9534 mL
50 mM 0.0876 mL 0.4381 mL 0.8763 mL 1.7525 mL 2.1907 mL
100 mM 0.0438 mL 0.2191 mL 0.4381 mL 0.8763 mL 1.0953 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 Angenomalin

[O-methylnotopterol, a new natural product from the roots and rhizomes of Notopterygium incisum].[Pubmed:20707067]

Zhongguo Zhong Yao Za Zhi. 2010 May;35(9):1134-6.

OBJECTIVE: To study the chemical constituents of ethyl acetate-soluble fraction from methanolic extract of the roots and rhizomes of Notopterygium incisum . METHOD: The chemical constituents were isolated and purified by various chromatographic methods, and their structures were identified by NMR and MS data analysis. RESULT: Five compounds were obtained and identified as falcarindiol (1), 8-hydroxy-l-methoxy-( Z) -9-heptadecene-4, 6-diyn-3-one (2) Angenomalin (3), scopoletin (4), O-methylnotopterol (5). CONCLUSION: Compound 5 was a new natural product and compounds 2-4 were isolated from the roots and rhizomes of N. incisum for the first time.

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