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Daphnicyclidin F

CAS# 385384-26-9

Daphnicyclidin F

2D Structure

Catalog No. BCN6400----Order now to get a substantial discount!

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Quality Control of Daphnicyclidin F

3D structure

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Daphnicyclidin F

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Chemical Properties of Daphnicyclidin F

Cas No. 385384-26-9 SDF Download SDF
PubChem ID 11732045 Appearance Powder
Formula C23H27NO5 M.Wt 397.47
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (2S,3R,5S,6R,10S)-5-hydroxy-2,6-dimethyl-21-oxo-14-oxa-8-azahexacyclo[11.6.1.15,19.02,10.03,8.017,20]henicosa-1(19),13(20),17-triene-18-carboxylate
SMILES CC1CN2CC3CCC4=C5C(=C(C6=C5C3(C2CC1(C6=O)O)C)C(=O)OC)CCO4
Standard InChIKey CBULSUOPAXBENF-VBIFSVJFSA-N
Standard InChI InChI=1S/C23H27NO5/c1-11-9-24-10-12-4-5-14-16-13(6-7-29-14)17(21(26)28-3)18-19(16)22(12,2)15(24)8-23(11,27)20(18)25/h11-12,15,27H,4-10H2,1-3H3/t11-,12-,15-,22-,23+/m1/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 Daphnicyclidin F

The stems of Daphniphyllum humile and D.teijsmanni.

Biological Activity of Daphnicyclidin F

DescriptionDaphnicyclidin F is a natural product from Daphniphyllum humile and D.teijsmanni.

Protocol of Daphnicyclidin F

Structure Identification
J Am Chem Soc. 2001 Nov 21;123(46):11402-8.

Daphnicyclidins A-H, novel hexa- or pentacyclic alkaloids from two species of Daphniphyllum.[Pubmed: 11707117]


METHODS AND RESULTS:
Eight highly modified Daphniphyllum alkaloids with unprecedented fused hexa- or pentacyclic skeletons, daphnicyclidin A,daphnicyclidin B, daphnicyclidin C, daphnicyclidin D, daphnicyclidin E, Daphnicyclidin F, daphnicyclidin G, daphnicyclidin H (1-8), have been isolated from the stems of Daphniphyllum humile and D.teijsmanni, and their structures were elucidated on the basis of spectroscopic data and chemical means.
CONCLUSIONS:
The stereochemistry was elucidated by combination of NOESY correlations, X-ray crystallographic data, and CD analyses.

Daphnicyclidin F Dilution Calculator

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Daphnicyclidin F Molarity Calculator

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Preparing Stock Solutions of Daphnicyclidin F

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5159 mL 12.5796 mL 25.1591 mL 50.3183 mL 62.8978 mL
5 mM 0.5032 mL 2.5159 mL 5.0318 mL 10.0637 mL 12.5796 mL
10 mM 0.2516 mL 1.258 mL 2.5159 mL 5.0318 mL 6.2898 mL
50 mM 0.0503 mL 0.2516 mL 0.5032 mL 1.0064 mL 1.258 mL
100 mM 0.0252 mL 0.1258 mL 0.2516 mL 0.5032 mL 0.629 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 Daphnicyclidin F

Daphnicyclidins A-H, novel hexa- or pentacyclic alkaloids from two species of Daphniphyllum.[Pubmed:11707117]

J Am Chem Soc. 2001 Nov 21;123(46):11402-8.

Eight highly modified Daphniphyllum alkaloids with unprecedented fused hexa- or pentacyclic skeletons, daphnicyclidins A-H (1-8), have been isolated from the stems of Daphniphyllum humile and D.teijsmanni, and their structures were elucidated on the basis of spectroscopic data and chemical means. The stereochemistry was elucidated by combination of NOESY correlations, X-ray crystallographic data, and CD analyses.

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