Pteroside D

CAS# 35943-38-5

Pteroside D

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Quality Control of Pteroside D

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Chemical structure

Pteroside D

3D structure

Chemical Properties of Pteroside D

Cas No. 35943-38-5 SDF Download SDF
PubChem ID 169738 Appearance Powder
Formula C21H30O8 M.Wt 410.5
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3S)-3-hydroxy-2,2,5,7-tetramethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3H-inden-1-one
SMILES CC1=C(C(=C2C(=C1)C(C(C2=O)(C)C)O)C)CCOC3C(C(C(C(O3)CO)O)O)O
Standard InChIKey TUGWHBZURNWRDG-LNZAMEHWSA-N
Standard InChI InChI=1S/C21H30O8/c1-9-7-12-14(19(27)21(3,4)18(12)26)10(2)11(9)5-6-28-20-17(25)16(24)15(23)13(8-22)29-20/h7,13,15-18,20,22-26H,5-6,8H2,1-4H3/t13-,15-,16+,17-,18+,20-/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 Pteroside D

The herbs of Pteris multifida

Biological Activity of Pteroside D

DescriptionStandard reference

Protocol of Pteroside D

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2012 Apr;37(7):946-50.

Sesquiterpenoids of Coniogramme maxima.[Pubmed: 22792795]


METHODS AND RESULTS:
Fifteen compounds were separated by chromatography technique. Their structures were determined by spectral data, including 10 sesquiterpenoids as (3S)-Pteroside D (1), epi-pterosin L (2), pterosin D (3), onitin (4), pterosin Z (5), onitisin (6), onitisin-glucopyranoside (7), onitin-15-O-beta-D-glucopyranoside (8), (2S,3R)-pterosin-L-2'-O-beta-D-glucopyranoside (9) and (3R)-peterosin D-3-O-beta-D-glucopyranoside (10). The other compounds were uracil (11), 3,4-dihydroxybenzaldehyde (12), 5-hydroxymethyl-2-furancarboxaldehyde (13), beta-sitosterol (14) and daucosterol (15).
CONCLUSIONS:
The above 15 compounds are separated from C. maxima for the first time, including 9 compounds being first separated from genus Coniogramme.

Pteroside D Dilution Calculator

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Pteroside D Molarity Calculator

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Preparing Stock Solutions of Pteroside D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.4361 mL 12.1803 mL 24.3605 mL 48.7211 mL 60.9013 mL
5 mM 0.4872 mL 2.4361 mL 4.8721 mL 9.7442 mL 12.1803 mL
10 mM 0.2436 mL 1.218 mL 2.4361 mL 4.8721 mL 6.0901 mL
50 mM 0.0487 mL 0.2436 mL 0.4872 mL 0.9744 mL 1.218 mL
100 mM 0.0244 mL 0.1218 mL 0.2436 mL 0.4872 mL 0.609 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 Pteroside D

[Sesquiterpenoids of Coniogramme maxima].[Pubmed:22792795]

Zhongguo Zhong Yao Za Zhi. 2012 Apr;37(7):946-50.

OBJECTIVE: To study sesquiterpenoids of Coniogramme maxima. METHOD: Chemical constituents were separated by chromatography and their structures were identified according to physicochemical property and spectrum data. RESULT: Fifteen compounds were separated by chromatography technique. Their structures were determined by spectral data, including 10 sesquiterpenoids as (3S)-Pteroside D (1), epi-pterosin L (2), pterosin D (3), onitin (4), pterosin Z (5), onitisin (6), onitisin-glucopyranoside (7), onitin-15-O-beta-D-glucopyranoside (8), (2S,3R)-pterosin-L-2'-O-beta-D-glucopyranoside (9) and (3R)-peterosin D-3-O-beta-D-glucopyranoside (10). The other compounds were uracil (11), 3,4-dihydroxybenzaldehyde (12), 5-hydroxymethyl-2-furancarboxaldehyde (13), beta-sitosterol (14) and daucosterol (15). CONCLUSION: The above 15 compounds are separated from C. maxima for the first time, including 9 compounds being first separated from genus Coniogramme.

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