Pterosin D

CAS# 34169-70-5

Pterosin D

Catalog No. BCN5269----Order now to get a substantial discount!

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Pterosin D:5mg Please Inquire In Stock
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Quality Control of Pterosin D

Number of papers citing our products

Chemical structure

Pterosin D

3D structure

Chemical Properties of Pterosin D

Cas No. 34169-70-5 SDF Download SDF
PubChem ID 147559 Appearance Powder
Formula C15H20O3 M.Wt 248.3
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R)-3-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one
SMILES CC1=C(C(=C2C(=C1)C(C(C2=O)(C)C)O)C)CCO
Standard InChIKey FITSCHPIOGIYJY-CYBMUJFWSA-N
Standard InChI InChI=1S/C15H20O3/c1-8-7-11-12(9(2)10(8)5-6-16)14(18)15(3,4)13(11)17/h7,13,16-17H,5-6H2,1-4H3/t13-/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 Pterosin D

The rhizoma of Cibotium barometz (L.) J.Sm.

Protocol of Pterosin D

Structure Identification
Tetrahedron Letters, 2003, 44(16):3249-3253.

Elisapterosins D and E: complex polycyclic diterpenes of the rare elisapterane class of natural products from the Caribbean sea whip Pseudopterogorgia elisabethae (Bayer).[Reference: WebLink]


METHODS AND RESULTS:
From the hexane extracts of a Colombian specimen of Pseudopterogorgia elisabethae (Bayer) we have isolated elisaPterosin D (2) and elisapterosin E (3), two structurally complex polycyclic diterpenes based on the rare elisapterane carbon skeleton. The structures of these scanty compounds were elucidated after interpretation of their combined spectroscopic data and NMR spectral comparisons with known elisapterane models.

Pterosin D Dilution Calculator

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Pterosin D Molarity Calculator

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Preparing Stock Solutions of Pterosin D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.0274 mL 20.1369 mL 40.2739 mL 80.5477 mL 100.6847 mL
5 mM 0.8055 mL 4.0274 mL 8.0548 mL 16.1095 mL 20.1369 mL
10 mM 0.4027 mL 2.0137 mL 4.0274 mL 8.0548 mL 10.0685 mL
50 mM 0.0805 mL 0.4027 mL 0.8055 mL 1.611 mL 2.0137 mL
100 mM 0.0403 mL 0.2014 mL 0.4027 mL 0.8055 mL 1.0068 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 Pterosin D

Chemical constituents analysis and antidiabetic activity validation of four fern species from Taiwan.[Pubmed:25622260]

Int J Mol Sci. 2015 Jan 22;16(2):2497-516.

Pterosins are abundant in ferns, and pterosin A was considered a novel activator of adenosine monophosphate-activated protein kinase, which is crucial for regulating blood glucose homeostasis. However, the distribution of pterosins in different species of ferns from various places in Taiwan is currently unclear. To address this question, the distribution of pterosins, glucose-uptake efficiency, and protective effects of pterosin A on beta-cells were examined. Our results showed that three novel compounds, 13-chloro-spelosin 3-O-beta-d-glucopyranoside (1), (3R)-Pterosin D 3-O-beta-d-(3'-p-coumaroyl)-glucopyranoside (2), and (2R,3R)-Pterosin L 3-O-beta-d-(3'-p-coumaroyl)-glucopyranoside (3), were isolated for the first time from four fern species (Ceratopteris thalictroides, Hypolepis punctata, Nephrolepis multiflora, and Pteridium revolutum) along with 27 known compounds. We also examined the distribution of these pterosin compounds in the mentioned fern species (except N. multiflora). Although all pterosin analogs exhibited the same effects in glucose uptake assays, pterosin A prevented cell death and reduced reactive oxygen species (ROS) production. This paper is the first report to provide new insights into the distribution of pterosins in ferns from Taiwan. The potential anti-diabetic activity of these novel phytocompounds warrants further functional studies.

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