Gnetulin

CAS# 152340-24-4

Gnetulin

Catalog No. BCN3401----Order now to get a substantial discount!

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Gnetulin: 5mg $903 In Stock
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Quality Control of Gnetulin

Number of papers citing our products

Chemical structure

Gnetulin

3D structure

Chemical Properties of Gnetulin

Cas No. 152340-24-4 SDF Download SDF
PubChem ID 49843576 Appearance Powder
Formula C30H26O8 M.Wt 514.5
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1Z)-2-(3,5-dihydroxyphenyl)-3-(4-hydroxy-3-methoxyphenyl)-1-[(4-hydroxy-3-methoxyphenyl)methylidene]-2,3-dihydroindene-4,6-diol
SMILES COC1=C(C=CC(=C1)C=C2C(C(C3=C(C=C(C=C23)O)O)C4=CC(=C(C=C4)O)OC)C5=CC(=CC(=C5)O)O)O
Standard InChIKey YUGHGAXRXHODHK-QPSGOUHRSA-N
Standard InChI InChI=1S/C30H26O8/c1-37-26-8-15(3-5-23(26)34)7-21-22-13-20(33)14-25(36)30(22)29(16-4-6-24(35)27(11-16)38-2)28(21)17-9-18(31)12-19(32)10-17/h3-14,28-29,31-36H,1-2H3/b21-7+
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 Gnetulin

The herbs of Gnetum montanum

Biological Activity of Gnetulin

DescriptionStandard reference

Protocol of Gnetulin

Structure Identification
Org Biomol Chem. 2014 Apr 14;12(14):2273-9.

Enzyme-promoted regioselective coupling oligomerization of isorhapontigenin towards the first synthesis of (±)-gnetulin.[Pubmed: 24569530]


METHODS AND RESULTS:
We report the first synthesis of a natural (±)-Gnetulin and an unnatural analogue of (±)-gnemonol M by using the regioselective oxidative coupling reactions of 5-tert-butyl-isorhapontigenin as the key step. Both the effects of different enzyme-catalyzed systems on the structures of coupling products and structural transformations of coupling products in the presence of several Lewis acids were systematically investigated.

Nat Prod Res. 2005 Jul;19(5):443-8.

Bioactive stilbene dimers from Gnetum cleistostachyum.[Pubmed: 15938189]


METHODS AND RESULTS:
Two new stilbene dimers, named bisisorhapontigenin A (1) and cis shegansu B (2), together with gnetuhainin P (3) and Gnetulin (4), were isolated from the lianas of Gnetum cleistostachyum C. Y. Cheng. Their structures were elucidated by means of spectroscopic evidences, including UV, IR, MS, 1H NMR, 13C NMR, NOE and 2D NMR, respectively. The pharmacological activities of compounds 1, 2 and 3 also have been tested.

Gnetulin Dilution Calculator

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Gnetulin Molarity Calculator

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Preparing Stock Solutions of Gnetulin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.9436 mL 9.7182 mL 19.4363 mL 38.8727 mL 48.5909 mL
5 mM 0.3887 mL 1.9436 mL 3.8873 mL 7.7745 mL 9.7182 mL
10 mM 0.1944 mL 0.9718 mL 1.9436 mL 3.8873 mL 4.8591 mL
50 mM 0.0389 mL 0.1944 mL 0.3887 mL 0.7775 mL 0.9718 mL
100 mM 0.0194 mL 0.0972 mL 0.1944 mL 0.3887 mL 0.4859 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 Gnetulin

Bioactive stilbene dimers from Gnetum cleistostachyum.[Pubmed:15938189]

Nat Prod Res. 2005 Jul;19(5):443-8.

Two new stilbene dimers, named bisisorhapontigenin A (1) and cis shegansu B (2), together with gnetuhainin P (3) and Gnetulin (4), were isolated from the lianas of Gnetum cleistostachyum C. Y. Cheng. Their structures were elucidated by means of spectroscopic evidences, including UV, IR, MS, 1H NMR, 13C NMR, NOE and 2D NMR, respectively. The pharmacological activities of compounds 1, 2 and 3 also have been tested.

Enzyme-promoted regioselective coupling oligomerization of isorhapontigenin towards the first synthesis of (+/-)-gnetulin.[Pubmed:24569530]

Org Biomol Chem. 2014 Apr 14;12(14):2273-9.

We report the first synthesis of a natural (+/-)-Gnetulin and an unnatural analogue of (+/-)-gnemonol M by using the regioselective oxidative coupling reactions of 5-tert-butyl-isorhapontigenin as the key step. Both the effects of different enzyme-catalyzed systems on the structures of coupling products and structural transformations of coupling products in the presence of several Lewis acids were systematically investigated.

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