Hedyotol D

CAS# 97465-80-0

Hedyotol D

Catalog No. BCN9270----Order now to get a substantial discount!

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Chemical structure

Hedyotol D

3D structure

Chemical Properties of Hedyotol D

Cas No. 97465-80-0 SDF Download SDF
PubChem ID 50909266 Appearance Powder
Formula C31H36O11 M.Wt 584.6
Type of Compound Lignans Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-(4-hydroxy-3-methoxyphenyl)-2-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]propane-1,3-diol
SMILES COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3C4COC(C4CO3)C5=CC(=C(C=C5)O)OC
Standard InChIKey DVTIDVKFFJRCAB-UHFFFAOYSA-N
Standard InChI InChI=1S/C31H36O11/c1-36-23-9-16(5-7-21(23)33)28(35)27(13-32)42-31-25(38-3)11-18(12-26(31)39-4)30-20-15-40-29(19(20)14-41-30)17-6-8-22(34)24(10-17)37-2/h5-12,19-20,27-30,32-35H,13-15H2,1-4H3
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.

Hedyotol D Dilution Calculator

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Hedyotol D Molarity Calculator

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Preparing Stock Solutions of Hedyotol D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.7106 mL 8.5529 mL 17.1057 mL 34.2114 mL 42.7643 mL
5 mM 0.3421 mL 1.7106 mL 3.4211 mL 6.8423 mL 8.5529 mL
10 mM 0.1711 mL 0.8553 mL 1.7106 mL 3.4211 mL 4.2764 mL
50 mM 0.0342 mL 0.1711 mL 0.3421 mL 0.6842 mL 0.8553 mL
100 mM 0.0171 mL 0.0855 mL 0.1711 mL 0.3421 mL 0.4276 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 Hedyotol D

Astrernestin, a novel aurone-phenylpropanoid adduct from the roots of Astragalus ernestii.[Pubmed:30990071]

Nat Prod Res. 2019 Apr 16:1-6.

Astragalus ernestii has been used as a substitute for Radix Astragali (Huang-Qi) in southwest China. To better understand the chemical rationale for the medicinal usage, the phytochemistry of A. ernestii was recently studied. As a result, a novel aurone-phenylpropanoid adduct astrernestin (1), together with five known phenoloids calycosin-7-O-beta-D-glucopyranoside (2), 4,4'-dimethoxy-3'-hydroxy-7,9':7',9-diepoxylignan-3-O-beta-D-glucopyranoside (3), syringaresinol-4-O-beta-D-monoglucoside (4), Hedyotol D 4''-O-beta-D-glucopyranoside (5) and trifolirhizin (6), were isolated from the roots of A. ernestii. The structure of compound 1 was elucidated by extensive spectroscopic analysis and optical rotation calculation.

[Lignans from barks of Ailanthus altissima].[Pubmed:28936846]

Zhongguo Zhong Yao Za Zhi. 2016 Dec;41(24):4615-4620.

Eleven lignans were isolated from the ethanol extract of the barks of Ailanthus altissima through various column chromatography methods including silica gel, Sephadex LH-20, ODS and HPLC. By physical, chemical and comprehensive spectroscopic methods, their structures were identified as (+)-neoolivil(1), prunustosanan AI (2), (7S,8R)-guaiacyl-glycerol-beta-O-4'-neolignan (3), (7R,8S)-guaiacyl-glycerol-beta-O-4'-neolignan (4), (7S,8R)-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy ]-1,3-propanediol(5), pinnatifidanin B V (6), pinnatifidanin B VI (7), (7R,7'R,7''S,8S,8'S,8''S)-4',4''-dihydroxy-3,3',3'',5-tetramethoxy-7,9':7',9-diep oxy-4,8''-oxy-8,8'-sesquineolignan-7'',9''-diol (8), Hedyotol D (9), 5-(2-propenyl)-7-methoxy-2-(3,4-methylenediovxyphenyl)benzofuran (10), and (7R,8S,7'E)-guaiacyl-glycerol-beta-O-4'-sinapyl ether(11).All of these compounds were isolated from this plant for the first time.

Anti-Complementary Components of Helicteres angustifolia.[Pubmed:27834928]

Molecules. 2016 Nov 10;21(11). pii: molecules21111506.

A first phenalenon derivative with an acetyl side chain at C-8, 8-acetyl-9-hydroxy-3-methoxy-7-methyl-1-phenalenon (compound 1), and a pair of new sesquilignan epimers at C-7'' of hedyotol C and Hedyotol D analogs, hedyotol C 7''-O-beta-d-glucopyranoside (compound 2) and Hedyotol D 7''-O-beta-d-glucopyranoside (compound 3) were isolated from the aerial parts of Helicteres angustifolia together with nine known compounds (4-12). Their structures were elucidated on the basis of spectroscopic methods, including mass spectroscopy, and 1D and 2D nuclear magnetic resonance. Eleven isolates exhibited anti-complementary activity. In particular, compounds 4 and 5 exhibited potent anti-complementary activities against the classical and alternative pathways with CH50 values of 0.040 +/- 0.009 and 0.009 +/- 0.002 mM, and AP50 values of 0.105 +/- 0.015 and 0.021 +/- 0.003 mM, respectively. The targets of compounds 4 and 5 in the complement activation cascade were also identified. In conclusion, the anti-complementary components of H. angustifolia possessed chemical diversity and consisted mostly of flavonoids and lignans in this study.

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