Hedyotol DCAS# 97465-80-0 |
- Hedyotol C
Catalog No.:BCN0538
CAS No.:97465-79-7
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| 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
Hedyotol D Molarity Calculator
| 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. | |||||
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- Cavaol E
Catalog No.:BCN9269
CAS No.:1233044-20-6
- Platyphyllonol 5-O-β-D-xylopyranoside
Catalog No.:BCN9268
CAS No.:288141-04-8
- Tatsinine
Catalog No.:BCN9267
CAS No.:90038-21-4
- 4-Demethyltraxillaside
Catalog No.:BCN9266
CAS No.:1691201-82-7
- Sepiumol E
Catalog No.:BCN9265
CAS No.:2412027-09-7
- Juncuenin A
Catalog No.:BCN9264
CAS No.:1161681-18-0
- Juncuenin B
Catalog No.:BCN9263
CAS No.:1161681-20-4
- (+)-Dalbergiphenol
Catalog No.:BCN9262
CAS No.:82358-44-9
- 9-Oxooctadeca-10,12-dienoic acid
Catalog No.:BCN9261
CAS No.:54232-58-5
- Gancaonin O
Catalog No.:BCN9260
CAS No.:129145-53-5
- Jasminoside
Catalog No.:BCN9259
CAS No.:82451-18-1
- threo-Guaiacylglycerol β-coniferyl ether
Catalog No.:BCN9258
CAS No.:168393-18-8
- Pregn-5-ene-3β,17α,20S-triol
Catalog No.:BCN9271
CAS No.:903-67-3
- 6-Methoxyspirotryprostatin B
Catalog No.:BCN9272
CAS No.:1031727-28-2
- 3-(3-Hydroxybutyl)phenol
Catalog No.:BCN9273
CAS No.:854464-95-2
- Phoyunbene B
Catalog No.:BCN9274
CAS No.:886747-62-2
- Effususol A
Catalog No.:BCN9275
CAS No.:1869082-58-5
- Machigline
Catalog No.:BCN9276
CAS No.:87264-30-0
- Cinnamolide
Catalog No.:BCN9277
CAS No.:23599-47-5
- Cassamedine
Catalog No.:BCN9278
CAS No.:16408-75-6
- Integracin A
Catalog No.:BCN9279
CAS No.:224186-03-2
- 2,7-Dihydroxy-1,6-dimethylpyrene
Catalog No.:BCN9280
CAS No.:468103-76-6
- 9,10-Didehydroeffususol A
Catalog No.:BCN9281
CAS No.:1869082-57-4
- Juncuenin D
Catalog No.:BCN9282
CAS No.:1161681-24-8
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.
