Dulcisxanthone BCAS# 869669-62-5 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
Cas No. | 869669-62-5 | SDF | Download SDF |
PubChem ID | N/A | Appearance | Yellow powder |
Formula | C24H26O6 | M.Wt | 410.5 |
Type of Compound | Xanthones | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
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. |
Dulcisxanthone B Dilution Calculator
Dulcisxanthone B Molarity Calculator
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. |
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
- Chasmanthin
Catalog No.:BCX0253
CAS No.:20379-19-5
- Sanggenon B
Catalog No.:BCX0252
CAS No.:81381-67-1
- Kaempferol 3-O-(2''-O-glucosyl)rutinoside
Catalog No.:BCX0251
CAS No.:55696-58-7
- Dehydrozingerone
Catalog No.:BCX0250
CAS No.:1080-12-2
- (2S,3S)-Pteroside C
Catalog No.:BCX0249
CAS No.:98855-62-0
- (2R,3S)-Pteroside C
Catalog No.:BCX0248
CAS No.:68399-16-6
- Pterosin L 2'-O-glucoside
Catalog No.:BCX0247
CAS No.:61102-11-2
- Pyridylpaeoniflorin
Catalog No.:BCX0246
CAS No.:1427054-19-0
- Malaysianol D
Catalog No.:BCX0245
CAS No.:1646330-59-7
- Bisacurone A
Catalog No.:BCX0244
CAS No.:127214-84-0
- ar-Turmerol
Catalog No.:BCX0243
CAS No.:1178899-16-5
- (S,E)-2-Methyl-6-(p-tolyl)hept-3-en-2-ol
Catalog No.:BCX0242
CAS No.:18383-55-6
- (E)-4-(4-Hydroxyphenyl)but-3-en-2-one
Catalog No.:BCX0255
CAS No.:22214-30-8
- (E)-α-Atlantone
Catalog No.:BCX0256
CAS No.:26294-59-7
- Arucadiol
Catalog No.:BCX0257
CAS No.:105037-85-2
- Suffruticosol B
Catalog No.:BCX0258
CAS No.:220936-87-8
- Sibiriquinone B
Catalog No.:BCX0259
CAS No.:723300-09-2
- Sanggenon O
Catalog No.:BCX0260
CAS No.:101664-32-8
- (2S,3S)-Pterosin S 14-O-glucoside
Catalog No.:BCX0261
CAS No.:62043-50-9
- Pruniflorone R
Catalog No.:BCX0262
CAS No.:1238102-65-2
- Assiguxanthone B
Catalog No.:BCX0263
CAS No.:197447-29-3
- N-(3-(4-Fluorophenyl)propyl)-7-hydroxycoumarin-3-carboxamide
Catalog No.:BCX0264
CAS No.:2136579-33-2
- Suffruticosol D
Catalog No.:BCX0265
CAS No.:1261292-11-8
- Isogarcinol
Catalog No.:BCX0266
CAS No.:71117-97-0
Isoprenylated xanthone and benzophenone constituents of the pericarp of Garcinia planchonii.[Pubmed:25632472]
Nat Prod Commun. 2014 Dec;9(12):1737-40.
A new xanthone, planchoxanthone (1), together with six known compounds, garcinianone A (2), cowanin (3), rubraxanthone (4), f-mangostin (5), Dulcisxanthone B (6), and guttiferone Q (7), were isolated from an n-hexane extract of the pericap of Garcinia planchonii. Their structures were elucidated using spectroscopic methods. Antioxidant activity of the isolated compounds was tested using the DPPH free radical scavenging assay.
Antioxidant xanthones from Cratoxylum cochinchinense.[Pubmed:17393660]
Nat Prod Res. 2006 Dec;20(14):1332-7.
A new xanthone named cratoxylumxanthone A (1), together with five known compounds: Dulcisxanthone B (2), alpha-mangostin (3), beta-mangostin (4), 2-geranyl-1,3,7-trihydroxy-4-(3-methylbut-2-enyl)xanthone (5) and tectochrystin (6), was isolated from Cratoxylum cochinchinense stems. The structure of new compound was characterized by 1D and 2D NMR techniques. The isolated compounds showed free radical scavenging against DPPH and lipid peroxidation inhibition.
Phenolic compounds from the fruit of Garcinia dulcis.[Pubmed:16111726]
Phytochemistry. 2005 Oct;66(19):2368-75.
Dulcinoside (1), dulcisisoflavone (2), dulcisxanthone A (3) and sphaerobioside acetate (6) together with 22 known compounds were isolated from the green fruit of G. dulcis. Dulcisflavan (4), Dulcisxanthone B (5) and isonormangostin (7) together with 22 known compounds were isolated from the ripe fruit. Compounds 6 and 7 were synthetic known compounds. Their structures were determined by spectroscopic methods. The radical scavenging and antibacterial activities of some of the compounds were investigated.