AverantinCAS# 5803-62-3 |
2D Structure
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 5803-62-3 | SDF | Download SDF |
PubChem ID | 22049 | Appearance | Powder |
Formula | C20H20O7 | M.Wt | 372.37 |
Type of Compound | Anthraquinones | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 1,3,6,8-tetrahydroxy-2-(1-hydroxyhexyl)anthracene-9,10-dione | ||
SMILES | CCCCCC(C1=C(C=C2C(=C1O)C(=O)C3=C(C=C(C=C3C2=O)O)O)O)O | ||
Standard InChIKey | WGPOPPKSQRZUTP-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C20H20O7/c1-2-3-4-5-12(22)17-14(24)8-11-16(20(17)27)19(26)15-10(18(11)25)6-9(21)7-13(15)23/h6-8,12,21-24,27H,2-5H2,1H3 | ||
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. |
Description | Averantin exhibits antifungal activity against Fusariumsolani, pathogenic fungus of P. notoginseng, with minimum inhibitory concentrations (MICs) of 16-32 ug/mL, and shows antibacterial activity against Bacillussubtilis with MICs of 16-32 ug/mL. |
Targets | Antifection |
In vitro | The antifungal metabolites obtained from the rhizospheric Aspergillus sp. YIM PH30001 against pathogenic fungi of Panax notoginseng.[Pubmed: 25022791 ]Nat Prod Res. 2014;28(24):2334-7.
|
Averantin Dilution Calculator
Averantin Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.6855 mL | 13.4275 mL | 26.855 mL | 53.71 mL | 67.1375 mL |
5 mM | 0.5371 mL | 2.6855 mL | 5.371 mL | 10.742 mL | 13.4275 mL |
10 mM | 0.2686 mL | 1.3428 mL | 2.6855 mL | 5.371 mL | 6.7138 mL |
50 mM | 0.0537 mL | 0.2686 mL | 0.5371 mL | 1.0742 mL | 1.3428 mL |
100 mM | 0.0269 mL | 0.1343 mL | 0.2686 mL | 0.5371 mL | 0.6714 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
- HOKU-81
Catalog No.:BCC1634
CAS No.:58020-43-2
- Epicorynoxidine
Catalog No.:BCN7554
CAS No.:58000-48-9
- Matairesinol
Catalog No.:BCN5789
CAS No.:580-72-3
- 2-Aminoquinoline
Catalog No.:BCC8555
CAS No.:580-22-3
- 3-Aminoquinoline
Catalog No.:BCC8620
CAS No.:580-17-6
- 6-Aminoquinoline
Catalog No.:BCC8766
CAS No.:580-15-4
- Uridine
Catalog No.:BCN4090
CAS No.:58-96-8
- alpha-Tocopherol acetate
Catalog No.:BCN5803
CAS No.:58-95-7
- Chlorothiazide
Catalog No.:BCC3752
CAS No.:58-94-6
- Hydrochlorothiazide
Catalog No.:BCC4786
CAS No.:58-93-5
- D-(+)-Xylose
Catalog No.:BCN1010
CAS No.:58-86-6
- Biotin
Catalog No.:BCC3585
CAS No.:58-85-5
- 24, 25-Dihydroxy VD2
Catalog No.:BCC1302
CAS No.:58050-55-8
- Miltefosine
Catalog No.:BCC4360
CAS No.:58066-85-6
- trans-3,4-Methylenedioxycinnamyl alcohol
Catalog No.:BCN1410
CAS No.:58095-76-4
- α-MSH
Catalog No.:BCC7420
CAS No.:581-05-5
- Suberosin
Catalog No.:BCN5791
CAS No.:581-31-7
- Anatabine
Catalog No.:BCN6899
CAS No.:581-49-7
- Isonicoteine
Catalog No.:BCN2152
CAS No.:581-50-0
- Undulatoside A
Catalog No.:BCN6773
CAS No.:58108-99-9
- Fmoc-Arg(NO2)-OH
Catalog No.:BCC2596
CAS No.:58111-94-7
- 1-(4-(3-Chloropropoxy)-3-methoxyphenyl)ethanone
Catalog No.:BCC8406
CAS No.:58113-30-7
- Aurantiamide
Catalog No.:BCN5790
CAS No.:58115-31-4
- SU 4312
Catalog No.:BCC7073
CAS No.:5812-07-7
The antifungal metabolites obtained from the rhizospheric Aspergillus sp. YIM PH30001 against pathogenic fungi of Panax notoginseng.[Pubmed:25022791]
Nat Prod Res. 2014;28(24):2334-7.
Eight anthraquinones (1-8), three xanthones (11-13) and two phenols (9-10) were isolated from Aspergillus sp. associated with Panax notoginseng, and their structures were determined as ziganein-1-methyl ether (1), 8-O-methylchrysophanol (2), averythrin (3), averufin (4), 8-O-methyl averufin (5), versicolorin B (6), Averantin (7), methyl-Averantin (8), arugosin C (9), diorcinol (10), sterigmatocystin (11), demethylsterigmatocystin (12) and dihydrosterigmatocystin (13) by spectroscopic analyses. Compounds 1, 2 and 5 were the novel isolates from genus Aspergillus. Compounds 3, 6 and 7 exhibited antifungal activity against Fusariumsolani, pathogenic fungus of P. notoginseng, with minimum inhibitory concentrations (MICs) of 16-32 mug/mL, and compounds 1, 3, 4, 7 and 9 showed antibacterial activity against Bacillussubtilis with MICs of 64-128 mug/mL, 16-32 mug/mL, 8-16 mug/mL, 16-32 mug/mL and 64-128 mug/mL, respectively. The metabolites showed the potential value in the research of antifungal agents, especially in searching for a biocontrol of diseases of P. notoginseng. The preliminary structure-activity relationships have been discussed for some of the compounds.