5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavoneCAS# 78417-26-2 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 78417-26-2 | SDF | Download SDF |
PubChem ID | 5496475 | Appearance | Yellow powder |
Formula | C18H16O8 | M.Wt | 360.3 |
Type of Compound | Flavonoids | Storage | Desiccate at -20°C |
Solubility | Soluble in DMSO and methanol; insoluble in water | ||
Chemical Name | 5,7-dihydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxychromen-4-one | ||
SMILES | COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(C(=C(C=C3O2)O)OC)O | ||
Standard InChIKey | PMBOOVZSTMWOFS-UHFFFAOYSA-N | ||
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 | 5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone is a natural product from Artemisia argyi. |
In vitro | Further characterization of foliar flavonoids in Crossostephium chinense and their geographic variation.[Pubmed: 24689280]Nat Prod Commun. 2014 Feb;9(2):163-4.
|
Structure Identification | Zhong Yao Cai. 2013 May;36(5):752-5.Chemical constituents from flowers of Gardenia jasminoides.[Pubmed: 24218967]To study the chemical constituents from flowers of Gardenia jasminoides. |
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone Dilution Calculator
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.7755 mL | 13.8773 mL | 27.7546 mL | 55.5093 mL | 69.3866 mL |
5 mM | 0.5551 mL | 2.7755 mL | 5.5509 mL | 11.1019 mL | 13.8773 mL |
10 mM | 0.2775 mL | 1.3877 mL | 2.7755 mL | 5.5509 mL | 6.9387 mL |
50 mM | 0.0555 mL | 0.2775 mL | 0.5551 mL | 1.1102 mL | 1.3877 mL |
100 mM | 0.0278 mL | 0.1388 mL | 0.2775 mL | 0.5551 mL | 0.6939 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
- Trequinsin hydrochloride
Catalog No.:BCC7333
CAS No.:78416-81-6
- Milrinone
Catalog No.:BCC4374
CAS No.:78415-72-2
- 1,7-Dihydroxy-2,3-dimethoxyxanthone
Catalog No.:BCN7523
CAS No.:78405-33-1
- MY-5445
Catalog No.:BCC6645
CAS No.:78351-75-4
- Pyranojacareubin
Catalog No.:BCN7429
CAS No.:78343-62-1
- Nocamycin I
Catalog No.:BCN1845
CAS No.:78339-49-8
- PCI-24781 (CRA-024781)
Catalog No.:BCC2155
CAS No.:783355-60-2
- MLN120B
Catalog No.:BCC1772
CAS No.:783348-36-7
- MRK 016
Catalog No.:BCC6070
CAS No.:783331-24-8
- H-D-1-Nal-OH
Catalog No.:BCC3281
CAS No.:78306-92-0
- 7-Ethylcamptothecin
Catalog No.:BCN2480
CAS No.:78287-27-1
- Ecliptasaponin A
Catalog No.:BCN3843
CAS No.:78285-90-2
- RGB-286638
Catalog No.:BCC5519
CAS No.:784210-87-3
- RGB-286638 free base
Catalog No.:BCC5520
CAS No.:784210-88-4
- Deacetyltaxol
Catalog No.:BCN2820
CAS No.:78432-77-6
- 19-Hydroxybaccatin III
Catalog No.:BCN4330
CAS No.:78432-78-7
- 7-Epi 10-Desacetyl Paclitaxel
Catalog No.:BCC1314
CAS No.:78454-17-8
- Enterolakton
Catalog No.:BCC8170
CAS No.:78473-71-9
- Praeruptorin E
Catalog No.:BCN2591
CAS No.:78478-28-1
- 7-Epi-10-deacetylcephalomannine
Catalog No.:BCN7673
CAS No.:78479-12-6
- N-trans-Feruloyl-3-methoxytyramine
Catalog No.:BCN4331
CAS No.:78510-19-7
- PSB 069
Catalog No.:BCC7416
CAS No.:78510-31-3
- Asperumine
Catalog No.:BCN2039
CAS No.:78513-20-9
- Dulcioic acid
Catalog No.:BCN4579
CAS No.:78516-69-5
Further characterization of foliar flavonoids in Crossostephium chinense and their geographic variation.[Pubmed:24689280]
Nat Prod Commun. 2014 Feb;9(2):163-4.
Foliar flavonoids of Crossostephium chinense in Japan and Taiwan were isolated and further characterized. Eighteen flavonoid aglycones, luteolin, apigenin, hispidulin, chrysoeriol, 5,7,4'-trihydroxy-6,3',5'-trimethoxyflavone, jaceosidin, cilsimaritin, quercetin 3-methyl ether, axillarin, chrysosplenol-D, cirsiliol, apometzgerin, 5,7,3'-trihydroxy-6,4',5'-trimethoxyflavone, luteolin 3',4'-dimethyl ether, cirsilineol, eupatilin, nepetin and 5,7,3',4'-tetrahydroxy-6,5'-dimethoxyflavone, were identified by UV, 1H and 13C NMR spectroscopic, LC-MS and HPLC comparisons w ith authentic samples. The compounds existed on the leaf surface. Four flavonoid glycosides, quercetin 3,7-di-O-glucoside, quercetin 3-O-rutinoside, luteolin 7-O-glucoside and apigenin 7-O-rutinoside, were also isolated as the intracellular flavonoids. It was shown by HPLC survey that variation of the species' flavonoids occurs among the collection sites.
[Chemical constituents from flowers of Gardenia jasminoides].[Pubmed:24218967]
Zhong Yao Cai. 2013 May;36(5):752-5.
OBJECTIVE: To study the chemical constituents from flowers of Gardenia jasminoides. METHODS: The compounds were isolated and purified by column chromatography and their structures were elucidated through spectroscopic techniques (NMR) and physicochemical properties. RESULTS: 15 compounds were isolated from flowers of G. jasminoides, and identified as 5, 7, 3'-trihydroxy-6, 4', 5'-trimethoxyflavone (1), 5, 7, 3', 5'- tetrahydroxy-6, 4'-dymethoxyflavone (2), kaempferol (3), quercetin (4), 3beta,23- dihydroxyurs-12-en-28-oic acid (5), 3beta,19alpha-dihydroxy-urs-12-en-28-oic acid (6), 3beta,19alpha,23-trihydroxy-urs-12-en-28-oic acid (7), emodin (8), physcion (9), crocin-I (10), beta-daucosterol (11), beta-sitosterol (12), stearic acid (13), palmitic acid (14), oleic acid (15). CONCLUSION: Compounds 1 - 15 are isolated from flowers of G. jasminoides and compounds 5 and 6 are isolated from genus Gardenia for the first time.