CitrusinolCAS# 112516-43-5 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 112516-43-5 | SDF | Download SDF |
PubChem ID | 44259051 | Appearance | Powder |
Formula | C20H16O6 | M.Wt | 352.34 |
Type of Compound | Flavonoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 3,5-dihydroxy-2-(4-hydroxyphenyl)-8,8-dimethylpyrano[2,3-h]chromen-4-one | ||
SMILES | CC1(C=CC2=C3C(=C(C=C2O1)O)C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)C | ||
Standard InChIKey | OKQQXHUICMLKQI-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C20H16O6/c1-20(2)8-7-12-14(26-20)9-13(22)15-16(23)17(24)18(25-19(12)15)10-3-5-11(21)6-4-10/h3-9,21-22,24H,1-2H3 | ||
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 | 1. Citrusinol exhibits cytotoxic activities against the HepG2 cell. |
Citrusinol Dilution Calculator
Citrusinol Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.8382 mL | 14.1908 mL | 28.3817 mL | 56.7634 mL | 70.9542 mL |
5 mM | 0.5676 mL | 2.8382 mL | 5.6763 mL | 11.3527 mL | 14.1908 mL |
10 mM | 0.2838 mL | 1.4191 mL | 2.8382 mL | 5.6763 mL | 7.0954 mL |
50 mM | 0.0568 mL | 0.2838 mL | 0.5676 mL | 1.1353 mL | 1.4191 mL |
100 mM | 0.0284 mL | 0.1419 mL | 0.2838 mL | 0.5676 mL | 0.7095 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
- Tubuloside A
Catalog No.:BCN2806
CAS No.:112516-05-9
- Neolinine
Catalog No.:BCN6564
CAS No.:112515-37-4
- Isoabsouline
Catalog No.:BCN1955
CAS No.:112513-34-5
- Absouline
Catalog No.:BCN1954
CAS No.:112513-33-4
- Picrasidine S
Catalog No.:BCN6006
CAS No.:112503-87-4
- Aristolactam FI
Catalog No.:BCN6005
CAS No.:112501-42-5
- 6-Aldehydo-isoophiopogonone A
Catalog No.:BCN6629
CAS No.:112500-90-0
- 5-Aminoisoquinoline
Catalog No.:BCC8736
CAS No.:1125-60-6
- 4,4-Pentamethylenepiperidine hydrochloride
Catalog No.:BCC6059
CAS No.:1125-01-5
- H-Glu(OcHex)-OH
Catalog No.:BCC2929
CAS No.:112471-82-6
- U-54494A hydrochloride
Catalog No.:BCC6668
CAS No.:112465-94-8
- 3-Phenyl-1-(pyrrol-1-yl)propan-1-one
Catalog No.:BCN4005
CAS No.:112448-69-8
- CI994 (Tacedinaline)
Catalog No.:BCC2159
CAS No.:112522-64-2
- ent-16alpha,17-Dihydroxyatisan-3-one
Catalog No.:BCN6607
CAS No.:112523-91-8
- Pioglitazone HCl
Catalog No.:BCC2278
CAS No.:112529-15-4
- 4-O-Methylepisappanol
Catalog No.:BCN3674
CAS No.:112529-37-0
- Mps1-IN-1
Catalog No.:BCC5590
CAS No.:1125593-20-5
- A 804598
Catalog No.:BCC6198
CAS No.:1125758-85-1
- SKLB610
Catalog No.:BCC3647
CAS No.:1125780-41-7
- 4-Allylpyrocatechol
Catalog No.:BCN6009
CAS No.:1126-61-0
- Iso-mogroside V
Catalog No.:BCN3047
CAS No.:1126032-65-2
- Dicyclanil
Catalog No.:BCC8938
CAS No.:112636-83-6
- U-73122
Catalog No.:BCC5199
CAS No.:112648-68-7
- Garcinone E
Catalog No.:BCN3604
CAS No.:112649-21-5
[Studies on constituents of rootsanel leaves from Desmodium blandum and their cytotoxic activity against growth of several tumor cells].[Pubmed:19160788]
Zhongguo Zhong Yao Za Zhi. 2008 Sep;33(18):2077-80.
OBJECTIVE: To investigate the chemical constituents of Desmodium blandum and their cytotoxic activity against the growth of several tumor cells. METHOD: Various chromatographic techniques including silica gel, Sephadex LH-20 column chromatography were employed for the isolation and purification of the constituents. The structures of compounds were elucidated by spectral analyses (IR, UV, NMR, MS). Their cytotoxic activity was then studied. RESULT: Eight compounds were isolated from the stems of D. blandum and identified as N, N-dimethyltryptamine (1), 5-methoxy-N, N-dimethyltryptamine (2), Citrusinol (3), yukovanol (4), (Z)-1-(4-hydroxy-2, 3-dimethoxyphenyl)-3-(4-hydroxyphenyl) propene (5), (Z)-1-(3-hydroxy-2, 4-dimethoxy-phenyl)-3-(4-hydroxy-3-methoxy-phenyl) propene (6), methylprotocatechuate (7), katuranin (8). CONCLUSION: Among these compounds, compound 6 was isolated from D. blandum for the first time. In the MTT test, compounds 2 and 6 exhibit cytotoxic activities against the KB cell, and compounds 3 and 6 exhibit the same activities against the HepG2 cell.