Home >> Research Area >>Natural Products>>Alkaloids>> Oxohydrastinine

Oxohydrastinine

CAS# 552-29-4

Oxohydrastinine

Catalog No. BCN3299----Order now to get a substantial discount!

Product Name & Size Price Stock
Oxohydrastinine: 5mg Please Inquire In Stock
Oxohydrastinine: 10mg Please Inquire In Stock
Oxohydrastinine: 20mg Please Inquire Please Inquire
Oxohydrastinine: 50mg Please Inquire Please Inquire
Oxohydrastinine: 100mg Please Inquire Please Inquire
Oxohydrastinine: 200mg Please Inquire Please Inquire
Oxohydrastinine: 500mg Please Inquire Please Inquire
Oxohydrastinine: 1000mg Please Inquire Please Inquire

Quality Control of Oxohydrastinine

Number of papers citing our products

Chemical structure

Oxohydrastinine

3D structure

Chemical Properties of Oxohydrastinine

Cas No. 552-29-4 SDF Download SDF
PubChem ID 160522 Appearance Powder
Formula C11H11NO3 M.Wt 205.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 6-methyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinolin-5-one
SMILES CN1CCC2=CC3=C(C=C2C1=O)OCO3
Standard InChIKey WIUVXEAALLSOQN-UHFFFAOYSA-N
Standard InChI InChI=1S/C11H11NO3/c1-12-3-2-7-4-9-10(15-6-14-9)5-8(7)11(12)13/h4-5H,2-3,6H2,1H3
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.

Source of Oxohydrastinine

The herbs of Thalictrum aquilegifolium

Biological Activity of Oxohydrastinine

Description1. Oxohydrastinine shows certain antibacterial activity in vitro.
TargetsAntifection

Oxohydrastinine Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

Oxohydrastinine Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Oxohydrastinine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.8733 mL 24.3665 mL 48.7329 mL 97.4659 mL 121.8324 mL
5 mM 0.9747 mL 4.8733 mL 9.7466 mL 19.4932 mL 24.3665 mL
10 mM 0.4873 mL 2.4366 mL 4.8733 mL 9.7466 mL 12.1832 mL
50 mM 0.0975 mL 0.4873 mL 0.9747 mL 1.9493 mL 2.4366 mL
100 mM 0.0487 mL 0.2437 mL 0.4873 mL 0.9747 mL 1.2183 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.

Organizitions Citing Our Products recently

 
 
 

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
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on Oxohydrastinine

Application of chromatography technology in the separation of active alkaloids from Hypecoum leptocarpum and their inhibitory effect on fatty acid synthase.[Pubmed:26544947]

J Sep Sci. 2015 Dec;38(23):4063-70.

A method that involved the combination of pH-zone-refining counter-current chromatography and semipreparative reversed-phase liquid chromatography has been established for the preparative separation of alkaloids from Hypecoum leptocarpum. From 1.2 g of crude sample, 31 mg N-feruloyltyramine, 27 mg Oxohydrastinine, 47 mg hydroprotopine, 25 mg leptopidine, and 18 mg hypecocarpine have been obtained. The structure of the new compound, hypecocarpine, is confirmed based on the analysis of spectroscopic data, including NMR, UV, and IR spectroscopy and positive electrospray ionization mass spectrometry. The known chemical structures were characterized on the basis of (1) H and (13) C NMR spectroscopy. The purities of the five alkaloids are all over 92.7% as determined by high-performance liquid chromatography. The alkaloids' cytotoxicity in breast cancer cells is assessed by using a Cell Counting Kit assay and their inhibitory effect on fatty acid synthase expression is assessed by a Western blot assay. These results suggest that leptopidine could suppress growth and induce cytotoxicity in breast cancer cells and that the cytotoxicity of leptopidine may be related to its inhibitory effect on fatty acid synthase expression.

One Step to Separate Five Alkaloids from Hypecoum leptocarpum by High-Speed Counter-Current Chromatography.[Pubmed:26499120]

J Chromatogr Sci. 2016 Mar;54(3):466-71.

High-speed counter-current chromatography (CCC) was firstly and successfully applied for the preparative separation and purification of alkaloids from crude extract of Hypecoum leptocarpum. After the measurement of partition coefficient of five target alkaloids in the two-phase solvent systems, the CCC was performed well with a two-phase solvent system composed of tetrachloromethane-chloroform-methanol-0.1 M HCl at a volume ratio of 1.5 : 2.5 : 3 : 2 (V/V/V/V). The upper phase was used as the stationary phase, and the lower phase was used as the mobile phase. From 120 mg crude extract, 5 mg leptopidine, 32 mg Oxohydrastinine, 27 mg (-)-N-methylanadine, 7 mg N-feruloyltyramine and 3 mg hypecoleptopine could be successfully separated. The amides alkaloid, N-feruloyltyramine, was firstly separated from H. leptocarpum. High-performance liquid chromatography analysis showed that the purity of each of the five target alkaloids was over 92%. Their chemical structures were confirmed by (1)H-NMR and (13)C-NMR data.

Keywords:

Oxohydrastinine,552-29-4,Natural Products, buy Oxohydrastinine , Oxohydrastinine supplier , purchase Oxohydrastinine , Oxohydrastinine cost , Oxohydrastinine manufacturer , order Oxohydrastinine , high purity Oxohydrastinine

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: