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Sanguinarine nitrate
Sanguinarine nitrate
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Sanguinarine nitrate
Price:
CAS No.: 4752-86-7
Catalog No.: CFN70372
Molecular Formula: C20H14N2O7
Molecular Weight: 394.3 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Chelidonium majus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Sanguinarine nitrate shows strong activity on Gram-negative bacteria.
Targets: Antifection
In vitro:
Journal of biological chemistry, 1986, 261(5):2034.
Biochemical and cross-resistance studies with HeLa cell mutants resistant to cardiac glycoside SC4453. Regulation of the resistant form of Na+/K+-ATPase in the mutant cells.[Reference: WebLink]
In HeLa cells, stable mutants which are between 25-to about 200-fold resistant to the cardiac glycoside derivative SC4453 (a digoxin analog which contains a pyridazine ring in place of a lactone ring in the C-17 position) have been isolated after a single step selection in the presence of the drug.
METHODS AND RESULTS:
Based on their cross-resistance pattern towards various cardiac glycosides, the mutants resistant to SC4453 (SCR mutants) appear to be of two different kinds and they differ from the two classes of ouabain-resistant mutants described previously (Gupta, R. S., and Chopra, A. (1985) J. Biol. Chem. 260, 6843-6850). One type of SCR mutants (designated as group C) exhibit a high degree of cross-resistance to all cardiac glycosides and their genins (viz. ouabain, digitoxin, digoxin, digoxigenin, convallatoxin, gitoxin, strophanthidin, and bufalin). In contrast, the second type of SCR mutant (group D) exhibit considerable resistance to only SC4453, digoxin, and digoxigenin, but showed very little or no cross-resistance to the other cardiac glycosides examined. The cross-resistance of the mutants towards cardiac glycosides was highly specific as they exhibited no cross-resistance towards a large number of other structurally and functionally related compounds (viz. ethacrynic acid, Sanguinarine nitrate, penicillic acid, methyl quinolizinum bromide, 5,5'-diphenylhydantoin, deoxycorticosterone, vanadium pentoxide, and adriamycin). The cellular uptake of 86Rb in the mutant cells was found to be resistant to specific cardiac glycosides. Studies on the sensitivity of plasma membrane Na+/K+-ATPase to cardiac glycosides show that about 10-15% of the enzymic activity in the mutant cells was highly resistant to inhibition by the specific drugs to which the mutants exhibit increased resistance. Very interestingly, when the mutant cells are grown in cardiac glycoside-containing medium, the resistant form of the enzyme accounts for about 50-60% of the total enzyme.
CONCLUSIONS:
These results show that both classes of SCR mutants are affected in Na+/K+-ATPase and that the amount of the resistant enzyme in the mutant cells is regulated in response to cardiac glycosides.
Postępy fitoterapii, 2012.
The effect of alkaloids and other groups of plant compounds on bacteria and fungi.[Reference: WebLink]
The studies included 35 substances belonging to alkaloids, coumarins, quinones, polyacetylenes, saponines and other chemical groups.
METHODS AND RESULTS:
It was documented that the strongest antibacterial activity on Gram-positive bacteria showed; shikonine and her derivates, berberine chloride, Sanguinarine nitrate, falkarionol, digitonine and usnic acid. The Sanguinarine nitrate and digitonine showed strong activity on Gram-negative bacteria. Imperatorine, Sanguinarine nitrate, sempervirine, galantamine hydrobromide, falkarinol, alantolactone and aristolochic acid showed the strong activity against yeast fungi and dermatophytes.
CONCLUSIONS:
The mentioned substances inhibited the growth of bacteria in concentration limits 1-250 μg/ml. The conducted studies show the possibility of the use some plant substances in medical practice.
Sanguinarine nitrate Description
Source: The herbs of Chelidonium majus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5361 mL 12.6807 mL 25.3614 mL 50.7228 mL 63.4035 mL
5 mM 0.5072 mL 2.5361 mL 5.0723 mL 10.1446 mL 12.6807 mL
10 mM 0.2536 mL 1.2681 mL 2.5361 mL 5.0723 mL 6.3403 mL
50 mM 0.0507 mL 0.2536 mL 0.5072 mL 1.0145 mL 1.2681 mL
100 mM 0.0254 mL 0.1268 mL 0.2536 mL 0.5072 mL 0.634 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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