Celosin I

CAS# 1807732-38-2

Celosin I

Catalog No. BCN8723----Order now to get a substantial discount!

Product Name & Size Price Stock
Celosin I: 5mg $75 In Stock
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Quality Control of Celosin I

Number of papers citing our products

Chemical structure

Celosin I

Chemical Properties of Celosin I

Cas No. 1807732-38-2 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C53H82O24 M.Wt 1103.2
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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 Celosin I

The herbs of Celosia argentea

Biological Activity of Celosin I

DescriptionCelosin H, celosin I, and celosin J could be used as chemical markers for the quality control of C. argentea seeds. Celosin I exhibited significant hepatoprotective effect on carbon tetrachloride-induced and N,N-dimethylformamide-induced hepatotoxicity in mice.
In vivo

Novel triterpenoid saponins from the seeds of Celosia argentea L.[Pubmed: 23157342 ]

Nat Prod Res. 2013 Aug;27(15):1353-60.


METHODS AND RESULTS:
Two new triterpenoid saponins Celosin I (1) and Celosin II (2) were isolated from the seeds of Celosia argentea L. (Amaranthaceae). The structures of the two new compounds were elucidated based on chemical analysis and spectral methods (IR, 1-D and 2-D NMR, ESI-MS, HR-ESI-MS).
CONCLUSIONS:
They exhibited significant hepatoprotective effect on carbon tetrachloride-induced and N,N-dimethylformamide-induced hepatotoxicity in mice.

Protocol of Celosin I

Structure Identification
J Asian Nat Prod Res. 2014;16(3):240-7.

New oleanane-type triterpenoid saponins isolated from the seeds of Celosia argentea.[Pubmed: 24456247]


METHODS AND RESULTS:
Three new oleanane-type triterpenoid saponins named celosin H, Celosin I, and celosin J were isolated from the seeds of Celosia argentea L. Their structures were characterized as 3-O-β-D-xylopyranosyl-(1 → 3)-β-D-glucuronopyranosyl-polygalagenin 28-O-β-D-glucopyranosyl ester, 3-O-β-D-glucuronopyranosyl-medicagenic acid 28-O-β-D-xylcopyranosyl-(1 → 4)-α-L-rhamnopyranosyl-(1 → 2)-β-D-fucopyranosyl ester, and 3-O-β-D-glucuronopyranosyl-medicagenic acid 28-O-α-L-arabinopyranosyl-(1 → 3)-[β-D-xylcopyranosyl-(1 → 4)]-α-L-rhamnopyranosyl-(1 → 2)-β-D-fucopyranosyl ester by NMR, MS, and chemical evidences, respectively.
CONCLUSIONS:
In our opinion, celosin H, Celosin I, and celosin J could be used as chemical markers for the quality control of C. argentea seeds.

Celosin I Dilution Calculator

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Celosin I Molarity Calculator

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Preparing Stock Solutions of Celosin I

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 0.9065 mL 4.5323 mL 9.0645 mL 18.1291 mL 22.6613 mL
5 mM 0.1813 mL 0.9065 mL 1.8129 mL 3.6258 mL 4.5323 mL
10 mM 0.0906 mL 0.4532 mL 0.9065 mL 1.8129 mL 2.2661 mL
50 mM 0.0181 mL 0.0906 mL 0.1813 mL 0.3626 mL 0.4532 mL
100 mM 0.0091 mL 0.0453 mL 0.0906 mL 0.1813 mL 0.2266 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.

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References on Celosin I

Dereplication-guided isolation of novel hepatoprotective triterpenoid saponins from Celosiae Semen by high-performance liquid chromatography coupled with electrospray ionization tandem quadrupole-time-of-flight mass spectrometry.[Pubmed:27721071]

J Pharm Biomed Anal. 2017 Jan 5;132:148-155.

Although natural products (NPs) from ethnomedical plants have played a vital role in modern drug discovery, separation and purification of bioactive compounds from plant extract is still challenging. In this study, a dereplication strategy using HPLC-QTOF-MS was employed to rapidly discover and highly targeted isolate the novel hepatoprotective triterpenoid saponins from the methanol extract of Celosiae Semen. Firstly, four known saponins, i.e. celosin H, Celosin I, celosin J, and pseudoginsenoside RT1 were selected as model compounds, and their fragmentation patterns in ESI-QTOF-MS/MS were characterized. Secondly, an HPLC-QTOF-MS/MS method was applied to chemically screen the saponins of interest, and thereby to guide the subsequent fraction and isolation procedure. Thirdly, the targeted isolation of desired compounds afforded two new triterpenoid saponins namely celosin K (1) and celosin L (2), which were structurally elucidated by combination of extensive NMR spectroscopic and chemical analyses. Finally, the protective effects of compounds 1 and 2 against APAP-induced hepatotoxicity in HepG2 cells were evaluated. These results indicate that the HPLC-QTOF-MS-guided isolation is an efficient methodology for isolating new NPs from medicinal plants through improving selectivity in separation and purification process.

Novel triterpenoid saponins from the seeds of Celosia argentea L.[Pubmed:23157342]

Nat Prod Res. 2013 Aug;27(15):1353-60.

Two new triterpenoid saponins Celosin I (1) and Celosin II (2) were isolated from the seeds of Celosia argentea L. (Amaranthaceae). The structures of the two new compounds were elucidated based on chemical analysis and spectral methods (IR, 1-D and 2-D NMR, ESI-MS, HR-ESI-MS). They exhibited significant hepatoprotective effect on carbon tetrachloride-induced and N,N-dimethylformamide-induced hepatotoxicity in mice.

Description

Celosin I, an oleanane-type triterpenoid saponin isolated from the seeds of Celosia argentea L, could be used as chemical markers for the quality control of C. argentea seeds. Celosin I exhibits significant hepatoprotective effect on carbon tetrachloride-induced and N,N-dimethylformamide-induced hepatotoxicity in mice.

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