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Gummiferin

$576

Brand : BIOFRON
Catalogue Number : BN-O0007
Specification : 98%(HPLC)
CAS number : 35988-42-2
Formula : C31H46O18S2
Molecular Weight : 770.8
PUBCHEM ID : 108174
Volume : 20mg

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Catalogue Number

BN-O0007

Analysis Method

Specification

98%(HPLC)

Storage

2-8°C

Molecular Weight

770.8

Appearance

Botanical Source

Structure Type

Category

SMILES

CC(C)CC(=O)OC1C(C(C(OC1OC2CC3(C4CCC5CC4(CCC3C(C2)(C(=O)O)C(=O)O)C(C5=C)O)C)CO)OS(=O)(=O)O)OS(=O)(=O)O

Synonyms

Carboxyatractyloside

IUPAC Name

15-hydroxy-7-[6-(hydroxymethyl)-3-(3-methylbutanoyloxy)-4,5-disulfooxyoxan-2-yl]oxy-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5,5-dicarboxylic acid

Density

Solubility

Flash Point

Boiling Point

Melting Point

InChl

InChl Key

AQFATIOBERWBDY-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:35988-42-2) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

30776590

Abstract

BACKGROUND:
As a widely used toxic traditional herbal medicine, the quality of the Fructus Xanthii must be well controlled to ensure the clinical therapeutic efficacy and safety.

AIMS:
A rapid, and sensitive using ultra-high performance liquid chromatography to triple quadrupole tandem mass spectrometry (UPLC-MS/MS) in selected reaction monitoring (SRM) mode was developed and validated for simultaneous quantitation of determination active and toxic ingredients form processed by stir-frying and raw materials of Fructus Xanthii.

METHODS:
Chromatographic separation of all targeted compound was performed on Waters ACQUITY UPLC HSS T3 column (50 mm × 2.1 mm, 1.8 μm). Moreover, the method was successfully applied in thirty-six samples of Fructus Xanthii collected from different sources in China. The processing method was optimized through Box-Behnken statistical design and response surface methodology.

RESULTS:
In this work, chemometrics was able to successfully discriminate and classify among samples. The optimal incubation conditions were as follows: under heating in a pot at 295 °C, medicine at 120 °C for 11.0 min with flipping frequently.

CONCLUSIONS:
Therefore, the established UPLC-QQQ-MS method in combination with chemometric analysis provides a rapid, flexible and reliable method for quality assessment of Fructus Xanthii. Importantly, the optimized experimental value of the processing process provides the basis for future research.

Copyright © 2018. Published by Elsevier GmbH.

KEYWORDS

Active and toxic ingredients; Chemometrics; Fructus Xanthii; UPLC-MS/MS

Title

Chemometrics coupled with UPLC-MS/MS for simultaneous analysis of markers in the raw and processed Fructus Xanthii, and application to optimization of processing method by BBD design.

Author

Jiang H1, Yang L1, Xing X1, Yan M1, Guo X1, Yang B1, Wang QH2, Kuang HX3.

Publish date

2019 Apr

PMID

29128544

Abstract

In order to evaluate the susceptibility of sheep to V. rubricaulis and to establish the clinical signs, serum biochemistry, and pathological findings, eight sheep were fed varying doses of V. rubricaulis. The onset of clinical signs occurred 6-48 h after the ingestion of V. rubricaulis. Clinical courses lasted 6-56 h after the ingestion of the plant. Serum activities of aspartate aminotransferase, gamma-glutamyl transferase, and alkaline phosphatase were highly elevated and glucose blood levels were low in affected sheep. Clinical signs consisted of apathy, anorexia, dry muzzle, respiratory distress, abdominal pain, and mushy feces with streaks of blood and mucus. Two sheep had neurological signs including muscle fasciculation, nystagmus, paddling movements, and blindness. Liver necrosis could be detected antemortem through liver biopsy. Five sheep died and three recovered. The liver was affected in all necropsied sheep; it increased in volume and had marked accentuation of the lobular pattern with red, depressed areas intercalated with a pale yellow network. Ascites and hydropericardium were consistent findings. Microscopically, centrilobular to massive coagulative necrosis was observed. Coagulative necrosis was also observed in a few proximal renal tubules. Microscopic lesions were not found in any other organs. The severity of liver lesions was proportional to the dose. Chemical analysis to detect carboxyatractyloside in V. rubricaulis plant material was negative. It is concluded that V. rubricaulis poisoning in sheep is clinically, biochemically, and pathologically characteristic of an acute hepatoxicosis.

Copyright © 2017 Elsevier Ltd. All rights reserved.

KEYWORDS

Acute liver failure; Hepatotoxicity; Poisonous plants; Sheep diseases; Vernonia rubricaulis

Title

Experimental poisoning by Vernonia rubricaulis in sheep.

Author

Godoy KCS1, Leal PV2, Araújo MA3, Souza AI4, Pott A5, Lee ST6, Barros CSL7, de Lemos RAA8.

Publish date

2018 Jan

PMID

28205519

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a common metabolic disorder in obese individuals. Adenine nucleotide translocase (ANT) exchanges ADP/ATP through the mitochondrial inner membrane, and Ant2 is the predominant isoform expressed in the liver. Here we demonstrate that targeted disruption of Ant2 in mouse liver enhances uncoupled respiration without damaging mitochondrial integrity and liver functions. Interestingly, liver specific Ant2 knockout mice are leaner and resistant to hepatic steatosis, obesity and insulin resistance under a lipogenic diet. Protection against fatty liver is partially recapitulated by the systemic administration of low-dose carboxyatractyloside, a specific inhibitor of ANT. Targeted manipulation of hepatic mitochondrial metabolism, particularly through inhibition of ANT, may represent an alternative approach in NAFLD and obesity treatment.

Title

Mitochondrial ATP transporter depletion protects mice against liver steatosis and insulin resistance.

Author

Cho J1, Zhang Y2, Park SY3, Joseph AM4, Han C4, Park HJ4, Kalavalapalli S5, Chun SK6, Morgan D7, Kim JS6, Someya S4, Mathews CE1, Lee YJ3, Wohlgemuth SE8, Sunny NE5, Lee HY3, Choi CS3,9, Shiratsuchi T2, Oh SP10, Terada N1.

Publish date

2017 Feb 16