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Aurantiamide benzoate
Aurantiamide benzoate
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Aurantiamide benzoate
Price:
CAS No.: 150881-02-0
Catalog No.: CFN91929
Molecular Formula: C32H30N2O4
Molecular Weight: 506.59 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Inula cappa
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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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: Aurantiamide benzoate exhibits moderate inhibitory activity against xanthine oxidase.
In vitro:
Yakugaku Zasshi. 2007 Feb;127(2):389-95.
Biological activity tests of chemical constituents from two Brazilian Labiatae plants.[Pubmed: 17268160]
We studied the bioactivities of constituents from two tropical medicinal plants, Cunila spicata and Hyptis fasciculata. These plants found in Brazil belong to the Labiatae family.
METHODS AND RESULTS:
Four known compounds obtained from these herbs were identified as 3alpha, 24-dihydoxylurs-12-en-28-oic acid, betulinic acid, aurantiamide acetate, and Aurantiamide benzoate by spectroscopic means. 3alpha, 24-Dihydoxylurs-12-en-28-oic acid has potent inhibitory activity against Streptococcus salivarius, Streptococcus pneumoniae, Streptococcus pyogenes, and Porphyromomas gingivalis. Aurantiamide benzoate exhibited moderate inhibitory activity against xanthine oxidase.
CONCLUSIONS:
It was clarified that herbs Cunila spicata and Hyptis fasciculata are effective against bronchitis and gout.
Aurantiamide benzoate Description
Source: The herbs of Inula cappa
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.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

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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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.974 mL 9.8699 mL 19.7398 mL 39.4797 mL 49.3496 mL
5 mM 0.3948 mL 1.974 mL 3.948 mL 7.8959 mL 9.8699 mL
10 mM 0.1974 mL 0.987 mL 1.974 mL 3.948 mL 4.935 mL
50 mM 0.0395 mL 0.1974 mL 0.3948 mL 0.7896 mL 0.987 mL
100 mM 0.0197 mL 0.0987 mL 0.1974 mL 0.3948 mL 0.4935 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.
Protocol
Structure Identification:
Zhong Yao Cai. 2005 Feb;28(2):102-4.
Studies on constituents from Ligularia narynensis.[Pubmed: 15981879]
To study the chemical constituents from Ligularia narynensis.
METHODS AND RESULTS:
The constituents were isolated and purified by column chromatography and the structures were identified by physicochemical properties and spectral analysis. Six compounds were obtained as Aurantiamide benzoate (1), aurantiamide acetate (2), 1-O-octacosanoylgerol (3), beta-sitosterol (4), daucesterol (5), ferulic acid (6).
CONCLUSIONS:
All these compounds were obtained from this plant for the first time. Compounds 1 and 2 were isolated for the first time from this genus.
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6-Methoxyluteolin

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