SMB01019

Amorfrutin A

≥90% (LC/MS-ELSD)

• Szinonimák: 2-hydroxy-4-methoxy-3-(3-methylbut-2-enyl)-6-(2-phenylethyl)benzoic acid, 3-hydroxy-4-isopentenyl-5-methoxybibenzyl-2-carboxylic acid
• Tapasztalati képlet (Hill-képlet): C₂₁H₂₄O₄
• CAS-szám: 80489-90-3
• Molekulatömeg: 340.41
• MDL-szám: MFCD23703108
• UNSPSC kód: 12352205
• NACRES: NA.25

Tulajdonságok

• biológiai forrás: plant
• Teszt: ≥90% (LC/MS-ELSD)
• Forma: solid
• molekulatömeg: 340.41
• oldhatóság: water: slightly soluble
• alkalmazás(ok): metabolomics; vitamins, nutraceuticals, and natural products
• tárolási hőmérséklet: −20°C
• SMILES string: O(C)c1c(c(c(c(c1)CCc2ccccc2)C(=O)O)O)CC=C(C)C
• InChI: 1S/C21H24O4/c1-14(2)9-12-17-18(25-3)13-16(19(20(17)22)21(23)24)11-10-15-7-5-4-6-8-15/h4-9,13,22H,10-12H2,1-3H3,(H,23,24)
• Nemzetközi kémiai azonosító kulcs: CTNFTPUIYFUXBE-UHFFFAOYSA-N

Leírás

Általános leírás

Amorfrutin A is a stilbenoid compound commonly present in plants like Glycyrrhiza foetida, Glycyrrhiza acanthocarpa, Cajanus cajan, and Amorpha fruticosa. Current research indicates that this naturally occurring metabolite possesses diverse biological activities, including anti-inflammatory, anticancer, antidiabetic, and antimicrobial properties.

Alkalmazás

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Biokémiai/fiziológiai hatások

According to the existing research, Amorfrutin-A demonstrated its ability to inhibit NF-κB activity, a pivotal regulator of genes governing a wide range of cellular functions, such as immune responses, apoptosis, tumor growth, and tissue development. Furthermore, it exhibits anti-inflammatory properties in colon cells by interacting with the nuclear receptor PPARγ, resulting in the reduced expression and secretion of inflammatory mediators. This suggests its potential for treating conditions like inflammatory bowel diseases. Additionally, it also exhibited antidiabetic activity through binding to and activating the nuclear receptor PPARγ.

Tulajdonságok és előnyök

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Egyéb megjegyzések

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Biztonsági adatok

• Tárolási osztály kódja: 11 - Combustible Solids
• WGK: WGK 3
• Lobbanási pont (F): Not applicable
• Lobbanási pont (C): Not applicable