SMB01019

Amorfrutin A

≥90% (LC/MS-ELSD)

Manufacturer: Sigma Aldrich

CAS Number: 80489-90-3

Synonym(S): 2-hydroxy-4-methoxy-3-(3-methylbut-2-enyl)-6-(2-phenylethyl)benzoic acid, 3-hydroxy-4-isopentenyl-5-methoxybibenzyl-2-carboxylic acid

Select a Size

Pack Size SKU Availability Price
1 MG SMB01019-1-MG In Stock ₹ 41,611.30

SMB01019 - 1 MG

₹ 41,611.30

In Stock

Quantity

1

Base Price: ₹ 41,611.30

GST (18%): ₹ 7,490.034

Total Price: ₹ 49,101.334

biological source

plant

Assay

≥90% (LC/MS-ELSD)

form

solid

mol wt

340.41

solubility

water: slightly soluble

application(s)

metabolomicsvitamins, nutraceuticals, and natural products

storage temp.

−20°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)

InChI key

CTNFTPUIYFUXBE-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
AH62037
80489-90-3 | 2-Hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-phenethylbenzoic acid
A2B Chem --

Description

  • General description: 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.
  • Application: It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
  • Biochem/physiol Actions: 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[1]. 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[2]. Additionally, it also exhibited antidiabetic activity through binding to and activating the nuclear receptor PPARγ[3].
  • Features and Benefits: High quality compound suitable for multiple research applicationsCompatible with HPLC and mass spectrometry techniques
  • Other Notes: For additional information on our range of Biochemicals, please complete this form.

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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SMB01019

≥90% (LC/MS-ELSD)...


biological source:
plant

Assay:
≥90% (LC/MS-ELSD)

form:
solid

mol wt:
340.41

solubility:
water: slightly soluble

application(s):
metabolomicsvitamins, nutraceuticals, and natural products

storage temp.:
−20°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)

InChI key:
CTNFTPUIYFUXBE-UHFFFAOYSA-N

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plant

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application(s):
metabolomicsvitamins, nutraceuticals, and natural products

storage temp.:
−20°C

InChI:
__

InChI key:
__

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1S/C27H30O15/c28-7-15-19(34)20(35)23(38)27(41-15)42-24-16(8-29)40-26(22(37)21(24)36)18-12(32)5-11(31)17-13(33)6-14(39-25(17)18)9-1-3-10(30)4-2-9/h1-6,15-16,19-24,26-32,34-38H,7-8H2/t15-,16-,19-,20+,21-,22-,23-,24-,26+,27+/m1/s1

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NDSUKTASTPEKBX-LXXMDOISSA-N

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InChI:
__

InChI key:
__