(E)-Cardamonin

Synonyms: Alpinetin chalcone, cardamomin

(E)-Cardamonin (Alpinetin chalcone, cardamomin) is a naturally occurring chalcone with strong anti-inflammatory activity. It is a novel TRPA1 antagonist with IC50 of 454 nM and also a NF-κB inhibitor.

(E)-Cardamonin Chemical Structure

(E)-Cardamonin Chemical Structure

CAS: 19309-14-9

Purity & Quality Control

Batch: S386701 DMSO] 87 mg/mL] false] ] ] false] ] ] false Purity: 99.81%
99.81

(E)-Cardamonin Related Products

Signaling Pathway

Choose Selective NF-κB Inhibitors

Biological Activity

Description (E)-Cardamonin (Alpinetin chalcone, cardamomin) is a naturally occurring chalcone with strong anti-inflammatory activity. It is a novel TRPA1 antagonist with IC50 of 454 nM and also a NF-κB inhibitor.
Targets
NF-κB [2]
(Cell-free assay)
TRPA1 [1]
(Cell-free assay)
454 nM
In vitro
In vitro Cardamonin inhibits cancer cell growth by inducing G2/M phase cell cycle arrest and apoptosis via accumulation of ROS. Cardamonin has been reported to have anti-inflammatory and anti-tumor activities. Cardamonin inhibits activation of the NF-κB pathway, which in turn triggers ROS accumulation to activate JNK mitogen-activated protein kinase (MAPK). Cardamonin inhibits viability of NPC cells. It induces G2/M phase arrest in CNE-2 cells. Cardamonin-induced accumulation of ROS is mediated through inhibition of the NF-κB pathway[2]. Cardamonin selectively blocks TRPA1 activation while did not interact with TRPV1 nor TRPV4 channel[1].
Cell Research Cell lines NPC cells
Concentrations 10 μM
Incubation Time 24, 48 and 72 h
Method Cell viability assay: NPC cells are treated with 10 μM cardamonin or 0.1% DMSO, absorbance is measured after 24, 48 and 72 h of treatment.
In Vivo
In vivo Cardamonin inhibits tumor growth in vivo without serious side effects[2].
Animal Research Animal Models Xenograft model (BALB/c nude mice)
Dosages 5 mg/kg
Administration i.p.

Chemical Information & Solubility

Molecular Weight 270.28 Formula

C16H14O4

CAS No. 19309-14-9 SDF --
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 87 mg/mL ( (321.88 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)


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In vivo
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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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