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Narciclasine STAT inhibitor

Cat.No.E1124

Narciclasine (Lycoricidinol), an isocarbostyril alkaloid, targets STAT3 via distinct mechanisms in tamoxifen-resistant breast cancer cells. This compound suppresses phosphorylation, activation, dimerization, and nuclear translocation of STAT3 by directly binding with the STAT3 SH2 domain and leads STAT3 degradation. It is a plant growth modulator. This chemical modulates the Rho/Rho kinase/LIM kinase/cofilin signaling pathway, greatly increasing GTPase RhoA activity as well as inducing actin stress fiber formation in a RhoA-dependent manner.
Narciclasine STAT inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 307.26

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Quality Control

Batch: E112401 DMSO]61 mg/mL]false]]]false]]]false Purity: 99.74%
99.74

Solubility

In vitro
Batch:

DMSO : 61 mg/mL (198.52 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

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In vivo
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Chemical Information, Storage & Stability

Molecular Weight 307.26 Formula

C14H13NO7

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 29477-83-6 -- Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
STAT3
In vitro

Narciclasine activates Rho and stress fibers in glioblastoma multiforme cells. The mean IC50 of ~50 nM calculated on the 6 human glioblastoma multiforme (U373, Hs683, GL19, GL5, GL16, GL17), The mean IC50 value of 47 nM for this compound across a panel of 60 cancer cell lines.

In vivo

Narciclasine significantly increases the survival of GL19 glioblastoma multiforme-bearing mice, and the survival of Hs683 glioblastoma multiforme-bearing mice.

References

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