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Inulicin

Catalog No. TQ0169   CAS 33627-41-7
Synonyms: 1-O-Acetylbritannilactone

Inulicin (1-O-Acetylbritannilactone), an active compound isolated from Inula Britannica L, inhibits VEGF-mediated activation of Src and FAK.

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Inulicin Chemical Structure
Inulicin, CAS 33627-41-7
Pack Size Availability Price/USD Quantity
1 mg In stock $ 51.00
5 mg In stock $ 163.00
10 mg In stock $ 250.00
25 mg In stock $ 418.00
50 mg In stock $ 623.00
100 mg In stock $ 887.00
1 mL * 10 mM (in DMSO) In stock $ 178.00
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Purity: 99.77%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Inulicin (1-O-Acetylbritannilactone), an active compound isolated from Inula Britannica L, inhibits VEGF-mediated activation of Src and FAK.
In vitro Inulicin (1-O-Acetylbritannilactone) inhibits angiogenesis and lung cancer cell growth through regulating VEGF-Src-FAK signaling. Inulicin dose-dependently inhibits vascular endothelial growth factor (VEGF)-induced proliferation, migration, and capillary structure formation of cultured human umbilical vascular endothelial cells (HUVECs). Significant high levels of Src and FAK phosphorylations are noticed in A549 cells, which are both inhibited by the treatment of Inulicin (5 μM and 10 μM). Src and FAK are both important for cancer cell proliferation. Thus, A549 cell growth, tested by MTT assay and clonogenicity assay, is remarkably inhibited by corresponding Inulicin treatment. The anti-A549 cell growth activity of Inulicin is again dose-dependent [1]. Inulicin (5, 10, 20 μM) has several concentration-dependent effects, including inhibition of lipopolysaccharide (LPS)-induced PGE2 production and COX-2 expression, and blockade of NF-κB activation and translocation. In addition, Inulicin directly inhibits the binding of active NF-κB to specific DNA cis-element [2].
In vivo Administration of a single dose of Inulicin (12 mg/kg/day) remarkably suppresses the growth of A549 xenografts in nude mice. In vivo, microvessels formation and Src activation are also significantly inhibited in Inulicin-treated xenograft tumors. A single dose of Inulicin (12 mg/kg/day, i.p.) dramatically inhibits the growth of A549 xenografts in nude mice. Further, the weights of Inulicin-treated tumors are remarkably lighter than that of vehicle-treated tumors [1].
Cell Research HUVECs or A549 cells are plated in 60 mm plates (300 cells/plate). After overnight incubation, cells are treated with applied agents (Inulicin; 5 μM and 10 μM) for 24 h. Cells are then washed, and fresh media are added. After 10 days of incubation, surviving colonies are fixed, stained, and manually counted [1].
Animal Research Male nude mice (4-6weeks old, BALB/c) are used. A549 cells (five million cells in 0.1 mL of culture medium) are subcutaneously injected at the right thigh of nude mice, and treatment is started when the tumors reach an average volume of about 100 mm3. Animals are randomized into two groups with 10 mice per group: (a) Vehicle; (b) 12 mg/kg of Inulicin. Inulicin is injected intraperitoneally (i.p.) daily. The mice are examined daily for toxicity/mortality relevant to treatment, and the tumor is measured with a caliper every two days. The tumor volume (in mm3) is calculated, and the tumor growth curve is presented. At the end of experiments, xenograft tumors are isolated through surgery and weighted [1].
Source
Synonyms 1-O-Acetylbritannilactone
Molecular Weight 308.37
Formula C17H24O5
CAS No. 33627-41-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: 45 mg/mL (145.93 mM), sonification is recommended.

TargetMolReferences and Literature

1. Zhengfu H, et al. 1-o-acetylbritannilactone (ABL) inhibits angiogenesis and lung cancer cell growth through regulating VEGF-Src-FAK signaling. Biochem Biophys Res Commun. 2015 Aug 21;464(2):422-7. 2. Liu YP, et al. Acetylbritannilactone suppresses lipopolysaccharide-induced vascular smooth muscle cell inflammatory response. Eur J Pharmacol. 2007 Dec 22;577(1-3):28-34.

Related compound libraries

This product is contained In the following compound libraries:
Tyrosine Kinase Inhibitor Library Immunology/Inflammation Compound Library Anti-Pancreatic Cancer Compound Library Natural Product Library for HTS Anti-Liver Cancer Compound Library Anti-Tumor Natural Product Library Anti-Inflammatory Traditional Chinese Medicine Compound Library NO PAINS Compound Library Anti-Cancer Metabolism Compound Library Selected Plant-Sourced Compound Library

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Keywords

Inulicin 33627-41-7 Angiogenesis Cytoskeletal Signaling Immunology/Inflammation Neuroscience NF-Κb Tyrosine Kinase/Adaptors NF-κB COX FAK Src Inhibitor inhibit Nuclear factor-κB Nuclear factor-kappaB 1-O-Acetylbritannilactone Cyclooxygenase inhibitor

 

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