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product name Aloeemodin


Description: Aloe emodin (also known as NSC 38628, Rhabarberone) is a hydroxyanthraquinone present in Aloe vera leaves, and has a specific in vitro and in vivo antitumor activity. It is an interferon-inducing agent with IC50 of about 1 μg/mL for JEV and of about 0.33 μg/mL for EV71. Aloe-emodin shows significant inhibitory activity against the P-388 leukemia in mice when administered as a suspension in acetone-Tween 80. Has a specific in vitro and in vivo antineuroectodermal tumor activity. Aloe-emodin treatment led to the dissociation of heat shock protein 90 (HSP90) and ER α and increased ER α ubiquitination.

References: Evid Based Complement Alternat Med. 2013;2013:376123; Carcinogenesis. 2012 Jul;33(7):1406-11; Eur J Pharmacol. 2014 Sep 5;738:125-32. 



Molecular Weight (MW)

270.24 
Formula

C15H10O5 
CAS No.

481-72-1 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 3 mg/mL (11.1 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

NSC 38628, Rhabarberone 

other peoduct :

In Vitro

In vitro activity: Aloe-emodin treatment led to the dissociation of heat shock protein 90 (HSP90) and ER α and increased ER α ubiquitination.  Protein fractionation results suggest that aloe-emodin tended to induce cytosolic ER α degradation. Aloe-emodin, a natural compound found in aloe, inhibited both proliferation and anchorage-independent growth of PC3 cells. Protein content analysis suggested that activation of the downstream substrates of mTORC2, Akt and PKCα, was inhibited by aloe-emodin treatment. Pull-down assay and in vitro kinase assay results indicated that aloe-emodin could bind with mTORC2 in cells and inhibit its kinase activity. Of three anthraquinone derivatives, aloe-emodin, with a lower cytotoxicity showed concentration-dependently reducing virus-induced cytopathic effect and inhibiting replication of influenza A in MDCK cells. Galectin-3 also inhibited influenza A virus replication. Proteomic analysis of treated cells indicated galectin-3 up-regulation as one anti-influenza A virus action by aloe-emodin. Since galectin-3 exhibited cytokine-like regulatory actions via JAK/STAT pathways, aloe-emodin also restored NS1-inhibited STAT1-mediated antiviral responses in transfected cells: e.g., STAT1 phosphorylation of interferon (IFN) stimulation response element (ISRE)-driven promoter, RNA-dependent protein kinase (PKR) and 25,-oligoadenylate synthetase (25,-OAS) expression. AE downregulated mRNA expression and promoter/gelatinolytic activity of Matrix Metalloproteinase (MMP)-2/9, as well as the RhoB expression at gene and protein level. AE suppressed the nuclear translocation and DNA binding of NF-κB. 


Kinase Assay:


Cell Assay

In Vivo Aloe-emodin also exhibited tumor suppression effects in vivo in an athymic nude mouse model. 
Animal model  
Formulation & Dosage  
References Evid Based Complement Alternat Med. 2013;2013:376123; Carcinogenesis. 2012 Jul;33(7):1406-11; Eur J Pharmacol. 2014 Sep 5;738:125-32.  

Pimavanserin

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Author: Sodium channel