Structure of Aloe emodin
CAS No.: 481-72-1
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Aloe-emodin, a natural product isolated and purified from the root of Rheum palmatum L. with a specific in vitro and in vivo anti-neuroectodermal tumor activity, reduces the toxicity and ROS induced by both monomeric and oligomeric Aβ species, appears to have some protective effect not only against hepatocyte death but also on the inflammatory response subsequent to lipid peroxidation and has a strong non-carcinogenic stimulant-laxative action when applied to the skin, although it may increase the carcinogenicity of some kind of radiation. Aloe-Emodine dose-dependently inhibited cleavage activity of the 3CLpro with IC50 value of 366μM in the cell-based assay.
Synonyms: Rhabarberone; 3-Hydroxymethylchrysazine; NSC 38628
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CAS No. : | 481-72-1 |
Formula : | C15H10O5 |
M.W : | 270.24 |
SMILES Code : | O=C1C2=C(C=CC=C2O)C(C3=CC(CO)=CC(O)=C13)=O |
Synonyms : |
Rhabarberone; 3-Hydroxymethylchrysazine; NSC 38628
|
MDL No. : | MFCD00017373 |
InChI Key : | YDQWDHRMZQUTBA-UHFFFAOYSA-N |
Pubchem ID : | 10207 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Description |
Aloe emodin (Rhabarberone) is a natural hydroxyanthraquinone with antitumor properties, capable of binding to and inhibiting the kinase activity of mTORC2, thus exerting antiproliferative effects and inducing apoptosis in cells[1].
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In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
HepG2 cells | 0, 50, 100, 200 μM | 0, 12, 24, 48, 72 hours | To evaluate the inhibitory effect of Aloe emodin on the growth of HepG2 cells. The results showed that AE inhibited the growth of HepG2 cells in a time- and concentration-dependent manner. | PMC10600456 |
Human lung non-small cell carcinoma cell line H460 | 40 μM | 16 hours | Investigated Aloe emodin-induced apoptosis, observed nuclear morphological changes and DNA fragmentation. | PMC1573035 |
Human lung squamous carcinoma cell line CH27 | 40 μM | 16 hours | Investigated Aloe emodin-induced apoptosis, observed nuclear morphological changes and DNA fragmentation. | PMC1573035 |
SW480 and HT-29 cells | 50 μM | 16 hours | AE only triggered apoptotic cell death in SW480 and HT-29 cells. | PMC9157280 |
HepG2 cells | 30 μM | 24 hours | To evaluate the effect of AE on cholesterol metabolism, it was found that 30 μM AE significantly inhibited SCAP and PCSK9 protein expression, upregulated LDLR expression, and promoted LDL uptake. | PMC7470781 |
H9C2 cells | 2 μM | 24 hours | To investigate the inhibitory effect of Aloe emodin on X-ray-induced mitochondrial dysfunction and mitophagy | PMC11653682 |
HT22 cells | 2, 4, 6 μM | 24 hours | To evaluate the protective effect of Aloe emodin on Aβ25-35-induced AD cell models and its promotion of cell proliferation. Results showed that 6 μM AE significantly increased cell viability and promoted DNA synthesis. | PMC11931456 |
HeLa cells | 25 μM and 50 μM | 24 hours | AE inhibited proliferation and migration and triggered caspase-dependent cell death of HeLa cells in a dose-dependent manner. | PMC9157280 |
HepG2 cells | 0, 50, 100, 200 μM | 24 hours | To evaluate the effect of Aloe emodin on apoptosis of HepG2 cells. The results showed that AE increased the proportion of early and late apoptotic HCC cells in a concentration-dependent manner. | PMC10600456 |
A375 and MCF7 cells | 50 μM | 24 or 48 hours | AE induced the GSDME activation in A375 and MCF7 cells. | PMC9157280 |
ARPE-19 cells | 0.2, 1.0 and 5.0 µg/mL | 48 hours | Inhibits VEGFA secretion in ARPE-19 cells under hypoxia condition | PMC5118782 |
TE-671 medulloblastoma cells | 0.14 μg/mL (IC50) | 48 hours | To evaluate the antiviral activity of aloe-emodin against enterovirus 71 (EV71), showing an IC50 of 0.14 μg/mL. | PMC7126984 |
HL-CZ promonocyte cells | 0.52 μg/mL (IC50) | 48 hours | To evaluate the antiviral activity of aloe-emodin against enterovirus 71 (EV71), showing an IC50 of 0.52 μg/mL. | PMC7126984 |
TE-671 medulloblastoma cells | 1.51 μg/mL (IC50) | 48 hours | To evaluate the antiviral activity of aloe-emodin against Japanese encephalitis virus (JEV), showing an IC50 of 1.51 μg/mL. | PMC7126984 |
HL-CZ promonocyte cells | 0.50 μg/mL (IC50) | 48 hours | To evaluate the antiviral activity of aloe-emodin against Japanese encephalitis virus (JEV), showing an IC50 of 0.50 μg/mL. | PMC7126984 |
HUVEC cells | 40, 20, 10 μM | 48 hours | Evaluate the effects of AE and EMD on HUVEC cells. The results showed that AE and EMD had minimal impact on the survival rate of HUVEC cells, with survival rates exceeding 80%. | PMC9694700 |
MCF-7 cells | 40, 20, 10 μM | 48 hours | Evaluate the effects of AE and EMD on adhesion, invasion, angiogenesis, and anoikis of MCF-7 cells. The results showed that AE and EMD could inhibit adhesion, invasion, and angiogenesis and induce anoikis of MCF-7 cells. | PMC9694700 |
A375 | 15 μM | 48 hours | Inhibited cell proliferation, disrupted glycolysis and oxidative phosphorylation, reduced TCA cycle intermediates | PMC11990439 |
COLO 794 | 15 μM | 48 hours | Inhibited cell proliferation, disrupted glycolysis and oxidative phosphorylation, reduced TCA cycle intermediates | PMC11990439 |
Mouse lung macrophages (MH-S) | 16 µg/ml | 5 hours | To evaluate the protective effect of Aloe emodin against S. aureus-mediated cell injury. Results showed that Aloe emodin significantly reduced cell death. | PMC6530610 |
Human lung epithelial cells (A549) | 16 µg/ml | 5 hours | To evaluate the protective effect of Aloe emodin against S. aureus-mediated cell injury. Results showed that Aloe emodin significantly reduced cell death. | PMC6530610 |
RAW264.7 cells | 300 μM | Assess the inhibitory effect of AE on inflammatory cytokines in LPS-stimulated RAW264.7 cells, results showed significant suppression of IL-6, IL-1β, and TNF-α upregulation | PMC10418438 | |
RAW264.7 cells | 0–300 μM | Evaluate the cytotoxicity of AE on RAW264.7 cells, results showed no significant toxicity at 0–300 μmol/L | PMC10418438 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
C57BL/6 mice | DSS-induced colitis model | Intragastric administration | 10, 20, 40 mg/kg | Once daily for 7 days | To evaluate the therapeutic effect of aloe emodin on colitis, results showed that aloe emodin significantly alleviated colitis symptoms and promoted mucosal healing | PMC11413701 |
Wistar rats | High-fat diet-induced hyperlipidemia model | Intragastric administration | 100 mg/kg | Once daily for 6 weeks | To evaluate the lipid-lowering effect of AE in hyperlipidemic rats, it was found that AE significantly reduced total cholesterol (TC) and low-density lipoprotein (LDL) levels in serum and liver, ameliorated hepatic lipid aggregation, and upregulated LDL receptor expression by inhibiting the PCSK9/LDLR pathway. | PMC7470781 |
Sprague-Dawley rats | Radiation-induced heart damage model | Intraperitoneal injection | 10 mg/kg | Once daily for 28 days | To evaluate the protective effect of Aloe emodin on radiation-induced heart damage | PMC11653682 |
C57BL/6 mice | CLP-induced sepsis model | Intraperitoneal injection | 0.1, 1.0, and 10 mg/kg | Once daily, continuous observation | Evaluate the therapeutic effect of AE on CLP-induced sepsis in mice, results showed AE significantly improved survival rate and reduced inflammatory response and organ damage | PMC10418438 |
Sprague-Dawley rats | PSD rat model induced by MCAO + CUMS | Oral gavage | 100 mg/kg | Once daily for 21 days | AE significantly improved behavioral function, reduced depression levels, improved brain tissue damage and lesions, increased the number of brain tissue neurons, decreased the contents of AQP3, AQP4, AQP5, GFAP, and TRPV4 in the brain and brain tissue, and increased the protein expressions of BDNF and NTF3 in PSprague-Dawley rats. | PMC10048947 |
APP/PS1 double transgenic mice | Alzheimer's disease model | Intragastric | 25, 50, 100 mg/kg | Once daily for 28 days | To evaluate the effect of Aloe emodin on cognitive dysfunction and hippocampal neuronal damage in AD model mice. Results showed that AE significantly improved cognitive function, reduced hippocampal damage, and activated mitophagy via the AMPK/PGC-1α/SIRT3 pathway. | PMC11931456 |
Guinea pigs | T. rubrum-caused tinea corporis model | Topical application | 10 μM | Once daily for three consecutive days | Evaluate the therapeutic efficacy of AE-mediated aPDT for T. rubrum-caused tinea corporis. Results showed that after three treatments, skin lesions were significantly improved, and fungal cells on the skin surface were completely inactivated. | PMC8867962 |
C57BL/6J mice | S. aureus pneumonia model | Hypodermic injection | 100 mg/kg | Every 8 hours for 72 hours | To evaluate the protective effect of Aloe emodin against S. aureus pneumonia. Results showed that Aloe emodin significantly reduced mortality in infected mice and decreased lung inflammation and bacterial colonization. | PMC6530610 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.70mL 0.74mL 0.37mL |
18.50mL 3.70mL 1.85mL |
37.00mL 7.40mL 3.70mL |
Tags: Aloe emodin | Rhabarberone | Ketones | Plant Standard | Other Compounds | 3CLpro | Organic Building Blocks | Anti-Infection | Small Molecule Positive Drugs | Drug Analysis | 481-72-1
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