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Chemical Structure| 481-74-3 Chemical Structure| 481-74-3

Structure of Chrysophanol
CAS No.: 481-74-3

Chemical Structure| 481-74-3

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Chrysophanol, a natural anthraquinone isolated from Dianella longifolia, is an EGFR/mTOR pathway inhibitor.

Synonyms: Chrysophanic acid; NSC 37132; Turkey Rhubarb

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Product Details of Chrysophanol

CAS No. :481-74-3
Formula : C15H10O4
M.W : 254.24
SMILES Code : O=C1C2=C(C=CC=C2O)C(C3=CC(C)=CC(O)=C13)=O
Synonyms :
Chrysophanic acid; NSC 37132; Turkey Rhubarb
MDL No. :MFCD00001208
InChI Key :LQGUBLBATBMXHT-UHFFFAOYSA-N
Pubchem ID :10208

Safety of Chrysophanol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P305+P351+P338

Isoform Comparison

Biological Activity

Target
  • mTOR

  • EGFR/ErbB1

In Vitro:

Cell Line
Concentration Treated Time Description References
HepG2 cells 12.5, 25, 50, 100, 120 μM 48 h To evaluate the cytotoxicity of chrysophanol on HepG2 cells, results showed that chrysophanol predominantly induced cell death through necrosis. PMC9476804
H9C2 cells 1, 10, 20 μM 12 h CHR significantly suppressed the DOX-induced cardiomyocyte injury including the reduction of cell viability, apoptosis and nuclear condensation. PMC6663922
Human podocytes (AB8/13 cells) 40 μM 48 h CHR significantly reversed high glucose (HG)-induced growth inhibition in AB8/13 cells and inhibited HG-promoted cell migration and inflammatory responses. PMC7678702
Caco-2 cells 0.025, 0.05, 0.1 mg/mL To investigate the bidirectional transport characteristics of chrysophanol in the Caco-2 cell monolayer model, results showed higher transport rates in RAI than in SKE, with ER values close to or above 1.5, suggesting it may be a substrate for ATP-binding cassette membrane transporters. PMC9975633
PC12 cells 10, 25, 50 μM 12 h To investigate the neuroprotective effect of chrysophanol (CHR) on PC12 treated with Aβ25-35. Results showed that CHR pretreatment significantly increased cell viability and reduced apoptosis. PMC7381772
Human sebocytes 0–100 μM 48 h To investigate the inhibitory effect of Chrysophanol on heat-induced lipogenesis, results showed that Chrysophanol concentration-dependently suppressed the expression of PPARγ and FAS and reduced lipid accumulation. PMC6555928

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Sprague-Dawley rats DOX-induced cardiomyopathy model Intragastric administration 5, 20, 40 mg/kg Once daily for 7 days Both CHR and 3AB significantly suppressed DOX-induced cardiac apoptosis, mitochondrial impairment and heart dysfunction. PMC6663922
C57BL/6 mice Diabetic nephropathy model Oral 50 mg/kg or 100 mg/kg Once daily for 4 weeks CHR significantly alleviated the symptoms of diabetic nephropathy, including reduced blood glucose, decreased renal inflammation and fibrosis, and inhibited the expression of TGF-β signaling pathway-related proteins. PMC7678702
Sprague-Dawley rats Single-pass intestinal perfusion model Intestinal perfusion 0.94 µg/mL Perfusion rate 0.2 mL/min, duration 120 minutes To study the absorption characteristics of chrysophanol in different intestinal segments, results showed the highest absorption coefficient in the colon, and higher Peff values in RAI than in SKE. PMC9975633

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.93mL

0.79mL

0.39mL

19.67mL

3.93mL

1.97mL

39.33mL

7.87mL

3.93mL

References

 

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