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Chemical Structure| 518-82-1 Chemical Structure| 518-82-1

Structure of Emodin
CAS No.: 518-82-1

Chemical Structure| 518-82-1

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Emodin (Frangula emodin), an anthraquinone derivative, is an anti-SARS-CoV compound that blocks the interaction between the SARS coronavirus spike protein and angiotensin-converting enzyme 2 (ACE2). Emodin inhibits casein kinase-2 (CK2) and has anti-inflammatory and anticancer effects. It is also a potent selective 11β-HSD1 inhibitor with IC50 values of 186 nM and 86 nM for human and mouse 11β-HSD1, respectively, and ameliorates metabolic disorders in diet-induced obese mice.

Synonyms: Frangula emodin; Archin; rheum emodin, 3-methyl-1,6,8-trihydroxyanthraquinone, Schuttgelb, and Persian Berry Lake.

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Product Details of Emodin

CAS No. :518-82-1
Formula : C15H10O5
M.W : 270.24
SMILES Code : O=C1C2=C(C=C(C)C=C2O)C(C3=CC(O)=CC(O)=C13)=O
Synonyms :
Frangula emodin; Archin; rheum emodin, 3-methyl-1,6,8-trihydroxyanthraquinone, Schuttgelb, and Persian Berry Lake.
MDL No. :MFCD00001207

Safety of Emodin

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Emodin

DNA
Hedgehog

Isoform Comparison

Biological Activity

Target
  • Dehydrogenase

Protocol

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

References

[1]Feng Y, Huang SL, et al, Leng Y. Emodin, a natural product, selectively inhibits 11beta-hydroxysteroid dehydrogenase type 1 and ameliorates metabolic disorder in diet-induced obese mice. Br J Pharmacol. 2010 Sep;161(1):113-26.

[2]Yim H, Lee YH, et al. Emodin, an anthraquinone derivative isolated from the rhizomes of Rheum palmatum, selectively inhibits the activity of casein kinase II as a competitive inhibitor. Planta Med. 1999 Feb;65(1):9-13.

[3]Liu JX, Zhang JH, et al. Emodin induces Panc-1 cell apoptosis via declining the mitochondrial membrane potential. Oncol Rep. 2012 Dec;28(6):1991-6.

[4]Song P, Kim JH, et al. Emodin regulates glucose utilization by activating AMP-activated protein kinase. J Biol Chem. 2013 Feb 22;288(8):5732-42.

[5]Tzeng TF, Lu HJ, et al. Emodin, a Naturally Occurring Anthraquinone Derivative, Ameliorates Dyslipidemia by Activating AMP-Activated Protein Kinase in High-Fat-Diet-Fed Rats. Evid Based Complement Alternat Med. 2012;2012:781812.

[6]Li RR, Liu XF, et al. Pharmacodynamics of Five Anthraquinones (Aloe-emodin, Emodin, Rhein, Chysophanol, and Physcion) and Reciprocal Pharmacokinetic Interaction in Rats with Cerebral Ischemia. Molecules. 2019 May 17;24(10). pii: E1898.

[7]Yim H, Lee YH, Lee CH, Lee SK. Emodin, an anthraquinone derivative isolated from the rhizomes of Rheum palmatum, selectively inhibits the activity of casein kinase II as a competitive inhibitor. Planta Med. 1999 Feb;65(1):9-13. doi: 10.1055/s-1999-13953. PMID: 10083837.

[8]Xing JY, Song GP, Deng JP, Jiang LZ, Xiong P, Yang BJ, Liu SS. Antitumor Effects and Mechanism of Novel Emodin Rhamnoside Derivatives against Human Cancer Cells In Vitro. PLoS One. 2015 Dec 18;10(12):e0144781. doi: 10.1371/journal.pone.0144781. PMID: 26682731; PMCID: PMC4684281.

[9]Li X, Wang H, Wang J, Chen Y, Yin X, Shi G, Li H, Hu Z, Liang X. Emodin enhances cisplatin-induced cytotoxicity in human bladder cancer cells through ROS elevation and MRP1 downregulation. BMC Cancer. 2016 Aug 2;16:578. doi: 10.1186/s12885-016-2640-3. PMID: 27485374; PMCID: PMC4971704.

 

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