Rheum emodi

Ethnobotanical Studies

Clinical Trials

Effect of rhubarb (Rheum emodi) in primary dysmenorrhoea: a single-blind randomized controlled trial.

Rehman H et al (2015).
J Complement Integr Med.
PubMed:
25367691

Studies

In Vitro Antioxidant and Inhibitory Study of Picrorhiza kurroa (Kutki), Syzygium aromaticum (Loung), Lawsonia inermis (Henna), Rheum emodi (Revand Chini), Curcuma longa (Haldi) Against Lipid Per-Oxidation in Mice Brain and Liver.

Summary

This study evaluated the antioxidant and protective properties of certain medicinal plants against oxidative stress in the brain and liver. , , and showed strong effects and could potentially help manage or prevent degenerative diseases.

Hassan F et al (2023).
Dose Response.
PubMed:
37900620

Growth inhibitory effect of selected quinones from Indian medicinal plants against Theileria annulata.

Kiriyanthan RM et al (2023).
Exp Parasitol.
PubMed:
37758051

Ameliorative impact of herbal formulation -Majoon-Dabeed-ul-ward and Sharbat-e-Deenar against CCl(4) induced liver toxicity via regulation of antioxidant enzymes and oxidative stress.

Shakya AK et al (2022).
Toxicol Res (Camb).
PubMed:
36337242

Effect of stress tolerance endophytic bacteria on the growth of Rheum emodi under abiotic stress.

Somal MK and Karnwal A (2022).
Plant Biol (Stuttg).
PubMed:
36000522

Antioxidant Activities of Bioactive Compounds Isolated from Rheum emodi Wall (Himalayan Rhubarb) Based on LC-DAD-ESI/MS and Preparative LC/MS System.

Park SK et al (2022).
Prev Nutr Food Sci.
PubMed:
35919565

Design, synthesis, cytotoxic, and anti-inflammatory activities of some novel analogues of aloe-emodin isolated from the rhizomes of Rheum emodi.

Dileep Kumar G et al (2022).
Nat Prod Res.
PubMed:
35021945

Phytochemical analysis, antioxidant and antibacterial potential of some selected medicinal plants traditionally utilized for the management of urinary tract infection.

Ur Rehman J et al (2021).
Pak J Pharm Sci.
PubMed:
34602432

Phytocompounds of Rheum emodi, Thymus serpyllum, and Artemisia annua Inhibit Spike Protein of SARS-CoV-2 Binding to ACE2 Receptor: In Silico Approach.

Summary

Scientists studied the potential of plant compounds to bind to the spike proteins of SARS-CoV-2 and its variants, as well as to the host receptors the virus uses to enter cells. They performed computer simulations and found that artemisinin had the strongest binding affinity with the spike proteins and was stable in simulations. Emodin had the best interactions with the host receptors. Both compounds were non-toxic. These results suggest that these plant compounds could inhibit SARS-CoV-2 infection and warrant further investigation as potential COVID-19 therapies.

Review COVID-19
Rolta R et al (2021).
Curr Pharmacol Rep.
PubMed:
34306988

Molecular docking studies of phytocompounds of Rheum emodi Wall with proteins responsible for antibiotic resistance in bacterial and fungal pathogens: in silico approach to enhance the bio-availability of antibiotics.

Rolta R et al (2022).
J Biomol Struct Dyn.
PubMed:
33225862

In silico screening of hundred phytocompounds of ten medicinal plants as potential inhibitors of nucleocapsid phosphoprotein of COVID-19: an approach to prevent virus assembly.

Summary

Researchers aimed to identify potential drug candidates for COVID-19 treatment by screening 100 phytocompounds for their binding affinity to the N-terminal domain of nucleocapsid phosphoprotein of SARS-CoV-2. Molecular docking and simulation techniques were used to study the interaction stability of the best three protein-ligand complexes. The phytocompounds which showed good binding affinity and met drug likeness properties and non-toxicity were identified as potential therapy for COVID-19. Alizarin, aloe-emodin, and anthrarufin were identified as the most promising phytocompounds and can be further tested for use as a potential drug to cure SARS-CoV-2 infection.

Rolta R et al (2021).
J Biomol Struct Dyn.
PubMed:
32851912

Antioxidant Activities of Stilbenoids from Rheum emodi Wall.

Chai YY et al (2012).
Evid Based Complement Alternat Med.
PubMed:
23193425