Sorrel (as plant) // Rumex acetosa L.

Family:
Polygonaceae
Approval state:
Approved
Number of articles retrieved:
1276
Number of processed references:
6
Compositions
#1: #2: #3: #4: Nepodin in the plant (plant part unspecified) #5: emodin-8-O-beta -D-glucopyranoside in aerial parts #6: chrysophanol in aerial parts #7: physcion in aerial parts #8: emodin in aerial parts #9: aloin in fruits, leaves and roots #10: anthracene derivatives in fruits #11: anthracene derivatives in leaves #12: anthracene derivatives in roots #13: sennoside A in fruits, leaves and roots #14: chrysophanol in fruits, leaves and roots #15: physcion in fruits, leaves and roots #16: rhein in leaves and roots #17: aloe-emodin in fruits, leaves and roots #18: emodin in fruits, leaves and roots #19: sennoside B in fruits, leaves and roots #20: oxalic acids in leaves
Endpoint Studies
#1: case report - mortality, unconsciousness
Genotoxicity
Composition #1: Sharma, Mrs. Manju., Rangaswami, S. Chemical components of the roots of Rumex acetosa: isolation of ω-acetoxyaloe emodin, a new 1,8-dihydroxyanthraquinone derivative. indian journal of chemistry, section b: organic chemistry including medicinal chemistry, 1977, vol. 15B, no. 10, p. 884–5. .
Composition #2: Sharma, Mrs. Manju., Rangaswami, S. Chemical components of the roots of Rumex acetosa: isolation of ω-acetoxyaloe emodin, a new 1,8-dihydroxyanthraquinone derivative. indian journal of chemistry, section b: organic chemistry including medicinal chemistry, 1977, vol. 15B, no. 10, p. 884–5. .
Composition #3: Sharma, Mrs. Manju., Rangaswami, S. Chemical components of the roots of Rumex acetosa: isolation of ω-acetoxyaloe emodin, a new 1,8-dihydroxyanthraquinone derivative. indian journal of chemistry, section b: organic chemistry including medicinal chemistry, 1977, vol. 15B, no. 10, p. 884–5. .
Composition #4: Hsiao, Pei-Ken., Ho, Li-I., Chen, Pi-Chu., Kuo, Hang-Chou. Botanical and chemical studies of Chinese herbal medicine "Yangti". yaoxue tongbao, 1980, vol. 15, no. 7, p. 48. .
Composition #5: Lee, NJ., Choi, JH., Koo, BS., Ryu, SY., Han, YH., Lee, SI., Lee, DU. Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa . biological & pharmaceutical bulletin, 2005, vol. 28, no. 11, p. 2158–2161. DOI: 10.1248/bpb.28.2158. [DOI link]
Composition #6: Lee, NJ., Choi, JH., Koo, BS., Ryu, SY., Han, YH., Lee, SI., Lee, DU. Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa . biological & pharmaceutical bulletin, 2005, vol. 28, no. 11, p. 2158–2161. DOI: 10.1248/bpb.28.2158. [DOI link]
Composition #7: Lee, NJ., Choi, JH., Koo, BS., Ryu, SY., Han, YH., Lee, SI., Lee, DU. Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa . biological & pharmaceutical bulletin, 2005, vol. 28, no. 11, p. 2158–2161. DOI: 10.1248/bpb.28.2158. [DOI link]
Composition #8: Lee, NJ., Choi, JH., Koo, BS., Ryu, SY., Han, YH., Lee, SI., Lee, DU. Antimutagenicity and cytotoxicity of the constituents from the aerial parts of Rumex acetosa . biological & pharmaceutical bulletin, 2005, vol. 28, no. 11, p. 2158–2161. DOI: 10.1248/bpb.28.2158. [DOI link]
Composition #9: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #10: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #11: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #12: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #13: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #14: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #15: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #16: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #17: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #18: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #19: Wegiera, Magdalena., Smolarz, Helena D., Wianowska, Dorota., Dawidowicz, Andrzej L. Anthracene derivatives in some species of Rumex L. genus. acta societatis botanicorum poloniae, 2007, vol. 76, no. 2, p. 103–108. .
Composition #20: Mithril, Charlotte., Dragsted, Lars Ove. Safety evaluation of some wild plants in the New Nordic Diet. food and chemical toxicology, 2012, vol. 50, no. 12, p. 4461–4467. DOI: 10.1016/j.fct.2012.09.016. [DOI link]
Endpoint study #1: Suckling, C.W. The recent case of poisoning by common sorrel (rumex acetosa). british medical journal, 1886, vol. 2, no. 1339, p. 436. DOI: 10.1136/bmj.2.1339.436. [DOI link]