Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In Nepal, healers treat indigestion and urinary complaints by drinking a warm root decoction prepared from Rumex nepalensis; dried roots are simmered for fifteen to twenty minutes and the liquid strained before use, as reported by Manandhar. In the eastern Himalayas of Bhutan, a leaf poultice is made to control swelling and promote wound healing; fresh leaves are crushed and applied directly, while the same part is also eaten as a cooked vegetable and used medicinally as an emollient, a practice recorded by Ghimire. Across Sikkim and northern West Bengal, communities prepare a decoction of the aerial parts or root for fever; decoctions are taken in small cups, while poultices of crushed leaves are used on swellings and wounds, as described by Ghimire. In parts of the Western Himalaya, roots are employed in a poultice for rheumatism and contusions, and a whole-plant decoction is taken for dysentery, documented by Ghimire, while an aerial-part decoction has been used for fever in similar regions.

A practical preparation for a mild decoction uses one to two teaspoons (about 2 to 4 grams) of dried Rumex nepalensis roots cut small and simmered in one cup (about 250 milliliters) of water for fifteen to twenty minutes; let cool, strain, and drink half to three-quarters of a cup. The same proportion can be used for a leaf poultice: mix one part freshly crushed leaves with two parts clean water to form a moist paste, apply to the area, cover with a soft cloth, and change two to three times daily. Because Rumex species contain oxalic acid, limit internal use to short courses and avoid if you have a history of calcium oxalate kidney stones; people with arthritis or gout should also use caution. The plant may interact with anticoagulants and blood‑sugar–lowering drugs and is not recommended during pregnancy or while nursing.

The traditional uses of Rumex nepalensis align with well‑established constituents present in several dock species: anthraquinones such as emodin, rhein, and chrysophanol, which have laxative effects; flavonoids and polyphenols that contribute to antioxidant and anti‑inflammatory actions; and oxalic acid, which can be moderately irritating and is central to the safety guidance above. These phytochemicals are reported in a profile of Himalayan dock species by Nair and Bhatt.

Rumex nepalensis remains in active use in village pharmacies and home gardens across Nepal, Bhutan, and Sikkim, and its extracts are under laboratory study for antimicrobial, anti‑inflammatory, and anti‑diabetic activities; dried roots and cut aerial parts are sold in local herbal markets, while tinctures and standardized extracts are increasingly offered by herbal companies in South Asia.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Rumex camptodon	Rech.f.	Beih. Bot. Centralbl. 49(2): 76 (1932)
Rumex bequaertii var. quarrei	(De Wild.) Robyns	Fl. Spermat. Parc Natl. Albert 1: 117 1948
Rumex quarrei	De Wild.	Pl. Bequaert. 5: 3 (1929)
Rumex bequaertii	De Wild.	Pl. Bequaert. 5: 2 (1929)
Rumex esquirolii	H.Lév.	Repert. Spec. Nov. Regni Veg. 11: 550 (1913)
Rumex ramulosus	Meisn.	Prodr. 14: 55 (1856)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Amharic	ቱልት
Chinese	牛耳大黄
Chinese	羊蹄
Chinese	土大黄
Chinese	羊蹄叶
Chinese	羊蹄实
Chinese	尼泊尔酸模
Chinese	尼泊爾酸模

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Rumex nepalensis var. remotiflorus	(Sam.) A.J.Li	Fl. Reipubl. Popularis Sin. 25(1): 161 (1998)

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Lesotho
  - Northern Provinces
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Madagascar

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen
- China
  - China North-central
  - China South-central
  - China Southeast
  - Qinghai
  - Tibet
- Eastern Asia
  - Japan
- Middle Asia
  - Tadzhikistan
- Western Asia
  - Afghanistan
  - Iran
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Myanmar
  - Vietnam
- Malesia
  - Jawa

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Yugoslavia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000403958
Tropicos	26001170
Flora of Italy	425
KEW	urn:lsid:ipni.org:names:697338-1
The Plant List	kew-2424706
Open Tree Of Life	1043326
Observations.org	135491
NCBI Taxonomy	174652
NBN Atlas	NHMSYS0000462979
IPNI	697338-1
iNaturalist	278468
GBIF	7291884
EPPO	RUMNE
EOL	2872862
Elurikkus	583962
USDA GRIN	32540
CMAUP	NPO574

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Medicinal ethnoveterinary plants used for treating livestock ailments in the omo-gibe and rift valley basins of Ethiopia

Wendimu A, Bojago E, Abrham Y

BMC Vet Res

30-Apr-2024

PMCID:	PMC11059770
doi:	10.1186/s12917-024-04019-6
PMID:	38689300

Plant cultural indicators of forest resources from the Himalayan high mountains: implications for improving agricultural resilience, subsistence, and forest restoration

Haq SM, Khoja AA, Waheed M, Pieroni A, Siddiqui MH, Bussmann RW

J Ethnobiol Ethnomed

24-Apr-2024

PMCID:	PMC11040985
doi:	10.1186/s13002-024-00685-w
PMID:	38659048

Isolation of quinic acid from dropped Citrus reticulata Blanco fruits: its derivatization, antibacterial potential, docking studies, and ADMET profiling

Heena, Kaushal S, Kaur V, Panwar H, Sharma P, Jangra R

Front Chem

18-Apr-2024

PMCID:	PMC11064019
doi:	10.3389/fchem.2024.1372560
PMID:	38698937

Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia

Seraw E, Melkamu Y, Masresha G

J Ethnobiol Ethnomed

17-Apr-2024

PMCID:	PMC11025143
doi:	10.1186/s13002-024-00678-9
PMID:	38632559

A dataset for fine-grained seed recognition

Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y

Sci Data

06-Apr-2024

PMCID:	PMC10998916
doi:	10.1038/s41597-024-03176-5
PMID:	38582756

Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023

Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Kafeero HM, Ssenku JE, Alemu SO, Walusansa A, Niyonzima N, Muwonge H

Integr Cancer Ther

06-Mar-2024

PMCID:	PMC10916491
doi:	10.1177/15347354241235583
PMID:	38445504

Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia

Nuro GB, Tolossa K, Giday M

J Exp Pharmacol

05-Mar-2024

PMCID:	PMC10929209
doi:	10.2147/JEP.S449496
PMID:	38476311

Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia

Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW

J Ethnobiol Ethnomed

28-Feb-2024

PMCID:	PMC10900619
doi:	10.1186/s13002-024-00666-z
PMID:	38419092

Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia

Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A

J Ethnobiol Ethnomed

22-Feb-2024

PMCID:	PMC10885532
doi:	10.1186/s13002-024-00651-6
PMID:	38389077

Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices

Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M

BMC Complement Med Ther

14-Feb-2024

PMCID:	PMC10865668
doi:	10.1186/s12906-024-04379-4
PMID:	38355544

Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia

Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E

J Ethnobiol Ethnomed

04-Jan-2024

PMCID:	PMC10768247
doi:	10.1186/s13002-023-00644-x
PMID:	38178202

Medicinal Plants in Treating Hepatitis B Among Communities of Central Region of Ethiopia

Beykaso G, Teklehaymanot T, Mulu A, Berhe N, Alemayehu DH, Giday M

Hepat Med

29-Dec-2023

PMCID:	PMC10759923
doi:	10.2147/HMER.S440351
PMID:	38170153

Prevalence of herbal and traditional medicine in Ethiopia: a systematic review and meta-analysis of 20-year studies

Tuasha N, Fekadu S, Deyno S

Syst Rev

13-Dec-2023

PMCID:	PMC10717384
doi:	10.1186/s13643-023-02398-9
PMID:	38093343

Molecular Signature of a Novel Alternanthera Yellow Vein Virus Variant Infecting the Ageratum conyzoides Weed in Oman

Shafiq M, Ondrasek G, Al-Sadi AM, Shahid MS

Viruses

04-Dec-2023

PMCID:	PMC10747960
doi:	10.3390/v15122381
PMID:	38140622

The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies

Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K

J Ethnobiol Ethnomed

30-Nov-2023

PMCID:	PMC10688143
doi:	10.1186/s13002-023-00631-2
PMID:	38037066

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Anthracenes
1,3,8-Trihydroxy-6-methyl-9(10H)-anthracenone	122635	Click to see	256.25	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Endocrocin	160483	Click to see	314.25	unknown	https://doi.org/10.1055/S-0030-1249779
> Benzenoids / Anthracenes / Anthraquinones
((2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(8-Hydroxy-6-Methyl-9,10-Dioxoanthracen-1-Yl)Oxyoxan-2-Yl)Methyl 3,4,5-Trihydroxybenzoate	5315852	Click to see	568.50	unknown	via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(8-hydroxy-6-methyl-9,10-dioxoanthracen-1-yl)oxyoxan-2-yl]methyl acetate	71452247	Click to see	458.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
[3,4,5-Trihydroxy-6-(8-hydroxy-6-methyl-9,10-dioxoanthracen-1-yl)oxyoxan-2-yl]methyl acetate	78072042	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC(=O)C)O)O)O	458.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
1,8-Dihydroxy-3-methyl-4a,9a-dihydroanthracene-9,10-dione	24867638	Click to see	256.25	unknown	via CMAUP database
Chrysophanol	10208	Click to see	254.24	unknown	via CMAUP database
Chrysophanol-8-O-beta-D-glucopyranoside [M+H]+	4483734	Click to see	416.40	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
Physcion	10639	Click to see	284.26	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
Pulmatin	442731	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O	416.40	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
[(2R,3S,4S,5R,6S)-6-(6,8-dihydroxy-3-methyl-9,10-dioxoanthracen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	162909929	Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC(=O)C)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O	474.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Citreorosein	361512	Click to see	286.24	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Emodin	3220	Click to see	270.24	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
Emodin 1-glucoside	13084799	Click to see	432.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Emodin 1-O-beta-D-glucoside	5319333	Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O	432.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Emodin-8-glucoside	99649	Click to see	432.40	unknown	https://doi.org/10.1055/S-0030-1249779
Emodin(1-)	25201450	Click to see	269.23	unknown	via CMAUP database
Glucofrangulin	318730	Click to see	432.40	unknown	https://doi.org/10.1055/S-0030-1249779
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol	125	Click to see C1=CC(=CC=C1CO)O	124.14	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
Nepodin	100780	Click to see	216.23	unknown	https://doi.org/10.1002/JLAC.18962910304 https://doi.org/10.1055/S-0030-1249779
Torachrysone	5321977	Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)O)OC	246.26	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane	11008	Click to see	450.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rosavin	9823887	Click to see	428.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Neral	643779	Click to see	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Illudanes and illudins / Melleolides and analogues
Armillaridin	51351607	Click to see CC1=C(C(=CC(=C1Cl)OC)O)C(=O)OC2CC3(C2(C(=CC4C3CC(C4)(C)C)C=O)O)C	448.90	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyl-5-tricyclo[8.7.0.02,7]heptadeca-1(17),11-dienyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101389367	Click to see	576.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
Bacopaside I	21599442	Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C	979.10	unknown	via CMAUP database
Bacopaside Ii	9876264	Click to see	929.10	unknown	via CMAUP database
Bacopaside III	15922618	Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)O)C)C)C	847.00	unknown	via CMAUP database
Bacopaside IV	10865594	Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C	767.00	unknown	via CMAUP database
Bacopaside N1	11949626	Click to see	797.00	unknown	via CMAUP database
Bacopaside N2	21574494	Click to see	797.00	unknown	via CMAUP database
Bacopaside V	11072737	Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C	767.00	unknown	via CMAUP database
Bacopaside X	10629555	Click to see	899.10	unknown	via CMAUP database
Bacoside A3	91827005	Click to see	929.10	unknown	via CMAUP database
Bacosine	71312547	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C	456.70	unknown	via CMAUP database
Bascopasaponin C	21599443	Click to see	899.10	unknown	via CMAUP database
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4S,5R,6S)-6-(7-acetyl-8-hydroxy-6-methylnaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methyl but-2-enoate	162925614	Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC3=C2C(=C(C(=C3)C)C(=O)C)O)O)O)O	446.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Rumexneposide A	71461206	Click to see CC=CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC3=C2C(=C(C(=C3)C)C(=O)C)O)O)O)O	446.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(7S,8S,9S,10R,13R,14S,16R,17R)-2,7,16-trihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate	16216753	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2C(C=C4C3C=C(C(=O)C4(C)C)O)O)C)C)C)O)O	572.70	unknown	via CMAUP database
Cucurbitacin E	5281319	Click to see	556.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methyldesmosterol	193567	Click to see	398.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltricyclo[8.7.0.02,7]heptadeca-1(17),11-dien-5-ol	101389368	Click to see	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone	5319972	Click to see	378.40	unknown	https://doi.org/10.1055/S-0030-1249779 https://doi.org/10.1016/J.PHYTOL.2010.05.005
Torachrysone 8-glucoside	14345578	Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC	408.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Torachrysone 8-O-Glucoside	11972479	Click to see	408.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
torachrysone-8-O-(acetyl)-glucoside	162867966	Click to see	450.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
> Organoheterocyclic compounds / Benzofurans
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3',4'-Dimethoxycinnamic acid	16848	Click to see	208.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
Ferulic acid glucoside	53978589	Click to see	356.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see	290.27	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(+)-Catechin 3-Gallate	5276454	Click to see	442.40	unknown	via CMAUP database
Epicatechin-3-Gallate	65056	Click to see	442.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one	11602329	Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC	328.27	unknown	https://doi.org/10.1002/JLAC.18962910304 https://doi.org/10.1016/J.PHYTOL.2010.05.005 https://doi.org/10.1055/S-0030-1249779
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[2,4,6-Trihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-1-propanone	19744872	Click to see	342.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol	5056	Click to see	228.24	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005
Resveratrol	445154	Click to see	228.24	unknown	https://doi.org/10.1016/J.PHYTOL.2010.05.005

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Rumex nepalensis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top