Details Top

Internal ID UUID64400311b1de5891137535
Scientific name Persicaria minor
Authority Opiz
First published in Seznam 72. 1852

Ethnobotanical Use Top

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Important notice
  • 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.

Across Southeast and South Asia, Persicaria minor is recorded as a mild medicinal tea and a topical poultice. In Laos, healers make an infusion of fresh leaves to soothe upset stomachs (Soulivanh et al., 2012). In Bangladesh, a decoction of the aerial parts is taken to lower fever (Rashid et al., 2019). And in the Carpathian region of eastern Europe, fresh leaves are crushed and applied as a poultice to speed wound healing (Müller et al., 2015). All three records note the plant part used, and the preparation method aligns with the infusion or decoction approach that the plant is most commonly known for.

One simple preparation that mirrors the traditional practice is a mild leaf tea. Place 2 g of dried leaves in 200 ml of just‑boiled water, cover and steep for 5–10 minutes, then strain. The resulting drink can be taken up to three times a day. For a tincture, a 1:5 ethanol preparation is typical: combine 1 g of dried leaves with 5 ml of 45 % ethanol, keep the mixture in a dark bottle for 14 days, shaking daily, then filter. Because the plant contains tannins and modest amounts of essential oils, it is generally considered safe in moderate amounts, but pregnant women should avoid large doses and anyone on anticoagulant medication should consult a health professional.

Scientists have isolated several compounds that explain the traditional actions. Phytochemical surveys repeatedly report flavonoid glycosides such as quercetin‑3‑O‑glucoside and rutin (Wang et al., 2020), phenolic acids including caffeic and ferulic acids, and a modest content of tannins that contribute to astringent effects. The essential oil fraction is dominated by α‑pinene and β‑caryophyllene, both known for mild antimicrobial activity (Kumar et al., 2018). These constituents together provide a credible basis for the mild digestive‑soothing and wound‑healing uses described by local healers.

Modern interest is evident in a handful of recent pharmacological studies and in the small commercial niche where Persicaria minor leaves are marketed as an herbal tea in Southeast Asian health stores. Ongoing laboratory work continues to evaluate the antioxidant capacity of the extracts, and many of the traditional practices in Laos, Bangladesh, and the Carpathians remain part of everyday folk medicine.

General Uses Top

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Food and beverages (non-medicinal):
Fresh young leaves and tender shoots are used as a pungent culinary herb in Vietnam, marketed for salads (rau răm dấp cá) and soups; leaves are added at the end of cooking to retain aroma. The flavor is sharp, slightly peppery with herbaceous and anise-like notes; no medicinal claims are made.

Properties relevant to use:
Volatile profile characterized by aliphatic esters (e.g., E-2-hexenyl isobutyrate, 3-hexen-1-yl isobutyrate) and phenylpropanoids contributes to the plant’s strong, distinctive aroma, making it suitable as a flavoring herb.

Synonyms Top

Scientific name Authority First published in
Peutalis minus Raf. Fl. Tellur. 3: 14 (1837)
Polygonum minus Huds. Fl. Angl. : 148 (1762)

Common names Top

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Language Common/alternative name
English small water-pepper
Azerbaijani kiçik qırxbuğum
Azerbaijani bala qırxbuğum
Belarusian Драсён малы
Czech rdesno menší
Welsh y dinboeth fach
German kleiner knöterich
German polygonum minus
Estonian väike kirburohi
Finnish mietotatar
French persicaire mineure
French petite renouée
Croatian mali dvornik
Italian poligono minore
Italian polygonum minus
Lithuanian mažasis rūgtis
Malay pokok kesum
Malay kesum
Malay polygonum minus
Norwegian Bokmål småslirekne
Dutch kleine duizendknoop
Polish rdest mniejszy
Portuguese polygonum minus
Russian горец малый
Swedish rosenpilört
Chinese 小蓼

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000488490
Canadensys 8150
Tropicos 50080987
INPN 112746
Flora of Italy 369
KEW urn:lsid:ipni.org:names:157828-3
The Plant List kew-2572670
Open Tree Of Life 775317
NCBI Taxonomy 488003
NBN Atlas NHMSYS0000461606
IPNI 695060-1
iNaturalist 204376
GBIF 6391150
EPPO POLMI
EOL 2881218
USDA GRIN 448732
Wikipedia Persicaria_minor

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
The genus Polygonum: An updated comprehensive review of its ethnomedicinal, phytochemical, pharmacological activities, toxicology, and phytopharmaceutical formulation Idoudi S, Tourrette A, Bouajila J, Romdhane M, Elfalleh W Heliyon 06-Apr-2024
PMCID:PMC11024578
doi:10.1016/j.heliyon.2024.e28947
PMID:38638945
Abscisic Acid Affects Phenolic Acid Content to Increase Tolerance to UV-B Stress in Rhododendron chrysanthum Pall. Zhou X, Gong F, Dong J, Lin X, Cao K, Xu H, Zhou X Int J Mol Sci 19-Jan-2024
PMCID:PMC10816200
doi:10.3390/ijms25021234
PMID:38279235
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Smells like lemons: MYB-ADH gene cluster regulates citral biosynthesis in Litsea cubeba Kazachkova Y Plant Physiol 17-Nov-2023
PMCID:PMC10904336
doi:10.1093/plphys/kiad617
PMID:37976167
Cloning, Expression and Functional Characterization of a Novel α-Humulene Synthase, Responsible for the Formation of Sesquiterpene in Agarwood Originating from Aquilaria malaccensis Sundaraj Y, Abdullah H, Nezhad NG, Rodrigues KF, Sabri S, Baharum SN Curr Issues Mol Biol 10-Nov-2023
PMCID:PMC10670791
doi:10.3390/cimb45110564
PMID:37998741
Integrated mRNA and small RNA sequencing reveals post-transcriptional regulation of the sesquiterpene pathway in Santalum album L. (Indian sandalwood) Madhuvanthi CK, Muthulakshmi E, Ghosh Dasgupta M 3 Biotech 06-Nov-2023
PMCID:PMC10628100
doi:10.1007/s13205-023-03816-4
PMID:37942052
Synergistic effects of flavonoids and paclitaxel in cancer treatment: a systematic review Asnaashari S, Amjad E, Sokouti B Cancer Cell Int 24-Sep-2023
PMCID:PMC10518113
doi:10.1186/s12935-023-03052-z
PMID:37743502
Green Synthesis of ZnO and Black TiO2 Materials and Their Application in Photodegradation of Organic Pollutants Nawaz R, Ullah H, Ghanim AA, Irfan M, Anjum M, Rahman S, Ullah S, Abdel Baki Z, Kumar Oad V ACS Omega 22-Sep-2023
PMCID:PMC10551907
doi:10.1021/acsomega.3c04229
PMID:37810725
Ethanolic Extract of Polygonum minus Protects Differentiated Human Neuroblastoma Cells (SH-SY5Y) against H2O2-Induced Oxidative Stress Sayuti NH, Zulkefli N, Tan JK, Saad N, Baharum SN, Hamezah HS, Bunawan H, Ahmed QU, Parveen H, Mukhtar S, Alsharif MA, Sarian MN Molecules 20-Sep-2023
PMCID:PMC10535396
doi:10.3390/molecules28186726
PMID:37764502
Comparison analysis of full-spectrum metabolomics revealed on the variation of potential metabolites of unscented, Chloranthus spicatus scented, and Osmanthus fragrans (Thunb.) Lour. scented Congou black teas Tang P, Wang JQ, Wang YF, Jin JC, Meng X, Zhu Y, Gao Y, Xu YQ Front Nutr 14-Aug-2023
PMCID:PMC10461629
doi:10.3389/fnut.2023.1234807
PMID:37645629
Presence of p25alpha-Domain in Seed Plants (Spermatophyta): Microbial/Animal Contaminations and/or Orthologs Orosz F Life (Basel) 30-Jul-2023
PMCID:PMC10455874
doi:10.3390/life13081664
PMID:37629521
Endophytic fungi: hidden treasure chest of antimicrobial metabolites interrelationship of endophytes and metabolites Jha P, Kaur T, Chhabra I, Panja A, Paul S, Kumar V, Malik T Front Microbiol 11-Jul-2023
PMCID:PMC10366620
doi:10.3389/fmicb.2023.1227830
PMID:37497538
Bioinformatic analysis of short-chain dehydrogenase/reductase proteins in plant peroxisomes Zhang Y, Wang X, Wang X, Wang Y, Liu J, Wang S, Li W, Jin Y, Akhter D, Chen J, Hu J, Pan R Front Plant Sci 09-Jun-2023
PMCID:PMC10288848
doi:10.3389/fpls.2023.1180647
PMID:37360717
Mercuric Chloride Induced Nephrotoxicity: Ameliorative Effect of Carica papaya Leaves Confirmed by Histopathology, Immunohistochemistry, and Gene Expression Studies Maria Francis Y, Karunakaran B, Ashfaq F, Yahia Qattan M, Ahmad I, Alkhathami AG, Idreesh Khan M, Varadhan M, Govindan L, Ponnusamy Kasirajan S ACS Omega 05-Jun-2023
PMCID:PMC10286259
doi:10.1021/acsomega.3c01045
PMID:37360438
Polyphenol supplementation and executive functioning in overweight and obese adults at risk of cognitive impairment: A systematic review and meta-analysis Farag S, Tsang C, Murphy PN PLoS One 25-May-2023
PMCID:PMC10212191
doi:10.1371/journal.pone.0286143
PMID:37228106

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Eicosane 8222 Click to see 282.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Pentadecane 12391 Click to see 212.41 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1R,3S,6S,7S,8S)-3,6,8-trimethyl-2-methylidenetricyclo[5.3.1.03,8]undecane 22211634 Click to see CC1CCC2(C(=C)C3CCC2(C1C3)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
1,6-Methanonaphthalene, decahydro-1,4,8a-trimethyl-9-methylene-, (1S,4S,4aS,6R,8aS)-(-)- 519743 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristelaidic acid 5312402 Click to see 226.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Myristoleic Acid 5281119 Click to see 226.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Oleic Acid 445639 Click to see 282.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Pentadecanoic Acid 13849 Click to see 242.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Stearic Acid 5281 Click to see 284.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol 8174 Click to see 158.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Lauryl Alcohol 8193 Click to see 186.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Pentadecanal 17697 Click to see 226.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Geranylacetone 1549778 Click to see 194.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
alpha-Thujene 17868 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Myrtenal 61130 Click to see 150.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(1R,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302226 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(5S)-2-methyl-5-[(2S)-6-methylhept-5-en-2-yl]cyclohexa-1,3-diene 12447832 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
beta-Guaiene 15560252 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Elemene 12309449 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
S-Curcumene 3083834 Click to see 202.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Sesquichamene 97829 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Thujopsene 442402 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2S,5S,6S,7R,8R,9R,12R)-5,8-diacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] benzoate 56677247 Click to see CC(=O)OC1CCC(C23C1(C(C(C(C2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)OC(=O)C5=CC=CC=C5)C)(C)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(-)-Aristolene 12309878 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7R,7aS,7bS)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 12305246 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Alloaromadendrene 12305247 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3R,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene 5317160 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2R,4aR,8aS)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 12304193 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(1R,6R)-alpha-himachalene 11367721 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
(4aR)-3,5,5-trimethyl-9-methylidene-2,4a,6,7,8,9a-hexahydro-1H-benzo[7]annulene 163188687 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 1202794 Click to see CC1=CCC2C(CCCC2(C1CO)C)(C)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Organoheterocyclic compounds / Epoxides
alpha-Humulene epoxide 14038843 Click to see CC1=CCCC2(C(O2)CC(C=CC1)(C)C)C 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Organoheterocyclic compounds / Naphthofurans
Drimenin 442202 Click to see 234.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)chromenylium-3-yl]oxy-6-methyloxane-3,4,5-triol 154497169 Click to see 417.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271663/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
3,5,3'-Trimethoxy-6,7:4',5'-bis(methylenedioxy)flavone 14704648 Click to see COC1=CC(=CC2=C1OCO2)C3=C(C(=O)C4=C(C5=C(C=C4O3)OCO5)OC)OC 400.30 unknown https://doi.org/10.1016/0031-9422(90)85309-4
5,3',4',5'-Tetramethoxy-6,7-methylenedioxyflavone 14704647 Click to see 386.40 unknown https://doi.org/10.1016/0031-9422(90)85309-4

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