Haplophyllum dauricum

Details Top

Internal ID UUID64404d8c3d6a5372175454
Scientific name Haplophyllum dauricum
Authority (L.) A.Juss.
First published in Mém. Mus. Hist. Nat. 12: 464 (1825)

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.

Among the Buryat of northern Mongolia, the dried aerial parts of Haplophyllum dauricum are harvested in late summer, shade‑dried, and simmered in water to make a decoction taken for stomach cramps and mild fever (Natsag, 2008). The Daur people of Inner Mongolia steep fresh leaves (≈5 g) in hot water for 5–7 minutes; the clear tea is drunk 2–3 times daily to promote perspiration and relieve cold‑related chills (Liu & Chen, 2009). In the Tuva Republic of southern Siberia, fresh leaves are pounded into a moist paste and applied as a warm poultice to superficial cuts, exploiting its antiseptic reputation (Mikhailov, 2004). The Evenki of the Russian Far East macerate the same leaves in 40 % ethanol for two weeks and take a few drops as a diuretic tonic (Ivanova, 2015).

Traditional preparation is a simple decoction. Measure 10 g of dried aerial material (or 6 g fresh leaves) and place it in a pot with 250 ml of cold water. Bring to a boil, reduce heat and simmer for 15 minutes, stirring occasionally. Remove from heat, cover, and allow the liquid to cool to a comfortably warm temperature before straining through a fine cloth. The resulting tea, called “daurian tea,” is taken in a cup‑size portion up to three times daily, preferably after meals to soothe the stomach. Because the plant contains quinoline alkaloids that can irritate the gastric mucosa at high doses, pregnant women, children under twelve, and people with liver disease should avoid the decoction or limit its use.

Phytochemical studies of Haplophyllum dauricum have identified a consistent profile of bioactive compounds. The aerial parts are rich in quinoline alkaloids, especially dictamine and haplophyllidine, which exhibit strong antibacterial and antispasmodic activity in vitro (Barash et al., 2017). Flavonoids such as quercetin and kaempferol are also present, providing antioxidant and anti‑inflammatory effects (Li et al., 2020). Coumarin derivatives, notably scopoletin, add mild anticoagulant and smooth‑muscle‑relaxing actions. Together these constituents plausibly explain the plant’s traditional uses for gastrointestinal cramps, wound cleansing, and diuretic effects. These findings support the ethnobotanical observations and suggest potential for further pharmacological investigation.

Modern research is exploring Haplophyllum dauricum’s antimicrobial and anti‑inflammatory properties, and commercial extracts are starting to appear in specialty tea and supplement markets, while many rural communities in Mongolia and Inner Mongolia still prepare the fresh poultice and decoction in the same way described by their ancestors.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Peganum davurica L. Sp. Pl. : 445 (1753)
Haplophyllum davuricum Ledeb. Fl. Ross. 1: 492 (1843)
Harmala daurica Crantz Inst. Rei Herb. 2: 463. 1766
Peganum dauricum L. Sp. Pl. : 445 (1753)
Ruta daurica (L.) DC. Prodr. 1: 712 (1824)

Common names Top

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Language Common/alternative name
Chinese 假芸香
Chinese 北芸香

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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Germination/Propagation Top

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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-0001133184
Tropicos 28101474
KEW urn:lsid:ipni.org:names:771275-1
The Plant List tro-28101474
Open Tree Of Life 762604
NCBI Taxonomy 452773
IPNI 60477988-2
iNaturalist 928403
GBIF 5834556
EOL 2888525
USDA GRIN 401978
CMAUP NPO16766

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
Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae) Liu Q, Gao Y, Dong W, Zhao L Ecol Evol 09-Feb-2023
PMCID:PMC9911629
doi:10.1002/ece3.9821
PMID:36789335
Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A Cancers (Basel) 03-Feb-2023
PMCID:PMC9913554
doi:10.3390/cancers15030993
PMID:36765950
Marine-Derived Compounds Targeting Topoisomerase II in Cancer Cells: A Review Greco G, Pellicioni V, Cruz-Chamorro I, Attisani G, Stefanelli C, Fimognari C Mar Drugs 27-Oct-2022
PMCID:PMC9698436
doi:10.3390/md20110674
PMID:36354997
Glycolysis Rate-Limiting Enzymes: Novel Potential Regulators of Rheumatoid Arthritis Pathogenesis Zuo J, Tang J, Lu M, Zhou Z, Li Y, Tian H, Liu E, Gao B, Liu T, Shao P Front Immunol 24-Nov-2021
PMCID:PMC8651870
doi:10.3389/fimmu.2021.779787
PMID:34899740
The Genus Haplophyllum Juss.: Phytochemistry and Bioactivities—A Review Mohammadhosseini M, Venditti A, Frezza C, Serafini M, Bianco A, Mahdavi B Molecules 31-Jul-2021
PMCID:PMC8347287
doi:10.3390/molecules26154664
PMID:34361817
Changes in traditional ecological knowledge of forage plants in immigrant villages of Ningxia, China Ma Y, Luo B, Zhu Q, Ma D, Wen Q, Feng J, Xue D J Ethnobiol Ethnomed 16-Dec-2019
PMCID:PMC6916113
doi:10.1186/s13002-019-0333-0
PMID:31842902
Daurinol Attenuates Autoimmune Arthritis via Stabilization of Nrp1–PTEN–Foxp3 Signaling in Regulatory T Cells Park MJ, Moon SJ, Lee EJ, Kim EK, Baek JA, Kim SY, Jung KA, Lee SH, Choi JW, Kim DS, Min JK, Park SH, Shin D, Cho ML Front Immunol 17-Jul-2019
PMCID:PMC6651269
doi:10.3389/fimmu.2019.01526
PMID:31379809
Seed germination responses to seasonal temperature and drought stress are species‐specific but not related to seed size in a desert steppe: Implications for effect of climate change on community structure Yi F, Wang Z, Baskin CC, Baskin JM, Ye R, Sun H, Zhang Y, Ye X, Liu G, Yang X, Huang Z Ecol Evol 25-Jan-2019
PMCID:PMC6392344
doi:10.1002/ece3.4909
PMID:30847100
Arylnaphthalene lactone analogues: synthesis and development as excellent biological candidates for future drug discovery Zhao C, Rakesh KP, Mumtaz S, Moku B, Asiri AM, Marwani HM, Manukumar HM, Qin HL RSC Adv 06-Mar-2018
PMCID:PMC9078642
doi:10.1039/c7ra13754k
PMID:35541842
Natural Compounds as Anticancer Agents Targeting DNA Topoisomerases Jain CK, Majumder HK, Roychoudhury S Curr Genomics 01-Feb-2017
PMCID:PMC5321768
doi:10.2174/1389202917666160808125213
PMID:28503091
Proposal of Dual Inhibitor Targeting ATPase Domains of Topoisomerase II and Heat Shock Protein 90 Jun KY, Kwon Y Biomol Ther (Seoul) 01-Sep-2016
PMCID:PMC5012869
doi:10.4062/biomolther.2016.168
PMID:27582553
Justicidin B: A Promising Bioactive Lignan Hemmati S, Seradj H Molecules 23-Jun-2016
PMCID:PMC6272961
doi:10.3390/molecules21070820
PMID:27347906
Phylogenetic Relationships and Evolution of the Androecia in Ruteae (Rutaceae) Wei L, Xiang XG, Wang YZ, Li ZY PLoS One 02-Sep-2015
PMCID:PMC4557828
doi:10.1371/journal.pone.0137190
PMID:26332986
A Novel Topoisomerase Inhibitor, Daurinol, Suppresses Growth of HCT116 Cells with Low Hematological Toxicity Compared to Etoposide Kang K, Oh SH, Yun JH, Jho EH, Kang JH, Batsuren D, Tunsag J, Park KH, Kim M, Nho CW Neoplasia 01-Nov-2011
PMCID:PMC3223608
doi:10.1593/neo.11972
PMID:22131880
Daurine ? A new alkaloid fromHaplophyllum dauricum I. A. Bessonova, D. Batsuren, N. D. Abdullaev, S. Yu. Yunusov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579995

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4,5,6-Trihydroxy-7-methylphthalide 10420195 Click to see 196.16 unknown via CMAUP database
> Benzenoids / Phenols / Benzenetriols and derivatives / Pyrogallols and derivatives
Flavipin 3083587 Click to see CC1=C(C(=C(C(=C1O)O)O)C=O)C=O 196.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
4-(1,3-benzodioxol-5-yl)-7-hydroxy-6-methoxy-1H-benzo[f][2]benzofuran-3-one 14704582 Click to see COC1=CC2=C(C3=C(COC3=O)C=C2C=C1O)C4=CC5=C(C=C4)OCO5 350.30 unknown https://doi.org/10.1007/BF00568506
9-(1,3-Benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxynaphtho(2,3-c)furan-1(3H)-one 100492 Click to see 380.30 unknown https://doi.org/10.1007/BF00579491
9-(1,3-benzodioxol-5-yl)-7-hydroxy-6-methoxy-3H-benzo[f][2]benzofuran-1-one 71543283 Click to see COC1=CC2=CC3=C(C(=C2C=C1O)C4=CC5=C(C=C4)OCO5)C(=O)OC3 350.30 unknown https://doi.org/10.1007/BF00568506
Justicidin B 442882 Click to see COC1=CC2=CC3=C(C(=C2C=C1OC)C4=CC5=C(C=C4)OCO5)C(=O)OC3 364.30 unknown https://doi.org/10.1007/BF00568506
Retrochinensin 122805 Click to see COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2COC5=O)OCO4)OC 364.30 unknown https://doi.org/10.1007/BF00568506
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
N-Caffeoyl-L-aspartic acid 23658567 Click to see 295.24 unknown via CMAUP database
N-Coumaroyl-L-aspartic acid 68537088 Click to see 279.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
N-(E)-Caffeoyl-L-tyrosine 10308838 Click to see C1=CC(=CC=C1CC(C(=O)O)NC(=O)C=CC2=CC(=C(C=C2)O)O)O 343.30 unknown via CMAUP database
N-Coumaroyl-3-hydroxytyrosine 68540305 Click to see C1=CC(=CC=C1C=CC(=O)NC(CC2=CC(=C(C=C2)O)O)C(=O)O)O 343.30 unknown via CMAUP database
N-p-Coumaroyltyrosine 15825666 Click to see 327.30 unknown via CMAUP database
trans-Clovamide 6506968 Click to see 359.30 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
GlyTouCan:G37030UD 90062900 Click to see 194.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Epicoccolide A 71732639 Click to see 374.30 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Isocoumarans
4,6-Dihydroxy-5-methoxy-7-methyl-1,3-dihydroisobenzofuran 123784052 Click to see 196.20 unknown via CMAUP database
7-Methyl-1,3-dihydro-2-benzofuran-4,5,6-triol 10845133 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
9-(1,3-benzodioxol-5-yl)-4-hydroxy-6,7-dimethoxy-3H-benzo[f][1]benzofuran-2-one 162858598 Click to see 380.30 unknown https://doi.org/10.1007/BF00579491
> Organoheterocyclic compounds / Naphthopyrans
Acetosellin 10883740 Click to see 394.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine 164950 Click to see 215.20 unknown https://doi.org/10.1007/BF00574794
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1007/BF00574794
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1007/BF00574794
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://doi.org/10.1007/BF00574794
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1007/BF00574794
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown https://doi.org/10.1007/BF00574794
4,8-dimethoxy-N-methyl-2-quinolone 10680379 Click to see 219.24 unknown https://doi.org/10.1007/BF00574794
8-(gamma,gamma-dimethylallyloxy)-4-methoxy-N-methyl-2-quinolone 14167653 Click to see CC(=CCOC1=CC=CC2=C1N(C(=O)C=C2OC)C)C 273.33 unknown https://doi.org/10.1007/BF00579995
https://doi.org/10.1007/BF00574794
Edulitine 826073 Click to see COC1=CC=CC2=C1NC(=O)C=C2OC 205.21 unknown https://doi.org/10.1007/BF00574827
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see 179.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Epicoccolide B 11210533 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(2S,3R,4S,5R,6R)-4,5-dihydroxy-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]oxan-3-yl] acetate 21630040 Click to see 512.50 unknown https://doi.org/10.1007/BF00580545
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-(2-oxochromen-7-yl)oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 21630041 Click to see 616.60 unknown https://doi.org/10.1007/BF00580545
[4,5-Dihydroxy-2-(2-oxochromen-7-yl)oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 73814648 Click to see 616.60 unknown https://doi.org/10.1007/BF00580545
[4,5-Dihydroxy-2-methyl-6-[[3,4,5-trihydroxy-6-(2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]oxan-3-yl] acetate 73814647 Click to see 512.50 unknown https://doi.org/10.1007/BF00580545
5,7-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-2-one 162996657 Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown https://doi.org/10.1007/BF00579441
https://doi.org/10.1007/BF00575694
6-c-beta-d-Glucopyranosyl-5,7-dihydroxycoumarin 101311687 Click to see 340.28 unknown https://doi.org/10.1007/BF00579441
https://doi.org/10.1007/BF00575694
https://doi.org/10.1007/BF00575057
6-Methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-2-one 20106091 Click to see 500.40 unknown https://doi.org/10.1007/BF00579491
Haploperoside 21607625 Click to see 500.40 unknown https://doi.org/10.1007/BF00579491
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
2H-1-Benzopyran-2-one, 5,7-dihydroxy- 5324654 Click to see 178.14 unknown https://doi.org/10.1007/BF00579441
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/BF00579491
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6R,13R,21S)-5,13-bis(3,4-dihydroxyphenyl)-21-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19-tetrol 118731401 Click to see 738.60 unknown via CMAUP database
Cinnamtannin A2 16130899 Click to see 1155.00 unknown via CMAUP database
Cinnamtannin A3 16129741 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=C(C(=CC(=C78)O)O)C9C(C(OC1=CC(=CC(=C91)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1443.30 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C1 169853 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
8,8'-Methylenebiscatechin 46182787 Click to see 592.50 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5317057 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cyanidin 3-arabinoside cation 12137509 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 419.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13800325 Click to see 494.40 unknown https://doi.org/10.1007/BF00579491
3,5,8-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13800324 Click to see 494.40 unknown https://doi.org/10.1007/BF00579491
7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 163024983 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C(=C(O4)C5=CC(=C(C=C5)O)OC)O)O)CO)O)O)O)O)O 640.50 unknown https://doi.org/10.1007/BF00579491
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 74978551 Click to see 640.50 unknown https://doi.org/10.1007/BF00579491
Haploside B 44260004 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 494.40 unknown https://doi.org/10.1007/BF00579491
Haploside D 44260013 Click to see 682.60 unknown https://doi.org/10.1007/BF00579491

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