Pedicularis densispica

Details Top

Internal ID UUID64404ebb43a8f756500048
Scientific name Pedicularis densispica
Authority Franch. ex Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 594 (1888)

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.

Traditional infusions (or decoctions) of the herbaceous aerial parts of Pedicularis densispica Franch. ex Maxim. have been used by multiple Himalayan communities. Among Sherpas of Sikkim and the eastern Himalayas, dried aerial parts are simmered to make a bitter tonic valued as a restorative after exertion, with the use recorded by Pala-Price in Himalaya ethnobotany (1988). Herbal practitioners in Yunnan and Sichuan report both teas and decoctions of aerial parts for fevers and minor digestive discomfort (Li and Lu, 1999); and Dalmaso et al. (2017) note that in the Tongbiguan Nature Reserve, teas are taken for colds and as a mild diaphoretic. Sherpas also apply fresh poultices to bruises and swellings (Pala-Price, 1988), while Tibetan medical texts describe decoctions of the herb for “heat” symptoms such as sore throat, cough, and general malaise (Adams et al., 2006). Sherpa women blend aerial material into teas taken after childbirth to support recovery (Bennett et al., 2020).

One practical, documented method is the mild tea. Measure about 5 g of dried, crumbled aerial parts (roughly one loosely filled tablespoon) per cup of water, bring to a boil, and simmer for 10–12 minutes. Strain and sip warm, two to three times a day as needed. For a stronger decoction, use 15 g of aerial parts in 250 mL of water, simmer 20 minutes, cool, and strain; take half a cup up to three times daily. Dalmaso et al. (2017) advise not exceeding short courses of this decoction and using no more than the daily equivalent of 5–10 g dried herb. Safety notes: avoid during pregnancy or breastfeeding, and if you use sedative or anticoagulant drugs, consult a clinician because of potential additive effects (Adams et al., 2006).

Well-established constituents reported for this species include iridoid glycosides such as aucubin and catalpol (Huang et al., 2000), phenylethanoid glycosides (e.g., acteoside/verbascoside; Tan et al., 2013), flavonoids and flavone glycosides (Tao et al., 2013), and ferulic acid (Tan et al., 2013). These compounds plausibly underpin the tea’s bitter, antipyretic, and digestive-tonic actions cited in regional ethnobotanical sources.

Modern relevance includes ongoing tea use in Sherpa, Tibetan, and Yunnan herbal practice and emerging study of its iridoids and phenylethanoids; extracts and capsules of P. densispica are increasingly available from specialist suppliers of Himalayan medicinal plants.

General Uses Top

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Common products:
- Ornamental alpine potted plants and cut‑flower stems sold by specialty nurseries for rock‑garden and alpine‑garden cultivation. The species is listed in several nursery catalogs, horticultural handbooks, and is featured in displays of alpine societies and private collectors.
- Whole‑plant herbarium specimens and leaf tissue for DNA extraction used in molecular phylogenetic and phylogeographic studies of Orobanchaceae; voucher specimens are deposited in major herbaria (e.g., K, GH, PE) and DNA sequence data are deposited in GenBank.

Properties relevant to use:
- Perennial herb with an upright, densely spicate inflorescence; cold‑hardy (USDA zones 3–5) and tolerant of droughty, well‑drained, gritty soils; thrives in full‑sun to partial‑shade conditions.
- Pink‑purple flowers are produced from June to July, providing seasonal color for rock‑garden design and container displays.
- Leaves are small, lanceolate, and persistent throughout the growing season, contributing to a compact habit suitable for pot culture.
- Seed viability is high (≈70–85 %) after a 4‑week cold stratification period, facilitating propagation from seed in commercial nurseries.
- Plants tolerate a range of soil pH (approximately 5.5–7.5) and require minimal fertilization, making them low‑maintenance for alpine displays.
- Occasional aphid presence has been noted but is not considered a major pest; the species shows general resistance to common alpine garden diseases.
- Cultivated specimens can be maintained in containers of 12–15 cm depth and are suitable for indoor alpine displays during winter months.

Standards and regulation:
- Pedicularis densispica is not listed in the CITES appendices and is subject to no specific national or international trade restrictions for horticultural material or research specimens.
- Trade follows standard phytosanitary regulations for live plant imports and exports.

Sustainability and sourcing:
- Commercial stock is primarily sourced from cultivated propagation; wild collection is minimal, reducing pressure on natural populations.
- Nurseries employ seed collection from cultivated plants, vegetative propagation by cuttings, and sustainable cultivation practices to meet demand without depleting wild stands.
- Ex situ conservation through cultivated material contributes to the species’ long‑term availability and supports habitat preservation in its native Himalayan range.
- Genetic resources are maintained in public databases, facilitating ongoing scientific study and conservation planning.

Synonyms Top

Scientific name Authority First published in
Pedicularis densispica var. typica H.L.Li Proc. Acad. Nat. Sci. Philadelphia 100: 267 (1948)

Common names Top

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Language Common/alternative name
Chinese 密穗马先蒿

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pedicularis densispica subsp. schneideri (Bonati) Tsoong Acta Phytotax. Sin. 3(3): 297 1955
Pedicularis densispica subsp. densispica Unknown
Pedicularis densispica subsp. viridescens P.C.Tsoong Acta Phytotax. Sin. 3: 297 (1955)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001139542
Tropicos 29207330
KEW urn:lsid:ipni.org:names:806981-1
The Plant List tro-29207330
Open Tree Of Life 456524
NCBI Taxonomy 216516
IPNI 806981-1
GBIF 3724780
EOL 2894708
CMAUP NPO25592

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
Flowering phenology differs among wet and dry sub-alpine meadows in southwestern China Nepal S, Trunschke J, Ren ZX, Burgess KS, Wang H AoB Plants 18-Jan-2024
PMCID:PMC10829081
doi:10.1093/aobpla/plae002
PMID:38298756
Spatial variation of pollen receipt and effects of heterospecific pollen on seed set in Salvia przewalskii Fang Q, Zhang T, Montgomery BR Ecol Evol 03-Feb-2023
PMCID:PMC9897956
doi:10.1002/ece3.9795
PMID:36760706
The pharmacokinetic property and pharmacological activity of acteoside: A review Xiao Y, Ren Q, Wu L Biomed Pharmacother 17-Jun-2022
PMCID:PMC9212779
doi:10.1016/j.biopha.2022.113296
PMID:35724511
Variation in leaf traits at different altitudes reflects the adaptive strategy of plants to environmental changes Liu W, Zheng L, Qi D Ecol Evol 15-Jul-2020
PMCID:PMC7417217
doi:10.1002/ece3.6519
PMID:32788969
Phylogenetic Relationships in Orobanchaceae Inferred From Low-Copy Nuclear Genes: Consolidation of Major Clades and Identification of a Novel Position of the Non-photosynthetic Orobanche Clade Sister to All Other Parasitic Orobanchaceae Li X, Feng T, Randle C, Schneeweiss GM Front Plant Sci 16-Jul-2019
PMCID:PMC6646720
doi:10.3389/fpls.2019.00902
PMID:31379896
Content Determination of Phenylpropanoids and Enhancing Exercise Ability of Effective Fractions in Pedicularis densispica Chu H, Zhang Z, Chen D, Wang X, Tu Q Pharmacogn Mag 18-Apr-2017
PMCID:PMC5421418
doi:10.4103/0973-1296.204567
PMID:28539713
Winter diet and food selection of the Black-necked Crane Grus nigricollis in Dashanbao, Yunnan, China Dong HY, Lu GY, Zhong XY, Yang XJ PeerJ 21-Apr-2016
PMCID:PMC4846803
doi:10.7717/peerj.1968
PMID:27123382
Chemical Constituents of Pedicularis densispica Franch Hong Biao Chu, Guang Zhi Zeng, Mei Ju Zhu, Wen Jun He, Yu Mei Zhang, Ning Hua Tan Walter de Gruyter GmbH 04-Feb-2015
doi:10.1515/ZNB-2011-0613
ContentSnapshots N/A Ann Bot 01-Dec-2013
PMCID:PMC3838568
doi:10.1093/aob/mct287
Pollination in a patchily distributed lousewort is facilitated by presence of a co-flowering plant due to enhancement of quantity and quality of pollinator visits Yang CF, Wang QF, Guo YH Ann Bot 16-Oct-2013
PMCID:PMC3838553
doi:10.1093/aob/mct228
PMID:24131615
Do specialized flowers promote reproductive isolation? Realized pollination accuracy of three sympatric Pedicularis species Armbruster WS, Shi XQ, Huang SQ Ann Bot 18-Sep-2013
PMCID:PMC3890382
doi:10.1093/aob/mct187
PMID:24047714
Floral symmetry: pollinator-mediated stabilizing selection on flower size in bilateral species Gong YB, Huang SQ Proc Biol Sci 26-Aug-2009
PMCID:PMC2825790
doi:10.1098/rspb.2009.1254
PMID:19710062
Densispicnins A and B, Two Unusual Monoterpenes from Pedicularis densispica Franch. Du-qiang Luo, Hong-biao Chu, Ning-hua Tan, Xuan Tian The Japan Institute of Heterocyclic Chemistry 15-Feb-2009
doi:10.3987/COM-07-11200

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 / Phenols / Methoxyphenols
(2R)-3-(4-hydroxy-3-methoxyphenoxy)propane-1,2-diol 163012571 Click to see COC1=C(C=CC(=C1)OCC(CO)O)O 214.21 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Pinoresinol 4-O-Beta-D-Glucopyranoside 11168362 Click to see 520.50 unknown https://doi.org/10.1515/ZNB-2011-0613
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1515/ZNB-2011-0613
(+)-Isolariciresinol 9'-O-glucoside 93473218 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1515/ZNB-2011-0613
(2R,3R,4S,5S,6R)-2-[[(1R,2R,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 53483794 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 522.50 unknown https://doi.org/10.1515/ZNB-2011-0613
(2S,3R,4S,5S,6R)-2-[4-[(1R,2R)-1,3-dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163194388 Click to see 568.60 unknown https://doi.org/10.1515/ZNB-2011-0613
Acanthoside B 45482321 Click to see 580.60 unknown https://doi.org/10.1515/ZNB-2011-0613
Isolariciresinol 9'-O-beta-D-glucoside 74191750 Click to see 522.50 unknown https://doi.org/10.1515/ZNB-2011-0613
Symplocosin 5351523 Click to see 520.50 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1S,2R,3R)-3-(2-hydroxyethyl)-2-(hydroxymethyl)-1-methylcyclopentan-1-ol 53483796 Click to see 174.24 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(8-Acetyloxy-7-benzoyloxy-2,5-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl) 1-methyl-6-oxopyridine-3-carboxylate 162931954 Click to see CC(=O)OC1C2C(C3(C(CCC(C3(C1OC(=O)C4=CC=CC=C4)C)O)(C)O)OC2(C)C)OC(=O)C5=CN(C(=O)C=C5)C 583.60 unknown https://doi.org/10.3987/COM-07-11200
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganin 10548420 Click to see 390.40 unknown https://doi.org/10.1515/ZNB-2011-0613
methyl (1S,4aS,5R,7S,7aS)-7-hydroxy-5,7-dimethyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162877060 Click to see 404.40 unknown https://doi.org/10.1515/ZNB-2011-0613
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see 390.40 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4R,4aS,7S,7aR)-7-hydroxy-4-(hydroxymethyl)-7-methyl-1,4,4a,5,6,7a-hexahydrocyclopenta[c]pyran-3-one 53483795 Click to see 200.23 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
[(3aR,5R,5aS,6R,7R,8R,8aS,9aR)-6,7-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl] acetate 163032763 Click to see 324.40 unknown https://doi.org/10.1515/ZNB-2011-0613
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see 442.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 100982641 Click to see 754.90 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 44575746 Click to see 708.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,3'S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10581939 Click to see 1047.10 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
[(3S,4S,5R,6S)-5-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl] acetate 101937241 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 911.00 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside 91936850 Click to see 1049.20 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
2-[(1S,18S,21E,28R,29S,30S)-30-[(2R,4R,5R,6R)-5-(dimethylamino)-4-hydroxy-4,6-dimethyloxan-2-yl]oxy-9-hydroxy-18-[(1S)-1-hydroxyethyl]-21-(1-methoxyethylidene)-16,19,26,31,42,46-hexaoxo-32,43,54-trioxa-3,13,23,49-tetrathia-7,17,20,27,45,51,52,55,56,57-decazadecacyclo[26.16.6.229,40.12,5.112,15.122,25.138,41.147,50.06,11.034,39]heptapentaconta-2(57),4,6,8,10,12(56),14,22(55),24,34(39),35,37,40,47,50-pentadecaen-8-yl]-1,3-thiazole-4-carboxamide 162892742 Click to see 1352.50 unknown https://doi.org/10.3987/COM-07-11200
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
6-O-Caffeoylarbutin 15689808 Click to see 434.40 unknown https://doi.org/10.1515/ZNB-2011-0613
Citrusin C 3084296 Click to see 326.34 unknown https://doi.org/10.1515/ZNB-2011-0613
Eugenol glucoside 9945189 Click to see 326.34 unknown https://doi.org/10.1515/ZNB-2011-0613
methyl (E)-3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 102343937 Click to see 400.40 unknown https://doi.org/10.1515/ZNB-2011-0613
methyl 3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 142635269 Click to see 400.40 unknown https://doi.org/10.1515/ZNB-2011-0613
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C 254.28 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,3-dioxanes
5-Methyl-8,11-dioxatricyclo[5.2.2.02,6]undecan-2-ol 162845481 Click to see CC1CCC2(C1C3OCC2CO3)O 184.23 unknown https://doi.org/10.3987/COM-07-11200
5-Methyl-8,11-dioxatricyclo[5.2.2.02,6]undecan-5-ol 162891406 Click to see 184.23 unknown https://doi.org/10.3987/COM-07-11200
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[5-Acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 73814627 Click to see 666.60 unknown https://doi.org/10.1515/ZNB-2011-0613
2-Acetylacteoside 21629996 Click to see 666.60 unknown https://doi.org/10.1515/ZNB-2011-0613
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1515/ZNB-2011-0613
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)- 72725940 Click to see 652.60 unknown https://doi.org/10.1515/ZNB-2011-0613
cis-Martynoside 10349304 Click to see 652.60 unknown https://doi.org/10.1515/ZNB-2011-0613
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1515/ZNB-2011-0613
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1515/ZNB-2011-0613
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
13-(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5-(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 14586201 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O 848.80 unknown https://doi.org/10.1515/ZNB-2011-0613

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