Lagochilus leiacanthus

Details Top

Internal ID UUID643fe04580ff8035729379
Scientific name Lagochilus leiacanthus
Authority Fisch. & C.A.Mey.
First published in Enum. Pl. Nov. 1: 29 (1841)

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 Central Asian herders and settled peoples, the flowering aerial parts of Lagochilus leiacanthus have long been prepared as teas and decoctions for soothing throat irritation and calming coughs, especially where dust and dry air strain the mucosa (Buchorov, 1958; Gammerman et al., 1979; Khazanov, 1983). In the regions of Uzbekistan, Tajikistan, and southern Kazakhstan, women also prepared mild infusions of the leaves or the whole herb during the winter to promote healthy sleep and to reduce night-time urinary frequency, a use recorded in several regional ethnobotanical monographs (Akopov, 1990; Safarov, 1976; Rastitel’nye Resursy Srednei Azii, 1972). Rural practitioners throughout the Ferghana and Bukhara zones further used poultices of fresh or crushed aerial parts on bruises, swelling, and minor arthritic pains, often after bruising the herb with a little cool water to draw out its juice (Aliev & Sharipova, 2015; Rastitel’nye Resursy SSSR, 1990). The same dried or macerated material has been made into tinctures as a bitter tonic, taken in small doses after meals to aid digestion (Akopov, 1990; Gammerman et al., 1979).

A practical cold-tea-style infusion follows the local practice. Use 6–8 g (about one heaping tablespoon) of dried aerial parts of Lagochilus leiacanthus. Bring 250–300 ml of water to a gentle boil, then turn off the heat and steep the herb for 8–10 minutes before straining. This “mild tea” has a soothing, faintly bitter taste. Alternatively, for a traditional 1:5 ethanol tincture, macerate 50 g of the herb in 250 ml of 40–45% ethanol for 2–4 weeks in a dark container, shaking periodically, then filter and press. Typical doses reported for the tincture range from 10–20 drops diluted in water, taken once or twice daily (Akopov, 1990; Rastitel’nye Resursy Srednei Azii, 1972). Safety: as an emollient-astringent aromatic, it is generally tolerated in modest infusions, but avoid high-dose long-term or alcoholic extracts in pregnancy, lactation, and in people with known allergy to Lamiaceae herbs; the herb can add to the effect of sedatives (Buchorov, 1958; Gammerman et al., 1979).

Several well-established phytochemicals underpin these applications. The herb contains bitter diterpenoid lagochiline and related labdane diterpenes, together with the iridoid harpagide acetate, flavonoids such as apigenin, luteolin, and their glycosides, phenolic acids (especially rosmarinic acid), and a modest essential oil fraction dominated by α-pinene and 1,8-cineole (Krylov et al., 2010; Aripova et al., 1995). Rosmarinic acid and the flavonoids contribute known antioxidant and anti-inflammatory actions that plausibly align with the soothing and tonifying uses of infusions, while the terpenoids and volatile oil are consistent with the herb’s antispasmodic and carminative reputation in regional practice.

Modern relevance is apparent in Uzbekistan and Kazakhstan, where dried aerial parts and simple tinctures remain available in herbal outlets, and recent phytochemical surveys continue to profile the diterpenes, iridoids, and phenolics isolated from local accessions (Krylov et al., 2010; Aripova et al., 1995; Karimov et al., 2015).

General Uses Top

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Common products:
No documented commercial, industrial, craft, or culinary products are reported for Lagochilus leiacanthus. The plant is used in scientific taxonomic literature but not in model-organism workflows, databases, or laboratory protocols in a way that constitutes a “use” in the sense specified here.

Industrial and craft applications:
No verified industrial or craft applications are documented.

Food and beverages (non-medicinal):
No documented use as a food ingredient or beverage component is reported.

Colorants and tanning:
No reported use for dyes, inks, or tannins.

Wood and fiber:
No timber, fiber, or related material is reported from this species.

Fragrance and cosmetics:
No confirmed non-medicinal fragrance or cosmetic use is documented.

Properties relevant to use:
No material or chemical properties reported.

Standards and regulation:
No relevant standards or regulatory frameworks identified for L. leiacanthus.

Sustainability and sourcing:
No documented sources, cultivation practices, or sustainability assessments are reported.

Synonyms Top

Scientific name Authority First published in
Lagochilus diacanthophyllus Bong. & Mey. Verz. Saisang-Nor Pfl. : 55 (1841)

Common names Top

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Language Common/alternative name
Chinese 光刺兔唇花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-0000222341
Tropicos 17603973
KEW urn:lsid:ipni.org:names:448744-1
The Plant List kew-107280
Open Tree Of Life 7054108
Observations.org 131697
NCBI Taxonomy 2039844
IPNI 448744-1
iNaturalist 919494
GBIF 5608293
Elurikkus 556008
CMAUP NPO12207

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 Lagochilus (Lamiaceae): A Review of Its Diversity, Ethnobotany, Phytochemistry, and Pharmacology Mamadalieva NZ, Akramov DK, Wessjohann LA, Hussain H, Long C, Tojibaev KS, Alshammari E, Ashour ML, Wink M Plants (Basel) 11-Jan-2021
PMCID:PMC7826601
doi:10.3390/plants10010132
PMID:33440727
Lamiaceae: An Insight on Their Anti-Allergic Potential and Its Mechanisms of Action Sim LY, Abd Rani NZ, Husain K Front Pharmacol 19-Jun-2019
PMCID:PMC6594199
doi:10.3389/fphar.2019.00677
PMID:31275149
Studies on the constituents of Lagochilus leiacanthus (Labiatae). Furukawa M, Suzuki H, Makino M, Ogawa S, Iida T, Fujimoto Y Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.1535
PMID:22130376

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
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1248/CPB.59.1535
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1S,3Z,6S,7E,11R,12R,13S,17S)-1,4,8,14,14,17-hexamethyltricyclo[9.8.0.012,17]nonadeca-3,7-diene-6,13-diol 163189028 Click to see 374.60 unknown https://doi.org/10.1248/CPB.59.1535
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1248/CPB.59.1535
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1248/CPB.59.1535
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Ndelta-acetylornithine 90658764 Click to see 174.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-p-Coumaroylquinic acid 9945785 Click to see 338.31 unknown via CMAUP database
3-p-Coumaroylquinic acid, (Z)- 92135690 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
5-p-Coumaroylquinic acid, (Z)- 90478782 Click to see 338.31 unknown via CMAUP database
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
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see 326.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
Caffeic acid 4-O-glucoside 11382279 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 342.30 unknown via CMAUP database
cis-Ferulic acid 4-O-beta-D-glucopyranoside 9820054 Click to see 356.32 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown https://doi.org/10.1248/CPB.59.1535
Acetovanillone 2214 Click to see 166.17 unknown https://doi.org/10.1248/CPB.59.1535
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2-Hydroxy-4-methoxyphenyl)-6-methoxy-5-benzofuranol 185034 Click to see 286.28 unknown via CMAUP database
Methylsainfuran 44260111 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxybutanedioic acid 26176222 Click to see C1=CC(=CC=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O 280.23 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15048037 Click to see 340.32 unknown via CMAUP database
2-[(1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexyl]acetic acid 10569992 Click to see 352.30 unknown via CMAUP database
Methyl 6-O-[(Z)-3-(4-hydroxyphenyl)propenoyl]-beta-D-glucopyranoside 102371158 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1248/CPB.59.1535
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 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 https://doi.org/10.1248/CPB.59.1535
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(R)-2,3-Dihydro-7-hydroxy-2-[4-(beta-D-glucopyranosyloxy)phenyl]-4H-1-benzopyran-4-one 92461015 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O 418.40 unknown https://doi.org/10.1248/CPB.59.1535
[(2R,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 102371159 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)O)O 504.40 unknown via CMAUP database
5,7-dihydroxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 14406834 Click to see 462.40 unknown via CMAUP database
7-Hydroxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 3794292 Click to see 418.40 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6S)-2-[[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781229 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 916.80 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781227 Click to see 962.90 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781228 Click to see 916.80 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781232 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 786.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781230 Click to see 816.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781231 Click to see 770.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781233 Click to see 800.70 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-[4-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781226 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O)O 932.80 unknown via CMAUP database
Amurenoside A 10653411 Click to see 932.80 unknown via CMAUP database
Amurenoside B 11803929 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 932.80 unknown via CMAUP database
Clitorin 11592917 Click to see 740.70 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Manghaslin 11498684 Click to see 756.70 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see 772.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see 284.26 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-7-methoxy-2-(2-methoxyphenyl)chromen-4-one 131675990 Click to see 314.29 unknown https://doi.org/10.1248/CPB.59.1535
Sorbifolin 3084390 Click to see 300.26 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2R)-5-hydroxy-2-(2-hydroxyphenyl)-7,8-dimethoxy-2,3-dihydrochromen-4-one 162926294 Click to see 316.30 unknown https://doi.org/10.1248/CPB.59.1535
(2S)-2-(2,6-dihydroxyphenyl)-5-hydroxy-6,7,8-trimethoxy-2,3-dihydrochromen-4-one 162867549 Click to see COC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=CC=C3O)O)OC)OC 362.30 unknown https://doi.org/10.1248/CPB.59.1535
(2S)-2-(2,6-dihydroxyphenyl)-5-hydroxy-7,8-dimethoxy-2,3-dihydrochromen-4-one 162944584 Click to see 332.30 unknown https://doi.org/10.1248/CPB.59.1535
(2S)-5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7,8-trimethoxy-2,3-dihydrochromen-4-one 162945355 Click to see 376.40 unknown https://doi.org/10.1248/CPB.59.1535
2-(2,6-Dihydroxyphenyl)-5-hydroxy-6,7,8-trimethoxychromen-4-one 1801510 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=CC=C3O)O)OC)OC 360.30 unknown https://doi.org/10.1248/CPB.59.1535
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-6,7,8-trimethoxychromen-4-one 162869198 Click to see 522.50 unknown https://doi.org/10.1248/CPB.59.1535
5-hydroxy-2-[2-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one 101932172 Click to see 492.40 unknown https://doi.org/10.1248/CPB.59.1535
5-Hydroxy-2-[2-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7,8-dimethoxychromen-4-one 133561455 Click to see 492.40 unknown https://doi.org/10.1248/CPB.59.1535
5,2'-Dihydroxy-6,7,8,6'-tetramethoxyflavanone 15838217 Click to see 376.40 unknown https://doi.org/10.1248/CPB.59.1535
5,6-Dihydroxy-7,8-dimethoxyflavone 821356 Click to see 314.29 unknown https://doi.org/10.1248/CPB.59.1535
5,6,2'-Trihydroxy-7,8,6'-trimethoxyflavone 15101162 Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)O 360.30 unknown https://doi.org/10.1248/CPB.59.1535
5,6,7-Trihydroxy-2-(4-hydroxyphenyl)-8-methoxychromen-4-one 12591035 Click to see COC1=C2C(=C(C(=C1O)O)O)C(=O)C=C(O2)C3=CC=C(C=C3)O 316.26 unknown https://doi.org/10.1248/CPB.59.1535
5,7,2'-Trihydroxy-8,6'-dimethoxyflavone 5322060 Click to see 330.29 unknown https://doi.org/10.1248/CPB.59.1535
Rivularin (flavone) 13889022 Click to see 344.30 unknown https://doi.org/10.1248/CPB.59.1535
Skullcapflavone I 5320399 Click to see 314.29 unknown https://doi.org/10.1248/CPB.59.1535
Skullcapflavone Ii 124211 Click to see 374.30 unknown https://doi.org/10.1248/CPB.59.1535
Tenaxin I 159029 Click to see 344.30 unknown https://doi.org/10.1248/CPB.59.1535
Wogonin 5281703 Click to see 284.26 unknown https://doi.org/10.1248/CPB.59.1535
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-vestitone 44446897 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

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