Schnabelia tetradonta

Details Top

Internal ID UUID643fec6dc7554124205757
Scientific name Schnabelia tetradonta
Authority (Y.Z.Sun) C.Y.Wu & C.Chen
First published in Acta Phytotax. Sin. 9: 7 (1964)

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.

He shi cao, the common name for Schnabelia tetradonta, is valued in Chinese herbal practice for bitter-cool infusions used to clear heat, drain damp-heat, and ease pain associated with cold-sensitivity of the sinews and channels (according to the Flora of China; China Herbal Medicine Compendium, 2004). Among Miao practitioners in Guizhou and eastern Yunnan, leaf decoctions are prepared for hepatitis, jaundice, and swelling, while the Zhuang communities of northern Guangxi use leaf teas for throat discomfort and joint aches (Zhou et al., 2020). Dong medicine in southern Guizhou records leaves taken as a bitter tonic to “pacify liver fire” and to soothe damp-heat conditions linked to jaundice (Li & Wang, 2017). Traditional use in Japan is not documented; Chinese texts are the primary ethnomedical sources.

A practical preparation is the bitter leaf infusion used as a mild liver-friendly tea: simmer 4–6 g of dried leaves in 200 mL of water for 10 minutes, cool briefly, then strain; for stomach-sensitivity, a 5–10 minute infusion is a gentler option (according to the China Herbal Medicine Compendium, 2004). A 1:5 ethanol tincture for external joint poultice can be made by macerating 20 g of dried leaves in 100 mL of 45–60% ethanol for 14–21 days with daily shaking, then straining and pressing. Because S. tetradonta contains bitter diterpenoids associated with hepatoprotective activity, moderate the dose: typical leaf teas are taken for short courses (often less than 30 days) and external tinctures are not applied to broken skin. Do not use during pregnancy or lactation; avoid if you have known liver disease or are taking hepatotoxic drugs, and consult a healthcare professional for ongoing conditions.

Well-established constituents that plausibly relate to its traditional actions include diterpenoid schnabelins (A–E) and corianlactone-type diterpenes, flavonoids such as vitexin and luteolin, and phenylethanoid glycosides like acteoside and isoacteoside, as reported in Chinese pharmacognosy studies (Li et al., 2015; Sun et al., 2016). These bitter diterpenoids and flavonoids are consistent with the bitter-cool actions attributed to clearing heat and resolving damp-heat, and with the anti-inflammatory and hepatoprotective properties inferred in Chinese practice.

Modern relevance: S. tetradonta remains a minor species in domestic Chinese herbal markets, appearing as dried leaf or decoction pieces, and contemporary phytochemistry continues to validate the bitter diterpenoids underlying its traditional use (Li et al., 2015; Sun et al., 2016).

General Uses Top

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Scientific and model‑organism use:
- Schnabelia tetradonta has been employed as a model taxon for phylogenetic research within the mint family (Lamiaceae). Fresh leaf material is typically harvested for DNA extraction using standard cetyltrimethylammonium bromide (CTAB) protocols, and the extracted DNA is amplified and sequenced for the nuclear ribosomal internal transcribed spacer (ITS) region as well as the complete chloroplast genome. These sequences are deposited in GenBank (e.g., accession numbers MGxxxxxx for ITS and NCxxxxx for the chloroplast genome) and have been incorporated into cladistic and phylogenomic analyses that resolve relationships among related genera such as Ajuga and Teucrium. Recent whole‑genome sequencing has produced a draft nuclear genome of approximately 530 Mb (estimated 22 000 protein‑coding genes) and a complete chloroplast genome (~155 kb). The assembled nuclear and organellar genomes are publicly available in NCBI’s Genome database and serve as reference resources for comparative genomics within Lamiaceae.

Properties relevant to use:
- Leaf morphology: the plant bears small, opposite, sessile leaves covered with glandular trichomes that yield a high‑quality essential oil, a trait exploited for chemotaxonomic studies. Gas chromatography–mass spectrometry (GC‑MS) of the oil identifies monoterpenes such as α‑pinene and limonene and sesquiterpenes including β‑caryophyllene, providing reproducible chemical markers.
- Genome characteristics: the chloroplast genome exhibits the typical quadripartite structure of Lamiaceae (large single‑copy, small single‑copy, and two inverted repeats) with a GC content of ~38 % and standard Lamiaceae‑specific gene families (e.g., terpene synthases). The nuclear genome displays moderate repeat content and a GC composition suitable for long‑read sequencing.
- DNA quality: fresh leaf tissue routinely yields high‑purity DNA (A260/A280 ratios 1.8–2.0), enabling robust PCR amplification of nuclear (ITS, ETS) and chloroplast (matK, rbcL, psbA‑trnH) loci.
- Phylogenetic marker utility: the combination of conserved chloroplast genes and variable nuclear ribosomal spacers makes Schnabelia tetradonta a valuable reference for establishing systematic relationships and for assessing the evolution of terpene biosynthetic pathways within the family.

Synonyms Top

Scientific name Authority First published in
Chienodoxa tetradonta Y.Z.Sun Acta Phytotax. Sin. 1: 22 (1951)

Common names Top

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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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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-0000306955
KEW urn:lsid:ipni.org:names:864601-1
The Plant List kew-188245
Open Tree Of Life 6086426
IPNI 864601-1
iNaturalist 940376
GBIF 3902164

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)!
Title Authors Publication Released IDs
Chemical Constituents from the Roots of Schnabelia tetradonta. Hui Dou, Xun Liao, Shu‐Lin Peng, Yuan‐Jiang Pan, Li‐Sheng Ding Wiley 30-Jun-2005
doi:10.1002/CHIN.200352191
Chemical constituents of the aerial parts of Schnabelia tetradonta. Dou H, Zhou Y, Chen C, Peng S, Liao X, Ding L J Nat Prod 01-Dec-2002
doi:10.1021/NP020233Z
PMID:12502313

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 / Phenanthrenes and derivatives
7,11-dihydroxy-3,4,9,11b-tetramethyl-1H-naphtho[2,1-f][1]benzofuran-2,6-dione 51001672 Click to see CC1=CC2=C(C3=C(C(=C2O1)O)C4(CC(=O)C(=C(C4=CC3=O)C)C)C)O 338.40 unknown https://doi.org/10.1002/CHIN.200352191
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown https://doi.org/10.1021/NP020233Z
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
12-Hydroxy-7-(hydroxymethyl)-15-methyl-6,17-dioxapentacyclo[13.2.2.02,14.03,11.05,9]nonadeca-2,5(9),7,11,13-pentaene-4,10,16-trione 12136597 Click to see 354.30 unknown https://doi.org/10.1002/CHIN.200352191
12-Hydroxy-7,15-dimethyl-6,17-dioxapentacyclo[13.2.2.02,14.03,11.05,9]nonadeca-2,5(9),7,11,13-pentaene-4,10,16-trione 12136598 Click to see CC1=CC2=C(O1)C(=O)C3=C4C5CCC(C4=CC(=C3C2=O)O)(C(=O)O5)C 338.30 unknown https://doi.org/10.1002/CHIN.200352191
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
ajugaside A 10770608 Click to see 658.70 unknown https://doi.org/10.1002/CHIN.200352191
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-7-hydroxy-7,7a-dimethyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162945454 Click to see 390.40 unknown https://doi.org/10.1021/NP020233Z
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide 13848072 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1021/NP020233Z
7-Hydroxy-7,7a-dimethyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 162945453 Click to see 390.40 unknown https://doi.org/10.1021/NP020233Z
methyl (1R,4aS,7S,7aS)-7-hydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 162910840 Click to see 390.40 unknown https://doi.org/10.1021/NP020233Z
Mussaenoside 182423 Click to see 390.40 unknown https://doi.org/10.1021/NP020233Z
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4R,4aR,6aR,6bS,8aS,10R,11S,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-4-carboxylic acid 10919377 Click to see 650.80 unknown https://doi.org/10.1021/NP020233Z
(3S,4R,4aS,6aR,6bS,8aS,10R,11S,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-10-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-4-carboxylic acid 163018422 Click to see CC12CCC3(C(=C1CC(C(C2)OC4C(C(C(C(O4)CO)O)O)O)(C)CO)CCC5C3(CCC6C5(CCC(C6(C)C(=O)O)O)C)C)C 650.80 unknown https://doi.org/10.1021/NP020233Z
3-Hydroxy-11-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-4-carboxylic acid 73880705 Click to see CC12CCC3(C(=C1CC(C(C2)OC4C(C(C(C(O4)CO)O)O)O)(C)CO)CCC5C3(CCC6C5(CCC(C6(C)C(=O)O)O)C)C)C 650.80 unknown https://doi.org/10.1021/NP020233Z
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3S,4S,5S,6R)-6-[[(2S,3R,4S,4aS,6aR,6bS,8R,8aS,12aR,14aR,14bR)-4-carboxy-2,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-7-oxo-1,2,3,4a,5,6,8,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 162908491 Click to see 664.80 unknown https://doi.org/10.1021/NP020233Z
(2R,4aR,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10929250 Click to see 504.70 unknown https://doi.org/10.1021/NP020233Z
(2R,4aR,6aR,6aS,6bR,8aS,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162919041 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)CO 504.70 unknown https://doi.org/10.1021/NP020233Z
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4S,4aR,6aR,6bS,8R,8aS,12aR,14aR,14bR)-4-carboxy-2,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-7-oxo-1,2,3,4a,5,6,8,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 11146764 Click to see CC1(CCC2C(C1)C3=CCC4C(C3(C(=O)C2O)C)(CCC5C4(CC(C(C5(C)C(=O)O)OC6C(C(C(C(O6)C(=O)O)O)O)O)O)C)C)C 664.80 unknown https://doi.org/10.1021/NP020233Z
10,11-Dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162919040 Click to see 504.70 unknown https://doi.org/10.1021/NP020233Z
6-[(4-Carboxy-2,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-7-oxo-1,2,3,4a,5,6,8,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 85415532 Click to see CC1(CCC2C(C1)C3=CCC4C(C3(C(=O)C2O)C)(CCC5C4(CC(C(C5(C)C(=O)O)OC6C(C(C(C(O6)C(=O)O)O)O)O)O)C)C)C 664.80 unknown https://doi.org/10.1021/NP020233Z
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1002/CHIN.200352191
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1002/CHIN.200352191
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/CHIN.200352191
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP020233Z
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 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 https://doi.org/10.1021/NP020233Z
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/CHIN.200352191
https://doi.org/10.1021/NP020233Z
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1002/CHIN.200352191
https://doi.org/10.1021/NP020233Z
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 https://doi.org/10.1002/CHIN.200352191
https://doi.org/10.1021/NP020233Z
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1002/CHIN.200352191
https://doi.org/10.1021/NP020233Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4R,5S,6S)-2-[4-(2-acetamidoethyl)phenoxy]-5-hydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (Z)-3-(4-methoxyphenyl)prop-2-enoate 11094024 Click to see 809.80 unknown https://doi.org/10.1021/NP020233Z
[(2S,3R,4R,5S,6R)-6-[(2S,3R,4S,5R,6R)-2-[4-(2-acetamidoethyl)phenoxy]-5-hydroxy-6-methyl-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (Z)-3-(4-methoxyphenyl)prop-2-enoate 163193722 Click to see 809.80 unknown https://doi.org/10.1021/NP020233Z
[6-[2-[4-(2-Acetamidoethyl)phenoxy]-5-hydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-methoxyphenyl)prop-2-enoate 85396853 Click to see 809.80 unknown https://doi.org/10.1021/NP020233Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-2-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 45027864 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1002/CHIN.200352191
Alyssonoside 6444250 Click to see 770.70 unknown https://doi.org/10.1002/CHIN.200352191
Forsythoside B 23928102 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1002/CHIN.200352191
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-methyloxan-2-yl]oxy-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163188454 Click to see 666.70 unknown https://doi.org/10.1021/NP020233Z
[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 131885703 Click to see 768.80 unknown https://doi.org/10.1002/CHIN.200352191
[4-[3,4-Dihydroxy-6-(hydroxymethyl)-5-methyloxan-2-yl]oxy-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163001998 Click to see 666.70 unknown https://doi.org/10.1021/NP020233Z
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 6-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)- 124222280 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown https://doi.org/10.1002/CHIN.200352191
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1021/NP020233Z
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1002/CHIN.200352191
> 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/10.1021/NP020233Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]-8-[(2S,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 162938769 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(CO5)O)O)O)O)O)O)O 534.50 unknown https://doi.org/10.1021/NP020233Z
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 10951585 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(CO5)O)O)O)O)O)O)O 534.50 unknown https://doi.org/10.1021/NP020233Z
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]-8-[(2S,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 162938761 Click to see 534.50 unknown https://doi.org/10.1021/NP020233Z
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]-8-[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 162938763 Click to see 534.50 unknown https://doi.org/10.1021/NP020233Z
Apigenin 6,8-di-c-alpha-l-arabinopyranoside 21576179 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(CO5)O)O)O)O)O)O)O 534.50 unknown https://doi.org/10.1021/NP020233Z
apigenin-6,8-C-dipentoside 14427338 Click to see 534.50 unknown https://doi.org/10.1021/NP020233Z

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