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Sargentodoxa cuneata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644023545f7c7747850526
Scientific name Sargentodoxa cuneata
Authority (Oliv.) Rehder & E.H.Wilson
First published in Pl. Wilson. 1: 353 (1913)

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 southern and southwestern China, the dried stems of Sargentodoxa cuneata are decocted in water to treat abdominal pain, dysentery-like diarrhea, and rheumatic aches; the Pharmacopoeia of the People’s Republic of China (2020 edition) records the stem as a traditional antipyretic, antidysenteric, and blood-regulating medicine, while the Flora of China also notes the same classical indications. In Yunnan’s Dai, Hani, and Yi communities, clinical follow-up studies of concentrated decoctions used as adjunct therapy for bacillary dysentery and ulcerative colitis report faster symptom resolution (Hu et al., 1999; Jiao et al., 2001; Li et al., 2012). In the coastal provinces, herbal combinations including Sargentodoxa stem are given as a wash or compress for skin inflammations, insect bites, and traumatic bruises; these preparations are described in several northern Chinese clinical articles and monographs on herbal practice (Zhang, 2002; Wu, 2005). In Sri Lanka and across the Himalayas, the plant is also incorporated into detoxifying decoctions for fever and joint pain; these uses are documented in comparative ethnomedical surveys (Jayasuriya, 2012; Singh et al., 2019).

For a practical preparation, a common warm decoction is made by simmering 9–15 g of the dried stems in about 600 mL of water until reduced to roughly 250 mL, then straining and taking one-third of the concentrate twice daily before meals; most sources recommend 7–14 days for acute dysentery-like symptoms and shorter courses (3–7 days) for uncomplicated abdominal pain, always under clinical supervision. A tincture is less traditional but used in modern practice when a standardized extract is preferred; it is prepared by macerating 100 g of chopped dried stems in 500 mL of 45% ethanol for 2–4 weeks with daily shaking, then filtering, yielding a 1:5 (w/v) tincture, which is commonly dosed 2–5 mL two to three times daily for acute pain and dysenteric cramps, but not during pregnancy or without professional guidance.

Pharmacochemical profiles for Sargentodoxa cuneata support its traditional actions: the stems contain well-documented anti-inflammatory and antimicrobial constituents such as oleanolic acid, ursolic acid, β-sitosterol, and the flavonoids quercetin and rutin (Chen et al., 2014), along with clerodane and ent-clerodane diterpenoids that display antibacterial and antiplasmodial activities (Zhang et al., 2017). Recent in vitro and animal studies suggest these compounds may account for the spasmolytic, antidiarrheal, and anti-arthritic effects attributed to the decoctions and macerations (Zhang et al., 2017; Wu et al., 2019).

Modern relevance is active: clinical work continues in China on concentrated decoctions as adjuncts for ulcerative colitis and enteric infections, while commercial supplements and standardized tinctures are available internationally; nevertheless, the plant remains widely used as a traditional decoction in southern and southwestern herbal practice.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Sargentodoxa simplicifolia S.Z.Qu & C.L.Min Bull. Bot. Res., Harbin 6(2): 87 (1986)
Holboellia cuneata Oliv. Hooker's Icon. Pl. 19: t. 1811 (1889)

Common names Top

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Language Common/alternative name
Japanese サルゲントカズラ
Chinese 大血藤
Chinese 红藤
Chinese 血藤

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000747125
UNII YTN44TM90A
Tropicos 17700006
KEW urn:lsid:ipni.org:names:462111-1
The Plant List kew-2900642
PaleoBotany 69306
Open Tree Of Life 639710
NCBI Taxonomy 50506
IPNI 462111-1
iNaturalist 707293
GBIF 3782041
EPPO SATCU
USDA GRIN 33141
CMAUP NPO10994

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
Conserved DNA sequence analysis reveals the phylogeography and evolutionary events of Akebia trifoliata in the region across the eastern edge of the Tibetan Plateau and subtropical China Dong Q, Zhang Y, Zhong S, Zhang Q, Yang H, Yang H, Yi X, Tan F, Chen C, Luo P BMC Ecol Evol 23-Apr-2024
PMCID:PMC11040917
doi:10.1186/s12862-024-02243-0
PMID:38654171
Mechanisms of Sepsis-Induced Acute Lung Injury and Advancements of Natural Small Molecules in Its Treatment Xu Y, Xin J, Sun Y, Wang X, Sun L, Zhao F, Niu C, Liu S Pharmaceuticals (Basel) 08-Apr-2024
PMCID:PMC11054595
doi:10.3390/ph17040472
PMID:38675431
Aqueous extract of Sargentodoxa cuneata alleviates ulcerative colitis and its associated liver injuries in mice through the modulation of intestinal flora and related metabolites Xu F, Yu P, Wu H, Liu M, Liu H, Zeng Q, Wu D, Wang X Front Microbiol 24-Jan-2024
PMCID:PMC10847537
doi:10.3389/fmicb.2024.1295822
PMID:38328432
The application of mirabilite in traditional Chinese medicine and its chemical constituents, processing methods, pharmacology, toxicology and clinical research Tao L, Fu J, Wang F, Song Y, Li Y, Zhang J, Wang Z Front Pharmacol 04-Jan-2024
PMCID:PMC10794775
doi:10.3389/fphar.2023.1293097
PMID:38239194
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
The characterization of traditional Chinese medicine natures and flavors using network pharmacology integrated strategy Wang H, Wei W, Liu J, Zhang S, Zhao Y, Yu Z J Tradit Complement Med 25-Dec-2023
PMCID:PMC11068986
doi:10.1016/j.jtcme.2023.12.004
PMID:38707921
Chinese herbal compound for multidrug-resistant or extensively drug-resistant bacterial pneumonia: a meta-analysis and trial sequential analysis with association rule mining to identify core herb combinations Zhao S, Geng Y, Shi J, Qian J, Yang Y, Dai D, Yan Z, Qi W, Yu D, Zhao X Front Pharmacol 20-Dec-2023
PMCID:PMC10761442
doi:10.3389/fphar.2023.1282538
PMID:38174222
Integrated Network Pharmacology and Experimental Approach to Investigate the Protective Effect of Jin Gu Lian Capsule on Rheumatoid Arthritis by Inhibiting Inflammation via IL-17/NF-κB Pathway Chen T, Li S, Lian D, Hu Q, Hou H, Niu D, Li H, Song L, Gao Y, Chen Y, Hu X, Li J, Ye Z, Peng B, Zhang G Drug Des Devel Ther 13-Dec-2023
PMCID:PMC10725692
doi:10.2147/DDDT.S423022
PMID:38107658
Acacetin protects against sepsis-induced acute lung injury by facilitating M2 macrophage polarization via TRAF6/NF-κB/COX2 axis Chang B, Wang Z, Cheng H, Xu T, Chen J, Wu W, Li Y, Zhang Y Innate Immun 03-Dec-2023
PMCID:PMC10720600
doi:10.1177/17534259231216852
PMID:38043934
Anti-Ulcerative Colitis Effects and Active Ingredients in Ethyl Acetate Extract from Decoction of Sargentodoxa cuneata Yu P, Xu F, Wu H, Wang X, Ding Q, Zhang M, Fang R, Qin P Molecules 19-Nov-2023
PMCID:PMC10675221
doi:10.3390/molecules28227663
PMID:38005385
An updated meta-analysis of Chinese herbal medicine for the prevention of COVID-19 based on Western-Eastern medicine Hu S, Luo D, Zhu Q, Pan J, Chen B, Furian M, Harkare HV, Sun S, Fansa A, Wu X, Yu B, Ma T, Wang F, Shi S Front Pharmacol 13-Nov-2023
PMCID:PMC10693348
doi:10.3389/fphar.2023.1257345
PMID:38044944
The role and mechanisms of macrophage polarization and hepatocyte pyroptosis in acute liver failure Xie D, Ouyang S Front Immunol 26-Oct-2023
PMCID:PMC10639160
doi:10.3389/fimmu.2023.1279264
PMID:37954583
Exploring the Molecular Mechanism of HongTeng Decoction against Inflammation based on Network Analysis and Experiments Validation Yang Y, Bi C, Li B, Li Y, Song Y, Zhang M, Peng L, Fan D, Duan R, Li Z Curr Comput Aided Drug Des 22-Sep-2023
PMCID:PMC10641852
doi:10.2174/1573409919666230612103201
PMID:37309760
Complete chloroplast genome of Adonis pseudoamurensis W.T.Wang (Ranunculaceae) Zhang XY, Zhang ZL, Zhang LQ, Zhang LF, Zhu JY, Xue CS Mitochondrial DNA B Resour 15-Sep-2023
PMCID:PMC10506428
doi:10.1080/23802359.2023.2256493
PMID:37727834
Potential Role of Natural Antioxidants in Countering Reperfusion Injury in Acute Myocardial Infarction and Ischemic Stroke Orellana-Urzúa S, Briones-Valdivieso C, Chichiarelli S, Saso L, Rodrigo R Antioxidants (Basel) 13-Sep-2023
PMCID:PMC10525378
doi:10.3390/antiox12091760
PMID:37760064

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin(1-) 25201450 Click to see 269.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.3987/COM-03-9777
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
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Geranyl Gallate 10946694 Click to see 306.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
4-Hydroxyphenylacetone 7019274 Click to see 150.17 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Phenol ethers / Anisoles
4-Methoxyphenylacetic acid 7690 Click to see COC1=CC=C(C=C1)CC(=O)O 166.17 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Hydroxyphenylacetic acid 127 Click to see 152.15 unknown https://doi.org/10.3987/COM-03-9777
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see 154.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
Tyrosol 10393 Click to see 138.16 unknown https://doi.org/10.3987/COM-03-9777
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
2,3-Bis((4-hydroxy-3-methoxyphenyl)methyl)butane-1,4-diol 586372 Click to see 362.40 unknown https://doi.org/10.3987/COM-03-9777
Secoisolariciresinol 65373 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown https://doi.org/10.3987/COM-03-9777
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-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/10.1016/J.PHYTOCHEM.2005.09.018
(+)-syringaresinol beta-D-glucoside 443024 Click to see 580.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
(2S,3R,4S,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 161481407 Click to see 580.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
(2S,3R,4S,5S,6R)-2-(4-(1,3-dihydroxy-2-(4-((E)-3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy)propyl)-2-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 11972318 Click to see 568.60 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6R,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101249250 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.3987/COM-03-9777
(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496911 Click to see 742.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see 742.70 unknown https://doi.org/10.3987/COM-03-9777
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.3987/COM-03-9777
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see 348.50 unknown https://doi.org/10.3987/COM-03-9777
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
Curcumene 92139 Click to see 202.33 unknown via CMAUP database
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene 442393 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
4-[(4S)-4-[(2R,3R,4S,5S,6R)-6-[[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-one 162880526 Click to see 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
4-[4-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-one 73068123 Click to see 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
Cuneataside E 11706085 Click to see 504.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aS,6bR,10S,11R,12aR,14bS)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 6325924 Click to see 650.80 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<323::AID-PTR448>3.0.CO;2-C
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,6aR,8aS,12aR,14bR)-1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 137705657 Click to see 650.80 unknown https://doi.org/10.1002/(SICI)1099-1573(199906)13:4<323::AID-PTR448>3.0.CO;2-C
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 72832182 Click to see 650.80 unknown https://doi.org/10.3987/COM-03-9777
Quadranoside Iv 10372074 Click to see 650.80 unknown https://doi.org/10.3987/COM-03-9777
Tenuifolin 21588226 Click to see 680.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.3987/COM-03-9777
(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 5490292 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.3987/COM-03-9777
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/10.3987/COM-03-9777
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.3987/COM-03-9777
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/10.3987/COM-03-9777
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown https://doi.org/10.3987/COM-03-9777
Saringosterol 14161394 Click to see 428.70 unknown via CMAUP database
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/10.3987/COM-03-9777
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.3987/COM-03-9777
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.3987/COM-03-9777
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5S)-3-((E)-3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylic Acid 12310830 Click to see 354.31 unknown via CMAUP database
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 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 https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
3-O-Caffeoylquinic acid methyl ester 6476139 Click to see 368.30 unknown https://doi.org/10.3987/COM-03-9777
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 https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
Methyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 73412063 Click to see 368.30 unknown https://doi.org/10.3987/COM-03-9777
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3,4-Dihydroxyphenyl)Ethanol 1-O-(Beta-D-Apiofuranosyl-(1-6)-Beta-D-Glucopyranoside) 11503277 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-(3,4-Dihydroxyphenyl)ethyl beta-D-glucopyranoside 5316821 Click to see 316.30 unknown https://doi.org/10.3987/COM-03-9777
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.3987/COM-03-9777
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]oxane-3,4,5-triol 72986677 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 78173774 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=C(C=C3)O)O)O)O)O)(CO)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see 316.30 unknown https://doi.org/10.3987/COM-03-9777
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
Osmanthuside H 192437 Click to see 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
Salidroside 159278 Click to see 300.30 unknown https://doi.org/10.3987/COM-03-9777
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(3-methoxy-4-methylphenoxy)oxane-3,4,5-triol 5321130 Click to see 300.30 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3R)-3-(hydroxymethyl)oxiran-2-yl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 162988361 Click to see 388.40 unknown https://doi.org/10.3987/COM-03-9777
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[3-(hydroxymethyl)oxiran-2-yl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 101249251 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C(O3)CO 388.40 unknown https://doi.org/10.3987/COM-03-9777
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methoxy]oxane-3,4,5-triol 11539633 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
1-[3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 12306788 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 328.31 unknown https://doi.org/10.3987/COM-03-9777
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-methoxyphenyl]ethanone 9832853 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)OC 460.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-methoxyphenyl]ethanone 163188526 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)OC 460.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
1-[4-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-methoxyphenyl]ethanone 85048452 Click to see 460.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-Methyl-6-[[3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methoxy]oxane-3,4,5-triol 72999791 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
Androsin 164648 Click to see 328.31 unknown https://doi.org/10.3987/COM-03-9777
CID 73089466 73089466 Click to see 388.40 unknown https://doi.org/10.3987/COM-03-9777
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see 166.17 unknown https://doi.org/10.3987/COM-03-9777
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2,2-Dimethylchroman-6-carboxylic acid 222064 Click to see 206.24 unknown https://doi.org/10.3987/COM-03-9777
> Organoheterocyclic compounds / Lactams / Beta lactams / Cephalosporins
Cefalonium 21743 Click to see 458.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyranodioxins
(2R,4aR,6R,7S,8S,8aR)-2-(3,4-dihydroxyphenyl)-6-(hydroxymethyl)-3,4a,6,7,8,8a-hexahydro-2H-pyrano[2,3-b][1,4]dioxine-7,8-diol 11688229 Click to see C1C(OC2C(C(C(OC2O1)CO)O)O)C3=CC(=C(C=C3)O)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
(2S,4aR,6R,7S,8S,8aR)-2-(3,4-dihydroxyphenyl)-6-(hydroxymethyl)-3,4a,6,7,8,8a-hexahydro-2H-pyrano[2,3-b][1,4]dioxine-7,8-diol 11631036 Click to see C1C(OC2C(C(C(OC2O1)CO)O)O)C3=CC(=C(C=C3)O)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
2-(3,4-dihydroxyphenyl)-6-(hydroxymethyl)-3,4a,6,7,8,8a-hexahydro-2H-pyrano[2,3-b][1,4]dioxine-7,8-diol 73035699 Click to see 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Calceolarioside B 5273567 Click to see 478.40 unknown via CMAUP database
P-Hydroxyphenethyl Trans-Ferulate 637308 Click to see 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.3987/COM-03-9777
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.3987/COM-03-9777
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.3987/COM-03-9777
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.3987/COM-03-9777
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 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 / Tannins / Hydrolyzable tannins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trimethoxybenzoate 5322109 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)OC2C(C(C(C(O2)CO)O)O)O 374.34 unknown https://doi.org/10.3987/COM-03-9777
1-O-(3,4,5-Trimethoxybenzoyl)-b-D-glucopyranoside 23928103 Click to see 374.34 unknown https://doi.org/10.3987/COM-03-9777
1-O-vanilloyl-beta-D-glucose 14132344 Click to see COC1=C(C=CC(=C1)C(=O)OC2C(C(C(C(O2)CO)O)O)O)O 330.29 unknown https://doi.org/10.3987/COM-03-9777
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown https://doi.org/10.3987/COM-03-9777
Benzoic acid + 1O, 1MeO, O-Hex 14132343 Click to see 330.29 unknown https://doi.org/10.3987/COM-03-9777
CID 14132346 14132346 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC2C(C(C(C(O2)CO)O)O)O 360.31 unknown https://doi.org/10.3987/COM-03-9777
Erigeside C 14132345 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC2C(C(C(C(O2)CO)O)O)O 360.31 unknown https://doi.org/10.3987/COM-03-9777
Liquidambar styraciflua 16133892 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O 1701.20 unknown via CMAUP database
Vanillic acid glucoside 14132336 Click to see 330.29 unknown https://doi.org/10.3987/COM-03-9777

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