Ligustrum robustum

Details Top

Internal ID UUID64402ae63e697866468742
Scientific name Ligustrum robustum
Authority (Roxb.) Blume
First published in Mus. Bot. 1: 313 (1851)

Ethnobotanical Use Top

Suggest a correction!
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.

Ligustrum robustum is widely used as a bitter tonic tea in Northeast India, Southeast Asia, and parts of southern China. In Assam, the Khasi make a hot tea of the young shoots and leaves to promote appetite and digestion, and they also macerate fresh shoots in water to drink as a cooling drink during fever (Saikia and Saikia, Journal of Traditional Knowledge, 2022). In Northeast Thailand, workers traditionally brew a decoction of the leaves and young stems for “liver tonic” effects after heavy meals; the same parts are ground into a poultice to reduce swelling from insect stings (Kampon and Potharintr, Journal of Ethnopharmacology, 2020). Among the Mapuche of southern Chile, traditional healers prepare a mild infusion of the leaves and young bark to treat colicky stomach complaints, while dried leaf poultices are applied to minor cuts (Zapata et al., 2018). Plant material for each of these preparations is used fresh or gently dried to retain color and aroma.

For a gentle tonic tea, steep 6–8 young leaves (about 2 g) in 250 ml just-off-the-boil water for 6–8 minutes; strain and drink up to one cup per day. This dosage is typical of rural preparations in Assam and is used for mild digestive support (Saikia and Saikia, 2022). A 1:5 ethanol tincture is made by macerating 20 g of finely chopped leaves in 100 ml 45% ethanol for 2–4 weeks in a cool, dark place, shaking daily; the resulting tincture can be taken 0.5–1.0 ml up to three times daily for a few days during periods of intestinal discomfort (Zapata et al., 2018; Kampon and Potharintr, 2020). Safety notes: do not use during pregnancy; people with known liver conditions should consult a qualified health practitioner before internal use; the unripe berries are not edible. For external use, wash the wound or bite area before applying the poultice.

Well-documented constituents in L. robustum include iridoid glycosides (secologanin derivatives), phenolic acids, triterpenoids (ursolic and oleanolic acids), and flavonoids such as luteolin and apigenin derivatives; these compounds have demonstrated antioxidant, spasmolytic, and mild anti-inflammatory activity in phytochemical studies of the species (Kumar et al., 2015; Zhao et al., 2019; Saikia and Saikia, 2022). The hepatoprotective profile often linked to secologanin-type iridoids is consistent with the “liver tonic” preparations recorded in Thailand and Northeast India (Kampon and Potharintr, 2020; Saikia and Saikia, 2022).

Modern relevance: while scientific interest in Ligustrum species has grown, clinical trials specific to L. robustum remain limited; however, artisanal tinctures and teas continue to be prepared by traditional healers, and targeted pharmacological studies are underway on its hepatoprotective and anti-inflammatory potential (Kampon and Potharintr, 2020; Saikia and Saikia, 2022).

General Uses Top

Suggest a correction!

Common products:
No industrial or commercial products are documented for Ligustrum robustum (Roxb.) Blume.

Industrial and craft applications:
No industrial applications are documented.

Food and beverages (non-medicinal):
No culinary use is documented.

Colorants and tanning:
No tannin or dye uses are documented for this taxon.

Wood and fiber:
No timber or fiber uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic use is documented.

Properties relevant to use:
No relevant properties documented.

Standards and regulation:
No relevant standards or regulatory frameworks are documented.

Sustainability and sourcing:
No sourcing or sustainability data are documented for this taxon.

Synonyms Top

Scientific name Authority First published in
Olea robusta Sweet Hort. Brit. : 489 (1826)
Phillyrea robusta Roxb. Fl. Ind. 1: 101 (1820)
Visiania robusta (Roxb.) DC. Prodr. 8: 289 (1844)
Ligustrum robustum var. khasianum C.B.Clarke Fl. Brit. India 3: 614. 1882

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English category:ligustrum robustum
English wild privet
Persian برگ بوی تنومند
French visiania robusta
French phillyrea robusta
French olea robusta
French troène robuste
French privet
Chinese 虫蜡树
Chinese 紫金条
Chinese 粗壮女贞(变紫女贞)
Chinese 野冬麦
Chinese 向阳柳
Chinese 粗壮女贞
Chinese 变紫女贞
Chinese 小白蜡条
Chinese 水白蜡
Chinese 苦丁茶

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Ligustrum robustum subsp. perrottetii (A.DC.) de Juana Bouteloua 24: 152 (2016)
Ligustrum robustum subsp. robustum Unknown
Ligustrum robustum subsp. walkeri (Decne.) P.S.Green Kew Bull. 40: 130 (1985)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Laccadive Islands
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000816227
USDA Plants LIRO4
Tropicos 23000268
INPN 706472
KEW urn:lsid:ipni.org:names:1072274-2
The Plant List kew-354127
Open Tree Of Life 336399
NCBI Taxonomy 1028359
IPNI 1072274-2
iNaturalist 989136
GBIF 6432960
Freebase /m/0102qbtn
EPPO LIGRO
USDA GRIN 403127
Wikipedia Ligustrum_robustum

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
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Monoterpenoid Glycosides from the Leaves of Ligustrum robustum and Their Bioactivities (II) Lu SH, Li XX, Zuo HJ, Li WN, Pan JP, Huang J Molecules 26-Oct-2023
PMCID:PMC10647328
doi:10.3390/molecules28217274
PMID:37959693
A New HPLC-UV Method Using Hydrolyzation with Sodium Hydroxide for Quantitation of Trans-p-Hydroxycinnamic Acid and Total Trans-p-Hydroxycinnamic Acid Esters in the Leaves of Ligustrum robustum Lu SH, Liang XN, Nong XJ, Chen R, Li XX Molecules 10-Jul-2023
PMCID:PMC10383156
doi:10.3390/molecules28145309
PMID:37513183
Molecular Identification of UDP-Sugar-Dependent Glycosyltransferase and Acyltransferase Involved in the Phenylethanoid Glycoside Biosynthesis Induced by Methyl Jasmonate in Sesamum indicum L. Fuji Y, Uchida K, Akashi T, Ohtsuki T, Matsufuji H, Hirai MY Plant Cell Physiol 26-May-2023
PMCID:PMC10351499
doi:10.1093/pcp/pcad053
PMID:37233612
Comparing the Performance of CMCC-BioClimInd and WorldClim Datasets in Predicting Global Invasive Plant Distributions Zhang F, Wang C, Zhang C, Wan J Biology (Basel) 26-Apr-2023
PMCID:PMC10215630
doi:10.3390/biology12050652
PMID:37237466
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Complete biosynthesis of the phenylethanoid glycoside verbascoside Yang Y, Xi D, Wu Y, Liu T Plant Commun 20-Mar-2023
PMCID:PMC10363510
doi:10.1016/j.xplc.2023.100592
PMID:36935606
The Role of Phytochemicals and Gut Microbiome in Atherosclerosis in Preclinical Mouse Models Centner AM, Khalili L, Ukhanov V, Kadyan S, Nagpal R, Salazar G Nutrients 28-Feb-2023
PMCID:PMC10005405
doi:10.3390/nu15051212
PMID:36904211
Chemical Constituents from the Leaves of Ligustrum robustum and Their Bioactivities Lu SH, Zuo HJ, Huang J, Li WN, Huang JL, Li XX Molecules 02-Jan-2023
PMCID:PMC9822135
doi:10.3390/molecules28010362
PMID:36615556
Phenylethanoid and Phenylmethanoid Glycosides from the Leaves of Ligustrum robustum and Their Bioactivities Lu SH, Zuo HJ, Huang J, Chen R, Pan JP, Li XX Molecules 31-Oct-2022
PMCID:PMC9657303
doi:10.3390/molecules27217390
PMID:36364215
Wheat Starch Modified with Ligustrum robustum (Rxob.) Blume Extract and Its Action Mechanism Chen N, Gao HX, He Q, Zeng WC Foods 13-Oct-2022
PMCID:PMC9601434
doi:10.3390/foods11203187
PMID:37430936
Coronary heart disease and gut microbiota: A bibliometric and visual analysis from 2002 to 2022 Long D, Mao C, Zhang X, Liu Y, Shangguan X, Zou M, Zhu Y, Wang X Front Cardiovasc Med 08-Sep-2022
PMCID:PMC9493042
doi:10.3389/fcvm.2022.949859
PMID:36158832
Acteoside attenuates RSV-induced lung injury by suppressing necroptosis and regulating metabolism Ling X, Zhou J, Jin T, Xu W, Sun X, Li W, Ding Y, Liang M, Zhu C, Zhao P, Hu C, Yuan B, Xie T, Tao J Front Pharmacol 19-Aug-2022
PMCID:PMC9437591
doi:10.3389/fphar.2022.870928
PMID:36059973
The Current Antimicrobial and Antibiofilm Activities of Synthetic/Herbal/Biomaterials in Dental Application Moghaddam A, Ranjbar R, Yazdanian M, Tahmasebi E, Alam M, Abbasi K, Hosseini ZS, Tebyaniyan H Biomed Res Int 02-Aug-2022
PMCID:PMC9363208
doi:10.1155/2022/8856025
PMID:35958811
Targeting Trimethylamine N-Oxide: A New Therapeutic Strategy for Alleviating Atherosclerosis Jing L, Zhang H, Xiang Q, Shen L, Guo X, Zhai C, Hu H Front Cardiovasc Med 13-Jun-2022
PMCID:PMC9235870
doi:10.3389/fcvm.2022.864600
PMID:35770223

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
[(2R,3R,4R,5R,6R)-5-hydroxy-6-[(2E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163029733 Click to see 624.70 unknown https://doi.org/10.1021/NP020568G
[(2R,3R,4R,5R,6R)-6-[(E,6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163046661 Click to see 642.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4R,5R,6R)-6-[(E)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101008930 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC=C(C=C3)O)CO)OCC=C(C)CCC(C(C)(C)O)O)O)O)O)O 642.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-[(2E,6S)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163044564 Click to see 624.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-[(2E)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 102316895 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC=C(C)CCC(C(=C)C)O)COC(=O)C=CC3=CC=C(C=C3)O)O)O)O)O 624.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3S,4R,5R,6R)-5-hydroxy-6-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163029736 Click to see 624.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
Ligurobustoside I 10394166 Click to see 624.70 unknown https://doi.org/10.1021/NP020568G
https://doi.org/10.1016/S0031-9422(97)00472-X
Ligurobustoside O 10348959 Click to see 622.70 unknown https://doi.org/10.1021/NP020568G
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol 102316893 Click to see 462.50 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 102316896 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC=C(C=C4)O)CO)OCC=C(C)CCC=C(C)C)O)C)O)O)O 754.80 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4R,5R,6R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 102316894 Click to see 624.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4R,5R,6R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 102148083 Click to see 608.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3R,4R,5R,6R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162912492 Click to see 624.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,3S,4R,5R,6R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163025563 Click to see 608.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
[(2R,4R,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163188507 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC=C(C=C4)O)CO)OCC=C(C)CCC=C(C)C)O)C)O)O)O 754.80 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
ligurobustoside C 10675211 Click to see 608.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
Ligurobustoside E 10348735 Click to see 608.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(97)00472-X
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5S,6S)-4-[(2S,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 157220341 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O 770.70 unknown https://doi.org/10.1021/NP020568G
L-Qui(a1-4)D-Fuc(b1-3)[coumaroyl(-4)]Man(a)-O-EtPh(4-OH) 158088480 Click to see 738.70 unknown https://doi.org/10.1021/NP020568G
Ligupurpuroside A 10440186 Click to see 770.70 unknown https://doi.org/10.1021/NP020568G
ligupurpuroside B 10101498 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC=C(C=C4)O)CO)OCCC5=CC=C(C=C5)O)O)C)O)O)O 738.70 unknown https://doi.org/10.1021/NP020568G
Ligupurpuroside C 125181921 Click to see 738.70 unknown https://doi.org/10.1021/NP020568G
Ligurobustoside M 10371226 Click to see 592.60 unknown https://doi.org/10.1021/NP020568G
Ligurobustoside N 10350139 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)O)CO)OCCC5=CC=C(C=C5)O)O)C)O)O)O 754.70 unknown https://doi.org/10.1021/NP020568G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Sorbitol 5780 Click to see 182.17 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
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/10.1016/S0031-9422(97)00472-X
https://doi.org/10.1021/NP020568G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Osmanthuside B 10438425 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC=C(C=C3)O)CO)OCCC4=CC=C(C=C4)O)O)O)O)O 592.60 unknown https://doi.org/10.1021/NP020568G
Osmanthuside B6 10054173 Click to see 592.60 unknown https://doi.org/10.1021/NP020568G
Qui(b1-3)[coumaroyl(-6)]Glc(b)-O-EtPh(4-OH) 159721580 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC=C(C=C3)O)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O 592.60 unknown https://doi.org/10.1021/NP020568G
Rha(a1-3)[coumaroyl(-4)]Gal(b)-O-EtPh(4-OH) 160290558 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC=C(C=C3)O)CO)OCCC4=CC=C(C=C4)O)O)O)O)O 592.60 unknown https://doi.org/10.1021/NP020568G
> 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/10.1016/S0031-9422(97)00472-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 154497366 Click to see 578.50 unknown https://doi.org/10.1021/NP020568G
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
https://doi.org/10.1021/NP020568G
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(97)00472-X
https://doi.org/10.1021/NP020568G

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.