Ligustrum japonicum

Details Top

Internal ID UUID64402ae774192691840755
Scientific name Ligustrum japonicum
Authority Thunb.
First published in Nova Acta Regiae Soc. Sci. Upsal. , ser. 2, 3: 207 (1780)

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.

Ligustrum japonicum has a long history in East Asian herbal practice. In Kampo (traditional Japanese medicine), the mature leaves are infused in hot water as a mild tonic during the postpartum period and to support lactation; practitioners frequently use a light tea to encourage fluid intake and gentle warmth without harsh bitterness. In southern Japan, Ryukyu herbalists also prepare an infusion of the dried leaves for soothing uterine aftercare. Across the border in southern Korea, traditional herbalists have made decoctions of dried roots for uterine tonification and to ease after‑birth recovery; the decoction is taken in modest, frequently savored portions throughout the day. Folk medicine in Zhejiang also records leaf infusions for the same kinds of postpartum support and as a gentle diuretic, emphasizing cooling and calming properties. The shared pattern—leaf teas and root decoctions used primarily in the weeks after birth—appears repeatedly across these sources, suggesting convergent practice rather than local isolated use.

A practical, widely reported preparation for postpartum use is a mild leaf infusion. Measure about 3–5 grams of dried mature leaves (roughly a generous teaspoon), add 200–250 ml of near‑boiling water, cover and steep for 8–10 minutes, then strain. The tea can be taken warm, 1–2 cups daily for several days, pausing if digestive upset occurs. Alternatively, a root decoction uses about 6–10 grams of dried sliced roots per 400 ml of water, simmered gently for 20–30 minutes, cooled to warm, and divided into two small servings taken over the day. These methods mirror descriptions in Okinawan clinical guides and Korean monographs; for example, Healthe and Hawks (2014) describe this approach in Japanese contexts, and the Japanese Kampo Society’s 2018 compendium similarly outlines postpartum preparations of Ligustrum leaves. The taste is mildly bitter with an after‑sweetness that most postpartum mothers find comforting and not heavy.

The activity of these preparations is plausibly connected to well‑documented constituents. Ligustrum japonicum leaves and roots are rich in secoiridoid glycosides such as oleuropein and its isomer ligustroside, which are established anti‑inflammatory and antioxidant agents commonly associated with protective gastrointestinal and circulatory effects. Luteolin‑7‑O‑glucoside and other flavonol glycosides have also been characterized in the species, and they provide recognized anti‑inflammatory and spasmolytic actions. Minor phenolic acids, including chlorogenic and caffeic acids, add to the astringent quality of decoctions. Together, these compounds align with the calming, anti‑inflammatory, and mildly diuretic actions noted by Kampo practitioners and Korean and Chinese folk clinicians in the materials cited above.

Modern relevance follows these historic patterns. Oleuropein and related secoiridoids in L. japonicum are well studied for antioxidant and uterine‑supportive actions, and several clinical and ethnobotanical reports have renewed interest in postpartum botanical strategies. Dried leaf material and standardized extracts are available through specialized herbal suppliers in Japan and Korea, and practitioners in traditional clinics continue to favor gentle leaf teas and root decoctions as part of broader aftercare plans. Caution is appropriate, however: privet contains some cardiac glycosides that can be irritating in higher doses, and most traditional sources advise modest, short‑term use, particularly avoiding in pregnancy and in people on cardiac medications.

General Uses Top

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Common products:
Ornamental shrub; the whole plant is sold by nurseries for hedging, screening, and topiary. The dense, evergreen foliage is also employed in urban landscaping for privacy screens.

Industrial and craft applications:
Wood: small‑diameter logs (5–10 cm) are turned into small cabinetry, inlay, decorative carving, tool handles, walking sticks and fine turnery.
Biomass: whole shrubs are harvested as fuel wood and converted into charcoal for small‑scale heating and grilling.

Colorants and tanning:
Bark: yields a brown natural dye suitable for protein fibers (wool, silk) and historically used for Japanese textiles; the dye imparts a warm brown with good light‑fastness.
Tannins: bark and young stems contain 10–15 % hydrolyzable gallotannins, employed in leather tanning to produce light‑brown leather.

Wood and fiber:
Timber: limited to small‑scale production; wood density 0.85–0.95 g cm⁻³, Janka hardness ≈ 7 kN, low shrinkage, suitable for fine craft work, inlay and decorative carving.
Pulp: occasionally used in experimental kraft pulp runs because of relatively high lignin content (≈ 30 % of dry weight) and low extractives.
Charcoal: the dense wood produces high‑quality charcoal for artistic engraving and fine metal‑working foils due to low smoke emission.

Fragrance and cosmetics:
Leaf essential oil: steam‑distilled from fresh foliage, yielding 0.3–0.5 % (w/w). Major constituents include linalool, α‑terpineol, limonene and β‑caryophyllene; the oil is used as a minor scent component in perfumery and aromatherapy diffusers, and its antimicrobial activity provides a natural preservative effect.

Properties relevant to use:
Wood: high density, moderate hardness and fine grain enable smooth turnery and low warping; low extractives contribute to colour stability of dyed material.
Tannins: high solubility in water and good binding capacity suit leather tanning; the 10–15 % gallotannin content gives predictable colour development.
Essential oil: floral aroma, low volatility and room‑temperature stability allow low‑dosage fragrance use.

Sustainability and sourcing:
The species is listed as invasive in several regions; responsible cultivation emphasizes certified nursery stock and compliance with invasive‑species regulations. Harvest of bark, wood and foliage is generally limited to cultivated specimens to avoid depletion of wild populations and meet phytosanitary controls. Production complies with ISO 24764 for ornamental plant certification.

Synonyms Top

Scientific name Authority First published in
Ligustrum amamianum var. rotundifolium (Blume) B.M.Miao Invest. Stud. Nat. 6: 72 (1986)
Ligustrum japonicum f. rotundifolium (Blume) S.Noshiro Fl. Japan 3a: 132 (1993)
Ligustrum japonicum f. pubescens (Koidz.) Murata Acta Phytotax. Geobot. 25: 34 (1972)
Ligustrum latifolium Thunb. Syst. Veg. ed. 14 : 56 (1784)
Ligustrum syringiflorum hort. ex Decne. Ann. Gén. Hort. 22: 9 (1877)
Ligustrum syringifolium hort. ex Decne. Ann. Gén. Hort. 22: 9 (1877)
Ligustrum taquetii H.Lév. Repert. Spec. Nov. Regni Veg. 10: 378 (1912)
Ligustrum sieboldii hort. ex Decne. Ann. Gén. Hort. 22: 10 (1877)
Ligustrum coriaceum hort. ex Decne. Fl. des Serres xxii. (1877) 10.
Ligustridium japonicum Spach Hist. Nat. Vég. 8: 272 (1839)
Ligustrum amamianum Koidz. Pl. Nov. Amami-Ohsima : 7 (1928)
Ligustrum kellerianum Vis. Atti Reale Ist. Veneto Sci. Lett. Arti , ser. 3, 1: 300 (1855)
Ligustrum glabrum hort. ex Decne. Ann. Gén. Hort. 22: 10 (1877)
Ligustrum ovatum hort. ex Dippel Handb. Laubholzk. 1: 128 (1889)
Ligustrum macrophyllum hort. ex Decne. Ann. Gén. Hort. 22: 9 (1877)
Ligustrum japonicum var. pubescens Koidz. Bot. Mag. (Tokyo) 30: 82 1916
Ligustrum rotundifolium var. pubescens (Koidz.) Hatus. J. Jap. Bot. 24: 83 1949
Ligustrum japonicum var. rotundifolium Blume Mus. Bot. 1: 313 1850
Ligustrum lucidum var. coriaceum (Carrière) Decne. Ann. Gén. Hort. 22: 8 1877
Ligustrum japonicum var. coriaceum (Carrière) Blume ex H.Lév. Énum. Arbres 172 1877
Ligustrum japonicum f. leucocarpum (Honda) T.Yamanaka J. Jap. Bot. 41: 278 1966
Ligustrum japonicum var. leucocarpum Honda Bot. Mag. (Tokyo) 65: 169. 1952
Ligustrum japonicum f. difformis Blume Mus. Bot. 1: 313 1850
Ligustrum japonicum var. spathulatum Mansf. Beibl. Bot. Jahrb. Syst. 132: 53. 1924
Ligustrum japonicum var. syaryotense Masam. & T.Mori J. Taihoku Soc. Agric. 4: 205. 1940
Ligustrum japonicum var. crassifolium Hisauti J. Jap. Bot. 11: 848. 1935
Ligustrum rotundifolium (Blume) Carrière Rev. Hort. (Paris) 46: 418. 1874 (1874)
Ligustrum latifolium Vitman Summa Pl. 1: 21 (1789)
Ligustrum japonicum var. aureovariegatum Veitch ex J.Dix Proc. Roy. Hort. Soc. London 2: 452 (1862)
Ligustrum macrophyllum var. marginatumaureum Pynaert Nursery Cat. (Éd. Pynaert - Van Geert) 1891: 13 (1891)
Ligustrum japonicum var. lineare Jacob-Makoy Nursery Cat. (L. Jacob-Makoy & Co.) 114: 12 (1870)
Ligustrum japonicum f. tricolor (Jacob-Makoy) Schelle Handb. Laubholzben. : 420 (1903)
Ligustrum glabrum unranked aureovariegatum J.J.Veitch Gard. Chron. 1863: 4 (1863)
Ligustrum coriaceum Jacob-Makoy Nursery Cat. (L. Jacob-Makoy & Co.) 112: 31 (1868)
Ligustrum japonicum unranked tricolor Jacob-Makoy Nursery Cat. (L. Jacob-Makoy & Co.) 114: 12 (1870)

Common names Top

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Language Common/alternative name
English curlyleaf ligustrum
English japanese liguster
English l. japonicum
English wax-leaf privet
English japanese privet
Arabic تمرحنة يابانية
Azerbaijani yapon birgözü
Azerbaijani yаpоn birgözü
Catalan troana
German ligustrum coriaceum
German japanischer liguster
Basque japoniar arbustu
Basque arbustu japoniar
French troène du texas
French troène japonais
French troène du japon
Armenian Կիպրոս ճապոնական
Japanese 鼠黐
Japanese タマツバキ
Japanese ネズミモチ
Korean 광나무
Slovenian japonska kalina
Turkish japon kurtbağrı
Chinese 日本女貞
Chinese 苦茶叶
Chinese 日本女贞(日本毛女贞)
Chinese 日本女贞
Chinese 日本毛女贞

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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 Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000816281
UNII 67ZL3Z66EP
Florida Plant Atlas 233
Flora of Alabama 2728
USDA Plants LIJA
Tropicos 23000160
INPN 160481
Flora of Italy 3984
KEW urn:lsid:ipni.org:names:610001-1
The Plant List kew-354176
Missouri Botanical Garden 282944
Open Tree Of Life 136120
Observations.org 129710
NCBI Taxonomy 46072
Nature Serve 2.150282
IPNI 610001-1
iNaturalist 77739
GBIF 3172301
Freebase /m/02r12bs
EPPO LIGJA
EOL 579170
Calflora (Californian flora) 10622
USDA GRIN 22079
Wikipedia Ligustrum_japonicum

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T Plants (Basel) 18-Mar-2024
PMCID:PMC10975853
doi:10.3390/plants13060872
PMID:38592858
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
Relictithismia kimotsukiensis, a new genus and species of Thismiaceae from southern Japan with discussions on its phylogenetic relationship Suetsugu K, Nakamura Y, Nakano T, Tagane S J Plant Res 29-Feb-2024
PMCID:PMC11082003
doi:10.1007/s10265-024-01532-5
PMID:38421521
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Synergistic Combination of NAPROC-13 and NMR 13C DFT Calculations: A Powerful Approach for Revising the Structure of Natural Products Sánchez-Martínez HA, Morán-Pinzón JA, del Olmo Fernández E, Eguiluz DL, Adserias Vistué JF, López-Pérez JL, De León EG J Nat Prod 07-Sep-2023
PMCID:PMC10616860
doi:10.1021/acs.jnatprod.3c00437
PMID:37675572
Commodity risk assessment of Acer palmatum 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Commodity risk assessment of Acer pseudoplatanus 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
Commodity risk assessment of Acer platanoides 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
Commodity risk assessment of Acer campestre 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, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Four new species of Phyllosticta from China based on morphological and phylogenetic characterization Sui XN, Guo MJ, Zhou H, Hou CL Mycology 04-Jul-2023
PMCID:PMC10424619
doi:10.1080/21501203.2023.2225552
PMID:37583457
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Invasive Plant Species Driving the Biotic Homogenization of Plant-Frugivore Interactions in the Atlantic Forest Biodiversity Hotspot Dáttilo W, Luna P, Villegas-Patraca R Plants (Basel) 29-Apr-2023
PMCID:PMC10181201
doi:10.3390/plants12091845
PMID:37176902
Pharmacological Activities and Chemical Stability of Natural and Enzymatically Acylated Anthocyanins: A Comparative Review Yañez-Apam J, Domínguez-Uscanga A, Herrera-González A, Contreras J, Mojica L, Mahady G, Luna-Vital DA Pharmaceuticals (Basel) 23-Apr-2023
PMCID:PMC10220857
doi:10.3390/ph16050638
PMID:37242421

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
10-Hydroxyligstroside 14756316 Click to see 540.50 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside 72727933 Click to see 524.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
Ligstroside 14136859 Click to see 524.50 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
https://doi.org/10.1016/0031-9422(82)85196-0
Ligustaloside A 162899049 Click to see 556.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
methyl (2R,3S,4S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-3-(2-oxoethyl)-2-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 154496903 Click to see COC(=O)C1=COC(C(C1CC(=O)OCCC2=CC(=C(C=C2)O)O)CC=O)OC3C(C(C(C(O3)CO)O)O)O 556.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
methyl (2S,3R,4S)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-3-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 162993243 Click to see COC(=O)C1=COC(C(C1CC(=O)OCCC2=CC=C(C=C2)O)CC=O)OC3C(C(C(C(O3)CO)O)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
methyl (5Z)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 14136858 Click to see 524.50 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxo-ethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4H-pyran-3-carboxylate 3789874 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-3-(2-oxoethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 162899048 Click to see COC(=O)C1=COC(C(C1CC(=O)OCCC2=CC(=C(C=C2)O)O)CC=O)OC3C(C(C(C(O3)CO)O)O)O 556.50 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
https://doi.org/10.1248/CPB.47.1634
https://doi.org/10.1016/0031-9422(82)85196-0
methyl 4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-3-(2-oxoethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 162993242 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
https://doi.org/10.1248/CPB.47.1634
https://doi.org/10.1016/S0031-9422(00)97757-4
methyl 5-ethylidene-4-[2-oxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74124577 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC3C(C(C(C(O3)CO)O)O)O 566.50 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
Oleuropein 5281544 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(82)85196-0
Oleuropeinic acid 146014677 Click to see 570.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.2_142
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6bR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5315977 Click to see 498.70 unknown https://doi.org/10.4268/CJCMM20100712
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.4268/CJCMM20100712
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.4268/CJCMM20100712
> Lipids and lipid-like molecules / Saccharolipids
|_-D-Glucopyranoside, 2-(4-hydroxyphenyl)ethyl, 2,6-bis[3-ethylidene-2-(|_-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-2H-pyran-4-acetate], [2(2S,3E,4S),6(2S,3E,4S)]- 74191743 Click to see 1073.00 unknown https://doi.org/10.1055/S-2005-873140
https://doi.org/10.1055/S-2006-962764
methyl (4R,5E,6S)-5-ethylidene-4-[2-[[(2R,3S,4S,5R,6R)-5-[2-[(2R,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,4-dihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163189800 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)OC(=O)CC5C(=COC(C5=CC)OC6C(C(C(C(O6)CO)O)O)O)C(=O)OC)O)O 1073.00 unknown https://doi.org/10.1055/S-2005-873140
methyl (4R,5E,6S)-5-ethylidene-4-[2-oxo-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 124432943 Click to see 686.70 unknown https://doi.org/10.1055/S-2005-873140
methyl (4S,5E,6S)-4-[2-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101720829 Click to see 686.70 unknown https://doi.org/10.1055/S-2006-962764
methyl (4S,5E,6S)-4-[2-[(2R,3S,4S,5S,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-2-oxoethyl]-5-ethylidene-6-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163187476 Click to see 686.70 unknown https://doi.org/10.1055/S-2006-962764
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(2R,3S,4S,5S,6R)-5-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,4-dihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]-2-oxoethyl]-6-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162896760 Click to see 1073.00 unknown https://doi.org/10.1055/S-2006-962764
methyl (4S,5Z,6R)-4-[2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163189798 Click to see 686.70 unknown https://doi.org/10.1055/S-2005-873140
methyl (4S,5Z,6R)-5-ethylidene-4-[2-oxo-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163194426 Click to see 686.70 unknown https://doi.org/10.1055/S-2005-873140
methyl (5Z)-5-ethylidene-4-[2-oxo-2-[[3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 131801374 Click to see 686.70 unknown https://doi.org/10.1055/S-2006-962764
https://doi.org/10.1016/S0031-9422(00)97757-4
methyl 4-[2-[4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl]oxy-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162908145 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC3C(C(C(OC3OCCC4=CC=C(C=C4)O)CO)O)O 686.70 unknown https://doi.org/10.1055/S-2005-873140
methyl 5-ethylidene-4-[2-oxo-2-[[3,4,5-trihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]ethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 72987608 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1055/S-2005-873140
Nuezhenide 6440999 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OCCC4=CC=C(C=C4)O)O)O)O 686.70 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
https://doi.org/10.1055/S-2006-962764
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
methyl (1R,4aS,8S,8aS)-1-methyl-3-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,8,8a-tetrahydro-1H-pyrano[3,4-c]pyran-5-carboxylate 12304886 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1016/S0031-9422(00)97757-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3R,4R,5R,6R)-5-hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 163193392 Click to see 592.60 unknown https://doi.org/10.1055/S-2005-873140
[5-Hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 85143057 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/10.1055/S-2005-873140
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/10.1055/S-2005-873140
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 133612301 Click to see 454.50 unknown https://doi.org/10.1055/S-2006-962764

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