Prunus lusitanica

Details Top

Internal ID UUID64403f64b2906965157280
Scientific name Prunus lusitanica
Authority L.
First published in Sp. Pl. : 473 (1753)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The principal commercial product of Prunus lusitanica is the live shrub, sold by nurseries as 1–3‑year‑old rooted cuttings or container‑grown specimens. Plants are marketed for their dense, glossy, evergreen foliage, making them suitable for hedging, privacy screens, and topiary. The species tolerates regular pruning, retains foliage through winter, and is well adapted to Mediterranean climates, enhancing its ornamental value.

Industrial and craft applications:
The shrub is produced on a commercial scale by horticultural nurseries to supply the landscaping industry. It is employed in large‑scale urban greening programs, private garden designs, and craft horticulture for shaping into formal topiary, clipped hedges, and ornamental knots. Its dense branching habit and tolerance to pruning make it a low‑maintenance option that reduces labor costs in landscape projects.

Properties relevant to use:
The evergreen leaves are leathery and retain chlorophyll throughout the year, providing continuous visual screening. The wood has a moderate density (≈0.7 g cm⁻³) typical of Rosaceae, with a high lignin‑cellulose ratio that confers durability for structural garden features. Leaf tissue contains condensed tannins (≈10 % of dry weight) and phenolic compounds quantified in phytochemical analyses, indicating potential for future leather‑tanning applications. The shrub shows moderate drought tolerance once established and responds well to repeated pruning, allowing controlled growth forms.

Standards and regulation:
There are no dedicated ISO, ASTM or EN standards for timber, leaf extracts or ornamental stock of P. lusitanica. Nursery trade is governed by the EU Plant Health Directive (EU 2016/2031) and national phytosanitary certification schemes, which require disease‑free propagation material and proper labeling. The species is not listed under CITES, and its wood is not subject to timber‑trade regulations such as the EU Timber Regulation. Any future commercial extraction of leaf tannins would need to comply with the EU REACH framework.

Sustainability and sourcing:
The IUCN Red List categorizes P. lusitanica as Least Concern, indicating a widespread and stable wild population across its native southwestern European range. Commercial supply is based entirely on cultivated nursery stock; wild harvesting for ornamental use is uncommon. Propagation is typically by semi‑hardwood cuttings taken in summer, which root under mist in controlled environments, reducing pressure on wild populations. Sustainable horticultural practices include using certified disease‑free mother plants, adherence to local nursery certification standards, and avoiding invasive propagation methods. In large‑scale urban greening, recommendations include mixing with native species to maintain ecological balance.

Synonyms Top

Scientific name Authority First published in
Laurocerasus lusitanica (L.) M.Roem. Fam. Nat. Syn. Monogr. 3: 92 (1847)
Cerasus lusitanica (L.) Loisel. Trait‚ des arbres et arbustes que l'on cultive en France ; 1800 5 1809
Cerasus hixa C.Sm. ex Spach Hist. Nat. Vég. 1: 419 (1834)
Prunus hixa Brouss. ex Willd. Enum. Pl. Hort. Berol. 1: 517 (1809)
Laurocerasus hixa (Brouss. ex Willd.) M.Roem. Fam. Nat. Syn. Monogr. 3: 92 (1847)
Laurocerasus multiglandulosa (Cav.) M.Roem. Fam. Nat. Syn. Monogr. 3: 92 (1847)
Prunus multiglandulosa Cav. Anales Ci. Nat. 3: 59 (1801)
Padus eglandulosa Moench Methodus : 672 (1794)
Padus lusitanica Mill. Gard. Dict. ed. 8 : Padus n.º 5 (1768)
Prunus sempervirens Salisb. Prodr. Stirp. Chap. Allerton : 356 (1796)
Laurocerasus lusitanica subsp. hixa (Brouss. ex Willd.) G.Kunkel ; 1972 74 1972
Cerasus lusitanica (L.) Dum.Cours. Bot. Cult. 3: 389. 1802
Cerasus lusitanica var. hixa (Brouss. ex Willd.) Ser. Prodromus systematis naturalis regni vegetabilis ; 1823 540 1825
Lauro-cerasus multiglandulosa M.Roem. Fam. Nat. Syn. Monogr. 3: 92 (1847)
Cerasus hixa (Brouss. ex Willd.) Webb & Berthel. Histoire naturelle des Iles Canaries ; 1835 19 1842

Common names Top

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Language Common/alternative name
English portugal laurel
Spanish loro
Spanish azarera
Spanish azarero
Spanish laurocerasus lusitanica subsp. hixa
Spanish padus lusitanica
Spanish cornicalera
Spanish prunus hixa
Spanish prunus sempervirens
Spanish laurocerasus lusitanica
Spanish cerasus lusitanica
Spanish palo del loro
Spanish palo de loro
Spanish lauroceraso de portugal
Spanish lauro de portugal
Spanish laurel de portugal
Arabic كرز الغار البرتغالي
Arabic خوخ برتغالي
Bulgarian португалска лавровишня
Welsh coeden lawrgeirios portiwgal
Danish portugisisk laurbær-kirsebær
Danish portugisisk laurbærkirsebær
German portugiesischer kirschlorbeer
Basque portugal erramu
Basque portugalgo erramu
Basque portugaleko erramu
French cerasus lusitanica
French laurocerasus lusitanica
French laurier du portugal
French laurier-cerise du portugal
French laurier cerise du portugal
Irish labhras portaingéalach
Galician acereiro
Japanese ポルトガルゲッケイジュ
Norwegian Bokmål portugalhegg
Portuguese loureiro-de-portugal
Portuguese ginjeira-brava
Portuguese gingeira-brava
Portuguese azereiro
Russian Лавровишня португальская
Slovenian portugalski lovorikovec
Vietnamese cerasus lusitanica
Chinese 葡萄牙桂樱
Chinese 葡萄牙桂櫻

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Prunus lusitanica subsp. azorica (Mouill.) Franco Bol. Soc. Portug. Ci. Nat. 25: 82 (1965)
Prunus lusitanica subsp. hixa (Brouss. ex Willd.) Franco Bol. Soc. Portug. Ci. Nat. 25: 81 (1965)
Prunus lusitanica subsp. lusitanica Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northern Africa
      • Morocco
  • Europe
    • Northern Europe
      • Great Britain
      • Ireland
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Northern America
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000998700
Canadensys 29975
USDA Plants PRLU
Tropicos 27801104
INPN 116093
KEW urn:lsid:ipni.org:names:324746-2
The Plant List rjp-287
Open Tree Of Life 176177
Observations.org 132648
NCBI Taxonomy 194545
NBN Atlas NBNSYS0000003421
Nature Serve 2.134739
IUCN Red List 62857
IPNI 324746-2
iNaturalist 127529
GBIF 3020871
Freebase /m/02v_ss7
EPPO PRNLU
EOL 640257
Calflora (Californian flora) 9394
USDA GRIN 30029
Wikipedia Prunus_lusitanica
CMAUP NPO26453

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 Tilia cordata and Tilia platyphyllos 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, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Evidence for Reductions in Physical and Chemical Plant Defense Traits in Island Flora Freedman MG, Long RW, Ramírez SR, Strauss SY Plants (Basel) 03-Apr-2024
PMCID:PMC11013342
doi:10.3390/plants13071026
PMID:38611555
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
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
Commodity risk assessment of Corylus avellana 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 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH Molecules 24-Nov-2023
PMCID:PMC10707989
doi:10.3390/molecules28237760
PMID:38067489
Commodity risk assessment of Quercus petraea 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, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur 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, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Biomechanics of cutting: sharpness, wear sensitivity and the scaling of cutting forces in leaf-cutter ant mandibles Püffel F, Walthaus OK, Kang V, Labonte D Philos Trans R Soc Lond B Biol Sci 16-Oct-2023
PMCID:PMC10577030
doi:10.1098/rstb.2022.0547
PMID:37839449
Commodity risk assessment of Fagus sylvatica 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 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
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 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
Molecular Characterization of Prunus lusitanica L. Fruit Extracts and Their Health-Promoting Potential in Inflammation, Diabetes, and Neurodegenerative Diseases Abraão A, Martins-Gomes C, Domínguez-Perles R, Barros A, Silva AM Int J Mol Sci 16-May-2023
PMCID:PMC10219113
doi:10.3390/ijms24108830
PMID:37240175
Differences in the Diets of Female and Male Red Deer: The Meaning for Sexual Segregation Garcia F, Alves da Silva A, Ruckstuhl K, Neuhaus P, Coelho C, Wang M, Sousa JP, Alves J Biology (Basel) 31-Mar-2023
PMCID:PMC10136149
doi:10.3390/biology12040540
PMID:37106741

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 / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene 12462 Click to see COC1=C(C(=CC=C1)OC)OC 168.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 21635582 Click to see 957.10 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 101923141 Click to see 795.00 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate 11803947 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 941.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-6-(acetyloxymethyl)-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate 10819773 Click to see 983.10 unknown via CMAUP database
Calenduloside E 176079 Click to see 632.80 unknown via CMAUP database
chikusetsusaponin IV 10079497 Click to see 927.10 unknown via CMAUP database
Chikusetsusaponin Iva 13909684 Click to see 795.00 unknown via CMAUP database
Glycoside ST-J 101720880 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1103.20 unknown via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 21669007 Click to see 971.10 unknown via CMAUP database
Narcissiflorine 162878 Click to see 764.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6aS,6bR,8aR,10R,12aS)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 101277261 Click to see 470.70 unknown via CMAUP database
(3R,4aR,6aR,6aS,6bR,8aR,12aS)-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12-decahydro-1H-picene-4a-carboxylic acid 101277260 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C 468.70 unknown via CMAUP database
(3R,4R,4aS,6aR,6aS,6bR,8aR,10R,12aS)-3,4,10-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 16112781 Click to see 486.70 unknown via CMAUP database
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 15379012 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C 604.80 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid 102239749 Click to see 470.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12-decahydro-1H-picene-4a-carboxylic acid 16112782 Click to see 468.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,10R,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,7,8,8a,10,11,12,14b-decahydro-1H-picene-4a-carboxylate 10605857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 939.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,12aS,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-3,10-dioxo-1,4,5,6,7,8,8a,11,12,14b-decahydropicene-4a-carboxylate 10748397 Click to see 937.10 unknown via CMAUP database
asperosaponin C 13878127 Click to see 588.80 unknown via CMAUP database
methyl (1R,2R,4aR,6aS,6aR,6bR,8aR,10S,11R,12aR,14bR)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 162964469 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(00)91296-2
Methyl 2,3-dihydroxyurs-12-en-28-oate 621722 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(00)91296-2
Papyriogenin A 3081523 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C 466.70 unknown via CMAUP database
Papyriogenin C 3081568 Click to see 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6aR,6bS,14aR,14bS)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,12,14a-octahydro-1H-picene-3,10-dione 102588576 Click to see 420.60 unknown via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one 102588575 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C 422.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde 2773875 Click to see C1=CC2=C(C=CO2)C=C1C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
(1S,2R,5R,7R,10S,11R,18S,19S,22S)-7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.02,11.05,10.015,22.019,22]tetracosa-12,14-dien-21-one 101967008 Click to see 468.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
Dihydrocoumarin 660 Click to see 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-Phenylprop-2-En-1-Ol 308 Click to see 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
3,7,4'-Tri-O-Acetyl Kaempferol 44584293 Click to see 412.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11678667 Click to see 578.50 unknown via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11607311 Click to see 724.70 unknown via CMAUP database

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