Details Top

Internal ID UUID643ffc9a2e7cd595597707
Scientific name Schinus molle
Authority L.
First published in Sp. Pl. : 388 (1753)

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.

Schinus molle leaves have long been prepared as infusions and decoctions to treat respiratory and fever conditions in several South American settings. In the Andean highlands of northern Chile, people make hot leaf infusions for colds and flu‑like fevers (Giordano et al., 1991). Among the Mapuche of southern Chile, leaf infusions are taken for colds and as a diaphoretic during fever (Del Vitto et al., 1997). In the temperate Lowlands of Argentina, leaf infusions are used for colds and sore throats (De Feo and Vitale, 2006). In all three cases the plant parts are the young or mature leaves, and the preparations are consumed as simple household teas. In parts of northwest Argentina and Bolivia, leaves are sometimes included in “maté” style beverages to improve digestion and address mild stomach upset (Voces et al., 1998). The preparation is straightforward: 2–3 g of dried leaf per cup, pour just‑boiled water, cover, and steep for 10–15 minutes; 1–3 cups per day is typical. People also chew fresh berries as a mouth freshener and remedy, but the infusions documented by the sources above are the most consistently reported. Active constituents reported for the species include monoterpenes such as α‑ and β‑phellandrene, limonene, and myrcene; sesquiterpenes such as β‑caryophyllene; and flavonoids like quercetin, which plausibly support the reported antibacterial and anti‑inflammatory effects. Modern relevance: leaf teas are still common in Andean households and appear in herbal commerce, and recent pharmacological studies on the species continue to focus on the anti‑microbial and antioxidant activity of these terpenes and flavonoids (Gómez et al., 2015).

General Uses Top

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Common products:
Schinus molle yields an essential oil, most commonly obtained by hydrodistillation of the mature fruit pericarp or leaves. A dried “pepper” spice is produced from the mature fruits. The species is widely planted as an ornamental and shade tree.

Industrial and craft applications:
The essential oil is used as a fragrance ingredient in perfumes and soaps, and as a scent in cleaning and household products. It is documented as a rodent repellent and as a grain protectant, showing activity against stored-product insects; commercial formulations based on this oil are registered as pest-control products in some markets. Resin or gum associated with the tree is cited as a component in natural varnishes and spirit varnishes.

Food and beverages (non-medicinal):
The mature fruits are processed into a culinary spice comparable to pepper (Piper nigrum). The spice is used as a seasoning and flavoring agent, including in alcoholic beverages; processors prepare ground or cracked products and may integrate the fruit in blends.

Colorants and tanning:
The bark yields brown natural dyes used in dyeing textiles and leather. While historical sources describe bark and leaf dyeing, quantitative tannin content and standardized dye performance data for S. molle are not well documented in the modern technical literature, limiting


its role in modern tanning.

Wood and fiber:
The wood is used for small turned objects, tool handles, and general carpentry, with reference to its workable grain and moderate density. It is not a major timber species but finds application where small sections and good finishing are required.

Fragrance and cosmetics:
The oil is primarily composed of limonene and alpha-phellandrene, imparting a characteristic fresh, citrus-peppery note suited to fragrance compounding. Typical concentrations in leave-on cosmetics are kept low due to phototoxicity concerns; the oil is commonly employed at low dose in soaps, detergents, and fine fragrance accords.

Properties relevant to use:
The essential oil’s high monoterpene content (limonene commonly above 30%, often 40–60%) provides strong odor impact and volatility, useful in perfumery and as a repellent. The fruit spice has sensory attributes comparable to Piper pepper and remains the principal non-volatile product. Wood properties are consistent with moderate-density hardwoods suitable for turning and finishing.

Standards and regulation:
IFRA guidance applies to fragrance use of S. molle leaf/fruit oil. National regulatory frameworks govern rodenticide and grain protectant uses where products are registered (e.g., EPA in the United States; European PPP Regulations in the EU). Food-grade spice processing is subject to national food standards for spices and dried fruits.

Sustainability and sourcing:
The species regenerates readily from seed and stump sprouting and tolerates arid to semi-arid conditions, making it available from wild-collection and small-holder agroforestry. Overharvesting for essential oil in some regions has led to local population pressure, prompting development of small-scale cultivation to supply perfume and grain-protection markets.

Synonyms Top

Scientific name Authority First published in
Schinus bituminosus Salisb. Prodr. Stirp. Chap. Allerton : 171 (1796)
Schinus molle var. huigan (Molina) Marchand Rev. Ancard. 164 1869
Schinus molle var. argentifolius Marchand Rev. Anacardiac. 163. 1869
Schinus occidentalis Sessé & Moc. Pl. Nov. Hisp. : 173 (1890)
Schinus molle var. huyngan (Molina) March. Rev. Anac. 164 1869

Common names Top

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Language Common/alternative name
English pepper tree
English peruvian peppertree
English american pepper
English california pepper tree
English false pepper
English peppercorn tree
English pepperina
English peruvian mastica
English peruvian pepper
Spanish pirú
Spanish piru
Spanish arbol de la pimienta
Spanish arbol de la pimienta falsa del peru
Spanish arbol de pimienta
Spanish Árbol de pimienta
Spanish arbol de pimiento
Spanish arbol del peru
Spanish falso pimentero
Spanish falso pimiento
Spanish lentisco del peru
Spanish lentisco del perú
Spanish pimentero de america
Spanish pimentero de américa
Spanish pimentero de americo
Spanish pimentero de américo
Spanish pimiento falso
Spanish pirul
Afrikaans peperboom
Amharic ትሩማንትሪ
Arabic فلفل رفيع الأوراق
Arabic فلفل زهري
Arabic فلفل ملطي
Arabic فلفل رفيع
Arabic متهدل
Arabic فلفل مستحي
Arabic فلفل كاذب
Arabic فلفل تربنتين
Arabic فلفل باكي
Arabic فلفل زهري
Arabic فلفل بيروي
Arabic فلفل بيروفي
ay mulli
Azerbaijani yumşaq şinus
Bulgarian мек шинус
Catalan pebre fals
Catalan fals pebrer
Catalan pebrer fals
Catalan pebrer bord
Czech pepř růžový
German molle-baum
German mollebaum
German peruanischer pfefferbaum
Persian فلفل پروئی
Finnish rosépippuri
Finnish perunroseepippuri
Finnish ruusupippuri
Finnish perunpippuripuu
Finnish roseepippuri
Finnish rosepippuri
French faux poivrier odorant
French faux-poivrier odorant
Hebrew פלפלון בכות
ht moye
Hungarian perui borsfa
Italian albero del pepe
Italian falso pepe
Italian pepe rosa
Japanese コショウボク
Korean 페퍼나무
Norwegian Bokmål peppertre
Dutch peruviaanse peperboom
Dutch false peper
Portuguese aroeira-brava
Quechua mulli
Quechua molle
Quechua kullash
Quechua kullas
Russian Перец перуанский
Russian Перуанский перец
Russian Шинус мягкий
Swedish rosépeppar
Swedish peruanskt pepparträd
Tamil மிளகு மரம்
Chinese 胡椒树
Chinese 肖乳香

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Schinus molle var. rusbyi F.A.Barkley Brittonia 5: 186 (1944)
Schinus molle var. molle

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
      • Canary Islands
      • Madeira
    • Middle Atlantic Ocean
      • Ascension
      • Saint Helena
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Somalia
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Angola
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Northern Provinces
    • West Tropical Africa
      • Guinea
      • Senegal
  • Asia-temperate
    • Arabian Peninsula
      • Yemen
    • Western Asia
      • Iraq
      • Palestine
  • Europe
    • Southeastern Europe
      • Greece
      • Italy
      • Sicilia
    • Southwestern Europe
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Florida
    • Southwestern U.S.A.
      • California
  • Southern America
    • Brazil
      • Brazil South
    • Caribbean
      • Cuba
      • Puerto Rico
    • Central America
      • El Salvador
      • Guatemala
    • Southern South America
      • Argentina Northeast
      • Chile North
      • Paraguay
      • Uruguay
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000435157
UNII 7NY65X282C
USDA Plants SCMO
Tropicos 1300267
INPN 121504
Flora of Italy 3035
KEW urn:lsid:ipni.org:names:71044-1
The Plant List kew-2480199
Open Tree Of Life 411495
Observations.org 134543
NCBI Taxonomy 43851
Nature Serve 2.139397
IUCN Red List 61984171
IPNI 71044-1
iNaturalist 57354
GBIF 3190642
Freebase /m/027gwc8
EPPO SCIMO
EOL 582275
Calflora (Californian flora) 7378
USDA GRIN 70668
Wikipedia Schinus_molle

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
In This Issue N/A Proc Natl Acad Sci U S A 30-Apr-2024
PMCID:PMC11067442
doi:10.1073/iti1824121
Risk assessment of Retithrips syriacus for the EU 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, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
The first peoples of the Atacama Desert lived among the trees: A 11,600- to 11,200-year-old grove and congregation site Ugalde PC, Joly D, Latorre C, Gayo EM, Labarca R, Simunovic M, McRostie V, Holliday VT, Quade J, Santoro CM Proc Natl Acad Sci U S A 22-Apr-2024
PMCID:PMC11067013
doi:10.1073/pnas.2320506121
PMID:38648488
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
Plants from Arid and Semi-Arid Zones of Mexico Used to Treat Respiratory Diseases: A Review Dávila-Rangel IE, Charles-Rodríguez AV, López-Romero JC, Flores-López ML Plants (Basel) 11-Mar-2024
PMCID:PMC10974781
doi:10.3390/plants13060792
PMID:38592789
The destructive subterranean termite Reticulitermes flavipes (Blattodea: Rhinotermitidae) can colonize arid territories Hernández-Teixidor D, Pérez-Morín A, Pestano J, Mora D, Fajardo S PeerJ 29-Feb-2024
PMCID:PMC10909367
doi:10.7717/peerj.16936
PMID:38435985
Poisoning by Nerium oleander L. in Franconia Geese Pugliese N, Tinelli A, Crescenzo G, Nieddu M, Baralla E, Schiavone A, Zizzo N, Samarelli R, Dessì F, Circella E, Zizzadoro C, Saleh MS, Camarda A Animals (Basel) 14-Feb-2024
PMCID:PMC10885877
doi:10.3390/ani14040612
PMID:38396580
Biodiversity and Structural Analysis of Woody Plant Species of Home Gardens in Basona Worana District, North Shoa Zone of Central Ethiopia Woldeyohannes A, Moges A Scientifica (Cairo) 08-Feb-2024
PMCID:PMC10869191
doi:10.1155/2024/5563636
PMID:38361969
Enhancement of Strawberry Shelf Life via a Multisystem Coating Based on Lippia graveolens Essential Oil Loaded in Polymeric Nanocapsules González-Moreno BJ, Galindo-Rodríguez SA, Rivas-Galindo VM, Pérez-López LA, Granados-Guzmán G, Álvarez-Román R Polymers (Basel) 26-Jan-2024
PMCID:PMC10857092
doi:10.3390/polym16030335
PMID:38337224
Evaluation of hepatoprotective and antidiarrheal activities of the hydromethanol crude extract and solvent fractions of Schinus molle L. (Anacardiaceae) leaf and fruit in mice Belayneh YM, Mengistu G, Hailay K Metabol Open 20-Jan-2024
PMCID:PMC10918422
doi:10.1016/j.metop.2024.100272
PMID:38455232
Psyllids in Natural Habitats as Alternative Resources for Key Natural Enemies of the Pear Psyllids (Hemiptera: Psylloidea) Horton DR Insects 06-Jan-2024
PMCID:PMC10816694
doi:10.3390/insects15010037
PMID:38249044
Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E J Ethnobiol Ethnomed 04-Jan-2024
PMCID:PMC10768247
doi:10.1186/s13002-023-00644-x
PMID:38178202
Pest categorisation of Pestalotiopsis microspora 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, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 21-Dec-2023
PMCID:PMC10733803
doi:10.2903/j.efsa.2023.8493
PMID:38130321
Essential-Oils-Loaded Biopolymeric Nanoparticles as Strategies for Microbial and Biofilm Control: A Current Status Romero-Montero A, Melgoza-Ramírez LJ, Ruíz-Aguirre JA, Chávez-Santoscoy A, Magaña JJ, Cortés H, Leyva-Gómez G, Del Prado-Audelo ML Int J Mol Sci 20-Dec-2023
PMCID:PMC10778842
doi:10.3390/ijms25010082
PMID:38203252
Prediction of Novel Natural Small Molecules From Schinus molle as an Inhibitor of PI3K Protein Target in Cancer Cells Using In Silico Screening Kumar U, Manivannan HP, Francis AP, Veeraraghavan VP, R G, Sankaran K Cureus 20-Dec-2023
PMCID:PMC10801101
doi:10.7759/cureus.50863
PMID:38259388

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1007/BF01100201
https://doi.org/10.1002/PTR.1834
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1996.9700558
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Octanoate 8091 Click to see 158.24 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl butyrate 5355856 Click to see CCCC(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1021/JF00116A075
Neryl hexanoate 12571389 Click to see CCCCCC(=O)OCC=C(C)CCC=C(C)C 252.39 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1996.9700558
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/JF00116A075
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/14786410802346223
https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1996.9700558
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1021/JF00116A075
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6R)-rel- 85568 Click to see 154.25 unknown https://doi.org/10.1007/BF02040199
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1996.9700558
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1997.9700813
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1996.9700558
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1997.9700813
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/14786410802346223
https://doi.org/10.1080/10412905.1997.9700813
https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1996.9700558
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00116A075
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1997.9700813
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1021/JF00116A075
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1021/JF00116A075
1,6-Dimethyl-4-(propan-2-yl)-1,2-dihydronaphthalene 5315609 Click to see 200.32 unknown https://doi.org/10.1021/JF00116A075
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/JF00116A075
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1021/JF00116A075
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1996.9700558
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700813
https://doi.org/10.1021/JF00116A075
alpha-Calacorene 12302243 Click to see 200.32 unknown https://doi.org/10.1021/JF00116A075
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1021/JF00116A075
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00116A075
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/JF00116A075
https://doi.org/10.1080/10412905.1996.9700558
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1021/JF00116A075
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1996.9700558
cis-beta-Guaiene 15560253 Click to see 204.35 unknown https://doi.org/10.1021/JF00116A075
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/JF00116A075
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1021/JF00116A075
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
gamma-Calacorene 14038842 Click to see CC1CC=C(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1021/JF00116A075
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF00116A075
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7aR,7bR)-1a,2,3,4,4a,5,7a,7b-Octahydro-1,1,7-trimethyl-4-methylene-1H-cycloprop(e)azulene 15923779 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(00)91153-1
(1aR,4aR,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,7a,7b-hexahydro-1aH-cyclopropa[e]azulene 154497743 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(00)91153-1
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1021/JF00116A075
beta-Spathulene 15923778 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(00)91153-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1021/JF00116A075
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1021/JF00116A075
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1021/JF00116A075
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/JF00116A075
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9700558
Germacrone 6436348 Click to see 218.33 unknown https://doi.org/10.1080/10412905.1996.9700558
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Isomasticadienonalic acid 131751752 Click to see 468.70 unknown https://doi.org/10.1055/S-2003-45096
Lanosta-7,24-dien-26-oic acid, 3-oxo-, methyl ester, (13alpha,14beta,1 7alpha,20S,24E)- 346345 Click to see 468.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
methyl (E,6R)-2-methyl-6-[(5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoate 162946601 Click to see CC(CCC=C(C)C(=O)OC)C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
methyl (E,6R)-2-methyl-6-[(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoate 162878721 Click to see CC(CCC=C(C)C(=O)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
methyl (E,6R)-6-[(3S,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoate 162856473 Click to see CC(CCC=C(C)C(=O)OC)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
methyl (E,6S)-2-methyl-7-oxo-6-[(5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoate 163049808 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
Methyl 2-methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoate 346347 Click to see 468.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
Methyl 2-methyl-7-oxo-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoate 163049807 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
methyl 6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoate 162856470 Click to see CC(CCC=C(C)C(=O)OC)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)89290-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(71)85052-5
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/10.1016/0031-9422(71)85052-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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/10.1002/PTR.1834
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Raffinose 439242 Click to see 504.40 unknown https://doi.org/10.1007/BF01100201
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Chamaejasmin 390362 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown https://doi.org/10.1055/S-2003-45096
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown https://doi.org/10.1007/BF01100201
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF01100201
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1002/PTR.1834
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(3S,5S,6R)-6-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate 163077302 Click to see 586.50 unknown https://doi.org/10.1002/PTR.1834
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.EJPHAR.2008.03.021
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.EJPHAR.2008.03.021
> Phenylpropanoids and polyketides / Tannins / Complex tannins
[2-[5,7-dihydroxy-4-oxo-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-4,5-dihydroxy-3-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]phenyl] 3,4,5-trihydroxybenzoate 162817587 Click to see 778.60 unknown https://doi.org/10.1002/PTR.1834

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