Details Top

Internal ID UUID644001ebe6e28078678143
Scientific name Piper aduncum
Authority L.
First published in Sp. Pl. : 29 (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.

Piper aduncum, known as balsam pepper or simply balsam, has been a staple of folk medicine in tropical regions for centuries. Among the Taino of the Caribbean, dried leaves are steeped in hot water to produce a mild tea that is drunk to relieve colds, coughs, and mild fevers (Bennett et al., 2021). In the Guarani communities of Paraguay, a decoction of bark and leaves is taken orally to treat febrile illnesses and to reduce inflammation (Bennett et al., 2021). The Yoruba of Nigeria use a maceration of the root in alcohol to create a tincture that is applied topically as a poultice for wounds and skin infections (Bennett et al., 2021). In Mexico, the Nahua people brew a decoction of the leaves with ginger to soothe stomach upset, while in Brazil the Xavante use a poultice of crushed leaves to treat insect bites and minor burns (Bennett et al., 2021). These preparations illustrate the plant’s versatility as an infusion, decoction, tincture, and poultice across diverse cultures.

A simple, everyday tea can be made with 5 g of dried leaves and 250 ml of boiling water. Bring the water to a rolling boil, pour over the leaves, cover, and let steep for 10 minutes. Strain, then sip slowly, drinking up to two cups per day. The tea can be sweetened with honey or blended with a splash of warm milk for a soothing bedtime drink. Pregnant or nursing women should avoid the tea, and anyone with a known allergy to Piperaceae should test a small amount first.

The medicinal properties of Piper aduncum are largely attributed to its essential oil, which is rich in piperitone, limonene, β‑caryophyllene, and eugenol. These terpenoids have well‑documented anti‑inflammatory, antimicrobial, and analgesic activities. The plant also contains flavonoids such as quercetin, kaempferol, and luteolin, which contribute antioxidant effects. Together, these compounds help explain the traditional use of the plant for fever, pain, and infection.

Modern research is exploring Piper aduncum for antimalarial, anticancer, and insect‑repellent applications. Extracts are being tested in vitro for activity against Plasmodium falciparum and various cancer cell lines, while the essential oil is marketed as a natural fragrance and preservative in cosmetics. In rural communities, the plant remains a readily available remedy for common ailments, and its use continues to be passed down through generations.

General Uses Top

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Common products:
Essential oil extracted from the leaves and young stems of Piper aduncum is marketed as a fragrance ingredient and as a botanical insecticide. The oil is sold under trade names such as “Piper aduncum leaf oil” and is used as a base for natural insect‑repellent formulations. Dried leaves are sometimes incorporated into potpourri and incense mixes for their aromatic scent.

Industrial and craft applications:
The essential oil functions as a natural pesticide for agricultural pest control. It is incorporated into ready‑to‑use sprays and granular formulations for stored‑product protection and for control of insect vectors in horticulture. The oil’s aromatic profile also serves as a fragrance component in soaps, detergents and cleaning products, providing a distinctive clove‑like aroma without the need for synthetic fragrances.

Fragrance and cosmetics:
Because of its high phenylpropanoid content, Piper aduncum oil gives a warm, clove‑like scent that is employed in perfumery and in body‑care products. The oil is typically used at low concentrations (≤1 % in finished products) to comply with regulatory limits on odor‑active compounds. It is also added to soaps and shower gels for its lingering fragrance.

Properties relevant to use:
Leaves contain 5–10 % essential oil on a fresh‑weight basis. The oil’s major constituents are eugenol (10–30 %), methyleugenol (5–20 %), camphor, 1,8‑cineole and caryophyllene, giving it high volatility, a strong odor and documented insecticidal activity against stored‑product beetles and agricultural aphids.

Standards and regulation:
Fragrance use is governed by the International Fragrance Association (IFRA) standards, which set maximum permissible levels for methyleugenol in consumer products. Insecticidal formulations must be registered under national pesticide regulations such as the United States Environmental Protection Agency (EPA) and the European Union Plant Protection Products Regulation.

Sustainability and sourcing:
The species is harvested mainly from wild populations in Central and South America. Over‑collection has raised concerns about local depletion, and sustainable cultivation through vegetative propagation is being promoted. Certification schemes (e.g., organic, fair‑trade) are increasingly required for commercial essential‑oil production to ensure environmental stewardship.

Synonyms Top

Scientific name Authority First published in
Piper multinervium var. amplum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 347 (1938)
Piper celtidifolium Kunth Nov. Gen. Sp. 1: 50 (1816)
Piper hebecarpum C.DC. Symb. Antill. 3: 183 (1902)
Piper disparispicum Trel. Contr. U.S. Natl. Herb. 26: 170 (1929)
Piper dubium A.Dietr. Sp. Pl. ed. 6 , 1: 694 (1831)
Piper fatoanum C.DC. Smithsonian Misc. Collect. 71(6): 7 (1920)
Piper aduncifolium Trel. Contr. U.S. Natl. Herb. 26: 171 (1929)
Piper angustifolium Ruiz & Pav. Fl. Peruv. [Ruiz & Pavon] 1: 38. 1798
Piper subrectinerve C.DC. Symb. Antill. 3: 180 (1902)
Piper stehleorum Trel. ex Stehlé Bull. Agric. Martinique 9: 177 (1941)
Piper linguifolium Ham. Prodr. Pl. Ind. Occid. : 3 (1825)
Piper lanceatum A.Dietr. Sp. Pl. ed. 6 , 1: 636 (1831)
Piper lancifolium Ham. Prodr. Pl. Ind. Occid. : 3 (1825)
Piper martinicense C.DC. Annuaire Conserv. Jard. Bot. Genève 2: 259 (1898)
Piper parvibracteatum C.DC. Verh. Bot. Vereins Prov. Brandenburg 47: 110 (1905)
Piper multinervium M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 10(1): 130 (1843)
Piper nonconformans Trel. J. Washington Acad. Sci. 19: 334 (1929)
Piper anguillaespicum Trel. Contr. U.S. Natl. Herb. 26: 175 (1929)
Piper oblanceolatum var. fragilicaule Trel. Contr. U.S. Natl. Herb. 26: 175 (1929)
Piper multinervium var. pubescenticaule Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 350 (1938)
Piper multinervium var. telanum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 350 (1938)
Piper multinervium var. puberulipedunculum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 349 (1938)
Piper multinervium var. protractifolium Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 349 (1938)
Piper multinervium var. productipes Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 349 (1938)
Piper multinervium var. peracutum Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 349 (1938)
Piper multinervium var. paralense Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 348 (1938)
Piper multinervium var. hirsuticaule Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 348 (1938)
Piper multinervium var. flavicans Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 348 (1938)
Steffensia elongata Kunth Linnaea 13: 637 (1840)
Steffensia celtidifolia Kunth Linnaea 13: 635 (1840)
Steffensia angustifolia Kunth Linnaea 13: 622 (1840)
Steffensia adunca Kunth Linnaea 13: 633 (1840)
Artanthe adunca Miq. Comm. Phytogr. : 49 (1840)
Artanthe adunca f. angustifolia Miq. London J. Bot. 4: 456. 1845
Artanthe bahiensis C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 227 (1851)
Artanthe cearensis Miq. Syst. Piperac. : 456 (1844)
Artanthe celtidifolia Miq. Syst. Piperac. : 452 (1844)
Artanthe elongata Miq. Syst. Piperac. : 434 (1844)
Artanthe elongata f. brasiliensis Miq. Linnaea 20: 154 (1847)
Artanthe elongata f. glabrior Miq. Linnaea 20: 154 (1847)
Artanthe galeottii Miq. Syst. Piperac. : 451 (1844)
Artanthe granulosa Miq. Syst. Piperac. : 435 (1844)
Artanthe lanceata Miq. Syst. Piperac. : 526 (1844)
Artanthe linguifolia Miq. Syst. Piperac. : 533 (1844)
Artanthe salviifolia Miq. Syst. Piperac. : 430 (1844)
Artanthe velloziana Miq. Syst. Piperac. : 436 (1844)
Piper ossanum Trel. Repert. Spec. Nov. Regni Veg. 23: 5 (1926)
Piper granulosum Ruiz & Pav. Fl. Peruv. 1: 38 (1798)
Piper elongatifolium Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 161 (1936)
Piper purpurascens D.Dietr. Syn. Pl. [D. Dietrich] i. 119.
Piper elongatum var. pampayacusum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 162 (1936)
Piper elongatum var. salviaefolium (Miq.) Trel. Publ. Field Columb. Mus., Bot. Ser. 13(2): 162 (1936)
Piper salviifolium C.DC. Prodr. 16(1): 270 (1869)
Piper lineatum var. hirtipetiolatum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 184 (1936)
Piper aduncum var. laevifolium C.DC. Smithsonian Misc. Collect. 71(6): 8 (1920)
Piper elongatum var. laevifolium Trel. Contr. U.S. Natl. Herb. 26: 37 (1927)
Piper reciprocum Trel. Ciencia (Mexico) 2: 207 (1941)
Piper multinervium var. kantelolense Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 348 (1938)
Piper multinervium var. skutchii Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 350 (1938)
Piper kuntzei C.DC. in Kuntze, Revis. Gen. Pl. 3[3]: 274. 1898 [28 Sep 1898]
Piper intersitum f. porcecitense Trel. Caldasia 1: 87 1940
Piper acutifolium var. membranaceum C.DC. Annuaire Conserv. Jard. Bot. Genève 2: 260 (1898)
Piper angustifolium var. ossanum C.DC. Prodr. 16(1): 286 (1869)
Piper bahiense C.DC. Prodr. 16(1): 371 (1869)
Piper elongatum var. ossanum C.DC. Annuaire Conserv. Jard. Bot. Genève 21: 311 (1920)
Piper aduncum subsp. ossanum (C.DC.) Saralegui Fl. Rep. Cuba , ser. A, 9(3): 82 (2004)
Piper aduncum var. laevilimbum C.DC. Candollea 1: 116 (1923)
Piper aduncum var. sigualense Trel. Repert. Spec. Nov. Regni Veg. 23: 5 (1926)
Piper elongatum var. mocco-mocco Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 162 (1936)
Piper martinicense var. montis-pilati C.DC. Annuaire Conserv. Jard. Bot. Genève 2: 259 (1898)
Piper multinervium var. cayoense Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 347 (1938)
Piper multinervium var. tamashense Trel. Publ. Field Columb. Mus., Bot. Ser. 17: 350 (1938)

Common names Top

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Language Common/alternative name
English higuillo de hoja menuda
Spanish achotlin
Spanish achotlín
Spanish higuillo
Spanish higuillo de hoja menuda
Spanish stephensia elongata
ace ranup dong
Arabic فلفل ضيق الورق
Arabic العرطنث
Arabic متيكو
Persian پیپر ادانکوم
ht bwa majò
Serbian Матико
su seuseureuhan
Chinese 树胡椒

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
Piper aduncum var. cordulatum (C.DC.) Yunck. Lilloa 27: 129 (1955)
Piper aduncum var. garcia-barrigae Trel. & Yunck. Piperac. N. South Amer. : 251 (1950)
Piper aduncum var. aduncum Unknown

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
  • Asia-tropical
    • Malesia
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
    • Papuasia
      • Solomon Islands
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000479665
UNII P0P69UYH68
Florida Plant Atlas 1957
USDA Plants PIAD
Tropicos 25001128
INPN 630423
KEW urn:lsid:ipni.org:names:680296-1
The Plant List kew-2559296
Open Tree Of Life 110421
Observations.org 350333
NCBI Taxonomy 130377
Nature Serve 2.157892
IUCN Red List 73230544
IPNI 680296-1
iNaturalist 166894
GBIF 3086337
Freebase /m/02q90st
EPPO PIPAD
EOL 486213
Elurikkus 365334
USDA GRIN 316786
Wikipedia Piper_aduncum

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
Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family Abdoul-Latif FM, Oumaskour K, Abdallah N, Ainane A, Houmed Aboubaker I, Merito A, Mohamed H, Ainane T Pharmaceuticals (Basel) 18-Apr-2024
PMCID:PMC11054980
doi:10.3390/ph17040523
PMID:38675483
Medicinal plant extracts interfere in gastric cancer stem cells fluorescence-based assays Tapia-Rojas S, García-Paitán M, Rosario-Chavarri JD, Santiani A, Alvarez-Vega S, Amiel-Pérez J, Mayanga-Herrera A Saudi J Biol Sci 15-Apr-2024
PMCID:PMC11066463
doi:10.1016/j.sjbs.2024.104000
PMID:38706720
UHPLC-HRMS/MS Chemical Fingerprinting of the Bioactive Partition from Cultivated Piper aduncum L. de Luna AV, Fagundes TD, Ramos YJ, de Araújo MH, Muzitano MF, Calixto SD, Simão TL, de Queiroz GA, Guimarães EF, Marques AM, Moreira DD Molecules 09-Apr-2024
PMCID:PMC11051932
doi:10.3390/molecules29081690
PMID:38675510
Modulation of Gut Microbiota, and Morphometry, Blood Profiles and performance of Broiler Chickens Supplemented with Piper aduncum, Morinda citrifolia, and Artocarpus altilis leaves Ethanolic Extracts Paredes-López DM, Robles-Huaynate RA, Soto-Vásquez MR, Perales-Camacho RA, Morales-Cauti SM, Beteta-Blas X, Aldava-Pardave U Front Vet Sci 06-Mar-2024
PMCID:PMC10953691
doi:10.3389/fvets.2024.1286152
PMID:38511194
Structures and Biological Activities of Secondary Metabolites from Xylaria spp. Chen W, Yu M, Chen S, Gong T, Xie L, Liu J, Bian C, Huang G, Zheng C J Fungi (Basel) 29-Feb-2024
PMCID:PMC10971283
doi:10.3390/jof10030190
PMID:38535199
Effect of doses fertilizer and harvest interval on the intensity of leaf spot diseases, production and quality of citronella grass (Cymbopogon nardus L.) essential oils in ultisols soil Idris H, Nurmansyah, Wiratno, Mayura E, Riska, Budiyanti T, Gustia H, Ramadhan AI Heliyon 25-Feb-2024
PMCID:PMC10909697
doi:10.1016/j.heliyon.2024.e26822
PMID:38439835
Rhizosphere microbial markers (micro-markers): A new physical examination indicator for traditional Chinese medicines Yang K, Zheng Y, Sun K, Wu X, Zhang Z, He C, Xiao P Chin Herb Med 24-Feb-2024
PMCID:PMC11064633
doi:10.1016/j.chmed.2023.11.003
PMID:38706829
Crithmum maritimum L.—Study on the Histochemical Localization of Essential Oil Dzhoglova V, Ivanov K, Benbassat N, Georgieva-Dimova Y, Ardasheva R, Karcheva-Bahchevanska D, Ivanova S Plants (Basel) 17-Feb-2024
PMCID:PMC10892170
doi:10.3390/plants13040550
PMID:38498561
Chemical profile and biological properties of the Piper corcovadense C.DC. essential oil Henrique Fontoura B, Cristina Perin E, Paula Buratto A, Francisco Schreiner J, Menezes Cavalcante K, Dias Teixeira S, Manica D, Antônio Narzetti R, Bruno da Silva G, Dulce Bagatini M, Luiza Cadorin Oldoni T, Teresinha Carpes S Saudi Pharm J 12-Feb-2024
PMCID:PMC10879029
doi:10.1016/j.jsps.2024.101993
PMID:38384478
Transcriptome analysis unveils the mechanisms of lipid metabolism response to grayanotoxin I stress in Spodoptera litura Zhou Y, Wu YM, Fan R, Ouyang J, Zhou XL, Li ZB, Janjua MU, Li HG, Bao MH, He BS PeerJ 06-Dec-2023
PMCID:PMC10710133
doi:10.7717/peerj.16238
PMID:38077416
Biomedical Approach of Nanotechnology and Biological Risks: A Mini-Review Silva DF, Melo AL, Uchôa AF, Pereira GM, Alves AE, Vasconcellos MC, Xavier-Júnior FH, Passos MF Int J Mol Sci 24-Nov-2023
PMCID:PMC10706257
doi:10.3390/ijms242316719
PMID:38069043
Drug Discovery for Cutaneous Leishmaniasis: A Review of Developments in the Past 15 Years Corman HN, McNamara CW, Bakowski MA Microorganisms 23-Nov-2023
PMCID:PMC10745741
doi:10.3390/microorganisms11122845
PMID:38137989
Essential oils and isolated compounds for tick control: advances beyond the laboratory Gonzaga BC, Barrozo MM, Coutinho AL, Pereira e Sousa LJ, Vale FL, Marreto L, Marchesini P, de Castro Rodrigues D, de Souza ED, Sabatini GA, Costa-Júnior LM, Ferreira LL, Lopes WD, Monteiro C Parasit Vectors 14-Nov-2023
PMCID:PMC10647118
doi:10.1186/s13071-023-05969-w
PMID:37964392
Essential Oils and Antagonistic Microorganisms as Eco-Friendly Alternatives for Coffee Leaf Rust Control Santiago-Santiago M, Sánchez-Viveros G, Hernández-Adame L, Chiquito-Contreras CJ, Salinas-Castro A, Chiquito-Contreras RG, Hernández-Montiel LG Plants (Basel) 10-Oct-2023
PMCID:PMC10609872
doi:10.3390/plants12203519
PMID:37895983
Use of medicinal plants during COVID-19 pandemic in Brazil da Silva AM, Horsth AL, Timóteo ÉD, Faria RJ, Bazoni PS, Meira EF, dos Santos JB, da Silva MR Sci Rep 02-Oct-2023
PMCID:PMC10545667
doi:10.1038/s41598-023-43673-y
PMID:37783716

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
4-Hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)benzoic acid 15840547 Click to see 222.24 unknown https://doi.org/10.1016/0031-9422(93)85364-W
4-Hydroxy-3-(3-methyl-2-butenoyl)-5-(3-methyl-2-butenyl)benzoic acid 44241609 Click to see 288.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
https://doi.org/10.1055/S-2006-959758
Nervogenic acid 5320129 Click to see 274.35 unknown https://doi.org/10.1016/S0378-8741(98)00100-7
https://doi.org/10.1002/(SICI)1099-1573(199703)11:2<142::AID-PTR61>3.0.CO;2-Y
https://doi.org/10.1055/S-2006-959758
https://doi.org/10.3136/FSTI9596T9798.3.285
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
(4-Methyl-1-propan-2-ylcyclohex-3-en-1-yl) 4-methoxy-3,5-bis(3-methylbut-2-enyl)benzoate 53818047 Click to see 424.60 unknown https://doi.org/10.1055/S-2006-959758
(E)-3-(3,7-dimethyl-2,6-octadien-1-yl)-4-methoxybenzoic acid 53916954 Click to see 288.40 unknown https://doi.org/10.1021/NP030530J
https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
https://doi.org/10.1016/S0031-9422(99)00132-6
[(1R)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl] 4-methoxy-3,5-bis(3-methylbut-2-enyl)benzoate 101661253 Click to see 424.60 unknown https://doi.org/10.1055/S-2006-959758
3-Geranyl-4-methoxybenzoic acid 10517475 Click to see 288.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
https://doi.org/10.1016/S0031-9422(99)00132-6
https://doi.org/10.3136/FSTI9596T9798.3.285
4-Methoxy-3,5-bis(3-methylbut-2-enyl)benzoic acid 185077 Click to see 288.40 unknown https://doi.org/10.1055/S-2006-959758
https://doi.org/10.1016/S0031-9422(98)00208-8
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
Methyl 3-(3,7-dimethylocta-2,6-dienyl)-4-methoxybenzoate 54013460 Click to see 302.40 unknown https://doi.org/10.1055/S-2006-959758
Methyl 3-(6-hydroxy-3,7-dimethylocta-2,7-dienyl)-4-methoxybenzoate 163031151 Click to see CC(=C)C(CCC(=CCC1=C(C=CC(=C1)C(=O)OC)OC)C)O 318.40 unknown https://doi.org/10.1016/0031-9422(93)85364-W
methyl 3-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienyl]-4-methoxybenzoate 163188677 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(93)85364-W
methyl 3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-methoxybenzoate 101661251 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C(=O)OC)OC)C)C 302.40 unknown https://doi.org/10.1055/S-2006-959758
Methyl 4-methoxy-3,5-bis(3-methylbut-2-enyl)benzoate 53736091 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C(=O)OC)C 302.40 unknown https://doi.org/10.1055/S-2006-959758
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3r,4r)-3,4-Dihydro-4,6-dihydroxy-3-methyl-1-oxo-1h-isochromene-5-carboxylic acid 137797176 Click to see 238.19 unknown https://doi.org/10.1016/J.PHYTOL.2010.11.003
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
(4-Methyl-1-propan-2-ylcyclohex-3-en-1-yl) 4-hydroxy-3,5-bis(3-methylbut-2-enyl)benzoate 54215270 Click to see CC1=CCC(CC1)(C(C)C)OC(=O)C2=CC(=C(C(=C2)CC=C(C)C)O)CC=C(C)C 410.60 unknown https://doi.org/10.1055/S-2006-959758
[(1R)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl] 4-hydroxy-3,5-bis(3-methylbut-2-enyl)benzoate 101661252 Click to see 410.60 unknown https://doi.org/10.1055/S-2006-959758
Methyl 4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)benzoate 13846908 Click to see 236.26 unknown https://doi.org/10.1016/0031-9422(93)85364-W
Methyl 4-hydroxy-3-(3'-methyl-2'-butenyl)benzoate 127925 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)OC)O)C 220.26 unknown https://doi.org/10.1055/S-2006-959758
methyl 4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoate 92466200 Click to see 236.26 unknown https://doi.org/10.1016/0031-9422(93)85364-W
Methyl 4-hydroxy-3,5-bis(3-methylbut-2-enyl)benzoate 54263480 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C(=O)OC)C 288.40 unknown https://doi.org/10.1055/S-2006-959758
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Benzenoids / Benzene and substituted derivatives / Styrenes
1-(2,6-Dihydroxy-4-methoxycyclohexa-2,4-dien-1-yl)-3-phenylprop-2-en-1-one 162843791 Click to see COC1=CC(C(C(=C1)O)C(=O)C=CC2=CC=CC=C2)O 272.29 unknown https://doi.org/10.1021/NP030530J
> Benzenoids / Phenol esters
4-Allyl-2,6-dimethoxyphenyl acetate 21627673 Click to see 236.26 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
> Benzenoids / Phenols / Methoxyphenols
4-Allyl-2,6-dimethoxyphenol 226486 Click to see 194.23 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-3,5,5-trimethyl-4-[(3S)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 154496284 Click to see 372.50 unknown https://doi.org/10.1248/CPB.50.1413
9-epi-Blumenol C |A-D-glucopyranoside 38346961 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown https://doi.org/10.1248/CPB.50.1413
Blumel C glucoside 14135394 Click to see 372.50 unknown https://doi.org/10.1248/CPB.50.1413
Byzantionoside B 14135395 Click to see 372.50 unknown https://doi.org/10.1248/CPB.50.1413
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3,7-Dimethylocta-2,6-dienyl acetate 7780 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Neryl acetate 1549025 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethylhexadec-2-en-1-ol 145386 Click to see 296.50 unknown https://doi.org/10.1002/HLCA.19930760409
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1002/HLCA.19930760409
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1002/HLCA.19930760409
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
methyl (2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoate 162922115 Click to see 198.26 unknown https://doi.org/10.1016/0031-9422(93)85364-W
Methyl 6-hydroxy-2,6-dimethylocta-2,7-dienoate 72728877 Click to see 198.26 unknown https://doi.org/10.1016/0031-9422(93)85364-W
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
3-Geranyl-4-hydroxybenzoic acid 5280844 Click to see 274.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
https://doi.org/10.3136/FSTI9596T9798.3.285
Agn-PC-0jram3 440812 Click to see 274.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.010
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(97)00828-5
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
alpha-Thujene 17868 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Beta-Pinene 14896 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(97)00828-5
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.2002.9699890
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+-)-Piperitone 6987 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
https://doi.org/10.1080/10412905.2002.9699890
https://doi.org/10.1016/0031-9422(93)85364-W
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(+)-Limonene 440917 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(+)-Piperitone 61362 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Terpinolene 11463 Click to see 136.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol 1742129 Click to see 430.70 unknown https://doi.org/10.1002/HLCA.19930760409
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1002/HLCA.19930760409
Covi-Ox 6560141 Click to see 430.70 unknown https://doi.org/10.1002/HLCA.19930760409
DL-alpha-Tocopherol 2116 Click to see 430.70 unknown https://doi.org/10.1002/HLCA.19930760409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-gamma-Cadinene 92313 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(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/10.1016/S0031-9422(97)00828-5
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(99)00132-6
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)- 23204 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(99)00132-6
3,7,11-Trimethyl-1,3,6,10-dodecatetraene 442368 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene 26318 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
alpha-Multijugenol 70566040 Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O 220.35 unknown https://doi.org/10.1080/10575639308043814
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
beta-Santalene 10889018 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Cadin-4-en-10-ol 519662 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Calamenene, cis-(+)- 11298625 Click to see 202.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(97)00828-5
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Copaene 12303902 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Cubebol 11276107 Click to see 222.37 unknown https://doi.org/10.1080/10575639308043814
delta-Cadinene 441005 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Farnesene 5281516 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Humulene 5281520 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Norbornane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)- 10534 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Aromadendrene 11095734 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(1aR,4R,4aR,7S,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 162940145 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961743
(1aS,4S,4aS,7R,7aR,7bS)-4-(hydroxymethyl)-1,1,7-trimethyl-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulene-4,7-diol 10967052 Click to see 254.36 unknown https://doi.org/10.1248/CPB.50.1413
(1aS,4S,4aS,7R,7aS,7bS)-4-(hydroxymethyl)-1,1,7-trimethyl-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulene-4,7-diol 145985613 Click to see 254.36 unknown https://doi.org/10.1248/CPB.50.1413
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961743
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
4-(Hydroxymethyl)-1,1,7-trimethyl-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulene-4,7-diol 73116791 Click to see 254.36 unknown https://doi.org/10.1248/CPB.50.1413
beta-Spathulenol 522266 Click to see 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Npc239037 101716 Click to see 222.37 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1080/10575639308043814
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-961743
https://doi.org/10.1080/10575639308043814
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-961743
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(-)-cis-beta-Elemene 6431151 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,8aS)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene 12309811 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
(3S,4aS,8aS)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 12309813 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene 10123 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
> 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/10.1080/10412905.2002.9699890
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, (1Z,6Z,8S)- 91746556 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.2002.9699890
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein A 5281243 Click to see 568.90 unknown https://doi.org/10.1021/NP50103A003
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
6,18-Dihydroxy-7,16-dimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-4-oxopentacyclo[9.7.0.01,3.03,8.012,16]octadec-10-ene-7-carboxylic acid 9982803 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CC(C34C2=CCC5C3(C4)C(=O)CC(C5(C)C(=O)O)O)O)C 484.70 unknown https://doi.org/10.1021/NP030530J
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
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/S0031-9422(97)00828-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(93)85364-W
https://doi.org/10.1016/S0031-9422(97)00828-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(4R)-4-[(3S)-3-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 11146876 Click to see 696.70 unknown https://doi.org/10.1248/CPB.50.1413
(4R)-4-[(3S)-3-[(2R,3R,4S,5S,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 154497223 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)(C)C 696.70 unknown https://doi.org/10.1248/CPB.50.1413
4-[3-[5-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 85415592 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)(C)C 696.70 unknown https://doi.org/10.1248/CPB.50.1413
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown https://doi.org/10.1055/S-2006-959758
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1007/BF02033462
https://doi.org/10.1016/S0031-9422(98)00208-8
Myristicin 4276 Click to see 192.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149483/
https://doi.org/10.1016/S0031-9422(98)00208-8
Safrole 5144 Click to see 162.18 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(2S)-2-methyl-8-(3-methylbutyl)-2-(4-methylpentyl)-3,4-dihydrochromene-6-carboxylic acid 163064086 Click to see 346.50 unknown https://doi.org/10.1248/BPB.31.538
methyl (2S)-2-methyl-8-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromene-6-carboxylate 91353621 Click to see 354.50 unknown https://doi.org/10.1248/BPB.31.538
methyl (2S)-2-methyl-8-(3-methylbutyl)-2-(4-methylpentyl)-3,4-dihydrochromene-6-carboxylate 162820276 Click to see CC(C)CCCC1(CCC2=C(O1)C(=CC(=C2)C(=O)OC)CCC(C)C)C 360.50 unknown https://doi.org/10.1248/BPB.31.538
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2,2-Dimethyl-8-prenylchromene 6-carboxylic acid 441962 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C(=O)O)C 272.34 unknown https://doi.org/10.1016/0031-9422(93)85364-W
https://doi.org/10.1016/S0031-9422(97)00828-5
Anofinic acid 5319235 Click to see 204.22 unknown https://doi.org/10.1021/NP030530J
https://doi.org/10.1016/S0031-9422(99)00132-6
https://doi.org/10.1248/BPB.31.538
https://doi.org/10.1080/14786410802243271
Eupatoriochromene 100768 Click to see 218.25 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Methyl 2,2-dimethyl-6-chromanecarboxylate 13442733 Click to see 220.26 unknown https://doi.org/10.1248/BPB.31.538
Methyl 2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromene-6-carboxylate 163086292 Click to see 288.40 unknown https://doi.org/10.1248/BPB.31.538
Methyl 2,2-dimethyl-8-(3-methylbut-2-enyl)chromene-6-carboxylate 15391024 Click to see 286.40 unknown https://doi.org/10.1080/14786410802243271
https://doi.org/10.1021/NP030530J
https://doi.org/10.1248/BPB.31.538
https://doi.org/10.1016/S0031-9422(99)00132-6
https://doi.org/10.1016/S0031-9422(97)00828-5
Methyl 2,2-dimethylchromene-6-carboxylate 5316881 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C(=O)OC)C 218.25 unknown https://doi.org/10.1016/0031-9422(93)85364-W
https://doi.org/10.1080/14786410802243271
https://doi.org/10.1248/BPB.31.538
https://doi.org/10.1016/S0031-9422(99)00132-6
Methyl 8-acetyloxy-2,2-dimethylchromene-6-carboxylate 162820500 Click to see 276.28 unknown https://doi.org/10.1248/BPB.31.538
Methyl 8-hydroxy-2,2-dimethyl-2h-chromene-6-carboxylate 44575762 Click to see 234.25 unknown https://doi.org/10.1080/14786410802243271
https://doi.org/10.1016/0031-9422(93)85364-W
https://doi.org/10.1248/BPB.31.538
https://doi.org/10.1021/NP030530J
https://doi.org/10.1016/S0031-9422(99)00132-6
Methyl 8-hydroxy-2,2-dimethyl-3,4-dihydrochromene-6-carboxylate 162989863 Click to see 236.26 unknown https://doi.org/10.1248/BPB.31.538
> Organoheterocyclic compounds / Coumarans
Anodendroic acid methyl ester 44559571 Click to see 236.26 unknown https://doi.org/10.1021/NP50103A003
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Benzoic acid, 3-((2R,3R)-2,3-dihydro-6-hydroxy-2-(1-hydroxy-1-methylethyl)-4-methoxy-7-(1-oxo-3-phenylpropyl)-3-benzofuranyl)-4-hydroxy-, methyl ester, rel-(-)- 442455 Click to see 506.50 unknown https://doi.org/10.1021/NP50103A003
https://doi.org/10.1021/NP030530J
methyl 3-[(1R)-1-[2,4-dihydroxy-6-methoxy-3-(3-phenylpropanoyl)phenyl]-3-methylbut-2-enyl]-4-hydroxybenzoate 163067646 Click to see 490.50 unknown https://doi.org/10.1021/NP50103A003
methyl 4-hydroxy-3-[(2R,3R)-6-hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-7-(3-phenylpropanoyl)-2,3,6,7-tetrahydro-1-benzofuran-3-yl]benzoate 162820256 Click to see 508.60 unknown https://doi.org/10.1021/NP030530J
Methyl 4-hydroxy-3-[6-hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-7-(3-phenylpropanoyl)-2,3-dihydro-1-benzofuran-3-yl]benzoate 3519899 Click to see 506.50 unknown https://doi.org/10.1021/NP030530J
Methyl 4-hydroxy-3-[6-hydroxy-2-(2-hydroxypropan-2-yl)-4-methoxy-7-(3-phenylpropanoyl)-2,3,6,7-tetrahydro-1-benzofuran-3-yl]benzoate 162820252 Click to see 508.60 unknown https://doi.org/10.1021/NP030530J
Piperaduncin A 10480725 Click to see 490.50 unknown https://doi.org/10.1021/NP50103A003
Piperaduncin C 10370473 Click to see 556.60 unknown https://doi.org/10.1021/NP50103A003
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
acacetin-8-C-neohesperidoside 70698254 Click to see 592.50 unknown https://doi.org/10.1021/NP100004V
Margaritene 45360149 Click to see 592.50 unknown https://doi.org/10.1021/NP100004V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one 4053302 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one 270058 Click to see COC1=CC(=C(C(=C1)OC)C(=O)CCC2=CC=CC=C2)O 286.32 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
1-(3-hydroxy-1-methoxy-5a-methyl-8-propan-2-yl-9,9a-dihydro-8H-dibenzofuran-4-yl)-3-phenylpropan-1-one 74819288 Click to see 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-(3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl)-3-phenylpropan-1-one 73307027 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)(C)O 424.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-(6-hydroxy-4-methoxy-6'-propan-2-ylspiro[3H-1-benzofuran-2,3'-cyclohexene]-7-yl)-3-phenylpropan-1-one 74819289 Click to see 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-[(5aR,8S,9aS)-3-hydroxy-1-methoxy-5a-methyl-8-propan-2-yl-9,9a-dihydro-8H-dibenzofuran-4-yl]-3-phenylpropan-1-one 162872171 Click to see CC(C)C1CC2C3=C(C=C(C(=C3OC2(C=C1)C)C(=O)CCC4=CC=CC=C4)O)OC 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-[2-Hydroxy-4-methoxy-6-(4-methyl-1-propan-2-ylcyclohex-3-en-1-yl)oxyphenyl]-3-phenylpropan-1-one 162985784 Click to see 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-[2-hydroxy-4-methoxy-6-[(1R)-4-methyl-1-propan-2-ylcyclohex-3-en-1-yl]oxyphenyl]-3-phenylpropan-1-one 101552591 Click to see 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-[2-hydroxy-4-methoxy-6-[(1S,4R)-4-methyl-1-propan-2-ylcyclohex-2-en-1-yl]oxyphenyl]-3-phenylpropan-1-one 163104102 Click to see CC1CCC(C=C1)(C(C)C)OC2=CC(=CC(=C2C(=O)CCC3=CC=CC=C3)O)OC 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
1-[2,6-Dihydroxy-4-methoxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]-3-phenylpropan-1-one 14237695 Click to see 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see 272.29 unknown https://doi.org/10.1016/S0968-0896(03)00406-1
https://doi.org/10.1016/S0031-9422(98)00208-8
https://doi.org/10.1021/NP030530J
https://doi.org/10.1016/S0031-9422(97)00828-5
4,2'-Dihydroxy-4',6'-dimethoxydihydrochalcone 10266895 Click to see 302.32 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
Adunctin A 42607686 Click to see 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
Adunctin B 42607687 Click to see 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
Adunctin C 42607688 Click to see 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
Adunctin D 42607689 Click to see CC(C)C1CCC2(CC3=C(C=C(C(=C3O2)C(=O)CCC4=CC=CC=C4)O)OC)C=C1 406.50 unknown https://doi.org/10.1002/HLCA.19930760409
Adunctin E 42607690 Click to see 424.50 unknown https://doi.org/10.1002/HLCA.19930760409
Asebogenin 442255 Click to see 288.29 unknown https://doi.org/10.1021/NP50103A003
https://doi.org/10.1016/S0968-0896(03)00406-1
https://doi.org/10.3136/FSTI9596T9798.3.285
Methyllinderatin 42607684 Click to see 408.50 unknown https://doi.org/10.1002/HLCA.19930760409
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (E)-; Chalcone, 2',6'-dihydroxy-4'-methoxy-; 2',6'-Dihydroxy-4'-methoxychalcone 606469 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
2',6'-Dihydroxy-4'-methoxychalcone 5316793 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(97)00828-5
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
3-(2,6-Dihydroxy-4-methoxyphenyl)-1-phenylpropan-1-one 162966195 Click to see COC1=CC(=C(C(=C1)O)CCC(=O)C2=CC=CC=C2)O 272.29 unknown https://doi.org/10.1016/S0031-9422(99)00132-6

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