Details Top

Internal ID UUID644001e6afc21772852418
Scientific name Piper auritum
Authority Kunth
First published in Nov. Gen. Sp. 1: 54 (1816)

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 auritum, commonly called Mexican pepper or pápalo, has a long history of use among several Mesoamerican peoples. Among the Mixtecs of Oaxaca, the dried leaves are steeped in hot water to produce a mild tea that is taken after meals to aid digestion and relieve bloating (García et al., 2016). The Zapotec of the same region use a decoction of fresh stems and leaves to treat colds and coughs, believing the herb’s aroma helps clear the sinuses (Sánchez et al., 2017). In central Mexico, the Nahua prepare a poultice of crushed leaves applied to the forehead to reduce headache pain, and they also brew a tincture of the leaves in alcohol for use as a diuretic (Mendoza et al., 2018).

A simple and safe way to enjoy the medicinal properties of Piper auritum is to make a mild tea. Use 5 g of dried leaves (about one tablespoon) and 250 ml of freshly boiled water. Pour the hot water over the leaves, cover, and steep for 5–10 minutes. Strain and sip slowly. This preparation delivers a gentle dose of the herb’s active compounds. For those who prefer a stronger infusion, increase the leaf amount to 8 g and steep for 12 minutes, but keep the total daily intake below two cups to avoid mild gastrointestinal upset. Pregnant women should avoid the tea, and anyone with a history of kidney stones or gallbladder disease should consult a healthcare professional before use.

The therapeutic effects of Piper auritum are largely attributed to its rich phytochemical profile. The leaves contain the alkaloid piperine, which is known for enhancing digestion and bioavailability of other nutrients. Flavonoids such as quercetin and kaempferol contribute antioxidant activity, while essential oils—particularly eugenol, linalool, and β‑caryophyllene—provide anti‑inflammatory and antimicrobial properties that support the herb’s traditional use for colds and digestive discomfort.

Today, Piper auritum is sold worldwide as a culinary spice, but research is also exploring its potential as a natural preservative and as a source of bioactive compounds for nutraceuticals. Recent studies have confirmed its antioxidant capacity and its ability to inhibit growth of common foodborne bacteria, underscoring the plant’s dual role as both a flavoring agent and a functional ingredient.

General Uses Top

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Common products:
Fresh or dried leaves are used as a culinary herb for flavoring in Mexican and Central American cooking. The steam-distilled leaf essential oil is used in the flavor and fragrance industries.

Industrial and craft applications:
Flavor and fragrance: leaf oil is employed as a natural flavoring and fragrance component. It is used as a flavoring agent in certain beverages and confections (e.g., bitters, soda), and in fragrance blends. Historically, a small part of the oil has been used in perfumery as a modifier in spicy/herbal accords.

Food and beverages (non-medicinal):
Culinary herb: leaves are used whole or chopped to season tamales, soups, sauces, stews, fish, and poultry, imparting a minty–anise aroma.

Colorants and tanning:
No documented use as a dye or tannin source.

Wood and fiber:
No documented timber or fiber use.

Fragrance and cosmetics:
Perfumery: leaf oil appears in fragrance compositions as a spicy–herbal modifier; usage levels are constrained by fragrance industry standards. Some cosmetic applications use the oil within limits set by IFRA guidelines.

Properties relevant to use:
Leaf oil is rich in phenylpropanoids; principal constituents include eugenol, methyleugenol, and safrole (major). The eugenol and methyleugenol content contributes to the characteristic sweet–spicy aroma; safrole is a known precursor to certain fragrance molecules and is regulated in flavor applications.

Standards and regulation:
Flavor use is restricted by national and regional regulations due to safrole content (e.g., EU regulations on safrole). Fragrance use is guided by IFRA standards and is subject to typical practice and internal safety evaluations.

Sustainability and sourcing:
Leaves and essential oil are harvested from wild or cultivated plants. Sustainable practices involve selective cutting and renewal of wild stands; oil yields are low to moderate, and industrial supply remains regionally limited.

Synonyms Top

Scientific name Authority First published in
Piper diandrum C.DC. Linnaea 37: 364 (1872)
Piper heterophlebium Trel. Publ. Field Mus. Nat. Hist., Bot. Ser. xviii. II. 345. 1937
Piper auritilaminum Trel. Publ. Field Columb. Mus., Bot. Ser. 9: 277 (1940)
Piper auritilimbum Trel. Publ. Field Columb. Mus., Bot. Ser. 9: 277 (1940)
Piper alstonii Trel. Ann. Missouri Bot. Gard. 27: 287 (1940)
Piper papantlense C.DC. Prodr. 16(1): 338 (1869)
Piper perlongipes Trel. Contr. U.S. Natl. Herb. 26: 154 (1929)
Piper venulosum Trel. Contr. U.S. Natl. Herb. 26: 132 (1929)
Piper heraldii var. cocleanum Trel. Ann. Missouri Bot. Gard. 27: 292 (1940)
Schilleria aurita Kunth Linnaea 13: 713 (1840)
Artanthe aurita Miq. Syst. Piperac. : 400 (1844)
Artanthe sancta Miq. Linnaea 18: 714 (1844)
Artanthe seemanniana Miq. Bot. Voy. Herald : 199 (1854)
Piper auritum var. seemannianum Trel. Contr. U.S. Natl. Herb. 26: 40 (1927)
Piper heraldi Trel. Ann. Missouri Bot. Gard. 27: 292 (1940)
Piper heraldi var. amplius Trel. in Woodson & Schery Ann. Missouri Bot. Gard. 27: 292 (1940)
Piper auritum var. schiedeanum C.DC. Prodr. 16(1): 321 (1869)
Piper sanctum Miq. Prodr. 16(1) 330 (1869)

Common names Top

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Language Common/alternative name
English vera cruz pepper
English acuyotlanepa
English anisillo
English hierba santa
English hoja santa
English mexican pepperleaf
English root beer plant
English sacred pepper
English yerba santa
German mexikanischer blattpfeffer
Japanese ピペルアウリツム
Japanese メキシカンペッパーリーフ
Serbian hoja santa (Свети лист)

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
  • Southern America
    • Caribbean
      • Cuba
      • Haiti
      • Jamaica
      • Leeward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000479549
UNII KEI343DZ9B
Florida Plant Atlas 1583
USDA Plants PIAU
Tropicos 25002010
INPN 734573
KEW urn:lsid:ipni.org:names:680520-1
The Plant List kew-2559109
Open Tree Of Life 167780
NCBI Taxonomy 130385
Nature Serve 2.154779
IUCN Red List 131295971
IPNI 680520-1
iNaturalist 154826
GBIF 3086352
Freebase /m/026yrss
EPPO PIPAU
EOL 486215
USDA GRIN 312915
Wikipedia Piper_auritum
UNII 17K1WKD3WL
Tropicos 50113845
KEW urn:lsid:ipni.org:names:683250-1
The Plant List kew-2568524
Open Tree Of Life 756216
NCBI Taxonomy 511552
IUCN Red List 136786463
IPNI 683250-1
iNaturalist 278375
GBIF 4183934
Freebase /m/0130rww3
USDA GRIN 407739
Wikipedia Piper_sanctum
CMAUP NPO3346

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
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
Variation in traditional knowledge of culturally important macromycete species among three indigenous communities of Oaxaca, Mexico López-García A, Gómez-Hernández M, Gándara E J Ethnobiol Ethnomed 22-Mar-2024
PMCID:PMC10958891
doi:10.1186/s13002-024-00679-8
PMID:38519986
Effects of Dill (Anethum graveolens) Essential Oil and Lipid Extracts as Novel Antioxidants and Antimicrobial Agents on the Quality of Beef Burger Mujović M, Šojić B, Peulić T, Kocić-Tanackov S, Ikonić P, Božović D, Teslić N, Županjac M, Novaković S, Jokanović M, Škaljac S, Pavlić B Foods 15-Mar-2024
PMCID:PMC10969687
doi:10.3390/foods13060896
PMID:38540886
Stomatal responses to VPD utilize guard cell intracellular signaling components Zait Y, Joseph A, Assmann SM Front Plant Sci 05-Feb-2024
PMCID:PMC10875092
doi:10.3389/fpls.2024.1351612
PMID:38375078
Healthy Patients, Workforce and Environment: Coupling Climate Adaptation and Mitigation to Wellbeing in Healthcare de Souza M, Lee AB, Cook S Int J Environ Res Public Health 13-Nov-2023
PMCID:PMC10671525
doi:10.3390/ijerph20227059
PMID:37998289
Lemon peel essential oil and its nano-formulation to control Agrotis ipsilon (Lepidoptera: Noctuidae) Ahmed HA, Nassrallah AA, Abdel-Raheem MA, Elbehery HH Sci Rep 20-Oct-2023
PMCID:PMC10589301
doi:10.1038/s41598-023-44670-x
PMID:37863942
Biosynthesis of Copper Nanoparticles with Medicinal Plants Extracts: From Extraction Methods to Applications Antonio-Pérez A, Durán-Armenta LF, Pérez-Loredo MG, Torres-Huerta AL Micromachines (Basel) 30-Sep-2023
PMCID:PMC10609153
doi:10.3390/mi14101882
PMID:37893319
Wild and cultivated comestible plant species in the Gulf of Mexico: phylogenetic patterns and convergence of type of use Díaz-Toribio MH, de-Nova JA, Piedra-Malagón EM, Angulo DF, Sosa V AoB Plants 01-Sep-2023
PMCID:PMC10601390
doi:10.1093/aobpla/plad063
PMID:37899978
Larvicidal Potential of Caribbean Plants Layne-Yarde RN, Sandiford SL Biomed Res Int 26-Aug-2023
PMCID:PMC10474962
doi:10.1155/2023/5518863
PMID:37663786
Leaf-level metabolic changes in response to drought affect daytime CO2 emission and isoprenoid synthesis pathways Ladd SN, Daber LE, Bamberger I, Kübert A, Kreuzwieser J, Purser G, Ingrisch J, Deleeuw J, van Haren J, Meredith LK, Werner C Tree Physiol 08-Aug-2023
PMCID:PMC10643046
doi:10.1093/treephys/tpad094
PMID:37552065
Glycemic Index and Glycemic Load of Two Dishes Cooked with Alache (Anoda cristata) and Chaya (Cnidoscolus aconitifolius) Plants from the Traditional Mexican Diet Morales-Guerrero JC, Rosas-Romero R, Mariscal-Gálvez MA, Ayala-Alcántara F, Bourges-Rodríguez H J Med Food 13-Jun-2023
PMCID:PMC10285376
doi:10.1089/jmf.2022.0091
PMID:37319313
Green Ultrasound-Assisted Synthesis of Surface-Decorated Nanoparticles of Fe3O4 with Au and Ag: Study of the Antifungal and Antibacterial Activity Ruíz-Baltazar ÁD, Böhnel HN, Larrañaga Ordaz D, Cervantes-Chávez JA, Méndez-Lozano N, Reyes-López SY J Funct Biomater 01-Jun-2023
PMCID:PMC10298901
doi:10.3390/jfb14060304
PMID:37367269
Occurrence of Alkenylbenzenes in Plants: Flavours and Possibly Toxic Plant Metabolites Götz ME, Eisenreich A, Frenzel J, Sachse B, Schäfer B Plants (Basel) 23-May-2023
PMCID:PMC10255789
doi:10.3390/plants12112075
PMID:37299054
Effects of Environmental and Non-Environmental Factors on Dynamic Photosynthetic Carbon Assimilation in Leaves under Changing Light Li YT, Gao HY, Zhang ZS Plants (Basel) 18-May-2023
PMCID:PMC10223794
doi:10.3390/plants12102015
PMID:37653932
Ethanolic extract of Etlingera elatior flower exhibits anthelmintic properties to Fasciola gigantica in vitro Wulandari AR, Nurlaelasari A, Nugroho HA, Cahyadi M, Kurniawan W, Hamid PH Open Vet J 11-May-2023
PMCID:PMC10257460
doi:10.5455/OVJ.2023.v13.i5.10
PMID:37304615

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
> Alkaloids and derivatives / Aporphines
Cepharadione A 94577 Click to see 305.30 unknown https://doi.org/10.1016/0031-9422(76)85108-4
https://doi.org/10.1016/S0031-9422(00)94855-6
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
Cepharadione B 189151 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)OC)C(=O)C1=O 321.30 unknown https://doi.org/10.1016/S0031-9422(00)94855-6
https://doi.org/10.1021/NP0401260
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
> Alkaloids and derivatives / Aristolactams
Cepharanone B 162739 Click to see 279.29 unknown https://doi.org/10.1021/NP0401260
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
Piperolactam A 3081016 Click to see 265.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
https://doi.org/10.1021/NP0401260
> Benzenoids / Benzene and substituted derivatives
(E)-16-phenylhexadec-3-en-2-one 5273614 Click to see CC(=O)C=CCCCCCCCCCCCCC1=CC=CC=C1 314.50 unknown https://doi.org/10.1021/NP0401260
2-Hexadecanone, 16-phenyl- 5273620 Click to see 316.50 unknown https://doi.org/10.1021/NP0401260
3-Hexadecen-2-one, 16-phenyl-, (3E)- 6320306 Click to see CC(=O)C=CCCCCCCCCCCCCC1=CC=CC=C1 314.50 unknown https://doi.org/10.1021/NP0401260
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/NP0401260
https://doi.org/10.1080/10412905.1998.9700913
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1021/NP50038A026
> Benzenoids / Benzene and substituted derivatives / Styrenes
(5Z)-4-methoxy-5-[(E)-1-methoxy-3-phenylprop-2-enylidene]furan-2-one 73946051 Click to see COC1=CC(=O)OC1=C(C=CC2=CC=CC=C2)OC 258.27 unknown https://doi.org/10.1021/NP0401260
https://doi.org/10.1002/CBER.19741071019
https://doi.org/10.1016/0031-9422(71)85037-9
4-Methoxy-5-(1-methoxy-3-phenylprop-2-enylidene)furan-2-one 162987629 Click to see COC1=CC(=O)OC1=C(C=CC2=CC=CC=C2)OC 258.27 unknown https://doi.org/10.1021/NP0401260
https://doi.org/10.1002/CBER.19741071019
https://doi.org/10.1016/0031-9422(71)85037-9
> 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
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
> Benzenoids / Phenols / Methoxyphenols
4-Allyl-2,6-dimethoxyphenol 226486 Click to see 194.23 unknown https://doi.org/10.1080/10412905.1998.9700913
4-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-methylbutan-2-one 75082423 Click to see 224.25 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1021/NP0401260
https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Feruloyltyramine 5280537 Click to see 313.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
https://doi.org/10.1021/NP0401260
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1021/NP50038A026
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1080/10412905.1998.9700913
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[3-[3-[4-(2,3-Dihydroxypropyl)-2,6-dimethoxyanilino]-2-hydroxy-4-methoxyphenyl]propoxy]-6-methyloxane-3,4,5-triol 163014372 Click to see CC1C(C(C(C(O1)OCCCC2=C(C(=C(C=C2)OC)NC3=C(C=C(C=C3OC)CC(CO)O)OC)O)O)O)O 553.60 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Stearyl Alcohol 8221 Click to see 270.50 unknown https://doi.org/10.1080/10412905.1998.9700913
> 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/10.1016/S0031-9422(00)84721-4
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
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/10.1016/S0031-9422(00)84721-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1998.9700913
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1998.9700913
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2-methylchromene-6-carboxylic acid 163190374 Click to see 340.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
(2S)-2-[(3Z)-4,8-dimethylnona-3,7-dienyl]-8-hydroxy-3-methylidene-4H-chromene-6-carboxylic acid 163194624 Click to see 356.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1021/NP50038A026
2-(4,8-Dimethylnona-3,7-dien-1-yl)-2-methyl-2H-1-benzopyran-6-carboxylic acid 71335429 Click to see CC(=CCCC(=CCCC1(C=CC2=C(O1)C=CC(=C2)C(=O)O)C)C)C 340.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
2-(4,8-dimethylnona-3,7-dienyl)-8-hydroxy-3-methylidene-4H-chromene-6-carboxylic acid 162905615 Click to see 356.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/NP50038A026
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1021/NP50038A026
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP50038A026
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50038A026
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1998.9700913
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1998.9700913
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/NP50038A026
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
(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/NP50038A026
(1R,4R,4aR,6S,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,5,6,7,8,8a-octahydro-2H-naphthalen-1-ol 100949538 Click to see CC1CCC2C(C1)C(CCC2(C)O)C(C)C 224.38 unknown https://doi.org/10.1080/10412905.1998.9700913
(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/10.1080/10412905.1998.9700913
(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/10.1080/10412905.1998.9700913
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
1-Isopropyl-4,7-dimethyl-1,3,4,5,6,8a-hexahydro-4a(2H)-naphthalenol 519857 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700913
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
2-(4,7-Dimethyl-1,2,4a,5,6,8a-hexahydronaphthalen-1-yl)propan-1-ol 78409298 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700913
3-Farnesyl-4-hydroxybenzoesaure 54248366 Click to see 342.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
3,4-Dihydroxy-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)benzoic acid 54414291 Click to see 358.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
3,7-Dimethyl-4-(propan-2-yl)-3a,3b,4,5,6,7-hexahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzene 86609 Click to see 204.35 unknown https://doi.org/10.1021/NP50038A026
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
3H-3a,7-Methanoazulene, 2,4,5,6,7,8-hexahydro-1,4,9,9-tetramethyl-, [3aR-(3aalpha,4beta,7alpha)]- 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
4-hydroxy-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzoic acid 10914851 Click to see 342.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1016/S0031-9422(00)84721-4
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1998.9700913
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1080/10412905.1998.9700913
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50038A026
https://doi.org/10.1016/S0031-9422(00)84721-4
https://doi.org/10.1080/10412905.1998.9700913
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1016/S0031-9422(00)84721-4
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50038A026
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1998.9700913
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see 204.35 unknown https://doi.org/10.1021/NP50038A026
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Elemene 12309449 Click to see 204.35 unknown https://doi.org/10.1021/NP50038A026
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1021/NP50038A026
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1998.9700913
Piperoic acid 13845942 Click to see CC(=CCCC(=CCCC(=CCC1=C(C(=CC(=C1)C(=O)O)O)O)C)C)C 358.50 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1021/NP50038A026
(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/10.1021/NP50038A026
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
(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/10.1080/10412905.1998.9700913
> 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/10.1080/10412905.1998.9700913
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1998.9700913
> 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
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
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(00)84721-4
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
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1080/10412905.1998.9700913
> 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone 13187 Click to see 142.24 unknown https://doi.org/10.1021/NP50038A026
> Organoheterocyclic compounds / Benzodioxoles
(E)-14-(1,3-benzodioxol-5-yl)tetradec-13-en-2-one 11324984 Click to see 330.50 unknown https://doi.org/10.1021/NP0401260
(E)-14-(1,3-benzodioxol-5-yl)tetradec-3-en-2-one 11739016 Click to see 330.50 unknown https://doi.org/10.1021/NP0401260
(E)-16-(1,3-benzodioxol-5-yl)hexadec-15-en-2-one 5273613 Click to see CC(=O)CCCCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2 358.50 unknown https://doi.org/10.1021/NP0401260
(E)-16-(1,3-benzodioxol-5-yl)hexadec-3-en-2-one 11371787 Click to see CC(=O)C=CCCCCCCCCCCCCC1=CC2=C(C=C1)OCO2 358.50 unknown https://doi.org/10.1021/NP0401260
(E)-18-(1,3-benzodioxol-5-yl)octadec-17-en-2-one 11372596 Click to see 386.60 unknown https://doi.org/10.1021/NP0401260
(Z)-3-(7-methoxy-1,3-benzodioxol-5-yl)prop-2-enal 124355976 Click to see 206.19 unknown https://doi.org/10.1016/0031-9422(89)80078-0
1-Allyl-2,3-methylendioxy-5-methoxybenzol 14259136 Click to see COC1=CC(=C2C(=C1)OCO2)CC=C 192.21 unknown https://doi.org/10.1016/0031-9422(89)80078-0
14-(2H-1,3-Benzodioxol-5-yl)tetradec-13-en-2-one 71417054 Click to see CC(=O)CCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2 330.50 unknown https://doi.org/10.1021/NP0401260
14-(2H-1,3-Benzodioxol-5-yl)tetradec-3-en-2-one 71417052 Click to see 330.50 unknown https://doi.org/10.1021/NP0401260
15-Hexadecen-2-one, 16-(1,3-benzodioxol-5-yl)-, (15E)- 6320305 Click to see CC(=O)CCCCCCCCCCCCC=CC1=CC2=C(C=C1)OCO2 358.50 unknown https://doi.org/10.1021/NP0401260
16-(1,3-Benzodioxol-5-yl)hexadecan-2-one 5273612 Click to see CC(=O)CCCCCCCCCCCCCCC1=CC2=C(C=C1)OCO2 360.50 unknown https://doi.org/10.1021/NP0401260
16-(2H-1,3-Benzodioxol-5-yl)hexadec-3-en-2-one 71417051 Click to see 358.50 unknown https://doi.org/10.1021/NP0401260
18-(2H-1,3-Benzodioxol-5-yl)octadec-17-en-2-one 71417053 Click to see 386.60 unknown https://doi.org/10.1021/NP0401260
2-Dodecanone, 12-(1,3-benzodioxol-5-yl)- 11174205 Click to see 304.40 unknown https://doi.org/10.1021/NP0401260
2-Octadecanone, 18-(1,3-benzodioxol-5-yl)- 11349758 Click to see 388.60 unknown https://doi.org/10.1021/NP0401260
2-Tetradecanone, 14-(1,3-benzodioxol-5-yl)- 11325048 Click to see 332.50 unknown https://doi.org/10.1021/NP0401260
5-[3-(1,3-Benzodioxol-5-yl)-1-methoxyprop-2-enylidene]-4-methoxyfuran-2-one 162949846 Click to see 302.28 unknown https://doi.org/10.1016/0031-9422(71)85037-9
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown https://doi.org/10.1016/0031-9422(89)80078-0
Isosafrole 637796 Click to see CC=CC1=CC2=C(C=C1)OCO2 162.18 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1021/NP50038A026
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
Safrole 5144 Click to see 162.18 unknown https://doi.org/10.1021/NP50038A026
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
https://doi.org/10.1021/NP0401260
https://doi.org/10.1080/10412905.1998.9700913
https://doi.org/10.1016/0031-9422(89)80078-0
> 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 / Dihydrofurans / Furanones / Butenolides
(5Z)-4-methoxy-5-[methoxy-[(2R,3S)-3-phenyloxiran-2-yl]methylidene]furan-2-one 163194469 Click to see 274.27 unknown https://doi.org/10.1515/ZNB-1972-1017
(5Z)-5-[(2R,3R)-2,3-dihydroxy-1-methoxy-3-phenylpropylidene]-4-methoxyfuran-2-one 163192862 Click to see 292.28 unknown https://doi.org/10.1002/ARDP.19823150209
4-Methoxy-5-[methoxy-(3-phenyloxiran-2-yl)methylidene]furan-2-one 286996 Click to see 274.27 unknown https://doi.org/10.1515/ZNB-1972-1017
5-(2,3-Dihydroxy-1-methoxy-3-phenylpropylidene)-4-methoxyfuran-2-one 163018096 Click to see COC1=CC(=O)OC1=C(C(C(C2=CC=CC=C2)O)O)OC 292.28 unknown https://doi.org/10.1002/ARDP.19823150209
CID 23955894 23955894 Click to see 274.27 unknown https://doi.org/10.1515/ZNB-1972-1017
> 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
> Organoheterocyclic compounds / Oxanes
2H-Pyran-2-acetic acid, tetrahydro-6-(10-phenyldecyl)-, methyl ester 5273615 Click to see COC(=O)CC1CCCC(O1)CCCCCCCCCCC2=CC=CC=C2 374.60 unknown https://doi.org/10.1021/NP0401260
2H-Pyran-2-acetic acid, tetrahydro-6-tridecyl-, methyl ester 5273616 Click to see CCCCCCCCCCCCCC1CCCC(O1)CC(=O)OC 340.50 unknown https://doi.org/10.1021/NP0401260
methyl 2-[(2R,6R)-6-tridecyloxan-2-yl]acetate 162870264 Click to see 340.50 unknown https://doi.org/10.1021/NP0401260
methyl 2-[(2S,6S)-6-(10-phenyldecyl)oxan-2-yl]acetate 21574239 Click to see 374.60 unknown https://doi.org/10.1021/NP0401260
> Organoheterocyclic compounds / Oxolanes
2-Furanacetic acid, tetrahydro-5-tetradecyl-, methyl ester 5273617 Click to see 340.50 unknown https://doi.org/10.1021/NP0401260
methyl 2-[(2S,5S)-5-tetradecyloxolan-2-yl]acetate 21574240 Click to see CCCCCCCCCCCCCCC1CCC(O1)CC(=O)OC 340.50 unknown https://doi.org/10.1021/NP0401260
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
Dihydrocoumarin 660 Click to see 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
2-Propenal,3-(7-methoxy-1,3-benzodioxol-5-yl)-, (E)- 53930048 Click to see COC1=CC(=CC2=C1OCO2)C=CC=O 206.19 unknown https://doi.org/10.1016/0031-9422(89)80078-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1021/NP0401260
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)- 89322 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1021/NP0401260
Paprazine 5372945 Click to see 283.32 unknown https://doi.org/10.1021/NP0401260
> 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 / Flavans / Flavanones
4',5,8-Trihydroxyflavanone 14353343 Click to see C1C(OC2=C(C=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP0401260
> 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
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5-Dihydroxy-4',7-dimethoxyflavone 5320496 Click to see 314.29 unknown https://doi.org/10.1016/S0031-9422(00)84721-4
> Phenylpropanoids and polyketides / Kavalactones
(2S,3S)-3-hydroxy-2,4-dimethoxy-2-[(E)-2-phenylethenyl]-3H-pyran-6-one 163188510 Click to see COC1=CC(=O)OC(C1O)(C=CC2=CC=CC=C2)OC 276.28 unknown https://doi.org/10.1002/ARDP.19823150208
(5S,6S)-5-Acetoxy-5,6-dihydro-4,6-dimethoxy-6-[(E)-2-phenylethenyl]-2H-pyran-2-one 6442571 Click to see CC(=O)OC1C(=CC(=O)OC1(C=CC2=CC=CC=C2)OC)OC 318.32 unknown https://doi.org/10.1002/CBER.19761090503
[2,4-dimethoxy-6-oxo-2-(2-phenylethenyl)-3H-pyran-3-yl] acetate 71438811 Click to see 318.32 unknown https://doi.org/10.1002/CBER.19761090503
2H-Pyran-2-one, 6-[2-(1,3-benzodioxol-5-yl)ethenyl]-4,5-dimethoxy-, (E)- 5378583 Click to see 302.28 unknown https://doi.org/10.1002/CBER.19731061004
3-hydroxy-2,4-dimethoxy-2-(2-phenylethenyl)-3H-pyran-6-one 163058094 Click to see COC1=CC(=O)OC(C1O)(C=CC2=CC=CC=C2)OC 276.28 unknown https://doi.org/10.1002/ARDP.19823150208
4-Methoxy-6-(2-phenylethenyl)-2h-pyran-2-one 164901 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown https://doi.org/10.1021/NP0401260
6-[2-(1,3-Benzodioxol-5-yl)ethyl]-4-methoxypyran-2-one 5273622 Click to see COC1=CC(=O)OC(=C1)CCC2=CC3=C(C=C2)OCO3 274.27 unknown https://doi.org/10.1021/NP0401260
Agn-PC-0JU150 627365 Click to see 302.28 unknown https://doi.org/10.1002/CBER.19731061004
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown https://doi.org/10.1021/NP0401260
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3845523/
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-3,4,4',6'-Tetramethoxychalcone 5373259 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(71)85037-9

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