Umbellularia californica

Details Top

Internal ID UUID6440475705727670296271
Scientific name Umbellularia californica
Authority (Hook. & Arn.) Nutt.
First published in N. Amer. Sylv. 1: 87 (1842)

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.

Among the Pomo of northern California, fresh or dried leaf material is steeped in hot water and drunk as a mild tea for coughs and colds (Moerman, 1998). The Yurok of the Klamath River region prepare a decoction of the leaves, simmering them for about 15 minutes to lower fever (Moerman, 1998). The Maidu of the Sierra Nevada brew a leaf tea for sore throats and stomach discomfort, often sweetening it with honey for children (Moerman, 1998). In all three traditions the plant part used is the foliage, and the method is a water‑based infusion or decoction.

A simple traditional tea can be made by placing 1 to 2 teaspoons (approximately 2–3 g) of dried Umbellularia californica leaves into a cup of fresh water, which measures about 240 mL (8 fl oz), bringing the water to a boil and then allowing it to cool to a gentle simmer. The leaves are steeped for 5–10 minutes, covered to retain the volatile oils, then strained. If desired, a teaspoon of honey can be stirred in before drinking. The resulting beverage is consumed warm, up to one cup two or three times daily. Because the leaves contain eucalyptol and other volatile terpenes, they should be used in moderation; pregnant women are advised to avoid large doses and individuals with a known allergy to bay‑leaf aromatics should discontinue use.

The pharmacological profile of Umbellularia californica is dominated by its essential‑oil composition, which includes the monoterpene eucalyptol (1,8‑cineole), α‑pinene, β‑pinene, camphor, and sabinene (Murray et al., 1995). These compounds are known antimicrobial agents and respiratory decongestants, matching the cough‑relief and fever‑lowering properties reported in ethnobotanical accounts. Their high eucalyptol content gives the leaf its characteristic camphor‑like aroma, and phytochemical surveys repeatedly confirm this profile.

Today the leaf is still harvested for culinary use under the name California bay leaf, and the essential oil is marketed as a natural expectorant and antimicrobial ingredient in complementary health products. The leaf is sold in specialty herb shops and online as a dried product, while the essential oil is bottled in small amber vials for aromatherapy. Recent laboratory work has confirmed antibacterial activity against Staphylococcus aureus and bronchodilatory effects in vitro, and in vitro assays have shown anti‑inflammatory activity, including inhibition of COX‑2 enzyme (Bennett et al., 2021). While commercial tinctures remain rare, a small number of herbalists continue to prepare the leaf tea as a traditional remedy, preserving the knowledge that has been handed down for generations.

General Uses Top

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Common products: Dried leaf spice, leaf essential oil, hardwood lumber, bark (tannins).
Industrial and craft applications: Hardwood is used for fine furniture, cabinetry, veneers, turned objects, musical instrument components, and boat interiors; leaf oil serves as a fragrance component in soaps, detergents, and other cleaning products.
Food and beverages (non-medicinal): Dried leaves are used as a culinary spice; leaf oil is employed as a flavoring agent in processed foods, sauces, and beverages.
Colorants and tanning: Bark contains hydrolyzable tannins used for leather tanning; leaf extracts yield natural brown dyes for protein fibers.
Wood and fiber: The dense, fine‑grained heartwood (≈0.90–0.95 g cm⁻³ at 12 % MC) is suitable for high‑quality wood products, sliced veneers, and fiberboard because of its high cellulose content.
Fragrance and cosmetics: Leaf essential oil, high in 1,8‑cineole, is used in perfumery for its camphoraceous note and in aromatherapy products.
Properties relevant to use: Leaf oil: 50–80 % 1,8‑cineole, strong monoterpene profile; wood: density, low shrinkage, fine grain; bark tannins: ~15 % dry weight, hydrolyzable, high leather‑tanning efficacy.
Standards and regulation: Leaf essential oil is evaluated against international essential‑oil standards (e.g., ISO 3215) for cineole content and purity; wood products follow standard moisture‑content tests (ASTM D 4442).
Sustainability and sourcing: Umbellularia californica occurs naturally in coastal forests of California and Oregon; commercial supply is mainly wild‑harvested. The species is listed as Least Concern (IUCN). Sustainable practices—selective logging, pruning, and hand‑picking—are promoted by state forest agencies to maintain populations and habitat.

Synonyms Top

Scientific name Authority First published in
Oreodaphne regalis Regel Gartenflora 5: 366 (1856)
Tetranthera causticans (Pasq.) Pasq. Nuovo Giorn. Bot. Ital. 1: 290 (1869)
Persea causticans Pasq. Cat. Ort. Bot. Napoli : 77 (1867)
Drimophyllum pauciflorum Nutt. N. Amer. Sylv. 1: 85 (1842)
Tetranthera californica Hook. & Arn. Bot. Beechey Voy. : 159 (1833)
Oreodaphne californica Nees Syst. Laur. : 463 (1836)
Umbellularia californica f. pendula Rehder J. Arnold Arbor. 1: 143. 1919
Umbellularia californica var. fresnensis Eastw. Leafl. W. Bot. 4: 166 (1945)
Litsea californica (Hook. & Arn.) Benth. & Hook.f. ex B.D.Jacks. Index Kew. 2: 100 (1894)

Common names Top

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Language Common/alternative name
English california laurel
Spanish tetranthera californica
Spanish laurel de california
Spanish sciadiodaphne
Czech okoličnatka kalifornská
German kalifornischer lorbeer
German berglorbeer
German kalifornischer berglorbeer
French laurier de californie
French myrte de l’orégon
French myrte de l'oregon
Croatian brdski lovor
Hungarian amerikai babér
Korean 움벨룰라리아
Norwegian Bokmål californialaurbær
Norwegian Nynorsk californialaurbær
Russian Умбеллюлярия
Ukrainian Умбелюларія
Ukrainian Умбелюларія каліфорнійська
Chinese 加州月桂
Chinese 加州月桂屬
Chinese 傘桂屬
Chinese 傘桂
Chinese 俄勒岡香桃木
Chinese 北美木姜子
Chinese 加州桂

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001071259
UNII Z9V57ME7RD
USDA Plants UMCA
Tropicos 17804222
INPN 160321
KEW urn:lsid:ipni.org:names:30189264-2
The Plant List tro-17804222
PFAF Umbellularia californica
Open Tree Of Life 913214
NCBI Taxonomy 3438
NBN Atlas NBNSYS0000042218
Nature Serve 2.144045
IUCN Red List 62572
IPNI 30189264-2
iNaturalist 48807
GBIF 5371727
Freebase /m/027fwl
FEIS plants/tree/umbcal
EPPO UMBCA
EOL 596841
Calflora (Californian flora) 8183
US Library of Congress sh85012493
USDA GRIN 40863
Wikipedia Umbellularia_californica

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_028538565.1 dmUmbCali1.0.hap2 Scaffold UCLA 2023-02-07 67 915.12 Mb

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
Phylogeography, origin and population structure of the self‐fertile emerging plant pathogen Phytophthora pseudosyringae Mullett MS, Harris AR, Scanu B, Van Poucke K, LeBoldus J, Stamm E, Bourret TB, Christova PK, Oliva J, Redondo MA, Talgø V, Corcobado T, Milenković I, Jung MH, Webber J, Heungens K, Jung T Mol Plant Pathol 08-Apr-2024
PMCID:PMC11002350
doi:10.1111/mpp.13450
PMID:38590129
Commodity risk assessment of Cornus alba and Cornus sanguinea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Kariampa P, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R EFSA J 12-Mar-2024
PMCID:PMC10928767
doi:10.2903/j.efsa.2024.8657
PMID:38476319
Pain Pathways: Linking Environmental Pollutants with Migraine-Associated Pain Signaling Schmidt S Environ Health Perspect 28-Feb-2024
PMCID:PMC10901286
doi:10.1289/EHP14416
PMID:38416538
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Unraveling the directional relationship of sleep and migraine-like pain Lillo Vizin RC, Kopruszinski CM, Redman PM, Ito H, Rau J, Dodick DW, Navratilova E, Porreca F Brain Commun 18-Feb-2024
PMCID:PMC10914446
doi:10.1093/braincomms/fcae051
PMID:38444905
Expanding the synthetic biology toolbox of Cupriavidus necator for establishing fatty acid production Mishra S, Perkovich PM, Mitchell WP, Venkataraman M, Pfleger BF J Ind Microbiol Biotechnol 16-Feb-2024
PMCID:PMC10926325
doi:10.1093/jimb/kuae008
PMID:38366943
Use of Aureobasidium in a sustainable economy Rensink S, van Nieuwenhuijzen EJ, Sailer MF, Struck C, Wösten HA Appl Microbiol Biotechnol 13-Feb-2024
PMCID:PMC10864419
doi:10.1007/s00253-024-13025-5
PMID:38349550
SOS: speed of stomata opening and closing is influenced by vapor pressure deficit Burgess AJ, Ugalde JM Plant Physiol 06-Feb-2024
PMCID:PMC11060658
doi:10.1093/plphys/kiae066
PMID:38319740
Potential mechanisms for osteopathic manipulative treatment to alleviate migraine-like pain in female rats Byrd K, Lund M, Pan Y, Chung BH, Child K, Fowler D, Burns-Martin J, Sanikommu M, Henderson H, Gregory C, Fleming RK, Xie JY Front Pain Res (Lausanne) 05-Feb-2024
PMCID:PMC10877942
doi:10.3389/fpain.2024.1280589
PMID:38380374
Overcoming Barriers to Medium Chain Fatty Alcohol Production Su Y, Mangus AM, Cordell WT, Pfleger BF Curr Opin Biotechnol 13-Jan-2024
PMCID:PMC10922944
doi:10.1016/j.copbio.2023.103063
PMID:38219523
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Xenobiotic Exposure and Migraine-Associated Signaling: A Multimethod Experimental Study Exploring Cellular Assays in Combination with Ex Vivo and In Vivo Mouse Models Rasmussen RH, Christensen SL, Calloe K, Nielsen BS, Rehfeld A, Taylor-Clark TE, Haanes KA, Taboureau O, Audouze K, Klaerke DA, Olesen J, Kristensen DM Environ Health Perspect 01-Nov-2023
PMCID:PMC10619430
doi:10.1289/EHP12413
PMID:37909725
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445

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 / Benzoic acid esters
Ethyl benzoate 7165 Click to see 150.17 unknown https://doi.org/10.1016/0031-9422(74)85146-0
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1016/0031-9422(74)85146-0
> 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/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1007/BF02657546
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tricaprin 69310 Click to see CCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCC)OC(=O)CCCCCCCCC 554.80 unknown https://doi.org/10.1007/BF02657546
Trilaurin 10851 Click to see CCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC 639.00 unknown https://doi.org/10.1007/BF02657546
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
(1R,5S)-4-(hydroxymethyl)-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one 92466631 Click to see 166.22 unknown https://doi.org/10.1016/S0031-9422(00)90381-9
(1R,5S)-4-Methyl-1-(1-methylethyl)bicyclo(3.1.0)hex-3-en-2-one 442504 Click to see 150.22 unknown https://doi.org/10.1016/S0031-9422(00)90381-9
https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
4-(Hydroxymethyl)-1-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one 73815092 Click to see 166.22 unknown https://doi.org/10.1016/S0031-9422(00)90381-9
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
beta-Thujene 520384 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
Pinocarvone 121719 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
Umbellulone 91195 Click to see CC1=CC(=O)C2(C1C2)C(C)C 150.22 unknown https://doi.org/10.1016/0031-9422(74)85146-0
https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/S0031-9422(00)90381-9
> 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/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(95)00094-1
https://doi.org/10.1016/0031-9422(74)85146-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
alpha-Santalene 94164 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Beta-Bisabolene 10104370 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene 10123 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
alpha-Selinene 10856614 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(74)85146-0
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Bufotenine 10257 Click to see 204.27 unknown https://doi.org/10.1016/S0031-9422(00)89642-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Ethyl 3-phenylprop-2-enoate 7649 Click to see 176.21 unknown https://doi.org/10.1016/0031-9422(74)85146-0
Ethyl cinnamate 637758 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1016/0031-9422(74)85146-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)89642-9
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 https://doi.org/10.1016/S0031-9422(00)89642-9
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)89642-9
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(00)89642-9
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(00)89642-9

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