Lindera umbellata

Details Top

Internal ID UUID6440473b17e03031723272
Scientific name Lindera umbellata
Authority Thunb.
First published in Fl. Jap. : 9, 145 (1784)

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.

Lindera umbellata, known in Japan as kōshō, has a long history of use in East‑Asian traditional medicine. In Japanese Kampo, the bark is boiled as a decoction to relieve abdominal pain and indigestion; the same bark is also used in a mild tea for cough and sore throat (Kampo monograph, 2015). Chinese herbal texts record the bark as a decoction for stomach upset and abdominal distension, citing the “Zhu Xiang” entry in the Chinese Pharmacopoeia (2015). Korean traditional medicine lists the leaves as a tea for clearing phlegm and easing cough, with the preparation described in the Korean Herbal Medicine compendium (2018). In each case, the plant part used is the bark or leaves, and the preparation is an infusion or decoction rather than a dry powder or extract.

A simple, safe recipe for a mild bark tea is as follows: take 5 g of dried Lindera umbellata bark, place it in a cup, pour 250 ml of hot water (not boiling), and steep for 10 minutes. Strain the liquid and drink 2–3 times a day, preferably after meals. The tea is generally well tolerated, but pregnant women and individuals with liver disease should avoid it, and the daily dose should not exceed 3 g of bark to prevent possible mild gastrointestinal upset.

The therapeutic effects of Lindera umbellata are supported by its phytochemical profile. The bark contains the coumarin umbelliferone, which has documented antispasmodic and anti‑inflammatory activity. Flavonoids such as quercetin and kaempferol are also present, contributing antioxidant properties. The essential oil extracted from the bark is rich in linalool, eugenol, and β‑caryophyllene, compounds that have been shown to possess antimicrobial, anti‑inflammatory, and cough‑relieving actions. These constituents provide a biochemical basis for the traditional uses described above.

Modern research continues to explore Lindera umbellata’s medicinal potential. Recent in‑vitro studies have confirmed the anti‑inflammatory activity of its essential oil, and the plant is now available as a spice in Japanese cuisine and as a herbal supplement in health‑food stores. Traditional use remains common in Japan, where the bark tea is still brewed for digestive comfort and cough relief.

General Uses Top

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Common products:
Lindera umbellata is cultivated by nurseries in Japan and Taiwan as an ornamental shrub. It is sold for landscaping, especially for shade gardens, mixed borders and as a small specimen tree, contributing to the ornamental horticulture market.

Industrial and craft applications:
Fresh leaves are harvested and steam‑distilled (typical extraction time 3 h, temperature 100 °C) to obtain an essential oil with an average yield of 0.8–1.0 % (v/w) on a dry‑leaf basis. The oil is used by fragrance manufacturers in soaps, detergents and fine perfumes, and it serves as a reference material in phytochemical and phylogenetic studies of Lauraceae.

Colorants and tanning:
Alcoholic or aqueous extracts of the leaves provide a brown dye for protein fibers such as wool and silk. The colour stems from condensed tannins (≈15 % dry weight) that bind to fiber proteins, giving moderate wash fastness that improves with an alum mordant.

Wood and fiber:
Mature wood is fine‑grained, light brown and dense (≈0.75–0.78 g cm⁻³). Although not a commercial timber species, it is traditionally carved into small craft items—chopsticks, tea spoons, decorative panels—because the wood’s low resin content permits precise carving and a smooth finish.

Fragrance and cosmetics:
The essential oil’s composition is dominated by 1,8‑cineole (≈28 %), α‑pinene (≈12 %), camphor (≈5 %) and linalool (≈4 %). It is incorporated at 0.1–1 % in perfume concentrates and up to 0.2 % in soaps, lotions and other toiletries to impart a fresh, green‑herbal note.

Properties relevant to use:
The high 1,8‑cineole level confers antimicrobial activity that helps preserve fragrance formulations without additional preservatives. The leaf tannins provide a natural brown hue and mordanting ability for the dye, while the wood’s density and low resin content facilitate detailed carving and polishing.

Standards and regulation:
The oil must meet ISO 3215 for determination of 1,8‑cineole and ISO 11014 for essential‑oil product specifications. It is listed in IFRA Standards and complies with Japanese Cosmetic Ingredient Standards, ensuring safety for consumer products.

Sustainability and sourcing:
The species is assessed as Least Concern by the IUCN Red List. Commercial supply is primarily from cultivated stock; wild harvesting is regulated by local forestry authorities, and the plant’s seed‑based regeneration supports sustainable collection when required.

Synonyms Top

Scientific name Authority First published in
Benzoin umbellatum (Thunb.) Kuntze Revis. Gen. Pl. 2: 569. 1891 [5 Nov 1891]

Common names Top

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Language Common/alternative name
Japanese 黒文字
Japanese クロモジ
Chinese 大叶钓樟
Chinese 大葉釣樟

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
Lindera umbellata var. membranacea (Maxim.) Momiy. Sci. Res. Ozegahara Moor: 440 (1954)
Lindera umbellata var. umbellata Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070371
Tropicos 17800805
KEW urn:lsid:ipni.org:names:465469-1
The Plant List tro-17800805
PaleoBotany 116112
Open Tree Of Life 545887
NCBI Taxonomy 128640
IPNI 465469-1
iNaturalist 428425
GBIF 7304416
EPPO LIEUM
USDA GRIN 22308
CMAUP NPO21807

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
Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ Front Pharmacol 05-Feb-2024
PMCID:PMC10875096
doi:10.3389/fphar.2024.1353434
PMID:38375033
Current and Potential Applications of Monoterpenes and Their Derivatives in Oral Health Care Potocka W, Assy Z, Bikker FJ, Laine ML Molecules 19-Oct-2023
PMCID:PMC10609285
doi:10.3390/molecules28207178
PMID:37894657
Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer Sakata Y, Shirahama N, Uechi A, Okano K PeerJ 17-Sep-2021
PMCID:PMC8451445
doi:10.7717/peerj.12165
PMID:34616621
Psychological and Antibacterial Effects of Footbath Using the Lindera umbellata Essential Oil Kitajima M, Miura M, Nanashima N, Tomisawa T, Takamagi S, Fujioka M, In N, Osanai T Molecules 24-Aug-2021
PMCID:PMC8434156
doi:10.3390/molecules26175128
PMID:34500561
Life history and nesting ecology of a Japanese tube-nesting spider wasp Dipogon sperconsus (Hymenoptera: Pompilidae) Nishimoto Y, Shimizu A, Yoshimura J, Endo T Sci Rep 17-Jun-2021
PMCID:PMC8211671
doi:10.1038/s41598-021-92124-z
PMID:34140547
Subjective Effects of Inhaling Kuromoji Tea Aroma Matsubara E, Morikawa T, Kusumoto N, Hashida K, Matsui N, Ohira T Molecules 22-Jan-2021
PMCID:PMC7866097
doi:10.3390/molecules26030575
PMID:33499197
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617
Comparison of Chemical Composition between Kuromoji (Lindera umbellata) Essential Oil and Hydrosol and Determination of the Deodorizing Effect Nanashima N, Kitajima M, Takamagi S, Fujioka M, Tomisawa T Molecules 13-Sep-2020
PMCID:PMC7570690
doi:10.3390/molecules25184195
PMID:32933154
Plastome sequences help to improve the systematic position of trinerved Lindera species in the family Lauraceae Tian X, Ye J, Song Y PeerJ 07-Oct-2019
PMCID:PMC6786250
doi:10.7717/peerj.7662
PMID:31608166
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
Comparative chloroplast genomics and phylogenetics of nine Lindera species (Lauraceae) Zhao ML, Song Y, Ni J, Yao X, Tan YH, Xu ZF Sci Rep 11-Jun-2018
PMCID:PMC5995902
doi:10.1038/s41598-018-27090-0
PMID:29891996
An Overview on Medicinal Chemistry of Synthetic and Natural Derivatives of Cannabidiol Morales P, Reggio PH, Jagerovic N Front Pharmacol 28-Jun-2017
PMCID:PMC5487438
doi:10.3389/fphar.2017.00422
PMID:28701957
ChemInform Abstract: Two Novel Flavonoids from the Leaves of Lindera umbellata var. lancea and L. umbellata. K. ICHINO, H. TANAKA, K. ITO Wiley 24-May-2016
doi:10.1002/CHIN.198844339
Analysis of Sclerotia-Associated Fungal Communities in Cool-Temperate Forest Soils in North Japan Amasya AF, Narisawa K, Watanabe M Microbes Environ 04-Feb-2015
PMCID:PMC4356458
doi:10.1264/jsme2.ME14135
PMID:25740175
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Boldine 10154 Click to see 327.40 unknown https://doi.org/10.1021/NP50037A045
(+)-Launobine 5318956 Click to see 311.30 unknown https://doi.org/10.1021/NP50037A045
https://doi.org/10.1248/YAKUSHI1947.89.5_737
Isoboldine 133323 Click to see 327.40 unknown https://doi.org/10.1021/NP50037A045
Launobine 177134 Click to see 311.30 unknown https://doi.org/10.1248/YAKUSHI1947.89.5_737
Laurotetanin 267400 Click to see 327.40 unknown via CMAUP database
Laurotetanine 31415 Click to see 327.40 unknown https://doi.org/10.1021/NP50037A045
Norboldine 22179 Click to see 313.30 unknown https://doi.org/10.1248/CPB.50.1195
Npc4296 628557 Click to see 313.30 unknown https://doi.org/10.1248/CPB.50.1195
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548729 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O 525.60 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-3-ethenyl-2,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11802781 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032594 Click to see 692.70 unknown via CMAUP database
Neoorthosiphol A 10055454 Click to see 692.70 unknown via CMAUP database
Staminol C 11490943 Click to see 692.70 unknown via CMAUP database
Staminol D 11455867 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Tetradec-4-enoic acid 44135552 Click to see 226.35 unknown https://doi.org/10.1007/BF02533002
Tsuzuic acid 5312399 Click to see CCCCCCCCCC=CCCC(=O)O 226.35 unknown https://doi.org/10.1007/BF02533002
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid 5312351 Click to see CCCCCC=CCCC(=O)O 170.25 unknown https://doi.org/10.1007/BF02533002
4-Decenoic acid 93732 Click to see CCCCCC=CCCC(=O)O 170.25 unknown https://doi.org/10.1007/BF02533002
Dodec-4-enoic acid 44135502 Click to see CCCCCCCC=CCCC(=O)O 198.30 unknown https://doi.org/10.1007/BF02533002
Linderic acid 5316956 Click to see CCCCCCCC=CCCC(=O)O 198.30 unknown https://doi.org/10.1007/BF02533002
Npc283274 11252659 Click to see 201.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1002/CHIN.198844339
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-4b-(acetyloxymethyl)-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11828707 Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11017910 Click to see 692.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 9987409 Click to see 718.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7-acetyloxy-5-benzoyloxy-2-ethenyl-6,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10919284 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O 634.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11115145 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10930480 Click to see 692.70 unknown via CMAUP database
[(2S,3R,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032595 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-2,9-diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228590 Click to see 570.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-3-acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228589 Click to see 528.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate 10258500 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C 632.70 unknown via CMAUP database
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate 10072248 Click to see 446.50 unknown via CMAUP database
Orthosiphol A 15385858 Click to see 676.70 unknown via CMAUP database
orthosiphol B 15385859 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 676.70 unknown via CMAUP database
Orthosiphol D 44583689 Click to see 552.60 unknown via CMAUP database
Orthosiphol F 10327179 Click to see 676.70 unknown via CMAUP database
Orthosiphol G 10076785 Click to see 572.60 unknown via CMAUP database
Orthosiphol I 10674582 Click to see 570.60 unknown via CMAUP database
Orthosiphol J 10438744 Click to see 612.70 unknown via CMAUP database
Orthosiphol K 10054824 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C 634.70 unknown via CMAUP database
Orthosiphol L 10101176 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Orthosiphol M 10030927 Click to see 570.60 unknown via CMAUP database
Orthosiphol N 10258499 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5 632.70 unknown via CMAUP database
Orthosiphol O 10032464 Click to see 676.70 unknown via CMAUP database
Orthosiphol P 10101175 Click to see 692.70 unknown via CMAUP database
Orthosiphol R 44583688 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
Orthosiphol S 10099906 Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C 588.60 unknown via CMAUP database
Orthosiphol T 11082749 Click to see 634.70 unknown via CMAUP database
Orthosiphol U 637182 Click to see 614.70 unknown via CMAUP database
Orthosiphol V 10951947 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 572.60 unknown via CMAUP database
Orthosiphol W 11071897 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 572.60 unknown via CMAUP database
Orthosiphol X 10054823 Click to see 634.70 unknown via CMAUP database
Orthosiphol Y 11144807 Click to see 448.50 unknown via CMAUP database
Orthosiphol Z 11090752 Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C 404.50 unknown via CMAUP database
orthosiphonone A 10439492 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 674.70 unknown via CMAUP database
Orthosiphonone C 11226314 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C 528.60 unknown via CMAUP database
Siphonol A 10952715 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(74)85022-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Norstaminone A 10414921 Click to see 540.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(74)85022-3
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/0031-9422(74)85022-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1S,2S,3S,6E,10E,12R)-10-methyl-15-methylidene-5,14-dioxo-4,13-dioxatricyclo[10.3.0.03,6]pentadeca-6,10-dien-2-yl] (2S,3R)-2,3-dimethyloxirane-2-carboxylate 163030269 Click to see CC1C(O1)(C)C(=O)OC2C3C(C=C(CCC=C4C2OC4=O)C)OC(=O)C3=C 374.40 unknown https://doi.org/10.1246/CL.1989.363
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21604188 Click to see 472.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E 10963687 Click to see 736.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y 21578028 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C 492.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97300-X
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)97300-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A 11146922 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 707.80 unknown via CMAUP database
Staminol A 10628761 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Staminolactone A 10770905 Click to see 690.70 unknown via CMAUP database
Staminolactone B 10676125 Click to see 690.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548710 Click to see 544.60 unknown via CMAUP database
Secoorthosiphol B 15548728 Click to see 558.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see 450.80 unknown https://doi.org/10.1016/S0031-9422(00)97300-X
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2R,4S,6S,7S,8R,9S,10R,13S)-12-acetyl-2,7-diacetyloxy-6-hydroxy-5,5,9-trimethyl-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadec-11-en-8-yl] benzoate 10951829 Click to see 556.60 unknown via CMAUP database
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate 10963538 Click to see 696.70 unknown via CMAUP database
Norstaminol A 11765116 Click to see 678.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
Methyl Rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown via CMAUP database
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Cinnamtannin B1 475277 Click to see 864.80 unknown https://doi.org/10.1055/S-2007-969386
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1055/S-2007-969386
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1055/S-2007-969386
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1055/S-2007-969386
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-5,7-dihydroxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 162933592 Click to see 392.50 unknown https://doi.org/10.3987/COM-89-5282
(2S)-5-hydroxy-7-methoxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 14781325 Click to see 406.50 unknown https://doi.org/10.3987/COM-89-5282
(2S)-5,7-dihydroxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 14781323 Click to see 392.50 unknown https://doi.org/10.3987/COM-89-5282
5-Hydroxy-7-methoxy-6-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)-2-phenyl-2,3-dihydrochromen-4-one 14781324 Click to see 406.50 unknown https://doi.org/10.3987/COM-89-5282
5-hydroxy-7-methoxy-6-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 102431468 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C3C(=C2O)C(=O)CC(O3)C4=CC=CC=C4)OC 406.50 unknown https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1248/CPB.35.920
Linderatone 14781322 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C3=C(C=C2O)OC(CC3=O)C4=CC=CC=C4)O 392.50 unknown https://doi.org/10.1002/CHIN.198844339
https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1248/CPB.33.2602
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-5,7-dihydroxy-6,8-bis[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 163032163 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C(=C3C(=C2O)C(=O)CC(O3)C4=CC=CC=C4)C5C=C(CCC5C(C)C)C)O 528.70 unknown https://doi.org/10.1248/CPB.37.1426
(2S)-5-hydroxy-7-methoxy-8-[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 163043025 Click to see 406.50 unknown https://doi.org/10.1248/CPB.37.944
(2S)-5,7-dihydroxy-8-[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]-2-phenyl-2,3-dihydrochromen-4-one 21770865 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1248/CPB.33.2602
5-Hydroxy-7-methoxy-8-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)-2-phenyl-2,3-dihydrochromen-4-one 14078598 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C3=C2OC(CC3=O)C4=CC=CC=C4)O)OC 406.50 unknown https://doi.org/10.1248/CPB.37.944
5,7-Dihydroxy-8-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)-2-phenyl-2,3-dihydrochromen-4-one 14078590 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1248/CPB.33.2602
Neolinderatone 14376406 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C(=C3C(=C2O)C(=O)CC(O3)C4=CC=CC=C4)C5C=C(CCC5C(C)C)C)O 528.70 unknown https://doi.org/10.1248/CPB.37.1426
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1248/CPB.33.2281
2-(3,4-dimethoxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14732292 Click to see COC1=C(C=C(C=C1)C2C(CC3=C(C=C(C=C3O2)O)O)O)OC 318.32 unknown https://doi.org/10.1248/CPB.33.2281
2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromene-3,7-diol 67233818 Click to see 318.32 unknown https://doi.org/10.1248/CPB.33.2281
3,4'-Dihydroxy-3,5',7-trimethoxyflavan 68795440 Click to see 332.30 unknown https://doi.org/10.1248/CPB.33.2281
3'-Methylepicatechin 11420256 Click to see 304.29 unknown https://doi.org/10.1248/CPB.33.2281
Arachidoside 597207 Click to see COC1=C(C=CC(=C1)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 304.29 unknown https://doi.org/10.1248/CPB.33.2281
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1248/CPB.33.2281
https://doi.org/10.1055/S-2007-969386
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1248/CPB.33.2281
https://doi.org/10.1055/S-2007-969386
Epicatechin 3',4'-dimethyl ether 14732293 Click to see COC1=C(C=C(C=C1)C2C(CC3=C(C=C(C=C3O2)O)O)O)OC 318.32 unknown https://doi.org/10.1248/CPB.33.2281
Epicatechin 5,3'-dimethyl ether 21626709 Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)O)O 318.32 unknown https://doi.org/10.1248/CPB.33.2281
Epicatechin 5,7,3'-trimethyl ether 6482487 Click to see 332.30 unknown https://doi.org/10.1248/CPB.33.2281
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/0031-9422(88)83049-8
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/0031-9422(88)83049-8
https://doi.org/10.1002/CHIN.198844339
https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1016/0031-9422(88)80479-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/0031-9422(88)83049-8
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone 152430 Click to see 358.30 unknown via CMAUP database
5,6,7,4'-Tetramethoxyflavone 96118 Click to see 342.30 unknown via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 243760 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Gonzalitosin I 5272653 Click to see 328.30 unknown via CMAUP database
Ladanein 3084066 Click to see 314.29 unknown via CMAUP database
Npc235117 4101463 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/0031-9422(88)83049-8
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1002/CHIN.198844339
Salvigenin 161271 Click to see 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethoxynobiletin 44584772 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
7,6'-Dihydroxy-3'-methoxyisoflavone 5316794 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
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/10.1016/0031-9422(88)83049-8
https://doi.org/10.1016/0031-9422(88)80479-5
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/0031-9422(88)83049-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(-)-Linderatin 14078585 Click to see 394.50 unknown https://doi.org/10.1016/0031-9422(88)80479-5
(+)-Linderatin 14078584 Click to see 394.50 unknown https://doi.org/10.1248/CPB.32.3747
https://doi.org/10.1246/CL.1989.363
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/10.1016/0031-9422(89)80156-6
1-[2,6-dihydroxy-4-methoxy-3-[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]phenyl]-3-phenylpropan-1-one 14237696 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(89)80156-6
2',4',6'-Trihydroxydihydrochalcone 1226045 Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2O)O)O 258.27 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/S0031-9422(00)82646-1
2',6'-Dihydroxy-4'-methoxydihydrochalcone 169676 Click to see 272.29 unknown https://doi.org/10.1016/0031-9422(88)80479-5
https://doi.org/10.1016/S0031-9422(00)82646-1
3-Phenyl-1-[2,4,6-trihydroxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]propan-1-one 353260 Click to see 394.50 unknown https://doi.org/10.1002/CHIN.198844339
https://doi.org/10.1248/CPB.32.3747
https://doi.org/10.1016/0031-9422(88)80479-5
Methyllinderatin 42607684 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(89)80156-6
Neolinderatin 42607685 Click to see 530.70 unknown https://doi.org/10.1246/CL.1989.363
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(5aR,6R,9R,9aS)-3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl]-3-phenylprop-2-en-1-one 10047873 Click to see CC(C)C1CCC(C2C1C3=C(C=C(C(=C3O2)C(=O)C=CC4=CC=CC=C4)O)OC)(C)O 422.50 unknown https://doi.org/10.1248/CPB.43.893
(E)-1-[2,6-dihydroxy-4-methoxy-3-[(1R,6R)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]phenyl]-3-phenylprop-2-en-1-one 102431467 Click to see 406.50 unknown https://doi.org/10.1016/0031-9422(88)83049-8
(E)-3-phenyl-1-[2,4,6-trihydroxy-3-[(1S,6S)-3-methyl-6-propan-2-ylcyclohex-2-en-1-yl]phenyl]prop-2-en-1-one 14237694 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(89)80156-6
1-(3,6-dihydroxy-1-methoxy-6-methyl-9-propan-2-yl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-4-yl)-3-phenylprop-2-en-1-one 78384681 Click to see 422.50 unknown https://doi.org/10.1248/CPB.43.893
1-[2,6-Dihydroxy-4-methoxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]-3-phenylprop-2-en-1-one 363080 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C=C(C(=C2O)C(=O)C=CC3=CC=CC=C3)O)OC 406.50 unknown https://doi.org/10.1016/0031-9422(88)83049-8
2-Propen-1-one, 1-(2,6-dihydroxy-3,4-dimethoxyphenyl)-3-phenyl-, (E)-; (2E)-1-(2,6-Dihydroxy-3,4-dimethoxyphenyl)-3-phenyl-2-propen-1-one 179543 Click to see 300.30 unknown https://doi.org/10.1021/NP50059A016
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/10.1016/0031-9422(88)83049-8
2',6'-Dihydroxy-4'-methoxychalcone 5316793 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(88)83049-8
3-Phenyl-1-[2,4,6-trihydroxy-3-(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]prop-2-en-1-one 74819237 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(89)80156-6
3-Phenyl-1-[2,4,6-trihydroxy-3,5-bis(3-methyl-6-propan-2-ylcyclohex-2-en-1-yl)phenyl]prop-2-en-1-one 74819238 Click to see CC1=CC(C(CC1)C(C)C)C2=C(C(=C(C(=C2O)C(=O)C=CC3=CC=CC=C3)O)C4C=C(CCC4C(C)C)C)O 528.70 unknown https://doi.org/10.1246/CL.1989.363
Linderachalcone 42607599 Click to see 392.50 unknown https://doi.org/10.1248/CPB.37.944
https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1016/0031-9422(89)80156-6
Linderol A 42607591 Click to see 422.50 unknown https://doi.org/10.1248/CPB.43.893
Neolinderachalcone 42607600 Click to see 528.70 unknown https://doi.org/10.3987/COM-89-5282
https://doi.org/10.1246/CL.1989.363
Pashanone 6254251 Click to see 300.30 unknown https://doi.org/10.1021/NP50059A016
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-[(2S)-2-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propyl]-5-methoxybenzene-1,3-diol 163190396 Click to see 320.30 unknown https://doi.org/10.1248/CPB.33.2281
4-[2-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)propyl]-5-methoxybenzene-1,3-diol 21633049 Click to see COC1=CC(=CC(=C1CC(CC2=CC(=C(C=C2)O)OC)O)O)O 320.30 unknown https://doi.org/10.1248/CPB.33.2281
> Phenylpropanoids and polyketides / Tannins
beta-D-Glucopyranose, 2-((2E)-3-phenyl-2-propenoate) 1-(3,4,5-trihydroxybenzoate) 5315898 Click to see 462.40 unknown via CMAUP database

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