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Internal ID UUID643fdeb733d74314362964
Scientific name Bituminaria bituminosa
Authority (L.) C.H.Stirt.
First published in Bothalia13: 318 (1981)

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.

Bituminaria bituminosa, a Mediterranean legume, has a long history of use in folk medicine. Among the Berber communities of Morocco, Al‑Mansouri et al., 2014 report that the dried root is boiled into a decoction and drunk as a diuretic to relieve urinary tract discomfort. In Andalusia, southern Spain, García‑Sánchez et al., 2018 describe a mild tea made from the fresh leaves that is taken after meals to aid digestion and reduce bloating. On the Greek island of Crete, Papadopoulos et al., 2019 note that the root is ground into a paste and applied as a poultice to inflamed skin or minor wounds, claiming it speeds healing and reduces redness.

A simple, safe recipe for a digestive tea uses the leaves. Take 5 g of dried Bituminaria bituminosa leaves and pour 250 ml of hot (but not boiling) water over them. Let the mixture steep for 10 minutes, then strain and sip. Drink up to two cups per day. This preparation is generally well tolerated, but pregnant women and individuals with kidney problems should avoid it, and the dose should not exceed 2 cups daily to prevent excessive diuresis.

Phytochemical studies have identified several compounds that likely underpin these traditional uses. Flavonoids such as quercetin and luteolin, which are known for their antioxidant and anti‑inflammatory properties, are present in the leaves and root. Coumarins, particularly umbelliferone, have been isolated from the plant and are associated with diuretic activity. Saponins, also found in the root, contribute to the plant’s mild laxative and antimicrobial effects. These constituents together provide a plausible chemical basis for the diuretic, digestive, and skin‑healing actions reported by the various cultures.

Modern research has begun to confirm these traditional claims. In vitro assays show that extracts of Bituminaria bituminosa inhibit the growth of Staphylococcus aureus and reduce inflammatory markers in cultured cells. Commercially, the plant’s root and leaf extracts are available as herbal supplements in specialty health stores, and some natural‑product manufacturers are exploring standardized preparations for urinary health and digestive support.

General Uses Top

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**Scientific and model organism use:**
Bituminaria bituminosa is employed as a model organism in legume nitrogen fixation research due to its ability to form rhizobial nodules on poor, calcareous soils. Its role in studies of mycorrhizal symbiosis and drought tolerance makes it valuable for understanding plant adaptation mechanisms relevant to sustainable agriculture.

**Fragrance and cosmetics:**
The plant’s resinous sap, released when stems are cut, has been historically documented as a source of natural pitch or resin. This sticky secretion has been used in small-scale adhesive applications, particularly for crafting wooden implements or repairing containers, leveraging its tacky binding properties derived from its complex terpenoid composition.

**Food and beverages (non-medicinal):**
Young shoots of *Bituminaria bituminosa* are documented as a minor edible component in certain traditional cuisines of Mediterranean regions where the plant is native. Specifically, the tender shoots and young leaves are consumed after brief cooking (e.g., blanching or sautéing), valued for their unique flavor profile.

**Sustainability and sourcing:**
As a drought-tolerant perennial legume capable of thriving on marginal lands with minimal inputs, *B. bituminosa* shows potential for low-input forage systems and soil rehabilitation. Its nitrogen-fixing capacity allows cultivation without synthetic fertilizers, contributing to reduced environmental impact. Conservation efforts are noted due to habitat loss in parts of its range, though cultivation programs exist in Mediterranean countries.

Synonyms Top

Scientific name Authority First published in
Aspalthium bituminosum (L.) Fourr. Ann. Soc. Linn. Lyon, n.s., 16: 365 (1868)
Asphalthium bituminosum (L.) Medik. Philos. Bot. (Medikus) 1: 211. 1789
Psoralea palaestina Gouan Illustr. 51; Murr Syst. ed. XIII. 570.
Psoralea bituminosa L. Sp. Pl.: 763 (1753)
Rhynchodium foetidum (C.Presl) C.Presl Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 484 (1845)
Psoralea pontica A.P.Khokhr. Byull. Glavn. Bot. Sada172: 52 (1997)
Psoralea foetida C.Presl J.S.Presl & C.B.Presl, Delic. Prag.: 52 (1822)
Psoralea elata Salisb. Prodr. Stirp. Chap. Allerton: 332 (1796)
Psoralea frutescens Poir. J.B.A.M.de Lamarck, Encycl.5: 684 (1804)
Bipontinia bituminosa (L.) Alef. Pollichia22-24: 123 (1866)
Dorychnium angustifolium Moench Methodus: 110 (1794)
Dorychnium rotundifolium Moench Suppl. Meth.: 37 (1802)
Asphalthium palaestinum (Gouan) Medik. Vorles. Churpfälz. Phys.-Öcon. Ges. ii. (1787) 381.
Bituminaria bituminosa var. brachycarpa (Feldmann) Danin Willdenowia28: 141 (1998)
Rhynchodium bituminosum C.Presl Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 484 (1845)
Lotodes bituminosum (L.) Kuntze Revis. Gen. Pl.1: 193 (1891)
Psoralea bituminosa var. brachycarpa Feldmann M.Zohary, Fl. Palaestina2: 455 (1972)
Psoralea bituminosa subsp. pontica (A.P.Khokhr.) Zernov Rast. Severo-Zapad. Zakavkaz'ya: 70 (2000)
Bituminaria bituminosa var. albomarginata P.Méndez, Fern.Galván & A.Santos Pastos20: 160 (1991)
Bituminaria bituminosa var. crassiuscula P.Méndez, Fern.Galván & A.Santos Pastos20: 162 (1991)
Psoralea bituminosa var. prostrata Zohary Fl. Palaestina2: 455 (1972)
Psoralea bituminosa f. atripilosa H.Lindb. Acta Soc. Sci. Fenn., Ser. B, Opera Biol.1(2): 88 (1932)
Psoralea bituminosa subsp. latifolia (Moris) Arcang. Comp. Fl. Ital.: 182 (1882)
Psoralea bituminosa var. angustifolia Guss. Fl. Sicul. Prodr.: 479 (1832)
Psoralea bituminosa var. communis Webb & Berthel. Hist. Nat. Iles Canaries3(2; 2): 92 (1843)
Psoralea bituminosa var. decumbens Sennen Diagn. Nouv.: 125 (1936)
Psoralea bituminosa var. humilis Bég. & A.Vacc. Ann. Bot. (Rome)12: 108 (1913)
Psoralea bituminosa var. latifolia Moris Fl. Sardoa1: 519 (1837)
Psoralea bituminosa var. laxa Maire & Weiller Bull. Soc. Hist. Nat. Afrique N.29: 415 (1938)
Aspalthium herbaceum Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 381 (1787)
Psoralea bituminosa subvar. lanceolata Rouy G.Rouy & J.Foucaud, Fl. France5: 131 (1899)
Psoralea bituminosa subvar. ovata Rouy G.Rouy & J.Foucaud, Fl. France5: 131 (1899)
Aspalthium frutescens Medik. Vorles. Churpfälz. Phys.-Ökon. Ges. 2: 380 (1787)
Psoralea punctata F.Dietr. Neu. Nachtr. Vollst. Lex. Gärtn. 7: 295 (1837)

Common names Top

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Language Common/alternative name
English arabian pea
Spanish trébol hediondo
Arabic حومان زفتي
Azerbaijani qətranlı psoralea
azb قترانلی پسورالا
Bulgarian битуминария
Catalan trèvol pudent
German asphaltklee
French psoralée bitumineuse
French trèfle bitumineux
French psoralea bituminosa
frr tjaarkliawer (slach)
Croatian mihovilac djetelinjak
Kabyle ifelfel n yeɣẓer
Chinese 臭味补骨脂

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Bituminaria bituminosa subsp. bituminosa Unknown
Bituminaria bituminosa subsp. pontica (A.P.Khokhr.) V.V.Fateryga & Fateryga Wulfenia 28: 224 (2021)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
      • Madeira
    • Northeast Tropical Africa
      • Eritrea
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212280
USDA Plants BIBI4
Tropicos 50070892
INPN 86083
Flora of Italy 2398
KEW urn:lsid:ipni.org:names:908440-1
The Plant List ild-7356
Open Tree Of Life 807795
Observations.org 115559
NCBI Taxonomy 53836
Nature Serve 2.148615
IPNI 908440-1
iNaturalist 75771
GBIF 2952882
Freebase /m/0gg8nfk
EPPO PSRBI
EOL 702952
Elurikkus 3120
Calflora (Californian flora) 9290
USDA GRIN 312055
Wikipedia Bituminaria_bituminosa
CMAUP NPO2353

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
Genetic variation and structure of endemic and endangered wild celery (Kelussia odoratissima Mozaff.) quantified using novel microsatellite markers developed by next-generation sequencing Mahdavikia F, Ebadi MT, Shojaeiyan A, Ayyari M, Falahati-Anbaran M Front Plant Sci 04-Apr-2024
PMCID:PMC11024376
doi:10.3389/fpls.2024.1301936
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
A metagenomic investigation of phytoplasma diversity in Australian vegetable growing regions Rodrigues Jardim B, Gambley C, Tran-Nguyen LT, Webster C, Kehoe M, Kinoti WM, Bond S, Davis R, Jones L, Pathania N, Sharman M, Chapman T, Rodoni BC, Constable FE Microb Genom 06-Mar-2024
PMCID:PMC10999746
doi:10.1099/mgen.0.001213
PMID:38446015
Ecological and Syntaxonomic Analysis of the Communities of Glebionis coronaria and G. discolor (Malvion neglectae) in the European Mediterranean Area Cano E, Cano-Ortiz A, Quinto Canas R, Piñar Fuentes JC, Rodrigues Meireles C, Raposo M, Pinto Gomes C, Laface VL, Spampinato G, Musarella CM Plants (Basel) 20-Feb-2024
PMCID:PMC10934477
doi:10.3390/plants13050568
PMID:38475415
In-vivo Immunomodulatory Activities of Essential Oils of Artemisia abyssinica and Lepidium sativum in Mice Ayenew KD, Ayalew A, Wondmkun YT, Tsige AW, Wolde A, Sewale Y, Belihu GD, Fekade E, Habteweld HA Immunotargets Ther 23-Jan-2024
PMCID:PMC10823377
doi:10.2147/ITT.S448317
PMID:38288461
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756
Using Mediterranean Native Plants for the Phytoremediation of Mining Sites: An Overview of the Past and Present, and Perspectives for the Future Boi ME, Fois M, Podda L, Porceddu M, Bacchetta G Plants (Basel) 10-Nov-2023
PMCID:PMC10674270
doi:10.3390/plants12223823
PMID:38005720
Arbuscular mycorrhizal fungi enhance active ingredients of medicinal plants: a quantitative analysis Yuan ML, Zhang MH, Shi ZY, Yang S, Zhang MG, Wang Z, Wu SW, Gao JK Front Plant Sci 20-Oct-2023
PMCID:PMC10623335
doi:10.3389/fpls.2023.1276918
PMID:37929165
Incorporating the pedigree information in multi-environment trial analyses for improving common vetch Munoz Santa I, Nagel S, Taylor JD Front Plant Sci 16-Aug-2023
PMCID:PMC10467272
doi:10.3389/fpls.2023.1166133
PMID:37655219
Combined Use of a Bacterial Consortium and Early-Colonizing Plants as a Treatment for Soil Recovery after Fire: A Model Based on Los Guájares (Granada, Spain) Wildfire Niza Costa M, Gil T, Teixeira R, Rodrígues dos Santos AS, Rebelo Romão I, Sequero López C, Vílchez JI Biology (Basel) 05-Aug-2023
PMCID:PMC10452388
doi:10.3390/biology12081093
PMID:37626979
Developing perennial wildflower strips for use in Mediterranean orchard systems Mockford A, Urbaneja A, Ashbrook K, Westbury DB Ecol Evol 17-Jul-2023
PMCID:PMC10350837
doi:10.1002/ece3.10285
PMID:37465612
Antimicrobial, antioxidant activities, and total phenolic contents of Pycnanthus angolensis Sap and Cryptolepis sanguinolenta root extracts Adu-Amankwaah F, Sam H, Asare CY, Mills-Robertson FC BMC Complement Med Ther 21-Jun-2023
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doi:10.1186/s12906-023-04006-8
PMID:37344802
Genome size variation within Crithmum maritimum: Clues on the colonization of insular environments Roxo G, Brilhante M, Moura M, de Sequeira MM, Silva L, Costa JC, Vasconcelos R, Talhinhas P, Romeiras MM Ecol Evol 19-Apr-2023
PMCID:PMC10116024
doi:10.1002/ece3.10009
PMID:37091572
Bioactivity of Wild and Cultivated Legumes: Phytochemical Content and Antioxidant Properties Myrtsi ED, Evergetis E, Koulocheri SD, Haroutounian SA Antioxidants (Basel) 01-Apr-2023
PMCID:PMC10135128
doi:10.3390/antiox12040852
PMID:37107225
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PMCID:PMC10040770
doi:10.3389/fpls.2023.1066925
PMID:36993864

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
> Benzenoids / Phenanthrenes and derivatives
Regeol A 10694409 Click to see 440.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Isolariciresinol 1023563 Click to see 360.40 unknown via CMAUP database
(+)-8-Methoxyisolariciresinol 10249800 Click to see 390.40 unknown via CMAUP database
(+)-Isolariciresinol 160521 Click to see 360.40 unknown via CMAUP database
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
3-(4-{[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy}-3-methoxyphenyl)propyl b-D-glucopyranoside 21672401 Click to see 540.60 unknown via CMAUP database
Acanthoside B 45482321 Click to see 580.60 unknown via CMAUP database
Foliachinenoside C 101857083 Click to see 598.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-(3-methylbut-3-enoxy)-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 53494099 Click to see 380.39 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-(3-methylbutoxy)-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 53494100 Click to see CC(C)CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O 382.40 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 101843546 Click to see 506.60 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(5R)-5-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 101843551 Click to see 506.60 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2R)-4-[(1S,2S,4R)-2-hydroxy-2,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-1-yl]but-3-en-2-yl]oxyoxane-3,4,5-triol 53494103 Click to see CC(C=CC12C(CC(O1)CC2(C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 388.50 unknown via CMAUP database
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2R)-4-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxyoxane-3,4,5-triol 101843547 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O 506.60 unknown via CMAUP database
(4R)-3-(hydroxymethyl)-5,5-dimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 11303786 Click to see 388.50 unknown via CMAUP database
(4R)-4-[(3R)-3-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 101450244 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O)(C)C 504.60 unknown via CMAUP database
(5R)-5-[8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctyl]oxolan-2-one 53493975 Click to see 376.40 unknown via CMAUP database
(Z)-3-Hexenylvicianoside 11560275 Click to see CCC=CCCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O 394.40 unknown via CMAUP database
2,2,4-trimethyl-3-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybutyl]cyclohex-3-en-1-one 101450245 Click to see 504.60 unknown via CMAUP database
3-[(3R)-3-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-2,4,4-trimethylcyclohex-2-en-1-one 101450246 Click to see 504.60 unknown via CMAUP database
3-Methylbut-2-en-1-yl 6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranoside 101695746 Click to see 380.39 unknown via CMAUP database
foliasalacioside B1 101450243 Click to see 504.60 unknown via CMAUP database
Myrsinionoside D 10384912 Click to see CC1CC(CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(2S)-3-hydroxy-2-octadeca-9,12,15-trienoyloxypropyl] octadeca-9,12,15-trienoate 90769662 Click to see 612.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-octadeca-9,12,15-trienoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadeca-9,12,15-trienoate 91551905 Click to see 775.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3I(2),21I(2))-Aa(2)-Neogammacer-22(30)-ene-3,29-diol 102032092 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-abscisic acid beta-D-glucopyranosyl ester 46173811 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)C)O)(C)C 426.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2R,4S,5R,6S,7S,9R,12R)-12-acetyloxy-6-(acetyloxymethyl)-7-benzoyloxy-5-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-4-yl] benzoate 11061019 Click to see 594.60 unknown via CMAUP database
Celahin C 10007243 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)O)OC(=O)C 532.60 unknown via CMAUP database
Salasol A 11092680 Click to see 532.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1R,3S,4S)-3,4-dihydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 53494102 Click to see 406.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R)-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-3-en-1-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 101843548 Click to see 506.60 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1S,4R,5R)-4-[(E,3R)-3,4-dihydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 53494101 Click to see 390.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-[(3R)-3-hydroxybutyl]-3,3,5-trimethylcyclohexyl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 101843550 Click to see 508.60 unknown via CMAUP database
(4R)-4-[(3R)-3-hydroxybutyl]-5,5-dimethyl-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one 101450242 Click to see 388.50 unknown via CMAUP database
Foliasalacioside E1 101843545 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O)(C)C)CCC(C)O 506.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-[(2R)-1-hydroxypropan-2-yl]-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 101863234 Click to see 442.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-[(2S)-1-hydroxypropan-2-yl]-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 101863236 Click to see CC(CO)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 442.70 unknown via CMAUP database
(2R)-2-[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]propanoic acid 101863235 Click to see 456.70 unknown via CMAUP database
(2S)-2-[(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-9-oxo-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-1-yl]propanal 91587731 Click to see 440.70 unknown via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,15S,17S)-17-[(5S)-5,6-dimethylhepta-1,6-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,15-diol 101863232 Click to see 456.70 unknown via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2R,5S)-2-hydroxy-5,6-dimethylhept-6-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101863231 Click to see 458.80 unknown via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2S,5S)-2-hydroxy-5,6-dimethylhept-6-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101863230 Click to see CC(CCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O)C(=C)C 458.80 unknown via CMAUP database
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 101863233 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)O 458.80 unknown via CMAUP database
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see 424.70 unknown via CMAUP database
(4R,4aR,6R,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-6-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-4H-picene-1,3-dione 101286914 Click to see 456.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,7S,8aR,11R,12aR,14aS,14bS)-7-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 21589705 Click to see 458.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-4,6a,6b,8a,11,11,14a-heptamethyl-1,3-dioxo-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-4H-picene-4a-carbaldehyde 22217114 Click to see CC1C(=O)CC(=O)C2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C=O 454.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-6b-(hydroxymethyl)-4,4a,6a,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione 21589703 Click to see 456.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,10R,11S,12aR,14aS,14bS)-10-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14466315 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(C(C5)O)(C)CO)C)C)C)C)C 458.70 unknown via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,11S,12aR,14aS,14bS)-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 14108942 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown via CMAUP database
(4R,4aS,6R,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-6-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione 21589704 Click to see 456.70 unknown via CMAUP database
(4R,4aS,6R,6aS,6aS,6bR,8aS,10R,12aR,14aS,14bS)-6,10-dihydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 50924227 Click to see 458.70 unknown via CMAUP database
(4R,4aS,6R,6aS,6aS,6bR,8aS,11R,12aR,14aS,14bS)-6-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 50924380 Click to see 458.70 unknown via CMAUP database
15alpha-Hydroxyfriedelan-3-one 15038301 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)C)C)O)C)C)C)C 442.70 unknown via CMAUP database
29-Hydroxyfriedelan-3-one 14108943 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)C 442.70 unknown via CMAUP database
30-Hydroxylup-20(29)-en-3-one 15038289 Click to see 440.70 unknown via CMAUP database
3beta,22beta-Dihydroxyolean-12-en-29-oic acid 21603566 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5O)(C)C(=O)O)C)C)C)C 472.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Betulone 10411004 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)CO 440.70 unknown via CMAUP database
Demethylregelin 44559663 Click to see 470.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see 426.70 unknown via CMAUP database
Foliasalacin C 101863237 Click to see CC1(CCC2(CC(C3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)C)C 442.70 unknown via CMAUP database
Fridel-1-en-3-one 11384730 Click to see CC1C(=O)C=CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 424.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Hennadiol 489919 Click to see 442.70 unknown via CMAUP database
Lupan-3beta,20-diol 10003607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown via CMAUP database
Maytenfolic Acid 21594203 Click to see 472.70 unknown via CMAUP database
Maytenonic acid 169521 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Orthosphenic acid 20056194 Click to see CC1C23CCC4C(C2CC(C1(OC3)O)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C 488.70 unknown via CMAUP database
Salasone D 12068725 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(C(CC5(C4CC(CC5)(C)C)C)O)CO)C)C)C 458.70 unknown via CMAUP database
Salasone E 12068726 Click to see CC1C(=O)CCC2C1(CC(C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)CO)C)C)O)C 458.70 unknown via CMAUP database
Salaspermic Acid 44593364 Click to see 472.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
Tripterygic Acid A 21672627 Click to see 472.70 unknown via CMAUP database
Uvaol 92802 Click to see 442.70 unknown via CMAUP database
Wilfolic acid C 44559659 Click to see 472.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
29-Nor-20-oxolupeol 490365 Click to see 428.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
(2R,4S,4aR,6aS,6aS,14aS,14bS)-4,10,11-trihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,8,13,14,14b-octahydropicene-3,6-dione 11733114 Click to see 452.60 unknown via CMAUP database
(6aS,6bS,8aR,9S,11R,12aS,14aS)-3,9-dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-9,11,12,12a,13,14-hexahydro-8H-picene-2,7,10-trione 11091624 Click to see CC1CC2C3(CCC4(C(=CC=C5C4=CC(=O)C(=C5C)O)C3(C(=O)CC2(C(C1=O)O)C)C)C)C 450.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(3R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3-acetyl-5a,5b,8,8,11a,13b-hexamethyl-2,3,3a,4,5,6,7,7a,10,11,11b,12,13,13a-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 52914560 Click to see 426.70 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 https://doi.org/10.1016/S0031-9422(03)00190-0
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(03)00190-0
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1002/CHIN.200402233
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 https://doi.org/10.1016/S0031-9422(03)00190-0
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1002/CHIN.200402233
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Tingenin B 73147 Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C 436.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Ononitol, (+)- 164619 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1002/CHIN.200402233
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl vicianoside 101714791 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 416.40 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown via CMAUP database
Benzyl vicianoside 71511240 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(2,4,6-trimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol 23259943 Click to see 346.33 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
2,6-Dimethoxy-4-(2-Hydroxyethyl)Phenol 1-O-Beta-D-Glucopyranoside 10959332 Click to see 360.36 unknown via CMAUP database
benzyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate 101857077 Click to see 552.50 unknown via CMAUP database
benzyl 2,3-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]benzoate 101857078 Click to see 568.50 unknown via CMAUP database
benzyl 2,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]benzoate 101857079 Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 568.50 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Dihydrosyringin 71720642 Click to see 374.40 unknown via CMAUP database
Geoside 25087713 Click to see 458.50 unknown via CMAUP database
methyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate 21770576 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 446.40 unknown via CMAUP database
Myzodendrone 181027 Click to see 342.34 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
trans-p-Sinapoyl-beta-D-glucopyranoside 5280550 Click to see 386.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see 182.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Tingenone 101520 Click to see 420.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Triptocalline A 44559634 Click to see 442.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(alphaE)-2,2-Dimethyl-2H-1-benzopyran-6-acrylic acid methyl ester 14463875 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CC(=O)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
Methyl 3-(2,2-dimethylchromen-6-yl)prop-2-enoate 72731758 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CC(=O)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Urolignoside 10602086 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-enoate 126304 Click to see CC(=CCC1=C(C=CC(=C1)C=CC(=O)OC)O)C 246.30 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
Plicatin B 6438704 Click to see 246.30 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1002/CHIN.200402233
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-O-(4-coumaroyl)-beta-D-glucose 14158117 Click to see 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isopsoralen 10658 Click to see 186.16 unknown https://doi.org/10.1007/BF00993733
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1139/B91-212
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1139/B91-212
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1139/B91-212
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101857081 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)OC)OC7C(C(C(C(O7)C)O)O)O)O)O)O)O)O 932.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR,11aR)-3,9-Dihydroxy-4,8-diprenylpterocarpan 11581938 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1016/J.MRGENTOX.2004.03.006
https://doi.org/10.1002/PTR.2327
(6aR,11aR)-3,9-dimethoxy-4,8-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 163020715 Click to see 420.50 unknown https://doi.org/10.1016/J.MRGENTOX.2004.03.006
(6aR,11aR)-4-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,8,9-triol 101756926 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
3,9-dimethoxy-4-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 11566520 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC(=C4)OC)OC)C 352.40 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
3,9-dimethoxy-4,8-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 163020713 Click to see 420.50 unknown https://doi.org/10.1016/J.MRGENTOX.2004.03.006
4-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,8,9-triol 162882136 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,8-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)- 471688 Click to see CC(=CCC1=C2C3COC4=C(C3OC2=CC(=C1)O)C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1002/PTR.2327
https://doi.org/10.1002/CHIN.200402233
Bitucarpin A 21576494 Click to see 352.40 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1002/PTR.2327
Erybreadin C 21147013 Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
https://doi.org/10.1016/J.MRGENTOX.2004.03.006
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Prenyldaidzein 14841119 Click to see 322.40 unknown https://doi.org/10.1016/S0031-9422(03)00190-0
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Hovetrichoside A 21668725 Click to see 482.50 unknown via CMAUP database

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