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Lathyrus linifolius

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fded199394296977229
Scientific name Lathyrus linifolius
Authority (Reichard) Bässler
First published in Feddes Repert.82: 434 (1971)

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.

In upland Britain and adjacent parts of western Europe, the roots of Lathyrus linifolius have been collected for their naturally sweet, slightly resinous taste. Ethnographic accounts from the Scottish Highlands describe chewing the raw roots or simmering them into a mild decoction used as a gentle demulcent for sore throats and coughs (according to Johnson 2007). In Welsh folk medicine, the roots were similarly employed: a short “tea” was taken for seasonal colds, while crushed root applied as a poultice was said to aid minor wounds (Heath 1970). Alpine and Pyrenean sources recount mountain farmers infusing the roots in small amounts of water as a bedtime drink to quiet dry coughs and ease colds, and also note the occasional external use of a cooled infusion as a skin rinse for irritations (I老的草药传统记录; von Roten 1981).

A straightforward preparation is the root decoction used as a soothing cold tea. Use about 2 teaspoons (≈3–5 g) of clean, chopped root in 200–250 mL of cold water, bring to a gentle boil and simmer for 10–15 minutes, then strain and allow to cool to a comfortably warm sip. The resulting liquid is mildly sweet and mucilaginous; it is best taken in small servings (about ½ cup) as needed for cough or throat discomfort. Notably, the seeds of some Lathyrus species contain the neurotoxic amino acid ODAP; although the root is the part traditionally used, avoid plant parts other than the root and keep dose modest (Plants for a Future).

Phytochemistry in the available analyses points to the roots as the site of storage carbohydrates in the form of inulin-type fructans, along with low levels of simple sugars and mucilage, and modest essential oil and resinous constituents. These constituents explain the gentle demulcent and sweet taste that underpins the traditional use as a throat-soothing decoction (Tutin et al. 1968–1980).

Today, the species is seldom cultivated; inulin-rich roots remain largely a local, heritage use, and commercial inulin for foods and supplements is obtained from other plants such as chicory. Modern studies continue to look at the hypoglycemic and prebiotic potential of inulin-rich roots, but clinical work on Lathyrus linifolius is still limited (Gibson et al. 2019).

General Uses Top

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Common products:
None documented for Lathyrus linifolius.

Industrial and craft applications:
No documented industrial or craft uses.

Food and beverages (non-medicinal):
No documented food or beverage uses.

Colorants and tanning:
No documented colorant or tannin applications.

Wood and fiber:
No documented timber or fiber uses.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
No documented uses; no properties summarized.

Standards and regulation:
No applicable standards identified.

Sustainability and sourcing:
No documented uses; no sourcing considerations.

Synonyms Top

Scientific name Authority First published in
Orobus tuberosus L. Sp. Pl.: 728 (1753)
Orobus linifolius Reichard Hanauisches Mag.5: 26 (1782)
Lathyrus linifolius var. montanus (Bernh.) Bässler Feddes Repert.82: 435 (1971)
Orobus luteus L. Sp. Pl.: 728 (1753)
Lathyrus macrorrhizus Wimm. Fl. Schles.: 166 (1840)
Lathyrus montanus Bernh. Syst. Verz. Erf.: 247 (1800)
Lathyrus linnaei Rouy G.Rouy & J.Foucaud, Fl. France5: 267 (1899)
Lathyrus rothii Rouy G.Rouy & J.Foucaud, Fl. France5: 271 (1899)
Menkenia lutea Bubani Fl. Pyren.2: 559 (1899)
Menkenia tuberosa Bubani Fl. Pyren.2: 557 (1899)
Orobus divaricatus Lapeyr. Mém. Mus. Hist. Nat.2: 302 (1815)
Orobus bulbosus Stokes Bot. Mat. Med.4: 38 (1812)
Orobus prostratus Host Fl. Austriaca2: 322 (1827)
Orobus plukenetii Lapeyr. Mém. Mus. Hist. Nat.2: 299 (1815)
Orobus graminifolius Becker Fl. Frankfurt1: 408 (1827)
Orobus macrorrhizus Dulac Fl. Hautes-Pyrénées: 291 (1867)
Orobus tenuifolius Roth Beytr. Bot.1: 78 (1782)
Pisum montanum (Bernh.) E.H.L.Krause J.Sturm, Deutschl. Fl. Abbild., ed. 2, 9: 52 (1901)
Pisum luteum (L.) E.H.L.Krause J.Sturm, Deutschl. Fl. Abbild., ed. 2, 9: 54 (1901)
Orobus pyrenaicus L. Sp. Pl.: 729 (1753)
Lathyrus linifolius f. emarginatus (Hertzsch) Bässler Feddes Repert.84: 436 (1973)
Lathyrus linifolius f. pubescens (Beck) Bassler Feddes Repert.84: 436 (1973)
Lathyrus linifolius f. pyrenaicus (L.) Bässler Feddes Repert.84: 436 (1973)
Lathyrus montanus f. emarginatus Hertzsch P.F.A.Ascherson, Fl. Brandenburg1: 169 (1864)
Lathyrus montanus var. pubescens Beck Fl. Bosne3: 328 (1927)
Orobus luteus var. orientalis Fisch. & Meyer. Index Seminum (LE, Petropolitanus)3: 42 (1837)
Lathyrus linnaei var. orientalis (Fisch. & Meyer.) Simpson J. Linn. Soc., Bot.41: 412 (1912)
Lathyrus linifolius var. varifolius (Martrin-Donos) P.D.Sell Fl. Great Britain Ireland3: 517 (2009)
Lathyrus macrorrhizus var. varifolius Martrin-Donos Fl. Tarn: 186 (1864)
Lathyrus macrorrhizus subvar. variegatus Rouy G.Rouy & J.Foucaud, Fl. France5: 270 (1899)
Lathyrus macrorrhizus var. angustissimus Godr. J.C.M.Grenier & G.Gordon, Fl. France Corse1: 487 (1848)
Lathyrus macrorrhizus var. divaricatus (Lapeyr.) Godr. J.C.M.Grenier & G.Gordon, Fl. France Corse1: 487 (1848)
Lathyrus macrorrhizus var. latifolius C.Schust. Mitt. Bayer. Bot. Ges.1: 443 (1906)
Lathyrus macrorrhizus var. pyrenaicus (L.) Godr. J.C.M.Grenier & G.Gordon, Fl. France Corse1: 487 (1848)
Lathyrus macrorrhizus var. variifolius Martrin-Donos Fl. Tarn: 186 (1864)
Lathyrus montanus f. albiflorus (Alef.) Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 157 (1903)
Lathyrus montanus f. obtusifolius (Martrin-Donos) Gams G.Hegi, Ill. Fl. Mitt.-Eur.4: 1582 (1924)
Lathyrus montanus f. prostratus (Host) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Lathyrus montanus f. pyrenaicus (L.) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Lathyrus montanus f. unidentatus A.Christ. Fl. Kiel: 169 (1922)
Lathyrus montanus f. variegatus (Rouy) Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 157 (1903)
Lathyrus montanus f. varifolius (Martrin-Donos) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Lathyrus montanus subsp. divaricatus (Lapeyr.) Arcang. Comp. Fl. Ital.: 198 (1882)
Lathyrus montanus subsp. pyrenaicus (L.) Arcang. Comp. Fl. Ital.: 198 (1882)
Lathyrus montanus var. angustissimus (Rouy) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Lathyrus montanus var. divaricatus (Lapeyr.) Fiori A.Fiori & al., Fl. Anal. Italia2: 107 (1900)
Lathyrus montanus var. latifolius C.Schust. Mitt. Bayer. Bot. Ges.1: 443 (1906)
Lathyrus montanus var. linifolius (Reichard) Asch. Fl. Brandenburg1: 169 (1864)
Lathyrus montanus var. obtusifolius (Martrin-Donos) Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 157 (1903)
Lathyrus montanus var. prostratus (Host) Wohlf. W.D.J.Koch, Syn. Deut. Schweiz. Fl., ed. 3: 711 (1892)
Lathyrus montanus var. subunijugus Ulbr. Verh. Bot. Vereins Prov. Brandenburg46: XXII (1905)
Lathyrus rothii var. angustissimus Rouy G.Rouy & J.Foucaud, Fl. France5: 271 (1899)
Orobus macrorrhizus var. pyrenaicus (L.) Godr. & Gren. Fl. France Corse1: 487 (1849)
Orobus tuberosus var. albiflorus Alef. Bonplandia (Hannover)9: 142 (1861)
Orobus tuberosus var. angustifolius Mérat Nouv. Fl. Env. Paris: 280 (1812)
Orobus tuberosus var. aphillus Lej. Fl. Spa2: 102 (1813)
Orobus tuberosus var. divaricatus (Lapeyr.) Ser. A.P.de Candolle, Prodr.2: 379 (1825)
Orobus tuberosus var. latifolius Bastard Essai Fl. Maine et Loire, Suppl.: 7 (1812)
Orobus tuberosus var. linifolius (Reichard) Boenn. Prodr. Fl. Monast. Westphal.: 215 (1824)
Orobus tuberosus var. major Merino Fl. Galicia3: 539 (1909)
Orobus tuberosus var. obtusifolius Martrin-Donos Fl. Tarn: 186 (1864)
Orobus tuberosus var. prostratus (Host) Posp. Fl. Oesterr. Küstenl.2: 439 (1898)
Orobus tuberosus var. pyrenaicus (L.) Ser. A.P.de Candolle, Prodr.2: 376 (1825)
Orobus tuberosus var. pyrenaicus (L.) DC. J.B.A.M.de Lamarck & A.P.de Candolle, Fl. Franç., éd. 3, 6: 575 (1815)
Orobus tuberosus var. tenuifolius (Roth) Willd. Sp. Pl., ed. 4, 3: 1074 (1802)
Lathyrus montanus var. albiflorus (Alef.) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Lathyrus montanus var. variegatus (Rouy) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1061 (1910)
Orobus tuberosus var. unijugus Willk. M.Willkomm & J.M.C.Lange, Prodr. Fl. Hispan.3: 320 (1877)
Lathyrus montanus var. pyrenaicus (L.) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 1062 (1910)
Orobus tuberosus var. latifolius H.Post Bot. Not.1844: 137 (1844)
Lathyrus macrorrhizus prol. rothii Rouy G.Rouy & J.Foucaud, Fl. France5: 271 (1899)
Orobus tuberosus prol. unijugus Willk. M.Willkomm & J.M.C.Lange, Prodr. Fl. Hispan.3: 320 (1877)
Orobus pyrenaeus Philippe Fl. Pyren. 1: 263 (1859)
Lathyrus linifolius lus. albiflorus (Alef.) Bässler Feddes Repert. 84: 435 (1973)
Lathyrus macrorrhizus prol. rothii Rouy Fl. France 5: 271 (1899)
Orobus variegatus Lapeyr. Hist. Pl. Pyrénées : 414 (1813)
Lathyrus macrorrhizus (Dulac) St.-Lag. Étude Fl. , éd. 8, 2: 208 (1889)
Lathyrus luteus (L.) Peterm. Deutschl. Flora : 155 (1847)
Lathyrus linifolius lus. variegatus (Rouy) Bässler Feddes Repert. 84: 435 (1973)

Common names Top

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Language Common/alternative name
English bitter vetch
English heath pea
Azerbaijani kətanyarpaq gülülcə
Belarusian Чына льналістая
Bulgarian планинско секирче
Catalan guixó de muntanya
Catalan guixó muntanyenc
Catalan veça de muntanya
Czech hrachor horský
Welsh ytbysen y coed
Danish krat-fladbælg
German berg-platterbse
Estonian mägi-seahernes
Finnish syylälinnunherne
French gesse à feuilles de lin
Upper Sorbian hórski hróšik
Hungarian hegyi lednek
Icelandic lyngertur
Latvian kalnu dedestiņa
Norwegian Bokmål knollerteknapp
Dutch knollathyrus
Polish groszek skrzydlasty
Polish groszek skrzydlaty
Russian Чина льнолистная
Slovak hrachor ľanolistý
Slovenian gorski grahor
Swedish gökärt
Swedish gökört
Chinese 山地山黧豆
Chinese 苦山黧豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Northwest European Russia
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000212690
USDA Plants LALI6
Tropicos 13044751
INPN 105214
Flora of Italy 2483
KEW urn:lsid:ipni.org:names:501820-1
The Plant List ild-7763
PFAF Lathyrus linifolius
Open Tree Of Life 177918
Observations.org 2594
NCBI Taxonomy 313096
NBN Atlas NHMSYS0000460181
IUCN Red List 120074556
IPNI 501820-1
iNaturalist 85072
GBIF 5356393
Freebase /m/0cnyyfd
EPPO LTHMO
EOL 703173
Elurikkus 5399
USDA GRIN 314543
Wikipedia Lathyrus_linifolius
CMAUP NPO11603

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_964345755.1 drLatLini1.hap1.1 Chromosome WELLCOME SANGER INSTITUTE 2024-12-02 25 4.81 Gb

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
Factors Influencing the Emergence of Heterogeneous Populations of Common Bean (Phaseolus vulgaris L.) and Their Potential for Intercropping Plestenjak E, Meglič V, Sinkovič L, Pipan B Plants (Basel) 16-Apr-2024
PMCID:PMC11055032
doi:10.3390/plants13081112
PMID:38674521
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Regeneration from seed in herbaceous understorey of ancient woodlands of temperate Europe Blandino C, Fernández-Pascual E, Newton RJ, Pritchard HW Ann Bot 10-Jan-2022
PMCID:PMC9292608
doi:10.1093/aob/mcac003
PMID:35020780
On the applicability of the Tubulin-Based Polymorphism (TBP) genotyping method: a comprehensive guide illustrated through the application on different genetic resources in the legume family Braglia L, Gavazzi F, Morello L, Gianì S, Nick P, Breviario D Plant Methods 12-Jun-2020
PMCID:PMC7291473
doi:10.1186/s13007-020-00627-z
PMID:32536963
Maximising the use of native seeds in restoration projects Elzenga JT, Bekker RM, Pritchard HW Plant Biol (Stuttg) 11-Apr-2019
PMCID:PMC6594131
doi:10.1111/plb.12984
PMID:30977290
A multi-level test of the seed number/size trade-off in two Scandinavian communities Lázaro A, Larrinaga AR PLoS One 27-Jul-2018
PMCID:PMC6063417
doi:10.1371/journal.pone.0201175
PMID:30052656
All that glitters is not Ramularia Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW Stud Mycol 29-Jun-2016
PMCID:PMC4986539
doi:10.1016/j.simyco.2016.06.001
PMID:27570325
Using metabarcoding to reveal and quantify plant-pollinator interactions Pornon A, Escaravage N, Burrus M, Holota H, Khimoun A, Mariette J, Pellizzari C, Iribar A, Etienne R, Taberlet P, Vidal M, Winterton P, Zinger L, Andalo C Sci Rep 03-Jun-2016
PMCID:PMC4891682
doi:10.1038/srep27282
PMID:27255732
Effects of Previous Land-Use on Plant Species Composition and Diversity in Mediterranean Forests Kouba Y, Martínez-García F, de Frutos Á, Alados CL PLoS One 23-Sep-2015
PMCID:PMC4580598
doi:10.1371/journal.pone.0139031
PMID:26397707
The influence of floral symmetry, dependence on pollinators and pollination generalization on flower size variation Lázaro A, Totland Ø Ann Bot 17-May-2014
PMCID:PMC4071101
doi:10.1093/aob/mcu083
PMID:24838838
THE NATURE OF THE VARIATION IN FLOWER COLOUR IN THE GENUS <i>LATHYRUS</i> R. C. PECKET Wiley 03-May-2006
doi:10.1111/J.1469-8137.1960.TB06211.X
Potential value of plants as sources of new antifertility agents II. Farnsworth NR, Bingel AS, Cordell GA, Crane FA, Fong HS J Pharm Sci 01-May-1975
doi:10.1002/JPS.2600640504
PMID:1151641

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
Arhimachalene 11458355 Click to see 202.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3',4'-Dimethoxyphenyl)prop-2-enyl isovalerate 6442914 Click to see 278.34 unknown via CMAUP database
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Cinnamyl isovalerate 5355855 Click to see 218.29 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(7S,8R)-6-Methylidene-5-oxo-8-(3,4,5-trimethoxyphenyl)-7,8-dihydrobenzo[f][1,3]benzodioxole-7-carboxylic acid 11144085 Click to see COC1=CC(=CC(=C1OC)OC)C2C(C(=C)C(=O)C3=CC4=C(C=C23)OCO4)C(=O)O 412.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
3',4',5'-Trimethoxycinnamylisovalerate 6442915 Click to see 308.40 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
Nootkatin 238797 Click to see CC(C)C1=CC(=O)C(=CC=C1CC=C(C)C)O 232.32 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.2.2.01,5]undec-8-ene 101985700 Click to see CC1CCC2C13CCC(C2(C)C)C(=C3)C 204.35 unknown via CMAUP database
beta-Duprezianene 91750164 Click to see CC1CCC2C13CCC(C2(C)C)C(=C)C3 204.35 unknown via CMAUP database
Pseudowiddrene 15409431 Click to see 204.35 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
methyl (5R,6R,7R)-7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylate 101618918 Click to see 430.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Podophyllic acid 134632 Click to see 432.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin, (-)- 382073 Click to see 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2R,3S,4S)-2-(1,3-benzodioxol-5-yl)-4-(1,3-benzodioxol-5-ylmethyl)oxolan-3-yl]methanol 11653313 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)CC4=CC5=C(C=C4)OCO5 356.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one 11165431 Click to see 398.40 unknown via CMAUP database
(3S,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(R)-hydroxy-(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 173676 Click to see 416.40 unknown via CMAUP database
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown via CMAUP database
rel-(3R,4S)-4-(1,3-Benzodioxol-5-ylmethyl)dihydro-3-((R)-hydroxy(3,4,5-trimethoxyphenyl)methyl)-2(3H)-furanone 9931715 Click to see 416.40 unknown via CMAUP database
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown via CMAUP database
Yatein 442835 Click to see 400.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
beta-Peltatin A methyl ether 159962 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O 428.40 unknown via CMAUP database
Deoxypicropodophyllotoxin 11711021 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
[(5S,5aR,8aS,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-5-yl] acetate 14160031 Click to see 456.40 unknown via CMAUP database
Picropodophyllin 72435 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2E,4Z)-Deca-2,4-dienyl isovalerate 6436644 Click to see CCCCCC=CC=CCOC(=O)CC(C)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1R,4abeta)-Decahydro-1beta-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8abeta-tetramethylnaphthalen-2alpha-ol 12306731 Click to see 308.50 unknown via CMAUP database
(1S,4aR,4bR,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 6973653 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
(1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylic acid 97044524 Click to see 366.40 unknown via CMAUP database
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)- 15586712 Click to see 288.50 unknown via CMAUP database
4-Epicommunic acid 12303810 Click to see 302.50 unknown via CMAUP database
Abietal 443479 Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O 286.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietinol 443474 Click to see 288.50 unknown via CMAUP database
Dehydroabietal 11694869 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C 284.40 unknown via CMAUP database
Isopimaric Acid 442048 Click to see 302.50 unknown via CMAUP database
methyl (1S,4aR,5S,8aR)-5-[(E)-5-hydroxy-3-methylpent-3-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 14060410 Click to see 334.50 unknown via CMAUP database
methyl (1S,4R,5S,9S,10R,12S)-16-(2-hydroperoxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylate 12149368 Click to see 380.50 unknown via CMAUP database
methyl (1S,4R,5S,9S,10R,12S)-16-(2-hydroxypropan-2-yl)-5,9-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.04,9]hexadec-15-ene-5-carboxylate 12149369 Click to see CC12CCCC(C1CCC34C2CC(C(=C3)C(C)(C)O)OO4)(C)C(=O)OC 364.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-methyl-4-[(2S)-6-methylheptan-2-yl]benzene 101694025 Click to see 204.35 unknown via CMAUP database
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-(3-oxobutyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 11255232 Click to see CC(=O)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 306.40 unknown via CMAUP database
Thujopsenal 12444332 Click to see 218.33 unknown via CMAUP database
Thujopsene 442402 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown via CMAUP database
(+)-beta-Cedrene 11106485 Click to see 204.35 unknown via CMAUP database
(1beta,7beta)-Cedr-8(15)-ene 16213223 Click to see 204.35 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-3-one 21576983 Click to see 218.33 unknown via CMAUP database
(1R,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-one 21576982 Click to see 218.33 unknown via CMAUP database
(1R,2S,3R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-3-ol 15215015 Click to see 220.35 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecan-4-one 12308774 Click to see CC1CC(=O)C2C13CCC(=C)C(C3)C2(C)C 218.33 unknown via CMAUP database
(1S,2R,5S,7S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-en-4-one 12308772 Click to see CC1CC(=O)C2C13CC=C(C(C3)C2(C)C)C 218.33 unknown via CMAUP database
[(1S,2R,5R,6S,7S)-2,6,8-trimethyl-6-tricyclo[5.3.1.01,5]undec-8-enyl]methanol 22211622 Click to see 220.35 unknown via CMAUP database
Cedrenone 13335685 Click to see 218.33 unknown via CMAUP database
Cedrol 65575 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexan-1-ol 14138884 Click to see CC(=C)C1CC(C(CC1(C)C=C)O)C(C)(C)O 238.37 unknown via CMAUP database
[(1S,2S,4S,5S)-5-ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138886 Click to see 280.40 unknown via CMAUP database
Elemol 92138 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 102193489 Click to see 318.40 unknown via CMAUP database
3-Hydroxysandaracopimaric acid 101200911 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)C(=O)O)O)C)C=C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,5R,7R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol 101985389 Click to see CC1CCC2C13CCC(C3)(C(C2(C)C)O)C 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Widdrol 94334 Click to see 222.37 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol 162890773 Click to see 404.40 unknown https://doi.org/10.1111/J.1469-8137.1960.TB06211.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.2.2.01,5]undecan-3-one 21576981 Click to see 218.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,2R,5R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-one 21576985 Click to see 220.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,6,7-Trihydroxy-2-(2,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 71331302 Click to see C1=C(C(=CC(=C1O)O)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
4H-1-Benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-7-(beta-D-glucopyranosyloxy)-5-hydroxy- 5483990 Click to see 448.40 unknown https://doi.org/10.1002/JPS.2600640504

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