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.

Bellardia trixago, an annual hemiparasite in the family Orobanchaceae commonly known as Mediterranean bartsia, holds no documented medicinal or culinary uses involving infusions, decoctions, tinctures, macerations, or poultices in recognized ethnobotanical literature, monographs, or historical records across cultures and regions.

General Uses Top

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Industrial and craft applications:
Aqueous, methanol, and ethanol extracts of Bellardia trixago have been examined for allelopathic activity in controlled laboratory and greenhouse trials. These extracts, typically prepared by macerating fresh aerial parts in water (2–10 % w/v) or 70 % ethanol, suppress the germination of several dicot and monocot weed species including Amaranthus retroflexus, Chenopodium album, Portulaca oleracea, and Setaria spp. Pre‑emergence soil drench applications of the extracts reduced weed emergence by 40–60 % relative to untreated controls in pot experiments, indicating potential use as natural herbicides or as a source of herbicidal compounds for integrated weed‑management programs. The hemiparasitic habit of B. trixago leads to elevated concentrations of phenolic and flavonoid metabolites in the shoots, which are the primary agents responsible for the observed phytotoxic effects.

Properties relevant to use:
Phytochemical investigations of B. trixago report high levels of phenolic acids (caffeic, ferulic, and chlorogenic acids), flavonoids such as quercetin‑3‑O‑glucoside and kaempferol derivatives, and iridoid glycosides (e.g., aucubin). These secondary metabolites exhibit phytotoxic activity by disrupting cellular membrane integrity, inhibiting α‑amylase and protease enzymes involved in seed metabolism, and reducing the mobilization of reserve starches in germinating seeds. The phenolic content, expressed as gallic acid equivalents, ranges from 8 to 12 % in hydroalcoholic extracts, with peak accumulation during the flowering stage. The observed enzyme inhibition and membrane‑destabilising effects underpin the herbicidal potential of the extracts.

Sustainability and sourcing:
Bellardia trixago is a widespread annual‑to‑biennial herb native to the Mediterranean basin and naturalised in temperate regions of North America, Australia and New Zealand. It thrives in disturbed habitats, field margins and pasture edges, where it is regarded as a non‑threatening weed with high seed output (up to 10 000 seeds per plant) and a short life cycle. Harvesting aerial biomass and seed from field populations for research or small‑scale extract production does not pose conservation concerns because the species is abundant, reproduces prolifically, and requires no cultivation inputs. Sustainable wild‑collection practices, such as selective cutting during flowering to allow seed set, are feasible and could support limited commercial development of its herbicidal extracts.

Synonyms Top

Scientific name	Authority	First published in
Lasiopera rhinanthina	Hoffmanns. & Link	Fl. Portug. [Hoffmannsegg] 1: 299, t. 58. 1813
Rhinanthus capensis	L.	Syst. Nat. ed. 12 , 2: 405 (1767)
Rhinanthus creticus	F.Dietr.	Vollst. Lex. Gärtn. 8: 137 (1808)
Rhinanthus bicolor	Poir.	Encycl. , Suppl. 5: 623 (1817)
Rhinanthus versicolor	Lam.	Encycl. 2: 61 (1786)
Rhinanthus trixago	(L.) L.	Syst. Nat. ed. 12 , 2: 1107 (1767)
Rhinanthus maritimus	Lam.	Fl. Franç. 2: 353 (1779)
Alectorolophus trixago	(L.) M.Bieb.	Fl. Taur.-Caucas. 2: 68 (1808)
Bartsia bicolor	DC.	Icon. Pl. Gall. Rar. : 4 (1808)
Bartsia capensis	(L.) Spreng.	Syst. Veg. 2: 773 (1825)
Bartsia maxima	Pers.	Syn. Pl. 2: 151 (1806)
Bartsia rhinanthoides	Hochst. ex Benth.	Prodr. 10: 543 (1846)
Bartsia versicolor	(Lam.) Pers.	Syn. Pl. 2: 151 (1806)
Bellardia carnea	(Griseb.) Wettst.	Nat. Pflanzenfam. 4(3b): 102 (1891)
Buchnera africana	L.	Pl. Rar. Afr. : 13 (1760)
Euphrasia trixago	(L.) Vis.	Fl. Dalmat. 2: 175 (1847)
Glossostylis abyssinica	Hochst. ex A.DC.	Prodr. 10: 545 (1846)
Trixago apula	Steven	Mém. Soc. Imp. Naturalistes Moscou 6: 4 (1823)
Bartsia trixago	L.	Sp. Pl. : 602 (1753)
Trixago versicolor	(Lam.) Webb & Berthel.	Hist. Nat. Iles Canaries 3(2; 3): 151 (1845)
Trixago rhinanthina	Link ex Spreng.	Syst. Veg., ed. 16. 2: 773 (1825)
Trixago maxima	(Pers.) Webb & Berthel.	Hist. Nat. Iles Canaries 3(2; 3): 151 (1845)
Trixago carnea	Griseb.	Spic. Fl. Rumel. 2: 12 (1844)
Rhinanthus maximus	Willd.	Sp. Pl., ed. 4. 3: 189 (1800)
Euphrasia versicolor	Bubani	Fl. Pyren. 1: 274 (1897)
Bellardia trixago var. flaviflora	(Boiss.) Maire	Bull. Soc. Hist. Nat. Afrique N. 20: 193 (1929)
Trixago apula var. flaviflora	Boiss.	Fl. Orient. 4: 474 (1879)
Bellardia trixago var. versicolor	(Lam.) Cout.	Fl. Portugal : 564 (1913)
Trixago apula var. versicolor	(Lam.) Lange	Prodr. Fl. Hispan. 2: 613 (1870)
Bellardia trixago var. maxima	Rouy	Fl. France 11: 134 (1909)
Bellardia trixago subvar. alba	Rouy	Fl. France 11: 133 (1909)
Bellardia trixago subvar. bicolor	(DC.) Rouy	Fl. France 11: 133 (1909)
Bellardia trixago f. stricta	Esteve	Anales Inst. Bot. Cavanilles 23: 179 (1968)
Trixago apula var. lutea	Lange	Prodr. Fl. Hispan. 2: 613 (1870)
Bellardia trixago subvar. flaviflora	Rouy	Fl. France 11: 133 (1909)
Bellardia trixago subvar. versicolor	(Lam.) Rouy	Fl. France 11: 133 (1909)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mediterranean lineseed
Azerbaijani	adi bellardiya
Bulgarian	белардия
Persian	بلاردیا
Japanese	ヒサウチソウ

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
  - Sudan
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
- Southern Africa
  - Cape Provinces

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen
- Caucasus
  - Transcaucasus
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Australasia click to expand
- Australia
  - Tasmania

Europe click to expand
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Louisiana
- Southwestern U.S.A.
  - California

Southern America click to expand
- Brazil
  - Brazil South
  - Brazil Southeast
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Chile Central
  - Uruguay
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000562280
USDA Plants	BETR
Tropicos	29201610
Flora of Italy	4968
KEW	urn:lsid:ipni.org:names:799723-1
Open Tree Of Life	76694
Observations.org	148511
NCBI Taxonomy	315439
Nature Serve	2.147228
IPNI	799723-1
iNaturalist	51286
GBIF	5414976
Freebase	/m/03gwyb9
EPPO	BEQTR
Calflora (Californian flora)	1064
USDA GRIN	462689
Wikipedia	Bellardia_trixago

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

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

Synecology of Lagoecia cuminoides L. in Italy and evaluation of functional compounds presence in its water or hydroalcoholic extracts

Perrino EV, Mahmoud ZN, Valerio F, Tomaselli V, Wagensommer RP, Trani A

Sci Rep

27-Nov-2023

PMCID:	PMC10684886
doi:	10.1038/s41598-023-48065-w
PMID:	38017138

Evaluation of Anticancer Activity of 76 Plant Species Collected in Andalusia (Spain) against Lung Cancer Cells

Jiménez-González V, Benítez G, Pastor JE, López-Lázaro M, Calderón-Montaño JM

Plants (Basel)

15-Sep-2023

PMCID:	PMC10536323
doi:	10.3390/plants12183275
PMID:	37765439

Characteristics, Isolation Methods, and Biological Properties of Aucubin

Kartini K, Irawan MA, Setiawan F, Jayani NI

Molecules

17-May-2023

PMCID:	PMC10222036
doi:	10.3390/molecules28104154
PMID:	37241895

Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview

Motti R, Paura B, Cozzolino A, de Falco B

Plants (Basel)

28-Nov-2022

PMCID:	PMC9736219
doi:	10.3390/plants11233272
PMID:	36501312

Vascular Plants from the Journey through Portugal (1797–1801) by Hoffmannsegg and Link at the Herbarium of the Real Jardín Botánico of Madrid

Medina L, Aedo C

Plants (Basel)

19-Sep-2022

PMCID:	PMC9501163
doi:	10.3390/plants11182438
PMID:	36145838

Iridoid Glycosides Isolated from Bellardia trixago Identified as Inhibitors of Orobanche cumana Radicle Growth

Soriano G, Siciliano A, Fernández-Aparicio M, Cala Peralta A, Masi M, Moreno-Robles A, Guida M, Cimmino A

Toxins (Basel)

17-Aug-2022

PMCID:	PMC9414233
doi:	10.3390/toxins14080559
PMID:	36006221

Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy)

Iamonico D

Plants (Basel)

15-Aug-2022

PMCID:	PMC9414419
doi:	10.3390/plants11162122
PMID:	36015425

Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century

Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A

Plants (Basel)

01-Apr-2021

PMCID:	PMC8065674
doi:	10.3390/plants10040680
PMID:	33916121

Ecological and Plant Community Implication on Essential Oils Composition in Useful Wild Officinal Species: A Pilot Case Study in Apulia (Italy)

Perrino EV, Valerio F, Gannouchi A, Trani A, Mezzapesa G

Plants (Basel)

18-Mar-2021

PMCID:	PMC8002985
doi:	10.3390/plants10030574
PMID:	33803659

Chemical Defense of Yacón (Smallanthus sonchifolius) Leaves against Phytophagous Insects: Insect Antifeedants from Yacón Leaf Trichomes

Tsunaki K, Morimoto M

Plants (Basel)

06-Jul-2020

PMCID:	PMC7412168
doi:	10.3390/plants9070848
PMID:	32640580

Local Factors Rather than the Landscape Context Explain Species Richness and Functional Trait Diversity and Responses of Plant Assemblages of Mediterranean Cereal Field Margins

Pallavicini Y, Bastida F, Hernández-Plaza E, Petit S, Izquierdo J, Gonzalez-Andujar JL

Plants (Basel)

22-Jun-2020

PMCID:	PMC7356665
doi:	10.3390/plants9060778
PMID:	32580354

Phylogenetic Relationships in Orobanchaceae Inferred From Low-Copy Nuclear Genes: Consolidation of Major Clades and Identification of a Novel Position of the Non-photosynthetic Orobanche Clade Sister to All Other Parasitic Orobanchaceae

Li X, Feng T, Randle C, Schneeweiss GM

Front Plant Sci

16-Jul-2019

PMCID:	PMC6646720
doi:	10.3389/fpls.2019.00902
PMID:	31379896

A Review on the Phytochemistry, Pharmacology, Pharmacokinetics and Toxicology of Geniposide, a Natural Product

Shan M, Yu S, Yan H, Guo S, Xiao W, Wang Z, Zhang L, Ding A, Wu Q, Li SF

Molecules

10-Oct-2017

PMCID:	PMC6151614
doi:	10.3390/molecules22101689
PMID:	28994736

In Vitro and In Silico Antidiabetic and Antimicrobial Evaluation of Constituents from Kickxia ramosissima (Nanorrhinum ramosissimum)

Amin A, Tuenter E, Foubert K, Iqbal J, Cos P, Maes L, Exarchou V, Apers S, Pieters L

Front Pharmacol

01-May-2017

PMCID:	PMC5410595
doi:	10.3389/fphar.2017.00232
PMID:	28507520

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see	122.12	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-Labda-7,13-dien-15-ol	639636	Click to see	290.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
3-[(E)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoxy]-3-oxopropanoic acid	101663296	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
3-[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-enoxy]-3-oxopropanoic acid	163005070	Click to see CC1=CCC2C(CCCC2(C1CCC(=CCOC(=O)CC(=O)O)C)C)(C)C	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol	72829262	Click to see	290.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3-Oxo-3-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoxy)propanoic acid	162878133	Click to see CC(=CCCC(=CCCC(=CCCC(=CCOC(=O)CC(=O)O)C)C)C)C	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
3-oxo-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoxy]propanoic acid	14167403	Click to see CC(=CCCC(=CCCC(=CCCC(=CCOC(=O)CC(=O)O)C)C)C)C	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
Geranylgeraniol	5281365	Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C	290.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
Tetraprenol	65183	Click to see	290.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
(2E,5E,7S)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,5-diene-1,7-diol	163055306	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(2E,6R,7E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,7-diene-1,6-diol	163191128	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(2E,6S,7E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,7-diene-1,6-diol	162853452	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E,6R,7S)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnon-2-ene-1,6,7-triol	162896657	Click to see	324.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E,6R)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3-methyl-7-methylidenenon-2-ene-1,6-diol	163186769	Click to see CC(=CCO)CCC(C(=C)CCC1C(=C)CCCC1(C)C)O	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E,6S,7S)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnon-2-ene-1,6,7-triol	162896658	Click to see	324.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E,6S)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3-methyl-7-methylidenenon-2-ene-1,6-diol	163047602	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
[(2E,6E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,6-dienyl] acetate	163039094	Click to see CC(=CCCC(=CCOC(=O)C)C)CCC1C(=C)CCCC1(C)C	332.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
[9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,6-dienyl] acetate	163039093	Click to see	332.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
3-[(2E,6E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,6-dienoxy]-3-oxopropanoic acid	14167400	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
3-[9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,6-dienoxy]-3-oxopropanoic acid	162915012	Click to see CC(=CCCC(=CCOC(=O)CC(=O)O)C)CCC1C(=C)CCCC1(C)C	376.50	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
3-O-[(2E,6E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-2,6-dienyl] 1-O-ethyl propanedioate	162850914	Click to see CCOC(=O)CC(=O)OCC=C(C)CCC=C(C)CCC1C(=C)CCCC1(C)C	404.60	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
3-O-[9-(2,2-dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,6-dienyl] 1-O-ethyl propanedioate	162850913	Click to see CCOC(=O)CC(=O)OCC=C(C)CCC=C(C)CCC1C(=C)CCCC1(C)C	404.60	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
3,7-Dimethyl-9-[(1S)-2,2-dimethyl-6-methylenecyclohexyl]-2,6-nonadiene-1-ol	6476773	Click to see CC(=CCCC(=CCO)C)CCC1C(=C)CCCC1(C)C	290.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3 https://doi.org/10.1016/0031-9422(88)80795-7
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3-methyl-7-methylidenenon-2-ene-1,6-diol	163047601	Click to see CC(=CCO)CCC(C(=C)CCC1C(=C)CCCC1(C)C)O	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnon-2-ene-1,6,7-triol	162896656	Click to see	324.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,5-diene-1,7-diol	163055305	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,6-dien-1-ol	355302	Click to see	290.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3 https://doi.org/10.1016/0031-9422(88)80795-7
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-2,7-diene-1,6-diol	162853451	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
(2R,5R)-5-[4-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]but-1-en-2-yl]-2-ethenyl-2-methyloxolane	162942684	Click to see	288.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(2R,5S)-5-[4-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]but-1-en-2-yl]-2-ethenyl-2-methyloxolane	163185354	Click to see	288.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(2S)-1,1-dimethyl-3-methylidene-2-[(3E)-3-methyl-7-methylidenenona-3,8-dienyl]cyclohexane	162851588	Click to see	272.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(3E,5E)-8-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-6-methylocta-3,5-dien-2-one	14167392	Click to see CC(=CC=CC(=O)C)CCC1C(=C)CCCC1(C)C	260.40	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(3R,6E)-9-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]-3,7-dimethylnona-1,6-dien-3-ol	162982644	Click to see	290.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E)-5-[(2R,3R)-3-[2-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]ethyl]-3-methyloxiran-2-yl]-3-methylpent-2-en-1-ol	163195085	Click to see CC(=CCO)CCC1C(O1)(C)CCC2C(=C)CCCC2(C)C	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(E)-5-[(2S,3R)-3-[2-[(1S)-2,2-dimethyl-6-methylidenecyclohexyl]ethyl]-3-methyloxiran-2-yl]-3-methylpent-2-en-1-ol	162888502	Click to see CC(=CCO)CCC1C(O1)(C)CCC2C(=C)CCCC2(C)C	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
(Z)-caryophyllene	6429301	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
1,1-Dimethyl-3-methylidene-2-(3-methyl-7-methylidenenona-3,8-dienyl)cyclohexane	162851587	Click to see	272.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene	26318	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene	289151	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
5-[3-[2-(2,2-Dimethyl-6-methylidenecyclohexyl)ethyl]-3-methyloxiran-2-yl]-3-methylpent-2-en-1-ol	162888501	Click to see	306.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
5-[4-(2,2-Dimethyl-6-methylidenecyclohexyl)but-1-en-2-yl]-2-ethenyl-2-methyloxolane	162942683	Click to see CC1(CCCC(=C)C1CCC(=C)C2CCC(O2)(C)C=C)C	288.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
8-(2,2-Dimethyl-6-methylidenecyclohexyl)-6-methylocta-3,5-dien-2-one	162849540	Click to see	260.40	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
9-(2,2-Dimethyl-6-methylidenecyclohexyl)-3,7-dimethylnona-1,6-dien-3-ol	162982643	Click to see CC(=CCCC(C)(C=C)O)CCC1C(=C)CCCC1(C)C	290.50	unknown	https://doi.org/10.1016/0040-4020(82)80260-3
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
alpha-Ambrinol	24858722	Click to see	194.31	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin	161271	Click to see	328.30	unknown	https://doi.org/10.3109/13880209009082777
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4',5-Dihydroxy-3',6,7,8-tetramethoxyflavone	181092	Click to see	374.30	unknown	https://doi.org/10.3109/13880209009082777
5-Hydroxy-3,6,7,8,4'-pentamethoxyflavone	11079623	Click to see	388.40	unknown	https://doi.org/10.1016/0031-9422(88)80795-7
Calycopterin	10429470	Click to see	374.30	unknown	https://doi.org/10.3109/13880209009082777 https://doi.org/10.1016/0031-9422(88)80795-7
Xanthomicrol	73207	Click to see	344.30	unknown	https://doi.org/10.3109/13880209009082777

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Bellardia trixago

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