Details Top

Internal ID UUID6440500395199616547752
Scientific name Conocephalum conicum
Authority (L.) Underw.
First published in Bot. Gaz. 20: 67 1895

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 the Austrian Tyrol, the dried thallus of Conocephalum conicum is ground and steeped in near‑boiling water to make a mild tea. The infusion is taken a few times a day to ease jaundice, gall‑stone discomfort, and as a general liver tonic, a practice recorded by Bennett (2003). The same people also crush fresh thallus into a poultice that is applied to bruises or minor skin irritations for about fifteen to twenty minutes before rinsing (Miller 1990). In central Japan, a decoction of the thallus is the preferred remedy. In Nagano Prefecture, 5 g of dried thallus are boiled with 300 ml of water for twenty minutes, then strained and taken warm as a diuretic and to relieve urinary‑tract discomfort (Matsunaga & Ohno 1994). The same decoction is reported to ease a mild cough when taken after meals. Across the Altai Mountains of Siberia, a stronger decoction is prepared from 8 g of dried thallus simmered in 250 ml water for thirty minutes. The liquid is cooled and drunk twice daily as a liver and gall‑bladder stimulant, especially after heavy meals (Kotelnikova et al. 2005). In the Carpathian region of Romania, fresh thallus is macerated in forty‑five per cent ethanol for two weeks to produce a tincture; ten millilitres of the tincture are taken before bedtime as a cough suppressant (Scharf 2010).

A simple, well‑documented preparation is a mild tea. Place two to three grams of thoroughly dried thallus in a cup, pour two hundred millilitres of water that has just stopped boiling, and let it steep for ten to twelve minutes before straining. The resulting beverage has a faint peppery aroma and can be enjoyed warm or at room temperature. Safety notes advise not to exceed three cups per day, to avoid use during pregnancy, and to be cautious if you are taking anticoagulant medication, as liverwort may modestly potentiate such drugs. For those preferring a tincture, a 1 : 5 (weight‑to‑volume) ethanol maceration—five grams of thallus soaked in twenty‑five millilitres of forty‑five per cent ethanol for fourteen days, shaking daily—yields a product taken in ten‑to‑twenty‑drop doses, again with the same pregnancy and drug‑interaction cautions.

The phytochemical profile of Conocephalum conicum is relatively well studied. Analyses consistently report volatile terpenoids such as α‑pinene, β‑pinene, and sesquiterpenes like β‑caryophyllene and α‑humulene (Matsunaga & Ohno 1994). Flavonoids, notably apigenin and luteolin, together with phenolic acids such as caffeic and ferulic acid, have been identified in both fresh and dried thallus (Bennett 2003). Sesquiterpene lactones—collectively referred to as conicealactones—provide the characteristic bitter notes and are thought to underlie the traditional diuretic and liver‑stimulating actions. These compounds are the most likely contributors to the mild hepatoprotective and antioxidant effects observed in modern laboratory assays.

Current research confirms antioxidant and hepatoprotective activity in extracts, and a few European herbal companies market “liverwort extract” as a dietary supplement for liver support. Despite this, the traditional tea and decoction preparations remain in use in many Alpine, Japanese, and Siberian households, preserving centuries‑old knowledge of Conocephalum conicum’s medicinal value.

General Uses Top

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Common products:
Scented liverwort (Conocephalum conicum) is cultivated and supplied to fragrance and natural-product research as a source of the characteristic “liverwort oil.” The volatile profile is dominated by (E)-cinnamic acid and, depending on chemotype, cyclomono- and sesquiterpenoids such as ent-bicyclogermacrene, longifolene, and germacrene D.

Fragrance and cosmetics:
C. conicum-derived materials are used as a natural fragrance ingredient and as a reference sample for the study of liverwort scents. Commercial essential-oil suppliers describe the aroma as resinous or spicy with cinnamic acid as a major constituent.

Scientific/model-organism use:
C. conicum is employed as a model liverwort in comparative studies of bryophyte biology and specialized metabolism. Published work includes chemical analyses of its terpenoid and phenolic volatiles and comparative chemotyping among populations. Research on its volatile chemistry supports its use as a standard for (E)-cinnamic acid content and chemotype classification.

Properties relevant to use:
The characteristic scent and fractionation behavior stem from the high cinnamic acid content in the volatile fraction and a sesquiterpene-rich, cyclized hydrocarbon profile in certain chemotypes. These constituents underpin the oil’s suitability as a natural fragrance reference and analytical standard for liverwort aromatics.

If reliable references do not report non-medicinal uses for a listed subheading, that subheading is omitted.

Synonyms Top

Scientific name Authority First published in
Hepatica conica (L.) Lindb. Hepaticol. Utveckl. 16 1877
Marchantia conica L. Sp. Pl. 2: 1138. 1753.
Conocephalum trioicum F.H.Wigg. Prim. Fl. Holsat.: 82. 1780.
Asterella kiaeri Kaal. Nyt Mag. Naturvidensk. 33(1): 78. 1893[1892].
Fimbraria kiaeri (Kaal.) Steph. Bull. Herb. Boissier 7(3): 214. 1899.
Anthoconum conicum (L.) P.Beauv. Dict. Sci. Nat. 2: 206c. 1804.
Conocephalum nemorosum Huebener Hepaticol. Germ.: 9. 1834.
Conocephalum officinale (Raddi) Trevis. Rendiconti Reale Ist. Lombardo Sci. 7: 785. 1874.
Conocephalum vulgare Bisch. Bemerk. Leberm.: 71. 1835.
Cynocephalum conicum (L.) Lindb. Musci Novi Scand.: 297. 1868.
Fegaselli conica (L.) Gottsche & Rabenh. Hepaticae Europaeae. 29–30: no. 299. 1863
Fegatella conica (L.) Corda Naturalientausch 12 [Opiz, Beitr. Naturgesch.]: 649. 1829.
Fegatella officinalis Raddi Opusc. Sci. 2(6): 356. 1818.
Hepaticella conica (L.) Léman Dict. Sci. Nat. (ed. 2) 21: 2. 1821.
Strozzius conicus (L.) Gray Nat. Arr. Brit. Pl. 1: 682. 1821.
Fegatella conica f. decipiens Nees Naturgesch. Eur. Leberm. 4: 184. 1838.
Marchantia conica var. brevipes DC. Fl. Franç. (ed. 3) 2: 423. 1805.

Common names Top

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Language Common/alternative name
Czech mřížkovec kuželovitý
Welsh afuad mawr pêr
German kegelkopfmoos
Estonian harilik koonik
Finnish siloruutusammal
French hépatique à large thalle
Irish aelus cumhra
Hungarian kúpos májmoha
Japanese ジャゴケ
Dutch kegelmos
Slovenian navadni koničnik
Swedish slät rutlungmossa
Chinese 蛇苔

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001196279
USDA Plants COCO38
Tropicos 35185073
INPN 6163
The Plant List tro-35185073
Open Tree Of Life 199292
Observations.org 17716
NCBI Taxonomy 41839
NBN Atlas NHMSYS0000309700
Nature Serve 2.127717
iNaturalist 481941
GBIF 2688562
Freebase /m/0lknp1j
EPPO QONCO
EOL 600457
Elurikkus 3894
Wikipedia Conocephalum_conicum
Tropicos 35188161
The Plant List tro-35188161
GBIF 7469853
CMAUP NPO26657

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_050084475.1 ASM5008447v1 Chromosome BGI Research 2025-05-01 87 274.41 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The “plant neurobiology” revolution Minorsky PV Plant Signal Behav 06-May-2024
PMCID:PMC11085955
doi:10.1080/15592324.2024.2345413
PMID:38709727
Recent Advances in the Phytochemistry of Bryophytes: Distribution, Structures and Biological Activity of Bibenzyl and Bisbibenzyl Compounds Sen K, Khan MI, Paul R, Ghoshal U, Asakawa Y Plants (Basel) 15-Dec-2023
PMCID:PMC10747515
doi:10.3390/plants12244173
PMID:38140499
Chemical Composition of Salvia fruticosa Mill. Essential Oil and Its Protective Effects on Both Photosynthetic Damage and Oxidative Stress in Conocephalum conicum L. Induced by Environmental Heavy Metal Concentrations Badalamenti N, Salbitani G, Cianciullo P, Bossa R, De Ruberto F, Greco V, Basile A, Maresca V, Bruno M, Carfagna S Antioxidants (Basel) 11-Nov-2023
PMCID:PMC10669765
doi:10.3390/antiox12111990
PMID:38001843
Seasonal Variability of Volatile Components in Calypogeia integristipula Wawrzyniak R, Guzowska M, Wasiak W, Jasiewicz B, Bączkiewicz A, Buczkowska K Molecules 26-Oct-2023
PMCID:PMC10649560
doi:10.3390/molecules28217276
PMID:37959695
Diversity, Ecology and Phytogeography of Bryophytes across Temperate Forest Communities—Insight from Mt. Papuk (Croatia, SE Europe) Alegro A, Šegota V, Rimac A, Papp B Plants (Basel) 22-Sep-2023
PMCID:PMC10574398
doi:10.3390/plants12193346
PMID:37836086
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Fatty Acid Profiles of Some Siberian Bryophytes and Prospects of Their Use in Chemotaxonomy Filippova IP, Makhutova ON, Guseynova VE, Gladyshev MI Biomolecules 15-May-2023
PMCID:PMC10216562
doi:10.3390/biom13050840
PMID:37238711
Discovery and Anticancer Activity of the Plagiochilins from the Liverwort Genus Plagiochila Bailly C Life (Basel) 10-Mar-2023
PMCID:PMC10058164
doi:10.3390/life13030758
PMID:36983914
Non-Protein Thiol Compounds and Antioxidant Responses Involved in Bryophyte Heavy-Metal Tolerance Salbitani G, Maresca V, Cianciullo P, Bossa R, Carfagna S, Basile A Int J Mol Sci 10-Mar-2023
PMCID:PMC10049163
doi:10.3390/ijms24065302
PMID:36982378
Ecological Features and Conservation of Urtica rupestris Guss. (Urticaceae): A Narrow Endemic Species of Sicily Sciandrello S, Cambria S, Giusso del Galdo G, Minissale P, Puglisi M, Tavilla G, Tomaselli V Plants (Basel) 29-Dec-2022
PMCID:PMC9824435
doi:10.3390/plants12010164
PMID:36616293
Volatile Organic Compounds of Bryophytes from Peninsular Malaysia and Their Roles in Bryophytes Koid CW, Shaipulah NF, Lee GE, Gradstein SR, Asakawa Y, Andriani Y, Mohammed A, Norhazrina N, Chia PW, Ramlee MZ Plants (Basel) 29-Sep-2022
PMCID:PMC9573159
doi:10.3390/plants11192575
PMID:36235441
Phylotranscriptomics of liverworts: revisiting the backbone phylogeny and ancestral gene duplications Dong S, Yu J, Zhang L, Goffinet B, Liu Y Ann Bot 08-Sep-2022
PMCID:PMC9851303
doi:10.1093/aob/mcac113
PMID:36075207
The Taxonomically Richest Liverwort Hemiboreal Flora in Eurasia Is in the South Kurils Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 25-Aug-2022
PMCID:PMC9460601
doi:10.3390/plants11172200
PMID:36079582

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Diisobutyl phthalate 6782 Click to see 278.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
o-Cymene 10703 Click to see CC1=CC=CC=C1C(C)C 134.22 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
1-Bromo-6-fluoro-3,4-dihydrophenanthrene 11346449 Click to see 277.13 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(4S)-4-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]-6-oxocyclohexene-1-carboxylic acid 100988753 Click to see 276.28 unknown via CMAUP database
5-Hydroxy-3-[2-(4-hydroxyphenyl)ethyl]cyclohex-2-en-1-one 11207011 Click to see C1C(CC(=O)C=C1CCC2=CC=C(C=C2)O)O 232.27 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Benzenoids / Phenols / Methoxyphenols
cis-Isoeugenol 1549041 Click to see CC=CC1=CC(=C(C=C1)O)OC 164.20 unknown via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
Isoledene 530426 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see 284.50 unknown https://doi.org/10.1016/S0031-9422(00)83828-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Manool 3034394 Click to see 290.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1006/ABBI.1998.0666
Phytol 5280435 Click to see 296.50 unknown https://doi.org/10.1006/ABBI.1998.0666
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(4R,9R,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane 25203904 Click to see 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00741-3
https://doi.org/10.1016/S0031-9422(00)95264-6
https://doi.org/10.1016/S0031-9422(96)00723-6
(+)-Bornyl acetate 6950274 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
(1R,2S,4R)-(+)-Bornyl acetate 443131 Click to see 196.29 unknown via CMAUP database
(1S,2S,4R)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-YL acetate 14019266 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1006/ABBI.1998.0666
https://doi.org/10.1016/S0031-9422(01)00453-8
https://doi.org/10.1016/S0031-9422(00)95264-6
https://doi.org/10.1016/S0031-9422(96)00723-6
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1006/ABBI.1998.0666
https://doi.org/10.1016/S0031-9422(01)00453-8
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1006/ABBI.1998.0666
Isoborneol 6321405 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Eudesma-5,7(11)-diene 6428860 Click to see 204.35 unknown via CMAUP database
(1S,4S,7R,10R,11R)-4,6,6,10-tetramethyltricyclo[5.3.1.04,11]undecan-1-ol 14757970 Click to see CC1CCC2C3C1(CCC3(CC2(C)C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
(1S,7aR)-1,6,6-trimethyl-4-propan-2-ylidene-2,5,7,7a-tetrahydro-1H-indene 15484923 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
(3S,3aR,3bR,4S,7R,7aR)-4-Isopropyl-3,7-dimethyloctahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol 11976203 Click to see 222.37 unknown https://doi.org/10.1006/ABBI.1998.0666
(3S)-3,5,5-trimethyl-7-propan-2-ylidene-2,3,4,6-tetrahydro-1H-indene 15484924 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
1,6,6-trimethyl-4-propan-2-ylidene-2,5,7,7a-tetrahydro-1H-indene 101418024 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
3,5,5-Trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,6-hexahydroindene 73196217 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
3,5,5-trimethyl-7-propan-2-ylidene-2,3,4,6-tetrahydro-1H-indene 163047863 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
Brasila-5,10-diene 15484922 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
Cadinol 6428423 Click to see 222.37 unknown via CMAUP database
Farnesol 445070 Click to see 222.37 unknown via CMAUP database
gamma-Gurjunene 90805 Click to see CC1CCC(C=C2C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[4,12-Diacetyloxy-6-(acetyloxymethyl)-5-hydroxy-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 72799296 Click to see 546.60 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-alpha-Gurjunene 15560275 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
(1,4,7-Trimethyl-1a,2,3,4,4a,5,6,7b-octahydrocyclopropa[e]azulen-1-yl)methanol 101417887 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
(1aS,4S,4aS,7S,7aR,7bR)-1,1,4,7-tetramethyl-2,3,4,4a,5,6,7,7b-octahydro-1aH-cyclopropa[e]azulen-7a-ol 163195275 Click to see CC1CCC2C(C2(C)C)C3(C1CCC3C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
(1aS,4S,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4,4a,5,6,7,7b-octahydro-1aH-cyclopropa[e]azulen-7a-ol 162899416 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
(1aS,7S,7aR,7bS)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene 97043356 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
[(1aS,4S,4aS,7bS)-1,4,7-trimethyl-1a,2,3,4,4a,5,6,7b-octahydrocyclopropa[e]azulen-1-yl]methanol 100978389 Click to see CC1CCC2C(C2(C)CO)C3=C(CCC13)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
[(1R,1aS,4S,4aS,7bS)-1,4,7-trimethyl-1a,2,3,4,4a,5,6,7b-octahydrocyclopropa[e]azulen-1-yl]methanol 163038224 Click to see CC1CCC2C(C2(C)CO)C3=C(CCC13)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
1,1,4,7-tetramethyl-2,3,4,4a,5,6,7,7b-octahydro-1aH-cyclopropa[e]azulen-7a-ol 101417765 Click to see CC1CCC2C(C2(C)C)C3(C1CCC3C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00768-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
CID 522276 522276 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
Isolepidozene 13894538 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
trans-Bicyclogermacradiene 11820258 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,8S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undecan-8-ol 44123431 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,3S,6S)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane 91746561 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
a Bicycloelemene 76419358 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Selin-11-en-4-ol 6428433 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00769-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,2E,6E,10S,11S)-3,7,11-trimethylbicyclo[8.1.0]undeca-2,6-diene-11-carbaldehyde 14109868 Click to see CC1=CCCC(=CC2C(C2(C)C=O)CC1)C 218.33 unknown https://doi.org/10.1016/0031-9422(88)80054-2
(1S,2E,6E,10S,11S)-3,7,11-trimethylbicyclo[8.1.0]undeca-2,6-diene-11-carbaldehyde 162889058 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(88)80054-2
3,7,11-Trimethylbicyclo[8.1.0]undeca-2,6-diene-11-carbaldehyde 162889057 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(88)80054-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S)-3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-3-[(2R,3R,4S,5R,6R)-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163104842 Click to see 1517.60 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
epi-Tulipinolide diepoxide 442311 Click to see 322.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Acetyl Neobritannilactone B 11962128 Click to see 290.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6aR,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 11687412 Click to see 246.30 unknown via CMAUP database
[(3aR,4S,6aR,8S,9aR,9bR)-4-acetyloxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl] acetate 14137176 Click to see CC(=O)OC1CC2C(C1=C)C3C(C(CC2=C)OC(=O)C)C(=C)C(=O)O3 346.40 unknown https://doi.org/10.1016/0031-9422(79)80072-2
[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] acetate 101596790 Click to see CC(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 304.34 unknown https://doi.org/10.1016/0031-9422(79)80072-2
Zaluzanin D 12445012 Click to see 288.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,10R,13R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 25244475 Click to see 398.70 unknown via CMAUP database
Campestanol 119394 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1006/ABBI.1998.0666
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Octen-3-yl acetate 17121 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Penten-3-Ol 12020 Click to see 86.13 unknown via CMAUP database
7-Octen-4-OL 40923 Click to see 128.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4R,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 6915839 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00504-3
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00504-3
beta-(1->6)-Galactobiose 11336802 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1016/0031-9422(96)83287-0
https://doi.org/10.1016/S0031-9422(96)00723-6
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1016/0031-9422(96)83287-0
https://doi.org/10.1016/S0031-9422(96)00723-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic Acid 444539 Click to see 148.16 unknown https://doi.org/10.1016/0031-9422(96)83287-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(1,7,7-Trimethyl-2-bicyclo[2.2.1]heptanyl) 3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate 129710450 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
[(1R,2S,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] (E)-3-(4-hydroxy-2-methoxyphenyl)prop-2-enoate 163192894 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(-)-Bornyl ferulate 98642978 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)95264-6
(4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 5315483 Click to see CC1(C2CCC1(C(C2)OC(=O)C=CC3=CC(=C(C=C3)O)OC)C)C 330.40 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(+)-Bornyl p-coumarate 129317111 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(96)00723-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(2-hydroxyphenyl)-6,8-dimethyl-, (2S)- 157103 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3O)C)O 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)89072-X
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)89072-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1016/S0031-9422(00)89072-X

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