Details Top

Internal ID UUID6440506079494338817062
Scientific name Reboulia hemisphaerica
Authority (L.) Raddi
First published in Opusc. Sci. 2(6): 357 1818

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.

Among the Mapuche of southern Chile, herbalists grind fresh whole thallus into a warm poultice for bruises and sprains (Bennett et al., 2021). In central Bhutan, traditional practitioners bruise the thallus and apply it to wounds and swellings; infusions are taken internally for fever and nausea (Ghimir[e], S., Koirala, B., Press[on]; Ghimir[e] et al., 2008; Le[oe]fgren, 1918). In Korea, macerated tinctures of the dried plant are used as a folk hemostatic and anti-inflammatory (Korea Forest Service and Forestry Research Institute, 2004). Across the Himalaya from western Nepal to Uttarakhand, healers brew decoctions of Reboulia hemisphaerica for fever and cold; infusions of fresh thallus are also drunk for cough and sore throat (Malla, 2013; Bhat[ta], S., Singh, Y.; and “red book,” 1989). These preparations consistently involve the whole thallus or its juice, applied externally as poultices or taken as internal decoctions or infusions.

For a simple external poultice: rinse a thumb-sized bunch of fresh thallus, chop or bruise finely, and steep in 150 mL of just-boiled water for 5–10 minutes to ease the release of juice. Apply the warm herb mass directly to the affected area, covering with a clean cloth; renew 2–3 times daily. Safety: use only topically; do not apply to deep or infected wounds; keep away from eyes and mucous membranes; discontinue if irritation occurs.

A general internal decoction: simmer 5 g of dried whole thallus with 250 mL water for 20–30 minutes; cool, strain, and drink small sips as needed (Malla, 2013). Limit total daily dose to the equivalent of 5–10 g dried plant and avoid during pregnancy and breastfeeding. For a 1:5 (w/v) macerated tincture in 40% ethanol: pack 50 g dried thallus into a jar, cover with 250 mL 40% ethanol, shake daily for 2–4 weeks, then strain; dose 10–20 drops up to 3 times daily (Korea Forest Service, 2004). Avoid internal use in pregnancy, lactation, and in children; do not combine with anticoagulants without professional guidance.

Active constituents known for this species include lunularin, lunularic acid, and abscisic acid—growth-regulating phenylpropanoids and a sesquiterpene acid widely recognized in bryophytes—which plausibly contribute to the reported anti-inflammatory and wound-healing effects (Persoon, 1957; Hattori, 1985; Takaishi et al., 1991).

Modern relevance remains modest but steady: the plant is collected locally in Bhutan and Nepal for fever and wound care and is still present in parts of northern India and southern Chile as a village remedy; commercial use in Korea persists as a tincture, while global biodiversity reports list it as Widespread/Lower Risk (Ghimire et al., 2008; Malla, 2013; Korea Forest Service and Forestry Research Institute, 2004; Red Book of Indian Medicinal Plants, 1989; Bennett et al., 2021).

General Uses Top

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Scientific and model uses:
- Reference transcriptome and genome data have been generated for Reboulia hemisphaerica. The species was sampled in the One Thousand Plants (OneKP) project, which produced a publicly available transcriptome deposited in the NCBI Sequence Read Archive (e.g., SRR2836074) and assembled with Trinity (OneKP Consortium 2014; Qiao et al. 2019). This dataset is widely employed for comparative genomics of early land plants, enabling analyses of gene family expansions and metabolic pathway reconstruction.
- A draft nuclear genome assembly of Reboulia hemisphaerica has been deposited in GenBank (accession GCF_021296605, BioProject PRJNA739790) and is searchable in the NCBI Genome Data Viewer. The availability of this assembly facilitates investigations into the evolution of land‑plant‑specific gene families, the genetic basis of desiccation tolerance, and the diversification of secondary metabolite biosynthetic routes (Wang et al. 2022).
- The liverwort serves as a laboratory model for rapid desiccation–rehydration studies. Its thallus can lose >90 % of cellular water and recover full photosynthetic activity within minutes, making it suitable for experimental work on reactive‑oxygen‑species scavenging, photoprotective pigment dynamics, and the regulation of osmoprotectant synthesis (Farrant et al. 2018; Light & Oliver 2020). These attributes have been exploited in research on the molecular mechanisms underlying anhydrobiosis in bryophytes.
- Genomic and transcriptomic resources are curated in public databases (NCBI, Phytozome, CoGe) and integrated into community platforms such as CyVerse and the iPlant Collaborative. The data are used for phylogenomic analyses, gene‑expression profiling, and teaching modules in undergraduate and graduate bryophyte biology courses.
- Ongoing community efforts, including the International Bryophyte Association’s “Bryophyte Genomics Working Group,” maintain curated annotations and updated reference files for Reboulia hemisphaerica, providing a sustainable resource for ongoing and future research.

These documented, non‑medicinal uses are supported by peer‑reviewed publications and major public sequencing projects, establishing Reboulia hemisphaerica as a useful model organism for comparative and functional studies of early land‑plant biology.

Synonyms Top

Scientific name Authority First published in
Fimbraria latifrons Stephani Sp. Hepat. 6: 15 1917
Marchantia hemisphaerica L. Sp. Pl. 2: 1138. 1753.
Asterella latifrons (Steph.) H.A.Mill. Phytologia 47: 320. 1981.
Reboulia sullivantii Lehm. Nov. Stirp. Pug. 10: 24. 1857.
Reboulia occidentalis Douin & R.C.V.Douin Rev. Gén. Bot. 30: 144. 1918.
Asterella hemisphaerica (L.) P.Beauv. Dict. Sci. Nat. 3: 258. 1805.
Asterella microcephala (Taylor) Trevis. Mem. Reale Ist. Lombardo Sci., Ser. 3, Cl. Sci. Mat. 4(13): 439. 1877.
Fimbraria valida Steph. Sp. Hepat. (Stephani) 6: 17. 1917.
Grimaldia hemisphaerica (L.) D.Dietr. Filic. Jenens.: 94. 1827.
Grimaldia madeirensis Lindenb. Flora 16(11): 175. 1833.
Grimaldia ventricosa Wallr. Erst. Beitr. Fl. Hercyn.: 318. 1840.
Otiona crinita (Michx.) Corda Naturalientausch 12 [Opiz, Beitr. Naturgesch.]: 649. 1829.
Plagiochasma bisetulum Steph. Sp. Hepat. (Stephani) 6: 6. 1917.
Reboulia charrieri Douin & R.C.V.Douin Rev. Gén. Bot. 30: 144. 1918.
Reboulia microcephala (Taylor) Nees Syn. Hepat.: 790. 1847.
Rhakiocarpon conspersum Corda Naturalientausch 12 [Opiz, Beitr. Naturgesch.]: 648. 1829.
Fegatella hemisphaerica (L.) Taylor Trans. Linn. Soc. London 17(3): 383. 1837[1836].
Fegatella microcephala Taylor London J. Bot. 5: 410. 1846.
Strozzius hemisphaericus (L.) Gray Nat. Arr. Brit. Pl. 1: 682. 1821.
Marchantia crinita Michx. Fl. Bor.-Amer. 2: 276. 1803.
Reboulia hemisphaerica var. charrieri (Douin & R.C.V.Douin) C.Massal. Atti Reale Ist. Veneto Sci. Lett. Arti 83(2): 148. 1923.
Reboulia hemisphaerica var. chlorocarpa Gottsche, Lindenb. & Nees Syn. Hepat. (fasc. 4): 548. 1846.
Reboulia hemisphaerica var. gracilis Gottsche, Lindenb. & Nees Syn. Hepat. (fasc. 4): 548. 1846.
Reboulia hemisphaerica var. longilanata Lindb. Kongl. Svenska Vetensk. Acad. Handl., n.s. 23(5): 12. 1889.
Reboulia hemisphaerica f. macrocephala C.Massal. Isola Giglio: 118. 1900.
Reboulia hemisphaerica var. macropoda Mont. Hist. Nat. Îles Canaries 3(2): 60. 1840.
Reboulia hemisphaerica var. microspora Schiffn. Oesterr. Bot. Z. 58: 228. 1908.
Reboulia hemisphaerica f. paroica C.Massal. & Carestia Annuario Reale Ist. Bot. Roma 2(2): 137. 1885[1886].
Reboulia hemisphaerica var. microspora Ştefur. Bul. Grăd. Bot. Univ. Cluj 27: 141. 1947.

Common names Top

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Language Common/alternative name
Czech koženka polokulovitá
Welsh afuad pengrwn
German halbkugeliges reboulmoos
Estonian paasrebuulia
Finnish lastusammal
Dutch schermlevermos
Swedish glanslungmossa
Chinese 石地钱
Chinese 石地錢

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Reboulia hemisphaerica subsp. acrogyna (R.M.Schust.) R.M.Schust. Hepat. Anthocerotae N. Amer. 6: 168. 1992.
Reboulia hemisphaerica subsp. australis R.M.Schust. Phytologia 56: 460. 1985.
Reboulia hemisphaerica subsp. dioica R.M.Schust. Phytologia 56: 462. 1985.
Reboulia hemisphaerica subsp. hemisphaerica
Reboulia hemisphaerica subsp. orientalis R.M.Schust. Phytologia 56: 461. 1985.

Varieties (abbr. var.) Top

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Name Authority First published in
Reboulia hemisphaerica var. fissisquama Herzog Symb. Sin. 5: 5. 1930.
Reboulia hemisphaerica var. hemisphaerica
Reboulia hemisphaerica var. pangiensis (Kashyap) Kashyap ex Kachroo J. Gauhati India Univ. 5: 121. 1954.
Reboulia hemisphaerica var. turkestanica C.E.O.Jensen ex Herzog Symb. Sin. 5: 5. 1930.

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-0001198412
Tropicos 35188343
The Plant List tro-35188343
GBIF 7973324
Tropicos 35203279
The Plant List tro-35203279
GBIF 7499801
Florida Plant Atlas 4821
USDA Plants REHE
Tropicos 35188345
INPN 6153
The Plant List tro-35188345
Open Tree Of Life 985279
Observations.org 17780
NCBI Taxonomy 37395
NBN Atlas NBNSYS0000036046
Nature Serve 2.124410
iNaturalist 56408
GBIF 2688584
EPPO RBLHE
EOL 600378
Elurikkus 6773

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_984653735.1 cmRebHemi8.1 Chromosome WELLCOME SANGER INSTITUTE 2026-07-10 36 258.94 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 complete chloroplast genome of Porella gracillima Mitt. (Porellaceae) and phylogenetic relationships to other bryophytes Lee JK, Park MJ, Park SJ, Park JS Mitochondrial DNA B Resour 21-Dec-2023
PMCID:PMC10763829
doi:10.1080/23802359.2023.2294898
PMID:38173922
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
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
Bioactive Compounds Produced by Endophytic Microorganisms Associated with Bryophytes—The “Bryendophytes” Stelmasiewicz M, Świątek Ł, Gibbons S, Ludwiczuk A Molecules 05-Apr-2023
PMCID:PMC10096483
doi:10.3390/molecules28073246
PMID:37050009
Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS Life (Basel) 04-Apr-2023
PMCID:PMC10145550
doi:10.3390/life13040948
PMID:37109477
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
Natural Products Targeting Liver X Receptors or Farnesoid X Receptor She J, Gu T, Pang X, Liu Y, Tang L, Zhou X Front Pharmacol 05-Jan-2022
PMCID:PMC8766425
doi:10.3389/fphar.2021.772435
PMID:35069197
“Efficacy–Nature–Structure” Relationship of Traditional Chinese Medicine Based on Chemical Structural Data and Bioinformatics Analysis Shao XX, Chen C, Liang MM, Yu ZY, Zhang FC, Zhou MJ, Wang ZG, Fu XJ ACS Omega 01-Dec-2021
PMCID:PMC8675060
doi:10.1021/acsomega.1c04440
PMID:34926906
Cytotoxicity, antimicrobial and antioxidant activities of mosses obtained from open habitats Wolski GJ, Sadowska B, Fol M, Podsędek A, Kajszczak D, Kobylińska A PLoS One 20-Sep-2021
PMCID:PMC8452054
doi:10.1371/journal.pone.0257479
PMID:34543304
Four Centuries of Medicinal Mosses and Liverworts in European Ethnopharmacy and Scientific Pharmacy: A Review Drobnik J, Stebel A Plants (Basel) 25-Jun-2021
PMCID:PMC8309153
doi:10.3390/plants10071296
PMID:34202287
Liverwort flora of Ayan – a gained link between subarctic and hemiboreal floras in West Okhotiya (Pacific Russia) Bakalin V, Klimova K, Bakalin D, Choi SS Biodivers Data J 01-Apr-2021
PMCID:PMC8032650
doi:10.3897/BDJ.9.e65199
PMID:33841022
Bibenzyls and bisbybenzyls of bryophytic origin as promising source of novel therapeutics: pharmacology, synthesis and structure-activity Nandy S, Dey A Daru 15-Aug-2020
PMCID:PMC7429097
doi:10.1007/s40199-020-00341-0
PMID:32803687
The complete chloroplast genome of Wiesnerella denudata (Mitt.) Steph. (Wiesnerellaceae, Marchantiophyta) Choi SS, Kwon W, Park J Mitochondrial DNA B Resour 03-Aug-2020
PMCID:PMC7782009
doi:10.1080/23802359.2020.1800431
PMID:33458082
The Increase of Simple Sequence Repeats during Diversification of Marchantiidae, An Early Land Plant Lineage, Leads to the First Known Expansion of Inverted Repeats in the Evolutionarily-Stable Structure of Liverwort Plastomes Sawicki J, Bączkiewicz A, Buczkowska K, Górski P, Krawczyk K, Mizia P, Myszczyński K, Ślipiko M, Szczecińska M Genes (Basel) 12-Mar-2020
PMCID:PMC7140840
doi:10.3390/genes11030299
PMID:32178248
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(-)-beta-Barbatene 14109424 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(+)-alpha-Barbatene 14037349 Click to see CC1=CCC2(CC1C3(C2(CCC3)C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(1R,2S,6S,7S)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.02,6]undec-8-ene 162904460 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(1R,4S,5R)-1,8-Dimethyl-4-(prop-1-en-2-yl)spiro[4.5]dec-7-ene 20055537 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(1R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene 5316209 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(4S)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene 12444487 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
1,4-Dimethyl-4-(1-methyl-2-methylidenecyclopentyl)cyclohexene 4475720 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
2,6,7-Trimethyl-10-methylidenetricyclo[5.3.1.02,6]undec-8-ene 101414595 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
4-(5,5-Dimethylcyclopenten-1-yl)-1,4-dimethylcyclohexene 14830702 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
4,8-Methanoazulene, 1,2,3,3a,4,5,8,8a-octahydro-3a,4,7,8a-tetramethyl-, (3aR,4R,8R,8aS)- 524193 Click to see CC1=CCC2(CC1C3(C2(CCC3)C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
4,8-Methanoazulene, decahydro-3a,4,8a-trimethyl-7-methylene-, (3aR,4R,8R,8aS)-rel- 524194 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
Bazzanene 179421 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
Beta-Barbatene 14109421 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
Gymnomitra-3(15),4-diene 15478921 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
Isobazzanene 14830703 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> Lignans, neolignans and related compounds
Marchantin C 5319272 Click to see 424.50 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
https://doi.org/10.1248/CPB.54.996
https://doi.org/10.1016/0031-9422(94)00860-V
Marchantin M 90667793 Click to see 454.50 unknown https://doi.org/10.1016/0031-9422(94)00860-V
Marchantin N 11754381 Click to see COC1=CC(=O)C2=C(C1=O)CCC3=CC=C(C=C3)OC4=C(C=CC(=C4)CCC5=CC(=CC=C5)O2)O 468.50 unknown https://doi.org/10.1016/0031-9422(94)00860-V
Marchantin O 101921656 Click to see 438.50 unknown https://doi.org/10.1016/0031-9422(94)00860-V
https://doi.org/10.1016/S0031-9422(99)00137-5
Marchantinquinone 10410864 Click to see C1CC2=C(C(=O)C=CC2=O)OC3=CC=CC(=C3)CCC4=CC(=C(C=C4)O)OC5=CC=C1C=C5 438.50 unknown https://doi.org/10.1016/0009-2797(95)03641-5
https://doi.org/10.1211/0022357001773913
https://doi.org/10.1016/0031-9422(94)00860-V
https://doi.org/10.1016/S0031-9422(99)00137-5
Riccardin C 10070992 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(82)83073-2
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
3-(2-Hydroxypropan-2-yl)-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-7-ol 4603262 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
https://doi.org/10.1016/0031-9422(94)00860-V
Zeorin 159931 Click to see 444.70 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
https://doi.org/10.1016/0031-9422(94)00860-V
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(10,11-Dihydroxy-2,6,8-trimethyl-2-tetracyclo[6.2.1.01,6.07,9]undecanyl)methyl acetate 73235296 Click to see CC(=O)OCC1(CCCC2(C13C(C4C2C4(C3O)C)O)C)C 294.40 unknown https://doi.org/10.1248/CPB.54.996
(1R,6R,7R,8R,9R,10R)-2,2,6,9-tetramethyltetracyclo[6.2.1.01,6.07,9]undecan-10-ol 163012806 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
(1R,6R,7R,8S,9R,10R,11S)-2,2,6,8-tetramethyltetracyclo[6.2.1.01,6.07,9]undecane-10,11-diol 162900532 Click to see 236.35 unknown https://doi.org/10.1248/CPB.54.996
[(1S,2S,6R,7R,8S,9R,10R,11S)-10,11-dihydroxy-2,6,8-trimethyl-2-tetracyclo[6.2.1.01,6.07,9]undecanyl]methyl acetate 162976986 Click to see 294.40 unknown https://doi.org/10.1248/CPB.54.996
2,2,6,8-Tetramethyltetracyclo[6.2.1.01,6.07,9]undecane-10,11-diol 73235295 Click to see CC1(CCCC2(C13C(C4C2C4(C3O)C)O)C)C 236.35 unknown https://doi.org/10.1248/CPB.54.996
2,2,6,9-Tetramethyltetracyclo[6.2.1.01,6.07,9]undecan-10-ol 73209729 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
Cyclomyltaylan-5alpha-ol 11117579 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,2R,5R)-2-methyl-5-[(1S)-1,2,2-trimethylcyclopentyl]bicyclo[3.1.0]hexan-2-ol 163186774 Click to see CC1(CCCC1(C)C23CCC(C2C3)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
2-Methyl-5-(1,2,2-trimethylcyclopentyl)bicyclo[3.1.0]hexan-2-ol 11106957 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Cuprenene 5316205 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/0031-9422(94)00860-V
(1aR,4aS,7R,8aS)-4a,8,8-trimethyl-2-methylidene-1a,3,4,5,6,7-hexahydro-1H-cyclopropa[j]naphthalen-7-ol 15488854 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
(4aR,5S,8S,8aR)-5-methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carbaldehyde 101921652 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(94)00860-V
(4aR,5S,8S,8aR)-5-methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid 101921655 Click to see CC1CCC(C2C1CCC(=C2)C(=O)O)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(94)00860-V
(5-Methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-2-yl)methanol 101417838 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(94)00860-V
(5-Methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-2-yl)methyl acetate 163011272 Click to see CC1CCC(C2C1CCC(=C2)COC(=O)C)C(=C)C 262.40 unknown https://doi.org/10.1016/0031-9422(94)00860-V
(6R)-3-Methylidene-6-(1,2,2-trimethylcyclopentyl)cyclohex-1-ene 71375071 Click to see CC1(CCCC1(C)C2CCC(=C)C=C2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(6S)-3-methylidene-6-[(1R)-1,2,2-trimethylcyclopentyl]cyclohexene 162919069 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(R)-3-Methylene-6-((S)-1,2,2-trimethylcyclopentyl)cyclohex-1-ene 25202927 Click to see CC1(CCCC1(C)C2CCC(=C)C=C2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
[(4aR,5S,8S,8aR)-5-methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-2-yl]methanol 101921653 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(94)00860-V
[(4aR,5S,8S,8aR)-5-methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-2-yl]methyl acetate 101921654 Click to see 262.40 unknown https://doi.org/10.1016/0031-9422(94)00860-V
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
1-methyl-4-[(1R)-1,2,2-trimethylcyclopentyl]cyclohexa-1,3-diene 71448973 Click to see CC1=CC=C(CC1)C2(CCCC2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
1-methyl-4-[(1S)-1,2,2-trimethylcyclopentyl]cyclohexa-1,4-diene 5316206 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(94)00860-V
1,3-Cyclohexadiene, 1-methyl-4-(1,2,2-trimethylcyclopentyl)- 12304250 Click to see CC1=CC=C(CC1)C2(CCCC2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
2-(8,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-1-yl)propan-2-ol 163034802 Click to see CC1CCCC2=CC=CC(C12C)C(C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
4a,8,8-trimethyl-2-methylidene-1a,3,4,5,6,7-hexahydro-1H-cyclopropa[j]naphthalen-7-ol 162901533 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
5-Methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carbaldehyde 101417932 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(94)00860-V
5-Methyl-8-prop-1-en-2-yl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid 14526684 Click to see CC1CCC(C2C1CCC(=C2)C(=O)O)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(94)00860-V
Cuparene 86895 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
Cyclopentanone, 2,2,3-trimethyl-3-(4-methylphenyl)-, (R)- 9813205 Click to see 216.32 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
gamma-Cuprenene 14830706 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(94)00860-V
Rulepidanol 15385763 Click to see CC1CCCC2=CC=CC(C12C)C(C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
Toluene, p-(1,2,2-trimethylcyclopentyl)-, (R)-(+)- 11084908 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
(1aR,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2,6,7,7b-tetrahydro-1aH-cyclopropa[a]naphthalene 21159127 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
1,1,7,7a-tetramethyl-5,6,7,7b-tetrahydro-1aH-cyclopropa[a]naphthalene 15625230 Click to see CC1CCC=C2C1(C3C(C3(C)C)C=C2)C 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
Rulepidadiene A 15625232 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(2S,6R)-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-2-ol 16079929 Click to see CC1=CCC2(CC1)C(=C)C(CCC2(C)C)O 220.35 unknown https://doi.org/10.1248/CPB.54.996
(6S,11S)-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-8-en-11-ol 16079927 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
5,5,9-Trimethyl-1-methylidenespiro[5.5]undec-8-en-11-ol 73235298 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
5,5,9-Trimethyl-1-methylidenespiro[5.5]undec-9-en-2-ol 73235300 Click to see 220.35 unknown https://doi.org/10.1248/CPB.54.996
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(Z,2R,5S)-5-ethyl-6-methylhept-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 11761435 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(91)85298-E
17-(5-ethyl-6-methylhept-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 122544 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(91)85298-E
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(91)85298-E
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6021 Click to see 268.23 unknown https://doi.org/10.1002/HLCA.201000423
beta-Inosine 135402037 Click to see C1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)O 268.23 unknown https://doi.org/10.1002/HLCA.201000423
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(1,2,6-Trimethyl-8-methylidene-11-tricyclo[5.3.1.02,6]undecanyl) acetate 162857607 Click to see CC(=O)OC1C2C(=C)CCC1(C3(C2(CCC3)C)C)C 262.40 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
[(1S,2S,6S,7R,11R)-1,2,6-trimethyl-8-methylidene-11-tricyclo[5.3.1.02,6]undecanyl] acetate 15819324 Click to see CC(=O)OC1C2C(=C)CCC1(C3(C2(CCC3)C)C)C 262.40 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1S,2R,6S,7S,9S)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-9-ol 14218181 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(91)85298-E
https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/S0031-9422(99)00137-5
(1S,2S,6S,7R,11R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109430 Click to see CC12CCCC1(C3(CCC(=C)C2C3O)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/S0031-9422(99)00137-5
(1S,2S,6S,7R,11R)-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undec-8-en-11-ol 10932993 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
(1S,2S,6S,7R,11S)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109432 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/S0031-9422(99)00137-5
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109431 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/S0031-9422(99)00137-5
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-9-ol 14218180 Click to see CC12CCCC1(C3(CC2C(=C)C(C3)O)C)C 220.35 unknown https://doi.org/10.1016/0031-9422(91)85298-E
https://doi.org/10.1016/S0031-9422(99)00205-8
https://doi.org/10.1016/S0031-9422(99)00137-5
1,2,6,8-Tetramethyltricyclo[5.3.1.02,6]undec-8-en-11-ol 85321042 Click to see CC1=CCC2(C(C1C3(C2(CCC3)C)C)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> 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/10.1002/HLCA.201000423
(2S,3R,4R,5R,6S)-2-[(2R,3R,4R,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101456594 Click to see 462.40 unknown https://doi.org/10.1002/HLCA.201000423
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101953021 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1002/HLCA.201000423
(2S,3R,4S,5R)-2-[(2R,3R,4R,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 101953019 Click to see 448.40 unknown https://doi.org/10.1002/HLCA.201000423
(2S,3R,4S,5R)-2-[(2R,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 101953020 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1002/HLCA.201000423
2-(3,4-Dihydroxyphenyl)ethyl beta-D-glucopyranoside 5316821 Click to see 316.30 unknown https://doi.org/10.1002/HLCA.201000423
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see 316.30 unknown https://doi.org/10.1002/HLCA.201000423
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(1S,2R,6S,7S,8S)-8-hydroxy-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undecan-9-one 101598592 Click to see 236.35 unknown https://doi.org/10.1016/0031-9422(91)85298-E
8-Hydroxy-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undecan-9-one 162966655 Click to see 236.35 unknown https://doi.org/10.1016/0031-9422(91)85298-E
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1R,2R,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-4-one 15488852 Click to see 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
(1S,2R,6S,7R,8R)-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undecan-9-one 14218187 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00587-7
https://doi.org/10.1016/S0031-9422(99)00205-8
(1S,2R,6S,7S)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-4-one 101357023 Click to see 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
(1S,2R,6S,7S)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-9-one 14218185 Click to see CC12CCCC1(C3(CC2C(=C)C(=O)C3)C)C 218.33 unknown https://doi.org/10.1016/0031-9422(91)85298-E
https://doi.org/10.1016/S0031-9422(99)00205-8
(1S,2R,6S,8R)-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undecan-9-one 163193283 Click to see CC1C2CC(CC1=O)(C3(C2(CCC3)C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-4-one 162952383 Click to see 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-9-one 14218184 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(91)85298-E
https://doi.org/10.1016/S0031-9422(99)00205-8
1,2,6,8-Tetramethyltricyclo[5.3.1.02,6]undecan-9-one 14218186 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1S,2S,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-one 15819323 Click to see 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-one 162902040 Click to see 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00205-8
> Organoheterocyclic compounds / Oxanes
(1R,3S,4S)-1',4,7,7-tetramethylspiro[2-oxabicyclo[2.2.1]heptane-3,4'-cyclohexene] 100984563 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
1',4,7,7-Tetramethylspiro[2-oxabicyclo[2.2.1]heptane-3,4'-cyclohexene] 163099895 Click to see CC1=CCC2(CC1)C3(CCC(C3(C)C)O2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(99)00137-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7,4'-dimethoxyflavone 5281601 Click to see 298.29 unknown https://doi.org/10.1016/0031-9422(91)85298-E

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