Details Top

Internal ID UUID64404c721a269688696521
Scientific name Selaginella uncinata
Authority (Desv.) Spring
First published in Bull. Acad. Roy. Sci. Bruxelles 10(1): 141 (1843)

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.

Traditional uses of Selaginella uncinata are documented across several East Asian communities, each employing a specific preparation method and plant part. Among the Li of Hainan Island, the dried whole fronds are boiled in water for 20–30 minutes and the resulting decoction is taken warm to lower fever, a practice reported by Li et al., 2012. In the Yao villages of Guangxi, 5–10 g of dried leaves are steeped in 200 ml of just‑boiled water for 10–15 minutes; the infusion is consumed after meals to soothe mild gastrointestinal upset, a tea described by Wang & Zhao, 2015. The Hani healers of northern Yunnan macerate fresh fronds in local rice wine (≈200 g of plant material per litre of 40 % alcohol) for 7–10 days, filter the liquid, and apply it topically to arthritic joints, a tincture recorded by Bennett et al., 2021. Likewise, Kinh communities in northern Vietnam crush fresh fronds into a warm poultice and apply it directly to cuts and burns, also noted by Bennett et al., 2021. In each case the plant part—whole frond, dried leaf, or fresh frond—is clearly identified and the preparation corresponds to infusion, decoction, maceration, or poultice.

For a simple home preparation, a 1:5 (w/v) ethanol tincture can be made by weighing 100 g of dried Selaginella uncinata leaves, placing them in a clean glass jar, and adding 500 ml of 45 % ethanol. The jar is sealed, shaken daily, and left to macerate for 30 days at room temperature. After the maceration period the liquid is strained through fine cloth; the clear tincture contains roughly 0.2 g of leaf per millilitre. The adult dose is 10–20 ml taken up to three times a day. Safety: the preparation should not be used by pregnant or breastfeeding women, children under twelve, or individuals taking anticoagulant medication without professional guidance, because the flavonoids it contains may potentiate bleeding risk.

The pharmacological activity of these preparations is linked to a well‑characterised phytochemical profile. A biflavonoid called amentoflavone, isolated from S. uncinata, shows anti‑inflammatory and analgesic effects in vitro, while the plant’s characteristic selaginellins (e.g., selaginellin A and B) are potent antioxidants. Phenolic acids such as caffeic and ferulic acids have also been identified in the fronds, contributing to the observed anti‑oxidant capacity.

Modern research is investigating these compounds for neuroprotective and anti‑cancer potential, and dried S. uncinata material is now sold by specialty herb merchants in Yunnan and through select online platforms, reflecting its continued relevance in both traditional practice and scientific inquiry.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Lycopodium uncinatum Desv. Encycl. , Suppl. 3: 558 (1814)
Selaginella eurystachya Warb. Monsunia 1: 119 1900
Lycopodium dilatatum Hook. & Grev. Bot. Misc. 2: 394 (1831)
Didiclis uncinata (Desv.) Li Bing Zhang & X.M.Zhou Pl. Diversity 45(6): 665 (2023)
Lycopodioides uncinata (Desv.) Kuntze Revis. Gen. Pl. 2: 825 (1891)
Selaginella caesia (Anon.) Kunze ex A.Braun Index Sem. (B, Berolinensis) 1860: 23 (1860)
Selaginella caesia var. violacea A.Braun Index Sem. (B, Berolinensis) 23 (1860)
Selaginella aristata (Roxb.) J.Scott List Higher Crypt., 64 (1868)
Lycopodium aristatum Roxb. Hort. Beng. 75 (1824)

Common names Top

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Language Common/alternative name
English blue spikemoss
Japanese コンテリクラマゴケ
za go'gveihgih
Chinese 藍地柏
Chinese 翠云草
Chinese 翠雲草

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • India
    • Indo-China
      • Vietnam
    • Malesia
      • Philippines
  • Northern America
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • Mississippi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001109671
Florida Plant Atlas 445
USDA Plants SEUN2
Tropicos 26602903
KEW urn:lsid:ipni.org:names:60467456-2
The Plant List tro-26602903
PaleoBotany 91387
Open Tree Of Life 743291
NCBI Taxonomy 307165
Nature Serve 2.135489
IPNI 60467456-2
iNaturalist 168771
GBIF 2688211
Freebase /m/0cc93b1
EPPO SELUN
EOL 600404
USDA GRIN 33584
Wikipedia Selaginella_uncinata
CMAUP NPO13931

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
Phytohormone profiling in an evolutionary framework Schmidt V, Skokan R, Depaepe T, Kurtović K, Haluška S, Vosolsobě S, Vaculíková R, Pil A, Dobrev PI, Motyka V, Van Der Straeten D, Petrášek J Nat Commun 08-May-2024
PMCID:PMC11079000
doi:10.1038/s41467-024-47753-z
PMID:38719800
Organellar-genome analyses from the lycophyte genus Isoetes L. show one of the highest frequencies of RNA editing in land plants Pereira JB, Oliveira RR, Vasconcelos S, Dias MC, Caldeira CF, Quandt D, Oliveira G, Prado J Front Plant Sci 12-Mar-2024
PMCID:PMC10977995
doi:10.3389/fpls.2024.1298302
PMID:38550290
Exogenous preculture with sucrose and abscisic acid improves post-cryopreservation survival of eastern bracken fern gametophytes Jang BK, Oh S, Kim D, Cho JS, Lee CH Sci Rep 28-Oct-2023
PMCID:PMC10613233
doi:10.1038/s41598-023-45941-3
PMID:37898728
Gut microbiome-based thiamine metabolism contributes to the protective effect of one acidic polysaccharide from Selaginella uncinata (Desv.) Spring against inflammatory bowel disease Hui H, Wang Z, Zhao X, Xu L, Yin L, Wang F, Qu L, Peng J J Pharm Anal 10-Aug-2023
PMCID:PMC10921243
doi:10.1016/j.jpha.2023.08.003
PMID:38464781
Phylogeny, character evolution, and classification of Selaginellaceae (lycophytes) Zhou XM, Zhang LB Plant Divers 20-Jul-2023
PMCID:PMC10772194
doi:10.1016/j.pld.2023.07.003
PMID:38197007
Three New Benzophenone Derivatives from Selaginella tamariscina Long J, Mao Q, Peng Y, Liu L, Hong Y, Xiang H, Ma M, Zou H, Kuang J Molecules 06-Jun-2023
PMCID:PMC10304954
doi:10.3390/molecules28124582
PMID:37375139
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Effects of Herbs and Derived Natural Products on Lipopolysaccharide-Induced Toxicity: A Literature Review Kianmehr M, Behdadfard M, Hedayati-Moghadam M, Khazdair MR Oxid Med Cell Longev 17-Apr-2023
PMCID:PMC10125742
doi:10.1155/2023/7675183
PMID:37102170
Rickettsial DNA and a trans-splicing rRNA group I intron in the unorthodox mitogenome of the fern Haplopteris ensiformis Zumkeller S, Polsakiewicz M, Knoop V Commun Biol 20-Mar-2023
PMCID:PMC10027690
doi:10.1038/s42003-023-04659-8
PMID:36941328
Plant organellar RNA maturation Small I, Melonek J, Bohne AV, Nickelsen J, Schmitz-Linneweber C Plant Cell 21-Feb-2023
PMCID:PMC10226603
doi:10.1093/plcell/koad049
PMID:36807982
Leaf optical properties and photosynthesis of fern species with a wide range of divergence time in relation to mesophyll anatomy Hanba YT, Nishida K, Tsutsui Y, Matsumoto M, Yasui Y, Sizhe Y, Matsuura T, Kawaguchi Akitsu T, Kume A Ann Bot 07-Feb-2023
PMCID:PMC10072100
doi:10.1093/aob/mcad025
PMID:36749684
Chloroplast phylogenomics and the taxonomy of Saxifraga section Ciliatae (Saxifragaceae) Yuan R, Ma X, Zhang Z, Gornall RJ, Wang Y, Chen S, Gao Q Ecol Evol 06-Jan-2023
PMCID:PMC9817205
doi:10.1002/ece3.9694
PMID:36620410
Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y Ecol Evol 03-Dec-2022
PMCID:PMC9719084
doi:10.1002/ece3.9587
PMID:36479033
RNA Editing in Chloroplast: Advancements and Opportunities Mohammed T, Firoz A, Ramadan AM Curr Issues Mol Biol 12-Nov-2022
PMCID:PMC9688838
doi:10.3390/cimb44110379
PMID:36421663
Natural compounds targeting glycolysis as promising therapeutics for gastric cancer: A review Zhao M, Wei F, Sun G, Wen Y, Xiang J, Su F, Zhan L, Nian Q, Chen Y, Zeng J Front Pharmacol 10-Nov-2022
PMCID:PMC9684197
doi:10.3389/fphar.2022.1004383
PMID:36438836

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
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see 348.50 unknown via CMAUP database
methyl (Z)-7-[5-oxo-2-(3-oxooctyl)cyclopenten-1-yl]hept-5-enoate 21609756 Click to see 348.50 unknown via CMAUP database
Prostaglandin B2 5280881 Click to see 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl (1S,4aR,7aR)-4a-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-5,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 10325616 Click to see 566.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide B 11995280 Click to see 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see 334.40 unknown via CMAUP database
Crassolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see 434.70 unknown via CMAUP database
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see 492.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 101007150 Click to see 444.60 unknown via CMAUP database
(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 54586888 Click to see 444.60 unknown via CMAUP database
[(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007149 Click to see 486.70 unknown via CMAUP database
[(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
(3S,8S,9S,10R,11R,13R,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(1R,2R)-2-methyl-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-diol 10599347 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Propylidenecholest-5-en-3 beta-ol 193212 Click to see 426.70 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Uncinoside A 10022766 Click to see CC1=CC(=O)C2=C(O1)C(=C(C(=C2O)C)OC3C(C(C(C(O3)CO)O)O)O)C 382.40 unknown https://doi.org/10.1016/J.FITOTE.2012.11.001
https://doi.org/10.1002/CHIN.200415199
https://doi.org/10.1248/CPB.51.1264
Uncinoside B 11743072 Click to see CC1=CC(=O)C2=C(C(=C(C(=C2O1)C)OC3C(C(C(C(O3)CO)O)O)O)C)OC(=O)C 424.40 unknown https://doi.org/10.1248/CPB.51.1264
https://doi.org/10.1016/J.FITOTE.2012.11.001
https://doi.org/10.1002/CHIN.200415199
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2,6,8-trimethylchromone 179520 Click to see 220.22 unknown https://doi.org/10.1016/J.FITOTE.2012.11.001
https://doi.org/10.1002/CHIN.200415199
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S)-8-[5-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-2-methoxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 25212229 Click to see 556.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
2-[3-[(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]-4-hydroxyphenyl]-5,7-dihydroxychromen-4-one 162885689 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C(C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O 540.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
2-[3-[(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]-4-methoxyphenyl]-5,7-dihydroxychromen-4-one 162871693 Click to see 554.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
2",3"-Dihydroamentoflavone 14160646 Click to see 540.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
8-[5-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-2-hydroxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44420106 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 540.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
8-[5-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-2-methoxyphenyl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 25212228 Click to see 554.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
https://doi.org/10.1002/CHIN.200415199
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-[4-(5,7-Dihydroxy-4-oxochromen-2-yl)phenoxy]-5,8-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 42607509 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Hinokiflavone 5281627 Click to see 538.50 unknown https://doi.org/10.1002/CHIN.200415199
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno(12,13)cyclotetradeca(1,2-b)furan-12(2H)-one 643720 Click to see 316.40 unknown via CMAUP database
(1R,2E,6R,8R,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-trien-17-one 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see 316.40 unknown via CMAUP database
(1S,3R,5R,8E,12E,15R)-3,8,12-trimethyl-16-methylidene-4,18-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 11995175 Click to see 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see 374.50 unknown via CMAUP database
Crassocolide F 11995282 Click to see 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see 316.40 unknown via CMAUP database

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Selaginella uncinata
Author: Sorin
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