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

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Synonyms Top

Scientific name Authority First published in
Lycopodium uncinatum Desv. Encycl. , Suppl. 3: 558 (1814)
Lycopodioides uncinatum (Desv. ex Poir.) Kuntze
Selaginella eurystachya Warb. Monsunia 1: 119 1900

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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No germination or propagation data was added yet.

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
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
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
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
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
A Comprehensive Evolutionary Study of Chloroplast RNA Editing in Gymnosperms: A Novel Type of G-to-A RNA Editing Is Common in Gymnosperms Huang KY, Kan SL, Shen TT, Gong P, Feng YY, Du H, Zhao YP, Wan T, Wang XQ, Ran JH Int J Mol Sci 16-Sep-2022
PMCID:PMC9505161
doi:10.3390/ijms231810844
PMID:36142757
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Excavation of Genes Responsive to Brassinosteroids by Transcriptome Sequencing in Adiantum flabellulatum Gametophytes Cai Z, Xie Z, Wang X, Zhang S, Wu Q, Yu X, Guo Y, Gao S, Zhang Y, Xu S, Wang H, Luo J Genes (Basel) 14-Jun-2022
PMCID:PMC9222622
doi:10.3390/genes13061061
PMID:35741824
Therapeutic potential of traditional Chinese medicine for the treatment of NAFLD: A promising drug Potentilla discolor Bunge Ji L, Li Q, He Y, Zhang X, Zhou Z, Gao Y, Fang M, Yu Z, Rodrigues RM, Gao Y, Li M Acta Pharm Sin B 11-May-2022
PMCID:PMC9513494
doi:10.1016/j.apsb.2022.05.001
PMID:36176915

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
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester 21609756 Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC 348.50 unknown via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O 348.50 unknown via CMAUP database
prostaglandin B2 5280881 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O 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 CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 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 CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C 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 CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C 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 COC(=O)C1=COC(C2C1(CC=C2COC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 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 CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide 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
Crassocolide B 11995280 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 492.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 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
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 101007150 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007149 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
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-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
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 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
(24E)-24-N-Propylidenecholesterol 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
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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/10.1002/CHIN.200415199
https://doi.org/10.1016/J.FITOTE.2012.11.001
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 CC1=CC(=O)C2=C(C(=C(C(=C2O1)C)O)C)O 220.22 unknown https://doi.org/10.1002/CHIN.200415199
https://doi.org/10.1016/J.FITOTE.2012.11.001
> 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 CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 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 COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)CC(O5)C6=CC=C(C=C6)O 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 COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)CC(O5)C6=CC=C(C=C6)O 554.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264561/
2",3"-Dihydroamentoflavone 14160646 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/
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 COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 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 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 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 CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=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 CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 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 CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
Crassocolide E 11995175 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Crassocolide F 11995282 Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C 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
ent-Sarcophine 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 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 CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database

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Sorin

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