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Details Top

Internal ID UUID64400a329a09b201562094
Scientific name Ardisia gigantifolia
Authority Stapf
First published in Bull. Misc. Inform. Kew 1906: 74 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ardisia kteniophylla Aug.DC. Repert. Spec. Nov. Regni Veg. 8: 354 (1910)
Ardisia kteniophylla var. microdonta Pit. Fl. Indo-Chine 3: 815 1930
Ardisia pseudoverticillata Merr. J. Arnold Arbor. 8: 13. 1927
Chloranthus kiangsiensis F.P.Metcalf Lingnan Sci. J. 20: 215 (1942)

Common names Top

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Language Common/alternative name
Chinese 走马胎
Chinese 走马胎叶
Chinese 山猪药
Chinese 走马风
Chinese 马胎
Chinese 走馬胎

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 South-central
      • China Southeast
      • Hainan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000544353
UNII WEC9M7UOAG
Tropicos 22001920
KEW urn:lsid:ipni.org:names:587033-1
The Plant List kew-2647985
Open Tree Of Life 675655
NCBI Taxonomy 213405
IPNI 587033-1
iNaturalist 343967
GBIF 5558418
EOL 2891543

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
Natural Products as New Approaches for Treating Bladder Cancer: From Traditional Medicine to Novel Drug Discovery Kang Y, Park C, Lee H, Kang S, Cheon C, Kim B Pharmaceutics 31-Mar-2023
PMCID:PMC10145408
doi:10.3390/pharmaceutics15041117
PMID:37111603
Inhibiting Angiogenesis by Anti-Cancer Saponins: From Phytochemistry to Cellular Signaling Pathways Majnooni MB, Fakhri S, Ghanadian SM, Bahrami G, Mansouri K, Iranpanah A, Farzaei MH, Mojarrab M Metabolites 22-Feb-2023
PMCID:PMC10052344
doi:10.3390/metabo13030323
PMID:36984763
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
Anti-colorectal cancer of Ardisia gigantifolia Stapf. and targets prediction via network pharmacology and molecular docking study Dai W, Yang J, Liu X, Mei Q, Peng W, Hu X BMC Complement Med Ther 09-Jan-2023
PMCID:PMC9827653
doi:10.1186/s12906-022-03822-8
PMID:36624500
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Chinese herbal medicine for the treatment of chronic fatigue syndrome: A systematic review and meta-analysis Zhang Y, Jin F, Wei X, Jin Q, Xie J, Pan Y, Shen W Front Pharmacol 29-Sep-2022
PMCID:PMC9557005
doi:10.3389/fphar.2022.958005
PMID:36249791
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
Combining DNA and HPTLC profiles to differentiate a pain relief herb, Mallotus repandus, from plants sharing the same common name, “Kho-Khlan” Thongkhao K, Tungphatthong C, Pichetkun V, Gaewtongliam S, Wiwatcharakornkul W, Sukrong S PLoS One 09-Jun-2022
PMCID:PMC9200221
doi:10.1371/journal.pone.0268680
PMID:35679267
Molecular phylogeny of Asian Ardisia (Myrsinoideae, Primulaceae) and their leaf-nodulated endosymbionts, Burkholderia s.l. (Burkholderiaceae) Yang CJ, Hu JM PLoS One 19-Jan-2022
PMCID:PMC8769342
doi:10.1371/journal.pone.0261188
PMID:35045070
Comparative genomic study on the complete plastomes of four officinal Ardisia species in China Xie C, An W, Liu S, Huang Y, Yang Z, Lin J, Zheng X Sci Rep 15-Nov-2021
PMCID:PMC8594775
doi:10.1038/s41598-021-01561-3
PMID:34782652
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Saponins in Cancer Treatment: Current Progress and Future Prospects Elekofehinti OO, Iwaloye O, Olawale F, Ariyo EO Pathophysiology 05-Jun-2021
PMCID:PMC8830467
doi:10.3390/pathophysiology28020017
PMID:35366261
Triterpenoid Saponin AG8 from Ardisia gigantifolia stapf. Induces Triple Negative Breast Cancer Cells Apoptosis through Oxidative Stress Pathway Mu LH, Wang LH, Yu TF, Wang YN, Yan H, Liu P, Yan C Oxid Med Cell Longev 13-Oct-2020
PMCID:PMC7584968
doi:10.1155/2020/7963212
PMID:33123316
Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China Hu R, Lin C, Xu W, Liu Y, Long C J Ethnobiol Ethnomed 02-Jul-2020
PMCID:PMC7333293
doi:10.1186/s13002-020-00387-z
PMID:32616044
Complete chloroplast genome sequence of Ardisia gigantifolia (Myrsinaceae), a vulnerable medicinal plant Shi Y, Liu B Mitochondrial DNA B Resour 13-Nov-2019
PMCID:PMC7707709
doi:10.1080/23802359.2019.1688727
PMID:33366306

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 / Phenol esters
(3-Hydroxy-5-pentadec-8-enylphenyl) acetate 163023980 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)OC(=O)C)O 360.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
[3-hydroxy-5-[(Z)-pentadec-8-enyl]phenyl] acetate 101474427 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)OC(=O)C)O 360.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
> Benzenoids / Phenols / Benzenediols / Resorcinols
2-(2,4-Dihydroxy-6-pentadec-8-enylphenyl)-3-heptadec-8-enyl-5-methoxycyclohexa-2,5-diene-1,4-dione 75104332 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=O)C=C(C1=O)OC)C2=C(C=C(C=C2O)O)CCCCCCCC=CCCCCCC 691.00 unknown https://doi.org/10.1002/HLCA.200900172
2-(2,4-dihydroxy-6-pentadecylphenyl)-3-[(Z)-heptadec-8-enyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 45258233 Click to see CCCCCCCCCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 693.00 unknown https://doi.org/10.1002/HLCA.200900172
2-(2,4-Dihydroxy-6-pentadecylphenyl)-3-heptadec-8-enyl-5-methoxycyclohexa-2,5-diene-1,4-dione 75104333 Click to see CCCCCCCCCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 693.00 unknown https://doi.org/10.1002/HLCA.200900172
2-(2,4-dihydroxy-6-tridecylphenyl)-3-[(Z)-heptadec-8-enyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 45258234 Click to see CCCCCCCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 665.00 unknown https://doi.org/10.1002/HLCA.200900172
2-(2,4-Dihydroxy-6-tridecylphenyl)-3-heptadec-8-enyl-5-methoxycyclohexa-2,5-diene-1,4-dione 75104334 Click to see CCCCCCCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 665.00 unknown https://doi.org/10.1002/HLCA.200900172
2-[(Z)-heptadec-8-enyl]-3-[2-[(Z)-heptadec-8-enyl]-4,6-dihydroxyphenyl]-6-methoxy-5-methylcyclohexa-2,5-diene-1,4-dione 44138732 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=C(C2=O)C)OC)CCCCCCCC=CCCCCCCCC 733.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
https://doi.org/10.1002/HLCA.200900172
2-[2,4-dihydroxy-6-[(Z)-pentadec-8-enyl]phenyl]-3-[(Z)-heptadec-8-enyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 45258232 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=O)C=C(C1=O)OC)C2=C(C=C(C=C2O)O)CCCCCCCC=CCCCCCC 691.00 unknown https://doi.org/10.1002/HLCA.200900172
2-Heptadec-8-enyl-3-(2-heptadec-8-enyl-4,6-dihydroxyphenyl)-6-methoxy-5-methylcyclohexa-2,5-diene-1,4-dione 74932131 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=C(C2=O)C)OC)CCCCCCCC=CCCCCCCCC 733.10 unknown https://doi.org/10.1002/HLCA.200900172
https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
3-[(Z)-heptadec-8-enyl]-2-[2-[(Z)-heptadec-8-enyl]-4,6-dihydroxyphenyl]-5-methoxycyclohexa-2,5-diene-1,4-dione 44138866 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 719.10 unknown https://doi.org/10.1002/HLCA.200900172
https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
3-[(Z)-heptadec-8-enyl]-4-[2-[(Z)-heptadec-8-enyl]-4,6-dihydroxyphenyl]-5-hydroxy-6-methylcyclohexa-3,5-diene-1,2-dione 44138867 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=O)C(=C2O)C)CCCCCCCC=CCCCCCCCC 719.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
3-[(Z)-heptadec-8-enyl]-4-[6-[(Z)-heptadec-8-enyl]-2,4-dihydroxy-3-methylphenyl]-5-hydroxy-6-methylcyclohexa-3,5-diene-1,2-dione 44138731 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=C(C(=C1C2=C(C(=O)C(=O)C(=C2O)C)CCCCCCCC=CCCCCCCCC)O)C)O 733.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
3-Heptadec-8-enyl-2-(2-heptadec-8-enyl-4,6-dihydroxyphenyl)-5-methoxycyclohexa-2,5-diene-1,4-dione 74932189 Click to see CCCCCCCCC=CCCCCCCCC1=C(C(=CC(=C1)O)O)C2=C(C(=O)C(=CC2=O)OC)CCCCCCCC=CCCCCCCCC 719.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
https://doi.org/10.1002/HLCA.200900172
5-(Z-heptadec-8-enyl) resorcinol 14235910 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
5-(Z-Heptadec-8-enyl)resorcinol 53774196 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
5-[(Z)-heptadec-8-enyl]-2-methyl-benzene-1,3-diol 23631090 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=C(C(=C1)O)C)O 360.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
5-Heptadec-8-enyl-2-methylbenzene-1,3-diol 74073051 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=C(C(=C1)O)C)O 360.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
5-Pentadec-8-enylbenzene-1,3-diol 5462454 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
5-Pentadecylresorcinol 76617 Click to see CCCCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
Bilobol 5281852 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
butyl (2R)-2-methylbutanoate 6997354 Click to see CCCCOC(=O)C(C)CC 158.24 unknown https://doi.org/10.1002/HLCA.200900172
https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
9-Hydroxy-2,6,8-trimethyltricyclo[5.3.1.01,5]undecane-6-carboxylic acid 163047268 Click to see CC1CCC2C13CC(C2(C)C(=O)O)C(C(C3)O)C 252.35 unknown https://doi.org/10.1002/HLCA.200900172
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4S,5R,8R,10S,13R,14R,17S,18R,20S)-2-hydroxy-10-[(2S,3R,4S,5S)-4-hydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(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-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 25147100 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)OC5C(C(C(C(O5)CO)O)O)O)OC6CCC7(C(C6(C)C)CCC8(C7CCC91C8(CC(C2(C9CC(CC2)(C)C=O)CO1)O)C)C)C)CO)O)O)O)O 1207.30 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
(1S,4S,5R,8R,10S,13R,14R,17S,18R,20S)-10-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(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]oxyoxan-2-yl]oxy-4,5,9,9,13,20-hexamethyl-2-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 73354154 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(=O)C1(C8CC(CC1)(C)C=O)CO9)C)C)C)CO)O)O)O)O 1043.20 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S,6R)-5-hydroxy-2-[(3S,4S,5R,6S)-4-hydroxy-6-[[(1S,2R,4S,5R,8R,10S,13R,14R,17S,18R)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl]oxy]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 162898428 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)OC5C(C(C(C(O5)CO)O)O)O)OC6CCC7(C(C6(C)C)CCC8(C7CCC91C8(CC(C2(C9CC(CC2)(C)C)CO1)O)C)C)C)CO)O)O)O)O 1193.40 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
10-[3,4-Dihydroxy-5-[5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5,9,9,13,20-hexamethyl-2-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 163011994 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)O)OC5CCC6(C(C5(C)C)CCC7(C6CCC89C7(CC(=O)C1(C8CC(CC1)(C)C=O)CO9)C)C)C)CO)O)O)O)O 1043.20 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
2-[5-Hydroxy-2-[4-hydroxy-6-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl)oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 75241346 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)OC5C(C(C(C(O5)CO)O)O)O)OC6CCC7(C(C6(C)C)CCC8(C7CCC91C8(CC(C2(C9CC(CC2)(C)C)CO1)O)C)C)C)CO)O)O)O)O 1193.40 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
2-Hydroxy-10-[4-hydroxy-5-[5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5,9,9,13,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-20-carbaldehyde 74396827 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(CO3)O)O)O)OC4COC(C(C4O)OC5C(C(C(C(O5)CO)O)O)O)OC6CCC7(C(C6(C)C)CCC8(C7CCC91C8(CC(C2(C9CC(CC2)(C)C=O)CO1)O)C)C)C)CO)O)O)O)O 1207.30 unknown https://doi.org/10.1016/J.CCLET.2009.12.029
> Lipids and lipid-like molecules / Saccharolipids
[3,5-Diacetyloxy-2-(acetyloxymethyl)-6-(2,3,4-trihydroxybutoxy)oxan-4-yl] hexadecanoate 85294273 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(C(OC(C1OC(=O)C)OCC(C(CO)O)O)COC(=O)C)OC(=O)C 648.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
https://doi.org/10.1002/HLCA.200900172
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3S,5S,8R,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2S,3R,4R,6R)-3-methoxy-6-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 44139361 Click to see CC1CC(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)OC7C(C(C(C(O7)CO)O)O)O 710.80 unknown https://doi.org/10.1002/HLCA.200900172
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,9R,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12315384 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
https://doi.org/10.1002/HLCA.200900172
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,4R,7R,8S,12R)-12-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-4-methyl-3,14-dioxatetracyclo[10.2.1.02,10.04,8]pentadec-2(10)-en-11-one 127035631 Click to see CC12CCC(C1CC3=C(O2)C4CC(C3=O)(CO4)O)C(=C)CO 306.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.04.004
https://doi.org/10.1002/HLCA.200900172
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
5-[(Z)-heptadec-8-enyl]-7-hydroxy-8-methylchromen-2-one 45258235 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=C(C2=C1C=CC(=O)O2)C)O 412.60 unknown https://doi.org/10.1002/HLCA.200900172
5-Heptadec-8-enyl-7-hydroxy-8-methylchromen-2-one 75104335 Click to see CCCCCCCCC=CCCCCCCCC1=CC(=C(C2=C1C=CC(=O)O2)C)O 412.60 unknown https://doi.org/10.1002/HLCA.200900172

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