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Euphorbia royleana

Euphorbia royleana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64403b952c084368032231
Scientific name Euphorbia royleana
Authority Boiss.
First published in Prodr. 15(2): 83 (1862)

Description Top

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Synonyms Top

Scientific name Authority First published in
Euphorbia pentagona Royle Ill. Bot. Himal. Mts. : 329 (1836)

Common names Top

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Language Common/alternative name
English churee
English danda thor
English royle's spurge
Nepali काने सिउँडी
szy nipaluma-masang
Chinese 霸王鞭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000964477
UNII M5R6ATY997
Tropicos 12800048
KEW urn:lsid:ipni.org:names:348095-1
The Plant List kew-81946
Open Tree Of Life 734807
NCBI Taxonomy 1130020
IPNI 348095-1
iNaturalist 418605
GBIF 3065786
Freebase /m/0n47c99
EOL 1144003
USDA GRIN 418371
Wikipedia Euphorbia_royleana
CMAUP NPO12595

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
An ethnoveterinary study on medicinal plants used by the Bai people in Yunlong County northwest Yunnan, China Gao H, Huang W, Zhao C, Xiong Y J Ethnobiol Ethnomed 13-Jan-2024
PMCID:PMC10787986
doi:10.1186/s13002-023-00633-0
PMID:38218888
Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK Sci Rep 03-Jan-2024
PMCID:PMC10764828
doi:10.1038/s41598-023-50287-x
PMID:38172161
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Electrochemical study on the effect of polar and non-polar extract of Artemisia vulgaris on the corrosion inhibition of mild-steel in an acidic medium Karki N, Neupane S, Gupta DK, Yadav AP RSC Adv 08-Mar-2023
PMCID:PMC9992942
doi:10.1039/d3ra00148b
PMID:36908543
Status Quo and Future Perspectives of Molecular and Genomic Studies on the Genus Biomphalaria—The Intermediate Snail Host of Schistosoma mansoni Au MF, Williams GA, Hui JH Int J Mol Sci 03-Mar-2023
PMCID:PMC10003693
doi:10.3390/ijms24054895
PMID:36902324
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Antitumor Effects of Esculetin, a Natural Coumarin Derivative, against Canine Mammary Gland Tumor Cells by Inducing Cell Cycle Arrest and Apoptosis Choi J, Yoo MJ, Park SY, Seol JW Vet Sci 22-Jan-2023
PMCID:PMC9961495
doi:10.3390/vetsci10020084
PMID:36851388
Diversity, distribution, and sustainability of traditional medicinal plants in Kaski district, western Nepal Khakurel D, Uprety Y, Ahn G, Cha JY, Kim WY, Lee SH, Rajbhandary S Front Pharmacol 20-Dec-2022
PMCID:PMC9807671
doi:10.3389/fphar.2022.1076351
PMID:36605393
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Ethnomedicinal study of medicinal plants used by Mizo tribes in Champhai district of Mizoram, India Laldingliani TB, Thangjam NM, Zomuanawma R, Bawitlung L, Pal A, Kumar A J Ethnobiol Ethnomed 24-Mar-2022
PMCID:PMC8944157
doi:10.1186/s13002-022-00520-0
PMID:35331291
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Study of Nutraceuticals and Phytochemicals for the Management of Alzheimer's Disease: A Review Ahmad SS, Khalid M, Kamal MA, Younis K Curr Neuropharmacol 15-Nov-2021
PMCID:PMC9185787
doi:10.2174/1570159X19666210215122333
PMID:33588732
Systematic Review of Polyherbal Combinations Used in Metabolic Syndrome Palla AH, Amin F, Fatima B, Shafiq A, Rehman NU, Haq IU, Gilani AU Front Pharmacol 07-Oct-2021
PMCID:PMC8529216
doi:10.3389/fphar.2021.752926
PMID:34690784
Ethnobotany of the Himalayas: Safeguarding Medical Practices and Traditional Uses of Kashmir Regions Bhat MN, Singh B, Surmal O, Singh B, Shivgotra V, Musarella CM Biology (Basel) 31-Aug-2021
PMCID:PMC8465354
doi:10.3390/biology10090851
PMID:34571728

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
> Benzenoids / Benzene and substituted derivatives
Benzyl mercaptan 7509 Click to see C1=CC=C(C=C1)CS 124.21 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1S,4R,5R,9S,10S,12R,15S)-9,15-diacetyloxy-4-hydroxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] benzoate 162881036 Click to see CC1CC23C(=O)C(C4(C5C(C5(C)C)C(C(C4=CC2(C1OC(=O)C)O3)O)OC(=O)C6=CC=CC=C6)OC(=O)C)C 538.60 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
> Benzenoids / Benzene and substituted derivatives / Biphenols
Euphorbetin 5317297 Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O 354.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Toluenes / Nitrotoluenes / Dinitrotoluenes
Musk ambrette 6753 Click to see CC1=C(C=C(C(=C1[N+](=O)[O-])OC)C(C)(C)C)[N+](=O)[O-] 268.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Spirangien A 11629035 Click to see CC=C(C)CC(C)C(C(C)C1C(C(CC2(O1)C(CC(C(O2)C(C)C(C(C)C=CC=CC=CC=CC=CC(CC(=O)O)OC)O)C)O)OC)C)O 703.00 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Roseoside 9930064 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1R,3R,4R,5R,7S,8S,9R,10Z,12S,13S,14S)-8,9,13-trihydroxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-4-yl] acetate 102022914 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1O)O3)C)O)O)OC(=O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14R)-4-acetyloxy-13-benzoyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-8-yl] benzoate 44179573 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)C5=CC=CC=C5)O3)C)O)OC(=O)C6=CC=CC=C6)OC(=O)C)C 616.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14R)-4-acetyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-8-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-13-yl] benzoate 44179574 Click to see CC=C(C)C(=O)OC1C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C(C1O)C)OC(=O)C5=CC=CC=C5)C)C)OC(=O)C 594.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4-acetyloxy-13-benzoyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-8-yl] benzoate 44179571 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)C5=CC=CC=C5)O3)C)O)OC(=O)C6=CC=CC=C6)OC(=O)C)C 616.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4-acetyloxy-3,6,6,10,14-pentamethyl-8,13-bis[[(E)-2-methylbut-2-enoyl]oxy]-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-9-yl] benzoate 44179495 Click to see CC=C(C)C(=O)OC1C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C(C1OC(=O)C5=CC=CC=C5)C)OC(=O)C(=CC)C)C)C)OC(=O)C 676.80 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4-acetyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-13-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-8-yl] (E)-2-methylbut-2-enoate 44179419 Click to see CC=C(C)C(=O)OC1C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C(C1O)C)OC(=O)C(=CC)C)C)C)OC(=O)C 572.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4-acetyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-13-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-8-yl] benzoate 44179498 Click to see CC=C(C)C(=O)OC1C(CC23C1(O2)C=C(C(C(C4C(C4(C)C)C(C(C3=O)C)OC(=O)C)OC(=O)C5=CC=CC=C5)O)C)C 594.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4-acetyloxy-9-hydroxy-3,6,6,10,14-pentamethyl-8-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-13-yl] benzoate 44179572 Click to see CC=C(C)C(=O)OC1C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C(C1O)C)OC(=O)C5=CC=CC=C5)C)C)OC(=O)C 594.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4,8-diacetyloxy-13-benzoyloxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-9-yl] benzoate 44179496 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)C5=CC=CC=C5)O3)C)OC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C)C 658.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4,8-diacetyloxy-3,6,6,10,14-pentamethyl-13-[(E)-2-methylbut-2-enoyl]oxy-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-9-yl] (E)-2-methylbut-2-enoate 44179420 Click to see CC=C(C)C(=O)OC1C(C2C(C2(C)C)C(C(C(=O)C34CC(C(C3(O4)C=C1C)OC(=O)C(=CC)C)C)C)OC(=O)C)OC(=O)C 614.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3R,4S,5R,7S,8S,9R,10E,12S,13S,14S)-4,8,13-triacetyloxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-9-yl] benzoate 44179497 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)C)O3)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)C 596.70 unknown https://doi.org/10.1021/NP800816N
[(1R,3S,4S,5R,7S,8R,9R,10E,12S,13S,14R)-8,9,13-triacetyloxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-4-yl] acetate 162894257 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1OC(=O)C)O3)C)OC(=O)C)OC(=O)C)OC(=O)C)C 534.60 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
[(1R,3S,4S,5R,7S,8R,9R,10E,12S,13S,14R)-8,9,13-trihydroxy-3,6,6,10,14-pentamethyl-2-oxo-16-oxatetracyclo[10.3.1.01,12.05,7]hexadec-10-en-4-yl] acetate 162950237 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1O)O3)C)O)O)OC(=O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
Ingol 42608245 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1O)O3)C)O)O)O)C 366.40 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
Ingol 12-acetate 536571 Click to see CC1CC23C(=O)C(C(C4C(C4(C)C)C(C(C(=CC2(C1O)O3)C)O)O)OC(=O)C)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(4R,6S,8R,9S,13S,18R)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-8-ol 5316859 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC)OC)O)OC)OC)COC 465.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dischidiol 102486662 Click to see CC(=C)C1(CCC2C(C1CCCO)(CCC3(C2(CCC4(C3CC(CC4)(C)C)C)C)C)C)O 444.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Euponin 5281465 Click to see CC=C(C)C(=O)OC1CC(=C2CC3C(C2C4C1C(=C)C(=O)O4)(O3)C)CO 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
CID 91895434 91895434 Click to see CC1(CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1)C)C)C 456.70 unknown via CMAUP database
Euphol 441678 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
Euphorbadienol 10863111 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown via CMAUP database
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
Monogynol B (6CI) 44586882 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(6S,7S,12S,16R)-7,12,16-trimethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 50986194 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown via CMAUP database
Cycloart-23-ene-3beta,25-diol 5470009 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4R,5R,6R)-2-[[(2R,3R,4S,5R,6R)-6-[[(1S,3R,6S,7S,8R,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-7-(hydroxymethyl)-7,12,16-trimethyl-6-[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-14-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 23304329 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CC4(C5CCC6C(C(CCC67C5(C7)CCC4(C3C(C)CCC(C(C)(C)O)O)C)OC8C(C(C(CO8)O)O)O)(C)CO)C)O)O)O)O)O)O 933.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,4R,5R,9S,10S,12R,15S)-4,9,15-triacetyloxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] 2-methylbutanoate 162817239 Click to see CCC(C)C(=O)OC1C2C(C2(C)C)C3(C(C(=O)C45CC(C(C4(O5)C=C3C1OC(=O)C)OC(=O)C)C)C)OC(=O)C 560.60 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
[(1S,4R,5R,9S,10S,12R,15S)-4,9,15-triacetyloxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] benzoate 162817241 Click to see CC1CC23C(=O)C(C4(C5C(C5(C)C)C(C(C4=CC2(C1OC(=O)C)O3)OC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C 580.60 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
[(1S,4S,5R,6R,9S,10R,12R)-6-acetyloxy-7,11-bis(acetyloxymethyl)-5-hydroxy-3,11-dimethyl-15-oxo-4-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl] (Z)-2-methylbut-2-enoate 45271602 Click to see CC=C(C)C(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)COC(=O)C)CC3)COC(=O)C)OC(=O)C)O)C 558.60 unknown https://doi.org/10.1021/NP800816N
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,4R,5R,9S,10S,12R,15S)-9,15-diacetyloxy-4-hydroxy-7,7,10,14-tetramethyl-11-oxo-16-oxapentacyclo[10.3.1.01,12.03,9.06,8]hexadec-2-en-5-yl] 2-methylbutanoate 162915787 Click to see CCC(C)C(=O)OC1C2C(C2(C)C)C3(C(C(=O)C45CC(C(C4(O5)C=C3C1O)OC(=O)C)C)C)OC(=O)C 518.60 unknown https://doi.org/10.1016/S0031-9422(00)80559-2
Ingenol 3-angelate 5,20-diacetate 45269949 Click to see CC=C(C)C(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3)COC(=O)C)OC(=O)C)O)C 500.60 unknown https://doi.org/10.1021/NP800816N
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2S)-2-(ethylamino)-2-thiophen-2-ylcyclohexan-1-one 73416012 Click to see CCNC1(CCCCC1=O)C2=CC=CS2 223.34 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Diacetone Alcohol 31256 Click to see CC(=O)CC(C)(C)O 116.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database

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