Erythroxylum hypericifolium - Unknown
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Internal ID UUID64401b909d84d211573001
Scientific name Erythroxylum hypericifolium
Authority Lam.
First published in Encycl. 2: 394 (1786)

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Synonyms Top

Scientific name Authority First published in
Erythroxylum hypericifolium var. microphyllum O.E.Schulz Pflanzenr. IV, 134: 151 1907

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
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Database ID/link to page
World Flora Online wfo-0000679893
Tropicos 100334881
INPN 706262
KEW urn:lsid:ipni.org:names:544068-1
The Plant List kew-2801454
Open Tree Of Life 6100286
IPNI 544068-1
GBIF 3693939
EPPO EYTHY

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Alkaloids of the genus Erythroxylum. Part 5. E. hypericifolium Lam. Root-bark Mansour S. Al-Said, William C. Evans, Raymond J. Grout Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19860000957
Alkaloids of Erythroxylum hypericifolium leaves Mansour S. Al-Said, William C. Evans, Raymond J. Grout Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80309-7
Alkaloids of Erythroxylum hypericifolium stem bark Mansour S. Al-Said, William C. Evans, Raymond J. Grout Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80086-X

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
> Alkaloids and derivatives
1-(1-Methylpyrrolidin-2-yl)acetone 94157 Click to see CC(=O)CC1CCCN1C 141.21 unknown https://doi.org/10.1016/0031-9422(89)80086-X
Cuscohygrine 1201543 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1016/0031-9422(89)80086-X
Cuskhygrine 441070 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1016/0031-9422(89)80086-X
Hygrine 440933 Click to see CC(=O)CC1CCCN1C 141.21 unknown https://doi.org/10.1016/0031-9422(89)80086-X
> Alkaloids and derivatives / Tropane alkaloids
[(1R,3R,5S,6R)-3-hydroxy-8-azabicyclo[3.2.1]octan-6-yl] 2-phenylacetate 11129086 Click to see C1C2CC(C(N2)CC1O)OC(=O)CC3=CC=CC=C3 261.32 unknown https://doi.org/10.1039/P19860000957
[(1S,5R)-3-acetyloxy-8-methyl-8-azabicyclo[3.2.1]octan-6-yl] 2-phenylacetate 163193379 Click to see CC(=O)OC1CC2CC(C(C1)N2C)OC(=O)CC3=CC=CC=C3 317.40 unknown https://doi.org/10.1016/0031-9422(89)80086-X
3beta-Phenylacetoxytropane 11086474 Click to see CN1C2CCC1CC(C2)OC(=O)CC3=CC=CC=C3 259.34 unknown https://doi.org/10.1016/0031-9422(89)80086-X
https://doi.org/10.1039/P19860000957
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1R,5R)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] benzoate 163193026 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C3=CC=CC=C3 261.32 unknown https://doi.org/10.1016/0031-9422(89)80086-X
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylated hydroquinones
Chrysogenester 139589899 Click to see CC1=CC(=C(C=C1O)CC=C(C)CCC=C(C)CCC(=O)OC)O 332.40 unknown https://doi.org/10.1016/0031-9422(89)80086-X
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Cyclopiamide C 122218853 Click to see CC(CC(=O)O)N1C(=O)C2=C(C1(C)C)C=C3C=CC=C4C3=C2C(=O)N4 338.40 unknown https://doi.org/10.1016/0031-9422(89)80309-7
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
[(1S,5R)-3-hydroxy-8-methyl-6-phenyl-8-azabicyclo[3.2.1]octan-1-yl] acetate 163190650 Click to see CC(=O)OC12CC(CC(N1C)C(C2)C3=CC=CC=C3)O 275.34 unknown https://doi.org/10.1016/0031-9422(89)80309-7

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