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Aspidosperma eburneum

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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 UUID643fea6070725893075470
Scientific name Aspidosperma eburneum
Authority Allem. ex Saldanha
First published in Ann. Sci. Nat., Bot. , sér. 5, 14: 213 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aspidosperma compactinervium Kuhlm. Anais Reunião Sul-Amer. Bot. 3: 87 (1938 publ. 1940)
Aspidosperma pruinosum Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 15: 132 (1940)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000290655
Tropicos 1802197
KEW urn:lsid:ipni.org:names:77361-1
The Plant List kew-17264
Open Tree Of Life 6067759
IPNI 77361-1
GBIF 3618654

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)!
Title Authors Publication Released IDs
Indole alkaloids from Aspidosperma pruinosum José J. Taveira, Domingos S. Nunes, Luzia Koike, Francisco de A.M. Reis Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83311-L
THE ALKALOIDS OF ASPIDOSPERMA DISCOLOR A. DC. FERREIRA JM, GILBERT B, OWELLEN RJ, DJERASSI C Experientia 01-Jan-1970
doi:10.1007/BF02151003
PMID:14101518

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 / Macroline alkaloids
Normacusine B 5318845 Click to see CC=C1CN2C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO 294.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
> Alkaloids and derivatives / Strychnos alkaloids
Curan-17-oic acid, 2,16-didehydro-19,20-dihydroxy-, methyl ester, (19S)- 614664 Click to see CC(C1(CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C(=O)OC)O)O 356.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
> Alkaloids and derivatives / Vallesaman alkaloids
Apparicine 5281349 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1007/BF02151003
> Alkaloids and derivatives / Yohimbine alkaloids
beta-Yohimbine 2866 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
CID 5458418 5458418 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
methyl (1S,15R,18S,19R,20S)-18-hydroxy-7-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 101630449 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3CC5C(C4)CCC(C5C(=O)OC)O 384.50 unknown https://doi.org/10.1016/0031-9422(92)83311-L
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2-[(2R,3Z,12bS)-3-ethylidene-9-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 101630448 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=C3C=C(C=C4)OC 326.40 unknown https://doi.org/10.1016/0031-9422(92)83311-L
2-[(2R,3Z,12bS)-3-ethylidene-9-methoxy-5-methyl-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-5-ium-2-yl]ethanol 101630860 Click to see CC=C1C[N+]2(CCC3=C(C2CC1CCO)NC4=C3C=C(C=C4)OC)C 341.50 unknown https://doi.org/10.1016/0031-9422(92)83311-L

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