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Aspidosperma oblongum

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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 UUID643fea6e573e0545963612
Scientific name Aspidosperma oblongum
Authority A.DC.
First published in Prodr. 8: 399 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Macaglia oblonga Kuntze Revis. Gen. Pl. 2: 416 (1891)
Aspidosperma kuhlmannii Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 12: 555 (1935)

Common names Top

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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
  • Southern America
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000291268
Tropicos 1800138
INPN 732579
KEW urn:lsid:ipni.org:names:77418-1
The Plant List kew-17324
Open Tree Of Life 72871
NCBI Taxonomy 1186084
IUCN Red List 169862304
IPNI 77418-1
GBIF 3617704
EOL 6852207

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
Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections Casciaro B, Calcaterra A, Cappiello F, Mori M, Loffredo MR, Ghirga F, Mangoni ML, Botta B, Quaglio D Toxins (Basel) 01-Sep-2019
PMCID:PMC6783983
doi:10.3390/toxins11090511
PMID:31480508
Aspidosperma de Guyane: Alcaloïdes des Graines de Aspidosperma oblongum G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, H. Jacquemin, S. K. Kan American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50029A019

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 / Corynanthean-type alkaloids
methyl (1S,18S,19S,20R)-18-hydroxy-1,3,11,12,14,17,18,19,20,21-decahydroyohimban-19-carboxylate 163087500 Click to see COC(=O)C1C(CC=C2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 352.40 unknown https://doi.org/10.1021/NP50029A019
> Alkaloids and derivatives / Yohimbine alkaloids
methyl (15R,18R,19R,20R)-18-hydroxy-11,12,14,15,16,17,18,19,20,21-decahydroyohimban-19-carboxylate 163188953 Click to see COC(=O)C1C(CCC2C1CC3=C4C(=C5C=CC=CC5=N4)CCN3C2)O 352.40 unknown https://doi.org/10.1021/NP50029A019
methyl (1S,13S,15R,18S,19R,20R)-18-hydroxy-13-oxido-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-13-ium-19-carboxylate 163191033 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CC[N+]3(C2)[O-])C5=CC=CC=C5N4)O 370.40 unknown https://doi.org/10.1021/NP50029A019
methyl (1S,15R,18R,19R,20R)-18-hydroxy-7-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163065733 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3CC5C(C4)CCC(C5C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP50029A019
methyl (1S,15S,18R,19R,20R)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 92460291 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1021/NP50029A019
methyl (1S,15S,18R,19R,20R)-18-hydroxy-7-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163065734 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3CC5C(C4)CCC(C5C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP50029A019
methyl (1S,15S,18S,19S,20R)-18-hydroxy-7-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163065732 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3CC5C(C4)CCC(C5C(=O)OC)O 384.50 unknown https://doi.org/10.1021/NP50029A019
Yohimbine beta-N-oxide 163184408 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CC[N+]3(C2)[O-])C5=CC=CC=C5N4)O 370.40 unknown https://doi.org/10.1021/NP50029A019

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