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Aspidosperma formosanum

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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 UUID643fea6206cf5317931652
Scientific name Aspidosperma formosanum
Authority Duarte
First published in Arq. Jard. Bot. Rio de Janeiro 19: 218 (1973)

Description Top

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Synonyms Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000290727
Tropicos 1801523
KEW urn:lsid:ipni.org:names:21974-2
The Plant List kew-17271
Open Tree Of Life 7626178
IPNI 21974-2
GBIF 3618523

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
Alkaloids of three Aspidosperma species Ruben M.F. Garcia, Keith S. Brown Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84426-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 / Aspidospermatan-type alkaloids
1-[(1R,9R,12R)-12-ethyl-6-hydroxy-5-methoxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5-trien-8-yl]ethanone 163001634 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=C4C=CC(=C5O)OC)C(=O)C 370.50 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(3,6-Dimethoxy-8-methyl-9-oxoxanthen-1-yl) acetate 86173730 Click to see CC1=CC(=CC2=C1C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC)OC 328.30 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
Lichexanthone 5358904 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC 286.28 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,12S,16R)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.02,10.03,8]hexadeca-2(10),3,5,7-tetraene 98042957 Click to see CCC1C2CCN(C1C3=C(C2=C)NC4=CC=CC=C43)C 266.40 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
(1S,12S,16S)-16-ethyl-15-methyl-11-methylidene-9,15-diazatetracyclo[10.3.1.02,10.03,8]hexadeca-2(10),3,5,7-tetraene 98042958 Click to see CCC1C2CCN(C1C3=C(C2=C)NC4=CC=CC=C43)C 266.40 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
[(1R,11R,12R)-16-ethyl-15-methyl-9,15-diazatetracyclo[10.3.1.02,10.03,8]hexadeca-2(10),3,5,7-tetraen-11-yl]methanol 162846496 Click to see CCC1C2CCN(C1C3=C(C2CO)NC4=CC=CC=C43)C 284.40 unknown https://doi.org/10.1016/S0031-9422(00)84426-X
Uleine, 1,13-dihydro-13-hydroxy- 622307 Click to see CCC1C2CCN(C1C3=C(C2CO)NC4=CC=CC=C43)C 284.40 unknown https://doi.org/10.1016/S0031-9422(00)84426-X

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