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Internal ID UUID643fd633c16ca890388456
Scientific name Ormosia coutinhoi
Authority Ducke
First published in Arch. Jard. Bot. Rio de Janeiro3: 136 (1922)

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Synonyms Top

Scientific name Authority First published in
Macroule coutinhoi (Ducke) Pierce Trop. Woods71: 2 (1942)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000168259
Tropicos 13011046
INPN 733753
KEW urn:lsid:ipni.org:names:176356-2
The Plant List ild-14584
Open Tree Of Life 702388
NCBI Taxonomy 1231560
IUCN Red List 62026772
IPNI 176356-2
iNaturalist 465975
GBIF 5355467
EOL 415970
USDA GRIN 436731

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Co-developing an international TLS network for the 3D ecological understanding of global trees: System architecture, remote sensing models, and functional prospects Lin Y, Filin S, Billen R, Mizoue N Environ Sci Ecotechnol 21-Feb-2023
PMCID:PMC10024182
doi:10.1016/j.ese.2023.100257
PMID:36941885
The isolation of 11-oxotetrahydrorhombifoline from <i>Ormosia coutinhoi</i> and a study of its mass spectrum Stewart McLean, A. G. Harrison, D. G. Murray Canadian Science Publishing 23-Apr-2011
doi:10.1139/V67-123
Alkaloid distribution in seeds of Ormosia, Pericopsis and Haplormosia A. Douglas Kinghorn, Raouf A. Hussain, Eugene F. Robbins, Manuel F. Balandrin, Charles H. Stirton, Stephen V. Evans Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83116-9

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 / Lupin alkaloids / Aloperine and related alkaloids / Ormosia-type alkaloids
(1S,2R,15S,16R,23R)-7,9,21-triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracos-13-ene 163069209 Click to see C1CCN2CC34CC(C2C1)C=C5C3N(CCC5)CN6C4CCCC6 327.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
(1S,2S,9R,10S)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-7-ene 163188814 Click to see C1CCNC(C1)C23CC(C=C4C2NCCC4)C5CCCCN5C3 315.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
1-Piperidin-2-yl-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-7-ene 76419204 Click to see C1CCNC(C1)C23CC(C=C4C2NCCC4)C5CCCCN5C3 315.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
7,9,21-Triazahexacyclo[11.9.1.11,15.02,7.09,23.016,21]tetracos-13-ene 163069205 Click to see C1CCN2CC34CC(C2C1)C=C5C3N(CCC5)CN6C4CCCC6 327.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Organoheterocyclic compounds / Quinolizidines / Quinolizidinones
(1R,2R,9S)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecane-8,10-dione 162848982 Click to see C=CCCN1CC2CC(C1=O)C(=O)N3C2CCCC3 262.35 unknown https://doi.org/10.1139/V67-123
11-But-3-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecane-8,10-dione 162848981 Click to see C=CCCN1CC2CC(C1=O)C(=O)N3C2CCCC3 262.35 unknown https://doi.org/10.1139/V67-123

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