Angylocalyx boutiqueanus
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Table of Contents
Details Top
| Internal ID | UUID643fdea0c6c12905001242 |
| Scientific name | Angylocalyx boutiqueanus |
| Authority | L.Touss. |
| First published in | Bull. Jard. Bot. État Bruxelles23: 380 (1953) |
Description Top
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Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Africa click to expand
-
West-central Tropical Africa
- Congo
- Gabon
- Zaïre
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West-central Tropical Africa
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000211897 |
| Tropicos | 13055737 |
| KEW | urn:lsid:ipni.org:names:474095-1 |
| The Plant List | ild-6983 |
| Open Tree Of Life | 3919913 |
| IUCN Red List | 19892557 |
| IPNI | 474095-1 |
| iNaturalist | 139771 |
| GBIF | 2952353 |
| EOL | 702777 |
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 | ||
|---|---|---|---|---|---|---|
| 2-hydroxymethyl-3,4-dihydroxypyrrolidine in fruits of angylocalyx boutiqueanus | Robert J. Nash, E. Arthur Bell, J. Michael Williams | Elsevier BV | 25-Jul-2002 |
|
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 |
|---|---|---|---|---|---|
| > Organoheterocyclic compounds / Pyrrolidines | |||||
| 1,4-Dideoxy-1,4-imino-d-arabinitol | 451991 | Click to see C1C(C(C(N1)CO)O)O | 133.15 | unknown | https://doi.org/10.1016/S0031-9422(00)81084-5 |
| 2-(Hydroxymethyl)pyrrolidine-3,4-diol | 1335 | Click to see C1C(C(C(N1)CO)O)O | 133.15 | unknown | https://doi.org/10.1016/S0031-9422(00)81084-5 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |