Leiotulus alexandrinus
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Table of Contents
Details Top
Internal ID | UUID643ff433b4f01684356928 |
Scientific name | Leiotulus alexandrinus |
Authority | Ehrenb. |
First published in | Linnaea 4: 399 (1829) |
Description Top
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Synonyms Top
Scientific name | Authority | First published in |
---|---|---|
Malabaila suaveolens | Coss. | Bull. Soc. Bot. France 19: 82 (1872 publ. 1873) |
Malabaila numidica | Coss. | Bull. Soc. Bot. France 9: 297 (1862) |
Peucedanum suaveolens | (Coss.) M.Hiroe | Umbell. World : 1577 (1979) |
Peucedanum numidicum | (Coss.) M.Hiroe | Umbell. World : 1575 (1979) |
Malabaila suaveolens var. numidica | (Coss.) Maire | Bull. Soc. Hist. Nat. Afrique N. 30: 345 1939 |
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
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Northern Africa
- Algeria
- Egypt
- Libya
- Morocco
- Tunisia
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Northern Africa
Links to other databases Top
Suggest others/fix!Database | ID/link to page |
---|---|
World Flora Online | wfo-0000360835 |
KEW | urn:lsid:ipni.org:names:844137-1 |
The Plant List | kew-2341713 |
IPNI | 844137-1 |
GBIF | 3628748 |
USDA GRIN | 467081 |
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)!
Title | Authors | Publication | Released | IDs | ||
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Comparative study of the flavonoids of some local members of the umbelliferae | Nabiel A.M. Saleh, Sabry I. El-Negoumy, Mohamed N. El-Hadidi, Hasnaa A. Hosni | Elsevier BV | 25-Jul-2002 |
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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 |
---|---|---|---|---|---|
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
Isorhamnetin | 5281654 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O | 316.26 | unknown | https://doi.org/10.1016/S0031-9422(00)84026-1 |
Collections Top
In private collections | 0 |
In public collections | 0 |