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Vepris natalensis

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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 UUID64405442b3bbe313896164
Scientific name Vepris natalensis
Authority (Sond.) Mziray
First published in Symb. Bot. Upsal. 30(1): 74 (1992)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cranzia natalensis Kuntze Revis. Gen. Pl. 1: 99 (1891)
Teclea natalensis (Sond.) Engl. Pflanzenw. Ost-Afrikas , C: 433 (1895)
Toddalia natalensis Sond. Fl. Cap. 1: 447 (1860)

Common names Top

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Language Common/alternative name
Afrikaans treurkersielemoen

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001227815
Tropicos 50052295
KEW urn:lsid:ipni.org:names:969502-1
The Plant List tro-50052295
IUCN Red List 146450776
IPNI 969502-1
iNaturalist 595988
GBIF 3834275
EOL 5625879

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
An azole, an amide and a limonoid from Vepris uguenensis (Rutaceae). Cheplogoi PK, Mulholland DA, Coombes PH, Randrianarivelojosia M Phytochemistry 01-Apr-2008
doi:10.1016/J.PHYTOCHEM.2007.12.013
PMID:18267321
Furoquinoline alkaloids from the southern African Rutaceae Teclea natalensis. Tarus PK, Coombes PH, Crouch NR, Mulholland DA, Moodley B Phytochemistry 01-Mar-2005
doi:10.1016/J.PHYTOCHEM.2004.12.023
PMID:15771894
South African plant extractives. Part II. Alkaloids of Teclea natalensis K. H. Pegel, Winifred G. Wright Royal Society of Chemistry (RSC) 20-Apr-2004
doi:10.1039/J39690002327

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 / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,3-Dioxolo[4,5-b]acridin-10(5H)-one, 6,11-dimethoxy-5-methyl- 628642 Click to see CN1C2=CC3=C(C(=C2C(=O)C4=C1C(=CC=C4)OC)OC)OCO3 313.30 unknown https://doi.org/10.1039/J39690002327
Evoxanthine 348484 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C4=C(C=C31)OCO4)OC 283.28 unknown https://doi.org/10.1039/J39690002327
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,7-Dimethoxy-8-((3-methylbut-2-en-1-yl)oxy)furo[2,3-b]quinoline 13970973 Click to see CC(=CCOC1=C(C=CC2=C1N=C3C(=C2OC)C=CO3)OC)C 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
https://doi.org/10.1016/J.PHYTOCHEM.2007.12.013
6-[(3,3-Dimethyloxiran-2-yl)methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline 11404711 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.12.013
6-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline 163091449 Click to see CC1(C(O1)COC2=C(C=C3C(=C2)C(=C4C=COC4=N3)OC)OC)C 329.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.12.013
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
https://doi.org/10.1016/J.PHYTOCHEM.2007.12.013
Flindersiamine 68221 Click to see COC1=C2C=COC2=NC3=C(C4=C(C=C31)OCO4)OC 273.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
Tecleanatalensine B 21580536 Click to see CC(=CCOC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)C 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.023
https://doi.org/10.1016/J.PHYTOCHEM.2007.12.013

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