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Vepris verdoorniana

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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 UUID643ffaa893d68541351868
Scientific name Vepris verdoorniana
Authority (Exell & Mendonça) Mziray
First published in Symb. Bot. Upsal. 30(1): 76 (1992)

Description Top

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Synonyms Top

Scientific name Authority First published in
Teclea verdoorniana Exell & Mendonça Consp. Fl. Angol. 1: 270 (1951)

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
  • Africa
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gabon
      • Gulf Of Guinea Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000420118
Tropicos 50052327
KEW urn:lsid:ipni.org:names:969514-1
The Plant List kew-2454401
Open Tree Of Life 6126703
IPNI 969514-1
GBIF 3833931
EOL 5625915

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
Nkolbisine, a New Furoquinoline Alkaloid, and 7-Deacetylazadirone From Teclea verdoorniana Johnson Foyere Ayafor, Joseph I. Okogun American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50020A012
Isolation and identification of three new phenolic furoquinoline alkaloids from Teclea verdoorniana Exell & Mendonça (Rutaceae) Johnson Foyere Ayafor, Joseph I. Okogun Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19820000909
Tecleaverdoornine: a new C-prenylated phenylated furoquinoline Joseph I. Okogun, J. Foyere Ayafor Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39770000652
Quinoline and indolopyridoquinazoline alkaloids from Vepris louisii J.Foyere Ayafor, B.Lucas Sondengam, B.Tchaleu Ngadjui Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83109-9

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
> Benzenoids / Benzene and substituted derivatives / Benzophenones
[2-(Methylamino)phenyl](2,4,6-trimethoxyphenyl)methanone 304461 Click to see CNC1=CC=CC=C1C(=O)C2=C(C=C(C=C2OC)OC)OC 301.34 unknown https://doi.org/10.1039/P19820000909
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1039/P19820000909
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP50020A012
https://doi.org/10.1039/P19820000909
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Azadirone II, 7-deacetyl 336015 Click to see CC1(C2CC(C3(C(C2(C=CC1=O)C)CCC4(C3=CCC4C5=COC=C5)C)C)O)C 394.50 unknown https://doi.org/10.1021/NP50020A012
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2R)-1-(4,7-dimethoxyfuro[2,3-b]quinolin-6-yl)oxy-3-methylbutane-2,3-diol 162911907 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1021/NP50020A012
10-(3-Hydroxy-3-methylbutyl)-8-methoxy-4,12,14-trioxa-2-azatetracyclo[7.7.0.03,7.011,15]hexadeca-1(16),2,5,7,9,11(15)-hexaen-16-ol 13970976 Click to see CC(C)(CCC1=C2C(=C(C3=C1OCO3)O)N=C4C(=C2OC)C=CO4)O 345.30 unknown https://doi.org/10.1039/P19820000909
https://doi.org/10.1016/0031-9422(82)83109-9
8-Methoxy-4,12,14-trioxa-2-azatetracyclo[7.7.0.03,7.011,15]hexadeca-1(16),2,5,7,9,11(15)-hexaen-16-ol 13970977 Click to see COC1=C2C=COC2=NC3=C(C4=C(C=C31)OCO4)O 259.21 unknown https://doi.org/10.1039/P19820000909
https://doi.org/10.1016/0031-9422(82)83109-9
Flindersiamine 68221 Click to see COC1=C2C=COC2=NC3=C(C4=C(C=C31)OCO4)OC 273.24 unknown https://doi.org/10.1039/C39770000652
https://doi.org/10.1039/P19820000909
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1039/P19820000909
Nkolbisine 157014 Click to see CC(C)(C(COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC)O)O 347.40 unknown https://doi.org/10.1021/NP50020A012
Tecleaverdoornine 152710 Click to see CC(=CCC1=C2C(=C(C3=C1OCO3)O)N=C4C(=C2OC)C=CO4)C 327.30 unknown https://doi.org/10.1039/P19820000909
https://doi.org/10.1039/C39770000652

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