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Vepris heterophylla

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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 UUID643ffaa9d76c4250442727
Scientific name Vepris heterophylla
Authority (Engl.) Letouzey
First published in Adansonia , n.s., 6: 246 (1966)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vepris sudanica (A.Chev.) Letouzey J. Agric. Trop. Bot. Appl. 8: 395 (1961)
Toddaliopsis heterophylla (Engl.) Engl. Bot. Jahrb. Syst. 54: 306 (1917)
Teclea sudanica A.Chev. Bull. Mus. Natl. Hist. Nat. , sér. 2, 5: 408 (1933)
Teclea heterophylla Engl. Veg. Erde 9(III 1): 756 (1915)
Teclea ferruginea A.Chev. Bull. Mus. Natl. Hist. Nat. , sér. 2, 5: 409 (1933)
Teclea campestris Engl. Bot. Jahrb. Syst. 54(4): 307. 1917 [13 Mar 1917]

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

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Burkina
      • Ghana
      • Mali
      • Niger
    • West-central Tropical Africa
      • Cameroon

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000420142
Tropicos 50048820
KEW urn:lsid:ipni.org:names:775493-1
The Plant List kew-2454457
NCBI Taxonomy 1762918
IUCN Red List 32202
IPNI 775493-1
iNaturalist 444682
GBIF 3834432
Freebase /m/02y__dn
EPPO VEPHE
Wikipedia Vepris_heterophylla
CMAUP NPO25624
Open Tree Of Life 5922757

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Evaluating Phytochemical Profiles, Cytotoxicity, Antiviral Activity, Antioxidant Potential, and Enzyme Inhibition of Vepris boiviniana Extracts Bakar K, Nilofar, Mohamed A, Świątek Ł, Hryć B, Sieniawska E, Rajtar B, Ferrante C, Menghini L, Zengin G, Polz-Dacewicz M Molecules 10-Nov-2023
PMCID:PMC10673197
doi:10.3390/molecules28227531
PMID:38005252
Chemistry, taxonomy and ecology of the potentially chimpanzee-dispersed Vepris teva sp.nov. (Rutaceae) endangered in coastal thicket in the Congo Republic Langat MK, Kami T, Cheek M PeerJ 23-Aug-2022
PMCID:PMC9415428
doi:10.7717/peerj.13926
PMID:36032959
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Herbal Medicine Use During Pregnancy: A Review of the Literature With a Special Focus on Sub-Saharan Africa El Hajj M, Holst L Front Pharmacol 09-Jun-2020
PMCID:PMC7296102
doi:10.3389/fphar.2020.00866
PMID:32581815
In vitro inhibitory effects of kaempferitrin on human liver cytochrome P450 enzymes Zhang N, Liu J, Chen Z, Dou W Pharm Biol 28-Aug-2019
PMCID:PMC6720019
doi:10.1080/13880209.2019.1656257
PMID:31456483
The acute diuretic effect of an ethanolic fraction of Phyllanthus amarus (Euphorbiaceae) in rats involves prostaglandins Yao AN, Kamagaté M, Amonkan AK, Chabert P, Kpahé F, Koffi C, Kouamé MN, Auger C, Kati-Coulibaly S, Schini-Kerth V, Die-Kakou H BMC Complement Altern Med 15-Mar-2018
PMCID:PMC5856278
doi:10.1186/s12906-018-2158-0
PMID:29544490
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
Phytotherapy of High Blood Pressure in Three Phytogeographic Regions of Cameroon Tsabang N, Yedjou CG, Tchounwou PB Pharm Anal Acta 30-Jan-2017
PMCID:PMC5648011
doi:10.4172/2153-2435.1000530
PMID:29057143
Diuretic and antioxidant activities of the aqueous extract of leaves of Vepris heterophylla (Engl.) R. Let (Rutaceae) in rats Ntchapda F, Bonabe C, Kemeta Azambou DR, Talla E, Dimo T BMC Complement Altern Med 13-Dec-2016
PMCID:PMC5154154
doi:10.1186/s12906-016-1439-8
PMID:27964714
Attitudes and use of medicinal plants during pregnancy among women at health care centers in three regions of Mali, West-Africa Nergard CS, Ho TP, Diallo D, Ballo N, Paulsen BS, Nordeng H J Ethnobiol Ethnomed 09-Oct-2015
PMCID:PMC4600315
doi:10.1186/s13002-015-0057-8
PMID:26453339
Traditional medicine practitioners’ knowledge and views on treatment of pregnant women in three regions of Mali Nordeng H, Al-Zayadi W, Diallo D, Ballo N, Paulsen BS J Ethnobiol Ethnomed 17-Sep-2013
PMCID:PMC3851135
doi:10.1186/1746-4269-9-67
PMID:24041441
Antioxidant Activities of Some Cameroonian Plants Extracts Used in the Treatment of Intestinal and Infectious Diseases Momeni J, Djialeu Ntchatchoua WP, Fadimatou, Akam MT, Ngassoum MB Indian J Pharm Sci 01-Jan-2010
PMCID:PMC2883220
doi:10.4103/0250-474X.62236
PMID:20582209
Phenolic compounds from Vepris heterophylla E. Gomes, G. Dellamonica, J. Gleye, Cl. Moulis, J. Chopin, E. Stanislas Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80188-5
Furoquinoline Alkaloids from Vepris heterophylla. Gomes ET, Travert S, Gleye J, Moulis C, Fourasté I, Stanislas E Planta Med 01-Aug-1994
doi:10.1055/S-2006-959512
PMID:17236063

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 / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-23-ethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaene 86310874 Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6 377.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown via CMAUP database
Sanguinarium 5154 Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6 332.30 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Adlumine 638255 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Adlumine 442155 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-13beta-Hydroxystylopine 6452886 Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O 339.30 unknown via CMAUP database
(+)-Isocorypalmine 71261649 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown via CMAUP database
(S)-Tetrahydrocolumbamine 440229 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
17-Methoxy-5,7-dioxa-1-azoniapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),2,4(8),9,11,14,16,18-octaen-16-ol 45490416 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)O 322.30 unknown via CMAUP database
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown via CMAUP database
Ophiocarpine 12313750 Click to see COC1=C(C2=C(C=C1)C(C3C4=CC5=C(C=C4CCN3C2)OCO5)O)OC 355.40 unknown via CMAUP database
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Noroxyhydrastinine 89047 Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2R)-1-(4,6-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methylbutane-2,3-diol 162984175 Click to see CC(C)(C(COC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)OC)O)O 347.40 unknown https://doi.org/10.1055/S-2006-959512
2,3-Butanediol, 1-((4,6-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy)-3-methyl-, (+)- 6452653 Click to see CC(C)(C(COC1=C(C=C2C(=C1)N=C3C(=C2OC)C=CO3)OC)O)O 347.40 unknown https://doi.org/10.1055/S-2006-959512
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1055/S-2006-959512
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Corypalline 280225 Click to see CN1CCC2=CC(=C(C=C2C1)O)OC 193.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 159894 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Methyl sinapate 5321318 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown https://doi.org/10.1016/0031-9422(83)80188-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1016/0031-9422(83)80188-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 4475102 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
6-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 162942272 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Glucoisovitexin 323971 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
8-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 14427440 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Vitexin 2''-O-beta-D-glucoside 5280641 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(83)80188-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(83)80188-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 102465037 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(83)80188-5

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