PlantaeDB Logo
Login Sign-up

Lophira alata

Lophira alata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643ffd6675dad012418275
Scientific name Lophira alata
Authority Banks ex C.F.Gaertn.
First published in Suppl. Carp. : 52 (1805)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lophira simplex G.Don Gen. Hist. 1: 814 (1831)
Lophira barberi Tiegh. J. Bot. (Morot) 15: 186 (1901)
Lophira africana Loud. ex G.Don Gen. Hist. 1: 814 (1831)
Lophira procera A.Chev. Vég. Ut. Afr. Trop. Franç. 5: 154 (1909)
Lophira alata var. procera (A.Chev.) Burtt Davy Forest Trees Timbers Brit. Emp. 2: 78 1933
Lophira barteri Tiegh. J. Bot. (Morot) 15: 186 (1901)
Lophira macrophylla Tiegh. J. Bot. (Morot) 15: 186 (1901)
Lophira thollonii Tiegh. J. Bot. (Morot) 15: 187 (1901)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English azobe
Spanish metel
Danish jerntræ
Danish azobé
German azobe
German azobé
German bongosi
German bongossi
Finnish siipibongossipuu
French azobé
French azobe
Hausa kujeme
Italian azobè
Japanese アソベ
Japanese ボンゴシ
ln bokole
Dutch azobe
Dutch azobé
Russian Лофира крылатая
Russian Лофира высокая

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • West Tropical Africa
      • Benin
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000443232
Tropicos 22800469
KEW urn:lsid:ipni.org:names:321039-1
The Plant List kew-2493774
Open Tree Of Life 5750805
NCBI Taxonomy 549775
IUCN Red List 33056
IPNI 321039-1
iNaturalist 186076
GBIF 3695610
Freebase /m/02xb9qm
EPPO LOHAL
EOL 5715979
USDA GRIN 22665
Wikipedia Lophira_alata

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
New Insights Into The Evolution of Chloroplast Genomes in Ochna Species (Ochnaceae, Malpighiales) Nhat Nam N, Hoang Danh N, Minh Thiet V, Do HD Evol Bioinform Online 15-Nov-2023
PMCID:PMC10655658
doi:10.1177/11769343231210756
PMID:38020533
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985
Human-induced land use changes and phosphorus limitation affect soil microbial biomass and ecosystem stoichiometry Awoonor JK, Dogbey BF, Salis I PLoS One 30-Aug-2023
PMCID:PMC10468095
doi:10.1371/journal.pone.0290687
PMID:37647326
Antimalarial Efficacy and Antioxidant Activity of Lophira lanceolata Stem Bark Ethanol Extract Using Plasmodium berghei Induced-Malaria in Swiss Albino's Mice Azizi MA, Nadia NA, Cedric Y, Sidiki NN, Guy-Armand GN, Esther DD, Sandra TN, Kevin TD, Payne VK J Parasitol Res 18-Aug-2023
PMCID:PMC10457170
doi:10.1155/2023/9400650
PMID:37637978
Improving the Autofluorescence of Lophira alata Woody Cells via the Removal of Extractives Yu Z, Xu D, Hu J, Chang S, Liu G, Huang Q, Han J, Li T, Liu Y, Wang X( Polymers (Basel) 01-Aug-2023
PMCID:PMC10422229
doi:10.3390/polym15153269
PMID:37571163
The complete chloroplast genome of Calophyllum soulattri Burm. f. (Calophyllaceae) Pahayo DG, Cadorna CA, Quimado MO, Rey JD Mitochondrial DNA B Resour 25-May-2023
PMCID:PMC10215020
doi:10.1080/23802359.2023.2215350
PMID:37250208
In Vitro Antiplasmodial, Cytotoxicity, and Antioxidant Activities of Lophira lanceolata (Ochnaceae): A Cameroonian Plant Commonly Used to Treat Malaria Abdel Azizi M, Christelle Nadia NA, Cedric Y, Guy-Armand GN, Aboubakar Sidiki NN, Jemimah Sandra TN, Alex Kevin TD, Payne VK J Trop Med 11-Feb-2023
PMCID:PMC9938790
doi:10.1155/2023/4061592
PMID:36820149
Effects of long-term Ailanthus altissima extract supplementation on fear, cognition and brain antioxidant levels Muhammad Abdur Rahman H, Javaid S, Ashraf W, Fawad Rasool M, Saleem H, Ali Khan S, Ul-Haq Z, Muhammad Muneeb Anjum S, Ahmad T, Alqahtani F, Ur Rehman A, Imran I Saudi Pharm J 15-Dec-2022
PMCID:PMC10023549
doi:10.1016/j.jsps.2022.12.003
PMID:36942273
Antibacterial potential of chalcones and its derivatives against Staphylococcus aureus da Silva L, Donato IA, Gonçalves CA, Scherf JR, dos Santos HS, Mori E, Coutinho HD, da Cunha FA 3 Biotech 01-Dec-2022
PMCID:PMC9712905
doi:10.1007/s13205-022-03398-7
PMID:36466769
Michael acceptor molecules in natural products and their mechanism of action Liang ST, Chen C, Chen RX, Li R, Chen WL, Jiang GH, Du LL Front Pharmacol 02-Nov-2022
PMCID:PMC9666775
doi:10.3389/fphar.2022.1033003
PMID:36408214
[1,2,4] Triazolo [3,4-a]isoquinoline chalcone derivative exhibits anticancer activity via induction of oxidative stress, DNA damage, and apoptosis in Ehrlich solid carcinoma-bearing mice WalyEldeen AA, El-Shorbagy HM, Hassaneen HM, Abdelhamid IA, Sabet S, Ibrahim SA Naunyn Schmiedebergs Arch Pharmacol 26-Jul-2022
PMCID:PMC9467967
doi:10.1007/s00210-022-02269-5
PMID:35881165
Research Status and Hotspots of Anticancer Natural Products Based on the Patent Literature and Scientific Articles Shen J, Li J, Yu P, Du G Front Pharmacol 17-Jun-2022
PMCID:PMC9247190
doi:10.3389/fphar.2022.903239
PMID:35784720
Improved wood species identification based on multi-view imagery of the three anatomical planes Rosa da Silva N, Deklerck V, Baetens JM, Van den Bulcke J, De Ridder M, Rousseau M, Bruno OM, Beeckman H, Van Acker J, De Baets B, Verwaeren J Plant Methods 11-Jun-2022
PMCID:PMC9188236
doi:10.1186/s13007-022-00910-1
PMID:35690828
Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants Ajao AA, Mukaila YO, Sabiu S Heliyon 25-Dec-2021
PMCID:PMC8733184
doi:10.1016/j.heliyon.2021.e08668
PMID:35024488
Phylogenetic Reassessment, Taxonomy, and Biogeography of Codinaea and Similar Fungi Réblová M, Kolařík M, Nekvindová J, Réblová K, Sklenář F, Miller AN, Hernández-Restrepo M J Fungi (Basel) 20-Dec-2021
PMCID:PMC8704094
doi:10.3390/jof7121097
PMID:34947079

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Arugosin H 11844239 Click to see CC1=CC(=C(C(=C1O)C=O)C(=O)C2=C(C=CC(=C2O)CC=C(C)C)O)O 356.40 unknown https://doi.org/10.1021/NP50070A029
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
(2R)-2-(7-hydroxy-4-oxochromen-3-yl)-3,3-bis(4-hydroxyphenyl)propanoic acid 101607250 Click to see C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=C(C3=O)C=CC(=C4)O)C(=O)O)O 418.40 unknown https://doi.org/10.1271/BBB1961.55.1151
Lophiraic acid 5487419 Click to see C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=C(C3=O)C=CC(=C4)O)C(=O)O)O 418.40 unknown https://doi.org/10.1271/BBB1961.55.1151
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(2,4-dihydroxyphenyl)-[(2S,3R,4S,5R)-5-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 162912725 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=C(C=C(C=C3)O)O)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 514.50 unknown https://doi.org/10.1016/S0040-4039(00)82195-4
(2,4-Dihydroxyphenyl)-[5-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 14162794 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=C(C=C(C=C3)O)O)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 514.50 unknown https://doi.org/10.1016/S0040-4039(00)82195-4
[(2R,3S,4S,5S)-4-(2,4-dihydroxybenzoyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 102056152 Click to see C1=CC(=CC=C1C2C(C(C(O2)C3=CC=C(C=C3)O)C(=O)C4=C(C=C(C=C4)O)O)C(=O)C5=C(C=C(C=C5)O)O)O 528.50 unknown https://doi.org/10.1016/0031-9422(92)83612-3
[(2S,3R,4S,5R)-5-[5-[(R)-[(2R,3R,3aR,4R,9bS)-7-hydroxy-2,4-bis(4-hydroxyphenyl)-3,3a,4,9b-tetrahydro-2H-furo[3,2-c]chromen-3-yl]-(2,4-dihydroxyphenyl)methyl]-2,4-dihydroxyphenyl]-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 162982736 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C5C(OC6=C(C5OC4C7=CC=C(C=C7)O)C=CC(=C6)O)C8=CC=C(C=C8)O)C9=C(C=C(C=C9)O)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1011.00 unknown https://doi.org/10.1016/0031-9422(92)83733-F
[(2S,3S,4S,5R)-5-[5-[(S)-[(2S,3S,3aS,4S,9bR)-7-hydroxy-2,4-bis(4-hydroxyphenyl)-3,3a,4,9b-tetrahydro-2H-furo[3,2-c]chromen-3-yl]-(2,4-dihydroxyphenyl)methyl]-2,4-dihydroxyphenyl]-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 101634666 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C5C(OC6=C(C5OC4C7=CC=C(C=C7)O)C=CC(=C6)O)C8=CC=C(C=C8)O)C9=C(C=C(C=C9)O)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1011.00 unknown https://doi.org/10.1016/0031-9422(92)83733-F
[(2S,3S,4S,5S)-5-[5-[(S)-[(2S,3S,3aS,4S,9bR)-7-hydroxy-2,4-bis(4-hydroxyphenyl)-3,3a,4,9b-tetrahydro-2H-furo[3,2-c]chromen-3-yl]-(2,4-dihydroxyphenyl)methyl]-2,4-dihydroxyphenyl]-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 101634667 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C5C(OC6=C(C5OC4C7=CC=C(C=C7)O)C=CC(=C6)O)C8=CC=C(C=C8)O)C9=C(C=C(C=C9)O)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1011.00 unknown https://doi.org/10.1016/0031-9422(92)83733-F
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Lithospermoside 10065132 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1016/S0305-1978(02)00187-4
> Organoheterocyclic compounds / Oxepanes
(1S,2R,5R,8R,9S)-4,4,8-trimethyl-13-oxatricyclo[6.3.2.02,5]tridecane-1,9-diol 163013188 Click to see CC1(CC2C1CCC3(C(CCC2(CO3)O)O)C)C 254.36 unknown https://doi.org/10.1016/0031-9422(92)83612-3
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(E)-1-(2,4-dihydroxyphenyl)-3-[(2S,3S)-3-[(2,4-dihydroxyphenyl)-methoxymethyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-one 101630348 Click to see COC(C1C(OC2=C1C=C(C=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)C4=CC=C(C=C4)O)C5=C(C=C(C=C5)O)O 526.50 unknown https://doi.org/10.1016/0031-9422(92)83612-3
(E)-3-[(2R,3S)-3-[(S)-[5-[(R)-[5-[(2R,3R,4R,5S)-4-(2,4-dihydroxybenzoyl)-5-(4-hydroxyphenyl)-3-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-2,4-dihydroxyphenyl]-[(2R,3S)-5-[(E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-enyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]methyl]-2,4-dihydroxyphenyl]-(2,4-dihydroxyphenyl)methyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 162896689 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C(OC5=C4C=C(C=C5)C=CC(=O)C6=C(C=C(C=C6)O)O)C7=CC=C(C=C7)O)C8=C(C=C(C(=C8)C(C9C(OC1=C9C=C(C=C1)C=CC(=O)C1=C(C=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=C(C=C(C=C1)O)O)O)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1503.50 unknown https://doi.org/10.1016/S0040-4039(99)00832-1
(E)-3-[3-[[5-[[5-[4-(2,4-dihydroxybenzoyl)-5-(4-hydroxyphenyl)-3-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-2,4-dihydroxyphenyl]-[5-[(E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-enyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]methyl]-2,4-dihydroxyphenyl]-(2,4-dihydroxyphenyl)methyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 16148290 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C(OC5=C4C=C(C=C5)C=CC(=O)C6=C(C=C(C=C6)O)O)C7=CC=C(C=C7)O)C8=C(C=C(C(=C8)C(C9C(OC1=C9C=C(C=C1)C=CC(=O)C1=C(C=C(C=C1)O)O)C1=CC=C(C=C1)O)C1=C(C=C(C=C1)O)O)O)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1503.50 unknown https://doi.org/10.1016/S0040-4039(99)00832-1
(E)-3-[3-[[5-[4-(2,4-dihydroxybenzoyl)-5-(4-hydroxyphenyl)-3-[(4-hydroxyphenyl)methyl]oxolan-2-yl]-2,4-dihydroxyphenyl]-(2,4-dihydroxyphenyl)methyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 16168529 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC(=C(C=C3O)O)C(C4C(OC5=C4C=C(C=C5)C=CC(=O)C6=C(C=C(C=C6)O)O)C7=CC=C(C=C7)O)C8=C(C=C(C=C8)O)O)C9=CC=C(C=C9)O)C(=O)C1=C(C=C(C=C1)O)O)O 1009.00 unknown https://doi.org/10.1016/0031-9422(92)80198-N
Lophirone D 14376455 Click to see C1=CC(=CC=C1C2=C(C3=C(O2)C=CC(=C3)C=CC(=O)C4=C(C=C(C=C4)O)O)C=O)O 400.40 unknown https://doi.org/10.1021/NP50070A029
Lophirone E 14376454 Click to see C1=CC(=CC=C1C2=CC3=C(O2)C=CC(=C3)C=CC(=O)C4=C(C=C(C=C4)O)O)O 372.40 unknown https://doi.org/10.1021/NP50070A029
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2,4-Dihydroxyphenyl)-[5-[3-(2,4-dihydroxyphenyl)-7,17-dihydroxy-11,21-bis(4-hydroxyphenyl)-10,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-4(9),5,7,14(19),15,17-hexaen-6-yl]-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 162970838 Click to see C1=CC(=CC=C1CC2C(C(OC2C3=CC4=C(C=C3O)OC5(C(C4C6=C(C=C(C=C6)O)O)C7C(OC8=C(C7O5)C=CC(=C8)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)C(=O)C1=C(C=C(C=C1)O)O)O 1009.00 unknown https://doi.org/10.1016/0031-9422(92)80198-N
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
3-[5-[(E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-enyl]-2-hydroxyphenyl]-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 14311191 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)C4=C(C=CC(=C4)C=CC(=O)C5=C(C=C(C=C5)O)O)O)O 510.50 unknown https://doi.org/10.1021/NP50070A029
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-[7-hydroxy-2-(4-hydroxyphenyl)-2H-chromen-3-yl]phenyl]prop-2-en-1-one 14756397 Click to see C1=CC(=CC=C1C2C(=CC3=C(O2)C=C(C=C3)O)C4=C(C=CC(=C4)C=CC(=O)C5=C(C=C(C=C5)O)O)O)O 494.50 unknown https://doi.org/10.1021/NP50070A029
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Lophirone A 5488805 Click to see C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=C(C3=O)C=CC(=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 510.50 unknown https://doi.org/10.1271/BBB1961.55.1151

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.