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Morinda lucida

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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 UUID643fe3a3e7804860870764
Scientific name Morinda lucida
Authority Benth.
First published in Niger Fl. : 406 (1849)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 黄茎巴戟

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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No forms added yet.

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
    • East Tropical Africa
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000246015
Tropicos 27907959
KEW urn:lsid:ipni.org:names:756419-1
The Plant List kew-129862
Open Tree Of Life 336207
NCBI Taxonomy 339305
IUCN Red List 156109487
IPNI 756419-1
GBIF 5339834
EOL 1110319
USDA GRIN 417533

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
Phenolic Content, Antioxidant Potential, and Antimicrobial Activity of Uvaria chamae (Annonaceae), a Food Plant from Burkina Faso Kaboré K, Dibala CI, Sama H, Diao M, Somda MK, Dicko MH Biochem Res Int 26-Mar-2024
PMCID:PMC10987249
doi:10.1155/2024/1289859
PMID:38567288
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Yupingfeng polysaccharide promote the growth of chickens via regulating gut microbiota Guan Y, Zheng W, Bai Y, Wu B Front Vet Sci 23-Feb-2024
PMCID:PMC10920335
doi:10.3389/fvets.2024.1337698
PMID:38464700
Predicting Plasmodium falciparum kinase inhibitors from antimalarial medicinal herbs using computational modeling approach Adelusi TI, Ojo TO, Bolaji OQ, Oyewole MP, Olaoba OT, Oladipo EK In Silico Pharmacol 19-Dec-2023
PMCID:PMC10730500
doi:10.1007/s40203-023-00175-z
PMID:38130691
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Medicinal plants used for management of diabetes and hypertension in Ghana Asafo-Agyei T, Appau Y, Barimah KB, Asase A Heliyon 29-Nov-2023
PMCID:PMC10703729
doi:10.1016/j.heliyon.2023.e22977
PMID:38076168
Therapeutic potentials of iridoids derived from Rubiaceae against in vitro and in vivo inflammation: A scoping review Jaafar A, Zulkipli MA, Mohd Hatta FH, Jahidin AH, Abdul Nasir NA, Hazizul Hasan M Saudi Pharm J 16-Nov-2023
PMCID:PMC10788517
doi:10.1016/j.jsps.2023.101876
PMID:38226349
Anti-malarial and haematological evaluation of the ethanolic, ethyl acetate and aqueous fractions of Chromolaena odorata Elebiyo TC, Oluba OM, Adeyemi OS BMC Complement Med Ther 09-Nov-2023
PMCID:PMC10634035
doi:10.1186/s12906-023-04200-8
PMID:37946127
In vitro trypanocidal activity of extracts and compounds isolated from Vitellaria paradoxa Bairy G, Ozzin-Kholy Zolipou CO, Nzoumbou-Boko R BMC Complement Med Ther 28-Sep-2023
PMCID:PMC10540432
doi:10.1186/s12906-023-04175-6
PMID:37770899
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
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
Allometric relationships between stem diameter, height and crown area of associated trees of cocoa agroforests of Ghana Asigbaase M, Dawoe E, Abugre S, Kyereh B, Ayine Nsor C Sci Rep 09-Sep-2023
PMCID:PMC10492788
doi:10.1038/s41598-023-42219-6
PMID:37689748
Herbs Used in Antimalarial Medicines: A Study in the Greater Accra Region of Ghana Nortey NN, Korsah S, Tagoe M, Apenteng JA, Owusu FA, Oppong J, Attah AE, Allotey S Evid Based Complement Alternat Med 19-Aug-2023
PMCID:PMC10460277
doi:10.1155/2023/6697078
PMID:37636997
From Plants to Psycho-Neurology: Unravelling the Therapeutic Benefits of Bioactive Compounds in Brain Disorders Grosso C, Santos M, Barroso MF Antioxidants (Basel) 11-Aug-2023
PMCID:PMC10451187
doi:10.3390/antiox12081603
PMID:37627598
Evaluation of α-Glucosidase Inhibition and Antihyperglycemic Activity of Extracts Obtained from Leaves and Flowers of Rumex crispus L. Aguila-Muñoz DG, Jiménez-Montejo FE, López-López VE, Mendieta-Moctezuma A, Rodríguez-Antolín J, Cornejo-Garrido J, Cruz-López MC Molecules 30-Jul-2023
PMCID:PMC10420655
doi:10.3390/molecules28155760
PMID:37570730

Phytochemical Profile Top

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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 / Anthracenes
8-Hydroxy-9,10-dimethoxyanthracene-2-carbaldehyde 163029200 Click to see COC1=C2C=CC(=CC2=C(C3=C1C=CC=C3O)OC)C=O 282.29 unknown https://doi.org/10.1016/0040-4020(73)80244-3
9,10-Dimethoxyanthracene-2-carbaldehyde 85793408 Click to see COC1=C2C=CC(=CC2=C(C3=CC=CC=C31)OC)C=O 266.29 unknown https://doi.org/10.1016/0040-4020(73)80244-3
https://doi.org/10.1039/C39720000405
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
2-Anthracenecarboxylic acid, 9,10-dihydro-1,3-dihydroxy-9,10-dioxo-, methyl ester 149791 Click to see COC(=O)C1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 298.25 unknown https://doi.org/10.1515/ZNB-1981-0925
> Benzenoids / Anthracenes / Anthraquinones
1-hydroxy-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 23786435 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 548.50 unknown https://doi.org/10.1515/ZNB-1981-0925
1-Hydroxy-2-methyl-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 74184160 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 548.50 unknown https://doi.org/10.1515/ZNB-1981-0925
1-Hydroxy-2-methylanthraquinone 160817 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 238.24 unknown https://doi.org/10.3109/13880209509055208
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.3109/13880209509055208
Anthraquinone base + 2O, MeOH, O-Hex-Pen 21917783 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1515/ZNB-1981-0925
Lucidin primeveroside 160180 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1515/ZNB-1981-0925
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1-Methyl-2,3-dihydroxyanthraquinone 11391150 Click to see CC1=C2C(=CC(=C1O)O)C(=O)C3=CC=CC=C3C2=O 254.24 unknown https://doi.org/10.3109/13880209509055208
1,6-Dihydroxy-5-methoxy-2-methylanthracene-9,10-dione 482558 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3OC)O)O 284.26 unknown https://doi.org/10.1515/ZNB-1981-0925
2-Hydroxy-3-(hydroxymethyl)anthraquinone 44445519 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C(=C3)CO)O 254.24 unknown https://doi.org/10.1055/S-2006-960473
3-Hydroxy-9,10-dioxo-anthracene-2-carbaldehyde 10198899 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C(=C3)C=O)O 252.22 unknown https://doi.org/10.1055/S-2006-960473
https://doi.org/10.1515/ZNB-1981-0925
6-Hydroxy-1-methoxy-2-methylanthracene-9,10-dione 44715573 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)OC 268.26 unknown https://doi.org/10.1055/S-2006-960473
9,10-Anthracenedione, 3-hydroxy-1-methoxy-2-(methoxymethyl)- 5319467 Click to see COCC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 298.29 unknown https://doi.org/10.1515/ZNB-1981-0925
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown https://doi.org/10.1016/0040-4020(73)80244-3
https://doi.org/10.3109/13880209509055208
https://doi.org/10.1039/C39720000405
Damnacanthal 2948 Click to see COC1=C2C(=CC(=C1C=O)O)C(=O)C3=CC=CC=C3C2=O 282.25 unknown https://doi.org/10.3109/13880209509055208
https://doi.org/10.1039/C39720000405
https://doi.org/10.1055/S-2006-961543
https://doi.org/10.1055/S-2006-960473
Damnacanthol 160474 Click to see COC1=C2C(=CC(=C1CO)O)C(=O)C3=CC=CC=C3C2=O 284.26 unknown https://doi.org/10.3109/13880209509055208
Digitolutein 160475 Click to see CC1=CC2=C(C(=C1O)OC)C(=O)C3=CC=CC=C3C2=O 268.26 unknown https://doi.org/10.1055/S-2006-961543
Lucidin ethyl ether 28578 Click to see CCOCC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 298.29 unknown https://doi.org/10.1055/S-2006-960473
Morindone 442756 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3O)O)O 270.24 unknown https://doi.org/10.3109/13880209509055208
Nordamnacanthal 160712 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)C=O)O 268.22 unknown https://doi.org/10.1055/S-2006-960473
https://doi.org/10.3109/13880209509055208
Rubiadin 1-methyl ether 96191 Click to see CC1=C(C=C2C(=C1OC)C(=O)C3=CC=CC=C3C2=O)O 268.26 unknown https://doi.org/10.1055/S-2006-960473
https://doi.org/10.1055/S-2006-961543
https://doi.org/10.3109/13880209509055208
https://doi.org/10.1039/C39720000405
Soranjidiol 124063 Click to see CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1016/0040-4020(73)80244-3
https://doi.org/10.1039/C39720000405
https://doi.org/10.1055/S-2006-960473
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1R,4R,8R,10R,11E,14S)-11-[(4-hydroxy-3-methoxyphenyl)methylidene]-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 163083638 Click to see COC1=C(C=CC(=C1)C=C2C3C4(C=CC5C4C(O3)OC=C5C(=O)OC)OC2=O)O 398.40 unknown https://doi.org/10.1016/S0031-9422(00)90940-3
methyl (1R,4R,8R,11E,14S)-11-[(4-hydroxy-3-methoxyphenyl)methylidene]-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 163189484 Click to see COC1=C(C=CC(=C1)C=C2C3C4(C=CC5C4C(O3)OC=C5C(=O)OC)OC2=O)O 398.40 unknown https://doi.org/10.1016/S0031-9422(00)90940-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-Succinylbenzoate 955 Click to see C1=CC=C(C(=C1)C(=O)CCC(=O)O)C(=O)O 222.19 unknown https://doi.org/10.1007/BF00391279

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