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Cochlospermum tinctorium

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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 UUID644032dd74edc771039557
Scientific name Cochlospermum tinctorium
Authority Perrier ex A.Rich.
First published in Fl. Seneg. Tent. : 99 (1831)

Description Top

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Synonyms Top

Scientific name Authority First published in
Maximilianea nilotica (Oliv.) Kuntze Revis. Gen. Pl. 1: 44 (1891)
Maximilianea tinctoria (Perrier ex A.Rich.) Kuntze Revis. Gen. Pl. 1: 44 1891
Cochlospermum niloticum Oliv. Fl. Trop. Afr. 1: 113 (1868)
Maximilianea tinctoria (Perrier ex A.Rich.) Kuntze Revis. Gen. Pl. 1: 44 (1891)

Common names Top

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Language Common/alternative name
dag bibilitutuɣu

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000902604
Tropicos 50040710
KEW urn:lsid:ipni.org:names:111537-1
The Plant List kew-44552
Open Tree Of Life 6114499
NCBI Taxonomy 2086539
IPNI 111537-1
iNaturalist 506189
GBIF 3702451
USDA GRIN 11019

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
Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS Plants (Basel) 04-Feb-2024
PMCID:PMC10857219
doi:10.3390/plants13030454
PMID:38337987
The Potential of Cochlospermum tinctorium, Flueggea virosa, and Waltheria indica Traditional Plants From Burkina Faso in Treating Periodontitis: A Systematic Review Diarra A, Agossa K, Youl EN Cureus 17-Jan-2024
PMCID:PMC10873538
doi:10.7759/cureus.52471
PMID:38371022
Pressurized Liquid Extraction for the Production of Extracts with Antioxidant Activity from Borututu (Cochlospermum angolense Welw.) Chipaca-Domingos HS, Ferreres F, Fornari T, Gil-Izquierdo A, Pessela BC, Villanueva-Bermejo D Foods 11-Mar-2023
PMCID:PMC10048227
doi:10.3390/foods12061186
PMID:36981113
The resource availability hypothesis (RAH) and cross-cultural patterns: which one explains West African Cochlospermum species’ uses in Benin? Favi GA, Dassou GH, Djidohokpin D, Ouachinou JM, Kpétikou CG, Gbedolo E, Anagonou A, Hidalgo-Triana N, Adomou AC J Ethnobiol Ethnomed 23-Aug-2022
PMCID:PMC9400265
doi:10.1186/s13002-022-00555-3
PMID:35999632
Extracts from Cabbage Leaves: Preliminary Results towards a “Universal” Highly-Performant Antibacterial and Antifungal Natural Mixture Arrais A, Testori F, Calligari R, Gianotti V, Roncoli M, Caramaschi A, Todeschini V, Massa N, Bona E Biology (Basel) 20-Jul-2022
PMCID:PMC9312816
doi:10.3390/biology11071080
PMID:36101458
Indigenous knowledge system associated with the uses of insects for therapeutic or medicinal purposes in two main provinces of Burkina Faso, West Africa Ouango M, Romba R, Drabo SF, Ouedraogo N, Gnankiné O J Ethnobiol Ethnomed 05-Jul-2022
PMCID:PMC9254572
doi:10.1186/s13002-022-00547-3
PMID:35790988
Molecular docking studies of phytochemicals from Terminalia chebula for identification of potential multi-target inhibitors of SARS-CoV-2 proteins Sarkar A, Agarwal R, Bandyopadhyay B J Ayurveda Integr Med 16-Feb-2022
PMCID:PMC8847108
doi:10.1016/j.jaim.2022.100557
PMID:35185301
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
Traditional medicinal plants used for treating emerging and re-emerging viral diseases in northern Nigeria Abubakar IB, Kankara SS, Malami I, Danjuma JB, Muhammad YZ, Yahaya H, Singh D, Usman UJ, Ukwuani-Kwaja AN, Muhammad A, Ahmed SJ, Folami SO, Falana MB, Nurudeen QO Eur J Integr Med 27-Nov-2021
PMCID:PMC9760313
doi:10.1016/j.eujim.2021.102094
PMID:36573184
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
A complementary food supplement from local food ingredients to enhance iron intake among children aged 6–59 months in Benin Affonfere M, Chadare FJ, Fassinou FT, Talsma EF, Linnemann AR, Azokpota P Food Sci Nutr 10-Jun-2021
PMCID:PMC8269688
doi:10.1002/fsn3.2358
PMID:34262740
Countrywide Survey of Plants Used for Liver Disease Management by Traditional Healers in Burkina Faso Tibiri A, Boria S, Traoré TK, Ouédraogo N, Nikièma A, Ganaba S, Compaoré JM, Ouédraogo I, Guissou IP, Carraz M Front Pharmacol 30-Nov-2020
PMCID:PMC7883685
doi:10.3389/fphar.2020.563751
PMID:33597863
Plants against Helicobacter pylori to combat resistance: An ethnopharmacological review Baker DA Biotechnol Rep (Amst) 21-May-2020
PMCID:PMC7248673
doi:10.1016/j.btre.2020.e00470
PMID:32477900
Impact of PPAR-Alpha Polymorphisms—The Case of Metabolic Disorders and Atherosclerosis Ruscica M, Busnelli M, Runfola E, Corsini A, Sirtori CR Int J Mol Sci 06-Sep-2019
PMCID:PMC6770475
doi:10.3390/ijms20184378
PMID:31489930
African Herbal Remedies with Antioxidant Activity: A Potential Resource Base for Wound Treatment Gulumian M, Yahaya ES, Steenkamp V Evid Based Complement Alternat Med 22-Nov-2018
PMCID:PMC6282146
doi:10.1155/2018/4089541
PMID:30595712

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0378-8741(87)90051-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3-Oxohexadecyl acetate 15726206 Click to see CCCCCCCCCCCCCC(=O)CCOC(=O)C 298.50 unknown https://doi.org/10.1016/0031-9422(91)83485-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Dodecanol 8193 Click to see CCCCCCCCCCCCO 186.33 unknown https://doi.org/10.1016/0031-9422(91)83485-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1-Hydroxy-3-hexadecanone 15726205 Click to see CCCCCCCCCCCCCC(=O)CCO 256.42 unknown https://doi.org/10.1016/0031-9422(91)83485-4
1-Hydroxyoctadecan-3-one 15726204 Click to see CCCCCCCCCCCCCCCC(=O)CCO 284.50 unknown https://doi.org/10.1016/0031-9422(91)83485-4
1-Nonadecanol 80281 Click to see CCCCCCCCCCCCCCCCCCCO 284.50 unknown https://doi.org/10.1016/0031-9422(91)83485-4
Dodecanoyl monoethanol 21588211 Click to see CCCCCCCCCCCC(=O)CCO 228.37 unknown https://doi.org/10.1021/NP020008H
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E,4E,6E,8E,10E,12E)-13-[(1R,6S)-1-hydroxy-2,2,6-trimethyl-4-oxocyclohexyl]-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid 101202075 Click to see CC1CC(=O)CC(C1(C=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)O)(C)C 398.50 unknown https://doi.org/10.1080/01483919808068324
https://doi.org/10.1021/NP020008H
https://doi.org/10.1016/S0031-9422(00)81841-5
https://doi.org/10.1016/0378-8741(92)90013-H
(2E,4E,6E,8E,10E,12E)-13-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid 101202074 Click to see CC1=CC(=O)CC(C1(C=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)O)(C)C 396.50 unknown https://doi.org/10.1080/01483919808068324
https://doi.org/10.1016/0378-8741(92)90013-H
https://doi.org/10.1016/S0031-9422(00)81841-5
https://doi.org/10.1021/NP020008H
13-(1-Hydroxy-2,2,6-trimethyl-4-oxocyclohexyl)-2,6,11-trimethyltrideca-2,4,6,8,10,12-hexaenoic acid 162891454 Click to see CC1CC(=O)CC(C1(C=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)O)(C)C 398.50 unknown https://doi.org/10.1021/NP020008H
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83485-4
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83485-4
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(91)83485-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(1R)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-2,6,11,15-tetramethylheptadeca-2,4,6,8,10,12,14,16-octaenoic acid 162844006 Click to see CC1=CC(=O)CC(C1(C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)C)O)(C)C 462.60 unknown https://doi.org/10.1016/S0031-9422(00)81841-5
(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(1S,6S)-1-hydroxy-2,2,6-trimethyl-4-oxocyclohexyl]-2,6,11,15-tetramethylheptadeca-2,4,6,8,10,12,14,16-octaenoic acid 14160635 Click to see CC1CC(=O)CC(C1(C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)C)O)(C)C 464.60 unknown https://doi.org/10.1016/S0031-9422(00)81841-5
(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-2,6,11,15-tetramethylheptadeca-2,4,6,8,10,12,14,16-octaenoic acid 14160633 Click to see CC1=CC(=O)CC(C1(C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)C)O)(C)C 462.60 unknown https://doi.org/10.1016/S0031-9422(00)81841-5
10-Hydroxy-9-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 73088393 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1021/NP020008H
17-(1-Hydroxy-2,2,6-trimethyl-4-oxocyclohexyl)-2,6,11,15-tetramethylheptadeca-2,4,6,8,10,12,14,16-octaenoic acid 162874704 Click to see CC1CC(=O)CC(C1(C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C)C)O)(C)C 464.60 unknown https://doi.org/10.1016/S0031-9422(00)81841-5
3-O-trans-p-Coumaroylalphitolic acid 11758552 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1021/NP020008H
9,10-Dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 12305767 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP020008H
Alphitolic acid 12305768 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP020008H
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1021/NP50064A039
https://doi.org/10.1016/0378-8741(92)90013-H
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Pentadecanone 61303 Click to see CCCCCCCCCCCCCC(=O)C 226.40 unknown https://doi.org/10.1016/0031-9422(91)83485-4
2-Tridecanone 11622 Click to see CCCCCCCCCCCC(=O)C 198.34 unknown https://doi.org/10.1016/0031-9422(91)83485-4
3-Hexadecanone 87789 Click to see CCCCCCCCCCCCCC(=O)CC 240.42 unknown https://doi.org/10.1016/0031-9422(91)83485-4
3-Octadecanone 87532 Click to see CCCCCCCCCCCCCCCC(=O)CC 268.50 unknown https://doi.org/10.1016/0031-9422(91)83485-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-[3,5-Di(tetradecanoyl)phenyl]hexadecan-1-one 15726207 Click to see CCCCCCCCCCCCCCCC(=O)C1=CC(=CC(=C1)C(=O)CCCCCCCCCCCCC)C(=O)CCCCCCCCCCCCC 737.20 unknown https://doi.org/10.1016/0031-9422(91)83485-4
> Organohalogen compounds / Vinyl halides / Vinyl bromides
1-Bromo-3,4,7,8-tetrachloro-3,7-dimethylocta-1,5-diene 72728369 Click to see CC(CCl)(C=CC(C(C)(C=CBr)Cl)Cl)Cl 354.90 unknown https://doi.org/10.1016/S0031-9422(00)81841-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2S,3S,4S,5S,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 76961739 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP020008H
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1016/0378-8741(87)90051-1

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