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Neoboutonia macrocalyx

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe42631c7a431363247
Scientific name Neoboutonia macrocalyx
Authority Pax
First published in Bot. Jahrb. Syst. 30: 339 (1901)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

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
      • Kenya
      • Tanzania
      • Uganda
    • South Tropical Africa
      • Malawi
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000249996
Tropicos 12805909
KEW urn:lsid:ipni.org:names:352470-1
The Plant List kew-133649
Open Tree Of Life 3913247
NCBI Taxonomy 1260343
IUCN Red List 144312642
IPNI 352470-1
GBIF 3070688
EOL 1153983

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
Chimpanzees select comfortable nesting tree species Lacroux C, Krief S, Douady S, Cornette R, Durand S, Aleeje A, Asalu E, Pouydebat E Sci Rep 07-Oct-2023
PMCID:PMC10560204
doi:10.1038/s41598-023-44192-6
PMID:37805595
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Density and characteristics of tree cavities inside and outside Volcanoes National Park, Rwanda Niringiyimana A, Nzarora A, Twahirwa JC, van der Hoek Y Ecol Evol 27-Oct-2022
PMCID:PMC9608801
doi:10.1002/ece3.9461
PMID:36311396
Repellent activity against Anopheles gambiae of the leaves of nesting trees in the Sebitoli chimpanzee community of Kibale National Park, Uganda Lacroux C, Pouydebat E, Rossignol M, Durand S, Aleeje A, Asalu E, Chandre F, Krief S Malar J 27-Sep-2022
PMCID:PMC9513939
doi:10.1186/s12936-022-04291-7
PMID:36163024
Antimalarial Activity of Extract and Fractions of Sauropus androgynus (L.) Merr. Ekasari W, Fatmawati D, Khoiriah SM, Baqiuddin WA, Nisa HQ, Maharupini AA, Wahyuni TS, Oktarina RD, Suhartono E, Sahu RK Scientifica (Cairo) 08-Sep-2022
PMCID:PMC9477630
doi:10.1155/2022/3552491
PMID:36119646
A chimpanzee enamel-diet δ13C enrichment factor and a refined enamel sampling strategy: Implications for dietary reconstructions Malone MA, MacLatchy LM, Mitani JC, Kityo R, Kingston JD J Hum Evol 15-Sep-2021
PMCID:PMC8478842
doi:10.1016/j.jhevol.2021.103062
PMID:34536662
Accommodating receptor flexibility and free energy calculation to reduce false positive binders in the discovery of natural products blockers of SARS-COV-2 spike RBD-ACE2 interface Ogedjo M, Onoka I, Sahini M, Shadrack DM Biochem Biophys Rep 25-May-2021
PMCID:PMC8148615
doi:10.1016/j.bbrep.2021.101024
PMID:34056140
Data on vegetation sampling in areas dominated by Pteridium aquilinum in Nyungwe forest, Western Province of Rwanda Senyanzobe JM, Mulei JM, Bizuru E, Nsengumuremyi C Data Brief 18-Jan-2021
PMCID:PMC7829135
doi:10.1016/j.dib.2021.106772
PMID:33532529
Impact of Pteridium aquilinum on vegetation in Nyungwe Forest, Rwanda Senyanzobe JM, Mulei JM, Bizuru E, Nsengimuremyi C Heliyon 03-Sep-2020
PMCID:PMC7481561
doi:10.1016/j.heliyon.2020.e04806
PMID:32944668
Antimalarial Plants Used across Kenyan Communities Omara T Evid Based Complement Alternat Med 12-Jun-2020
PMCID:PMC7306085
doi:10.1155/2020/4538602
PMID:32617107
The potential of anti-malarial compounds derived from African medicinal plants: a review of pharmacological evaluations from 2013 to 2019 Bekono BD, Ntie-Kang F, Onguéné PA, Lifongo LL, Sippl W, Fester K, Owono LC Malar J 18-May-2020
PMCID:PMC7236213
doi:10.1186/s12936-020-03231-7
PMID:32423415
Wood and meat as complementary sources of sodium for Kanyawara chimpanzees (Pan troglodytes) Venable EM, Machanda Z, Hagberg L, Lucore J, Otali E, Rothman JM, Uwimbabazi M, Wrangham R Am J Phys Anthropol 24-Feb-2020
PMCID:PMC7180133
doi:10.1002/ajpa.24029
PMID:32091137
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
On the hunt for the alternate host of Hemileia vastatrix Koutouleas A, Jørgen Lyngs Jørgensen H, Jensen B, Lillesø JB, Junge A, Ræbild A Ecol Evol 23-Nov-2019
PMCID:PMC6912922
doi:10.1002/ece3.5755
PMID:31871671
Traditional ecological knowledge and flood risk management: A preliminary case study of the Rwenzori Bwambale B, Muhumuza M, Nyeko M Jamba 31-May-2018
PMCID:PMC6014233
doi:10.4102/jamba.v10i1.536
PMID:29955272

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Glycidol esters
[(1R,2S,4R,5S,6S,10S,11R,12R,14S,16R)-4-(dodecanoyloxymethyl)-5,6,11-trihydroxy-8,12,15,15-tetramethyl-7-oxo-3-oxapentacyclo[9.5.0.02,4.06,10.014,16]hexadec-8-en-14-yl] hexadecanoate 16681403 Click to see 801.10 unknown https://doi.org/10.1021/NP0604174
[4-(Dodecanoyloxymethyl)-5,6,11-trihydroxy-8,12,15,15-tetramethyl-7-oxo-3-oxapentacyclo[9.5.0.02,4.06,10.014,16]hexadec-8-en-14-yl] hexadecanoate 73307173 Click to see CCCCCCCCCCCCCCCC(=O)OC12CC(C3(C4C=C(C(=O)C4(C(C5(C(C3C1C2(C)C)O5)COC(=O)CCCCCCCCCCC)O)O)C)O)C 801.10 unknown https://doi.org/10.1021/NP0604174
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
[(1R,2S,6R,10S,11R,13S,15R)-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] pentadecanoate 16681404 Click to see 572.80 unknown https://doi.org/10.1021/NP0604174
[(1R,2S,6R,10S,11R,13S,15R)-8-(dodecanoyloxymethyl)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] hexadecanoate 16681475 Click to see CCCCCCCCCCCCCCCC(=O)OC12CC(C3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)COC(=O)CCCCCCCCCCC)O)C 769.10 unknown https://doi.org/10.1021/NP0604174
[1,6-Dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] pentadecanoate 73307174 Click to see CCCCCCCCCCCCCCC(=O)OC12CC(C3(C(C1C2(C)C)C=C(CC4(C3C=C(C4=O)C)O)CO)O)C 572.80 unknown https://doi.org/10.1021/NP0604174
[8-(Dodecanoyloxymethyl)-1,6-dihydroxy-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] hexadecanoate 73307213 Click to see 769.10 unknown https://doi.org/10.1021/NP0604174
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(1R,2S,4R,5S,6S,10S,11R,12R,14S,16R)-5,6,11-trihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethyl-7-oxo-3-oxapentacyclo[9.5.0.02,4.06,10.014,16]hexadec-8-en-14-yl] tetradecanoate 102086222 Click to see 590.80 unknown https://doi.org/10.1021/NP0604174
[5,6,11-Trihydroxy-4-(hydroxymethyl)-8,12,15,15-tetramethyl-7-oxo-3-oxapentacyclo[9.5.0.02,4.06,10.014,16]hexadec-8-en-14-yl] tetradecanoate 162989483 Click to see 590.80 unknown https://doi.org/10.1021/NP0604174

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