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Myrianthus serratus

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 UUID643ff5b8c2060647176402
Scientific name Myrianthus serratus
Authority (Trécul) Benth. & Hook.f.
First published in Gen. Pl. 3: 379 (1880)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Dicranostachys serrata Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 85 (1847)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Myrianthus serratus var. letestui Ruiter Bull. Jard. Bot. Natl. Belg. 46: 492 (1976)
Myrianthus serratus var. serratus

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Burkina
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000374687
Tropicos 21301883
KEW urn:lsid:ipni.org:names:584399-1
The Plant List kew-2369424
Open Tree Of Life 5749377
NCBI Taxonomy 1781622
IUCN Red List 147036328
IPNI 584399-1
GBIF 7316414
Wikipedia Myrianthus_serratus

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
The Occurrence and Biological Activity of Tormentic Acid—A Review Olech M, Ziemichód W, Nowacka-Jechalke N Molecules 22-Jun-2021
PMCID:PMC8270333
doi:10.3390/molecules26133797
PMID:34206442
An E-ring γ-lactone pentacyclic triterpene from Myrianthus serratus David Lontsi, Ngninzeko Fernande Ngounou, Azefack Leon Tapondjou, Beibam Lucas Sondengam, Bernard Bodo, Marie-Therese Martin Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00292-1

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 alcohol esters
Oct-2-enyl acetate 102248 Click to see 170.25 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162935281 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC 632.90 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1S,4S,5R,8R,10R,11R,13R,14R,18S,19S,20R)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracos-16-en-11-yl] acetate 100956041 Click to see 512.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Benthamic acid methyl ester 601647 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Euscaphic Acid Methyl Ester 14314584 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Maslinic acid methyl ester 13653327 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
methyl (1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 457300 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Methyl 3-epimaslinate 609113 Click to see 486.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Tormentic Acid Methyl Ester 14314585 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1
Urs-12-en-28-oic acid, 2,3,19-trihydroxy-, methyl ester, (2alpha,3beta)- 601648 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC 502.70 unknown https://doi.org/10.1016/S0031-9422(98)00292-1

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