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Drypetes gossweileri

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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 UUID644038d96542f023667826
Scientific name Drypetes gossweileri
Authority S.Moore
First published in J. Bot. 58: 271 (1920)

Description Top

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Synonyms Top

Scientific name Authority First published in
Drypetes arinozacia J.D.Kenn. Unknown Publ.
Drypetes armoracia Pax & K.Hoffm. Pflanzenr. , IV, 147, XV: 275 (1922)

Common names Top

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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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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
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000946498
Tropicos 12804142
KEW urn:lsid:ipni.org:names:345047-1
The Plant List kew-64890
Open Tree Of Life 3909858
NCBI Taxonomy 2708818
IPNI 345047-1
GBIF 3075913
EOL 1145774

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
Megaherbivores modify forest structure and increase carbon stocks through multiple pathways Berzaghi F, Bretagnolle F, Durand-Bessart C, Blake S Proc Natl Acad Sci U S A 23-Jan-2023
PMCID:PMC9945987
doi:10.1073/pnas.2201832120
PMID:36689651
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154
Beyond the Bark: An Overview of the Chemistry and Biological Activities of Selected Bark Essential Oils Graf M, Stappen I Molecules 27-Oct-2022
PMCID:PMC9654741
doi:10.3390/molecules27217295
PMID:36364121
Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria Odebunmi CA, Adetunji TL, Adetunji AE, Olatunde A, Oluwole OE, Adewale IA, Ejiwumi AO, Iheme CE, Aremu TO Plants (Basel) 10-Oct-2022
PMCID:PMC9573491
doi:10.3390/plants11192667
PMID:36235532
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
Chemical composition, in vitro antioxidant and anti-inflammatory properties of essential oils of four dietary and medicinal plants from Cameroon Ndoye Foe FM, Tchinang TF, Nyegue AM, Abdou JP, Yaya AJ, Tchinda AT, Essame JL, Etoa FX BMC Complement Altern Med 07-Apr-2016
PMCID:PMC4823886
doi:10.1186/s12906-016-1096-y
PMID:27056828
Evidence of a link between taboos and sacrifices and resource scarcity of ritual plants Quiroz D, van Andel T J Ethnobiol Ethnomed 08-Jan-2015
PMCID:PMC4326513
doi:10.1186/1746-4269-11-5
PMID:25573058
Antifungal Activity and Acute Toxicity of Stem Bark Extracts of Drypetes Gossweileri S. Moore-Euphorbiaceae from Cameroon Ngouana V, Fokou PV, Foudjo BU, Ngouela SA, Boyom FF, Zollo PH Afr J Tradit Complement Altern Med 02-Apr-2011
PMCID:PMC3252230
doi:10.4314/ajtcam.v8i3.65300
PMID:22468013
Chemical constituents of Drypetes gossweileri and their enzyme inhibitory and anti-fungal activities Athar Ata, Damaris S. Tan, Wadim L. Matochko, Julius K. Adesanwo Elsevier BV 09-Nov-2010
doi:10.1016/J.PHYTOL.2010.10.007
Phenolic constituents from Drypetes armoracia. Wandji J, Tillequin F, Mulholland DA, Temgoua AD, Wansi JD, Seguin E, Fomum ZT Phytochemistry 01-Jun-2003
doi:10.1016/S0031-9422(02)00630-1
PMID:12770597
Sterolic and triterpenoidic constituents of stem bark of Drypetes gossweileri. Dupont MP, Llabrés G, Delaude C, Tchissambou L, Gastmans JP Planta Med 01-Jun-1997
doi:10.1055/S-2006-957678
PMID:17252356

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
> Benzenoids / Anthracenes / Anthraquinones
2,3-Dihydroxy-9,10-dihydroanthracene-1,4-dione 135404238 Click to see C1C2=CC=CC=C2CC3=C1C(=O)C(=C(C3=O)O)O 242.23 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
4-Hydroxybenzyl cyanide 26548 Click to see C1=CC(=CC=C1CC#N)O 133.15 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Hydroxyphenylacetic acid 127 Click to see C1=CC(=CC=C1CC(=O)O)O 152.15 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
> Benzenoids / Phenols / Methoxyphenols
3,4,5-Trimethoxyphenol 69505 Click to see COC1=CC(=CC(=C1OC)OC)O 184.19 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1055/S-2006-957678
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
methyl (2S)-3-[(1R,2S,4aS,4bR,6aR,10aS,10bS,12aS)-2-ethyl-2,4b,6a,9,9,10b,12a-heptamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-1-yl]-2-methylpropanoate 163046747 Click to see CCC1(CCC2C(C1CC(C)C(=O)OC)(CCC3(C2(CCC4(C3CC(CC4)(C)C)C)C)C)C)C 472.80 unknown https://doi.org/10.1055/S-2006-957678
Methyl 3-(2-ethyl-2,4b,6a,9,9,10b,12a-heptamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-1-yl)-2-methylpropanoate 163046746 Click to see CCC1(CCC2C(C1CC(C)C(=O)OC)(CCC3(C2(CCC4(C3CC(CC4)(C)C)C)C)C)C)C 472.80 unknown https://doi.org/10.1055/S-2006-957678
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] octadecanoate 73188074 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)C=CC(CC)C(C)C)C)C 679.20 unknown https://doi.org/10.1055/S-2006-957678
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,4,5,6,6a,7,8,9,10,12,12a,13,14b-tetradecahydropicene-3,14-dione 162907005 Click to see CC1C(=O)CCC2C1(CCC3C2(C(=O)CC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
7-Oxofriedelin 21596176 Click to see CC1C(=O)CCC2C1(CC(=O)C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
Drypemolundein B 101084580 Click to see CC1C(=O)CCC2C1(CCC3C2(C(=O)CC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Putranjivadione 634915 Click to see CC1C(=O)CCC2C1(CC(=O)C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
Stigmast-5-en-3-ol, octadecanoate, (3beta)- 13828710 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 681.20 unknown https://doi.org/10.1055/S-2006-957678
Stigmasterol 3-stearate 13828746 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)C=CC(CC)C(C)C)C)C 679.20 unknown https://doi.org/10.1055/S-2006-957678
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2006-957678
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
N-beta-d-glucopyranosyl-p-hydroxy-phenylacetamide 162866738 Click to see C1=CC(=CC=C1CC(=O)NC2C(C(C(C(O2)CO)O)O)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.007
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Gerontoxanthone C 14259059 Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)CC=C(C)C)(C)C 396.40 unknown https://doi.org/10.1055/S-2006-957678
> Phenylpropanoids and polyketides / Phenylpropanoic acids
(E,4S,5R,6S)-2-benzyl-4,5,6,7-tetrahydroxyhept-2-enoic acid 163187198 Click to see C1=CC=C(C=C1)CC(=CC(C(C(CO)O)O)O)C(=O)O 282.29 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
(E,4S,5S,6R)-2-benzyl-4,5,7-trihydroxy-6-methylhept-2-enoic acid 163190350 Click to see CC(CO)C(C(C=C(CC1=CC=CC=C1)C(=O)O)O)O 280.32 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
2-Benzyl-4,5,6,7-tetrahydroxyhept-2-enoic acid 73117149 Click to see C1=CC=C(C=C1)CC(=CC(C(C(CO)O)O)O)C(=O)O 282.29 unknown https://doi.org/10.1016/S0031-9422(02)00630-1
2-Benzyl-4,5,7-trihydroxy-6-methylhept-2-enoic acid 162859696 Click to see CC(CO)C(C(C=C(CC1=CC=CC=C1)C(=O)O)O)O 280.32 unknown https://doi.org/10.1016/S0031-9422(02)00630-1

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