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Cylicodiscus gabunensis

Cylicodiscus gabunensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd792da506803919244
Scientific name Cylicodiscus gabunensis
Authority Harms
First published in H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam., Nachtr. 1: 192 (1897)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piptadenia gabunensis (Harms) Roberty Bull. Inst. Fondam. Afrique Noire, Sér. A, Sci. Nat.16: 343 (1954)
Cyrtoxiphus staudtii Harms H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam., Nachtr. 1: 204 (1897)

Common names Top

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Language Common/alternative name
Akan denya
Japanese オカン
Russian Окан
Chinese 加蓬圆盘豆
Chinese 加蓬圓盤豆

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
      • Ghana
      • Ivory Coast
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000174888
Tropicos 13057203
KEW urn:lsid:ipni.org:names:489319-1
The Plant List ild-21
Open Tree Of Life 659690
NCBI Taxonomy 204972
IUCN Red List 62021855
IPNI 489319-1
GBIF 2977092
EOL 643184
USDA GRIN 436014

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
Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M Heliyon 21-Mar-2024
PMCID:PMC10999872
doi:10.1016/j.heliyon.2024.e28247
PMID:38590891
Assembly, annotation and analysis of the chloroplast genome of the Algarrobo tree Neltuma pallida (subfamily: Caesalpinioideae) Caycho E, La Torre R, Orjeda G BMC Plant Biol 16-Nov-2023
PMCID:PMC10652460
doi:10.1186/s12870-023-04581-5
PMID:37974117
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
Anti-Onchocercal Properties of Extracts of Scoparia dulcis and Cylicodiscus gabunensis Tiku TE, Samje M, Mfonku N, Cho-Ngwa F J Trop Med 16-Nov-2022
PMCID:PMC9683978
doi:10.1155/2022/4279689
PMID:36438180
Selective and clear-cut logging have varied imprints on tree community structure in a moist semi-deciduous forest in Ghana Addo-Fordjour P, Afram IS, Oppong J Heliyon 04-Nov-2022
PMCID:PMC9649955
doi:10.1016/j.heliyon.2022.e11393
PMID:36387494
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
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
Antibiotic resistance modifying ability of phytoextracts in anthrax biological agent Bacillus anthracis and emerging superbugs: a review of synergistic mechanisms Dassanayake MK, Khoo TJ, An J Ann Clin Microbiol Antimicrob 02-Dec-2021
PMCID:PMC8641154
doi:10.1186/s12941-021-00485-0
PMID:34856999
Genome skimming reveals novel plastid markers for the molecular identification of illegally logged African timber species Mascarello M, Amalfi M, Asselman P, Smets E, Hardy OJ, Beeckman H, Janssens SB PLoS One 11-Jun-2021
PMCID:PMC8195358
doi:10.1371/journal.pone.0251655
PMID:34115787
A review of Cameroonian medicinal plants with potentials for the management of the COVID-19 pandemic Fongnzossie Fedoung E, Biwole AB, Nyangono Biyegue CF, Ngansop Tounkam M, Akono Ntonga P, Nguiamba VP, Essono DM, Forbi Funwi P, Tonga C, Nguenang GM, Kemeuze V, Sonwa DJ, Tsabang N, Bouelet IS, Tize Z, Boum AT, Momo Solefack MC, Betti JL, Nouga Bissoue A, Lehman LG, Mapongmetsem PM, Nneme Nneme L, Ngono Ngane RA, Ngogang Yonkeu J 26-Mar-2021
PMCID:PMC7994110
doi:10.1007/s13596-021-00567-6
Hybrid capture of 964 nuclear genes resolves evolutionary relationships in the mimosoid legumes and reveals the polytomous origins of a large pantropical radiation Koenen EJ, Kidner C, de Souza ÉR, Simon MF, Iganci JR, Nicholls JA, Brown GK, de Queiroz LP, Luckow M, Lewis GP, Pennington RT, Hughes CE Am J Bot 30-Nov-2020
PMCID:PMC7839790
doi:10.1002/ajb2.1568
PMID:33253423
Natural Products as Sources of Antimalarial Drugs: Ethnobotanical and Ethnopharmacological Studies Oladeji OS, Oluyori AP, Bankole DT, Afolabi TY Scientifica (Cairo) 09-May-2020
PMCID:PMC7238349
doi:10.1155/2020/7076139
PMID:32455050
Discovery, synthesis and antibacterial evaluation of phenolic compounds from Cylicodiscus gabunensis Aldulaimi O, Drijfhout F, Uche FI, Horrocks P, Li WW BMC Complement Altern Med 24-Jul-2019
PMCID:PMC6651987
doi:10.1186/s12906-019-2589-2
PMID:31340805
Evaluation of cytotoxic effects and acute and chronic toxicity of aqueous extract of the seeds of Calycotome villosa (Poiret) Link (subsp. intermedia) in rodents Lyoussi B, Cherkaoui Tangi K, Morel N, Haddad M, Quetin-Leclercq J Avicenna J Phytomed 01-Mar-2018
PMCID:PMC5885326
PMID:29632843
Smallholder Farmers' Livelihood Security Options amidst Climate Variability and Change in Rural Ghana Yamba S, Appiah DO, Pokuaa-Siaw L, Asante F Scientifica (Cairo) 03-Dec-2017
PMCID:PMC5733969
doi:10.1155/2017/1868290
PMID:29348969

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 / Prenol lipids / Sesquiterpenoids / Guaianes
(8S,8aR)-5-[(2S)-1-hydroxypropan-2-yl]-3,8-dimethyl-6,7,8,8a-tetrahydro-1H-azulen-2-one 163085216 Click to see CC1CCC(=CC2=C(C(=O)CC12)C)C(C)CO 234.33 unknown https://doi.org/10.1016/0040-4020(95)00720-S
https://doi.org/10.1016/0031-9422(90)80194-L
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 162898435 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)C)C(=O)O 899.10 unknown https://doi.org/10.1016/0031-9422(90)85229-9
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aR,13bR)-9-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 162993638 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)O)O)C)C(=O)O 767.00 unknown https://doi.org/10.1016/0031-9422(91)85129-N
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162978015 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 899.10 unknown https://doi.org/10.1016/0031-9422(91)85129-N
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] (4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162905999 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)C)(CCC6C5(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)(C)C)OC1C(C(C(C(O1)CO)O)O)O)O)O 1207.30 unknown https://doi.org/10.1016/0031-9422(91)85129-N
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl] (4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162928809 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)C)(CCC6C5(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O 1369.50 unknown https://doi.org/10.1016/0031-9422(91)85129-N
[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] 10-[4-[4,5-dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162905997 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)C)(CCC6C5(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)(C)C)OC1C(C(C(C(O1)CO)O)O)O)O)O 1207.30 unknown https://doi.org/10.1016/0031-9422(91)85129-N
[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl] 10-[4-[4,5-dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162928807 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)C)(CCC6C5(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O 1369.50 unknown https://doi.org/10.1016/0031-9422(91)85129-N
10-[4-[4,5-Dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-11-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162978014 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 899.10 unknown https://doi.org/10.1016/0031-9422(91)85129-N
9-[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 162993636 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)O)O)C)C(=O)O 767.00 unknown https://doi.org/10.1016/0031-9422(91)85129-N
9-[4-[4,5-Dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 162898432 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)O)OC8C(C(C(CO8)O)O)O)O)C)C(=O)O 899.10 unknown https://doi.org/10.1016/0031-9422(90)85229-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 14707301 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1016/0040-4020(95)00720-S
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aR,13bR)-9-hydroxy-5a-(hydroxymethyl)-5b,8,8,11a-tetramethyl-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 162959407 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1016/0031-9422(90)80194-L
6,10,10,25,29,29-Hexamethyl-17,35-dioxanonacyclo[18.14.2.02,15.02,19.05,14.06,11.021,34.024,33.025,30]hexatriaconta-15,21(34)-diene-3,22-dione 73155758 Click to see CC1(CCCC2(C1CCC3C2CC(=O)C45C3=COCC4C6COC5C7=C6C(=O)CC8C7CCC9C8(CCCC9(C)C)C)C)C 600.90 unknown https://doi.org/10.1016/0040-4020(95)00720-S
9-Hydroxy-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 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0040-4020(95)00720-S
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0040-4020(95)00720-S
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0040-4020(95)00720-S
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0040-4020(95)00720-S
Urs-12-ene-3,28-diol, (3beta)- 3266408 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1248/CPB.58.1100
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1248/CPB.58.1100

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