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Greenwayodendron suaveolens

Greenwayodendron suaveolens - 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 UUID64401ec038dd0507013826
Scientific name Greenwayodendron suaveolens
Authority (Engl. & Diels) Verdc.
First published in Adansonia , n.s., 9: 90 (1969)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polyalthia suaveolens Engl. & Diels Monogr. Afrik. Pflanzen-Fam. 6: 42 (1901)
Polyalthia mortehanii De Wild. Bull. Jard. Bot. État Bruxelles 4: 384 (1914)
Xylopia otunga Exell J. Bot. 69: 99 (1931)
Greenwayodendron suaveolens var. gabonica (Pellegr. ex Le Thomas) Verdc. Adansonia n.s., 9: 90 1969
Polyalthia suaveolens var. gabonica Pellegr. ex Le Thomas Mém. Mus. Natl. Hist. Nat. 16: 206 (1969)
Polyalthia aubrevillei Ghesq. ex Aubrév. Fl. For. Cote d'Ivoire i. 114 (1936), in clavi, gallice.

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
    • East Tropical Africa
      • Uganda
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000708834
Tropicos 1601043
KEW urn:lsid:ipni.org:names:73282-1
The Plant List kew-2831998
Open Tree Of Life 956932
NCBI Taxonomy 235734
IUCN Red List 62584
IPNI 73282-1
iNaturalist 132965
GBIF 3156191
EOL 305203
USDA GRIN 463421
Wikipedia Greenwayodendron_suaveolens

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
Complete chloroplast genome of two nutmeg species, Myristica argentea Warb. 1891 and Myristica fatua Houtt. 1774 (Myristicaceae) Kusuma J, Couderc M, Scarcelli N, Duminil J Mitochondrial DNA B Resour 19-Jul-2023
PMCID:PMC10361002
doi:10.1080/23802359.2023.2233154
PMID:37485420
A Divergent Polyene Cyclization for the Total Synthesis of Greenwayodendrines, Greenwaylactams, Polysin and Polyveoline Plangger I, Pinkert T, Wurst K, Magauer T Angew Chem Int Ed Engl 15-Jun-2023
PMCID:PMC7614870
doi:10.1002/anie.202307719
PMID:37318945
Assessing plant diversity change in logged and unlogged dense semi-deciduous production forest of eastern Cameroon Hubert Kpoumie Mounmemi, Mensah Ekué MR, Funwi Preasious Forbi, Roger Kabelong Banoho LP, Tiokeng B, Maffo Maffo NL, Lagarde Jean Betti, Carole Mireil Votio Tchoupou, Amandine Flore Yonkeu Ntonmen, Taedoumg HE, Zapfack L Heliyon 12-May-2023
PMCID:PMC10199262
doi:10.1016/j.heliyon.2023.e16199
PMID:37215910
Medicinal Plants as Therapeutic Alternatives to Combat Mycobacterium tuberculosis: A Comprehensive Review Gautam S, Qureshi KA, Jameel Pasha SB, Dhanasekaran S, Aspatwar A, Parkkila S, Alanazi S, Atiya A, Khan MM, Venugopal D Antibiotics (Basel) 08-Mar-2023
PMCID:PMC10044459
doi:10.3390/antibiotics12030541
PMID:36978408
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
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
Plant Terpenoids as Hit Compounds against Trypanosomiasis Durão R, Ramalhete C, Madureira AM, Mendes E, Duarte N Pharmaceuticals (Basel) 10-Mar-2022
PMCID:PMC8951850
doi:10.3390/ph15030340
PMID:35337138
Ethnobotanical Survey of Local Flora Used for Medicinal Purposes among Indigenous People in Five Areas in Lagos State, Nigeria Lawal IO, Rafiu BO, Ale JE, Majebi OE, Aremu AO Plants (Basel) 25-Feb-2022
PMCID:PMC8912796
doi:10.3390/plants11050633
PMID:35270103
A Review on Medicinal Plants Used in the Management of Headache in Africa Frimpong EK, Asong JA, Aremu AO Plants (Basel) 28-Sep-2021
PMCID:PMC8539318
doi:10.3390/plants10102038
PMID:34685845
Endophytic Fungi from Alstonia boonei De Wild and Greenwayodendron suaveolens (Engl. and Diels) Verdc. subsp. Suaveolens Possess Inhibitory Activity against Pneumonia Causing Bacteria Demeni PC, Betote PH, Kom CW, Tchamgoue EN, Ndedi Moni ED, Foumane Maniepi JS, Agbor GA, Nyegue MA Evid Based Complement Alternat Med 05-Aug-2021
PMCID:PMC8360735
doi:10.1155/2021/9966323
PMID:34394399
Seedling recruitment under isolated trees in a tea plantation provides a template for forest restoration in eastern Africa Ndangalasi HJ, Martínez-Garza C, Harjo TC, Pedigo CA, Wilson RJ, Cordeiro NJ PLoS One 06-May-2021
PMCID:PMC8101954
doi:10.1371/journal.pone.0250859
PMID:33956837
Individualistic evolutionary responses of Central African rain forest plants to Pleistocene climatic fluctuations Helmstetter AJ, Béthune K, Kamdem NG, Sonké B, Couvreur TL Proc Natl Acad Sci U S A 04-Dec-2020
PMCID:PMC7768702
doi:10.1073/pnas.2001018117
PMID:33277432
Complete chloroplast genome sequence and phylogenetic analysis of Annona reticulata Niu YF, Li KX, Liu J Mitochondrial DNA B Resour 09-Oct-2020
PMCID:PMC7782357
doi:10.1080/23802359.2020.1829131
PMID:33458233
The complete chloroplast genome of Annona muricata L.: a tropical fruit with important medicinal properties Niu YF, Li KX, Liu J Mitochondrial DNA B Resour 16-Sep-2020
PMCID:PMC7781942
doi:10.1080/23802359.2020.1820394
PMID:33458156
Investigating the direct and indirect effects of forest fragmentation on plant functional diversity Zambrano J, Cordeiro NJ, Garzon-Lopez C, Yeager L, Fortunel C, Ndangalasi HJ, Beckman NG PLoS One 02-Jul-2020
PMCID:PMC7331995
doi:10.1371/journal.pone.0235210
PMID:32614922

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
> Alkaloids and derivatives / Aporphines
(12S,13S)-13-methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-16-ol 163004742 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)O)OC)OCO3 325.40 unknown https://doi.org/10.1055/S-0028-1097383
(12S,13S)-13,16-dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 10065797 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)OC)OC)OCO3 339.40 unknown https://doi.org/10.1055/S-0028-1097383
(12S,13S)-13,16-dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 162976414 Click to see COC1C2C3=C(C4=C1C=C(C=C4)OC)C5=C(C=C3CCN2)OCO5 325.40 unknown https://doi.org/10.1055/S-0028-1097383
13-Methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-16-ol 163004741 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)O)OC)OCO3 325.40 unknown https://doi.org/10.1055/S-0028-1097383
13-Methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 75072032 Click to see COC1C2C3=C(C4=CC=CC=C14)C5=C(C=C3CCN2)OCO5 295.30 unknown https://doi.org/10.1055/S-0028-1097383
13,16-Dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 431012 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)OC)OC)OCO3 339.40 unknown https://doi.org/10.1055/S-0028-1097383
13,16-Dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 162976413 Click to see COC1C2C3=C(C4=C1C=C(C=C4)OC)C5=C(C=C3CCN2)OCO5 325.40 unknown https://doi.org/10.1055/S-0028-1097383
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown https://doi.org/10.1055/S-0028-1097383
Oxostephanine 343547 Click to see COC1=CC=CC2=C1C(=O)C3=NC=CC4=CC5=C(C2=C43)OCO5 305.30 unknown https://doi.org/10.1055/S-0028-1097383
Pachypodantine 44566390 Click to see COC1C2C3=C(C4=CC=CC=C14)C5=C(C=C3CCN2)OCO5 295.30 unknown https://doi.org/10.1016/S0040-4039(00)94990-6
https://doi.org/10.1055/S-0028-1097383
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(-)-Oliveroline 12444634 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 295.30 unknown https://doi.org/10.1055/S-0028-1097383
16-Methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-13-ol 13891890 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1055/S-0028-1097383
7-Methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaen-13-ol 15560262 Click to see CN1CCC2=C3C1C(C4=CC=CC=C4C3=C5C(=C2OC)OCO5)O 325.40 unknown https://doi.org/10.1055/S-0028-1097383
7-Methyl-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4',5':4,5]benzo[1,2,3-de]quinolin-8-ol 431013 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3 295.30 unknown https://doi.org/10.1055/S-0028-1097383
Guatterine 10358947 Click to see CN1CCC2=C3C1C(C4=CC=CC=C4C3=C5C(=C2OC)OCO5)O 325.40 unknown https://doi.org/10.1055/S-0028-1097383
Oliveridine 13891891 Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=C4C=CC(=C5)OC)O)OCO3 325.40 unknown https://doi.org/10.1055/S-0028-1097383
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-[(1R,2S,3S)-2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propanoic acid 163193076 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCC(=O)O 353.50 unknown https://doi.org/10.1021/NP040165B
3-[(1S,2R,3R)-2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propan-1-ol 46831720 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCCO 339.50 unknown https://doi.org/10.1021/NP1001225
3-[2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propan-1-ol 75215103 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCCO 339.50 unknown https://doi.org/10.1021/NP1001225
3-[2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propanoic acid 85432447 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCC(=O)O 353.50 unknown https://doi.org/10.1021/NP1001225
https://doi.org/10.1021/NP040165B
methyl 3-[(1S,2R,3R)-2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propanoate 46831975 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCC(=O)OC 367.50 unknown https://doi.org/10.1021/NP1001225
methyl 3-[2-(1H-indol-3-ylmethyl)-2,3-dimethyl-6-propan-2-ylidenecyclohexyl]propanoate 75215187 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCC(=O)OC 367.50 unknown https://doi.org/10.1021/NP1001225
Suaveolindole 11199009 Click to see CC1CCC(=C(C)C)C(C1(C)CC2=CNC3=CC=CC=C32)CCC(=O)O 353.50 unknown https://doi.org/10.1021/NP1001225
https://doi.org/10.1021/NP040165B
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
12,13,17,17-Tetramethyl-3-azapentacyclo[10.7.1.02,10.04,9.016,20]icosa-2(10),4,6,8,16(20)-pentaen-18-ol 75215102 Click to see CC1CCC2=C3C1(CC4=C(C3CC(C2(C)C)O)NC5=CC=CC=C45)C 335.50 unknown https://doi.org/10.1021/NP1001225
Pentacyclindole 46831719 Click to see CC1CCC2=C3C1(CC4=C(C3CC(C2(C)C)O)NC5=CC=CC=C45)C 335.50 unknown https://doi.org/10.1021/NP1001225
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
(1,13,17,17-Tetramethyl-2-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7,9-tetraen-16-yl) acetate 5258383 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC4=CC5=CC=CC=C5N43)C)C 379.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
(1R,12S,13S,18R)-1,13,17,17-tetramethyl-2-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7,9-tetraen-16-one 46871703 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC4=CC5=CC=CC=C5N43)C)C 335.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
(2S,4aS,5R,6R)-5-(1H-indol-2-ylmethyl)-1,1,5,6-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-2-ol 163036227 Click to see CC1CC=C2C(C1(C)CC3=CC4=CC=CC=C4N3)CCC(C2(C)C)O 337.50 unknown https://doi.org/10.1016/S0040-4039(00)94990-6
1,13,17,17-Tetramethyl-2-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7,9-tetraen-16-one 75228509 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC4=CC5=CC=CC=C5N43)C)C 335.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
3-O-acetylgreenwayodendrin 46891355 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC4=CC5=CC=CC=C5N43)C)C 379.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
5-(1H-indol-2-ylmethyl)-1,1,5,6-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-2-ol 163036226 Click to see CC1CC=C2C(C1(C)CC3=CC4=CC=CC=C4N3)CCC(C2(C)C)O 337.50 unknown https://doi.org/10.1016/S0040-4039(00)94990-6
Greenwayodendrin-3-one 46891354 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC4=CC5=CC=CC=C5N43)C)C 335.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(2S,4aS,5R,6R)-5-(1H-indol-3-ylmethyl)-1,1,5,6-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-2-ol 163188043 Click to see CC1CC=C2C(C1(C)CC3=CNC4=CC=CC=C43)CCC(C2(C)C)O 337.50 unknown https://doi.org/10.1016/S0040-4039(00)94990-6
(2S,5R,6R,8aR)-5-(1H-indol-3-ylmethyl)-1,1,5,6-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-2-ol 21602731 Click to see CC1CCC2C(=CCC(C2(C)C)O)C1(C)CC3=CNC4=CC=CC=C43 337.50 unknown https://doi.org/10.1021/NP1001225
5-(1H-indol-3-ylmethyl)-1,1,5,6-tetramethyl-2,3,4,4a,6,7-hexahydronaphthalen-2-ol 163038595 Click to see CC1CC=C2C(C1(C)CC3=CNC4=CC=CC=C43)CCC(C2(C)C)O 337.50 unknown https://doi.org/10.1016/S0040-4039(00)94990-6
5-(1H-indol-3-ylmethyl)-1,1,5,6-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-2-ol 73798648 Click to see CC1CCC2C(=CCC(C2(C)C)O)C1(C)CC3=CNC4=CC=CC=C43 337.50 unknown https://doi.org/10.1021/NP1001225
> Organoheterocyclic compounds / Indoles and derivatives / Indolines / 2,3-Cyclopentanoindolines
(1R,2S,10S,12S,13R,16R,18R)-1,13,17,17-tetramethyl-9-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7-trien-16-ol 46871719 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC4C3C5=CC=CC=C5N4)C)C 339.50 unknown https://doi.org/10.1016/S0040-4039(01)92418-9
https://doi.org/10.1016/J.BMCL.2010.04.145
1-(16-Hydroxy-1,13,17,17-tetramethyl-9-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7-trien-9-yl)ethanone 75238640 Click to see CC(=O)N1C2CC3C4(CCC(C(C4CCC3(C2C5=CC=CC=C51)C)(C)C)O)C 381.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
1-[(1R,2S,10S,12S,13R,16R,18R)-16-hydroxy-1,13,17,17-tetramethyl-9-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7-trien-9-yl]ethanone 46871720 Click to see CC(=O)N1C2CC3C4(CCC(C(C4CCC3(C2C5=CC=CC=C51)C)(C)C)O)C 381.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
1,13,17,17-Tetramethyl-9-azapentacyclo[10.8.0.02,10.03,8.013,18]icosa-3,5,7-trien-16-ol 13819235 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC4C3C5=CC=CC=C5N4)C)C 339.50 unknown https://doi.org/10.1016/J.BMCL.2010.04.145
https://doi.org/10.1016/S0040-4039(01)92418-9

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