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Duguetia confinis

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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 UUID64401895663e0855466329
Scientific name Duguetia confinis
Authority (Engl. & Diels) Chatrou
First published in Changing Genera : 67 (1998)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pachypodanthium confine Engl. & Diels Notizbl. Königl. Bot. Gart. Berlin 3: 55 (1900)
Unona confinis Pierre ex Engl. & Diels Notizbl. Königl. Bot. Gart. Berlin 3: 55 (1900)
Pachypodanthium confine var. sargosii (R.E.Fr.) Le Thomas Fl. Gabon 16: 106 1969
Pachypodanthium sargosii R.E.Fr. Ark. Bot. , prepr., a.s., 3: 38 (1953)

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-central Tropical Africa
      • Cabinda
      • Cameroon
      • Congo
      • Gabon

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000657823
Tropicos 50159677
KEW urn:lsid:ipni.org:names:1003560-1
The Plant List kew-2779079
Open Tree Of Life 902136
NCBI Taxonomy 294148
IUCN Red List 61984644
IPNI 1003560-1
GBIF 3157560
EOL 1053959
USDA GRIN 463419

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
Duguetia confinis Engl. & Diels (Annonaceae) inhibitory and cytotoxic effects on breast adenocarcinoma growth both in vitro and in vivo Nkuimi OB, Silihe KK, Tabi YO, Ngo Pambe JC, Njamen D, Zingue S Heliyon 24-Jan-2024
PMCID:PMC10839804
doi:10.1016/j.heliyon.2024.e24410
PMID:38317996
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review Frezza C, Venditti A, Toniolo C, De Vita D, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Serafini M, Bianco A Molecules 03-Jan-2020
PMCID:PMC6983269
doi:10.3390/molecules25010197
PMID:31947789
Gut microbiomes of wild great apes fluctuate seasonally in response to diet Hicks AL, Lee KJ, Couto-Rodriguez M, Patel J, Sinha R, Guo C, Olson SH, Seimon A, Seimon TA, Ondzie AU, Karesh WB, Reed P, Cameron KN, Lipkin WI, Williams BL Nat Commun 03-May-2018
PMCID:PMC5934369
doi:10.1038/s41467-018-04204-w
PMID:29725011
A mega-phylogeny of the Annonaceae: taxonomic placement of five enigmatic genera and support for a new tribe, Phoenicantheae Guo X, Tang CC, Thomas DC, Couvreur TL, Saunders RM Sci Rep 04-Aug-2017
PMCID:PMC5544705
doi:10.1038/s41598-017-07252-2
PMID:28779135
An alkaloid, two conjugate sesquiterpenes and a phenylpropanoid from Pachypodanthium confine Engl. and Diels. Mathouet H, Elomri A, Lameiras P, Daïch A, Vérité P Phytochemistry 01-Jul-2007
doi:10.1016/J.PHYTOCHEM.2007.04.001
PMID:17544038
Composition and anti-plasmodial activities of essential oils from some Cameroonian medicinal plants. Boyom FF, Ngouana V, Zollo PH, Menut C, Bessiere JM, Gut J, Rosenthal PJ Phytochemistry 01-Dec-2003
doi:10.1016/J.PHYTOCHEM.2003.08.004
PMID:14599525
Oxoaporphine alkaloids from Duguetia eximia Otto R. Gottlieb, Aderbal F. Magalhães, Eva G. Magalhães, José G.S. Maia, Anita J. Marsaioli Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94260-2

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
(12R,13S)-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 163005059 Click to see COC1C2C3=C(C4=CC=CC=C14)C5=C(C=C3CCN2)OCO5 295.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
1-[(12S,13R)-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-hexaen-11-yl]ethanone 162870534 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)OC)OCO3 337.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
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/10.1016/J.PHYTOCHEM.2007.04.001
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10,11-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol 162887410 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)O 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
2,10,11-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-3-ol 12309269 Click to see COC1=C(C=C2CN3CCC4=CC(=C(C=C4C3CC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
3,10,11-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol 14021682 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)O 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
Discretine 821491 Click to see COC1=C(C=C2CN3CCC4=CC(=C(C=C4C3CC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
> Benzenoids / Benzene and substituted derivatives / Benzylethers
1,2,4-trimethoxy-5-[(1R)-1-methoxyethyl]benzene 163047606 Click to see CC(C1=CC(=C(C=C1OC)OC)OC)OC 226.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
> Benzenoids / Naphthalenes
(1R)-6,7,8-trimethoxy-1-(2,4,5-trimethoxyphenyl)-1,2-dihydronaphthalene 162870528 Click to see COC1=CC(=C(C=C1C2CC=CC3=CC(=C(C(=C23)OC)OC)OC)OC)OC 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
> Benzenoids / Phenol esters
Eugenol acetate 7136 Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC 206.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Benzenoids / Phenol ethers / Anisoles
2,4,5-Trimethoxystyrene 152219 Click to see COC1=CC(=C(C=C1C=C)OC)OC 194.23 unknown https://doi.org/10.1016/S0031-9422(00)94260-2
> Benzenoids / Tetralins
(1S)-6,7,8-trimethoxy-1-(2,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydronaphthalene 163028563 Click to see COC1=CC(=C(C=C1C2CCCC3=CC(=C(C(=C23)OC)OC)OC)OC)OC 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
1-[(1R)-3-(4,8-dimethylnona-3,7-dienyl)cyclohex-3-en-1-yl]-2,4,5-trimethoxybenzene 162886081 Click to see CC(=CCCC(=CCCC1=CCCC(C1)C2=CC(=C(C=C2OC)OC)OC)C)C 398.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
1-[(1R)-3-[(3E)-4,8-dimethylnona-3,7-dienyl]cyclohex-3-en-1-yl]-2,4,5-trimethoxybenzene 44519714 Click to see CC(=CCCC(=CCCC1=CCCC(C1)C2=CC(=C(C=C2OC)OC)OC)C)C 398.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
1-[(1R)-3-[(3Z)-4,8-dimethylnona-3,7-dienyl]cyclohex-3-en-1-yl]-2,4,5-trimethoxybenzene 163191380 Click to see CC(=CCCC(=CCCC1=CCCC(C1)C2=CC(=C(C=C2OC)OC)OC)C)C 398.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene 5315589 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
alpha-Cadinene, (+)- 12306048 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see C12C3C4C1C5(C2C3=C45)O 118.13 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Organoheterocyclic compounds / Epoxides
(4E,7E)-1,5,9,9-Tetramethyl-12-oxabicyclo[9.1.0]dodeca-4,7-diene 22559443 Click to see CC1=CCCC2(C(O2)CC(C=CC1)(C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.004
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.04.001

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