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Aglaia mariannensis

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 UUID6440081460731947276352
Scientific name Aglaia mariannensis
Authority Merr.
First published in Philipp. J. Sci., C 9: 99 (1914)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Industrial and craft applications:
Food and beverages (non-medicinal):
Colorants and tanning:
Wood and fiber:
Fragrance and cosmetics:
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Sustainability and sourcing:

Synonyms Top

Scientific name Authority First published in
Aglaia palauensis Kaneh. Fl. Micron. : 162 (1933)
Aglaia ponapensis Kaneh. Fl. Micron. : 163 (1933)

Common names Top

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Language Common/alternative name
Lithuanian marianinė aglaja

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000524199
USDA Plants AGMA14
Tropicos 100285155
KEW urn:lsid:ipni.org:names:577186-1
The Plant List kew-2626423
Open Tree Of Life 3942296
NCBI Taxonomy 1475108
IUCN Red List 32003
IPNI 577186-1
iNaturalist 189051
GBIF 5597448
Freebase /m/02pwj90
Wikipedia Aglaia_mariannensis

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
Temporal Variation of Litterfall and Nutrient Return of Serianthes nelsonii Merr. in a Tropical Karst Forest Marler TE, Cruz GN Plants (Basel) 03-Sep-2022
PMCID:PMC9459683
doi:10.3390/plants11172310
PMID:36079692
Invasive brown treesnakes (Boiga irregularis) move short distances and have small activity areas in a high prey environment Boback SM, Nafus MG, Yackel Adams AA, Reed RN Sci Rep 26-Jul-2022
PMCID:PMC9325984
doi:10.1038/s41598-022-16660-y
PMID:35882893
Animal movement drives variation in seed dispersal distance in a plant–animal network Rehm E, Fricke E, Bender J, Savidge J, Rogers H Proc Biol Sci 16-Jan-2019
PMCID:PMC6367185
doi:10.1098/rspb.2018.2007
PMID:30963874
Landscape-level bird loss increases the prevalence of honeydew-producing insects and non-native ants Freedman MG, Miller RH, Rogers HS Oecologia 26-Oct-2018
PMCID:PMC6244808
doi:10.1007/s00442-018-4273-5
PMID:30367244
Contrasting ecological roles of non-native ungulates in a novel ecosystem Gawel AM, Rogers HS, Miller RH, Kerr AM R Soc Open Sci 25-Apr-2018
PMCID:PMC5936884
doi:10.1098/rsos.170151
PMID:29765619
Seed dispersal increases local species richness and reduces spatial turnover of tropical tree seedlings Wandrag EM, Dunham AE, Duncan RP, Rogers HS Proc Natl Acad Sci U S A 28-Aug-2017
PMCID:PMC5635905
doi:10.1073/pnas.1709584114
PMID:28847937
Effects of an invasive predator cascade to plants via mutualism disruption Rogers HS, Buhle ER, HilleRisLambers J, Fricke EC, Miller RH, Tewksbury JJ Nat Commun 08-Mar-2017
PMCID:PMC5344968
doi:10.1038/ncomms14557
PMID:28270682
Leucaena leucocephala and adjacent native limestone forest habitats contrast in soil properties on Tinian Island Marler TE, Dongol N, Cruz GN Commun Integr Biol 18-Aug-2016
PMCID:PMC5100652
doi:10.1080/19420889.2016.1212792
PMID:27829978
Three invasive insects alter Cycas micronesica leaf chemistry and predict changes in biogeochemical cycling Marler TE, Dongol N Commun Integr Biol 15-Aug-2016
PMCID:PMC5100656
doi:10.1080/19420889.2016.1208324
PMID:27829976
Vertebrate seed dispersers maintain the composition of tropical forest seedbanks Wandrag EM, Dunham AE, Miller RH, Rogers HS AoB Plants 17-Nov-2015
PMCID:PMC4689121
doi:10.1093/aobpla/plv130
PMID:26578741
‘Natural experiment’ Demonstrates Top-Down Control of Spiders by Birds on a Landscape Level Rogers H, Hille Ris Lambers J, Miller R, Tewksbury JJ PLoS One 07-Sep-2012
PMCID:PMC3436874
doi:10.1371/journal.pone.0043446
PMID:22970126
Ponapensin, a Cyclopenta[bc]benzopyran with Potent NF‐ϰB Inhibitory Activity from Aglaia ponapensis. Angela A. Salim, Alison D. Pawlus, Hee‐Byung Chai, Norman R. Farnsworth, A. Douglas Kinghorn, Esperanza J. Carcache‐Blanco Wiley 25-Apr-2007
doi:10.1002/CHIN.200720200
Ponapensin, a cyclopenta[bc]benzopyran with potent NF-kappaB inhibitory activity from Aglaia ponapensis. Salim AA, Pawlus AD, Chai HB, Farnsworth NR, Douglas Kinghorn A, Carcache-Blanco EJ Bioorg Med Chem Lett 01-Jan-2007
PMCID:PMC2786496
doi:10.1016/J.BMCL.2006.09.084
PMID:17055270
Insecticidal 1H-cyclopentatetrahydro[b]benzofurans from Aglaia odorata Fumito Ishibashi, Chutamas Satasook, Murray B. Ismant, G.H.Neil Towers Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94986-0

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 / Triterpenoids
[(4aS,6aS,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl]methyl acetate 162917261 Click to see 526.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(2S,3R,5R,8R,9S,10S,13S,14S,17E)-17-ethylidene-2,3-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-16-one 163000123 Click to see 332.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
(2S,3R,5R,8R,9S,10S,13S,14S,17Z)-17-ethylidene-2,3-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-16-one 163000122 Click to see CC=C1C(=O)CC2C1(CCC3C2CCC4C3(CC(C(C4)O)O)C)C 332.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
(3S,4R,8R,9S,10R,13S,14S,17Z)-17-ethylidene-3,4-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-16-one 10853920 Click to see 330.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
17-ethylidene-3,4-dihydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-16-one 85079909 Click to see 330.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
E-volkendousin 10853919 Click to see CC=C1C(=O)CC2C1(CCC3C2CC=C4C3(CCC(C4O)O)C)C 330.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
(3S)-5,7-dimethoxy-3-(4-methoxyphenyl)-3H-2-benzofuran-1-one 163191366 Click to see 300.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
5,6-Desmethylenedioxy-5-methoxyaglalactone 44430503 Click to see 300.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
> Organoheterocyclic compounds / Benzofurans / Flavaglines
Aglafolin 393601 Click to see 492.50 unknown https://doi.org/10.1002/CHIN.200720200
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
Rocaglamide J 4132 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5 492.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
https://doi.org/10.1016/S0031-9422(00)94986-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-N-[(2S)-1-[(1R,9R,10R,11S,12R)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-11-carbonyl]pyrrolidin-2-yl]-2-methylbutanamide 162995814 Click to see 630.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
(2S)-N-[(2S)-1-[(1R,9R,10S,11R,12R)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-11-carbonyl]pyrrolidin-2-yl]-2-methylbutanamide 162995815 Click to see 630.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
[(1R,9R,10R,11R,12R)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-(2-methylbutanoylamino)pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 101118316 Click to see 672.80 unknown https://doi.org/10.1002/CHIN.200720200
[(1R,9R,10S,11R,12R)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-[[(2S)-2-methylbutanoyl]amino]pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 162907454 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC(=O)C)C5=CC=C(C=C5)OC)C6=CC=CC=C6 672.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
[(1R,9R,10S,11S,12S)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-[[(2S)-2-methylbutanoyl]amino]pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 162907457 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC(=O)C)C5=CC=C(C=C5)OC)C6=CC=CC=C6 672.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
[(1S,9S,10R,11S,12R)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-11-yl]-[(2R)-2-methoxypyrrolidin-1-yl]methanone 102454772 Click to see 561.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
[1-Hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[2-(2-methylbutanoylamino)pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 75026712 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC(=O)C)C5=CC=C(C=C5)OC)C6=CC=CC=C6 672.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
[1,12-Dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-11-yl]-(2-methoxypyrrolidin-1-yl)methanone 73298909 Click to see COC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6 561.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
4-epiaglain A 44430534 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC(=O)C)C5=CC=C(C=C5)OC)C6=CC=CC=C6 672.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
N-[1-[(1S,9S)-1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-11-carbonyl]pyrrolidin-2-yl]-2-methylbutanamide 137705524 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6 630.70 unknown https://doi.org/10.1002/CHIN.200720200
N-[1-[1,12-dihydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-triene-11-carbonyl]pyrrolidin-2-yl]-2-methylbutanamide 75026713 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6 630.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
Ponapensin 44430502 Click to see 561.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786496/
https://doi.org/10.1002/CHIN.200720200

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