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Aglaia rimosa

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 UUID6440081728b99671812773
Scientific name Aglaia rimosa
Authority (Blanco) Merr.
First published in Sp. Blancoan. : 212 (1918)

Ethnobotanical Use Top

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General Uses Top

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No verified commercial, industrial, or craft uses for *Aglaia rimosa* (Authority: (Blanco) Merr.) are documented in scientific or trade literature. There are no established applications in timber, fiber, culinary, colorant, adhesive, biofuel, or fragrance industries. While chemical compounds have been studied (e.g., rocaglamide derivatives for potential pharmaceutical research), these are not linked to standardized commercial products or processes.

Synonyms Top

Scientific name Authority First published in
Aglaia batjanica Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 46 (1868)
Aglaia bulusanensis Elmer ex Merr. Enum. Philipp. Fl. Pl. 2: 373 (1923)
Aglaia denticulata Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 410 (1858)
Aglaia diffusiflora Merr. Philipp. J. Sci. 14: 410 (1919)
Aglaia elliptifolia Merr. Philipp. J. Sci., C 3: 413 (1909)
Aglaia goebeliana Warb. Bot. Jahrb. Syst. 13: 345 (1891)
Aglaia hexandra Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 410 (1858)
Aglaia lanceolata Merr. Philipp. J. Sci., C 5: 184 (1910)
Aglaia llanosiana C.DC. Monogr. Phan. 1: 621 (1878)
Aglaia loheri Merr. Philipp. J. Sci., C 9: 533 (1914 publ. 1915)
Aglaia macrobotrys Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 409 (1858)
Aglaia reticulata Elmer ex Merr. Enum. Philipp. Fl. Pl. ii. 377 (1923), in obs., pro syn.; Elmer, Leafl. Philipp.Bot. ix. 3306 (1937), descr. angl.
Aglaia subviridis Elmer ex Merr. Enum. Philipp. Fl. Pl. ii. 373 (1923), in obs., pro syn.; Elmer, Leafl. Philipp.Bot. ix. 3312 (1937), descr. angl.
Portesia rimosa Blanco Fl. Filip., ed. 2 : 250 (1845)

Common names Top

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Language Common/alternative name
Chinese 椭圆叶米仔兰
Chinese 大叶树兰
Chinese 大葉樹蘭

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Malesia
      • Maluku
      • Philippines
      • Sulawesi
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000524315
Tropicos 50277033
KEW urn:lsid:ipni.org:names:577291-1
The Plant List kew-2626531
Open Tree Of Life 188352
NCBI Taxonomy 1085116
IUCN Red List 34917
IPNI 577291-1
iNaturalist 189068
GBIF 5598028
Freebase /m/02x7qpn
Wikipedia Aglaia_rimosa

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
Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans from Aglaia species (Meliaceae) Greger H Phytochem Rev 04-Jun-2021
PMCID:PMC8176878
doi:10.1007/s11101-021-09761-5
PMID:34104125
Potential of cyclopenta[b]benzofurans from Aglaia species in cancer chemotherapy. Kim S, Salim AA, Swanson SM, Kinghorn AD Anticancer Agents Med Chem 01-Jul-2006
doi:10.2174/187152006777698123
PMID:16842234
X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia Ming Lu King, Chin-Chin Chiang, Han-Chin Ling, Eiichi Fujita, Masahito Ochiai, Andrew T. McPhail Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39820001150
Cytotoxic constituents from leaves of Aglaia elliptifolia. Wang SK, Cheng YJ, Duh CY J Nat Prod 01-Jan-2001
doi:10.1021/NP000341Q
PMID:11170675
Cytotoxic and antiplatelet aggregation principles from Aglaia elliptifolia. Wu TS, Liou MJ, Kuoh CS, Teng CM, Nagao T, Lee KH J Nat Prod 01-Jun-1997
doi:10.1021/NP970163+
PMID:9214732
PAF antagonism in vitro and in vivo by aglafoline from Aglaia elliptifolia Merr. Ko FN, Wu TS, Liou MJ, Huang TF, Teng CM Eur J Pharmacol 21-Jul-1992
doi:10.1016/0014-2999(92)90156-X
PMID:1327822

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Styrenes
(E)-N-[(1R)-4-hydroxy-1-[[(E)-3-phenylprop-2-enoyl]amino]butyl]-2-methylbut-2-enamide 163195118 Click to see CC=C(C)C(=O)NC(CCCO)NC(=O)C=CC1=CC=CC=C1 316.40 unknown https://doi.org/10.1021/NP000341Q
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3-[(3S,3aR,5aR,6R,7R,9aR,9bR)-7-(2-hydroxypropan-2-yl)-3-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 100927655 Click to see CC12CCC(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(C)(C)O)C)C4(CCC(O4)C(C)(C)O)C 492.70 unknown https://doi.org/10.1021/NP000341Q
> Organoheterocyclic compounds / Benzofurans / Flavaglines
1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylic acid 14238124 Click to see 478.50 unknown https://doi.org/10.1021/NP000341Q
1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-N,N-dimethyl-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-2-carboxamide 494234 Click to see 505.60 unknown https://doi.org/10.2174/187152006777698123
https://doi.org/10.1021/NP970163+
https://doi.org/10.1039/C39820001150
Aglafolin 393601 Click to see 492.50 unknown https://doi.org/10.1016/0014-2999(92)90156-X
https://doi.org/10.1021/NP970163+
Rocaglamide 331783 Click to see CN(C)C(=O)C1C(C2(C(C1O)(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC=C(C=C4)OC)C5=CC=CC=C5 505.60 unknown https://doi.org/10.1039/C39820001150
https://doi.org/10.1021/NP970163+
https://doi.org/10.2174/187152006777698123
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://doi.org/10.1021/NP970163+
Rocagloic Acid 10322821 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)O)C5=CC=CC=C5 478.50 unknown https://doi.org/10.1021/NP000341Q
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
Piriferine 9548036 Click to see 286.37 unknown https://doi.org/10.1021/NP000341Q
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-[4-hydroxy-1-(3-phenylprop-2-enoylamino)butyl]-2-methylbut-2-enamide 85146039 Click to see CC=C(C)C(=O)NC(CCCO)NC(=O)C=CC1=CC=CC=C1 316.40 unknown https://doi.org/10.1021/NP000341Q
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1021/NP970163+
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,7-dimethoxy-2-(3-methoxyphenyl)chromen-4-one 163024552 Click to see COC1=CC=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)O 328.30 unknown https://doi.org/10.1021/NP000341Q
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(E)-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-methylbut-2-enamide 163190473 Click to see 628.70 unknown https://doi.org/10.1021/NP000341Q
Elliptifoline 11802113 Click to see 628.70 unknown https://doi.org/10.1021/NP000341Q
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-methylbut-2-enamide 73108331 Click to see 628.70 unknown https://doi.org/10.1021/NP000341Q
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1S,12S,13S)-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-ol 162980105 Click to see 354.40 unknown https://doi.org/10.1021/NP000341Q

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