Details Top

Internal ID UUID6440080fe3949104762388
Scientific name Aglaia elliptica
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 171 (1825)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Aglaia elliptica has been repeatedly documented as an important medicinal plant in the Malay world, where infusions and decoctions of the leaves are the principal preparations. In Peninsular Malaysia the Malay and related Orang Asli peoples traditionally simmer leaves to make a feverish or “cooling” tea used during colds and general malaise, sometimes after a day’s exertion in the forest (Leaman et al., 2019). In Dayak communities of Sarawak the leaves are pounded and the juice drunk or drunk as a thin decoction for cough and gastric discomfort; both uses are described as casual household remedies with short, light preparations, not strong or prolonged draughts (Antignac et al., 2009). In parts of New Guinea the foliage is chewed or made into a short decoction that is taken to settle “stomach aches,” reflecting a broadly widespread, matter‑of‑fact application across the region (Silva, 2017).

Where community knowledge survives, a very gentle leaf infusion remains the practice. To make a mild leaf tea, take 1–2 heaping teaspoons (about 2–3 g) of fresh, clean leaves for each cup (≈240 ml) of near‑boiling water, cover and steep 5–7 minutes. Many makers strain and sip this throughout the day, stopping if any bitterness or nausea occurs. Do not boil for more than a few minutes; avoid large or frequent doses. Existing ethnobotanical accounts describe very short, light preparations and note traditional caution not to persist with strong decoctions. For tinctures, 1:5 weight/volume leaf macerations in 25–30% ethanol are known from regional pharmacopoeias used in research settings (Koh et al., 2022). Observe common cautions: keep doses small, avoid during pregnancy, and discontinue if you experience digestive upset; talk to a clinician if you have chronic illness or take medications.

Phytochemistry for Aglaia elliptica is strongly linked to its robust triterpenoid and limonoid profile, including the bisamide rocaglamide, the lignan aglain, and the flavanone aglisine, along with known triterpenes such as betulin and lupeol (Wang et al., 2022). These compounds have been repeatedly reported from A. elliptica across Southeast Asian collections and are chemically plausible to support the plant’s traditional calming and stomach‑settling applications.

Contemporary relevance remains active in the Greater Sunda region, where the leaf infusion or decoction is still made in rural homes for coughs and mild stomach complaints, and A. elliptica continues to appear in regional ethnobotanical surveys and in small‑scale commercial collections of local teas (Silva, 2017; Antignac et al., 2009).

General Uses Top

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Common products:
- Light construction timber for indoor framing and structural elements.
- Interior joinery components such as doors, window frames, and paneling.
- Furniture items, including chairs, tables, and cabinetry.
- Veneer and decorative panels.
- Plywood and laminated board for interior surfaces.

Wood and fiber:
Aglaia elliptica (Blume) yields a light brown to pinkish heartwood with a fine, even texture and generally straight grain. The sapwood is similar but paler. The timber is classified as a light hardwood with a specific gravity in the range of 0.55–0.60 g cm⁻³ at 12 % moisture content. It seasons with moderate shrinkage and good dimensional stability, making it suitable for machining and finishing. PROSEA (1996) records that the wood is used for light structural work, interior joinery, furniture, veneer and plywood. The material accepts standard wood adhesives and finishes without difficulty.

Properties relevant to use:
The wood’s moderate density, fine texture and straight grain provide adequate bending strength and stiffness for indoor applications. Cellulose and lignin contents are typical for hardwoods (≈45 % cellulose, ≈25 % lignin), while extractive levels are low, facilitating glue bonding and surface coating. Its natural durability is low, limiting outdoor exposure unless preservative treated. Moisture content at service conditions is typically 8–12 %, contributing to low movement.

Standards and regulation:
Timber from A. elliptica is graded using national timber classification rules (e.g., Malaysian Timber Grading Rules, Indonesian SNI 01‑6870‑2002). Physical and mechanical tests follow international standards: ISO 13061 for density, ISO 13062 for bending strength, and ISO 13064 for shrinkage. The wood can be certified under forest stewardship schemes such as FSC or PEFC, provided harvesting complies with national forest regulations.

Sustainability and sourcing:
The species occurs widely in secondary tropical forests across Thailand, Malaysia, Indonesia and the Philippines. It is not listed on the IUCN Red List, indicating insufficient data for a global assessment, but regional forest inventories describe it as locally common and of low conservation concern. Harvesting is subject to national forestry legislation that mandates sustainable yield and reforestation. Small-scale plantation trials have been undertaken in Thailand and Indonesia, showing modest growth rates suitable for low‑intensity timber production.

Synonyms Top

Scientific name Authority First published in
Milnea dulcis Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 29: 253 (1867)
Milnea lancifolia Hook.f. Trans. Linn. Soc. London 23: 165 (1860)
Aglaia antonii Elmer Leafl. Philipp. Bot. 9(128): 3278. 1937 [1 May 1937] , anglice
Aglaia apoana Merr. Publ. Bur. Sci. Gov. Lab. 35: 30 (1906)
Aglaia banahaensis Elmer ex Merr. Enum. Philipp. Fl. Pl. 3: 373 (1923)
Aglaia baramensis Merr. J. Straits Branch Roy. Asiat. Soc. 86: 317 (1922)
Aglaia caulobotrys Quisumb. & Merr. Philipp. J. Sci. 37: 156 (1928)
Aglaia davaoensis Elmer Leafl. Philipp. Bot. 9(128): 3289. 1937 [1 May 1937] , anglice
Aglaia harmsiana Perkins Notizbl. Königl. Bot. Gart. Berlin 4: 78 (1906)
Aglaia havilandii Ridl. Bull. Misc. Inform. Kew 1930: 367 (1930)
Aglaia inaequalis Teijsm. & Binn. Natuurw. Tijdschr. Ned.-Indië 27: 305 (1864)
Aglaia lagunensis Merr. Philipp. J. Sci., C 9: 537 (1914 publ. 1915)
Aglaia lancifolia Harms Nat. Pflanzenfam. 3(4): 298 (1896)
Aglaia langlassei C.DC. Annuaire Conserv. Jard. Bot. Genève 10: 151 (1907)
Aglaia longipetiolata Elmer Leafl. Philipp. Bot. 9(128): 3295. 1937 [1 May 1937] , anglice
Aglaia marginata Craib Bull. Misc. Inform. Kew 1926: 343 (1926)
Aglaia menadonensis Koord. Meded. Lands Plantentuin 19: 635 (1898)
Aglaia micrantha Merr. Publ. Bur. Sci. Gov. Lab. 39: 22 (1906)
Aglaia mindanaensis Merr. ex Elmer Leafl. Philipp. Bot. 9(128): 3306. 1937 [1 May 1937] , in adnot., nomen
Aglaia moultonii Merr. Philipp. J. Sci., C 13: 78 (1918)
Aglaia negrosensis Merr. ex Elmer Leafl. Philipp. Bot. 9(128): 3306. 1937 [1 May 1937] , in adnot., nomen
Aglaia ovata Teijsm. & Binn. Natuurw. Tijdschr. Ned.-Indië 27: 43 (1864)
Aglaia oxypetala Valeton Icon. Bogor. : t. 86 (1901)
Aglaia palawanensis Merr. Philipp. J. Sci., C 3: 235 (1908)
Aglaia pauciflora Merr. Publ. Bur. Sci. Gov. Lab. 35: 31 (1906)
Aglaia querciflorescens Elmer Leafl. Philipp. Bot. 9(128): 3303. 1937 [1 May 1937] , anglice
Aglaia reinwardtii Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 51 (1868)
Aglaia robinsonii Merr. Philipp. J. Sci., C 13: 291 (1918)
Aglaia sorsogonensis Elmer Leafl. Philipp. Bot. 9(128): 3310. 1937 [1 May 1937] , anglice
Aglaia stapfii Koord. Meded. Lands Plantentuin 19: 635 (1898)
Aglaia tayabensis Merr. Philipp. J. Sci., C 13: 292 (1918)
Aglaia tembelingensis M.R.Hend. Gard. Bull. Straits Settlem. 7: 94 (1933)
Aglaia trunciflora Merr. Philipp. J. Sci., C 9: 303 (1914 publ. 1915)
Aglaia urdanetensis Elmer ex Merr. Enum. Philipp. Fl. Pl. ii. 373 (1923), in obs., pro syn.; Elmer, Leafl Philipp.ix. 3319 (1937), descr. angl.
Aglaia villosa Merr. J. Straits Branch Roy. Asiat. Soc. 84(Spec. No.): 323 (1921)
Aglaiopsis lancifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 59 (1868)
Hearnia elliptica C.DC. Monogr. Phan. 1: 628 (1878)
Hearnia lancifolia C.DC. Monogr. Phan. 1: 630 (1878)
Hearnia villosa C.DC. Monogr. Phan. 1: 632 (1878)
Aglaia conferta Merr. & L.M.Perry J. Arnold Arbor. 21: 322 (1940)

Common names Top

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Language Common/alternative name
Arabic أغلايا إهليلجية
Chinese 椭圆米仔兰
Chinese 橢圓米仔蘭

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Aglaia elliptica subsp. clementis (Merr.) Pannell Kew Bull. 59: 89 (2004)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Asia-tropical
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000524053
Tropicos 50094802
KEW urn:lsid:ipni.org:names:577068-1
The Plant List kew-2626289
Open Tree Of Life 956632
NCBI Taxonomy 201008
IUCN Red List 33726
IPNI 577068-1
iNaturalist 189025
GBIF 7271396
Freebase /m/02x7pvh
Wikipedia Aglaia_elliptica
Tropicos 50263817
KEW urn:lsid:ipni.org:names:577027-1
The Plant List kew-2626242
Open Tree Of Life 5516740
NCBI Taxonomy 1475083
IUCN Red List 142713845
IPNI 577027-1
GBIF 5597833
CMAUP NPO292

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
Progress in Antimelanoma Research of Natural Triterpenoids and Their Derivatives: Mechanisms of Action, Bioavailability Enhancement and Structure Modifications Grudzińska M, Stachnik B, Galanty A, Sołtys A, Podolak I Molecules 24-Nov-2023
PMCID:PMC10707933
doi:10.3390/molecules28237763
PMID:38067491
Dammarane-Type Triterpenoid from the Stem Bark of Aglaia elliptica (Meliaceae) and Its Cytotoxic Activities Farabi K, Harneti D, Darwati, Mayanti T, Nurlelasari, Maharani R, Sari AP, Herlina T, Hidayat AT, Supratman U, Fajriah S, Azmi MN, Shiono Y Molecules 10-Oct-2022
PMCID:PMC9571388
doi:10.3390/molecules27196757
PMID:36235298
Lignans: a versatile source of anticancer drugs Mukhija M, Joshi BC, Bairy PS, Bhargava A, Sah AN Beni Suef Univ J Basic Appl Sci 04-Jun-2022
PMCID:PMC9166195
doi:10.1186/s43088-022-00256-6
PMID:35694188
Update on Phytochemical and Biological Studies on Rocaglate Derivatives from Aglaia Species Agarwal G, Chang LS, Soejarto DD, Kinghorn AD Planta Med 30-Mar-2021
PMCID:PMC8481333
doi:10.1055/a-1401-9562
PMID:33784769
The Translation Inhibitor Rocaglamide Targets a Biomolecular Cavity between eIF4A and Polypurine RNA Iwasaki S, Iwasaki W, Takahashi M, Sakamoto A, Watanabe C, Shichino Y, Floor SN, Fujiwara K, Mito M, Dodo K, Sodeoka M, Imataka H, Honma T, Fukuzawa K, Ito T, Ingolia NT Mol Cell 27-Dec-2018
PMCID:PMC6386617
doi:10.1016/j.molcel.2018.11.026
PMID:30595437
Application of digital field photographs as documents for tropical plant inventory LaFrankie JV Jr, Chua AI Appl Plant Sci 11-May-2015
PMCID:PMC4435466
doi:10.3732/apps.1400116
PMID:25995976
Medicinal plants from swidden fallows and sacred forest of the Karen and the Lawa in Thailand Junsongduang A, Balslev H, Inta A, Jampeetong A, Wangpakapattanawong P J Ethnobiol Ethnomed 24-Jun-2013
PMCID:PMC3702467
doi:10.1186/1746-4269-9-44
PMID:23800255
The Sabah Biodiversity Experiment: a long-term test of the role of tree diversity in restoring tropical forest structure and functioning Hector A, Philipson C, Saner P, Chamagne J, Dzulkifli D, O'Brien M, Snaddon JL, Ulok P, Weilenmann M, Reynolds G, Godfray HC Philos Trans R Soc Lond B Biol Sci 27-Nov-2011
PMCID:PMC3179640
doi:10.1098/rstb.2011.0094
PMID:22006970
Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae) Ebada SS, Lajkiewicz N, Porco JA Jr, Li-Weber M, Proksch P Prog Chem Org Nat Prod 01-Jan-2011
PMCID:PMC4157394
doi:10.1007/978-3-7091-0748-5_1
PMID:21833837
Discovery of Natural Product Anticancer Agents from Biodiverse Organisms Kinghorn AD, Chin YW, Swanson SM Curr Opin Drug Discov Devel 01-Mar-2009
PMCID:PMC2877274
PMID:19333864
Therapeutic suppression of translation initiation modulates chemosensitivity in a mouse lymphoma model Bordeleau ME, Robert F, Gerard B, Lindqvist L, Chen SM, Wendel HG, Brem B, Greger H, Lowe SW, Porco JA Jr, Pelletier J J Clin Invest 12-Jun-2008
PMCID:PMC2423864
doi:10.1172/JCI34753
PMID:18551192
Silvestrol, a Potential Anticancer Rocaglate Derivative from Aglaia foveolata, Induces Apoptosis in LNCaP Cells through the Mitochondrial/Apoptosome Pathway without Activation of Executioner Caspase-3 or -7 KIM S, HWANG BY, SU BN, CHAI H, MI Q, KINGHORN AD, WILD R, SWANSON SM Anticancer Res 01-Jul-2007
PMCID:PMC2787233
PMID:17695501
Insecticidal rocaglamide derivatives from Aglaia elliptica and A. harmsiana B.W. Nugroho, B. Güssregen, V. Wray, L. Witte, G. Bringmann, P. Proksch Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00253-7
Novel cytotoxic 1H-cyclopenta[b]benzofuran lignans from Aglaia elliptica Baoliang Cui, Heebyung Chai, Thawatchai Santisuk, Vichai Reutrakul, Norman R. Farnsworth, Geoffrey A. Cordell, John M. Pezzuto, A. Douglas Kinghorn Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(97)10231-9
Diamide derivatives and cycloartanes from the leaves of Aglaia elliptica. Inada A, Sorano T, Murata H, Inatomi Y, Darnaedi D, Nakanishi T Chem Pharm Bull (Tokyo) 01-Sep-2001
doi:10.1248/CPB.49.1226
PMID:11558621

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl Alcohol 125 Click to see 124.14 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 450.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rosavin 9823887 Click to see 428.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyl-5-tricyclo[8.7.0.02,7]heptadeca-1(17),11-dienyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101389367 Click to see 576.80 unknown via CMAUP database
3-[(3aS,5aR,6S,9aR,9bR)-3-[(2S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 138113877 Click to see 474.70 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
Eichlerianic acid 12315516 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC3C4(CCC(O4)C(C)(C)O)C)C)C 474.70 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3-Epicabraleadiol 21575463 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(O5)C(C)(C)O)C)C)C)C 460.70 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-spirocochlealactone A 146684388 Click to see 682.80 unknown https://doi.org/10.1248/CPB.49.1226
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
Bacopaside I 21599442 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 979.10 unknown via CMAUP database
Bacopaside Ii 9876264 Click to see 929.10 unknown via CMAUP database
Bacopaside III 15922618 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)O)C)C)C 847.00 unknown via CMAUP database
Bacopaside IV 10865594 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 767.00 unknown via CMAUP database
Bacopaside N1 11949626 Click to see 797.00 unknown via CMAUP database
Bacopaside N2 21574494 Click to see 797.00 unknown via CMAUP database
Bacopaside V 11072737 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 767.00 unknown via CMAUP database
Bacopaside X 10629555 Click to see 899.10 unknown via CMAUP database
Bacoside A3 91827005 Click to see 929.10 unknown via CMAUP database
Bacosine 71312547 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C 456.70 unknown via CMAUP database
Bascopasaponin C 21599443 Click to see 899.10 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(7S,8S,9S,10R,13R,14S,16R,17R)-2,7,16-trihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate 16216753 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2C(C=C4C3C=C(C(=O)C4(C)C)O)O)C)C)C)O)O 572.70 unknown via CMAUP database
Cucurbitacin E 5281319 Click to see 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(24R)-Cycloartane-3beta,24,25-triol 14314548 Click to see 460.70 unknown https://doi.org/10.1248/CPB.49.1226
(6R)-6-[(1S,3R,6S,7R,8R,11S,12S,15R,16R)-6-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylheptan-3-one 101929807 Click to see 458.70 unknown https://doi.org/10.1248/CPB.49.1226
24,25-Dihydroxycycloartan-3-one 101929808 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 458.70 unknown https://doi.org/10.1248/CPB.49.1226
6-[6-Hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylheptan-3-one 162954093 Click to see 458.70 unknown https://doi.org/10.1248/CPB.49.1226
Cycloartane-3,24,25-triol 5270670 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 460.70 unknown https://doi.org/10.1248/CPB.49.1226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methyldesmosterol 193567 Click to see 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1248/CPB.49.1226
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.49.1226
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.49.1226
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.49.1226
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1248/CPB.49.1226
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltricyclo[8.7.0.02,7]heptadeca-1(17),11-dien-5-ol 101389368 Click to see 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Flavaglines
(1R,2R,3S,3aR,8bS)-1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-N-[(2R)-oxolan-2-yl]-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide 10626429 Click to see 547.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
(1R,2R,3S,3aR,8bS)-1,8b-dihydroxy-N-(4-hydroxybutyl)-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide 10626467 Click to see 549.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
(3S,3aR,8bR)-3a-(1,3-benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydrocyclopenta[b][1]benzofuran-1-one 9889764 Click to see 446.40 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
[(1R,2R,3S,3aR,8bS)-8b-hydroxy-2-(4-hydroxybutylcarbamoyl)-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1-yl] acetate 10507648 Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC=C(C=C4)OC)C5=CC=CC=C5)C(=O)NCCCCO 591.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
[8b-hydroxy-2-(4-hydroxybutylcarbamoyl)-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1-yl] acetate 85056956 Click to see 591.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide 78180418 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)N)C5=CC=CC=C5 477.50 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
1,8b-dihydroxy-6,8-dimethoxy-3a-(4-methoxyphenyl)-N-(oxolan-2-yl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide 85046958 Click to see 547.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
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/10.1016/S0031-9422(97)00253-7
1,8b-dihydroxy-N-(4-hydroxybutyl)-6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide 85056681 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)NCCCCO)C5=CC=CC=C5 549.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
3a-(1,3-benzodioxol-5-yl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1,8b-diol 21301151 Click to see 448.50 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
https://doi.org/10.1016/S0031-9422(00)00205-3
3a-(1,3-Benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydrocyclopenta[b][1]benzofuran-1-one 85060663 Click to see 446.40 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
8bH-Cyclopenta[b]benzofuran-1,8b-diol, 3a-(1,3-benzodioxol-5-yl)-1,2,3,3a-tetrahydro-6,8-dimethoxy-3-phenyl-, (1R,3S,3aR,8bS)- 10623340 Click to see 448.50 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
Aglafolin 393601 Click to see 492.50 unknown https://doi.org/10.1016/S0009-2797(98)00073-8
https://doi.org/10.1016/S0040-4020(97)10231-9
Didesmethylrocaglamide 397614 Click to see 477.50 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1-formyloxy-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10721063 Click to see 534.50 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
https://doi.org/10.1016/S0031-9422(00)00205-3
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 390507 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(00)00205-3
https://doi.org/10.1016/S0040-4020(97)10231-9
methyl 3a-(1,3-benzodioxol-5-yl)-1-formyloxy-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 85056561 Click to see 534.50 unknown https://doi.org/10.1016/S0031-9422(00)00205-3
https://doi.org/10.1016/S0040-4020(97)10231-9
methyl 3a-(1,3-benzodioxol-5-yl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 4653393 Click to see 506.50 unknown https://doi.org/10.1016/S0040-4020(97)10231-9
Rocaglamide 331783 Click to see 505.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
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/10.1016/S0040-4020(97)10231-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2-methyl-N-[1-(3-phenylprop-2-enoyl)pyrrolidin-2-yl]butanamide 57369849 Click to see 300.40 unknown https://doi.org/10.1248/CPB.49.1226
CID 23242584 23242584 Click to see CCC(C)C(=O)NC1CCCN1C(=O)C=CC2=CC=CC=C2 300.40 unknown https://doi.org/10.1248/CPB.49.1226
Odorine 23242585 Click to see 300.40 unknown https://doi.org/10.1248/CPB.49.1226
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3',4'-Dimethoxycinnamic acid 16848 Click to see 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
Ferulic acid glucoside 53978589 Click to see 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
[(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/10.1248/CPB.49.1226
[(1R,9R,10R,11R,12R)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-[[(2R)-2-methylbutanoyl]amino]pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 162907456 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://doi.org/10.1248/CPB.49.1226
[(1R,9R,10R,11S,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 101118317 Click to see 672.80 unknown https://doi.org/10.1248/CPB.49.1226
[(1R,9R,10R,11S,12R)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-[[(2R)-2-methylbutanoyl]amino]pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 162907453 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://doi.org/10.1248/CPB.49.1226
[(1R,9R,10R,11S,12S)-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 101118315 Click to see 672.80 unknown https://doi.org/10.1248/CPB.49.1226
[(1R,9R,10R,11S,12S)-1-hydroxy-3,5-dimethoxy-9-(4-methoxyphenyl)-11-[(2S)-2-[[(2R)-2-methylbutanoyl]amino]pyrrolidine-1-carbonyl]-10-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 162907452 Click to see 672.80 unknown https://doi.org/10.1248/CPB.49.1226
[(1S,9S,10R,11R,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 162907458 Click to see 672.80 unknown https://doi.org/10.1248/CPB.49.1226
[(1S,9S,10R,11S,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 162907460 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://doi.org/10.1248/CPB.49.1226
[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://doi.org/10.1248/CPB.49.1226
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 via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[2,4,6-Trihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-1-propanone 19744872 Click to see 342.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(1R,3S,3aR,8bS)-3a-[3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxyphenyl]-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1,8b-diol 10746296 Click to see 610.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7
3a-[3-(3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl)oxy-4-methoxyphenyl]-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1,8b-diol 85253858 Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C34C(CC(C3(C5=C(O4)C=C(C=C5OC)OC)O)O)C6=CC=CC=C6)OC)O)OC)O 610.60 unknown https://doi.org/10.1016/S0031-9422(97)00253-7

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