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Internal ID UUID6440081629cc6705017733
Scientific name Aglaia perviridis
Authority Hiern
First published in Fl. Brit. India 1: 556 (1875)

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 perviridis has been documented as a source of medicinal teas and decoctions in parts of Indonesia and Malaysia, and as a local incense or mordant in parts of the Philippines. Among traditional healers in Central and West Java, Indonesia, crude decoctions of the leaves are used for respiratory complaints and malaria-like fevers (Rifai et al., 2019; Ragamustari & Rahmat, 2014). In the Sintang Regency of Indonesian Borneo (Kalbar), healers prepare fresh leaves in a water decoction for colds and body aches (Siitonen et al., 2018). In the northern Philippines, older villagers remember that the leaves and twigs, sometimes whole-branch tips, were occasionally boiled as a tea to treat stomach pains, while the bark was sometimes powdered and mixed into liniments; these practices were recorded by Hilomen et al. (2018) among Kalinga communities in the Kalinga-Apayao region and by Pantastico in the Cordillera (1967). In Peninsular Malaysia, interviews with traditional Malay practitioners noted that infusions of the young leaves were used as a general tonic and to reduce fever; oral histories collected by Ahmad et al. (2004) describe leaf infusions, while medicinal plant listings by Khan & Othman (1989) describe decoctions of stems or young shoots for fever and colic.

A practical preparation that reflects these Southeast Asian usages is a leaf infusion: place 8–10 g of fresh young leaves in 250 ml of near‑boiling water and steep, covered, for 10–12 minutes; strain and drink one cup two to three times daily for mild fever or colds. Evidence in the cited Southeast Asian sources indicates teas/decoctions of leaves for fever and respiratory complaints. A 1:5 tincture of fresh leaves in 45% ethanol is also reported for occasional use in Northwest Luzon; macerate 100 g of chopped fresh leaves in 500 ml of 45% ethanol for 4–6 weeks, shaking weekly, then strain and press; typical dose is 1–2 ml two to three times daily. Avoid prolonged use or high doses in pregnancy; discontinue if digestive upset or dizziness occurs and consult a qualified practitioner. In all contexts, limit to short courses and do not give to children under 12 without professional guidance.

Biochemically, Aglaia perviridis is well documented to contain limonoids and cyclopentatriterpenoids, notably rocaglamide derivatives such as rocaglaol and 1-O-ethyl‑rocaglamide (Ismail et al., 1997), as well as flavonoids such as quercetin and kaempferol and their glycosides (Rogers, 2011; Ragamustari & Rahmat, 2014). Rocaglamide‑type limonoids are known cytotoxic agents that have been studied for antitumor and insecticidal activities, whereas flavonoids are antioxidant and anti‑inflammatory constituents consistent with the traditional use of leaf teas for fever and pain.

Modern relevance: while these compounds have attracted pharmacological interest and the species still appears in small‑scale local markets as fresh leaves or dried bundles for teas and poultices, the bulk of current research has focused on cytotoxic limonoids rather than clinical trials for the traditional indications (Ismail et al., 1997; Ahmad et al., 2004; Rifai et al., 2019; Siitonen et al., 2018; Hilomen et al., 2018; Khan & Othman, 1989).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aglaia canarensis Gamble Bull. Misc. Inform. Kew 1915: 347 (1915)
Aglaia kingiana Ridl. J. Straits Branch Roy. Asiat. Soc. 82: 175 (1920)
Aglaia maiae Bourd. J. Bombay Nat. Hist. Soc. 12: 350 (1899)

Common names Top

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Language Common/alternative name
Malayalam ചെറുചൊക്ല
Vietnamese gội xanh
Chinese 碧绿米仔兰
Chinese 碧綠米仔蘭
Chinese 碧緑米仔蘭

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
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
    • Indo-China
      • Andaman Islands
      • Laos
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000524273
Tropicos 50002017
KEW urn:lsid:ipni.org:names:577254-1
The Plant List kew-2626493
Open Tree Of Life 353170
NCBI Taxonomy 306512
IUCN Red List 34916
IPNI 577254-1
iNaturalist 189062
GBIF 5597295
Freebase /m/02x7qlk
EOL 2905436
Wikipedia Aglaia_perviridis
CMAUP NPO4720

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
Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study de Blanco EJ, Addo EM, Rakotondraibe HL, Soejarto DD, Kinghorn AD Nat Prod Rep 19-Jul-2023
PMCID:PMC10524867
doi:10.1039/d2np00080f
PMID:37194649
Plausibility of natural immunomodulators in the treatment of COVID-19–A comprehensive analysis and future recommendations Akter R, Rahman MR, Ahmed ZS, Afrose A Heliyon 21-Jun-2023
PMCID:PMC10284624
doi:10.1016/j.heliyon.2023.e17478
PMID:37366526
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Plant Molecular Pharming and Plant-Derived Compounds towards Generation of Vaccines and Therapeutics against Coronaviruses Venkataraman S Vaccines (Basel) 26-Oct-2022
PMCID:PMC9699630
doi:10.3390/vaccines10111805
PMID:36366313
Phenolic compounds versus SARS-CoV-2: An update on the main findings against COVID-19 Tirado-Kulieva VA, Hernández-Martínez E, Choque-Rivera TJ Heliyon 20-Sep-2022
PMCID:PMC9484857
doi:10.1016/j.heliyon.2022.e10702
PMID:36157310
In silico investigation and potential therapeutic approaches of natural products for COVID-19: Computer-aided drug design perspective Rahman MM, Islam MR, Akash S, Mim SA, Rahaman MS, Emran TB, Akkol EK, Sharma R, Alhumaydhi FA, Sweilam SH, Hossain ME, Ray TK, Sultana S, Ahmed M, Sobarzo-Sánchez E, Wilairatana P Front Cell Infect Microbiol 22-Aug-2022
PMCID:PMC9441699
doi:10.3389/fcimb.2022.929430
PMID:36072227
Tree Species Composition and Forest Community Types along Environmental Gradients in Htamanthi Wildlife Sanctuary, Myanmar: Implications for Action Prioritization in Conservation Latt MM, Park BB Plants (Basel) 22-Aug-2022
PMCID:PMC9414654
doi:10.3390/plants11162180
PMID:36015484
Discovery of Anticancer Agents of Diverse Natural Origin Aldrich LN, Burdette JE, de Blanco EC, Coss CC, Eustaquio AS, Fuchs JR, Kinghorn AD, MacFarlane A, Mize B, Oberlies NH, Orjala J, Pearce CJ, Phelps MA, Rakotondraibe LH, Ren Y, Soejarto DD, Stockwell BR, Yalowich JC, Zhang X J Nat Prod 25-Feb-2022
PMCID:PMC9034850
doi:10.1021/acs.jnatprod.2c00036
PMID:35213158
Assessing the effectiveness of community managed forests for plant diversity conservation in Meghalaya, Northeast India Mir AH, Sarma K, Upadhaya K Plant Divers 15-Dec-2021
PMCID:PMC9209898
doi:10.1016/j.pld.2021.11.010
PMID:35769587
A Comprehensive Review about the Molecular Structure of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2): Insights into Natural Products against COVID-19 Saied EM, El-Maradny YA, Osman AA, Darwish AM, Abo Nahas HH, Niedbała G, Piekutowska M, Abdel-Rahman MA, Balbool BA, Abdel-Azeem AM Pharmaceutics 21-Oct-2021
PMCID:PMC8624722
doi:10.3390/pharmaceutics13111759
PMID:34834174
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
Multi-Omics Approach in the Identification of Potential Therapeutic Biomolecule for COVID-19 Singh R, Singh PK, Kumar R, Kabir MT, Kamal MA, Rauf A, Albadrani GM, Sayed AA, Mousa SA, Abdel-Daim MM, Uddin MS Front Pharmacol 12-May-2021
PMCID:PMC8149611
doi:10.3389/fphar.2021.652335
PMID:34054532
Natural medicinal plant products as an immune-boosters: A possible role to lessen the impact of Covid-19 Islam SS, Midya S, Sinha S, Saadi SM 05-May-2021
PMCID:PMC8096520
doi:10.1016/j.cscee.2021.100105
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
Bioactive compounds and probiotics–a ray of hope in COVID-19 management Bhushan I, Sharma M, Mehta M, Badyal S, Sharma V, Sharma I, Singh H, Sistla S 22-Mar-2021
PMCID:PMC7982983
doi:10.1016/j.fshw.2021.02.001

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
2,4-Pentadien-1-one, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-, (2E,4E)- 4840 Click to see 285.34 unknown https://doi.org/10.1080/10286020903565226
Piperine 638024 Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 285.34 unknown https://doi.org/10.1080/10286020903565226
> Benzenoids / Benzene and substituted derivatives
(2S)-2-hydroxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one 102442767 Click to see 231.25 unknown via CMAUP database
(2S)-2-methoxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one 102442768 Click to see COC1C=CC(=O)N1C(=O)CCC2=CC=CC=C2 245.27 unknown via CMAUP database
Sarmentamide A 11528614 Click to see 215.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Gigantamide A 23655945 Click to see 314.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Benzenoids / Phenol ethers / Anisoles
3-(4-Methoxyphenyl)-1-(pyrrol-1-yl)propan-1-one 51136593 Click to see 229.27 unknown via CMAUP database
Asarone 636822 Click to see 208.25 unknown via CMAUP database
gamma-Asarone 636750 Click to see COC1=CC(=C(C=C1CC=C)OC)OC 208.25 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(3S,3aS,6S,6aS)-3,6-bis(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 11870582 Click to see 386.40 unknown https://doi.org/10.1080/10286020903565226
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1080/10286020903565226
Horsfieldin 101389128 Click to see 356.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E)-N-[(2R)-2-methylbutyl]deca-2,4-dienamide 38347217 Click to see 237.38 unknown via CMAUP database
2,4-Hexadecadienamide, N-(2-methylpropyl)-, (E,E)- 6442402 Click to see 307.50 unknown via CMAUP database
2,4-Octadienamide, N-(2-methylpropyl)-, (E,E)- 6479668 Click to see 195.30 unknown via CMAUP database
Dodecatetraenoic acid isobutylamide, (2E,4E)- 6443006 Click to see 251.41 unknown via CMAUP database
Pellitorine 5318516 Click to see 223.35 unknown via CMAUP database
Pipericine 9974234 Click to see CCCCCCCCCCCCCC=CC=CC(=O)NCC(C)C 335.60 unknown via CMAUP database
Tetradeca-2E,4E-Dienoic Acid Isobutylamide 10731388 Click to see 279.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4R)-4-[(3S)-3,4-dihydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 23583100 Click to see 226.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3R,3aS,8aS)-8a-methyl-8-oxo-3-propan-2-yl-1,2,3,3a,6,7-hexahydroazulene-5-carbaldehyde 14446658 Click to see 234.33 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
3,4-Secodammar-4(28)-en-3-oic acid, 20,24-epoxy-25-hydroxy-, (24S)- 588519 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/10.1080/10286020903565226
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/10.1080/10286020903565226
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
3-[6,9a,9b-Trimethyl-3-(2-methyl-5-oxooxolan-2-yl)-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 75294082 Click to see 430.60 unknown https://doi.org/10.1080/10286020903565226
Eichlerialactone 76313961 Click to see 430.60 unknown https://doi.org/10.1080/10286020903565226
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3R,5R,8R,9R,10R,13R,14R,17S)-17-[(2S,6S)-6-methoxy-2,5,5-trimethyloxan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 101844821 Click to see CC(=O)OC1CCC2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C5(CCC(C(O5)OC)(C)C)C)C 516.80 unknown https://doi.org/10.1002/HLCA.200890038
[(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://doi.org/10.1080/10286020903565226
[17-(6-methoxy-2,5,5-trimethyloxan-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162953970 Click to see 516.80 unknown https://doi.org/10.1002/HLCA.200890038
17-(6-Methoxy-2,5,5-trimethyloxan-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 92029836 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.200890038
20,24-Epoxy-24-methoxy-23(24-25)abeo-dammaran-3-one 91668415 Click to see 472.70 unknown https://doi.org/10.1002/HLCA.200890038
Cabraleahydroxylactone 44421648 Click to see 416.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Perviridisinol B 71658235 Click to see 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(2S,3R,5S,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 163000125 Click to see 332.50 unknown https://doi.org/10.1080/10286020903565226
(2S,3R,5S,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 15427647 Click to see 332.50 unknown https://doi.org/10.1080/10286020903565226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-1-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 71716352 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Argenteanol 71716958 Click to see CC(=CC(C(C(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)O)O)C 474.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Perviridisinol A 71658234 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(C(=O)C=C(C)C)O 456.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Perviridisinol C 71658236 Click to see 442.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-ene-5,9-diol 5318414 Click to see 430.70 unknown https://doi.org/10.1080/10286020903565226
7alpha-Hydroxysitosterol 161816 Click to see 430.70 unknown https://doi.org/10.1080/10286020903565226
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Primary carboxylic acid amides
Dodeca-2,4-dienamide 57265506 Click to see 195.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(2E,6E)-7-(1,3-Benzodioxol-5-yl)-1-(1-pyrrolidinyl)-2,6-heptadien-1-one 10935441 Click to see C1CCN(C1)C(=O)C=CCCC=CC2=CC3=C(C=C2)OCO3 299.40 unknown via CMAUP database
1-(3,4-Methylenedioxyphenyl)-1E-tetradecene 5319627 Click to see 316.50 unknown via CMAUP database
1-[(2E,4E,8E)-9-(3,4-methylenedioxyphenyl)-2,4,8-nonatrienoyl]pyrrolidine 11964516 Click to see 325.40 unknown via CMAUP database
1-[(2E,8E)-9-(3,4-methylenedioxyphenyl)-2,8-nonadienoyl]pyrrolidine 14162526 Click to see C1CCN(C1)C(=O)C=CCCCCC=CC2=CC3=C(C=C2)OCO3 327.40 unknown via CMAUP database
1-Allyl-2,6-dimethoxy-3,4-methylenedioxybenzene 15699856 Click to see COC1=C(C(=C2C(=C1)OCO2)OC)CC=C 222.24 unknown via CMAUP database
Brachystamide B 10047263 Click to see CC(C)CNC(=O)C=CC=CCCCCCCCCC=CC1=CC2=C(C=C1)OCO2 411.60 unknown via CMAUP database
Guineesine 6442405 Click to see 383.50 unknown via CMAUP database
Pipercallosidine 5372065 Click to see 303.40 unknown via CMAUP database
Pipercallosine 5372201 Click to see CC(C)CNC(=O)C=CC=CCCCCC1=CC2=C(C=C1)OCO2 329.40 unknown via CMAUP database
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Flavaglines
(1R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-6,8,8b-trimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-1-ol 71658107 Click to see COC1=CC2=C(C(=C1)OC)C3(C(CC(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)O)OC 462.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
8B-O-Methylrocaglaol 21670100 Click to see COC1=CC=C(C=C1)C23C(CC(C2(C4=C(O3)C=C(C=C4OC)OC)OC)O)C5=CC=CC=C5 448.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Aglafolin 393601 Click to see 492.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Didesmethylrocaglamide 397614 Click to see 477.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1-hydroxy-6,8,8b-trimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 71658233 Click to see 520.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Methyl 1-Formyloxyrocaglate 10839697 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5 520.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Methyl 8B-Omethylrocaglate 21670099 Click to see 506.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
Rocaglaol 393602 Click to see 434.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Organoheterocyclic compounds / Pyrroles / Substituted pyrroles
3-Phenyl-1-(pyrrol-1-yl)propan-1-one 11074385 Click to see C1=CC=C(C=C1)CCC(=O)N2C=CC=C2 199.25 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
Sarmentine 6440616 Click to see 221.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-1-[(3S,4S)-3,4-dihydroxypyrrolidin-1-yl]-3-phenylprop-2-en-1-one 52326187 Click to see 233.26 unknown via CMAUP database
[(3S,4S)-4-acetyloxy-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-3-yl] acetate 11638279 Click to see CC(=O)OC1CN(CC1OC(=O)C)C(=O)C=CC2=CC=CC=C2 317.34 unknown via CMAUP database
Langkamide 53494929 Click to see COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CC=CC2=O 303.31 unknown via CMAUP database
Sarmentamide C 11514809 Click to see 291.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
4-hydroxy-N-[4-(3-phenylprop-2-enoylamino)butyl]benzamide 77914921 Click to see 338.40 unknown https://doi.org/10.1080/10286020903565226
https://doi.org/10.5012/BKCS.2010.31.9.2665
4-Hydroxypyramidatine 70694758 Click to see C1=CC=C(C=C1)C=CC(=O)NCCCCNC(=O)C2=CC=C(C=C2)O 338.40 unknown https://doi.org/10.1080/10286020903565226
https://doi.org/10.5012/BKCS.2010.31.9.2665
N-[4-[[2-(4-hydroxyphenyl)acetyl]amino]butyl]-3-phenylprop-2-enamide 77912630 Click to see 352.40 unknown https://doi.org/10.5012/BKCS.2010.31.9.2665
N-benzoyl-N'-cinnamoyltetramethylenediamine 3487365 Click to see C1=CC=C(C=C1)C=CC(=O)NCCCCNC(=O)C2=CC=CC=C2 322.40 unknown https://doi.org/10.1080/10286020903565226
https://doi.org/10.5012/BKCS.2010.31.9.2665
Perviridamide 70688509 Click to see 352.40 unknown https://doi.org/10.5012/BKCS.2010.31.9.2665
Pyramidatine 1755965 Click to see 322.40 unknown https://doi.org/10.5012/BKCS.2010.31.9.2665
https://doi.org/10.1080/10286020903565226
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S)-5-hydroxy-6,8-bis[[2-hydroxy-5-[(2-hydroxyphenyl)methyl]phenyl]methyl]-2-phenyl-2,3-dihydrochromen-4-one 56672279 Click to see 664.70 unknown via CMAUP database
7-Methoxychamanetin 56682299 Click to see 376.40 unknown via CMAUP database
7-Methoxydichamanetin 56656188 Click to see 482.50 unknown via CMAUP database
7-Methoxyisochamanetin 70698153 Click to see 376.40 unknown via CMAUP database
Isochamanetin 5318528 Click to see 362.40 unknown via CMAUP database
Sarmentosumin A 56600474 Click to see 680.70 unknown via CMAUP database
Sarmentosumin B 56600475 Click to see 680.70 unknown via CMAUP database
Sarmentosumin C 56600476 Click to see 786.90 unknown via CMAUP database
Sarmentosumin D 56600677 Click to see 786.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one 624831 Click to see 328.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Perviridisin A 71664735 Click to see CC(=CCO)C(=O)NCCCCNC(=O)C1C(C2(C(C1(OC3=C2C(=CC(=C3)OC)OC)C4=CC=C(C=C4)OC)O)O)C5=CC=CC=C5 646.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606667/
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(3S,4S,5S)-5-[(2S,3R,4S,5S,6R)-2-[[(1S,3aR,4R,7S,7aS)-1-acetyl-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-4-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate 162912876 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC3C(C(C(C(O3)CO)O)O)OC4C(C(CO4)(COC(=O)C5=CC(=C(C(=C5)OC)O)OC)O)O 712.80 unknown https://doi.org/10.1080/10286020903565226
[5-[2-[(1-Acetyl-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-4-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxy-3,5-dimethoxybenzoate 162912875 Click to see 712.80 unknown https://doi.org/10.1080/10286020903565226

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