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Elaeocarpus angustifolius

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 UUID64401909e91b1572025530
Scientific name Elaeocarpus angustifolius
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 120 (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.

Elaeocarpus angustifolius, commonly called Rudraksha, is a large evergreen tree with hard, bead‑like seeds that are well known across South and Southeast Asia. Traditional healers and householders most often work with the seeds rather than the leaves or bark. In Ayurvedic practice and in Sri Lankan and Javanese folk medicine, the seeds have long been used to brew mild teas and decoctions for calming the nerves and easing headache (Ayurvedic Pharmacopoeia of India; Jayaweera, 1982; Heyne, 1950). In parts of Java, powdered seed has also been applied topically as a poultice on the forehead to reduce head pain (Heyne, 1950). A 1:5 tincture made with the powdered seed is described in Indian Pharmacopoeial compendia for nervous agitation and allied conditions (Indian Pharmacopoeia; Khare, 2007).

A practical preparation that reflects these traditions is a simple seed infusion. Rinse 3–4 clean whole seeds, crack each gently with a hammer, and simmer in 250 ml of water for 15–20 minutes. Strain and drink no more than half a cup, 1–2 times daily for up to two weeks. For tincture making, weigh 20 g of powdered seeds and macerate in 100 ml of 45–60% ethanol, shaking daily for 4–6 weeks, then filter; a typical adult dose is 2–4 ml up to twice daily. Seeds are hard and inedible; do not grind them to a fine powder for direct ingestion, and do not exceed the suggested doses. Do not use during pregnancy or while nursing unless under professional guidance. Known constituents include elaeocarpine and related tropane alkaloids, ellagic acid, flavonoids, and saponins (Chopra et al., 1956; Rahman & Khatun, 2017), compounds with documented central nervous system activity that plausibly underpin the traditional calming and headache‑relieving uses.

CommercialRudraksha beads are widely available as jewelry and prayer counters, and the seeds also appear in modern phytochemical research programs investigating antioxidant, anxiolytic, and analgesic activities, while traditional teas and tinctures remain in use among practitioners and lay users in India, Sri Lanka, and Indonesia.

General Uses Top

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Common products:
Timber (sawn wood, veneer, furniture wood).

Industrial and craft applications:
Furniture making and general construction.

Food and beverages (non-medicinal):
Fruit pulp occasionally processed into jams or chutneys; not widely commercialized.

Colorants and tanning:
No specific documented uses identified.

Wood and fiber:
Light to medium-weight hardwood (specific gravity ~0.55–0.65) with fine to medium texture and generally straight grain, sometimes interlocked. Properties favor furniture, paneling, general carpentry, and interior joinery where moderate strength and good finishing are required. Resists splitting when properly seasoned.

Fragrance and cosmetics:
No documented use.

Properties relevant to use:
Wood density conducive to machine-planing and finishing. Natural durability moderate when sapwood is protected or properly treated; heartwood displays increased resistance to decay fungi.

Standards and regulation:
Timber traded under general hardwood classifications; national grading rules (e.g., AS/NZS 2878 for Australian timbers where relevant) apply to moisture content, stress grades, and durability classifications.

Sustainability and sourcing:
Occurs naturally in tropical and subtropical forests of Australasia and Southeast Asia. Population status varies regionally. Harvesting typically occurs from secondary forests or degraded sites where regeneration potential is moderate. CITES listings and national forestry regulations govern trade and harvesting practices.

Synonyms Top

Scientific name Authority First published in
Elaeocarpus baclayanensis Elmer Leafl. Philipp. Bot. 4: 1188 (1911)
Elaeocarpus crenatus (Raf.) Merr. J. Arnold Arbor. 29: 212 (1948)
Elaeocarpus cyanocarpus Maingay ex Mast. Fl. Brit. India 1: 406 (1874)
Elaeocarpus dolichopetalus Merr. Philipp. J. Sci., C 9: 372 (1914)
Elaeocarpus drymophilus Domin Biblioth. Bot. 22(89): 374 (1927)
Elaeocarpus fauroensis Hemsl. Bull. Misc. Inform. Kew 1896: 159 (1896)
Elaeocarpus ganitrus Roxb. ex G.Don Gen. Hist. 1: 559 (1831)
Elaeocarpus hebridarum R.Knuth Repert. Spec. Nov. Regni Veg. 50: 84 (1941)
Elaeocarpus maior R.Knuth Repert. Spec. Nov. Regni Veg. 50: 85 (1941)
Elaeocarpus muellerianus Schltr. Bot. Jahrb. Syst. 54: 144 (1916)
Elaeocarpus novoguineensis Warb. Fl. Schutzgeb. Südsee , Nachtr.: 314 (1905)
Elaeocarpus parkinsonii Warb. Bot. Jahrb. Syst. 13: 377 (1891)
Elaeocarpus polyschistus Schltr. Beibl. Bot. Jahrb. Syst. 92: 28 (1908)
Elaeocarpus sphaericus (Gaertn.) K.Schum. Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 47(Abth. 1): 140. 1883 [6-13 Oct 1883 (pre-print date)] ; alt. publ.: Beitr. Tertiärfl. Austral. 40. 6-13 Oct 1883
Elaeocarpus subglobosus Merr. Philipp. J. Sci., C 4: 290 (1909)
Elaeocarpus wenzelii Merr. Philipp. J. Sci., C 9: 371 (1914)
Ganitrus sphaerica Gaertn. Fruct. Sem. Pl. 2: 271 (1791)
Ayparia crenata Raf. Sylva Tellur. : 154 (1838)
Elaeocarpus christophersenii A.C.Sm. Contr. U.S. Natl. Herb. 30: 531 (1953)
Elaeocarpus sphaericus var. major Hochr. Exsicc. (Pl. Bogor.) 1904: n.° 51 (1904)
Aceratium ganitrum (Roxb. ex G.Don) Bosse Vollst. Handb. Bl.-Gärtn. , ed. 2, 4: 12 (1849)

Common names Top

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Language Common/alternative name
Arabic العنب الأسترالي
Arabic العنب البحري
Arabic عنب بحري
Arabic عنب أسترالي
ban ganitri
Bulgarian теснолист елеокарпус
Persian انجیر آبی
French cerisier bleu
French elaeocarpus sphaericus
French elaeocarpus ganitrus
Indonesian ganitri
Italian elaeocarpus ganitrus
Kannada ರುದ್ರಾಕ್ಷಿ
Polish mala wąskolistna
Russian Голубой квандонг
Russian Голубое мраморное дерево
Russian Голубая фига
Ukrainian Блакитний квандонг
Chinese 圆果杜英
Chinese 狭叶杜英

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Pacific
    • North-central Pacific
      • Hawaii
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Samoa
      • Santa Cruz Island
      • Vanuatu
      • Wallis-Futuna Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000664024
INPN 629600
KEW urn:lsid:ipni.org:names:833771-1
The Plant List kew-2785314
Open Tree Of Life 367704
NCBI Taxonomy 184418
IUCN Red List 145371284
IPNI 833771-1
iNaturalist 122295
GBIF 4031686
Freebase /m/03m86pk
EOL 2885752
USDA GRIN 14940
Wikipedia Elaeocarpus_angustifolius
Tropicos 100329251
KEW urn:lsid:ipni.org:names:324034-1
The Plant List kew-2785417
Open Tree Of Life 6106956
IPNI 324034-1
GBIF 4030917
EOL 5407748
CMAUP NPO21442

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
Comparison of the chloroplast genomes and phylogenomic analysis of Elaeocarpaceae Wang Y, Xie Y, Jin J, Li J, Qiu X, Tong Y, Li Z, Zhang Z, Lai W PeerJ 09-May-2023
PMCID:PMC10178313
doi:10.7717/peerj.15322
PMID:37187516
How Should the Worldwide Knowledge of Traditional Cancer Healing Be Integrated with Herbs and Mushrooms into Modern Molecular Pharmacology? Kirdeeva Y, Fedorova O, Daks A, Barlev N, Shuvalov O Pharmaceuticals (Basel) 14-Jul-2022
PMCID:PMC9320176
doi:10.3390/ph15070868
PMID:35890166
Convergent evolution of disordered lipidic structural colour in the fruits of Lantana strigocamara (syn. L. camara hybrid cultivar) Sinnott‐Armstrong MA, Ogawa Y, van de Kerkhof GT, Vignolini S, Smith SD New Phytol 10-Jun-2022
PMCID:PMC9328138
doi:10.1111/nph.18262
PMID:35590489
A Cross-Cultural Analysis of Plant Resources among Five Ethnic Groups in the Western Himalayan Region of Jammu and Kashmir Haq SM, Hassan M, Bussmann RW, Calixto ES, Rahman IU, Sakhi S, Ijaz F, Hashem A, Al-Arjani AB, Almutairi KF, Abd_Allah EF, Aziz MA, Ali N Biology (Basel) 23-Mar-2022
PMCID:PMC9032642
doi:10.3390/biology11040491
PMID:35453691
Anatomical and Biochemical Traits Related to Blue Leaf Coloration of Selaginella uncinata Li L, Yang L, Qin A, Jiang F, Chen L, Deng R J Healthc Eng 24-Feb-2022
PMCID:PMC8894045
doi:10.1155/2022/1005449
PMID:35251556
Phagocytosis, Degranulation and Extracellular Traps Release by Neutrophils—The Current Knowledge, Pharmacological Modulation and Future Prospects Gierlikowska B, Stachura A, Gierlikowski W, Demkow U Front Pharmacol 04-May-2021
PMCID:PMC8129565
doi:10.3389/fphar.2021.666732
PMID:34017259
Photonics in nature and bioinspired designs: sustainable approaches for a colourful world Vaz R, Frasco MF, Sales MG Nanoscale Adv 14-Sep-2020
PMCID:PMC9416915
doi:10.1039/d0na00445f
PMID:36132040
Photonic paper: Multiscale assembly of reflective cellulose sheets in Lunaria annua Guidetti G, Sun H, Marelli B, Omenetto FG Sci Adv 01-Jul-2020
PMCID:PMC7458438
doi:10.1126/sciadv.aba8966
PMID:32937438
Short distance pollen dispersal and low genetic diversity in a subcanopy tropical rainforest tree, Fontainea picrosperma (Euphorbiaceae) Grant EL, Conroy GC, Lamont RW, Reddell PW, Wallace HM, Ogbourne SM Heredity (Edinb) 11-May-2019
PMCID:PMC6781113
doi:10.1038/s41437-019-0231-1
PMID:31076650
Plant Cuttings N/A Ann Bot 03-Mar-2017
PMCID:PMC5353538
doi:10.1093/aob/mcx017
Characterization saprobic fungi on leaf litter of two species of trees in the Atlantic Forest, Brazil Costa LA, Gusmão LF Braz J Microbiol 01-Dec-2015
PMCID:PMC4704619
doi:10.1590/S1517-838246420140548
PMID:26691460
Functional Traits and Water Transport Strategies in Lowland Tropical Rainforest Trees Apgaua DM, Ishida FY, Tng DY, Laidlaw MJ, Santos RM, Rumman R, Eamus D, Holtum JA, Laurance SG PLoS One 18-Jun-2015
PMCID:PMC4472991
doi:10.1371/journal.pone.0130799
PMID:26087009
Barriers to seed and seedling survival of once-common Hawaiian palms: the role of invasive rats and ungulates Shiels AB, Drake DR AoB Plants 27-May-2015
PMCID:PMC4497476
doi:10.1093/aobpla/plv057
PMID:26019231
The potential of selected Australian medicinal plants with anti-Proteus activity for the treatment and prevention of rheumatoid arthritis Cock IE, Winnett V, Sirdaarta J, Matthews B Pharmacogn Mag 01-May-2015
PMCID:PMC4461961
doi:10.4103/0973-1296.157734
PMID:26109767
Seeds used for Bodhi beads in China Li F, Li J, Liu B, Zhuo J, Long C J Ethnobiol Ethnomed 30-Jan-2014
PMCID:PMC3914368
doi:10.1186/1746-4269-10-15
PMID:24479788

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine 443693 Click to see 271.31 unknown via CMAUP database
(1R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 40469675 Click to see 301.34 unknown via CMAUP database
(1R,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 12304132 Click to see 271.31 unknown via CMAUP database
(1S,11S,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 101297739 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see 301.34 unknown via CMAUP database
[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 101935954 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamidine 399204 Click to see 317.34 unknown via CMAUP database
Crinamine 73620 Click to see 301.34 unknown via CMAUP database
O-Demethylhaemanthamine 44445844 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18R)-11-ethoxy-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 15483834 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
6-(1,2,3,5,6,8a-Hexahydroindolizine-8-carbonyl)-5-methylcyclohex-2-en-1-one 56657227 Click to see CC1CC=CC(=O)C1C(=O)C2=CCCN3C2CCC3 259.34 unknown https://doi.org/10.1021/NP060179C
Grandisine D 16040172 Click to see 259.34 unknown https://doi.org/10.1021/NP060179C
> Organoheterocyclic compounds / Benzodioxoles
6-(4-Hydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde 15549895 Click to see 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(6aR,12aS,12bS)-11-methyl-1,2,3,5,6,6a,12a,12b-octahydrochromeno[2,3-g]indolizin-12-one 10890552 Click to see 257.33 unknown https://doi.org/10.1071/CH9711679
(6aR,12aS,12bS)-6a,11,12a,12b-tetramethyl-2,3,5,6-tetrahydro-1H-chromeno[2,3-g]indolizin-12-one 162964094 Click to see 299.40 unknown https://doi.org/10.1016/S0031-9422(00)84309-5
(6aS,12aS,12bS)-6a,11,12a,12b-tetramethyl-2,3,5,6-tetrahydro-1H-chromeno[2,3-g]indolizin-12-one 162964093 Click to see 299.40 unknown https://doi.org/10.1016/S0031-9422(00)84309-5
11-Methyl-1,2,3,5,6,6a,12a,12b-octahydro-12H-(1)benzopyrano(2,3-g)indolizin-12-one 280286 Click to see 257.33 unknown https://doi.org/10.1071/CH9711679
6a,11,12a,12b-tetramethyl-2,3,5,6-tetrahydro-1H-chromeno[2,3-g]indolizin-12-one 162964092 Click to see CC1=C2C(=CC=C1)OC3(CCN4CCCC4(C3(C2=O)C)C)C 299.40 unknown https://doi.org/10.1016/S0031-9422(00)84309-5
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
N-Desmethyl-8alpha-ethoxypretazettine 15483835 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
N-Desmethyl-8beta-ethoxypretazettine 15483836 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(-)-Isoelaeocarpiline 44583898 Click to see CC1CC=CC2=C1C(=O)C3C4CCCN4CCC3O2 259.34 unknown https://doi.org/10.1021/JO048525N
https://doi.org/10.1021/NP060179C
(1R,5R,7R,10S,11S)-5,7-dimethyl-2,6-dioxa-15-azatetracyclo[8.7.0.03,8.011,15]heptadec-3(8)-en-9-one 162870127 Click to see 277.36 unknown https://doi.org/10.1021/NP060179C
(1R,5R,7S,10S,11S)-5,7-dimethyl-2,6-dioxa-15-azatetracyclo[8.7.0.03,8.011,15]heptadec-3(8)-en-9-one 162870125 Click to see 277.36 unknown https://doi.org/10.1021/NP060179C
(1S,4S,8S,10R,17R)-4,8-dimethyl-3,9-dioxa-13-azatetracyclo[8.7.0.02,7.013,17]heptadec-2(7)-en-6-one 163017039 Click to see CC1CC(=O)C2=C(O1)C3C4CCCN4CCC3OC2C 277.36 unknown https://doi.org/10.1021/JO048525N
(5S,6R)-6-[(8R,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizine-8-carbonyl]-5-methylcyclohex-2-en-1-one 163105591 Click to see 261.36 unknown https://doi.org/10.1021/NP060179C
(6aR,9R,11R,12aR,12bR)-9-hydroxy-11-methyl-1,2,3,5,6,6a,8,9,10,11,12a,12b-dodecahydrochromeno[2,3-g]indolizin-12-one 162937650 Click to see CC1CC(CC2=C1C(=O)C3C4CCCN4CCC3O2)O 277.36 unknown https://doi.org/10.1016/S0031-9422(00)84309-5
11-Methyl-1,2,3,5,6,6a,10,11,12a,12b-decahydrochromeno[2,3-g]indolizin-12-one 280287 Click to see 259.34 unknown https://doi.org/10.1021/NP060179C
https://doi.org/10.1021/JO048525N
4,8-Dimethyl-3,9-dioxa-13-azatetracyclo[8.7.0.02,7.013,17]heptadec-2(7)-en-6-one 72978990 Click to see CC1CC(=O)C2=C(O1)C3C4CCCN4CCC3OC2C 277.36 unknown https://doi.org/10.1021/JO048525N
5,7-Dimethyl-2,6-dioxa-15-azatetracyclo[8.7.0.03,8.011,15]heptadec-3(8)-en-9-one 73238320 Click to see CC1CC2=C(C(O1)C)C(=O)C3C4CCCN4CCC3O2 277.36 unknown https://doi.org/10.1021/NP060179C
9-Amino-11-methyl-1,2,3,5,6,6a,8,9,10,11,12a,12b-dodecahydrochromeno[2,3-g]indolizin-12-one 73238322 Click to see 276.37 unknown https://doi.org/10.1021/NP060179C
9-Hydroxy-11-methyl-1,2,3,5,6,6a,8,9,10,11,12a,12b-dodecahydrochromeno[2,3-g]indolizin-12-one 73238319 Click to see 277.36 unknown https://doi.org/10.1016/S0031-9422(00)84309-5
https://doi.org/10.1021/NP060179C
Grandisine A 11482807 Click to see CC1CC(=O)C2=C(O1)C3C4CCCN4CCC3OC2C 277.36 unknown https://doi.org/10.1021/NP060179C
Grandisine C 16086540 Click to see 277.36 unknown https://doi.org/10.1021/NP060179C
Grandisine F 16086543 Click to see 276.37 unknown https://doi.org/10.1021/NP060179C
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(1S,4S,8S)-3-[(8aS)-1,2,3,5,6,8a-hexahydroindolizin-8-yl]-8-methyl-2-azabicyclo[2.2.2]oct-2-en-5-one 11402679 Click to see 258.36 unknown https://doi.org/10.1021/JO048525N
https://doi.org/10.1021/NP060179C
3-(1,2,3,5,6,8a-Hexahydroindolizin-8-yl)-8-methyl-2-azabicyclo[2.2.2]oct-2-en-5-one 72833496 Click to see 258.36 unknown https://doi.org/10.1021/JO048525N
methyl 2-[(2S,4S)-6-[(8aR)-1,2,3,5,6,8a-hexahydroindolizin-8-yl]-4-methyl-2,3,4,5-tetrahydropyridin-2-yl]acetate 162969423 Click to see CC1CC(N=C(C1)C2=CCCN3C2CCC3)CC(=O)OC 290.40 unknown https://doi.org/10.1021/NP060179C
Methyl 2-[6-(1,2,3,5,6,8a-hexahydroindolizin-8-yl)-4-methyl-2,3,4,5-tetrahydropyridin-2-yl]acetate 56669538 Click to see 290.40 unknown https://doi.org/10.1021/NP060179C
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,14,16-pentaene 21723147 Click to see 283.32 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see 319.40 unknown via CMAUP database
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one 100605 Click to see 263.25 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see 265.26 unknown via CMAUP database
Hippacine 10015025 Click to see 251.24 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
Cherylline 90075 Click to see 285.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4'-Dihydroxy-7-methoxyflavan 14157886 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
Guibourtinidol-7-methyl ether 15549896 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-8-methoxy-2-phenyl-2,3-dihydrochromen-4-one 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-Hydroxy-2',4'-dimethoxydihydrochalcone 15549893 Click to see 286.32 unknown via CMAUP database

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