Details Top

Internal ID UUID64405a95f162b510314671
Scientific name Stenocereus thurberi
Authority (Engelm.) Buxb.
First published in in Bot. Stud. 12: 101. 1961.

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Fresh fruit of Stenocereus thurberi, sold as a fresh produce item.
- Processed fruit products: juice, jam, syrup, and dried fruit snacks.
- Plant material supplied to research institutions as a source of DNA; a draft reference genome (∼1.2 Gb) has been released for evolutionary and CAM‑photosynthesis studies.

Food and beverages (non-medicinal):
The mature fruits are harvested in late summer. After cleaning and peeling, the pulp is crushed to obtain juice that is pasteurized (typically at 90 °C for 2 min), filtered, and packaged as a beverage, or boiled with sugar to produce jam, fruit butter, or syrup. Dried pieces are marketed as a snack. The juice can also be concentrated for use in flavored beverages, dairy products, and frozen desserts. The fruit contains approximately 85 % water, about 12 % soluble sugars (Brix ≈ 12), and has an acidic pH of 4.5–5.0, giving a sweet‑tart flavor suitable for confectionery and beverage formulations. No medicinal claims are associated with these products.

Properties relevant to use:
High moisture content yields a juice extraction efficiency of roughly 70 % (by weight). The sugar concentration provides natural sweetness, reducing the need for added sugars in processed products. The organic acid profile stabilizes flavor after heat treatment. The low titratable acidity (~0.3 % citric acid equivalent) contributes to a mild tartness that balances sweetness, making the fruit suitable for applications ranging from drinks to confectionery. Seeds contain a small amount (≈ 5 % of seed weight) of oil rich in linoleic acid, but commercial oil extraction is not currently undertaken.

Standards and regulation:
Fresh and processed cactus‑fruit products are regulated as produce or fruit juices under the U.S. Food and Drug Administration (21 CFR 110) and Codex Alimentarius (CXS 192‑1995). Processing facilities must implement Hazard Analysis and Critical Control Points (HACCP) and meet ISO 22000 food‑safety management requirements for international trade. Mexican fruit‑juice producers must also comply with NMX‑AA‑164‑SCFI‑2015, which specifies maximum allowable microbial loads.

Sustainability and sourcing:
Stenocereus thurberi is classified as “Least Concern” on the IUCN Red List (2021). Wild harvesting occurs selectively in late summer to avoid over‑exploitation. In recent years, small orchards have been established in northern Mexico for commercial fruit production, decreasing pressure on wild populations. International trade of live plants is regulated under CITES; the species is not listed, but exporters must obtain phytosanitary certificates from the Mexican Servicio Nacional de Sanidad, Inocuidad y Calidad Agroalimentaria (SENASICA). No CITES restrictions apply.

Synonyms Top

Scientific name Authority First published in
Neolemaireocereus thurberi (Engelm.) Backeb. in Cactaceae (Berlin) 1943-1944: 10. 1944.
Pilocereus thurberi Engelm. ex Rümpler Handb. Cacteenk.: 689. 1885.
Cereus thurberi Engelm. in Amer. J. Sci. Arts, ser. 2 17: 234–235. 1854.
Lemaireocereus thurberi (Engelm.) Britton & Rose in Contr. U.S. Natl. Herb. 12(10): 426. 1909.
Marshallocereus thurberi (Engelm.) Backeb. in Cact. Succ. J. (Los Angeles) 23: 121. 1951.
Rathbunia thurberi (Engelm.) P.V.Heath in Calyx 2(3): 103. 1992.
Cereus thurberi var. monstrosus Dams in Monatsschr. Kakteenk. 14: 182. 1904.
Glandulicereus thurberi (Engelm.) Guiggi in Cactology 3: 7. 2012.
Rathbunia thurberi f. cristata P.V.Heath in Calyx 2: 103. 1992.
Rathbunia thurberi f. dichotoma P.V.Heath in Calyx 2: 103. 1992.
Stenocereus thurberi f. cristatus (P.V.Heath) P.V.Heath in Calyx 5: 100. 1996.
Stenocereus thurberi f. dichotomus (P.V.Heath) P.V.Heath in Calyx 5: 100. 1996.

Common names Top

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Language Common/alternative name
English organpipe cactus
English organ pipe cactus
Spanish pilocereus thurberi
Spanish lemaireocereus thurberi
Spanish rathbunia thurberi
Spanish marshallocereus thurberi
Spanish pitayo dulce
German orgelpfeifenkaktus
Persian کاکتوس لولهای
Hebrew אורגן פייפ קקטוס
Japanese オルガンパイプサボテン
Korean 대왕각
Korean 오르간파이프선인장
lb uergelpäifekaktus
Dutch orgelpijpcactus
Swedish orgelpipekaktus
Chinese 茶柱
Chinese 管風琴仙人掌果
Chinese 风琴管仙人掌
Chinese 大王阁

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Stenocereus thurberi subsp. littoralis (K.Brandegee) N.P.Taylor in Cactaceae Consensus Init. 5: 13. 1998.
Stenocereus thurberi subsp. thurberi

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Northern America
    • Mexico
      • Mexico Northeast
      • Mexico Northwest
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001287223
USDA Plants STTH3
Tropicos 5100601
KEW urn:lsid:ipni.org:names:244652-2
The Plant List tro-5100601
Open Tree Of Life 322813
NCBI Taxonomy 171973
Nature Serve 2.128983
IUCN Red List 151842
IPNI 244652-2
iNaturalist 82005
GBIF 3084384
Freebase /m/0fw4l2
EPPO SVCTH
EOL 491487
USDA GRIN 406666
Wikipedia Stenocereus_thurberi
CMAUP NPO20383

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_002740465.2 Sthu_v2 Scaffold The University of Arizona 2025-07-30 27 905.18 Mb

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
Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 Strickland LE, Thompson RS, Shafer SL, Bartlein PJ, Pelltier RT, Anderson KH, Schumann RR, McFadden AK Sci Data 12-Jan-2024
PMCID:PMC10786896
doi:10.1038/s41597-023-02616-y
PMID:38216580
Nanoparticles of Betalain–Gelatin with Antioxidant Properties by Coaxial Electrospraying: Preparation and Characterization Figueroa-Enriquez CE, Rodríguez-Félix F, Plascencia-Jatomea M, Sánchez-Escalante A, Vargas-López JM, Tapia-Hernández JA, Canizales-Rodríguez DF, Castro-Enriquez DD, Ruiz-Cruz S, Santos-Sauceda I, Burruel-Ibarra SE, Pompa-Ramos JL ACS Omega 23-Oct-2023
PMCID:PMC10634192
doi:10.1021/acsomega.3c04021
PMID:37969967
Pre-contact Agave domesticates – living legacy plants in Arizona’s landscape Hodgson WC, Jane Rosenthal E, Salywon AM Ann Bot 10-Oct-2023
PMCID:PMC10799993
doi:10.1093/aob/mcad113
PMID:37815005
Agri-silvicultures of Mexican Arid America Andablo-Reyes AD, Moreno-Calles AI, Cancio-Coyac BA, Gutiérrez-Coatecatl E, Rivero-Romero AD, Hernández-Cendejas G, Casas A J Ethnobiol Ethnomed 14-Sep-2023
PMCID:PMC10503103
doi:10.1186/s13002-023-00612-5
PMID:37710240
The CAM lineages of planet Earth Gilman IS, Smith JA, Holtum JA, Sage RF, Silvera K, Winter K, Edwards EJ Ann Bot 12-Sep-2023
PMCID:PMC10799995
doi:10.1093/aob/mcad135
PMID:37698538
Are 150 km of open sea enough? Gene flow and population differentiation in a bat-pollinated columnar cactus Arenas S, Búrquez A, Bustamante E, Scheinvar E, Eguiarte LE PLoS One 29-Jun-2023
PMCID:PMC10309638
doi:10.1371/journal.pone.0282932
PMID:37384637
New Functional Foods with Cactus Components: Sustainable Perspectives and Future Trends Monteiro SS, Almeida RL, Santos NC, Pereira EM, Silva AP, Oliveira HM, Pasquali MA Foods 27-Jun-2023
PMCID:PMC10340198
doi:10.3390/foods12132494
PMID:37444232
Global change impacts on cacti (Cactaceae): current threats, challenges and conservation solutions Hultine KR, Hernández-Hernández T, Williams DG, Albeke SE, Tran N, Puente R, Larios E Ann Bot 21-Mar-2023
PMCID:PMC10799997
doi:10.1093/aob/mcad040
PMID:36861500
Antioxidant and Antimicrobial Effect of Biodegradable Films Containing Pitaya (Stenocereus thurberi) Extracts during the Refrigerated Storage of Fish Castro-Enríquez D, Miranda JM, Trigo M, Rodríguez-Félix F, Aubourg SP, Barros-Velázquez J Antioxidants (Basel) 21-Feb-2023
PMCID:PMC10044973
doi:10.3390/antiox12030544
PMID:36978792
Physiological and life history changes associated with seasonal adaptation in the cactophilic Drosophila mojavensis Shaible TM, Matzkin LM Biol Open 26-Oct-2022
PMCID:PMC9637388
doi:10.1242/bio.059610
PMID:36285699
Deciphering the genetic and functional diversity of cultivable bacteria from chasmophytic pigweed (Chenopodium album) from Tsomoriri, Ladakh, India Das S, Verma S, Choudhary P, Singh R, Saxena AK 3 Biotech 23-Aug-2022
PMCID:PMC9399335
doi:10.1007/s13205-022-03278-0
PMID:36032512
Ortholog genes from cactophilic Drosophila provide insight into human adaptation to hallucinogenic cacti Padró J, De Panis DN, Luisi P, Dopazo H, Szajnman S, Hasson E, Soto IM Sci Rep 01-Aug-2022
PMCID:PMC9343604
doi:10.1038/s41598-022-17118-x
PMID:35915153
Effectiveness of Two Universal Angiosperm Probe Sets Tested In Silico for Caryophyllids Taxa with Emphasis on Cacti Species Chincoya DA, Solórzano S Genes (Basel) 24-Mar-2022
PMCID:PMC9032312
doi:10.3390/genes13040570
PMID:35456376
Evolutionary Genetics of Cacti: Research Biases, Advances and Prospects Franco FF, Amaral DT, Bonatelli IA, Romeiro-Brito M, Telhe MC, Moraes EM Genes (Basel) 01-Mar-2022
PMCID:PMC8952820
doi:10.3390/genes13030452
PMID:35328006
Acuity and summation strategies differ in vinegar and desert fruit flies Currea JP, Frazer R, Wasserman SM, Theobald J iScience 16-Dec-2021
PMCID:PMC8741510
doi:10.1016/j.isci.2021.103637
PMID:35028530

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 / Harmala alkaloids
1-Methoxymethyl-Beta-Carboline 5382686 Click to see COCC1=NC=CC2=C1NC3=CC=CC=C23 212.25 unknown via CMAUP database
3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid 5375436 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 240.26 unknown via CMAUP database
7-Methoxy-Beta-Carboline-1-Propionic Acid 12082492 Click to see 270.28 unknown via CMAUP database
Methyl 9H-pyrido(3,4-b)indole-1-carboxylate 597266 Click to see 226.23 unknown via CMAUP database
n-Pentyl beta-carboline-1-propionate 11404122 Click to see CCCCCOC(=O)CCC1=NC=CC2=C1NC3=CC=CC=C23 310.40 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Hydroxy-9-medroxycanthin-6-one 11448499 Click to see 266.25 unknown via CMAUP database
1-Hydroxycanthin-6-one 86014459 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3O 236.22 unknown via CMAUP database
12-Hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 70649326 Click to see 266.25 unknown via CMAUP database
13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 637482 Click to see C1=CC2=C(C=C1OC3C(C(C(C(O3)CO)O)O)O)N4C(=O)C=CC5=NC=CC2=C54 398.40 unknown via CMAUP database
13-Methoxy-6-methyl-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-4,7,9(16),10(15),11,13-hexaene-2,3-dione 10912909 Click to see CN1C=CC2=C3C1=CC(=O)C(=O)N3C4=C2C=CC(=C4)OC 280.28 unknown via CMAUP database
3-(Hydroxymethyl)-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 86249531 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C(=CC4=NC=C3)CO 250.25 unknown via CMAUP database
3,13-Dimethoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 86176124 Click to see 280.28 unknown via CMAUP database
4,5-Dihydrocanthin-6-one 76316632 Click to see 222.24 unknown via CMAUP database
4,5-Dimethoxycanthin-6-One 638215 Click to see 280.28 unknown via CMAUP database
5-Hydroxymethyl-9-methoxycanthin-6-one 11300467 Click to see 280.28 unknown via CMAUP database
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
6H-Indolo(3,2,1-de)(1,5)naphthyridin-6-one, 10-methoxy- 158928 Click to see COC1=CC2=C(C=C1)N3C(=O)C=CC4=NC=CC2=C43 250.25 unknown via CMAUP database
8-Hydroxy-9-methoxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one 85654132 Click to see COC1=C(C2=C(C=C1)C3=C4N2C(=O)C=CC4=NC=C3)O 266.25 unknown via CMAUP database
9-Methoxy-6H-indolo(3,2,1-de)(1,5)naphthyridin-6-one 9881423 Click to see 250.25 unknown via CMAUP database
9-Methoxycanthin-6-one-N-oxide 44593495 Click to see 266.25 unknown via CMAUP database
9,10-Dimethoxycanthin-6-one 10446368 Click to see COC1=C(C=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3)OC 280.28 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine L 5324104 Click to see 250.25 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
p-Hydroxybenzoate 54675830 Click to see 137.11 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate 54694262 Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O 197.16 unknown via CMAUP database
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
6,6'-Dihydroxy-(1,1'-biphenyl)-3,3'-dicarboxylic acid 76328834 Click to see 274.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
(1R,2R)-1-[4-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]-3-methoxyphenyl]propane-1,2,3-triol 101225308 Click to see 376.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)- 11063784 Click to see 214.21 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
4-[[(3R,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol 15560085 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Laurycolactone A 46878902 Click to see 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1alpha,4abeta,10aalpha)]- 1201531 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Pedunculoside 14286954 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1R,2S,3S,7R,9R,12R,13R,14S,15R,16R,17S)-3,7,12,13,15,16-hexahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione 118708398 Click to see 412.40 unknown via CMAUP database
(1R,2S,3S,7S,8R,9S,12R,13R,14S,15R,16R,17S)-3,8,12,13,15,16-hexahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione 44614657 Click to see CC1C(C(C2C3(C(C(C4C2(C1(C(C(=O)O4)O)O)C)O)C(=CC(=O)C3O)C)C)O)O 412.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,13S,14R,15R,17S)-3,15-dihydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11,16-trione 76332506 Click to see 362.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,13S,14R,15S,17S)-3,15-dihydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11,16-trione 10992082 Click to see CC1C2CC(=O)OC3C2(C(C(=O)C1O)C4(C(C3)C(=CC(=O)C4O)C)C)C 362.40 unknown via CMAUP database
(1R,4R,5R,6S,7R,8R,11R,13S,16S,17S,18S,19R)-4,5,7,8,16,17-hexahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-9-one 101637224 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)O)O)CO2)C(=CC(C4O)O)C)C)O)O 412.40 unknown via CMAUP database
(1R,4R,5R,6S,7R,8R,11R,13S,17S,18S,19R)-4,5,7,8,17-pentahydroxy-14,18-dimethylspiro[3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-6,2'-oxirane]-9,16-dione 13936702 Click to see 424.40 unknown via CMAUP database
(1R)-1,3abeta,11beta-Trihydroxy-2alpha,4beta-diacetoxy-3alpha,8,11abeta-trimethyl-1beta,11cbeta-(epoxymethano)-1,2,3,3a,4,5,6abeta,7aalpha,10,11,11a,11balpha,11c-tridecahydro-6-oxa-7H-benzo[de]anthracene-5,10-dione 44614656 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)OC(=O)C)O)CO2)C(=CC(=O)C4O)C)C)O)OC(=O)C 494.50 unknown via CMAUP database
(1S,2R,6R,9R,10S,11R,12R,15R)-11-hydroxy-2,6,9,15-tetramethyl-13-oxatetracyclo[10.2.1.02,10.05,9]pentadec-4-ene-3,8,14-trione 11109942 Click to see CC1CC(=O)C2(C1=CC(=O)C3(C2C(C4C(C3C(=O)O4)C)O)C)C 318.40 unknown via CMAUP database
(1S,2R,9R,10R,11R,12R,15R)-11-hydroxy-2,6,9,15-tetramethyl-13-oxatetracyclo[10.2.1.02,10.05,9]pentadeca-4,6-diene-3,8,14-trione 52325751 Click to see 316.30 unknown via CMAUP database
[(1R,2S,3S,7S,9R,12R,13R,14S,15R,16R,17S)-3,13,15,16-tetrahydroxy-2,6,14,17-tetramethyl-4,11-dioxo-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-en-12-yl] acetate 100931036 Click to see 438.50 unknown via CMAUP database
13-alpha-(21)-Epoxyeurycomanone 13936703 Click to see 424.40 unknown via CMAUP database
13,21-Dihydroeurycomanone 13936707 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)O)O)CO2)C(=CC(=O)C4O)C)C)O)O 410.40 unknown via CMAUP database
14,15beta-Dihydroxyklaineanone 10883790 Click to see 396.40 unknown via CMAUP database
15beta-Hydroxyklaineanone 21677660 Click to see CC1C2C(C(=O)OC3C2(C(C(C1O)O)C4(C(C3)C(=CC(=O)C4O)C)C)C)O 380.40 unknown via CMAUP database
Eurycomanol 14396865 Click to see 410.40 unknown via CMAUP database
Eurycomanol 2-O-|A-D-glucopyranoside 101637225 Click to see 572.60 unknown via CMAUP database
Eurycomanone 13936691 Click to see 408.40 unknown via CMAUP database
Laurycolactone B 46878903 Click to see 316.30 unknown via CMAUP database
methyl (1S,2R,8R,9R,10R,11R,12R,15R)-8,11-dihydroxy-2,6,9,15-tetramethyl-3,14-dioxo-13-oxatetracyclo[10.2.1.02,10.05,9]pentadeca-4,6-diene-8-carboxylate 15884867 Click to see CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(C=C4C)(C(=O)OC)O)C)C)O 376.40 unknown via CMAUP database
Pasakbumin D 14589373 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(CO)O)O)(OC5)O)C)O 442.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1R,2R,3R,6R,7S,8R,9S,12S,13R,14R,15R,16R)-3,6,8,14,15-pentahydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-4-en-11-one 101499157 Click to see 368.40 unknown via CMAUP database
(1R,2S,3S,7S,8R,9S,12S,13R,14R,15R,16R)-3,8,14,15-tetrahydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-5-ene-4,11-dione 14589371 Click to see 366.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,12S,13R,14R,15R,16R)-3,14,15-trihydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-5-ene-4,11-dione 102377055 Click to see 350.40 unknown via CMAUP database
Eurycolactone F 10938426 Click to see 408.40 unknown via CMAUP database
Eurycomaoside 11283976 Click to see 530.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(E,6R)-6-[(2R,5S)-5-[(2R,5R)-5-[(2S,5R)-5-[(E,2R)-6-hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl]-2-methyloxolan-2-yl]oxolan-2-yl]-5-methyloxolan-2-yl]-2-methylhept-3-ene-2,6-diol 44585468 Click to see 540.70 unknown via CMAUP database
(E,6S)-6-[(2R,5S)-5-[(2R,5R)-5-[(2S,5R)-5-[(E,2S)-6-hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl]-2-methyloxolan-2-yl]oxolan-2-yl]-5-methyloxolan-2-yl]-2-methylhept-3-ene-2,6-diol 10896840 Click to see 540.70 unknown via CMAUP database
14-Deacetyl eurylene 11786187 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C(CCC(C2(CCC(O2)C(C)(CCC=C(C)C)O)C)OC(=O)C)O)O)C 552.80 unknown via CMAUP database
Eurylene 179304 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C(CCC(C2(CCC(O2)C(C)(CCC=C(C)C)O)C)OC(=O)C)OC(=O)C)O)C 594.80 unknown via CMAUP database
Teurilene 185415 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C2CCC(O2)C3(CCC(O3)C(C)(CCC=C(C)C)O)C)O)C 492.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,2R,10R,11R,12R,13R,16R)-12-hydroxy-2,6,10,16-tetramethyl-9,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadeca-4,6-diene-3,8,15-trione 10336848 Click to see 332.30 unknown via CMAUP database
(1S,2R,3R,8S,9S,10R,11S,12R,13R,16R)-3,8,9,12-tetrahydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-5-ene-4,15-dione 44612898 Click to see 366.40 unknown via CMAUP database
(1S,2R,4R,5S,8S,9S,10R,11R,12R,13R,16R)-4,8,9,12-tetrahydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,15-dione 44612900 Click to see 366.40 unknown via CMAUP database
(1S,2R,6R,9S,10R,11R,12R,13R,16R)-9,12-dihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-4-ene-3,8,15-trione 76314382 Click to see CC1CC(=O)C(C2(C1=CC(=O)C3(C2C(C4C(C3C(=O)O4)C)O)C)C)O 348.40 unknown via CMAUP database
5,6-Dehydroeurycomalactone 15173195 Click to see 346.40 unknown via CMAUP database
6alpha-Hydroxyeurycomalactone 10067332 Click to see 364.40 unknown via CMAUP database
7alpha-Hydroxyeurycomalactone 46878901 Click to see CC1C2C(C3C4(C(CC(C3(C1C(=O)O2)C)O)C(=CC(=O)C4O)C)C)O 350.40 unknown via CMAUP database
Eurycolactone E 636592 Click to see 350.40 unknown via CMAUP database
Eurycomalactone 441793 Click to see CC1C2C(C3C4(C(CC(=O)C3(C1C(=O)O2)C)C(=CC(=O)C4O)C)C)O 348.40 unknown via CMAUP database
Eurycomalide B 46878940 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Npc122922 76332505 Click to see 556.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one 92446370 Click to see COC1=C(C=CC(=C1)C(=O)C(CO)O)O 212.20 unknown via CMAUP database
2-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)ethanone 87530 Click to see 182.17 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Eurycomalin A 102004690 Click to see 406.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1R,5S,6S,7R,8R,11R,13S,17S,18S,19R)-5,7,8,17-tetrahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.05,19.013,18]nonadec-14-ene-4,9,16-trione 78210165 Click to see 408.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid 938 Click to see 123.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3,5,6,7,8,3',4'-Heptamethoxyflavone 150893 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(1S,2S)-1,2-bis(3-methoxy-4-oxidanyl-phenyl)propane-1,3-diol 12468617 Click to see 320.30 unknown via CMAUP database

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