Pachycereus pringlei - Unknown
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Internal ID UUID643ff839e7d46273574241
Scientific name Pachycereus pringlei
Authority (S.Watson) Britton & Rose
First published in in Contr. U.S. Natl. Herb. 12: 422. 1909.

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Synonyms Top

Scientific name Authority First published in
Pilocereus pringlei (S.Watson) F.A.C.Weber Dict. Hort. 2: 966. 1898.
Pachycereus calvus (Engelm. ex J.M.Coult.) Britton & Rose in Contr. U.S. Natl. Herb. 12: 420. 1909.
Pachycereus pringlei f. cristatus P.V.Heath in Calyx 2: 107. 1992.
Pachycereus pringlei f. constrictus P.V.Heath in Calyx 2: 107. 1992.
Pachycereus pringlei f. calvus (Engelm. ex J.M.Coult.) P.V.Heath in Calyx 2: 107. 1992.
Pachycereus titan (Engelm. ex J.M.Coult.) Britton & Rose in Contr. U.S. Natl. Herb. 12: 422. 1909.
Cereus calvus Engelm. ex J.M.Coult. in Contr. U.S. Natl. Herb. 3(7): 409. 1896.
Cereus pringlei S.Watson in Proc. Amer. Acad. Arts 20: 368. 1885.
Cereus pringlei var. calvus M.E.Jones in Contr. W. Bot. 18: 60. 1933.
Cereus titan Engelm. ex J.M.Coult. in Contr. U.S. Natl. Herb. 3: 409. 1896.

Common names Top

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Language Common/alternative name
English elephant cactus
English mexican giant cardon
Spanish cardon
Spanish sagueso
Spanish sahuaso
Bulgarian кардон
German sagueso
German sahuaso
Basque kardoi erraldoi
Persian کاکتوس خرطومی
guc yosuu
Hindi पैकिसेरियस प्रिंगलेइ
Japanese ブリンチュウ
Punjab ہاتھی تھور
Swedish krusbärspelarkaktus
Tamil பாக்கிசீரியசு பிரிங்கிலீ
Chinese 武伦柱
Chinese 武倫柱果

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000398337
Tropicos 50145266
KEW urn:lsid:ipni.org:names:179828-2
The Plant List kew-2414408
Open Tree Of Life 141048
NCBI Taxonomy 154437
IUCN Red List 151996
IPNI 179828-2
iNaturalist 199206
GBIF 7282285
Freebase /m/025s0kt
EOL 5181979
USDA GRIN 417540
Wikipedia Pachycereus_pringlei
CMAUP NPO2505

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_002740445.1 Ppri_v1.3 Scaffold The University of Arizona 2017-10-31 20.0x 600.49 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
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
Assembly and Function of Seed Endophytes in Response to Environmental Stress Wang YL, Zhang HB J Microbiol Biotechnol 30-May-2023
PMCID:PMC10580892
doi:10.4014/jmb.2303.03004
PMID:37311706
Physiology, genomics, and evolutionary aspects of desert plants Mohanta TK, Mohanta YK, Kaushik P, Kumar J J Adv Res 07-May-2023
PMCID:PMC10982872
doi:10.1016/j.jare.2023.04.019
PMID:37160225
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
Trioecy is maintained as a time-stable mating system in the pink sea urchin Toxopneustes roseus from the Mexican Pacific Díaz-Martínez JP, Mejía-Gutiérrez LM, Islas-Villanueva V, Benítez-Villalobos F Sci Rep 10-Dec-2022
PMCID:PMC9741619
doi:10.1038/s41598-022-26059-4
PMID:36496463
Marine subsidies produce cactus forests on desert islands Wilder BT, Becker AT, Dettman DL Sci Rep 12-Oct-2022
PMCID:PMC9556768
doi:10.1038/s41598-022-21133-3
PMID:36224217
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
Transcriptional analysis of Ceratopteris richardii young sporophyte reveals conservation of stem cell factors in the root apical meristem Aragón-Raygoza A, Herrera-Estrella L, Cruz-Ramírez A Front Plant Sci 11-Aug-2022
PMCID:PMC9413220
doi:10.3389/fpls.2022.924660
PMID:36035690
Coalescent‐based species delimitation in North American pinyon pines using low‐copy nuclear genes and plastomes Montes J, Peláez P, Moreno‐Letelier A, Gernandt DS Am J Bot 08-May-2022
PMCID:PMC9321694
doi:10.1002/ajb2.1847
PMID:35526278
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
Unraveling the development behind unisexual flowers in Cylindropuntia wolfii (Cactaceae) Ramadoss N, Orduño-Baez A, Portillo C, Steele S, Rebman J, Flores-Rentería L BMC Plant Biol 02-Mar-2022
PMCID:PMC8889693
doi:10.1186/s12870-022-03431-0
PMID:35236303
De Novo Transcriptome of Mammillaria bombycina (Cactaceae) under In Vitro Conditions and Identification of Glyoxalase Genes Enríquez-González C, Garcidueñas-Piña C, Castellanos-Hernández OA, Enríquez-Aranda S, Loera-Muro A, Ocampo G, Pérez-Molphe Balch E, Morales-Domínguez JF Plants (Basel) 31-Jan-2022
PMCID:PMC8838482
doi:10.3390/plants11030399
PMID:35161380

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 COC1=CC2=C(C=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 270.28 unknown via CMAUP database
methyl 9H-pyrido[3,4-b]indole-1-carboxylate 597266 Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 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 COC1=CC2=C(C=C1)C3=C4N2C(=O)C=CC4=NC=C3O 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
1,6-Diazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16),10,12,14-hexaen-2-one 76316632 Click to see C1CC(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4 222.24 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 COC1=C(C=C2C3=C4C(=NC=C3)C=CC(=O)N4C2=C1)O 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
2,9-Dimethoxy-1H-4,10b-diazafluoranthene-1-one 86176124 Click to see COC1=CC2=C(C=C1)C3=C4N2C(=O)C(=CC4=NC=C3)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
5-Hydroxymethyl-9-methoxycanthin-6-one 11300467 Click to see COC1=CC2=C(C=C1)C3=C4N2C(=O)C(=CC4=NC=C3)CO 280.28 unknown via CMAUP database
5-Methoxycanthin-6-one 259218 Click to see COC1=CC2=NC=CC3=C2N(C1=O)C4=CC=CC=C34 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-Methoxycanthin-6-one 9881423 Click to see COC1=CC2=C(C=C1)C3=C4N2C(=O)C=CC4=NC=C3 250.25 unknown via CMAUP database
9-Methoxycanthin-6-one N-oxide 44593495 Click to see COC1=CC2=C(C=C1)C3=C4N2C(=O)C=CC4=[N+](C=C3)[O-] 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 C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=[N+](C=C3)[O-] 236.22 unknown via CMAUP database
Methyl nigakinone 638215 Click to see COC1=C(C(=O)N2C3=CC=CC=C3C4=C2C1=NC=C4)OC 280.28 unknown via CMAUP database
Picrasidine L 5324104 Click to see CN1C=CC2=C3C1=CC(=O)C(=O)N3C4=CC=CC=C24 250.25 unknown via CMAUP database
Picrasidine Q 54714262 Click to see COC1=C(C2=NC=CC3=C2N(C1=O)C4=CC=CC=C34)O 266.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
4-Hydroxybenzoate 54675830 Click to see C1=CC(=CC=C1C(=O)O)[O-] 137.11 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 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 COC1=CC(=CC(=C1O)OC)C(=O)O 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 C1=CC(=C(C=C1C(=O)O)C2=C(C=CC(=C2)C(=O)O)O)O 274.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
(2R,3R)-3-[3-Methoxy-4-[2-methoxy-4-(3-hydroxy-1-propenyl)phenoxy]phenyl]propane-1,2,3-triol 101225308 Click to see COC1=C(C=CC(=C1)C=CCO)OC2=C(C=C(C=C2)C(C(CO)O)O)OC 376.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
threo-Guaiacylglycerol 11063784 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 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 COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Laurycolactone A 46878902 Click to see CC1C2C(C3C4(C(CC(=O)C3(C1C(=O)O2)C)C(=CC4=O)C)C)O 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 CC1C(C(C2C3(C1(C(C(=O)OC3CC4(C2(C(C(=O)C=C4C)O)C)O)O)O)C)O)O 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 CC1C2CC(=O)OC3C2(C(C(=O)C1O)C4(C(C3)C(=CC(=O)C4O)C)C)C 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)-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 CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(=O)C=C4C)C)C)O 316.30 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
13alpha(21)-Epoxyeurycomanone 13936702 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C6(C4(C(C(=O)O3)O)O)CO6)O)(OC5)O)C)O 424.40 unknown via CMAUP database
14,15beta-Dihydroxyklaineanone 10883790 Click to see CC1C(C(C2C3(C(CC4C2(C1(C(C(=O)O4)O)O)C)C(=CC(=O)C3O)C)C)O)O 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
15beta-O-Acetyl-14-hydroxyklaineanone 100931036 Click to see CC1C(C(C2C3(C(CC4C2(C1(C(C(=O)O4)OC(=O)C)O)C)C(=CC(=O)C3O)C)C)O)O 438.50 unknown via CMAUP database
Eurycomanol 14396865 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(=C)C4(C(C(=O)O3)O)O)O)(OC5)O)C)O)O 410.40 unknown via CMAUP database
Eurycomanol 2-O-beta-D-glucopyranoside 101637225 Click to see CC1=CC(C(C2(C1CC3C45C2C(C(C(=C)C4(C(C(=O)O3)O)O)O)(OC5)O)C)O)OC6C(C(C(C(O6)CO)O)O)O 572.60 unknown via CMAUP database
Eurycomanone 13936691 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(=C)C4(C(C(=O)O3)O)O)O)(OC5)O)C)O 408.40 unknown via CMAUP database
Laurycolactone B 46878903 Click to see CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(=O)C=C4C)C)C)O 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 B 13936703 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C6(C4(C(C(=O)O3)O)O)CO6)O)(OC5)O)C)O 424.40 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 CC1C(C(C2C3(C(C=CC(C3C(C4C2(C1C(=O)O4)C)O)(C)O)O)C)O)O 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 CC1C(C(C2C3(C1C(=O)OC3C(C4C2(C(C(=O)C=C4C)O)C)O)C)O)O 366.40 unknown via CMAUP database
6-Dehydrolongilactone 102377055 Click to see CC1C(C(C2C3(C(CC4C2(C1C(=O)O4)C)C(=CC(=O)C3O)C)C)O)O 350.40 unknown via CMAUP database
Eurycolactone F 10938426 Click to see CC1C(C(C2C3(C1C(=O)OC3C(C4C2(C(C(=O)C=C4C)O)C)OC(=O)C)C)O)O 408.40 unknown via CMAUP database
Eurycomaoside 11283976 Click to see CC1C(C(C2C3(C(C=CC(C3C(C4C2(C1C(=O)O4)C)O)(C)O)OC5C(C(C(C(O5)CO)O)O)O)C)O)O 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 CC1(CCC(O1)C(C)(CC=CC(C)(C)O)O)C2CCC(O2)C3(CCC(O3)C(C)(CC=CC(C)(C)OO)O)C 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 CC1(CCC(O1)C(C)(CC=CC(C)(C)O)O)C2CCC(O2)C3(CCC(O3)C(C)(CC=CC(C)(C)OO)O)C 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 CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(OC(=O)C=C4C)C)C)O 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 CC1C2C(C3C(C1C(=O)O2)(C(C(=O)C4=C(CC(C(C34C)O)O)C)O)C)O 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 CC1C2C(C3C4(C(C(C(=O)C3(C1C(=O)O2)C)O)C(=CC(C4O)O)C)C)O 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 CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(C(=O)C=C4C)O)C)C)O 346.40 unknown via CMAUP database
6alpha-Hydroxyeurycomalactone 10067332 Click to see CC1C2C(C3C4(C(C(C(=O)C3(C1C(=O)O2)C)O)C(=CC(=O)C4O)C)C)O 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 CC1C2C(C3C4(C(CC(=O)C3(C1C(=O)O2)C)C(=CC(C4O)O)C)C)O 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 CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(C(C=C4C)O)O)C)C)O 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 C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 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
Isoaloeresin D 76332505 Click to see CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(C)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC=C(C=C4)O)OC 556.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 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 COC1=C(C=CC(=C1)C(=O)CO)O 182.17 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Eurycomalin A 102004690 Click to see CC(=C)C1CC2=C(O1)C(=CC(=C2)C(=O)O)C3=CC(=CC4=C3OC(C4)C(=C)C)C(=O)O 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 CC1C2(C(C(=O)OC3C24COC(=O)C1(C4C5(C(C3)C(=CC(=O)C5O)C)C)O)O)O 408.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid 938 Click to see C1=CC(=CN=C1)C(=O)O 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 COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3,5,6,7,8,3',4'-Heptamethphoxyflavone 150893 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC 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 COC1=C(C=CC(=C1)C(CO)C(C2=CC(=C(C=C2)O)OC)O)O 320.30 unknown via CMAUP database

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