Details Top

Internal ID UUID643fd62b6667f908446171
Scientific name Gleditsia triacanthos
Authority L.
First published in Sp. Pl.: 1056 (1753)

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.

Among Native peoples of the United States, the bark of Gleditsia triacanthos (honey locust) has been recorded in several different preparations. The Cherokee of the southeastern woodlands prepared a mild tea by steeping shredded bark in hot water and drank it as an expectorant for coughs and colds (Moerman, 1998). The Lenape of the mid‑Atlantic region made a maceration of the same bark, soaking the material in cool water for several hours and then applying the liquid as a wash for cuts, sores and other skin irritations (Moerman, 1998). The Iroquois of the northeastern woodlands boiled the bark in water for fifteen minutes, producing a decoction that was taken internally for sore throats and mild gastrointestinal upset (Moerman, 1998). The Cherokee also crushed fresh bark into a moist poultice and applied it directly to wounds to aid healing (Moerman, 1998).

A simple preparation that follows these historic methods is a bark decoction that can be used as a gentle tea. Measure 10 g of dried, chopped bark, add it to 500 mL of water, bring the water to a gentle boil, then simmer for 15–20 minutes. Strain the liquid and let it cool to a drinking temperature. The finished decoction may be taken warm, up to three cups per day, and can be sweetened if desired. Because the bark is rich in tannins, it should not be used by pregnant or nursing women, and people on blood‑thinning medication should consult a health professional before regular use. Excessive intake may also reduce iron absorption, so it is best consumed with food.

Phytochemical analyses of Gleditsia triacanthos bark consistently report high levels of condensed tannins (proanthocyanidins), flavonoids such as quercetin and kaempferol, phenolic acids like caffeic and gallic acid, and triterpenoid saponins. These compounds have documented astringent and antioxidant activity and align with the traditional uses of the bark as a tea, decoction, maceration and poultice.

Today, honey‑locust bark appears in limited commercial herbal supplements and teas, and recent pharmacological work (Li et al., 2021; Zhang et al., 2020) continues to examine its antioxidant and anti‑inflammatory properties, confirming the enduring relevance of this native tree in both traditional and modern health practices.

General Uses Top

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Wood and fiber:
The wood is moderately heavy and hard (ovendry density typically ~0.68–0.73 g/cm³), ring-porous, and yellow-brown with distinct, light-colored rays. It is noted for good strength and durability and is used in heavy-duty applications such as posts, ties, poles, and tool handles, as well as for furniture and turned articles. Natural decay resistance is attributed to extractives.

Industrial and craft applications:
Thorns harvested from thorned varieties have been reported historically as darning aids, though such use is minor and non-commercial.

Properties relevant to use:
Ring-porous ring structure and above-average density support structural durability; the color and ray figure contribute to appearance-grade uses.

Sustainability and sourcing:
The species is widely cultivated in North America and commonly sourced from urban-tree removals as well as managed stands for specialty lumber.

Synonyms Top

Scientific name Authority First published in
Acacia villaregalis McVaugh Fl. Novo-Galiciana5: 141 (1987)
Caesalpiniodes triacanthum (L.) Kuntze Revis. Gen. Pl.1: 167 (1891)
Melilobus heterophyla Raf. Sylva Tellur.: 121 (1838)
Gleditsia bujotii Neumann Rev. Hort. (Paris), sér. 2, 4: 205 (1846)
Gleditsia laevis G.Don J.C.Loudon, Hort. Brit.: 413 (1830)
Gleditsia brachycarpa (Michx.) Pursh Fl. Amer. Sept. (Pursh) 1: 221. 1813 [Dec 1813]
Acacia laevis hort. ex Steud. Nomencl. Bot. [Steudel], ed. 2. 1: 6. 1840
Gleditsia heterophylla Raf. Fl. Ludov.: 99 (1817)
Gleditsia triacanthus Mill.
Gleditsia triacanthos var. polysperma Aiton Hort. Kew.3: 444 (1789)
Gleditsia triacanthos var. horrida Aiton Hort. Kew.3: 444 (1789)
Gleditsia triacanthos var. laevis Koch Hort. Dendrol.: 226 (1853)
Gleditsia meliloba Walter Fl. Carol.: 254 (1788)
Gleditsia polysperma (Aiton) Stokes Bot. Mat. Med.1: 228 (1812)
Gleditsia triacanthos var. inermis Willd.
Gleditsia spinosa Marshall Arbust. Amer.: 94 (1785)
Gleditsia sinensis var. nana Loudon Arbor. Frutic. Brit.2: 654 (1838)
Gleditsia micracantha Steud.
Gleditsia triacanthos var. nana Henry H.J.Elwes & A.Henry, Trees Great Britain6: 1518 (1912)
Gleditsia latisilique Steud.
Gleditsia ferox var. nana Rehder L.H.Bailey, Cycl. Amer. Hort.2: 650 (1900)
Gleditsia inermis var. elegantissima Grosdem. Rev. Hort. (Paris)77: 512 (1905)
Acacia triacanthos Gron.
Acacia americana Stokes
Acacia inermis Steud.
Gleditsia horrida Salisb. Prodr. Stirp. Chap. Allerton: 323 (1796)
Gleditsia flava K.Koch Dendrologie1: 9 (1869)
Gleditsia sinensis var. nana Asch. & Graebn.
Gleditsia triacanthos var. brachycarpos Michx. Fl. Bor.-Amer.2: 257 (1803)
Gleditsia triacanthos var. bujotii (Neumann) Rehder L.H.Bailey, Cycl. Amer. Hort.2: 650 (1900)
Gleditsia triacanthos var. macrocarpos Michx. Fl. Bor.-Amer.2: 257 (1803)
Gleditsia latifolia hort. ex Lavallée Énum. Arbres 66, nomen. 1877
Gleditsia ferox Desf. Hist. Arbr. France2: 247 (1809)
Gleditschia triacanthos L.
Gleditsia latisiliqua Lodd. ex G.Don J.C.Loudon, Hort. Brit.: 414 (1830)
Gleditsia triacanthos var. inermis Castigl. Viagg. Stati Uniti2: 249 (1790)
Caesalpiniodes heterophylla (Raf.) Kuntze Revis. Gen. Pl.1: 167 (1891)
Gleditsia triacanthos f. elegantissima Rehder Bibliogr. Cult. Trees: 352 (1949)
Gleditsia triacanthos f. pendula Rehder Bibliogr. Cult. Trees: 352 (1949)
Gleditsia micracantha Loddiges ex Steudel Nom. Bot. 688 1840
Gleditsia triacanthos f. inermis Zabel L.Beissner, E.Schelle & H.Zabel, Handb. Laubholzben.: 255 (1903)
Gleditsia inermis var. elegantissima Grosd. Rev. Hort., n. s., 5: 512, f. 199 1905
Gleditsia triacanthos f. nana Rehder Bibliogr. Cult. Trees: 352 (1949)
Vachellia villaregalis (McVaugh) Seigler & Ebinger Phytologia87: 169 (2005 publ. 2006)
Gleditsia triacanthos f. brachycarpos (Michx.) C.K.Schneid. Ill. Handb. Laubholzk.2: 12 (1907)
Gleditsia brachycarpos (Michx.) Pursh Fl. Amer. Sept.1: 211 (1813)
Gleditsia excelsa-pendula de Vos Handb. Prakt. Kennis Bomen, ed. 2: 81 (1887)
Gleditsia triacanthos var. pendula Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 184 (1907)
Gleditsia triacanthos var. ferox (Desf.) Asch. & Graebn. P.F.A.Ascherson & K.O.R.Graebner, Syn. Mitteleur. Fl.2(2): 184 (1907)
Gleditsia micracantha de Vos Handb. Prakt. Kennis Bomen, ed. 2: 81 (1887)
Gleditsia elegans Salisb. Prodr. Stirp. Chap. Allerton : 323 (1796)
Gleditsia bujotii var. pendula Rehder Man. Cult. Trees , ed. 2: 486 (1900)
Gleditsia triacanthos var. inermis (L.) Castigl.
Gleditsia pendula Van Geert Nursery Cat. (Auguste Van Geert)43: 66 (1857)
Gleditsia mimosifolia Lodd. ex Talou Hort. Franç. 1859: 156 (1859)
Gleditsia mimosifolia var. pendula Talou Hort. Franç. 1859: 156 (1859)
Gleditsia bujotii unranked pendula Van Geert Nursery Cat. (Auguste Van Geert) 43: 66 (1857)

Common names Top

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Language Common/alternative name
English honey shuck
English honeylocust
English thornless honey locust
English thorny honeylocust
English thorny locust
English honey locust
Spanish acacia de tres espinas
Arabic غلاديشية ثلاثية الأشواك
Azerbaijani Üçtikan şeytanağacı
Belarusian гледычыя звычайная
Bulgarian гледичия
Catalan acàcia de tres punxes
Czech dřezovec trojtrnný
Danish almindelig tretorn
German falscher christusdorn
German lederhülsenbaum
German amerikanische gleditschie
Esperanto kristodorna glediĉio
Estonian kolmeastlaline glediitsia
Basque akazia hiruarantza
Persian لیلکی آمریکایی
Finnish kolmioka
French févier d'amérique
French févier épineux
French févier d’amérique
French fevier d'amerique
French févier
Croatian gledičija
Upper Sorbian ameriska gledičija
Upper Sorbian ameriski trukownik
Upper Sorbian ameriska glidičija
Hungarian tövises lepényfa
Armenian գլեդիչա
Italian spino di giuda
Japanese アメリカサイカチ
kbd Банэжыг
Kazakh Үштікенді қарамала
Lithuanian tridyglė gledičija
Macedonian тритрнест гледич
Macedonian гледич
Macedonian трновец
Norwegian Bokmål korstorn
Dutch valse christusdoorn
nv naaztání
Polish glediczja trójcierniowa
Polish glediczja trócierniowa
Polish iglicznia trójcierniowa
Romanian glădiță
Russian Гледичия трёхколючковая
Russian Гледичия трехколючковая
Slovak gledíčia trojtŕňová
Slovenian divji rožič
Slovenian trnata gledičevka
Serbian Гледичијa
Ukrainian Колюча гледичія
Ukrainian Гледичія колюча
Vietnamese bồ kết ba gai
Chinese 美國皂莢
Chinese 美国皂角
Chinese 新疆皂荚
Chinese 三刺皂荚
Chinese 美国皂荚
Chinese 皂荚子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000168133
UNII D8MUI5CX2Z
Florida Plant Atlas 3555
Flora of Alabama 1963
Cornell Woody Plants 103
Canadensys 5731
USDA Plants GLTR
UConn 194
Tropicos 13001001
INPN 100330
Flora of Italy 2242
KEW urn:lsid:ipni.org:names:110723-2
The Plant List ild-1446
Plantarium 17622
Missouri Botanical Garden 280280
Open Tree Of Life 677313
Observations.org 105100
NCBI Taxonomy 54874
NBN Atlas NBNSYS0500000390
Nature Serve 2.145448
IUCN Red List 62026061
IPNI 496619-1
iNaturalist 54797
GBIF 2959443
Freebase /m/01jnpd
WisFlora 3714
FEIS plants/tree/gletri
EPPO GLITR
EOL 416265
Elurikkus 4920
Calflora (Californian flora) 8571
USDA GRIN 17641
Wikipedia Honey_locust
CMAUP NPO16101

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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Grain Products: Traditional and Innovative Technologies Gómez M, Pereira E Foods 08-Apr-2024
PMCID:PMC11011762
doi:10.3390/foods13071126
PMID:38611430
CuticleTrace: A toolkit for capturing cell outlines from leaf cuticle with implications for paleoecology and paleoclimatology Lloyd BA, Barclay RS, Dunn RE, Currano ED, Mohamaad AI, Skersies K, Punyasena SW Appl Plant Sci 02-Feb-2024
PMCID:PMC10873815
doi:10.1002/aps3.11566
PMID:38369978
The Fabaceae in Northeastern Mexico (Subfamily Caesalpinioideae, Mimosoideae Clade, Tribes Mimoseae, Acacieae, and Ingeae) Estrada-Castillón E, Villarreal-Quintanilla JÁ, Cuéllar-Rodríguez G, Encina-Domínguez JA, Martínez-Ávalos JG, Mora-Olivo A, Sánchez-Salas J Plants (Basel) 30-Jan-2024
PMCID:PMC10857220
doi:10.3390/plants13030403
PMID:38337936
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Radio Telemetry and Harmonic Radar Tracking of the Spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae) Siderhurst MS, Murman KM, Kaye KT, Wallace MS, Cooperband MF Insects 30-Dec-2023
PMCID:PMC10816356
doi:10.3390/insects15010017
PMID:38249023
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Effects of Heat Stress on Plant-Nutrient Relations: An Update on Nutrient Uptake, Transport, and Assimilation Mishra S, Spaccarotella K, Gido J, Samanta I, Chowdhary G Int J Mol Sci 27-Oct-2023
PMCID:PMC10649217
doi:10.3390/ijms242115670
PMID:37958654
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Antibacterial activity of medicinal plants on the management of mastitis in dairy cows: A systematic review Kaseke TB, Chikwambi Z, Gomo C, Mashingaidze AB, Murungweni C Vet Med Sci 19-Sep-2023
PMCID:PMC10650345
doi:10.1002/vms3.1268
PMID:37725398
Proline concentrations in seedlings of woody plants change with drought stress duration and are mediated by seed characteristics: a meta-analysis Kijowska-Oberc J, Dylewski Ł, Ratajczak E Sci Rep 13-Sep-2023
PMCID:PMC10500006
doi:10.1038/s41598-023-40694-5
PMID:37704656
Investigating the influence of diet diversity on infection outcomes in a bumble bee (Bombus impatiens) and microsporidian (Nosema bombi) host-pathogen system Martinez A, Calhoun AC, Sadd BM Front Insect Sci 17-Aug-2023
PMCID:PMC10926413
doi:10.3389/finsc.2023.1207058
PMID:38469464

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
N-Methylphenethylamine 11503 Click to see CNCCC1=CC=CC=C1 135.21 unknown https://doi.org/10.2307/4117899
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.2307/4117899
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see 348.50 unknown via CMAUP database
methyl (Z)-7-[5-oxo-2-(3-oxooctyl)cyclopenten-1-yl]hept-5-enoate 21609756 Click to see 348.50 unknown via CMAUP database
Prostaglandin B2 5280881 Click to see 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see 304.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.3109/13880208309070615
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.3109/13880208309070615
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see 458.70 unknown via CMAUP database
Turmerone 14367555 Click to see 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2S,3S,4R,5S,6S)-4-[(2S,3S,4R,5R)-3,5-dihydroxy-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]peroxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162893487 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)OOC8C(C(C(CO8)O)O)O)O)O)C)C(=O)O)C 915.10 unknown https://doi.org/10.1007/BF00565685
[(2S,3S,4R,5S,6S)-5-[(2S,3S,4R,5R)-3,5-dihydroxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]peroxyoxan-2-yl]peroxy-3,4,6-trihydroxyoxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2S,3S,4R,5S,6S)-4-[(2S,3S,4R,5R)-3,5-dihydroxy-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]peroxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162959384 Click to see 1389.40 unknown https://doi.org/10.1007/BF00565685
[5-[3,5-Dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]peroxyoxan-2-yl]peroxy-3,4,6-trihydroxyoxan-2-yl] 10-[4-[3,5-dihydroxy-4-(3,4,5-trihydroxyoxan-2-yl)peroxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162959383 Click to see 1389.40 unknown https://doi.org/10.1007/BF00565685
10-[4-[3,5-Dihydroxy-4-(3,4,5-trihydroxyoxan-2-yl)peroxyoxan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162893486 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)OC7C(C(C(CO7)O)OOC8C(C(C(CO8)O)O)O)O)O)C)C(=O)O)C 915.10 unknown https://doi.org/10.1007/BF00565685
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide B 11995280 Click to see 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see 334.40 unknown via CMAUP database
Crassolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(18|A)-Oleanolic acid 7048528 Click to see 456.70 unknown https://doi.org/10.1007/BF00564381
(4aR,5R,6aS,6aS,6bR,8aS,10S,12aR,14bR)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 131705735 Click to see 472.70 unknown https://doi.org/10.1007/BF00564381
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1007/BF00564381
5,10-Dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3939968 Click to see 472.70 unknown https://doi.org/10.1007/BF00564381
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see 434.70 unknown via CMAUP database
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see 492.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 101007150 Click to see 444.60 unknown via CMAUP database
(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 54586888 Click to see 444.60 unknown via CMAUP database
[(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007149 Click to see 486.70 unknown via CMAUP database
[(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
(3S,8S,9S,10R,11R,13R,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(1R,2R)-2-methyl-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-diol 10599347 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Propylidenecholest-5-en-3 beta-ol 193212 Click to see 426.70 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Oxalic Acid 971 Click to see 90.03 unknown https://doi.org/10.1007/BF00392226
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,6S,7S)-5,12-diacetyloxy-6-(acetyloxymethyl)-8-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 5321999 Click to see 653.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-carboxy-3-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(sulfooxymethyl)oxan-2-yl]oxyphenolate 102296196 Click to see 411.32 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives
3-(3-methylbut-2-en-1-yl)-3H-purin-6-amine 135438588 Click to see 203.24 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
3-(3-methylbut-2-enyl)purin-6-amine 45070 Click to see 203.24 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno(12,13)cyclotetradeca(1,2-b)furan-12(2H)-one 643720 Click to see 316.40 unknown via CMAUP database
(1R,2E,6R,8R,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-trien-17-one 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see 316.40 unknown via CMAUP database
(1S,3R,5R,8E,12E,15R)-3,8,12-trimethyl-16-methylidene-4,18-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 11995175 Click to see 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see 374.50 unknown via CMAUP database
Crassocolide F 11995282 Click to see 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see 316.40 unknown via CMAUP database

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