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

Description Top

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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)

Common names Top

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Language Common/alternative name
English thornless honey locust
English honey locust
English honey shuck
English thorny locust
English thorny honeylocust
English honeylocust
Spanish caesalpiniodes triacanthum
Spanish gleditsia triacanthus
Spanish gleditsia sinensis var nana
Spanish gleditsia micracantha
Spanish gleditsia latisilique
Spanish gleditsia inermis var. elegantissima
Spanish gleditsia inermis var elegantissima
Spanish gleditsia bujotii var pendula
Spanish acacia de tres espinas
Spanish gleditsia spinosa
Spanish acacia laevis
Spanish gleditsia flava
Spanish gleditsia elegans
Spanish acacia inermis
Spanish gleditsia horrida
Spanish acacia triacanthos
Spanish gleditsia dioicuas
Arabic غلاديشية ثلاثية الأشواك
Azerbaijani Üçtikan şeytanağacı
Belarusian гледычыя звычайная
Bulgarian гледичия
Catalan acàcia de tres punxes
Czech dřezovec trojtrnný
Danish almindelig tretorn
German amerikanische gleditschie
German lederhülsenbaum
German falscher christusdorn
Esperanto kristodorna glediĉio
Estonian kolmeastlaline glediitsia
Basque akazia hiruarantza
Persian لیلکی آمریکایی
Finnish kolmioka
French févier d’amérique
French févier épineux
French fevier d'amerique
French févier
French févier d'amérique
Croatian gledičija
Upper Sorbian ameriska gledičija
Upper Sorbian ameriska glidičija
Upper Sorbian ameriski trukownik
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 гледич
Macedonian тритрнест гледич
Norwegian Bokmål korstorn
Dutch valse christusdoorn
nv naaztání
Polish gleditsia triacantha
Polish iglicznia trójcierniowa
Polish glediczja trócierniowa
Polish glediczja trójcierniowa
Portuguese acacia americana
Romanian glădiță
Russian Гледичия трехколючковая
Russian Гледичия трёхколючковая
Slovak gledíčia trojtŕňová
Serbian Гледичијa
Ukrainian Гледичія колюча
Ukrainian gleditchia triacanthos
Ukrainian Колюча гледичія
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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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

Suggest others/fix!
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
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
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
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
Commodity risk assessment of Fagus sylvatica 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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Commodity risk assessment of Acer campestre 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, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Strategies for the Management of Aggressive Invasive Plant Species Lorenzo P, Morais MC Plants (Basel) 28-Jun-2023
PMCID:PMC10346621
doi:10.3390/plants12132482
PMID:37447043
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Larvicidal Activities of Allium sativum L. and Zingiber officinale Rosc. Extracts against Filariasis Vectors in Hadiya Zone, Ethiopia Assemie A, Gemeda T Biomed Res Int 31-May-2023
PMCID:PMC10247325
doi:10.1155/2023/6636837
PMID:37292452
The Antibacterial and Wound Healing Properties of Natural Products: A Review on Plant Species with Therapeutic Potential against Staphylococcus aureus Wound Infections Morguette AE, Bartolomeu-Gonçalves G, Andriani GM, Bertoncini GE, de Castro IM, Spoladori LF, Bertão AM, Tavares ER, Yamauchi LM, Yamada-Ogatta SF Plants (Basel) 29-May-2023
PMCID:PMC10255540
doi:10.3390/plants12112147
PMID:37299127
Assessing the Spontaneous Spread of Climate-Adapted Woody Plants in an Extensively Maintained Collection Garden Szabó K, Gergely A, Tóth B, Szilágyi K Plants (Basel) 15-May-2023
PMCID:PMC10224429
doi:10.3390/plants12101989
PMID:37653906
Multigene Phylogeny and Pathogenicity Trials Revealed Alternaria alternata as the Causal Agent of Black Spot Disease and Seedling Wilt of Pecan (Carya illinoinensis) in South Africa Achilonu CC, Marais GJ, Ghosh S, Gryzenhout M Pathogens 02-May-2023
PMCID:PMC10223959
doi:10.3390/pathogens12050672
PMID:37242342
King rail (Rallus elegans) home range and microhabitat characteristics in western Lake Erie coastal marshes Brewer DE, Gehring TM, Garcia MM, Shirkey BT, Simpson JW, Fournier AM Ecol Evol 26-Apr-2023
PMCID:PMC10133529
doi:10.1002/ece3.10043
PMID:37122771

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
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester 21609756 Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC 348.50 unknown via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O 348.50 unknown via CMAUP database
prostaglandin B2 5280881 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O 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 CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 304.50 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 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 CCCCCCCCCCCC(=O)O 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 CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C 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
(S)-Turmerone 14367555 Click to see CC1=CCC(=CC1)C(C)CC(=O)C=C(C)C 218.33 unknown via CMAUP database
Secogorgosterol 386853 Click to see CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C 458.70 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 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)OC9C(C(C(C(O9)O)OOC1C(C(C(CO1)O)OOC1C(C(C(C(O1)CO)O)O)O)O)O)O)C 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 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)OC9C(C(C(C(O9)O)OOC1C(C(C(CO1)O)OOC1C(C(C(C(O1)CO)O)O)O)O)O)O)C 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 CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide 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
Crassocolide B 11995280 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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 CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O)C 472.70 unknown https://doi.org/10.1007/BF00564381
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-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 7048528 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF00564381
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 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 CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O)C 472.70 unknown https://doi.org/10.1007/BF00564381
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 492.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 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
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 101007150 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007149 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
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-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
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 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
(24E)-24-N-Propylidenecholesterol 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
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Oxalic Acid 971 Click to see C(=O)(C(=O)O)O 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 CC(=O)OCC12C(CCC(C13C(C(C(C2OC(=O)C4=CN=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)(C)O)OC(=O)C 653.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3,5-Dihydroxy-4-[(6-O-sulfonato-beta-D-glucopyranosyl)oxy]benzoic acid 102296196 Click to see C1=C(C=C(C(=C1O)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O)[O-])C(=O)O 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 CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C 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 CC(=CCN1C=NC(=N)C2=C1N=CN2)C 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 CC(=CCN1C=NC(=C2C1=NC=N2)N)C 203.24 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 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 CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=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 CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 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 CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
Crassocolide E 11995175 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Crassocolide F 11995282 Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C 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
ent-Sarcophine 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 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 CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database

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