Medicago arabica - Unknown
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Details Top

Internal ID UUID643fdefeab3ca304221051
Scientific name Medicago arabica
Authority (L.) Huds.
First published in Fl. Angl.: 288 (1762)

Description Top

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Medicago arabica, commonly known as the spotted medick, spotted burclover, or heart clover, is a flowering plant in the pea and bean family Fabaceae. It is native to the Mediterranean basin, but is found throughout the world, usually in clifftop grasslands and grassy places. It is a low-growing plant with spotted trifoliate leaves and pale yellow flowers that appear between April and August. The fruits are legumes, strangely coiled and sharply spiny. It has a symbiotic relationship with the bacterium Sinorhizobium medicae, which is capable of nitrogen fixation.

Synonyms Top

Scientific name Authority First published in
Medicago polymorpha var. arabica L. Sp. Pl.: 780 (1753)
Medicago cordata Desr. J.B.A.M.de Lamarck, Encycl.3: 636 (1792)
Medicago talyschensis Latsch. Zametki Sist. Geogr. Rast.27: 76 (1969)
Medicago maculata Sibth.
Medica arabica (L.) Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 386 (1787)
Medicago maculata Hook. & Arn. Bot. Beechey Voy. 330. 1838 [Dec 1838]
Medicago arabica f. purpurea Burkart in Cabrera Colecç. Ci. Inst. Nac. Tecnol. Agropecu4(3a): 560 (1967)
Medicago arabica subsp. inermis Ricker Bull. Bur. Pl. Industr. U.S.D.A.267: 33 (1913)
Medicago arabica f. elegans Kožuharov Izv. Bot. Inst. (Sofia)15: 152 (1965)
Medicago arabica f. heptacycla Urb. Verh. Bot. Vereins Prov. Brandenburg15: 74 (1873)
Medicago arabica f. pastoralis Kožuharov Izv. Bot. Inst. (Sofia)15: 152 (1965)
Medicago arabica var. longispina Rouy G.Rouy & J.Foucaud, Fl. France5: 35 (1899)
Medicago arabica var. minor Lojac. & Pojark. Malpighia20: 203 (1906)
Medicago maculata var. tetraphylla Desp. Fl. Sarthe: 51 (1838)
Medicago maculata var. tetraphylla N.H.F.Desp. Fl. Sarthe: 51 (1838)

Common names Top

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Language Common/alternative name
English spotted medick
English heart clover
English spotted burclover
Spanish trebol silvestre
Spanish trébol silvestre
Spanish trébol manchado
Spanish trebol manchado
Spanish mielga pintada
Spanish lucerna de arabia
Spanish carretón manchado
Arabic فصة عربية
Bulgarian арабска люцерна
Catalan herba de la taca
Czech tolice arabská
Welsh maglys brith
German arabischer schneckenklee
German gefleckter schneckenklee
Esperanto arabia medikago
Estonian araabia lutsern
Persian یونجه عربی
Finnish laikkumailanen
French luzerne d'arabie
French luzerne tachée
Upper Sorbian arabiska šlinčina
Armenian Առվույտ արաբական
Japanese メディカゴ・アラビカ
Latvian arābijas lucerna
Dutch gevlekte rupsklaver
Swedish fläcklusern
Ukrainian Люцерна арабська
Vietnamese linh lăng Ả rập
Chinese 紫斑苜蓿
Chinese 阿拉伯苜蓿
Chinese 褐斑苜蓿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

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-0000213417
Florida Plant Atlas 1815
Flora of Alabama 2010
Canadensys 5828
USDA Plants MEAR
Tropicos 13066794
INPN 107574
Flora of Italy 2591
KEW urn:lsid:ipni.org:names:58427-3
The Plant List ild-8482
Open Tree Of Life 525750
Observations.org 7041
NCBI Taxonomy 70936
NBN Atlas NHMSYS0000460629
Nature Serve 2.131378
IPNI 60465999-2
iNaturalist 61012
GBIF 2965527
Freebase /m/02vmcgw
EPPO MEDAB
EOL 703751
Elurikkus 5659
Calflora (Californian flora) 5381
USDA GRIN 23555
Wikipedia Medicago_arabica

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_946800305.1 drMedArab1.1 Chromosome WELLCOME SANGER INSTITUTE 2022-09-15 44.0x 491.62 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
Characterization and phylogenetic analysis of the complete chloroplast genome of Asterothamnus centraliasiaticus Novopokr. (Asteraceae: Asterothamnus) Li Z, Liu Y, Ma Y Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810623
doi:10.1080/23802359.2024.2306207
PMID:38274851
Diploid Nuclei Occur throughout the Life Cycles of Pucciniales Fungi Talhinhas P, Carvalho R, Tavares S, Ribeiro T, Azinheira H, Ramos AP, Silva MD, Monteiro M, Loureiro J, Morais-Cecílio L Microbiol Spectr 08-Jun-2023
PMCID:PMC10433954
doi:10.1128/spectrum.01532-23
PMID:37289058
Do Patches of Flowering Plants Enhance Insect Pollinators in Apple Orchards? Barda M, Karamaouna F, Kati V, Perdikis D Insects 19-Feb-2023
PMCID:PMC9960344
doi:10.3390/insects14020208
PMID:36835777
Disadvantaged Economic Conditions and Stricter Border Rules Shape Afghan Refugees’ Ethnobotany: Insights from Kohat District, NW Pakistan Shah AA, Badshah L, Khalid N, Shah MA, Manduzai AK, Faiz A, De Chiara M, Mattalia G, Sõukand R, Pieroni A Plants (Basel) 28-Jan-2023
PMCID:PMC9918957
doi:10.3390/plants12030574
PMID:36771658
GPS Tracking to Monitor the Spatiotemporal Dynamics of Cattle Behavior and Their Relationship with Feces Distribution Hassan-Vásquez JA, Maroto-Molina F, Guerrero-Ginel JE Animals (Basel) 12-Sep-2022
PMCID:PMC9495034
doi:10.3390/ani12182383
PMID:36139243
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M Molecules 16-Jun-2022
PMCID:PMC9230627
doi:10.3390/molecules27123863
PMID:35744986
Legumes of the Sardinia Island: Knowledge on Symbiotic and Endophytic Bacteria and Interactive Software Tool for Plant Species Determination Muresu R, Porceddu A, Concheri G, Stevanato P, Squartini A Plants (Basel) 06-Jun-2022
PMCID:PMC9183093
doi:10.3390/plants11111521
PMID:35684293
The complete chloroplast genome of Medicago arabica (Fabaceae) Jiao Y, He X, Shen Y, Chao Y, Zhang T Mitochondrial DNA B Resour 23-Apr-2022
PMCID:PMC9045773
doi:10.1080/23802359.2022.2067498
PMID:35493715
Diet Selection by the Italian Hare (Lepus corsicanus de Winton, 1898) in Two Protected Coastal Areas of Latium Freschi P, Fascetti S, Riga F, Rizzardini G, Fortebraccio M, Ragni M, Paolino R, Cosentino C Animals (Basel) 09-Mar-2022
PMCID:PMC8944817
doi:10.3390/ani12060687
PMID:35327084
Genetic Diversity and Differentiation of Eleven Medicago Species from Campania Region Revealed by Nuclear and Chloroplast Microsatellites Markers Djedid IK, Terzaghi M, Brundu G, Cicatelli A, Laouar M, Guarino F, Castiglione S Genes (Basel) 31-Dec-2021
PMCID:PMC8774365
doi:10.3390/genes13010097
PMID:35052437
Separation and Quantification of Selected Sapogenins Extracted from Nettle, White Dead-Nettle, Common Soapwort and Washnut Ligor M, Kiełbasa A, Ratiu IA, Buszewski B Molecules 20-Dec-2021
PMCID:PMC8708431
doi:10.3390/molecules26247705
PMID:34946786
Feeding Preferences of the Italian Roe Deer (Capreolus capreolus italicus Festa, 1925) in a Coastal Mediterranean Environment Freschi P, Fascetti S, Riga F, Rizzardini G, Musto M, Cosentino C Animals (Basel) 26-Jan-2021
PMCID:PMC7912300
doi:10.3390/ani11020308
PMID:33530361
Phylogeny and Species Delimitation of Chinese Medicago (Leguminosae) and Its Relatives Based on Molecular and Morphological Evidence Chen J, Wu G, Shrestha N, Wu S, Guo W, Yin M, Li A, Liu J, Ren G Front Plant Sci 13-Jan-2021
PMCID:PMC7874099
doi:10.3389/fpls.2020.619799
PMID:33584760
Pest categorisation of Diabrotica undecimpunctata howardi Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Kertész V, Maiorano A, Streissl F, MacLeod A EFSA J 11-Dec-2020
PMCID:PMC7729658
doi:10.2903/j.efsa.2020.6358
PMID:33318768

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-[(17S,18S,19S,20R)-17-acetyloxy-20-[(2S,3S,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-carboxy-18,19,21-trihydroxy-16-methylhenicosyl]-6-hydroxybenzoic acid 197691 Click to see CC(CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O)C(C(C(C(CO)OC2C(C(C(C(O2)CO)O)O)OC(=O)C)O)O)(C(=O)O)OC(=O)C 816.90 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-11-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163047851 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C(=O)O)C)C)C 959.10 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-11-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 163008044 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(CO5)O)O)O)O)C)CC=C6C3(CCC7(C6CC(CC7)(C)COC8C(C(C(C(O8)CO)O)O)O)C(=O)O)C)C)C 959.10 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-11-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163045154 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)C 827.00 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 162851135 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(CO7)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 943.10 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-2-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 11549167 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 648.80 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-11-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,4,6a,6b,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 162931394 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C(=O)O)C)C)C 943.10 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,14b-hexamethyl-11-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 163043014 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(CO5)O)O)O)C)CC=C6C3(CCC7(C6CC(CC7)(C)COC8C(C(C(C(O8)CO)O)O)O)C(=O)O)C)C)C 943.10 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 163009656 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(CO7)O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown https://doi.org/10.1021/JF8036984
(2S,3S,4S,5R,6R)-6-[[(3S,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 162952440 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(CO7)O)O)O)C)C)C2C1)C)C(=O)O)C 780.90 unknown https://doi.org/10.1021/JF8036984
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101726448 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 783.00 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 76401272 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 783.00 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 4643550 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 767.00 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
6-[(8a-Carboxy-2-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 73003231 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 648.80 unknown https://doi.org/10.1021/JF8036984
6-[(8a-Carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 13919558 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(CO7)O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-11-[[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163047850 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C(=O)O)C)C)C 959.10 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-11-[[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-4,4,6a,6b,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 162931393 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C(=O)O)C)C)C 943.10 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-11-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 163008043 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(CO5)O)O)O)O)C)CC=C6C3(CCC7(C6CC(CC7)(C)COC8C(C(C(C(O8)CO)O)O)O)C(=O)O)C)C)C 959.10 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-2-hydroxy-4,4,6a,6b,11,14b-hexamethyl-11-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163045153 Click to see CC1(C2CCC3(C(C2(CC(C1OC4C(C(C(C(O4)C(=O)O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)C 827.00 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 162952439 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(CO7)O)O)O)C)C)C2C1)C)C(=O)O)C 780.90 unknown https://doi.org/10.1021/JF8036984
6-[[8a-Carboxy-4,4,6a,6b,11,14b-hexamethyl-11-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 163043013 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(CO5)O)O)O)C)CC=C6C3(CCC7(C6CC(CC7)(C)COC8C(C(C(C(O8)CO)O)O)O)C(=O)O)C)C)C 943.10 unknown https://doi.org/10.1021/JF8036984
beta-D-Glucopyranosyl (3beta,4alpha)-3-[(2-O-beta-D-glucopyranosyl-alpha-L-arabinopyranosyl)oxy]-23-hydroxyolean-12-en-28-oate 101623722 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 929.10 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
beta-D-Glucopyranosyl (3beta,4alpha)-3-[(O-alpha-L-arabinopyranosyl-(1-->2)-O-beta-D-glucopyranosyl-(1-->2)-alpha-L-arabinopyranosyl)oxy]-23-hydroxyolean-12-en-28-oate 101726449 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1061.20 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
Calendulaglycoside F 5104673 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown https://doi.org/10.1021/JF8036984
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown https://doi.org/10.1021/JF8036984
CID 5087640 5087640 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown https://doi.org/10.1021/JF8036984
HN-saponin F 14101171 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 767.00 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
Medicoside F 131752993 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 929.10 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
Medicoside I 74177087 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1061.20 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown https://doi.org/10.1021/JF8036984
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1016/0305-1978(73)90022-7
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown https://doi.org/10.1016/0305-1978(73)90022-7
Zeaxanthin 5280899 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 568.90 unknown https://doi.org/10.1016/0305-1978(73)90022-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101726447 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C 620.80 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162917532 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)O)C 899.10 unknown https://doi.org/10.1021/JF8036984
10-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13878149 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 767.00 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
11-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 133053421 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(CO6)O)O)O)O)C)C)C2C1)C)C(=O)O)C 620.80 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
9-(Hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 4483448 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 604.80 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
Cauloside A 441928 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 604.80 unknown https://doi.org/10.1021/JF030446+
https://doi.org/10.1021/JF8036984
Cauloside C 13878151 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 767.00 unknown https://doi.org/10.1021/JF8036984
https://doi.org/10.1021/JF030446+
Medicoside C 14779979 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)O)C 899.10 unknown https://doi.org/10.1021/JF8036984
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Chrysoeriol glucuronide 14630703 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/0305-1978(82)90048-5
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1016/0305-1978(82)90048-5

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