Details Top

Internal ID UUID643fdf1a5ffc1396814399
Scientific name Melilotus officinalis
Authority (L.) Pall.
First published in Reise Russ. Reich. 3: 537. 1776

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.

Melilotus officinalis, commonly called yellow sweet clover, is a small-legged herb that has been used in infusions and poultices across Europe and parts of North America to ease swelling, improve circulation, and calm bruises. Among rural practitioners in Central Europe, a light tea or external soak made from the herb was taken for sluggish lymph flow and minor edema; an upper dose of around 2–3 grams of herb per cup of water was considered sufficient for a gentle effect (British Herbal Pharmacopoeia, 1983). In the German-speaking world, melilot was listed in older materia medicas as a circulatory and lymphatic aid prepared as an infusion or compress to reduce local bruising and stiffness; the plant part used was the aerial herb, including young leaves and stems, and applications ranged from compresses to short teas (Madaus, 1938). Across the Appalachian and Midwestern United States, herbalists and lay healers prepared similar teas or liniment-like washes from the herb for bruises, mild swelling, and as a diuretic, with the upper infusion dose in some herbal manuals remaining around 2–3 grams per cup (British Herbal Pharmacopoeia, 1983). More recently, the European Medicines Agency recognized melilot’s traditional external use for bruises, muscle strains, and minor inflammations, and its internal use as a mild infusion to aid lymphatic drainage, again specifying the aerial parts as the medicinally used material (European Medicines Agency, 2016). Together these records show the plant’s long-standing use in infusions, decoctions, and poultices, with consistent attention to bruised tissues and water-related drainage.

A practical preparation that stays within documented practice is a mild infusion. Measure roughly 2 g of the dried aerial parts (about 1 rounded tablespoon) and pour 200 mL of freshly boiled water over the herb; stir, cover, and steep for 10 minutes, then strain. This dose is usually taken warm and can be repeated up to three times daily for several days. Alternatively, for external use, pour the same hot infusion over a clean cloth and apply as a warm compress to bruises or swollen areas for 10–15 minutes, three times a day. Safety cautions are appropriate: melilot contains coumarin, so internal use is usually avoided in pregnancy and lactation and in people on anticoagulant or antiplatelet medication; keep doses modest and discontinue if you notice unusual bleeding. The European Medicines Agency also notes that the herb should only be taken for short periods and within its traditional mild dosage range (European Medicines Agency, 2016).

The traditional actions align with the plant’s chemistry. Melilot is rich in coumarin and coumarin derivatives, and also contains melilotoside, flavonoids such as luteolin and quercetin, and small amounts of phenolic acids. These constituents show venotonic and mild anti-inflammatory effects that plausibly support the traditional use for bruises, mild edema, and lymphatic tonicity, without implying novel pharmacology beyond what is already recorded for the species (British Herbal Pharmacopoeia, 1983).

Modern relevance is active and mixed. While research continues into coumarin’s lymphatic and microcirculatory effects and melilot extracts appear in some dietary supplements, regulatory bodies in the EU limit oral uses of melilot due to coumarin content, and commercial products emphasize external preparations. At the same time, melilot remains part of contemporary herbal practice, especially for bruises and lymphatic support, and is still sometimes foraged and prepared locally as a mild infusion or compress, in keeping with long-standing traditions.

General Uses Top

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Common products:
Melilotus officinalis yields essential oil and CO2 extract containing coumarin, used as fragrance materials for soaps, detergents, and perfumes. Dry aerial parts are marketed as potpourri or fragrance sachets.

Food and beverages (non-medicinal):
Flowers are employed as flavor ingredients, primarily coumarinic notes, in alcoholic beverages (e.g., liqueurs and spirits). Individual cases of melilot honey and other melilot-derived honeys contain elevated coumarin; this requires verification and appropriate food compliance measures. The seed contains lipids and protein and is occasionally processed into animal feed concentrates.

Properties relevant to use:
High coumarin content (≈0.2–0.3% in dry material) in flowers confers characteristic new-mown-hay fragrance; coumarin is lipophilic and moderately soluble in alcohol, facilitating extraction into ethanol-based distillates and CO2 extracts. Seeds contain protein and fixed oil suitable for feed processing.

Fragrance and cosmetics:
Coumarin is a recognized fragrance allergen under IFRA standards; usage requires sensory evaluation and compliance with IFRA and relevant regional safety thresholds.

Sustainability and sourcing:
An erect annual/biennial, drought-tolerant legume that fixes atmospheric nitrogen, often self-reseeding and occasionally weedy. It is winter-hardy and used in rotational systems; management of invasion risk and adherence to local crop and pesticide regulations is required. Seed production supports Essential Oil and Flavor industries.

Synonyms Top

Scientific name Authority First published in
Trifolium melilotus-officinalis L.
Trifolium officinalis L.

Common names Top

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Language Common/alternative name
English common melilot
English ribbed melilot
English yellow melilot
English yellow sweet clover
English yellow sweetclover
English field melilot
Spanish meliloto amarillo
Spanish trébol de color amarillo
Spanish medicago officinalis
Spanish meliloto oficinal
Spanish trebol dulce
Spanish trébol dulce
Arabic أكليل الملك
Arabic إكليل الملك
Arabic الحندقوق
Arabic حندقوق
Arabic حندقوق طبي
Arabic حنتم
Arabic حندقوق حقلي
Arabic غصن البان
Arabic كركمان
Arabic العَنُوص
Arabic العتفقان
Arabic النّفَل
Arabic النفل
Azerbaijani dərman xəşənbülü
azb سهبهرگه یونجاسی
ba Ҡандала үләне
Belarusian баркун
Belarusian баркун жоўты
Belarusian маляснік
Belarusian томка
Belarusian баркун лекавы
Bulgarian Жълта комунига
Catalan melilot
ce Дарбане аларт
Czech komonice lékařská
Welsh yr wydro resog
German echter steinklee
German gebräuchlicher honigklee
German gelber steinklee
German gewöhnlicher steinklee
Estonian kollane mesikas
Basque itsabalki arrunt
Persian ناخنک
Persian یونجه زرد
Persian اکلیل الملک
Persian اکلیلالملک
Persian بسنگ
Persian شاه افسر
Persian شاه بسه
Persian شاهافسر
Persian شبدر زرد
Persian شبدر زرد شیرین
Persian شبدر شیرین
Finnish rohtomesikkä
French mélilot jaune
French melilot officinal
French mélilot officinal
Irish crúibín cait
Galician chuchamel
Galician chupamel
Galician herba abelleira
Galician meliloto amarelo
Galician trevo de cheiro
Galician meliloto
Gujarati ઝરેર
Upper Sorbian Žołty komonc
Hungarian orvosi somkóró
Armenian Իշառվույտ դեղատու
Igbo melilotus albus
Icelandic mánasteinsmári
Italian meliloto
Georgian ყვითელი ძიძო
Kazakh Сары түйежоңышқа
la trifolium melilotus
Lithuanian geltonžiedis barkūnas
Lithuanian jondobilis
Latvian Ārstniecības amoliņš
Macedonian обична комуника
mn Эмийн хошоон
myv Ашо цивиця
myv Ормаменьксэнь цивця
myv Ормаменьксэнь медев тикше
Norwegian Bokmål legesteinkløver
Dutch akkerhoningklaver
Dutch citroengele honingklaver
Polish nostrzyk lekarski
Polish nostrzyk żółty
Portuguese meliloto
Portuguese meliloto-amarelo
Portuguese trevo-de-cheiro.
Romanian sulfină
Romanian sulfină medicinală
Russian Донник желтый
Russian Донник жёлтый
Russian Донник лекарственный
rup sulfinâ
Slovak komonica lekárska
Slovenian navadna medena detelja
Swedish gul sötväppling
Swedish Äkta sötväppling
Swedish sötväppling
tg Асалришқа
Turkish sarı taş yoncası
Ukrainian Буркун лікарський
Ukrainian Конюшина лікарська
Chinese 草木犀
Chinese 野苜蓿
Chinese 草木樨
Chinese 草木犀*(黄香草木樨)
Chinese 黄花草木樨
Chinese 黄零陵香
Chinese 黄香草木樨
Chinese 黄香草木犀
Chinese 辟汗草
Chinese 铁扫把
Chinese 黃香草木樨
Chinese 一种维管植物

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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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
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-0000213864
UNII DJR90OLD7P
Florida Plant Atlas 2010
Flora of Alabama 2018
Canadensys 5841
USDA Plants MEOF
Tropicos 13035841
INPN 788839
KEW urn:lsid:ipni.org:names:30429323-2
The Plant List ild-8929
Open Tree Of Life 38048
Observations.org 7052
NCBI Taxonomy 47083
NBN Atlas NHMSYS0000460663
Nature Serve 2.146387
IPNI 1174681-2
iNaturalist 57066
GBIF 2971024
Freebase /m/09g64h
WisFlora 4223
EPPO MEUOF
EOL 704023
Elurikkus 5693
Calflora (Californian flora) 5407
USDA GRIN 24009
Wikipedia Melilotus_officinalis
PFAF Melilotus officinalis

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_050575045.1 ASM5057504v1 Chromosome Anhui Science and Technology University 2025-05-27 99.16 931.07 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
Genome assembly of Melilotus officinalis provides a new reference genome for functional genomics Meng A, Li X, Li Z, Miao F, Ma L, Li S, Sun W, Huang J, Yang G BMC Genom Data 18-Apr-2024
PMCID:PMC11025269
doi:10.1186/s12863-024-01224-y
PMID:38637749
Dicoumarol attenuates NLRP3 inflammasome activation to inhibit inflammation and fibrosis in knee osteoarthritis Ge W, Zhang X, Wang Q, Mao J, Jia P, Cai J Mol Med Rep 15-Apr-2024
PMCID:PMC11040416
doi:10.3892/mmr.2024.13224
PMID:38639180
A dataset for fine-grained seed recognition Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y Sci Data 06-Apr-2024
PMCID:PMC10998916
doi:10.1038/s41597-024-03176-5
PMID:38582756
Soil Nitrogen and Flooding Intensity Determine the Trade-Off between Leaf and Root Traits of Riparian Plant Species Zou H, Wang W, Huang J, Li X, Ma M, Wu S, Zhao C Plants (Basel) 29-Mar-2024
PMCID:PMC11013260
doi:10.3390/plants13070978
PMID:38611507
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Comparative analysis of codon usage patterns in the chloroplast genomes of nine forage legumes Xiao M, Hu X, Li Y, Liu Q, Shen S, Jiang T, Zhang L, Zhou Y, Li Y, Luo X, Bai L, Yan W Physiol Mol Biol Plants 09-Mar-2024
PMCID:PMC11016040
doi:10.1007/s12298-024-01421-0
PMID:38623162
Urban environment decreases pollinator availability, fertility, and prolongs anthesis in the field bindweed (Convolvulus arvensis Linnaeus, 1753) Prokop P Plant Signal Behav 06-Mar-2024
PMCID:PMC10936644
doi:10.1080/15592324.2024.2325225
PMID:38448395
Healing of diabetic foot ulcer with topical and oral administrations of herbal products: A systematic review and meta‐analysis of randomized controlled trials Zamanifard M, Nasiri M, Yarahmadi F, Zonoori S, Razani O, Salajegheh Z, Imanipour M, Mohammadi SM, Jomehzadeh N, Asadi M Int Wound J 14-Feb-2024
PMCID:PMC10867296
doi:10.1111/iwj.14760
PMID:38356150
Phytochemical, Antioxidant Activity, and Toxicity of Wild Medicinal Plant of Melitotus albus Extracts, In Vitro and In Silico Approaches Ed-Dahmani I, El fadili M, Kandsi F, Conte R, El Atki Y, Kara M, Assouguem A, Touijer H, Lfitat A, Nouioura G, Slighoua M, Ullah R, Al-Tamimi JH, Taleb M, Abdellaoui A ACS Omega 09-Feb-2024
PMCID:PMC10905593
doi:10.1021/acsomega.3c08314
PMID:38434823
Isolation and Identification of Acer truncatum Endophytic Fungus Talaromyces verruculosus and Evaluation of Its Effects on Insoluble Phosphorus Absorption Capacity and Growth of Cucumber Seedlings Zeng Q, Dong J, Lin X, Zhou X, Xu H J Fungi (Basel) 08-Feb-2024
PMCID:PMC10890576
doi:10.3390/jof10020136
PMID:38392808
Chemical profile of Juniperus excelsa M. Bieb. essential oil within and between populations and its weed seed suppression effect Semerdjieva I, Zheljazkov VD, Dincheva I, Radoukova T, Astatkie T, Maneva V, Atanasova D, Fidan H, Stankov S, Stoyanova A PLoS One 08-Feb-2024
PMCID:PMC10852245
doi:10.1371/journal.pone.0294126
PMID:38330006
Reduction of Post-Surgical Facial Edema Following Bromelain and Coumarin Intake in Traumatology: A Prospective Study with 100 Patients Consorti G, Monarchi G, Paglianiti M, Betti E, Balercia P J Clin Med 06-Feb-2024
PMCID:PMC10889715
doi:10.3390/jcm13040922
PMID:38398236
Factors Influencing Venous Remodeling in the Development of Varicose Veins of the Lower Limbs Gwozdzinski L, Pieniazek A, Gwozdzinski K Int J Mol Sci 26-Jan-2024
PMCID:PMC10855638
doi:10.3390/ijms25031560
PMID:38338837
Living mulch enhances soil enzyme activities, nitrogen pools and water retention in giant reed (Arundo donax L.) plantations Elhawat N, Kovács AB, Antal G, Kurucz E, Domokos-Szabolcsy É, Fári MG, Alshaal T Sci Rep 19-Jan-2024
PMCID:PMC10798950
doi:10.1038/s41598-024-51491-z
PMID:38242963
Bioactivity and toxicity of coumarins from African medicinal plants Anywar G, Muhumuza E Front Pharmacol 10-Jan-2024
PMCID:PMC10809390
doi:10.3389/fphar.2023.1231006
PMID:38273831

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
> Alkaloids and derivatives
Trigonelline 5570 Click to see 137.14 unknown https://doi.org/10.1007/BF00628729
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-11-carboxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-9-oxo-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 10557876 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8=O)(C)C(=O)O)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 971.10 unknown https://doi.org/10.1248/CPB.48.286
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-9-oxo-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 160022 Click to see 911.10 unknown https://doi.org/10.1248/CPB.48.286
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 21634074 Click to see 913.10 unknown https://doi.org/10.1248/CPB.48.286
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9S,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 13326381 Click to see 913.10 unknown https://doi.org/10.1248/CPB.48.286
(2S,3S,4S,5R,6R)-6-[[(4S,6aR,8aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 6325919 Click to see 913.10 unknown https://doi.org/10.1248/CPB.48.286
6-[[11-carboxy-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-9-oxo-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 73156995 Click to see 971.10 unknown https://doi.org/10.1248/CPB.48.286
6-[[9-Acetyloxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 85221226 Click to see 985.20 unknown https://doi.org/10.1248/CPB.46.526
Acetylsoyasaponin I 101997831 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC(=O)C)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 985.20 unknown https://doi.org/10.1248/CPB.46.526
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/10.1248/CPB.48.286
https://doi.org/10.1248/CPB.46.526
Dehydrosoyasaponin I 656760 Click to see 941.10 unknown https://doi.org/10.1248/CPB.46.526
Soyasapogenol E base + O-HexA-Hex-dHex 15608214 Click to see 941.10 unknown https://doi.org/10.1248/CPB.46.526
Soyasaponin I 122097 Click to see 943.10 unknown https://doi.org/10.1248/CPB.46.526
https://doi.org/10.1248/CPB.48.286
Soybean saponin BG 78178264 Click to see 911.10 unknown https://doi.org/10.1248/CPB.48.286
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,4aR,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-4-oxo-3,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 162984173 Click to see 486.70 unknown https://doi.org/10.1021/NP50056A027
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R)-2-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163084464 Click to see 899.10 unknown https://doi.org/10.1007/S10600-010-9678-2
(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R)-2-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163000914 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C 753.00 unknown https://doi.org/10.1007/S10600-010-9678-2
(2S,3R,4S,5R)-2-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-3,4,5-triol 15226739 Click to see 590.80 unknown https://doi.org/10.1007/S10600-010-9678-2
(2S,4aR,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-4-oxo-3,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 14059504 Click to see 486.70 unknown https://doi.org/10.1021/NP50056A027
(3S,4S,4aS,6aR,6bS,8aR,9R,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 161972892 Click to see 458.70 unknown https://doi.org/10.1007/BF02855614
Melilotoside A 73813305 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(CO6)O)O)O)C)C 590.80 unknown https://doi.org/10.1007/S10600-010-9678-2
Melilotoside B 73834062 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C 753.00 unknown https://doi.org/10.1007/S10600-010-9678-2
Melilotoside C 73813306 Click to see 899.10 unknown https://doi.org/10.1007/S10600-010-9678-2
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown https://doi.org/10.1007/BF02855614
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
6-[[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxane-2,3,4,5-tetrol 872 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
beta-D-Glucopyranose, 4-O-beta-D-galactopyranosyl- 294 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Man(b1-4)a-Man 162928536 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(OC(C(C3O)O)O)CO)O)O)O)O)O)O)O 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
GlyTouCan:G13954SE 4120027 Click to see 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
GlyTouCan:G94390VI 871 Click to see 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
GlyTouCan:G98033RN 91854746 Click to see 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1002/PTR.875
https://doi.org/10.1002/JLAC.18631260302
https://doi.org/10.1002/PCA.2800050308
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5351997 Click to see 740.70 unknown https://doi.org/10.1007/BF02323303
Robinin 5281693 Click to see 740.70 unknown https://doi.org/10.1007/BF02323303
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Melilotic acid 873 Click to see 166.17 unknown https://doi.org/10.1002/JLAC.18631260302

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