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

Description Top

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Melilotus officinalis, commonly known as sweet yellow clover, is a species of legume native to Eurasia and introduced to North America, Africa, and Australia. It is an annual or biennial plant that grows up to 4-6 feet tall and has three leaflets on its leaves. It prefers calcareous loamy and clay soils with a pH above 6.5, and is often found in open disturbed land, prairies, and savannahs. Sweet clover contains coumarin which can convert to a powerful anticoagulant toxin when the plant becomes moldy, and can be fatal to cattle. It is used as a forage crop, cover crop, and source of nectar for honey bees, and has been used to treat soils contaminated with dioxins. It can be managed by mulching, hand-pulling, mowing, herbicide applications, and prescribed burns.

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
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
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
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
Ukrainian конюшина лікарська
Ukrainian буркун лікарський
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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Name Authority First published in
Melilotus officinalis subsp. albus (Medik.) H.Ohashi & Tateishi Sci. Rep. Tohoku Univ. Ser. 4, 38(4): 319 (1984):.

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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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

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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

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
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
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
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
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
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
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
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
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Natural Product-Based Glycolysis Inhibitors as a Therapeutic Strategy for Epidermal Growth Factor Receptor–Tyrosine Kinase Inhibitor-Resistant Non-Small Cell Lung Cancer Park W, Han JH, Wei S, Yang ES, Cheon SY, Bae SJ, Ryu D, Chung HS, Ha KT Int J Mol Sci 09-Jan-2024
PMCID:PMC10815680
doi:10.3390/ijms25020807
PMID:38255882
Impact of cellulose and lignin on restoration of vegetation and soil chemical properties for saline-alkali soil of songnen plain Fu F, Luo J, Zhao L, Yang F, Wang N PLoS One 02-Jan-2024
PMCID:PMC10760773
doi:10.1371/journal.pone.0296366
PMID:38165910
Quercetin: A Potential Polydynamic Drug Georgiou N, Kakava MG, Routsi EA, Petsas E, Stavridis N, Freris C, Zoupanou N, Moschovou K, Kiriakidi S, Mavromoustakos T Molecules 17-Dec-2023
PMCID:PMC10745404
doi:10.3390/molecules28248141
PMID:38138630
Rhamnogalacturonan I with β-(1,4)-Galactan Side Chains as an Ever-Present Component of Tertiary Cell Wall of Plant Fibers Chernova T, Mikshina P, Petrova A, Ibragimova N, Ageeva M, Gorshkova T Int J Mol Sci 08-Dec-2023
PMCID:PMC10743774
doi:10.3390/ijms242417253
PMID:38139081
Redundant and scattered genetic determinants for coumarin biodegradation in Pseudomonas sp. strain NyZ480 Gu Y, Li T, Zhou NY Appl Environ Microbiol 10-Oct-2023
PMCID:PMC10617510
doi:10.1128/aem.01109-23
PMID:37815346
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
Trigonelline 5570 Click to see C[N+]1=CC=CC(=C1)C(=O)[O-] 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,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 15608214 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)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 941.10 unknown https://doi.org/10.1248/CPB.46.526
(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 CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8=O)(C)C)C)C)C)C)C(=O)O)O)O)O)O)O)O)O 911.10 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 CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)O)O)O)O)O 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 CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)O)O)O)O)O 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 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
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 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
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.46.526
https://doi.org/10.1248/CPB.48.286
Dehydrosoyasaponin I 656760 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)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 941.10 unknown https://doi.org/10.1248/CPB.46.526
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/10.1248/CPB.46.526
https://doi.org/10.1248/CPB.48.286
Soybean saponin BG 78178264 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8=O)(C)C)C)C)C)C)C(=O)O)O)O)O)O)O)O)O 911.10 unknown https://doi.org/10.1248/CPB.48.286
Wistariasaponin C 21634074 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)O)O)O)O)O 913.10 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 CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5=O)(C)C(=O)O)C)C)C)(C)CO)O 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 CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(COC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)O)O)CO)O)O)O)O)O 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 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
(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 CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5=O)(C)C(=O)O)C)C)C)(C)CO)O 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 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
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 CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(COC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)O)O)CO)O)O)O)O)O 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
Cellobiose 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
Melibiose 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
4-a-Isomaltosylglucose 4120027 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
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
Maltotriose 871 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
Man(b1-4)Man(b1-4)a-Man 91854746 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown https://doi.org/10.1016/S0008-6215(00)90811-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown https://doi.org/10.1002/JLAC.18631260302
https://doi.org/10.1002/PCA.2800050308
https://doi.org/10.1002/PTR.875
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol, robinoside 5351997 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1007/BF02323303
Robinin 5281693 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1007/BF02323303
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-Hydroxybenzenepropanoic acid 873 Click to see C1=CC=C(C(=C1)CCC(=O)O)O 166.17 unknown https://doi.org/10.1002/JLAC.18631260302

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