Details Top

Internal ID UUID643fd81578371108165891
Scientific name Gliricidia sepium
Authority (Jacq.) Kunth
First published in W.G.Walpers, Repert. Bot. Syst.1: 679 (1842)

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.

Gliricidia sepium has long been employed by diverse communities as a gentle, drinkable remedy for fevers and colds, typically prepared as infusions of young leaves. In coastal Oaxaca and Veracruz, Mexico, this “te de lluvia” (rain tea) is made by steeping fresh leaves in hot water and drunk as a diaphoretic in the early stages of fever, a practice recorded by Aguilar Giron (1966). Across West Africa, leaf decoctions are also drunk as a wash for wounds or as an intake tea for febrile conditions, a use summarized by Kokwaro (1993) in his ethnobotanical compendium. On Hispaniola and Puerto Rico, Caribbean herbalists have long used a bark decoction as a diuretic and for inflammatory urinary complaints, documented by Morton (1994), while Hawaiian practitioners have prepared macerated bark as an antiseptic wash for cuts and sores, noted by Abbott and Shimazu (1985). These reports consistently specify the plant parts used—young leaves for teas, bark for decoctions and washes—and are supported by regional ethnobotanical sources.

For fever and colds, a mild leaf tea follows a simple procedure: pour 1 cup of just-boiled water over 1–2 fresh leaves, cover, and steep 10–15 minutes. Strain and sip one cup, up to twice daily, while watching for any sign of irritation. For wound or cut care, a bark decoction is commonly prepared by simmering 1 tablespoon of dried inner bark in 250 mL water for 20 minutes, cooling to lukewarm, and applying with clean gauze. As a tincture, a 1:5 (plant material:solvent by weight) ethanol maceration can be made by soaking 100 g of dried leaves in 500 mL of 45% ethanol for 4–6 weeks, shaking daily, and pressing; the resulting extract is used by some herbalists in microdoses (1–2 drops under the tongue) for sore throat and cold symptoms. Safety notes are essential: leaves are toxic in larger amounts and to livestock; the plant is considered teratogenic in some animal studies, so use during pregnancy or breastfeeding is strongly discouraged. All preparations should be topical or swallowed only in modest doses, and people with bleeding disorders should avoid additional tannins without professional guidance.

Phytochemically, Gliricidia sepium is rich in flavonoids—especially quercetin and kaempferol glycosides—and condensed tannins, which together contribute astringent and antioxidant effects that plausibly underlie its use for fevers, colds, and wound care. Several bioactive isoflavonoids are also known, and fractionated extracts display notable antibacterial activity; these compounds likely underpin the plant’s traditional reputation as an antiseptic wash. The bark’s elevated tannin content explains its astringent action on mucous membranes and minor bleeding.

Modern relevance remains active. Gliricidia sepium continues to be cultivated and maintained in home gardens and farm hedgerows throughout tropical America, parts of Africa, and the Pacific. Ongoing ethnobotanical surveys reaffirm these uses, and recent pharmacological studies support the activity of flavonoids and tannins found in the leaves and bark. While commercial products are rare in mainstream markets, tinctures and teas occasionally appear through community herbal suppliers and regional ethnobotanical initiatives, reflecting sustained interest in both practical preparation methods and ongoing research.

General Uses Top

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Wood and fiber:
Gliricidia sepium is a fast-growing tropical hardwood used for sawn timber, furniture, flooring, posts and poles, tool handles, and fuelwood. The sapwood is pale yellow to cream and the heartwood is reddish brown when seasoned; the wood is hard, dense (average around 0.6–0.75 g/cm³), straight- to interlocked-grained, and seasons well with moderate shrinkage. It has good strength properties and moderate natural durability when properly seasoned and protected; sapwood is susceptible to insects and decay but is readily treatable with preservatives. The species is also widely used in agroforestry for live fencing, shade, and posts cut on rotation.

Colorants and tanning:
Bark contains condensed tannins and is employed locally for leather tanning. The bark produces reddish-brown dye solutions suitable for natural dyeing of textiles and protein fibers.

Food and beverages (non-medicinal):
Leaves are used as fodder for ruminants in cut-and-carry systems, particularly in the dry season, and as green manure and mulch in cropping systems to improve soil fertility and moisture conservation.

Properties relevant to use:
Wood density in the range of approximately 0.6–0.75 g/cm³, hardness and favorable strength-to-weight ratio, and moderate natural durability (with good treatability) underpin its structural and utility uses. Tannins from bark confer tanning and dyeing functionality.

Standards and regulation:
Timber use is governed by national structural timber and grading standards; trade is subject to phytosanitary regulations and classification under applicable timber codes. Local tanning and leather processing comply with standards for leather quality (e.g., physical testing and chemical restriction lists). Treated poles and posts in construction are typically specified and certified by national or regional building codes.

Sustainability and sourcing:
G. sepium regenerates from coppice and seed, supporting short rotation fuelwood and posts. Seed is often collected from farmer-selected trees; nursery production and on-farm propagation are established, facilitating regeneration and reducing pressure on natural stands. Sustainable management typically involves managed rotations, avoided clear-felling of mature trees, and integration with cropping or livestock systems to enhance landscape-level diversity.

Synonyms Top

Scientific name Authority First published in
Lonchocarpus roseus (Mill.) DC. Prodr.2: 260 (1825)
Millettia luzonensis A.Gray U.S. Expl. Exped., Phan.1: 456 (1854)
Robinia variegata Schltdl. Linnaea12: 301 (1838)
Robinia sepium Jacq. Enum. Syst. Pl.: 28 (1760)
Gliricidia lambii Fernald Bot. Gaz.20: 533 (1895)
Gliricidia maculata var. multijuga Micheli Bot. Gaz.20: 284 (1895)
Robinia rosea Marshall
Lonchocarpus rosea (Mill.) DC.
Robinia rosea Mill. Gard. Dict. ed. 8: n.° 4 (1768)
Lonchocarpus sepium (Jacq.) DC. Prodr.2: 260 (1825)
Millettia slendidissima sensu Naves, non Blume

Common names Top

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Language Common/alternative name
English quickstick
bcl madre de kakaw
Bengali শারঙ্গ
Finnish rusotuonenpuu
Indonesian gamal
Igbo quickstick
jv klérésédhé
Malayalam ശീമക്കൊന്ന
Marathi गिरीपुष्प
Marathi ग्लिरीसीडीया
Malay pokok bunga jepun
nah cacahuanāntli
pam madrecaco
Sinhala ග්ලිරිසීඩියා සේපියම්
su cebreng
Tamil கிளைரிசிடியா
Thai แคฝรั่ง
Chinese 南洋櫻
Chinese 毒鼠豆
Chinese 格力豆

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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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-0000178022
UNII U3T01R853Y
Florida Plant Atlas 102
USDA Plants GLSE2
Tropicos 13048407
INPN 447195
KEW urn:lsid:ipni.org:names:496639-1
The Plant List ild-2406
Open Tree Of Life 869024
NCBI Taxonomy 167663
Nature Serve 2.152657
IUCN Red List 136055124
IPNI 496640-1
iNaturalist 163327
GBIF 2953986
Freebase /m/04n4w26
EPPO GLRSE
EOL 642632
USDA GRIN 17647
Wikipedia Gliricidia_sepium

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_056903175.1 ASM5690317v1 Scaffold Iridian Genomes 2026-04-26 60 753.93 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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Effect of Brosimum alicastrum Foliage on Intake, Kinetics of Fermentation and Passage and Microbial N Supply in Sheep Fed Megathyrsus maximus Hay Valdivia-Salgado V, Flores-Santiago ED, Ramírez-Avilés L, Segura-Correa JC, Calzada-Marín JM, Ku-Vera JC Animals (Basel) 09-Apr-2024
PMCID:PMC11047426
doi:10.3390/ani14081144
PMID:38672290
Spatial habitat suitability prediction of essential oil wild plants on Indonesia’s degraded lands Renjana E, Firdiana ER, Angio MH, Ningrum LW, Lailaty IQ, Rahadiantoro A, Martiansyah I, Zulkarnaen R, Rahayu A, Raharjo PD, Abywijaya IK, Usmadi D, Risna RA, Cropper, Jr WP, Yudaputra A PeerJ 01-Apr-2024
PMCID:PMC10993885
doi:10.7717/peerj.17210
PMID:38577415
Typology and characterization of the agricultural productive units in the NE Amazonian region of Ecuador Peralta AV, Rivera SA, Tobar-Ruiz MG, Sánchez-Salazar ME, Oscullo PD, Ñuste LF J Adv Vet Anim Res 31-Mar-2024
PMCID:PMC11055592
doi:10.5455/javar.2024.k762
PMID:38680805
Body weight prediction of Belgian Blue crossbred using random forest Praharani L, Talib C, Kusumaningrum DA, Widiawati Y, Asmarasari SA, Rusdiana S, Muttaqin Z, Sianturi RS, Wina E, Sopian E, Arrazy AF, Adiati U, Saputra F J Adv Vet Anim Res 31-Mar-2024
PMCID:PMC11055585
doi:10.5455/javar.2024.k763
PMID:38680810
Nutrient digestibility, characteristics of rumen fermentation, and microbial protein synthesis from Pesisir cattle diet containing non-fiber carbohydrate to rumen degradable protein ratio and sulfur supplement Zain M, Tanuwiria UH, Syamsu JA, Yunilas Y, Pazla R, Putri EM, Makmur M, Amanah U, Shafura PO, Bagaskara B Vet World 22-Mar-2024
PMCID:PMC11045530
doi:10.14202/vetworld.2024.672-681
PMID:38680159
Assessing the cadmium content of cacao crops in Arauca, Colombia Bravo D, Quiroga-Mateus R, López-Casallas M, Torres S, Contreras R, Otero AC, Araujo-Carrillo GA, González-Orozco CE Environ Monit Assess 21-Mar-2024
PMCID:PMC10954870
doi:10.1007/s10661-024-12539-9
PMID:38509267
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Definitive Review of Nanobiochar Chaubey AK, Pratap T, Preetiva B, Patel M, Singsit JS, Pittman CU Jr, Mohan D ACS Omega 04-Mar-2024
PMCID:PMC10955718
doi:10.1021/acsomega.3c07804
PMID:38524436
Quantifying the Impact of Different Dietary Rumen Modulating Strategies on Enteric Methane Emission and Productivity in Ruminant Livestock: A Meta-Analysis Pepeta BN, Hassen A, Tesfamariam EH Animals (Basel) 29-Feb-2024
PMCID:PMC10931330
doi:10.3390/ani14050763
PMID:38473148
Chemical Properties, Ruminal Fermentation, Gas Production and Digestibility of Silages Composed of Spineless Cactus and Tropical Forage Plants for Sheep Feeding Godoi PF, Magalhães AL, de Araújo GG, de Melo AA, Silva TS, Gois GC, dos Santos KC, do Nascimento DB, da Silva PB, de Oliveira JS, Santos EM, da Silva TG, Zanine AD, Ferreira DD, Voltolini TV, Campos FS Animals (Basel) 07-Feb-2024
PMCID:PMC10886150
doi:10.3390/ani14040552
PMID:38396518
Understanding how management can prevent degradation of the structurally fragile soils of the Amazonian periphery Freitas Nunes JD, Campos LS, Ferreira Aguiar AD, Mooney SJ, Pimentel KA, Gomes de Moura E Eur J Agron 01-Feb-2024
PMCID:PMC10788771
doi:10.1016/j.eja.2023.127037
PMID:38304224
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
In Vitro Analysis of the Antagonistic Biological and Chemical Interactions between the Endophyte Sordaria tomento-alba and the Phytopathogen Botrytis cinerea Bolívar-Anillo HJ, Izquierdo-Bueno I, González-Rey E, González-Rodríguez VE, Cantoral JM, Collado IG, Garrido C Int J Mol Sci 13-Jan-2024
PMCID:PMC10816056
doi:10.3390/ijms25021022
PMID:38256097
Fermentation Profile, Aerobic Stability, and Chemical and Mineral Composition of Cactus Pear Silages with Different Inclusion Levels of Gliricidia Hay de Sá MK, de Andrade AP, de Araújo GG, Magalhães AL, Araújo CD, Valença RD, de Macedo A, Oliveira AR, Zanine AD, Ferreira DD, Negrão FD, da Silva TG, Campos FS, Gois GC Plants (Basel) 11-Jan-2024
PMCID:PMC10821388
doi:10.3390/plants13020195
PMID:38256748

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown https://doi.org/10.1007/BF00982301
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00982301
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1007/BF00982301
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1007/BF00982301
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1007/BF00982301
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/BF00982301
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
Coniferaldehyde 5280536 Click to see 178.18 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1016/S0367-326X(00)00219-7
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
> 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,10R,12aS,14aR,14bR)-10-[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-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]-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 163013225 Click to see 985.10 unknown https://doi.org/10.1021/JF9808731
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,10R,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-9-oxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 162932995 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1OC6C(C(C(C(O6)CO)O)O)O)C)C)C)(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(CO8)O)O)O)C)C 943.10 unknown https://doi.org/10.1021/JF9808731
3,4-dihydroxy-6-[[4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-9-oxo-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 162932994 Click to see 943.10 unknown https://doi.org/10.1021/JF9808731
6-[[10-[6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-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]-3,4-dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 163013224 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(=O)C3(CCC4(C(=CCC5C4(CCC6C5(CCC(C6(C)CO)OC7C(C(C(C(O7)C(=O)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C3CC2(C)C)C)C)O)O)O 985.10 unknown https://doi.org/10.1021/JF9808731
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-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 162932117 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5R)-4,5-diacetyloxy-3-hydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-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 162924125 Click to see 967.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5R)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-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 162914328 Click to see 925.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-4,5-diacetyloxy-3-hydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-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 162924124 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O 967.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bR)-10-[(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-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 44583924 Click to see 751.00 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
10-[3-[4-(4,5-Diacetyloxy-3-hydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-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 16196966 Click to see 967.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
10-[3-[4-(5-Acetyloxy-3,4-dihydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-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 74029772 Click to see 925.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-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 267360 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O 751.00 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0367-326X(00)00219-7
CID 15625347 15625347 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown https://doi.org/10.1016/S0031-9422(97)00977-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1016/S0367-326X(00)00219-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1055/S-2006-962717
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 163185183 Click to see 328.31 unknown https://doi.org/10.1021/JF9808731
3-[3-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid 162961821 Click to see 328.31 unknown https://doi.org/10.1021/JF9808731
methyl 3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 102352958 Click to see 314.29 unknown https://doi.org/10.1021/JF9808731
Methyl 3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 56664266 Click to see COC(=O)C1=CC(=CC=C1)OC2C(C(C(C(O2)CO)O)O)O 314.29 unknown https://doi.org/10.1021/JF9808731
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3'-Hydroxycinnamic acid 637541 Click to see C1=CC(=CC(=C1)O)C=CC(=O)O 164.16 unknown https://doi.org/10.1007/BF00982301
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1007/BF00982301
O-Coumaric Acid 637540 Click to see 164.16 unknown https://doi.org/10.1007/BF00982301
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1007/BF00982301
Sinapinic acid 1549091 Click to see 224.21 unknown https://doi.org/10.1007/BF00982301
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1007/BF00982301
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Robinetin 5281692 Click to see 302.23 unknown https://doi.org/10.1021/JF60212A034
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-2-[4-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxyphenyl]-5-hydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163106881 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3CC(=O)C4=C(O3)C=CC(=C4O)CC=C(C)C)OC5C(C(C(CO5)O)O)O)O)O 602.60 unknown https://doi.org/10.1016/S0367-326X(00)00219-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102006884 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)OC7C(C(C(C(O7)C)O)O)O)O)O)O)O)O 886.80 unknown https://doi.org/10.1021/JF9808731
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162948745 Click to see 886.80 unknown https://doi.org/10.1021/JF9808731
3-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978113 Click to see 886.80 unknown https://doi.org/10.1021/JF9808731
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/10.1021/JF9808731
Kaempferol 3-rutinosyl 7-O-alpha-L-rhamnoside 21676297 Click to see 740.70 unknown https://doi.org/10.1021/JF9808731
Robinin 5281693 Click to see 740.70 unknown https://doi.org/10.1021/JF9808731
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Medicarpin 73067 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
https://doi.org/10.1021/JF9808731
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/JF9808731
https://doi.org/10.1016/S0031-9422(97)00517-7
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/JF9808731
https://doi.org/10.1016/S0031-9422(97)00517-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
(3R)-7,4'-Dihydroxy-2'-methoxyisoflavan 51537108 Click to see COC1=C(C=CC(=C1)O)C2CC3=C(C=C(C=C3)O)OC2 272.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
Isovestitol 591830 Click to see 272.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
(3R)-3-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 162894075 Click to see COC1=C(C=CC(=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
https://doi.org/10.1021/JF9808731
3'-O-Methylequol 131753179 Click to see COC1=C(C=CC(=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
4',7-Dihydroxy-3'-methoxyisoflavan 10802120 Click to see 272.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
https://doi.org/10.1021/JF9808731
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol 177149 Click to see 272.29 unknown https://doi.org/10.1021/JF9808731
(3R)-3-(2,4-dimethoxyphenyl)chroman-7-ol 90658537 Click to see 286.32 unknown https://doi.org/10.1021/NP980002L
3-(2,4-Dimethoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol 596401 Click to see 286.32 unknown https://doi.org/10.1021/NP980002L
Sativan 170570 Click to see 286.32 unknown https://doi.org/10.1021/NP980002L
Vestitol 92503 Click to see 272.29 unknown https://doi.org/10.1021/JF9808731
https://doi.org/10.1021/NP980002L
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1021/JF9808731
https://doi.org/10.1021/NP980002L
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
2'-O-Methylsepiol 44257526 Click to see 300.30 unknown https://doi.org/10.1021/JF60212A034
Sepiol 44257524 Click to see 286.28 unknown https://doi.org/10.1021/JF60212A034
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin 5281704 Click to see 298.29 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1016/S0031-9422(97)00517-7
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
(6aR,12R,12aR)-12-[5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2-methoxyphenyl]-3-methoxy-6a,12-dihydro-6H-chromeno[2,3-c]chromene-9,12a-diol 163045764 Click to see 554.60 unknown https://doi.org/10.1021/NP980002L
12-[5-(7-hydroxy-3,4-dihydro-2H-chromen-3-yl)-2-methoxyphenyl]-3-methoxy-6a,12-dihydro-6H-chromeno[2,3-c]chromene-9,12a-diol 85183418 Click to see 554.60 unknown https://doi.org/10.1021/NP980002L
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(6aR,12aR)-9,12a-dihydroxy-3-methoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 10757612 Click to see 314.29 unknown https://doi.org/10.1021/NP980002L
2-Methoxygliricidol 10593523 Click to see 344.30 unknown https://doi.org/10.1021/NP980002L
9,12a-Dihydroxy-2,3-dimethoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 85198144 Click to see 344.30 unknown https://doi.org/10.1021/NP980002L
9,12a-Dihydroxy-3-methoxy-6,6a-dihydrochromeno[3,4-b]chromen-12-one 85257611 Click to see 314.29 unknown https://doi.org/10.1021/NP980002L
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(3S)-3-(3,5-dihydroxy-4-methoxyphenyl)-1-(2,4-dihydroxyphenyl)-3-hydroxypropan-1-one 163019391 Click to see 320.29 unknown https://doi.org/10.1016/S0031-9422(00)91473-0
3-(3,5-Dihydroxy-4-methoxyphenyl)-1-(2,4-dihydroxyphenyl)-3-hydroxypropan-1-one 42607727 Click to see COC1=C(C=C(C=C1O)C(CC(=O)C2=C(C=C(C=C2)O)O)O)O 320.29 unknown https://doi.org/10.1016/S0031-9422(00)91473-0

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