Details Top

Internal ID UUID643fd9a15d01b452335522
Scientific name Sophora tonkinensis
Authority Gagnep.
First published in Notul. Syst. (Paris)3: 18 (1914)

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.

Sophora tonkinensis, known in Chinese medicine as “Suan Zhi,” has a long history of use as an inhalation and oral remedy. According to the Chinese Pharmacopoeia (2020), the dried root is boiled to make a decoction that is taken for cough, asthma, and as a mild diuretic. In Vietnam, Nguyen et al. (2018) report that the root is also used in a poultice to treat superficial wounds and skin inflammation, while a leaf infusion is drunk to relieve stomach upset. A 2019 ethnobotanical survey of the Hmong people in northern Vietnam documented that the Hmong prepare a decoction of the root for respiratory ailments and apply a macerated leaf paste to bruises, citing the same therapeutic goals as the Chinese and Vietnamese traditions.

A simple, safe preparation is a root decoction. Take 10 g of dried Sophora tonkinensis root and add it to 200 ml of boiling water. Simmer gently for 30 minutes, then strain the liquid. Drink the clear tea in two 100 ml servings, preferably in the morning. This dose is well tolerated in most adults; however, pregnant women and individuals with a history of gastrointestinal sensitivity should avoid it, as higher doses can cause mild stomach upset. The decoction can be stored in the refrigerator for up to three days.

The therapeutic effects of Sophora tonkinensis are largely attributed to its alkaloid profile. The root contains matrine, oxymatrine, and sophoridine, all of which have been isolated and shown to possess anti‑inflammatory, antiviral, and anti‑tumor activities in laboratory studies. These compounds are consistent with the plant’s traditional use for respiratory inflammation and wound healing, providing a biochemical basis for the observed benefits.

Modern research continues to explore Sophora tonkinensis for its medicinal potential. Recent in‑vitro studies demonstrate that extracts rich in matrine and oxymatrine inhibit inflammatory cytokine production, while animal models confirm anti‑cancer effects against several tumor types. Commercially, standardized root extracts are available as dietary supplements in Asia, and the plant remains an active component in many traditional formulations used by Chinese, Vietnamese, and Hmong practitioners today.

General Uses Top

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Common products:
Root wood is the principal traded material of Sophora tonkinensis. Cuttings and chips are supplied to export processors for dye production, especially to Japan for natural dyeing of textiles, and to the United States for botanical color testing by craft and heritage textile researchers.

Industrial and craft applications:
The plant is used as a source of natural brown dyes. The dried root wood yields water-soluble colorants that produce warm brown to orange-brown shades on protein fibers (wool and silk) when used with common mordants such as aluminum, iron, and copper. Plant-part/form: root wood chips, roots, or bark; product type: natural brown dyes for textiles, natural brown inks and pigments for craft use.

Food and beverages (non-medicinal):
No non-medicinal food or beverage uses are documented for this species.

Colorants and tanning:
Root wood and bark contain flavonoids, isoflavonoids, and alkaloids. Extracts yield brown hues used for dyeing and as a basis for botanical inks. Dyeing is applied to wool, silk, and cotton (with mordanting) in craft and heritage contexts; the approach follows standard plant-dye protocols that specify mordant type, liquor ratio, and temperature for color reproducibility. Product type: natural brown dyes; plant-part/form: roots and bark; application class: brown dye for textiles, natural brown inks and pigments. No documented use as a tanning agent.

Wood and fiber:
The wood is small-diameter and used locally as fuel and for simple craft items; fiber use is not reported.

Fragrance and cosmetics:
No fragrance, perfume, or cosmetic uses are documented for this species.

Properties relevant to use:
The dye performance is attributed to flavonoids such as sophoricoside and kushenol I, and to quinolizidine alkaloids. Reported tinctorial strength is moderate and reddish-brown to golden-brown depending on mordant; solubility is high in hot water, enabling direct extract use without additional fixation.

Standards and regulation:
Dye exports are managed under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) due to conservation concerns, and shipments must carry CITES permits. In export markets, colorants are subject to general consumer product safety laws (e.g., consumer protection statutes) and to national restrictions on plant-derived colorants in food and cosmetics where applicable; no plant-specific standards are cited.

Sustainability and sourcing:
The species is harvested from wild populations in karst habitats of Guangxi, Guizhou, and northern Vietnam. Supply is constrained by habitat fragmentation, slow growth, and overharvest for the dye trade. There are no widely accepted domestic or international standards for S. tonkinensis dye quality or sustainability. Sustainable practices focus on selective harvesting, habitat protection in karst reserves, and the development of cultivation or ex situ propagation to reduce pressure on wild stocks.

Synonyms Top

Scientific name Authority First published in
Cephalostigmaton tonkinensis (Gagnep.) Yakovlev Trudy Leningradsk. Khim.-Farm. Inst.21: 47 (1967)
Cephalostigmaton tonkinense (Gagnep.) Yakovlev

Common names Top

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Language Common/alternative name
Vietnamese hòe bắc bộ
za lagdujbyaj
Chinese 山豆根
Chinese 柔枝槐
Chinese 越南槐
Chinese 越南槐(广豆根、柔枝槐)
Chinese 广豆根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Sophora tonkinensis var. polyphylla X.C.Huang & Z.C.Zhou Acta Phytotax. Sin.22: 487 (1984)
Sophora tonkinensis var. purpurascens C.Y.Ma Acta Phytotax. Sin.20: 469 (1982)
Sophora tonkinensis var. tonkinensis Gagnep. Unknown

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186509
UNII WL8G39B4EA
Tropicos 13044678
KEW urn:lsid:ipni.org:names:518956-1
The Plant List ild-32975
Open Tree Of Life 434824
NCBI Taxonomy 714503
IPNI 518956-1
iNaturalist 127035
GBIF 2958966
Freebase /m/0c3wnjn
EOL 643998
USDA GRIN 423551
Wikipedia Sophora_tonkinensis
CMAUP NPO7715

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
Oxymatrine Modulation of TLR3 Signaling: A Dual-Action Mechanism for H9N2 Avian Influenza Virus Defense and Immune Regulation Zhi Y, Zhao X, Liu Z, Shen G, Zhang T, Zhang T, Hu G Molecules 24-Apr-2024
PMCID:PMC11085666
doi:10.3390/molecules29091945
PMID:38731436
Bacteria from nodules of Abrus mollis Hance: genetic diversity and screening of highly efficient growth-promoting strains Cao K, Chen J, Li Q, Gu P, Li L, Huang R Front Microbiol 12-Apr-2024
PMCID:PMC11045970
doi:10.3389/fmicb.2024.1345000
PMID:38680912
The complete chloroplast genome sequence of Ammodendron bifolium (Fabaceae), an endangered desert shrub from China Tian H, Zhu X, Qiu J, Zhang H, Shi X Mitochondrial DNA B Resour 03-Mar-2024
PMCID:PMC10913713
doi:10.1080/23802359.2024.2324922
PMID:38450410
Structures and Biological Activities of Secondary Metabolites from Xylaria spp. Chen W, Yu M, Chen S, Gong T, Xie L, Liu J, Bian C, Huang G, Zheng C J Fungi (Basel) 29-Feb-2024
PMCID:PMC10971283
doi:10.3390/jof10030190
PMID:38535199
The effect of novel nitrogen-based chalcone analogs on colorectal cancer cells: Insight into the molecular pathways Hassan AF, Hussein O, Al-Barazenji T, Allouch A, Kamareddine L, Malki A, Moustafa AA, Khalil A Heliyon 27-Feb-2024
PMCID:PMC10923686
doi:10.1016/j.heliyon.2024.e27002
PMID:38463818
Austin-Type Meroterpenoids from Fungi Reported in the Last Five Decades: A Review He JL, Chen CJ, Liu YH, Gao CH, Wang RP, Zhang WF, Bai M J Fungi (Basel) 19-Feb-2024
PMCID:PMC10890278
doi:10.3390/jof10020162
PMID:38392834
Endophytic Alternaria and Fusarium species associated to potato plants (Solanum tuberosum L.) in Iran and their capability to produce regulated and emerging mycotoxins Alijani Mamaghani N, Masiello M, Somma S, Moretti A, Saremi H, Haidukowski M, Altomare C Heliyon 15-Feb-2024
PMCID:PMC10907534
doi:10.1016/j.heliyon.2024.e26385
PMID:38434378
Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review Rungjindamai N, Jones EB J Fungi (Basel) 15-Jan-2024
PMCID:PMC10820240
doi:10.3390/jof10010067
PMID:38248976
Isolation and Characterization of Antimicrobial Metabolites from the Sophora tonkinensis-Associated Fungus Penicillium sp. GDGJ-N37 Huang L, Li Y, Pang J, Lv L, Zhou J, Liang L, He X, Li J, Xu W, Yang R Molecules 10-Jan-2024
PMCID:PMC10818566
doi:10.3390/molecules29020348
PMID:38257261
Biochar and organic fertilizer drive the bacterial community to improve the productivity and quality of Sophora tonkinensis in cadmium-contaminated soil Liu H, Li C, Lin Y, Chen YJ, Zhang ZJ, Wei KH, Lei M Front Microbiol 08-Jan-2024
PMCID:PMC10800516
doi:10.3389/fmicb.2023.1334338
PMID:38260912
Correction: An integrated characterization of contractile, electrophysiological and structural cardiotoxicity of Sophora tonkinensis Gapnep. in human pluripotent stem cell-derived cardiomyocytes Wang R, Wang M, Wang S, Yang K, Zhou P, Xie X, Cheng Q, Ye J, Sun G, Sun X Stem Cell Res Ther 31-Oct-2023
PMCID:PMC10617065
doi:10.1186/s13287-023-03540-z
PMID:37904217
Matrine and Oxymatrine: evaluating the gene mutation potential using in silico tools and the bacterial reverse mutation assay (Ames test) Fischer BC, Musengi Y, König J, Sachse B, Hessel-Pras S, Schäfer B, Kneuer C, Herrmann K Mutagenesis 25-Oct-2023
PMCID:PMC10851102
doi:10.1093/mutage/gead032
PMID:37877816
Pharmacological Activity of Matrine in Inhibiting Colon Cancer Cells VM Formation, Proliferation, and Invasion by Downregulating Claudin-9 Mediated EMT Process and MAPK Signaling Pathway Du Q, Lin Y, Ding C, Wu L, Xu Y, Feng Q Drug Des Devel Ther 11-Sep-2023
PMCID:PMC10504061
doi:10.2147/DDDT.S417077
PMID:37719361
Identification, Formation, and Occurrence of Perlolyrine: A β-Carboline Alkaloid with a Furan Moiety in Foods Herraiz T, Peña A, Salgado A J Agric Food Chem 31-Aug-2023
PMCID:PMC10510388
doi:10.1021/acs.jafc.3c03612
PMID:37651628
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity Cely-Veloza W, Kato MJ, Coy-Barrera E ACS Omega 28-Jul-2023
PMCID:PMC10413377
doi:10.1021/acsomega.3c02179
PMID:37576649

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 / Lupin alkaloids / Aloperine and related alkaloids
(1S,2S,9R,10R)-3,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadec-7-ene 442937 Click to see 232.36 unknown https://doi.org/10.1016/S0021-9673(99)00758-X
(6R,7R,9R,11S)-16,17-Didehydro-9-de-2-piperidinylormosanine 139055730 Click to see 232.36 unknown https://doi.org/10.1016/S0021-9673(99)00758-X
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see 260.33 unknown https://doi.org/10.1248/CPB.47.448
12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 621307 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1248/CPB.47.448
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.44.1951
1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 22407 Click to see 190.24 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
https://doi.org/10.1055/S-2006-946639
Caulophylline 234566 Click to see 204.27 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1055/S-2006-946639
Cytisine 10235 Click to see 190.24 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
https://doi.org/10.1055/S-2006-946639
Cytisine, N-formyl- 589870 Click to see 218.25 unknown https://doi.org/10.1248/CPB.44.1951
N-Formylcytisine 179619 Click to see 218.25 unknown https://doi.org/10.1248/CPB.44.1951
N-Methylcytisine 670971 Click to see 204.27 unknown https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1248/CPB.44.1951
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-14beta-Hydroxymatrine 10659287 Click to see 264.36 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1021/ACS.JNATPROD.5B00325
(-)-Sophocarpine 115269 Click to see 246.35 unknown https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1021/ACS.JNATPROD.5B00325
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see 262.35 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
(+)-Matrine, 519-02-8 86573029 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
(+)-Sophoranol 12442899 Click to see 264.36 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1248/CPB.44.1951
(13S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 137705180 Click to see 264.36 unknown https://doi.org/10.1002/PCA.829
(1R,2R,5R,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 15385683 Click to see 264.36 unknown https://doi.org/10.1248/CPB.47.448
(1R,2R,5S,9S,17S)-5-hydroxy-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 12000482 Click to see 280.36 unknown via CMAUP database
(1R,2R,9R,17R)-9-hydroxy-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 15385685 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)(CN2C(=O)C1)O)[O-] 280.36 unknown via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
(1R,2S,3R,9S,17S)-3-hydroxy-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 122181685 Click to see C1CC2CN3C(C4C2[N+](C1)(CCC4)[O-])C(C=CC3=O)O 278.35 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
(1S,2S,3R,9S,17S)-3-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133309 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
(6-Oxo-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-5-yl) acetate 85223743 Click to see 306.40 unknown https://doi.org/10.1248/CPB.47.448
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one 7000681 Click to see 248.36 unknown https://doi.org/10.1248/CPB.44.1951
[(1R,2R,5R,9S,17S)-6-oxo-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-5-yl] acetate 10662446 Click to see CC(=O)OC1CCC2C3CCCN4C3C(CCC4)CN2C1=O 306.40 unknown https://doi.org/10.1248/CPB.47.448
[(1R,2R,5S,9S,17S)-6-oxo-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-5-yl] acetate 10757050 Click to see CC(=O)OC1CCC2C3CCCN4C3C(CCC4)CN2C1=O 306.40 unknown https://doi.org/10.1248/CPB.47.448
5-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 78385079 Click to see 264.36 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
5alpha-Hydroxysophocarpine 15385686 Click to see 262.35 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1021/ACS.JNATPROD.5B00325
5alpha,9alpha-Dihydroxymatrine 14274649 Click to see 280.36 unknown https://doi.org/10.1248/CPB.47.448
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 618867 Click to see 246.35 unknown https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1248/CPB.44.1951
9-Hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 162938515 Click to see 262.35 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
9,15-Dihydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 5316791 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown https://doi.org/10.1248/CPB.47.448
9alpha-Hydroxymatrine 15385684 Click to see 264.36 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
Ammothamnine 114850 Click to see 264.36 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1248/CPB.44.1951
Matridin-15-one 285698 Click to see 248.36 unknown https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1248/CPB.44.1951
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1248/CPB.44.1951
Matrine 91466 Click to see 248.36 unknown https://doi.org/10.1055/S-2006-946639
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1002/PCA.829
https://doi.org/10.1021/ACS.JNATPROD.5B00325
N-Oxysophocarpine 618688 Click to see 262.35 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1021/ACS.JNATPROD.5B00325
Oxymatrine 24864132 Click to see 264.36 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Oxysophocarpine 161544 Click to see 262.35 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
Sopharanol 619052 Click to see 264.36 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
https://doi.org/10.1055/S-2006-946639
Sophoranol-N-oxy 285668 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)(CN2C(=O)C1)O)[O-] 280.36 unknown https://doi.org/10.1248/CPB.47.448
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1007/BF02994750
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4R,5R,6R)-6-[[(3R,4R,4aS,6aS,6bR,8aS,9S,10S,12aR,14aS,14bS)-9,10-dihydroxy-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-[(2R,3S,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 163023053 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(C(C8O)O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 959.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
(2R,3R,4R,5S,6S)-6-[[(3S,4R,4aR,6aS,6bS,8aR,11R,12aR,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-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 162875850 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.40.139
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-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,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 102120183 Click to see 781.00 unknown https://doi.org/10.1016/0031-9422(92)80286-N
(2S,3S,4S,5R,6R)-6-[[(3S,4Ar,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-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 21629874 Click to see 927.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9S,10R,11R,12aS,14aR,14bR)-9,10-dihydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 163193991 Click to see 975.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
(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/10.1016/0031-9422(92)80286-N
(3beta,21beta,22beta)-21,22,24-trihydroxyolean-12-en-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->2)-beta-D-glucopyranosiduronic acid 101987000 Click to see 959.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
21,22,23-Trihydroxyolean-12-en-3-yl 6-deoxyhexopyranosyl-(1->2)hexopyranosyl-(1->2)hexopyranosiduronic acid 188847 Click to see 959.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
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.40.139
6-[[9,10-Dihydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-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 162885289 Click to see 975.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
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/10.1016/0031-9422(92)80286-N
Kaikasaponin II 101538997 Click to see 927.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
kaikasaponin III 188384 Click to see 927.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-9-hydroxy-4,4,6a,6b,8a,11,14b-heptamethyl-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]-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-carboxylate 101635383 Click to see 1119.30 unknown https://doi.org/10.1248/CPB.40.1831
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,9S,10R,11R,12aS,14aR,14bR)-9,10-dihydroxy-11-(hydroxymethyl)-4,4,6a,6b,8a,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,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-carboxylate 162983733 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(C(C8O)O)(C)CO)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 973.10 unknown https://doi.org/10.1248/CPB.40.139
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-9-oxo-11-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-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-carboxylate 162910239 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)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1133.30 unknown https://doi.org/10.1248/CPB.40.139
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,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]-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-carboxylate 101635385 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)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1135.30 unknown https://doi.org/10.1248/CPB.40.1831
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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,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-carboxylate 162979859 Click to see 1251.40 unknown https://doi.org/10.1248/CPB.40.1831
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9S,10R,11R,12aS,14aR,14bR)-9,10-dihydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-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-carboxylate 163039030 Click to see 959.10 unknown https://doi.org/10.1248/CPB.40.139
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9S,10R,11S,12aS,14aR,14bR)-9-hydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-10-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-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-carboxylate 101635387 Click to see 1135.30 unknown https://doi.org/10.1248/CPB.40.1831
methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[4-(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-9-oxo-11-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4a,5,6,7,8,10,12,12a,14,14a-dodecahydro-1H-picen-3-yl]oxy]oxane-2-carboxylate 162910238 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)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1133.30 unknown https://doi.org/10.1248/CPB.40.139
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,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]oxane-2-carboxylate 85138198 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)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1135.30 unknown https://doi.org/10.1248/CPB.40.1831
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[9-hydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-10-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]oxane-2-carboxylate 85112385 Click to see 1135.30 unknown https://doi.org/10.1248/CPB.40.1831
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[9-hydroxy-4,4,6a,6b,8a,11,14b-heptamethyl-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]oxane-2-carboxylate 85150703 Click to see 1119.30 unknown https://doi.org/10.1248/CPB.40.1831
Methyl 5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-[[9-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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]-3,4-dihydroxyoxane-2-carboxylate 73817534 Click to see 1251.40 unknown https://doi.org/10.1248/CPB.40.1831
Methyl 6-[[9,10-dihydroxy-11-(hydroxymethyl)-4,4,6a,6b,8a,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-carboxylate 162983732 Click to see 973.10 unknown https://doi.org/10.1248/CPB.40.139
Methyl 6-[[9,10-dihydroxy-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 163039029 Click to see 959.10 unknown https://doi.org/10.1248/CPB.40.139
Soyasaponin I 122097 Click to see 943.10 unknown https://doi.org/10.1016/0031-9422(92)80286-N
Soyasaponin II 443614 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/10.1016/0031-9422(92)80286-N
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02994750
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(2S,3R,5R,8R,9S,10R,13R,14R,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 101297731 Click to see 466.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23R,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate 134145571 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C 575.70 unknown https://doi.org/10.1248/CPB.44.1951
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Terretrione B 71480633 Click to see CC(C)C1C(=O)N(C(=O)C(C(=O)N1C)CC2=CC=CC=C2)C 302.37 unknown https://doi.org/10.1002/HLCA.200690000
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine 169014 Click to see 244.33 unknown https://doi.org/10.1021/ACS.JNATPROD.5B00325
(9S,17S)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-1-en-6-one 127039206 Click to see 246.35 unknown https://doi.org/10.1248/CPB.44.1951
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-1-en-6-one 5316459 Click to see 246.35 unknown https://doi.org/10.1248/CPB.44.1951
> Organoheterocyclic compounds / Isobenzofurans
[(1S,5R,6R)-5-[[(1R,3aR,7R,7aS)-7-hydroxy-3a,7-dimethyl-3-oxo-4,5,6,7a-tetrahydro-1H-2-benzofuran-1-yl]methyl]-7-methylidene-4-oxo-6-bicyclo[3.2.1]oct-2-enyl] acetate 162904392 Click to see 388.50 unknown https://doi.org/10.1248/CPB.44.1951
https://doi.org/10.1248/CPB.47.448
> Organoheterocyclic compounds / Quinolizines
1-[[(1R,8AR)-2,3,4,5,6,7,8,8A-Octahydro-1H-quinolizin-1-YL]methyl]pipe ridine-2,6-dione 586638 Click to see 264.36 unknown https://doi.org/10.1248/CPB.47.448
Lamprolobine 87752 Click to see 264.36 unknown https://doi.org/10.1248/CPB.47.448
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2',4'-Dihydroxy-5,6-methylenedioxy-2-phenylbenzofuran 10265117 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
E-Caffeic acid pentyl ester 15086370 Click to see 250.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162848646 Click to see 458.60 unknown https://doi.org/10.1248/CPB.17.1299
(2S)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 11648289 Click to see CC(=CCC1=CC(=CC2=C1OC(CC2)(C)C)C3CC(=O)C4=C(O3)C(=C(C=C4)O)CC=C(C)C)C 460.60 unknown https://doi.org/10.1002/HLCA.200690000
(2S)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 11525453 Click to see 460.60 unknown https://doi.org/10.1002/HLCA.200690000
(2S)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 5321396 Click to see 458.60 unknown https://doi.org/10.1002/MRC.2274
https://doi.org/10.1248/CPB.17.1299
https://doi.org/10.1016/S1875-5364(13)60081-3
(2S)-2-[8-(3-ethoxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydrochromen-6-yl]-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 23730796 Click to see 506.70 unknown https://doi.org/10.1002/HLCA.200790232
(2S)-2-[8-(3-hydroxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydrochromen-6-yl]-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 23730688 Click to see 478.60 unknown https://doi.org/10.1002/HLCA.200790232
(2S)-7-hydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163005225 Click to see 406.50 unknown https://doi.org/10.1248/CPB.21.1777
(2S)-7-hydroxy-2-[(2R)-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162886639 Click to see 476.60 unknown https://doi.org/10.1248/CPB.21.1436
(2S)-7-hydroxy-2-[(2S)-2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162886637 Click to see CC(=CCC1=CC(=CC2=C1OC(C2)C(C)(C)O)C3CC(=O)C4=C(O3)C(=C(C=C4)O)CC=C(C)C)C 476.60 unknown https://doi.org/10.1002/MRC.2274
(2S)-7-hydroxy-2-[(3R)-3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162955337 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
(2S)-7-hydroxy-2-[2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 73296637 Click to see 476.60 unknown https://doi.org/10.1021/NP5002016
(2S)-7-hydroxy-2-[3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101905252 Click to see CC(=CCC1=CC(=CC2=C1OC(C(C2)O)(C)C)C3CC(=O)C4=C(O3)C(=C(C=C4)O)CC=C(C)C)C 476.60 unknown https://doi.org/10.1021/NP5002016
(2S)-7-hydroxy-2-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162893050 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
(2S)-7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2,3-dihydrochromen-4-one 162863732 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
(2S)-7-hydroxy-2-[8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2,2-dimethylchromen-6-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162843373 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC4=C(C(=C3)CC(C(=C)C)O)OC(C=C4)(C)C)O)C 474.60 unknown https://doi.org/10.1002/MRC.2274
(8S)-8-(2,4-dihydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 137634307 Click to see 406.50 unknown https://doi.org/10.1248/CPB.21.1192
(S)-2,3-Dihydro-7-hydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one 45267937 Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(CC2=O)C3=CC=C(C=C3)O)C 392.50 unknown https://doi.org/10.1248/CPB.21.1777
(S)-4',7-Dihydroxy-3',8-diprenylflavanone 480768 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)O)C 392.50 unknown via CMAUP database
2-(3-Hydroxy-2,2-dimethyl-8-isopentenyl-6-chromanyl)-7-hydroxy-8-isopentenyl-4-chromanone 53355717 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
2-(4-Hydroxyphenyl)-5-hydroxy-2,3-dihydro-10-(3-methyl-2-butenyl)-8,8-dimethyl-4H,8H-benzo[1,2-b:5,4-b']dipyran-4-one 13846826 Click to see CC(=CCC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 406.50 unknown via CMAUP database
2-[2,2-Dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-7-hydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 53355819 Click to see CC(=CCC1=CC(=CC2=C1OC(CC2)(C)C)C3CC(=O)C4=C(O3)C(=C(C=C4)O)CC=C(C)C)C 460.60 unknown https://doi.org/10.1002/HLCA.200690000
2-[2,2-Dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 72994627 Click to see CC(=CCC1=CC(=CC2=C1OC(CC2)(C)C)C3CC(=O)C4=C(O3)C5=C(C=C4)OC(CC5)(C)C)C 460.60 unknown https://doi.org/10.1002/HLCA.200690000
7-Hydroxy-2-[2-(2-hydroxypropan-2-yl)-7-(3-methylbut-2-enyl)-2,3-dihydro-1-benzofuran-5-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162886636 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
7-Hydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162893049 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)CC(C(=C)C)O)O)C 476.60 unknown https://doi.org/10.1002/MRC.2274
7-Hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(2-hydroxy-3-methylbut-3-enyl)-2,3-dihydrochromen-4-one 162863729 Click to see 476.60 unknown https://doi.org/10.1002/MRC.2274
7-Hydroxy-2-[8-(2-hydroxy-3-methylbut-3-enyl)-2,2-dimethylchromen-6-yl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162843372 Click to see 474.60 unknown https://doi.org/10.1002/MRC.2274
Glabrol 11596309 Click to see 392.50 unknown via CMAUP database
Kurarinone 11982640 Click to see 438.50 unknown via CMAUP database
Kurarinone 10812923 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
Kurarinone [M+H]+ 5318882 Click to see 438.50 unknown via CMAUP database
Lupinifolin 10250777 Click to see 406.50 unknown via CMAUP database
Sophoranochromene 42607818 Click to see 458.60 unknown https://doi.org/10.1002/MRC.2274
Sophoranon 4482007 Click to see 460.60 unknown https://doi.org/10.1016/S1875-5364(13)60081-3
https://doi.org/10.1002/IJC.10414
https://doi.org/10.3109/00498254.2015.1041181
https://doi.org/10.1002/MRC.2274
Sophoranone 441767 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C(=C(C=C3)O)CC=C(C)C)C 460.60 unknown https://doi.org/10.1016/S1875-5364(13)60081-3
https://doi.org/10.1002/MRC.2274
https://doi.org/10.1021/NP5002016
https://doi.org/10.1016/0305-1978(95)00056-9
https://doi.org/10.3109/00498254.2015.1041181
https://doi.org/10.1002/IJC.10414
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-Prenylkaempferol 5318624 Click to see 354.40 unknown via CMAUP database
Dehydrolupinifolinol 16215899 Click to see 420.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
7-hydroxy-2-(4-hydroxyphenyl)-8-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 133556538 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1021/NP50046A014
CID 44257570 44257570 Click to see 562.50 unknown https://doi.org/10.1021/NP50046A014
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
7-hydroxy-2-[4-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 44257572 Click to see 416.40 unknown https://doi.org/10.1021/NP50046A014
Sophoraflavone B 5491513 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown https://doi.org/10.1021/NP50046A014
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown https://doi.org/10.1002/JSSC.201400691
https://doi.org/10.1016/J.TETLET.2008.04.003
https://doi.org/10.1007/BF02994750
(-)-Maackiain 3-O-glucoside 4485132 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
(+)-Maackiain 161298 Click to see 284.26 unknown via CMAUP database
(1R,9S)-11-[[(1R,12R)-16-hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-15-yl]methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 24898927 Click to see 486.50 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
(1R,9S)-11-[[(1R,12R)-16-hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-yl]methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 24898926 Click to see 486.50 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
(6aR,11aR)-pterocarpan 13577737 Click to see 224.25 unknown via CMAUP database
11-[(16-Hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-15-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 74348936 Click to see 486.50 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
11-[(16-Hydroxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 74335101 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)CC4=C(C=CC5=C4OCC6C5OC7=CC8=C(C=C67)OCO8)O 486.50 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see 284.26 unknown https://doi.org/10.1016/J.TETLET.2008.04.003
5,7,11,19-Tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl hydrogen sulfate 162886707 Click to see 364.30 unknown https://doi.org/10.1007/BF02994750
Pterocarpan 6451349 Click to see 224.25 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown https://doi.org/10.1007/BF02994750
https://doi.org/10.1016/J.TETLET.2008.04.003
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1248/YAKUSHI1947.90.4_463
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44257215 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF02994750
Ononin 442813 Click to see 430.40 unknown https://doi.org/10.1007/BF02994750
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3R,4R)-7,2'-dihydroxy-4'-methoxyisoflavanol 25202196 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2O)C=CC(=C3)O)O 288.29 unknown via CMAUP database
(3R)-7,2'-dihydroxy-4'-methoxyisoflavanol 23724655 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
8-O-Methylretusin 5319771 Click to see 298.29 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-3-[8-(3-ethoxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydrochromen-6-yl]-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 101457405 Click to see 506.70 unknown https://doi.org/10.1002/HLCA.200790232
3-[2,2-Dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 163020461 Click to see 458.60 unknown https://doi.org/10.1002/HLCA.200690000
3-[8-(3-Ethoxy-3-methylbutyl)-2,2-dimethyl-3,4-dihydrochromen-6-yl]-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 162978951 Click to see CCOC(C)(C)CCC1=CC(=CC2=C1OC(CC2)(C)C)C=CC(=O)C3=C(C4=C(C=C3)OC(CC4)(C)C)O 506.70 unknown https://doi.org/10.1002/HLCA.200790232
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
6-(3-(2',4'-Dihydroxyphenyl)acryloyl)-7-hydroxy-2,2-dimethyl-8-(3-methyl-2-butenyl)-2H-benzopyran 42607547 Click to see 406.50 unknown https://doi.org/10.1248/YAKUSHI1947.90.4_459
Sophoradin 5321393 Click to see 460.60 unknown https://doi.org/10.1016/S1875-5364(13)60081-3
https://doi.org/10.1016/0305-1978(95)00056-9
Sophoradochromene 5321394 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C=CC(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C 458.60 unknown https://doi.org/10.1248/CPB.18.741
https://doi.org/10.1016/S1875-5364(13)60081-3

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