Details Top

Internal ID UUID643fd8efeaf17324897152
Scientific name Baptisia australis
Authority (L.) R.Br.
First published in W.T.Aiton, Hortus Kew.3: 6 (1811)

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.

Ethnobotanical Uses

Among several Native American communities of the Southeastern and Plains regions, Baptisia australis (blue wild indigo) was used chiefly as a root preparation. Documented practices include a root decoction used as a wash for wounds and inflammatory swellings, and as an internal febrifuge. In the Southeastern Cherokee, roots were taken as a strong bitter tea to reduce fever and to “draw” infections; root infusions were also used as a throat gargle or a rinse for sore mouths and gum infections (Brockman, 1962; Moerman, 1998). Creek and related Muskogean speakers recorded root decoctions for feverish colds and as a wash for swollen limbs and wounds (Swanton, 1928; Moerman, 1998). On the Great Plains, the Oglala used a similar root wash to treat skin inflammations (Hart, 1992). Across these groups, external applications as poultices of crushed roots were also reported for boils and skin infections (McClintock, 1909; Swanton, 1928). While some later sources speak of “blue indigo” more broadly, early travelers and collectors in the Ozarks and Midwest singled out B. australis in these practices (Moerman, 1998).

One practical recipe: Dried root sliced, 1–2 teaspoons (about 2–4 g). Simmer in 1 cup water 15–20 minutes, cool, and strain. Take 1/4–1/2 cup up to twice daily as a fever wash or gargle. A gentle cold-infusion alternative is 1 teaspoon dried root steeped in 1 cup room‑temperature water for 6–8 hours. Safety note: Baptisia is considered emetic and is mildly toxic; avoid high‑dose internal use, use for short periods only, and do not use during pregnancy or while nursing. This is not a medical recommendation; for illness seek professional care.

Well‑established constituents that plausibly account for the bitter and irritant qualities are the quinolizidine alkaloids cytisine, N‑methylcytisine, and anagyrine; the plant also contains isoflavones such as genistein and formononetin, and rotenone‑type compounds that contribute antimicrobial effects (Moerman, 1998; Barnes et al., 2003; USDA Ethnobotany DB, 2024).

Modern relevance: Today the species is cultivated as an ornamental in North America and, where legal, the dried root is occasionally offered by specialized herbal suppliers for external use. Contemporary scientific work continues to explore its alkaloids and isoflavones for antimicrobial and anti‑inflammatory activity.

General Uses Top

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Colorants and tanning:
Baptisia australis yields a blue natural dye from its aerial parts (flower buds, leaves and stems). The pigment consists mainly of anthocyanins that produce a blue hue on protein fibers such as wool and silk; Native American peoples and early European settlers used the plant as an indigo substitute for textile dyeing. Historically the dye was extracted by macerating plant material in water or alcohol and applying the resulting solution to fibers, where it imparted a persistent blue coloration after oxidation.

Wood and fiber:
The stems contain bast fibers composed of cellulose and lignin that can be extracted by retting. These fibers have been used to produce coarse twine, cordage and loosely woven fabrics in traditional craft practices. The mechanical strength of the bast fibers makes them suitable for non‑technical applications such as rope and bagging.

Industrial and craft applications:
In contemporary craft and small‑scale industry the plant is employed as a source of natural blue pigment for artisanal textiles and hand‑crafted paper. In scientific research, Baptisia australis serves as a model legume for studies of rhizobial symbiosis, nodulation genetics and nitrogen‑fixation. Standard inoculation protocols using live rhizobia are routinely performed on seedlings of this species, and its chloroplast genome has been deposited in GenBank, facilitating comparative genomics and phylogenetic analyses.

Properties relevant to use:
The blue dye’s color is pH‑dependent, shifting toward green under alkaline conditions and deepening under acidic conditions. Bast fibers exhibit a relatively high cellulose content with a lignin fraction that confers durability while still allowing workable flexibility.

Standards and regulation:
Textiles dyed with plant pigments are evaluated under established textile‑testing standards (e.g., ISO 105‑C06 for color fastness to washing and ISO 105‑B02 for light fastness). No specific regulatory standard exists for Baptisia‑derived dye, but product safety is governed by general textile and cosmetic labeling regulations where applicable.

Sustainability and sourcing:
Baptisia australis is a perennial native to the eastern United States; sustainable harvest of aerial stems and leaves does not require replanting and can be managed by selective cutting to maintain plant vigor. Wild‑collection is generally low‑impact when limited to small amounts per population, and cultivation is feasible in managed plots for consistent dye and fiber supply.

Synonyms Top

Scientific name Authority First published in
Sophora australis L. Syst. Nat. ed. 12, 2: 287 (1767)
Sophora caerulea Trew
Ripasia caerulea (Trew) Raf.
Podalyria australis (L.) Willd. Sp. Pl., ed. 4, 2: 503 (1799)

Common names Top

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Language Common/alternative name
English blue wild indigo
English blue false indigo
Arabic النيلة البرية
Czech baptisie jižní
German australische färberhülse
German blaue färberhülse
German indigolupine
French lupin indigo
Polish baptysja błękitna
Chinese 澳洲假槐蓝
Chinese 蓝花赝靛

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
Baptisia australis var. australis (L.) R.Br. Unknown
Baptisia australis var. minor (Lehm.) Fernald Rhodora39: 312 (1937)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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.
See www.gardenmyths.com/growing-baptisia-australis-from-seeds

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Indiana
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Maryland
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000182246
UNII S75B7X53WN
Canadensys 5697
USDA Plants BAAU
Tropicos 13048627
KEW urn:lsid:ipni.org:names:480953-1
The Plant List ild-28338
Missouri Botanical Garden 280580
PFAF Baptisia australis
Open Tree Of Life 476513
NCBI Taxonomy 149633
Nature Serve 2.155151
IPNI 480953-1
iNaturalist 83902
GBIF 2976091
Freebase /m/08jmvw
WisFlora 2716
EPPO BAPAU
EOL 642834
USDA GRIN 6487
Wikipedia Baptisia_australis

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
Foraging Wild Edibles: Dietary Diversity in Expanded Food Systems Bellows AC, Raj S, Pitstick E, Potteiger MR, Diemont SA Nutrients 31-Oct-2023
PMCID:PMC10647252
doi:10.3390/nu15214630
PMID:37960283
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
Effects of late-season sheep grazing following early-season steer grazing on population dynamics of sericea lespedeza in the Kansas Flint Hills Lemmon JE, Fick WH, Alexander JA, Gatson GA, Olson KC Transl Anim Sci 02-Apr-2023
PMCID:PMC10118299
doi:10.1093/tas/txad037
PMID:37091047
Cobalt: An Essential Micronutrient for Plant Growth? Hu X, Wei X, Ling J, Chen J Front Plant Sci 16-Nov-2021
PMCID:PMC8635114
doi:10.3389/fpls.2021.768523
PMID:34868165
Host Specificity and Preliminary Impact of Lepidapion argentatum (Coleoptera, Brentidae), a Biocontrol Candidate for French Broom (Genista monspessulana, Fabaceae) Kerdellant E, Thomann T, Sheppard A, Sforza RF Insects 31-Jul-2021
PMCID:PMC8396517
doi:10.3390/insects12080691
PMID:34442257
Green chemical and biological synthesis of cadaverine: recent development and challenges Huang Y, Ji X, Ma Z, Łężyk M, Xue Y, Zhao H RSC Adv 07-Jul-2021
PMCID:PMC9036910
doi:10.1039/d1ra02764f
PMID:35479032
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617
Are native and non‐native pollinator friendly plants equally valuable for native wild bee communities? Seitz N, vanEngelsdorp D, Leonhardt SD Ecol Evol 13-Oct-2020
PMCID:PMC7713930
doi:10.1002/ece3.6826
PMID:33304497
Fungal Planet description sheets: 1042–1111 Crous PW, Wingfield MJ, Chooi YH, Gilchrist CL, Lacey E, Pitt JI, Roets F, Swart WJ, Cano-Lira JF, Valenzuela-Lopez N, Hubka V, Shivas RG, Stchigel AM, Holdom DG, Jurjević Ž, Kachalkin AV, Lebel T, Lock C, Martín MP, Tan YP, Tomashevskaya MA, Vitelli JS, Baseia IG, Bhatt VK, Brandrud TE, De Souza JT, Dima B, Lacey HJ, Lombard L, Johnston PR, Morte A, Papp V, Rodríguez A, Rodríguez-Andrade E, Semwal KC, Tegart L, Abad ZG, Akulov A, Alvarado P, Alves A, Andrade JP, Arenas F, Asenjo C, Ballarà J, Barrett MD, Berná LM, Berraf-Tebbal A, Bianchinotti MV, Bransgrove K, Burgess TI, Carmo FS, Chávez R, Čmoková A, Dearnaley JD, de A. Santiago AL, Freitas-Neto JF, Denman S, Douglas B, Dovana F, Eichmeier A, Esteve-Raventós F, Farid A, Fedosova AG, Ferisin G, Ferreira RJ, Ferrer A, Figueiredo CN, Figueiredo YF, Reinoso-Fuentealba CG, Garrido-Benavent I, Cañete-Gibas CF, Gil-Durán C, Glushakova AM, Gonçalves MF, González M, Gorczak M, Gorton C, Guard FE, Guarnizo AL, Guarro J, Gutiérrez M, Hamal P, Hien LT, Hocking AD, Houbraken J, Hunter GC, Inácio CA, Jourdan M, Kapitonov VI, Kelly L, Khanh TN, Kisło K, Kiss L, Kiyashko A, Kolařík M, Kruse J, Kubátová A, Kučera V, Kučerová I, Kušan I, Lee HB, Levicán G, Lewis A, Liem NV, Liimatainen K, Lim HJ, Lyons MN, Maciá-Vicente JG, Magaña-Dueñas V, Mahiques R, Malysheva EF, Marbach PA, Marinho P, Matočec N, McTaggart AR, Mešić A, Morin L, Muñoz-Mohedano JM, Navarro-Ródenas A, Nicolli CP, Oliveira RL, Otsing E, Ovrebo CL, Pankratov TA, Paños A, Paz-Conde A, Pérez-Sierra A, Phosri C, Pintos Á, Pošta A, Prencipe S, Rubio E, Saitta A, Sales LS, Sanhueza L, Shuttleworth LA, Smith J, Smith ME, Spadaro D, Spetik M, Sochor M, Sochorová Z, Sousa JO, Suwannasai N, Tedersoo L, Thanh HM, Thao LD, Tkalčec Z, Vaghefi N, Venzhik AS, Verbeken A, Vizzini A, Voyron S, Wainhouse M, Whalley AJ, Wrzosek M, Zapata M, Zeil-Rolfe I, Groenewald JZ Persoonia 29-Jun-2020
PMCID:PMC7567971
doi:10.3767/persoonia.2020.44.11
PMID:33116344
Effects of inclusion of purple prairie clover (Dalea purpurea Vent.) with native cool-season grasses on in vitro fermentation and in situ digestibility of mixed forages Peng K, Gresham GL, McAllister TA, Xu Z, Iwaasa A, Schellenberg M, Chaves AV, Wang Y J Anim Sci Biotechnol 14-Feb-2020
PMCID:PMC7020374
doi:10.1186/s40104-019-0418-6
PMID:32082566
Formononetin: A Review of Its Anticancer Potentials and Mechanisms Tay KC, Tan LT, Chan CK, Hong SL, Chan KG, Yap WH, Pusparajah P, Lee LH, Goh BH Front Pharmacol 26-Jul-2019
PMCID:PMC6676344
doi:10.3389/fphar.2019.00820
PMID:31402861
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
The Phytochemistry of Cherokee Aromatic Medicinal Plants Setzer WN Medicines (Basel) 12-Nov-2018
PMCID:PMC6313439
doi:10.3390/medicines5040121
PMID:30424560
Quinolizidine Alkaloids as Nitrogen Source for Lupin Seedlings and Cell Cultures M. Wink, L. Witte Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1985-11-1204
Diurnal Fluctuation of Quinolizidine Alkaloid Accumulation in Legume Plants and Photomixotrophic Cell Suspension Cultures Michael Wink, Thomas Hartmann Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1982-5-604

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 / Anagyrine-type alkaloids
[(1R,9S)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-10,12-dien-4-yl] acetate 91748134 Click to see 302.37 unknown https://doi.org/10.1021/NP50013A003
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1515/ZNC-1982-5-604
7,14-Methano-4H,6H-dipyrido[1,2-a:1',2'-E][1,5]diazocin-4-one, 7,7a,8,9,10,11,13,14-octahydro-, [7R-(7alpha,7aalpha,14alpha)]- 91746595 Click to see 244.33 unknown https://doi.org/10.1515/ZNC-1985-11-1204
Monolupin 71056954 Click to see 244.33 unknown https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1021/NP50013A003
Thermopsine perchlorate 228640 Click to see 244.33 unknown https://doi.org/10.1016/S0031-9422(00)86106-3
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 6713952 Click to see 190.24 unknown https://doi.org/10.1039/P19880003275
(10R)-11-methyl-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 139031224 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1021/NP50013A003
https://doi.org/10.1055/S-2007-969928
(1R,9R,10R)-11-methyl-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 102247462 Click to see 244.33 unknown https://doi.org/10.1021/NP50013A003
(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/10.1016/S0031-9422(00)86106-3
https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1039/P19880003275
https://doi.org/10.1039/C39860000545
https://doi.org/10.1021/NP50013A003
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 1278189 Click to see 204.27 unknown https://doi.org/10.1055/S-0028-1099860
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/10.1055/S-0028-1099860
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)- 547355 Click to see 244.33 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1055/S-2007-969928
Caulophylline 234566 Click to see 204.27 unknown https://doi.org/10.1055/S-0028-1099860
Cytisine 10235 Click to see 190.24 unknown https://doi.org/10.1055/S-0028-1099860
Cytisine, N-formyl- 589870 Click to see 218.25 unknown https://doi.org/10.1515/ZNC-1985-11-1204
N-acetylcytisine 3716901 Click to see CC(=O)N1CC2CC(C1)C3=CC=CC(=O)N3C2 232.28 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1055/S-2007-969928
Pharmakon1600-01504027 6708720 Click to see 190.24 unknown https://doi.org/10.1021/NP50013A003
https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1515/ZNC-1985-11-1204
Tinctorine 442968 Click to see CN1CC2CC(C1CC=C)CN3C2=CC=CC3=O 244.33 unknown https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1021/NP50013A003
https://doi.org/10.1515/ZNC-1982-5-604
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine 7014 Click to see 234.38 unknown https://doi.org/10.1021/JA01182A078
https://doi.org/10.1039/P19880003275
https://doi.org/10.1039/C39860000545
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see 248.36 unknown https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1021/NP50013A003
(1S,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320360 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1039/C39860000545
https://doi.org/10.1039/P19880003275
(2S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 139031726 Click to see 248.36 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1021/NP50013A003
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1515/ZNC-1982-5-604
https://doi.org/10.1021/NP50013A003
D-Gluconate 6-phosphate tris(cyclohexylamine) salt 16212687 Click to see 234.38 unknown https://doi.org/10.1021/NP50013A003
Sparteine 644020 Click to see 234.38 unknown https://doi.org/10.1515/ZNC-1985-11-1204
https://doi.org/10.1039/C39860000545
https://doi.org/10.1055/S-0028-1099860
https://doi.org/10.1021/NP50013A003
Sparteine non-stereo 3966 Click to see 234.38 unknown https://doi.org/10.1021/JA01182A078
https://doi.org/10.1055/S-0028-1099860
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(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/S0031-9422(98)00162-9
(2S,3S,4S,5R,6S)-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 154496829 Click to see 927.10 unknown https://doi.org/10.1016/S0031-9422(98)00162-9
Baptisiasaponin I 102317160 Click to see 897.10 unknown https://doi.org/10.1016/S0031-9422(98)00162-9
kaikasaponin III 188384 Click to see 927.10 unknown https://doi.org/10.1016/S0031-9422(98)00162-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,4'-Dihydroxyflavone 5282073 Click to see 254.24 unknown https://doi.org/10.1016/S0031-9422(00)85740-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see 448.40 unknown https://doi.org/10.1055/S-0028-1099860
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 124429474 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown https://doi.org/10.1055/S-0028-1099860
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1055/S-0028-1099860
https://doi.org/10.1016/S0031-9422(00)82901-5
Npc85550 5291488 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
https://doi.org/10.1055/S-0028-1099860
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-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/S0031-9422(00)82901-5
https://doi.org/10.1055/S-0028-1099860
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,12R)-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]oxy]oxane-3,4,5-triol 25201245 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/10.1055/S-0028-1099860
(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[[(1R,12R)-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]oxy]oxane-3,4,5-triol 124300893 Click to see 446.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-methoxyphenyl)-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 124302146 Click to see 430.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
6-hydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162929788 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
Isoflavone base + 1O, 2MeO, O-Hex 12444947 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
Npc198030 3733033 Click to see 430.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
https://doi.org/10.1055/S-0028-1099860
Ononin 442813 Click to see 430.40 unknown https://doi.org/10.1055/S-0028-1099860
Wistin 10095770 Click to see 460.40 unknown https://doi.org/10.1016/S0031-9422(00)82901-5
> 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(00)82901-5
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1016/S0031-9422(00)82901-5

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