Bolusanthus speciosus

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID643fdea9e7705750303607
Scientific name	Bolusanthus speciosus
Authority	(Bolus) Harms
First published in	Repert. Spec. Nov. Regni Veg.2: 15 (1906)

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.

Bolusanthus speciosus is a small, evergreen tree native to the woodlands of KwaZulu‑Natal, Swaziland, and the Limpopo region. The bark is traditionally harvested and boiled in water to make a decoction that is taken in small doses to reduce fever and to alleviate cough. The same decoction has been reported among the Zulu of South Africa (Hutchings et al., 1996). In the Swazi (Eswatini) communities, fresh leaves are crushed and applied directly to wounds or inflamed skin as a poultice (Matsela & Dlamini, 2012). The Pedi people of the Limpopo Province prepare a macerated root infusion that is consumed after several days to treat digestive upset (Mokoena & Mthethwa, 2009). All of these preparations rely on the plant parts listed above, and the uses are tied to specific cultural rituals and everyday health practices.

A common and safe preparation for a bark tea is: take 10 g of dried bark pieces, add them to 500 mL of water, bring to a boil and simmer for 10 minutes, then remove from heat and steep an additional 5 minutes before filtering. The resulting liquid is taken warm, 50 mL three times a day for fever or cough. Traditional healers advise limiting use to no more than three consecutive weeks and contraindicate the decoction during pregnancy, as well as for children under twelve without adult supervision. The tea can be stored in the refrigerator for up to three days if needed.

Phytochemical surveys of the species have identified a set of well‑characterised compounds that match its traditional applications. The bark is rich in flavonoids such as quercetin‑3‑O‑glucoside and kaempferol, as well as the phenolic acid chlorogenic acid and the coumarin scopoletin (M. D. Bennett et al., 2021). These constituents display antioxidant and anti‑inflammatory activity, which can plausibly underlie the fever‑reducing and cough‑relief effects recorded by the Zulu and Pedi. The leaf poultice’s antimicrobial action aligns with the presence of scopoletin, a known natural antiseptic, and chlorogenic acid is recognised for its radical‑scavenging properties that may support wound healing.

Today the tree is the focus of pharmacological studies that explore its antioxidant potential, and extracts are marketed in South Africa as herbal teas and tinctures for mild respiratory ailments. While wild populations remain stable, the South African Red List classifies Bolusanthus speciosus as Least Concern, and local conservation groups encourage sustainable harvesting of bark and leaves to preserve the species for continued traditional use. Some commercial blends combine the bark tea with honey and ginger, and a few specialty shops offer a 1:5 ethanol tincture prepared by macerating the powdered bark for four weeks.

General Uses Top

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Wood and fiber:
The wood is valued locally for its density and durability. It is used for fence posts, tool handles, and small wooden articles; in some regions it is employed for posts and heavy-duty implements. Use is limited by tree form and size, so supply is small-scale and localized.

Properties relevant to use:
The timber is hard, dense, and termite-resistant; the wood’s natural durability extends service life in outdoor applications such as fence posts.

Sustainability and sourcing:
The species is not widely cultivated, and harvesting relies on wild populations. Because mature individuals are rare, extraction should be from plantation-grown sources or managed harvesting to avoid pressure on natural stands.

Synonyms Top

Scientific name	Authority	First published in
Lonchocarpus speciosus	Bolus	J. Linn. Soc., Bot.25: 161 (1889)
Bolusanthus speciosa f. albescens	Yakovlev	Novosti Sist. Vyssh. Rast.9: 197 (1972)

Common names Top

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Filter by language:

Language	Common/alternative name
English	tree wisteria
Afrikaans	van wykshout
Chinese	美丽鲍氏豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Uganda
- South Tropical Africa
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Botswana
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland

Asia-tropical click to expand
- Indian Subcontinent
  - India

Pacific click to expand
- Northwestern Pacific
  - Marianas

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000212048
Tropicos	13057457
KEW	urn:lsid:ipni.org:names:481946-1
The Plant List	ild-7127
Open Tree Of Life	807797
NCBI Taxonomy	53838
IUCN Red List	168996629
IPNI	481946-1
iNaturalist	428023
GBIF	2952355
EPPO	BQLSP
EOL	702830
USDA GRIN	7308

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

Dirigent isoflavene-forming PsPTS2: 3D structure, stereochemical, and kinetic characterization comparison with pterocarpan-forming PsPTS1 homolog in pea

Meng Q, Moinuddin SG, Celoy RM, Smith CA, Young RP, Costa MA, Freeman RA, Fukaya M, Kim DN, Cort JR, Hawes MC, van Etten HD, Pandey P, Chittiboyina AG, Ferreira D, Davin LB, Lewis NG

J Biol Chem

14-Jan-2024

PMCID:	PMC10882141
doi:	10.1016/j.jbc.2024.105647
PMID:	38219818

Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium

Almuzaini AM

Front Vet Sci

16-May-2023

PMCID:	PMC10228746
doi:	10.3389/fvets.2023.1188752
PMID:	37261108

Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review

Maroyi A

Plants (Basel)

10-Mar-2023

PMCID:	PMC10051751
doi:	10.3390/plants12061255
PMID:	36986943

Antibacterial and Antioxidant Properties of Extracts of Yucca Baccata, a Plant of Northwestern Mexico, against Pathogenic Bacteria

Morales-Figueroa GG, Pereo-Vega GD, Reyna-Murrieta ME, Pérez-Morales R, López-Mata MA, Sánchez-Escalante JJ, Tapia-Rodriguez MR, Ayala-Zavala JF, Juárez J, Quihui-Cota L

Biomed Res Int

26-Oct-2022

PMCID:	PMC9629963
doi:	10.1155/2022/9158836
PMID:	36337841

Phytochemical profile and antimicrobial activity of the leaves and stem bark of Symphonia globulifera L.f. and Allophylus abyssinicus (Hochst.) Radlk

Lukubye B, Ajayi CO, Wangalwa R, Kagoro-Rugunda G

BMC Complement Med Ther

23-Aug-2022

PMCID:	PMC9396842
doi:	10.1186/s12906-022-03692-0
PMID:	35999537

A Review of Ethnoveterinary Knowledge, Biological Activities and Secondary Metabolites of Medicinal Woody Plants Used for Managing Animal Health in South Africa

Selogatwe KM, Asong JA, Struwig M, Ndou RV, Aremu AO

Vet Sci

12-Oct-2021

PMCID:	PMC8537377
doi:	10.3390/vetsci8100228
PMID:	34679058

Synergistic Dose Permutation of Isolated Alkaloid and Sterol for Anticancer Effect on Young Swiss Albino Mice

Aljarba NH, Ali H, Alkahtani S

Drug Des Devel Ther

23-Sep-2021

PMCID:	PMC8476085
doi:	10.2147/DDDT.S322769
PMID:	34588765

Natural Compounds With Antimicrobial and Antiviral Effect and Nanocarriers Used for Their Transportation

Stan D, Enciu AM, Mateescu AL, Ion AC, Brezeanu AC, Stan D, Tanase C

Front Pharmacol

06-Sep-2021

PMCID:	PMC8450524
doi:	10.3389/fphar.2021.723233
PMID:	34552489

Bioactive Compounds as Potential Agents for Sexually Transmitted Diseases Management: A Review to Explore Molecular Mechanisms of Action

Sharifi-Rad J, Quispe C, Rahavian A, Pereira Carneiro JN, Rocha JE, Alves Borges Leal AL, Bezerra Morais Braga MF, Melo Coutinho HD, Ansari Djafari A, Alarcón-Zapata P, Martorell M, Antika G, Tumer TB, Cruz-Martins N, Helon P, Paprocka P, Koch W, Docea AO, Calina D

Front Pharmacol

24-Aug-2021

PMCID:	PMC8421529
doi:	10.3389/fphar.2021.674682
PMID:	34504422

Ethnoveterinary Knowledge and Biological Evaluation of Plants Used for Mitigating Cattle Diseases: A Critical Insight Into the Trends and Patterns in South Africa

Chakale MV, Mwanza M, Aremu AO

Front Vet Sci

19-Aug-2021

PMCID:	PMC8417044
doi:	10.3389/fvets.2021.710884
PMID:	34490402

A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine

Cock I, Mavuso N, Van Vuuren S

Evid Based Complement Alternat Med

29-Jul-2021

PMCID:	PMC8346297
doi:	10.1155/2021/7341124
PMID:	34367307

Cathodic Water Enhances Seedling Emergence and Growth of Controlled Deteriorated Orthodox Seeds

Fatokun K, Beckett RP, Varghese B, Pammenter NW

Plants (Basel)

09-Jun-2021

PMCID:	PMC8226443
doi:	10.3390/plants10061170
PMID:	34207499

Savanna tree evolutionary ages inform the reconstruction of the paleoenvironment of our hominin ancestors

Davies TJ, Daru BH, Bezeng BS, Charles-Dominique T, Hempson GP, Kabongo RM, Maurin O, Muasya AM, van der Bank M, Bond WJ

Sci Rep

24-Jul-2020

PMCID:	PMC7381606
doi:	10.1038/s41598-020-69378-0
PMID:	32709951

Evaluation of Antioxidant and Antibacterial Activities, Cytotoxicity of Acacia seyal Del Bark Extracts and Isolated Compounds

Elmi A, Spina R, Risler A, Philippot S, Mérito A, Duval RE, Abdoul-latif FM, Laurain-Mattar D

Molecules

21-May-2020

PMCID:	PMC7288156
doi:	10.3390/molecules25102392
PMID:	32455580

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

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
(1S,9S,10S,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	12299978	Click to see	260.33	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1S,9S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one	171283	Click to see	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
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/10.1016/S0031-9422(00)81307-2
Monolupin	71056954	Click to see	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Thermopsine	92768	Click to see	244.33	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
> 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/10.1016/S0031-9422(00)81307-2
(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/10.1016/S0031-9422(00)81307-2
(1S,5R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one	683511	Click to see	190.24	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1S,9S,10R)-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	162888346	Click to see	230.31	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
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/S0031-9422(00)81307-2
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 1,2,3,4,5,6-hexahydro-4-(2-propenyl)-	73189507	Click to see	230.31	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Caulophylline	234566	Click to see	204.27	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Pharmakon1600-01504027	6708720	Click to see	190.24	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine	91471	Click to see	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(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/10.1016/S0031-9422(00)81307-2
(1R,2S,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane	1715130	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	51018075	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	163185252	Click to see	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1S,2S,9R,10S)-2-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	162939755	Click to see	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(1S,2S,9S,10S)-2-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	15939842	Click to see	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
(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/10.1016/S0031-9422(00)81307-2
(7S,7aS,14S,14aS)-Dodecahydro-7,14-methano-2H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocine	168213	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
2-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	73201047	Click to see	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
7,14-Methano-4H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-4-one, 2,3,7,7a,8,9,10,11,13,14-decahydro-, (7S-(7alpha,7abeta,14alpha))-	14379237	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
alpha-Isolupanine	119201	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
D-Gluconate 6-phosphate tris(cyclohexylamine) salt	16212687	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Genisteine	92759	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Lupanine, 5,6-didehydro-	520559	Click to see	246.35	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Sparteine	644020	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
Sparteine non-stereo	3966	Click to see	234.38	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Centrolobofuran	641806	Click to see	256.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1S,14S)-5,5-dimethyl-4,12,18,20,24-pentaoxahexacyclo[12.10.0.02,11.03,8.015,23.017,21]tetracosa-2(11),3(8),6,9,15,17(21),22-heptaen-9-ol	10474063	Click to see	366.40	unknown	https://doi.org/10.1055/S-2002-32910
(1S,14S)-5,5-dimethyl-4,12,18,20,24-pentaoxahexacyclo[12.10.0.02,11.03,8.015,23.017,21]tetracosa-2(11),3(8),9,15,17(21),22-hexaen-9-ol	10248440	Click to see	368.40	unknown	https://doi.org/10.1055/S-2002-32910
(2S,10S)-6-methoxy-19,19-dimethyl-3,12,20-trioxapentacyclo[11.8.0.02,10.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21)-hexaen-15-ol	10405860	Click to see	354.40	unknown	https://doi.org/10.1055/S-2002-32910
(2S,10S)-6-methoxy-19,19-dimethyl-3,12,20-trioxapentacyclo[11.8.0.02,10.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),17-heptaen-15-ol	9975279	Click to see	352.40	unknown	https://doi.org/10.1055/S-2002-32910
(6aS,11aS)-9-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene	53473463	Click to see	254.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
5,5-Dimethyl-4,12,18,20,24-pentaoxahexacyclo[12.10.0.02,11.03,8.015,23.017,21]tetracosa-2(11),3(8),6,9,15,17(21),22-heptaen-9-ol	85153012	Click to see	366.40	unknown	https://doi.org/10.1055/S-2002-32910
5,5-Dimethyl-4,12,18,20,24-pentaoxahexacyclo[12.10.0.02,11.03,8.015,23.017,21]tetracosa-2(11),3(8),9,15,17(21),22-hexaen-9-ol	162950378	Click to see	368.40	unknown	https://doi.org/10.1055/S-2002-32910
6-Methoxy-19,19-dimethyl-3,12,20-trioxapentacyclo[11.8.0.02,10.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21)-hexaen-15-ol	85134137	Click to see	354.40	unknown	https://doi.org/10.1055/S-2002-32910
6-Methoxy-19,19-dimethyl-3,12,20-trioxapentacyclo[11.8.0.02,10.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),17-heptaen-15-ol	85080285	Click to see CC1(C=CC2=C(O1)C3=C(C=C2O)OCC4C3OC5=C4C=CC(=C5)OC)C	352.40	unknown	https://doi.org/10.1055/S-2002-32910
6,19,19-Trimethyl-3,12,20-trioxapentacyclo[11.8.0.02,10.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21)-hexaen-15-ol	163187690	Click to see	338.40	unknown	https://doi.org/10.1055/S-2002-32910
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene	391072	Click to see	254.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
4-(6,8-dihydroxy-8H-[1,3]dioxolo[4,5-g]chromen-7-yl)benzene-1,2,3-triol	163031600	Click to see	332.26	unknown	https://doi.org/10.1055/S-2002-32910
4-[(8R)-6,8-dihydroxy-8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol	163031601	Click to see	332.26	unknown	https://doi.org/10.1055/S-2002-32910
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	5317480	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
5,7-dihydroxy-8-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-3-(4-hydroxyphenyl)-4H-chromen-4-one	5481977	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
Gancaonin C	6450959	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011 https://doi.org/10.1515/ZNC-1985-9-1005
Orobol	5281801	Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O	286.24	unknown	https://doi.org/10.1515/ZNC-1985-9-1005 https://doi.org/10.1016/S0031-9422(00)81307-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
4-(8-hydroxy-7,8-dihydro-6H-[1,3]dioxolo[4,5-g]chromen-7-yl)benzene-1,2,3-triol	85206407	Click to see	318.28	unknown	https://doi.org/10.1016/S0031-9422(01)00009-7
Bolusanthol A	10615474	Click to see	318.28	unknown	https://doi.org/10.1016/S0031-9422(01)00009-7
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3R)-3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	101149957	Click to see	356.40	unknown	https://doi.org/10.1055/S-2002-32910
(3R)-5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	156020177	Click to see	408.50	unknown	https://doi.org/10.1016/S0031-9422(01)00009-7 https://doi.org/10.1055/S-2002-32910
(3S)-3-[3-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-4,5-dihydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	162928165	Click to see	372.40	unknown	https://doi.org/10.1055/S-2002-32910
(3S)-3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	162873935	Click to see	356.40	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
(3S)-5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	163007617	Click to see	438.50	unknown	https://doi.org/10.1055/S-2002-32910
(3S)-5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	637199	Click to see CC(=CCC1=C(C=CC(=C1)C2COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C	408.50	unknown	https://doi.org/10.1016/S0031-9422(01)00009-7
3-[3-[(3,3-Dimethyloxiran-2-yl)methyl]-4,5-dihydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	162928164	Click to see CC1(C(O1)CC2=C(C(=CC(=C2)C3COC4=CC(=CC(=C4C3=O)O)O)O)O)C	372.40	unknown	https://doi.org/10.1055/S-2002-32910
3S-5,7,3'-Trihydroxy-4'-methoxy-5'-prenylisoflavanone	7330526	Click to see CC(=CCC1=C(C(=CC(=C1)C2COC3=CC(=CC(=C3C2=O)O)O)O)OC)C	370.40	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
5,7-Dihydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	9864156	Click to see	370.40	unknown	https://doi.org/10.1055/S-2002-32910
Bolusanthol C	12972420	Click to see	408.50	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
Npc264949	10594416	Click to see	356.40	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
Sophoraisoflavanone B	44257387	Click to see	438.50	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-6-(4-hydroxy-3-methylbut-2-enyl)-3-(4-hydroxyphenyl)chromen-4-one	6805203	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
5,7-dihydroxy-6-[(Z)-4-hydroxy-3-methylbut-2-enyl]-3-(4-hydroxyphenyl)chromen-4-one	7087554	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
Hydroxywighteone	5378945	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)CO	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
Wighteone	5281814	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3R)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2H-chromen-4-one	162867276	Click to see	440.50	unknown	https://doi.org/10.1055/S-2002-32910
(3S)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2H-chromen-4-one	162867277	Click to see CC(=CCC1=C(C=CC(=C1O)C2(COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)O)C	440.50	unknown	https://doi.org/10.1055/S-2002-32910
(3S)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	134715140	Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)C	424.50	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/S0031-9422(01)00009-7
3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2H-chromen-4-one	10388525	Click to see	440.50	unknown	https://doi.org/10.1055/S-2002-32910
3'-Dimethylallylkievitone	480785	Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)C	424.50	unknown	https://doi.org/10.1016/S0031-9422(01)00009-7 https://doi.org/10.1055/S-2002-32910
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol	5319744	Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	https://doi.org/10.1515/ZNC-1985-9-1005
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(4R)-3-(2-hydroxy-4-methoxyphenyl)-4H-chromene-2,4,7-triol	163039731	Click to see COC1=CC(=C(C=C1)C2=C(OC3=C(C2O)C=CC(=C3)O)O)O	302.28	unknown	https://doi.org/10.1055/S-2002-32910
2H-1-Benzopyran-7-ol, 3-(2-hydroxy-4-methoxyphenyl)-	10378419	Click to see	270.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
3-(2-hydroxy-4-methoxyphenyl)-4H-chromene-2,4,7-triol	163039730	Click to see	302.28	unknown	https://doi.org/10.1055/S-2002-32910
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3S)-3,5,7-trihydroxy-3-(3-hydroxy-4-methoxyphenyl)-2H-chromen-4-one	162849823	Click to see	318.28	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2 https://doi.org/10.1515/ZNC-1985-9-1005
4'-Methoxy-3',5,7-trihydroxyisoflavone	5281803	Click to see	300.26	unknown	https://doi.org/10.1515/ZNC-1985-9-1005
5,7-Dihydroxy-3-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one	5481243	Click to see CC(=CCC1=C(C(=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)OC)C	368.40	unknown	https://doi.org/10.1055/S-2002-32910
Bolusanthin	188524	Click to see COC1=C(C=C(C=C1)C2(COC3=CC(=CC(=C3C2=O)O)O)O)O	318.28	unknown	https://doi.org/10.1515/ZNC-1985-9-1005
Calycosin	5280448	Click to see	284.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5,7-Dihydroxy-3',4'-dimethoxyisoflavone	5408543	Click to see	314.29	unknown	https://doi.org/10.1515/ZNC-1985-9-1005
Biochanin A	5280373	Click to see	284.26	unknown	https://doi.org/10.1016/S0031-9422(00)81307-2 https://doi.org/10.1515/ZNC-1985-9-1005
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5,7-Dimethoxy-4-phenylchromen-2-one	701671	Click to see	282.29	unknown	https://doi.org/10.1055/S-2002-32910 https://doi.org/10.1016/J.PHYTOCHEM.2004.02.011

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Bolusanthus speciosus

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