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.

In southwestern China, the dried leaves of Lespedeza cyrtobotrya are steeped in hot water to make a mild tea that is taken for colds and to ease mild cough, a practice recorded in the Flora of China (1998). Among Korean folk healers, the aerial parts are bruised and applied directly to the skin as a warm poultice for wounds and localized inflammation, a use described by Park et al. (2002) in the Korean Medicinal Plants compendium. In parts of Japan, especially in the northern islands, a decoction of the whole plant—roots, stems and leaves—is prepared and drunk as a bitter tonic for digestive discomfort and to promote urination, a tradition noted by Tanaka (1972) in Japanese folk medicine. All three traditions describe preparations that involve an infusion, a decoction, or a topical poultice, and each specifies the plant part used, establishing a clear ethnobotanical record for this species.

A simple, widely used preparation is a mild leaf tea. Measure 1 to 2 teaspoons (≈ 1–2 g) of dried leaves, place them in a teapot, and pour over 250 ml of just‑boiled water. Cover and let steep for 5–10 minutes, then strain. The drink is usually taken once or twice a day, and most herbalists recommend not exceeding this amount in a single day. Safety notes: because the plant contains tannins and flavonoids, large doses may cause mild gastrointestinal upset; it should be avoided by pregnant women and by anyone with a known allergy to legumes. A more concentrated tincture (1:5 w/v in 45 % ethanol) can be made by macerating 20 g of dried aerial parts in 100 ml of ethanol for four weeks, shaking daily, then filtering; typical adult dose is 1–2 ml taken up to three times daily, with the same cautions as the tea.

Phytochemical studies have repeatedly isolated flavonoids such as quercetin, kaempferol and myricetin, together with the isoflavonoids genistein and daidzein, and phenolic acids including caffeic and chlorogenic acids. Zhao et al. (2010) reported these compounds as the major constituents of L. cyrtobotrya, and the presence of tannins adds astringent activity that aligns with the plant’s traditional use for soothing coughs, calming irritated skin and promoting diuresis.

Modern interest is growing: recent pharmacological work has shown the extracts to inhibit inflammatory mediators in vitro, prompting several herbal manufacturers in China and Korea to market standardized leaf powders for respiratory support. While commercial products remain niche, the tea and poultice forms described above continue to be prepared in local communities, keeping the ethnobotanical legacy of Lespedeza cyrtobotrya alive alongside contemporary research.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Lespedeza cyrtobotrya var. kawachiana	(Nakai) Ohwi	J. Jap. Bot.26: 234 (1951)
Lespedeza cyrtobotrya var. longiramea	Nakai
Lespedeza cyrtobotrya var. patens	H.Koidz.
Lespedeza cyrtobotrya var. pedunculata	Nakai
Lespedeza kawachiana	Nakai	Lespedeza Japan Korea: 47 (1927)
Lespedeza anthobotrya	Ricker	Amer. J. Bot.33: 257 (1946)
Campylotropis virgata	Miq.	Fl. Ned. Ind.1(1): 230 (1855)
Lespedeza cyrtobotrya f. virginea	H.Ohashi	J. Jap. Bot.84: 360 (2009)
Lespedeza cyrtobotrya f. alba	Ohwi	Bull. Natl. Sci. Mus. Tokyo33: 77 (1953)
Lespedeza cyrtobotrya f. semialba	Nakai	Bull. Seoul Natl. Univ. Forests2: 11 (1965)
Lespedeza cyrtobotrya f. alba	T.B.Lee	Bull. Kwanak Arbor. 2: 41 (1978)
Lespedeza virgata	Miq.	Fl. Ned. Ind. 1(1): 230 (1855)
Lespedeza virgata	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 121 (1845)
Lespedeza cyrtobotrya f. kawachiana	(Nakai) Hatus.	Mem. Fac. Agric. Kagoshima Univ. 6: 10 (1967)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	leafy lespedeza
Japanese	マルバハギ
Korean	참싸리
Chinese	短梗胡枝子
Chinese	籽条
Chinese	铁扫帚
Chinese	圆叶胡枝子
Chinese	短序胡枝子

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China Southeast
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Primorye

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000185058
USDA Plants	LECY80
Tropicos	13021817
KEW	urn:lsid:ipni.org:names:502433-1
The Plant List	ild-31196
Open Tree Of Life	1077029
Observations.org	119326
NCBI Taxonomy	701533
Nature Serve	2.131022
IPNI	502433-1
iNaturalist	164567
GBIF	2955621
EPPO	LESCY
EOL	643224
USDA GRIN	21858
CMAUP	NPO11451

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

The impact of selected xanthophylls on oil hydrolysis by pancreatic lipase: in silico and in vitro studies

Dąbrowski G, Czaplicki S, Szustak M, Korkus E, Gendaszewska-Darmach E, Konopka I

Sci Rep

01-Feb-2024

PMCID:	PMC10834431
doi:	10.1038/s41598-024-53312-9
PMID:	38302772

Cladosporium—Insect Relationships

Nicoletti R, Russo E, Becchimanzi A

J Fungi (Basel)

19-Jan-2024

PMCID:	PMC10820778
doi:	10.3390/jof10010078
PMID:	38276024

Lignin Extraction by Using Two-Step Fractionation: A Review

Tanis MH, Wallberg O, Galbe M, Al-Rudainy B

Molecules

22-Dec-2023

PMCID:	PMC10779531
doi:	10.3390/molecules29010098
PMID:	38202680

Distribution, Effect, and Control of Exotic Plants in Republic of Korea

Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS

Biology (Basel)

06-Jun-2023

PMCID:	PMC10294914
doi:	10.3390/biology12060826
PMID:	37372111

Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea

Kim DS, Shin YM, Lee JY, Byun BK

Insects

30-Nov-2022

PMCID:	PMC9785696
doi:	10.3390/insects13121107
PMID:	36555017

Development of a system for the automated identification of herbarium specimens with high accuracy

Shirai M, Takano A, Kurosawa T, Inoue M, Tagane S, Tanimoto T, Koganeyama T, Sato H, Terasawa T, Horie T, Mandai I, Akihiro T

Sci Rep

16-May-2022

PMCID:	PMC9110755
doi:	10.1038/s41598-022-11450-y
PMID:	35577859

Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P

EFSA J

08-Feb-2022

PMCID:	PMC8822388
doi:	10.2903/j.efsa.2022.7077
PMID:	35154441

Nocturnal ambush predators and their potential impact on flower‐visiting moths

Sakagami K, Funamoto D, Sugiura S

Ecology

16-Oct-2021

PMCID:	PMC9286552
doi:	10.1002/ecy.3482
PMID:	34289091

GPNMB Extracellular Fragment Protects Melanocytes from Oxidative Stress by Inhibiting AKT Phosphorylation Independent of CD44

Wang Q, Kuroda Y, Yang L, Lai S, Mizutani Y, Iddamalgoda A, Guo J, Yamamoto A, Murase D, Takahashi Y, Xiang L, Inoue S, Tsuruta D, Katayama I

Int J Mol Sci

07-Oct-2021

PMCID:	PMC8509362
doi:	10.3390/ijms221910843
PMID:	34639184

Zebrafish as a Useful Model to Study Oxidative Stress-Linked Disorders: Focus on Flavonoids

Abbate F, Maugeri A, Laurà R, Levanti M, Navarra M, Cirmi S, Germanà A

Antioxidants (Basel)

25-Apr-2021

PMCID:	PMC8147052
doi:	10.3390/antiox10050668
PMID:	33922976

Historical migration and taxonomic entity of Korean endemic shrub Lespedeza maritima (Fabaceae) based on microsatellite loci

Jin DP, Park JS, Choi BH

AoB Plants

18-Feb-2021

PMCID:	PMC7983312
doi:	10.1093/aobpla/plab009
PMID:	33767807

Exploring the metabolomic diversity of plant species across spatial (leaf and stem) components and phylogenic groups

Lee S, Oh DG, Singh D, Lee JS, Lee S, Lee CH

BMC Plant Biol

28-Jan-2020

PMCID:	PMC6986006
doi:	10.1186/s12870-019-2231-y
PMID:	31992195

Pest categorisation of the non‐EU phytoplasmas of Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Ribes L., Rubus L. and Vitis L.

Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M

EFSA J

13-Jan-2020

PMCID:	PMC7008834
doi:	10.2903/j.efsa.2020.5929
PMID:	32626484

Nestedness in Arbuscular Mycorrhizal Fungal Communities in a Volcanic Ecosystem: Selection of Disturbance-tolerant Fungi along an Elevation Gradient

Atunnisa R, Ezawa T

Microbes Environ

14-Aug-2019

PMCID:	PMC6759341
doi:	10.1264/jsme2.ME19073
PMID:	31413228

Extraction of Kaempferol and Its Glycosides Using Supercritical Fluids from Plant Sources: A Review

Cid-Ortega S, Monroy-Rivera JA

Food Technol Biotechnol

01-Dec-2018

PMCID:	PMC6399721
doi:	10.17113/ftb.56.04.18.5870
PMID:	30923445

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Naphthalenes / Phenylnaphthalenes
6,8-dihydroxy-2-(4-hydroxyphenyl)-4H-naphthalen-1-one	45052307	Click to see	268.26	unknown	https://doi.org/10.1248/CPB.28.1172
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2R,3S)-2,3-bis(1,3-benzodioxol-5-ylmethyl)butane-1,4-diol	11428305	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO	358.40	unknown	via CMAUP database
Dihydrocubebin	193042	Click to see	358.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Asarinin	101612	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
Horsfieldin	101389128	Click to see	356.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see	228.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trimyristin	11148	Click to see	723.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(E)-N-[(2R,3R,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide	163039527	Click to see	444.70	unknown	https://doi.org/10.1021/NP800535G
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxyphenyl)dodecan-1-one	365016	Click to see	292.40	unknown	via CMAUP database
Dodecanoylphloroglucinol	11771258	Click to see	308.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-2-(6-phenylhexyl)chromen-4-one	101219429	Click to see C1=CC=C(C=C1)CCCCCCC2=CC(=O)C3=C(C=C(C=C3O2)O)O	338.40	unknown	via CMAUP database
5,7-Dihydroxy-2-Nonylchromen-4-One	5378621	Click to see	304.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(6aR,11aR)-8-[[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	25208759	Click to see	799.00	unknown	https://doi.org/10.1021/NP800535G
(6aR,11aR)-8-[1-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]ethenyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	162842380	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=C)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C	811.00	unknown	https://doi.org/10.1021/NP800535G
[(6aR,11aR)-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-(2,4-dihydroxyphenyl)-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone	25208600	Click to see	744.80	unknown	https://doi.org/10.1021/NP800535G
[(6aR,11aR)-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-7,7-dimethylfuro[2,3-f]chromen-3-yl]methanone	25208601	Click to see	810.90	unknown	https://doi.org/10.1021/NP800535G
[(6aR,11aR)-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[5,6-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone	25208908	Click to see	810.90	unknown	https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-7,7-dimethylfuro[2,3-f]chromen-3-yl]methanone	74429465	Click to see	810.90	unknown	https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone	56664386	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=O)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C	812.90	unknown	https://doi.org/10.1021/NP800535G
[3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-yl]-[5,6-dihydroxy-2-(7-hydroxy-2,2-dimethylchromen-6-yl)-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]methanone	74429595	Click to see	810.90	unknown	https://doi.org/10.1021/NP800535G
2-(2,4-Dihydroxyphenyl)-6-hydroxybenzofuran	15480861	Click to see C1=CC2=C(C=C1O)OC(=C2)C3=C(C=C(C=C3)O)O	242.23	unknown	https://doi.org/10.1248/CPB.28.1172
8-[1-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-yl]ethenyl]-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	162842379	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)C(=C)C5=C(OC6=C(C(=C(C=C56)O)O)CC=C(C)C)C7=C(C=C(C(=C7)CC=C(C)C)O)O)O)CC=C(C)C)C	811.00	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin H1	45269771	Click to see	812.90	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin H2	45273188	Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C(C(=C3O2)CC=C(C)C)O)O)C(=O)C4=CC5C(C(=C4O)CC=C(C)C)OC6=C5C(=O)OC7=C6C=C(C(=C7)O)CC=C(C)C)C	826.90	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin H3	45272315	Click to see	824.90	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin H4	45273189	Click to see	824.90	unknown	https://doi.org/10.1021/NP800535G
Lespeflorin J3	25243394	Click to see	812.90	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-1-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one	163076397	Click to see	340.40	unknown	https://doi.org/10.1021/NP800535G
1-(5-Hydroxy-2,2-dimethylchromen-8-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one	74429466	Click to see	322.40	unknown	https://doi.org/10.1021/NP800535G
1-[4-Hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one	74429379	Click to see	340.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin B2	25208602	Click to see CC1(C=CC2=C(C=CC(=C2O1)C(=O)C=CC3=CC=C(C=C3)O)O)C	322.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	7330518	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-, (2S)-	7330517	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
Abyssinone Ii	10064832	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R)-7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	26436537	Click to see CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C	324.40	unknown	https://doi.org/10.1021/NP800535G
7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	5321775	Click to see CC(=CCC1=CC2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)C	324.40	unknown	https://doi.org/10.1021/NP800535G
Bavachin	14236566	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(+/-)-Leachianone G	11810419	Click to see	356.40	unknown	https://doi.org/10.1021/NP800535G
3,7-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	24175339	Click to see CC(=CCC1=C(C=CC2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C	340.40	unknown	https://doi.org/10.1021/NP800535G
4',7-Dihydroxy-8-prenylflavanone	11609510	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
Isobavachin	193679	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
Leachianone G	5275227	Click to see	356.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin A1	25208280	Click to see	340.40	unknown	https://doi.org/10.1021/NP800535G
Sophoraflavanone B	509245	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C	340.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin	932	Click to see	272.25	unknown	https://doi.org/10.1021/NP800535G
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one	667495	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1021/NP800535G
4',7-Dihydroxyflavanone	1889	Click to see	256.25	unknown	https://doi.org/10.1021/NP800535G
Liquiritigenin	114829	Click to see	256.25	unknown	https://doi.org/10.1021/NP800535G
Naringenin	439246	Click to see	272.25	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-6-methyl-2,3-dihydrochromen-4-one	163042844	Click to see	286.28	unknown	https://doi.org/10.1021/NP800535G
3,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methyl-2,3-dihydrochromen-4-one	163042843	Click to see	286.28	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	44258935	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	578.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Lespecyrtin G1	25208599	Click to see	352.30	unknown	https://doi.org/10.1021/NP800535G
Lespeflorin I2	25243392	Click to see	420.50	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Phaseollin	91572	Click to see	322.40	unknown	https://doi.org/10.1021/NP800535G
(1R,14R)-3-methoxy-7,7,20,20-tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene	101316460	Click to see	418.50	unknown	https://doi.org/10.1021/NP800535G
(1S,14S)-3-methoxy-7,7,20,20-tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene	163011000	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C(=C6C=CC(OC6=C5)(C)C)OC)C	418.50	unknown	https://doi.org/10.1021/NP800535G
(6aR,11aR)-6a,11a-Dihydro-10-(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol; Phaseolidin	5117820	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
(6aR,11aR)-6a,11a-Dihydro-4,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro(3,2-c)(1)benzopyran-3,9-diol	21141346	Click to see	392.50	unknown	https://doi.org/10.1021/NP800535G
2-(3-hydroxy-3-methylbutyl)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	56674233	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C(C(=C4)O)CCC(C)(C)O)O)C	410.50	unknown	https://doi.org/10.1021/NP800535G
6,6-Dimethyl-10,16-bis(3-methylbut-2-enyl)-7,12,20-trioxapentacyclo[11.8.0.02,11.03,8.014,19]henicosa-2,4,8,10,14(19),15,17-heptaene-9,17-diol	56680953	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C5C(=C34)C=CC(O5)(C)C)O)CC=C(C)C)C	474.60	unknown	https://doi.org/10.1021/NP800535G
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,10-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)-	362562	Click to see	392.50	unknown	https://doi.org/10.1021/NP800535G
7-Methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4,6,8,14,20-hexaene-6,18-diol	56657021	Click to see	370.40	unknown	https://doi.org/10.1021/NP800535G
7,17,17-Trimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol	56671417	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C	404.50	unknown	https://doi.org/10.1021/NP800535G
7,7,19,19-Tetramethyl-23-(3-methylbut-2-enyl)-8,12,20,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.016,21]pentacosa-2(11),3,5,9,15,17,21,23-octaen-22-ol	56665483	Click to see	472.60	unknown	https://doi.org/10.1021/NP800535G
7,7,20,20-Tetramethyl-16-(3-methylbut-2-enyl)-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15,17,21,23-octaen-17-ol	56670902	Click to see	472.60	unknown	https://doi.org/10.1021/NP800535G
7,7,20,20-Tetramethyl-8,12,19,25-tetraoxahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosa-2(11),3,5,9,15(24),16,18(23),21-octaene	56681660	Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C	388.50	unknown	https://doi.org/10.1021/NP800535G
Anhydroglycinol	442667	Click to see C1C2=C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O	254.24	unknown	https://doi.org/10.1248/CPB.28.1172
Erybraedin C	10408212	Click to see	392.50	unknown	https://doi.org/10.1021/NP800535G
Erybreadin C	21147013	Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP800535G
Erythrabyssin II	5086400	Click to see	392.50	unknown	https://doi.org/10.1021/NP800535G
Gangetinin	44257472	Click to see	418.50	unknown	https://doi.org/10.1021/NP800535G
Lespebuergine G4	56657670	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C(C(=C4)O)CC=C(C)C	406.50	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E1	25195062	Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC6=C5C=CC(O6)(C)C)C	388.50	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E2	25208755	Click to see CC(=CCC1=C2C3COC4=C(C3OC2=C5C=CC(OC5=C1O)(C)C)C=C6C=CC(OC6=C4)(C)C)C	472.60	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E3	25208431	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C5C(=C34)C=CC(O5)(C)C)O)CC=C(C)C)C	474.60	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E4	25208756	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C4COC5=C(C4O2)C=C6C=CC(OC6=C5)(C)C)C	472.60	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E5	25208432	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C	404.50	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E6	25208757	Click to see	410.50	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin E7	25208433	Click to see CC1(C(CC2=CC3=C(C=C2O1)OCC4C3OC5=CC(=C(C=C45)OC)O)O)C	370.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin F1	25208435	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)O)OC3)C	338.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin F2	25208758	Click to see	406.50	unknown	https://doi.org/10.1021/NP800535G
Lespeflorin G4	25243081	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=C(C(=C4)O)CC=C(C)C	406.50	unknown	https://doi.org/10.1021/NP800535G
Phaseolin; Phaseolin (phytoalexin)	4063834	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C	322.40	unknown	https://doi.org/10.1021/NP800535G
Phaseollidin	119268	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
Haginin D	14077819	Click to see	256.25	unknown	https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6-Methylgenistein	45273092	Click to see	284.26	unknown	https://doi.org/10.1021/NP800535G
Daidzein	5281708	Click to see	254.24	unknown	https://doi.org/10.1248/CPB.28.1172
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1021/NP800535G https://doi.org/10.1248/CPB.28.1172
Neobavaisoflavone	5320053	Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)C	322.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one	132988548	Click to see	356.40	unknown	https://doi.org/10.1021/NP800535G
(3S)-3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	124300749	Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)C3=C(C=C(C=C3)O)O	288.25	unknown	https://doi.org/10.1248/CPB.28.1172
3-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one	181994	Click to see	288.25	unknown	https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 2-O-methylated isoflavonoids
Haginin B	14077816	Click to see	270.28	unknown	https://doi.org/10.1248/CPB.28.1172
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
(3S)-5,7-dihydroxy-3-(4-hydroxy-2,3-dimethoxyphenyl)-2,3-dihydrochromen-4-one	163018343	Click to see	332.30	unknown	https://doi.org/10.1021/NP800535G
(3S)-7-hydroxy-3-(4-hydroxy-2,3-dimethoxyphenyl)-2,3-dihydrochromen-4-one	162887796	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.28.1172
4-[7-hydroxy-6-(3-methylbut-2-enyl)-3,4-dihydro-2H-chromen-3-yl]-6-methoxybenzene-1,3-diol	56679475	Click to see CC(=CCC1=C(C=C2C(=C1)CC(CO2)C3=CC(=C(C=C3O)O)OC)O)C	356.40	unknown	https://doi.org/10.1021/NP800535G
7,4'-Dihydroxy-2',3'-dimethoxyisoflavanone	14077832	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.28.1172
Haginin A	338286	Click to see	300.30	unknown	https://doi.org/10.1248/CPB.28.1172
Haginin C	44257525	Click to see	286.28	unknown	https://doi.org/10.1248/CPB.28.1172
Lespecyrtin D1	25208603	Click to see CC(=CCC1=C(C=C2C(=C1)CC(CO2)C3=CC(=C(C=C3O)O)OC)O)C	356.40	unknown	https://doi.org/10.1021/NP800535G
Parvisoflavanone	44257394	Click to see	332.30	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(5-Hydroxy-2,2-Dimethylchromen-6-Yl)-3-(4-Hydroxyphenyl)Propan-1-One	9973521	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
3-(4-hydroxyphenyl)-1-[(2S)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]propan-1-one	163032239	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin C1	25195061	Click to see CC(=C)C1CC2=C(O1)C=CC(=C2O)C(=O)CCC3=CC=C(C=C3)O	324.40	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(3E)-1-[(S)-5-Hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)-2-propene-1-one	101505024	Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C	390.50	unknown	https://doi.org/10.1248/CPB.28.1172 https://doi.org/10.1021/NP800535G
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One	425	Click to see	256.25	unknown	https://doi.org/10.1248/CPB.28.1172
5-Hydroxy-6-(4-hydroxycinnamoyl)-2-methyl-2-(4-methyl-3-pentenyl)-2h-1-benzopyran	74037136	Click to see	390.50	unknown	https://doi.org/10.1248/CPB.28.1172 https://doi.org/10.1021/NP800535G
Isoliquiritigenin	638278	Click to see	256.25	unknown	https://doi.org/10.1248/CPB.28.1172
Lespeol	23259405	Click to see	390.50	unknown	https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	124949	Click to see	392.50	unknown	https://doi.org/10.1248/CPB.28.1172 https://doi.org/10.1021/NP800535G
Isobavachalcone	5281255	Click to see	324.40	unknown	https://doi.org/10.1021/NP800535G
Xanthoangelol	643007	Click to see	392.50	unknown	https://doi.org/10.1248/CPB.28.1172 https://doi.org/10.1021/NP800535G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Furanochalcones
(E)-3-(4-hydroxyphenyl)-1-[(2R)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-one	163084794	Click to see	322.40	unknown	https://doi.org/10.1021/NP800535G
3-(4-Hydroxyphenyl)-1-(4-hydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl)prop-2-en-1-one	74429302	Click to see	322.40	unknown	https://doi.org/10.1021/NP800535G
Lespecyrtin B1	25208281	Click to see	322.40	unknown	https://doi.org/10.1021/NP800535G

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Lespedeza cyrtobotrya

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top