Lespedeza floribunda

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Synonyms

Common Names

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Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID643fdbd7a55ac163449714
Scientific name	Lespedeza floribunda
Authority	Bunge
First published in	Uchen. Zap. Imp. Kazansk. Univ.1835(4): 164 (1835)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Lespedeza floribunda var. alopecuroides	Franch.	Pl. Delavay.: 169 (1890)
Lespedeza stollasae	L.H.Bailey	Gentes Herbarum1: 32 (1920)

Common names Top

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Language	Common/alternative name
Chinese	多花胡枝子
Chinese	铁鞭草
Chinese	白毛蒿花
Chinese	米汤草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Qinghai
- Eastern Asia
  - Japan
  - Korea
- Mongolia
  - Mongolia

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000197885
Tropicos	13021825
KEW	urn:lsid:ipni.org:names:502457-1
The Plant List	ild-44407
Open Tree Of Life	636153
NCBI Taxonomy	587870
IUCN Red List	19891575
IPNI	502457-1
iNaturalist	129676
GBIF	2955761
EOL	648474
USDA GRIN	21863
CMAUP	NPO13293

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

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

Addressing the Relationship between Leaf Nitrogen and Carbon Isotope Discrimination from the Three Levels of Community, Population and Individual

Wang S, Han Y, Jia Y, Chen Z, Wang G

Plants (Basel)

04-Apr-2023

PMCID:	PMC10097192
doi:	10.3390/plants12071551
PMID:	37050177

Feeding habits and habitat use of barking deer (Muntiacus vaginalis) in Himalayan foothills, Pakistan

Habiba U, Anwar M, Khatoon R, Hussain M, Khan KA, Khalil S, Bano SA, Hussain A

PLoS One

15-Jan-2021

PMCID:	PMC7810515
doi:	10.1371/journal.pone.0245279
PMID:	33450743

The effect of slope aspect on vegetation attributes in a mountainous dry valley, Southwest China

Yang J, El-Kassaby YA, Guan W

Sci Rep

05-Oct-2020

PMCID:	PMC7536199
doi:	10.1038/s41598-020-73496-0
PMID:	33020576

New Compounds from the Roots of Corsican Calicotome Villosa (Poir.) Link.: Two Pterocarpans and a Dihydrobenzofuran

Palu DS, Paoli M, Casabianca H, Casanova J, Bighelli A

Molecules

30-Jul-2020

PMCID:	PMC7435676
doi:	10.3390/molecules25153467
PMID:	32751545

Influence of Afforestation on the Species Diversity of the Soil Seed Bank and Understory Vegetation in the Hill-Gullied Loess Plateau, China

Wang N, Jiao J, Jia Y, Wang D

Int J Environ Res Public Health

24-Oct-2017

PMCID:	PMC5664785
doi:	10.3390/ijerph14101285
PMID:	29064405

How long should the fully hillside-closed forest protection be implemented on the Loess Plateau, Shaanxi, China?

Hou L, Hou S

PeerJ

04-Sep-2017

PMCID:	PMC5588796
doi:	10.7717/peerj.3764
PMID:	28890857

Synthesis of Psoralidin derivatives and their anticancer activity: First synthesis of Lespeflorin I

Pahari P, Saikia UP, Das TP, Damodaran C, Rohr J

Tetrahedron

09-Jun-2016

PMCID:	PMC5044874
doi:	10.1016/j.tet.2016.04.066
PMID:	27698514

Diversity of Woodland Communities and Plant Species along an Altitudinal Gradient in the Guancen Mountains, China

Meng D, Zhang JT, Li M

ScientificWorldJournal

01-Apr-2012

PMCID:	PMC3329947
doi:	10.1100/2012/398765
PMID:	22566768

Melanin synthesis inhibitors from Lespedeza floribunda.

Mori-Hongo M, Takimoto H, Katagiri T, Kimura M, Ikeda Y, Miyase T

J Nat Prod

27-Feb-2009

doi:	10.1021/NP800395J
PMID:	19132934

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Lespeflorin C7	25243326	Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)C(=O)C(CC3=CC=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.1021/NP800395J
> Organoheterocyclic compounds / Naphthopyrans
Pannorin	54692973	Click to see CC1=CC2=CC(=CC(=C2C3=C1C(=CC(=O)O3)O)O)O	258.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Lespeflorin F1	25242926	Click to see COC1=C(C=CC(=C1OC)O)C2=CC3=C(O2)C(=C(C=C3)O)OC	316.30	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin F2	25243079	Click to see CC(=CCC1=C2C(=CC(=C1O)OC)C(=C(O2)C3=C(C=C(C=C3)O)O)CO)C	370.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin J1	25243393	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=C(C(=C5C(=C4)C6COC7=C(C6O5)C=CC(=C7CC=C(C)C)O)CC=C(C)C)O)C	812.90	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin J2	25243077	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=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)OC)O)O)CC=C(C)C)O)C	758.80	unknown	https://doi.org/10.1021/NP800395J
lespeflorin J3	25243394	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/NP800395J
Lespeflorin J4	25243395	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)OC)O)O)CC=C(C)C)C	758.80	unknown	https://doi.org/10.1021/NP800395J
> 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/NP800395J
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/NP800395J
Bavachin	14236566	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/NP800395J
Cajaflavanone	42607935	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C	406.50	unknown	https://doi.org/10.1021/NP800395J
Erythrisenegalone	15224381	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC=C(C=C4)O)O)C	406.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin B1	25243246	Click to see CC(=CCC1=CC2=C(C=C1O)OC(C(C2=O)O)C3=CC(=C(C=C3)O)CC=C(C)C)C	408.50	unknown	https://doi.org/10.1021/NP800395J
Macarangaflavanone B	14309760	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C	408.50	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(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/10.1021/NP800395J
Euchrenone a3	45269666	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)CC=C(C)C)O)C	490.60	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin A1	25243164	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(CC2=O)C3=CC=C(C=C3)OC)C	406.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin A2	25243165	Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)OC)O)C	338.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin A3	25243166	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(CC2=O)C3=CC4=C(C=C3)OC(C=C4)(C)C)C	458.60	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin B2	23958195	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(C(C2=O)O)C3=CC=C(C=C3)O)C	408.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin B3	25243247	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(C(C2=O)O)C3=CC(=C(C=C3)O)CC=C(C)C)C	476.60	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin B4	25243248	Click to see CC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)O)C	492.60	unknown	https://doi.org/10.1021/NP800395J
Prostratol	45268825	Click to see CC(=CCC1=CC2=C(C(=C1O)CC=C(C)C)OC(CC2=O)C3=CC(=C(C=C3)O)CC=C(C)C)C	460.60	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Lespeflorin A4	25243167	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC(CC3=O)C4=C(C=C(C=C4)O)OC)O)C	368.40	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Lespeflorin I1	25243000	Click to see CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)C	352.30	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin I2	25243392	Click to see CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4=C(C(=C(C=C34)O)O)CC=C(C)C)C	420.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin I3	25243076	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3=O)C	366.40	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(2S,11S)-17,17-dimethyl-6-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol	154496538	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C	390.50	unknown	https://doi.org/10.1021/NP800395J
(2S,11S)-17,17-dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol	161690659	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1021/NP800395J
(6aS,11aS)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	124351123	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP800395J
4-Prenylphaseollidin	21141346	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C	392.50	unknown	https://doi.org/10.1021/NP800395J
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,8-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)-	471688	Click to see CC(=CCC1=C2C3COC4=C(C3OC2=CC(=C1)O)C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP800395J
CID 10408212	10408212	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP800395J
Erybraedin A	362562	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)O)C	392.50	unknown	https://doi.org/10.1021/NP800395J
erybraedin B	44257439	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C	390.50	unknown	https://doi.org/10.1021/NP800395J
Erybreadin B	45268827	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C	390.50	unknown	https://doi.org/10.1021/NP800395J
Folitenol	15840592	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G1	25242927	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=CC(=C(C=C34)OC)O)O)C	354.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G10	25242998	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=CC(=C4)O	338.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G11	25243327	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C5C=CC(OC5=C(C=C34)O)(C)C)C	406.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G12	25243328	Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C4COC5=C(C4O3)C=CC(=C5)OC)C	352.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G2	25243080	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)O)OC)CC=C(C)C)C	422.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G3	25242995	Click to see CC(=CCC1=C(C2=C(C=C1O)OCC3C2OC4=C(C(=C(C=C34)O)OC)CC=C(C)C)OC)C	452.50	unknown	https://doi.org/10.1021/NP800395J
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/NP800395J
Lespeflorin G5	25227611	Click to see CC1=CC2=C(C(=C1O)CC=C(C)C)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O	406.50	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G6	45270490	Click to see CC1=CC2=C(C(=C1OC)CC=C(C)C)OC3C2COC4=C3C=CC(=C4)O	352.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G7	25243162	Click to see CC(=CCC1=C2C(=CC(=C1O)OC)C3COC4=C(C3O2)C=CC(=C4)O)C	354.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G8	25242997	Click to see CC(=CCC1=C2C(=CC(=C1OC)O)C3COC4=C(C3O2)C=CC(=C4)OC)C	368.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin G9	25243163	Click to see CC(=CCC1=C2C(=CC(=C1O)OC)C3COC4=C(C3O2)C=CC(=C4)OC)C	368.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin H1	25242999	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)OC)OC3)C	352.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin H2	25227612	Click to see CC1(C=CC2=C3C(=CC(=C2O1)O)C4=C(O3)C5=C(C=C(C=C5)OC)OC4)C	350.40	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein	5280961	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O	270.24	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
Lespeflorin D1	25227610	Click to see CC(=CCC1=C(C=CC2=C1OCC(C2=O)C3=C(C(=C(C=C3)O)CC=C(C)C)OC)O)C	422.50	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 8-O-methylated isoflavonoids
Lespeflorin E1	25243078	Click to see COC1=C(C=CC(=C1OC)O)C2=CC3=C(C(=C(C=C3)O)OC)OC2	330.30	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Lespeflorin C1	25243249	Click to see CC(=CCC1=CC(=C(C=C1O)O)C(=O)C(CC2=CC=C(C=C2)O)O)C	342.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin C2	25243250	Click to see CC(=CCC1=CC(=C(C=C1O)O)C(=O)C(CC2=CC=C(C=C2)OC)O)C	356.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin C5	25243324	Click to see CC1=C(C(=CC(=C1O)C(=O)C(CC2=CC=C(C=C2)O)O)CC=C(C)C)O	356.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin C6	25243325	Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)C)O)C(=O)C(CC2=CC=C(C=C2)O)O)C	410.50	unknown	https://doi.org/10.1021/NP800395J
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
Lespeflorin C3	25243322	Click to see CC(=CCC1=CC(=C(C=C1O)OC)C(=O)C(CC2=CC=C(C=C2)O)O)C	356.40	unknown	https://doi.org/10.1021/NP800395J
Lespeflorin C4	25243323	Click to see CC(=CCC1=CC(=C(C=C1O)OC)C(=O)C(CC2=CC=C(C=C2)OC)O)C	370.40	unknown	https://doi.org/10.1021/NP800395J

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Lespedeza floribunda

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top