Common products:
Caragana sinica is cultivated as an ornamental shrub in horticulture. It is listed in Chinese plant catalogs and referenced in the Flora of China as a decorative species valued for its bright yellow flowers and tolerance of poor soils. Nurseries propagate seedlings for use in private gardens, public landscaping, and urban green spaces where a hardy, low‑maintenance shrub is required. The plant is also sold for use in living fences, hedgerows, and privacy screens due to its dense, upright habit and spiny branches.

Industrial and craft applications:
In ecological restoration projects across China, Caragana sinica is employed for soil stabilization and erosion control. Regional restoration guidelines cite the species as a pioneer plant capable of establishing on degraded sites, including abandoned mining areas, highway embankments, and riverine banks. Its deep root system and ability to fix atmospheric nitrogen improve soil structure and fertility, facilitating the establishment of later‑successional species. The shrub is sometimes harvested for small‑diameter fuelwood in rural settings, although this use is secondary to its primary role in land reclamation.

Properties relevant to use:
Caragana sinica forms symbiotic nodules with Rhizobium, allowing it to fix nitrogen and contribute to soil fertility. It exhibits drought tolerance and can grow on nutrient‑poor, sandy, or loamy soils. The species reaches a mature height of 1–3 m and produces a branching canopy that provides ground cover within two to three years under favorable conditions. Its seeds are small, dark, and retain high viability for several years when stored under cool, dry conditions, making seed‑based propagation reliable for large‑scale planting.

Sustainability and sourcing:
The species propagates readily from seed, and commercial nurseries maintain mother plants for seed collection. As it is not listed as threatened by the IUCN Red List and occurs naturally in several provinces of China, it can be sourced sustainably for restoration and ornamental markets. Harvest for fuelwood is limited to small branches and does not compromise overall population health when managed responsibly.

Synonyms Top

Scientific name	Authority	First published in
Caragana chamlagu	Lam.	Encycl.1: 616 (1785)
Caragana chamlayu	Lam.
Robinia sinica	Buc'hoz	Pl. Nouv. Découv.: 24 (1784)
Robinia sinensis	Buc'hoz	ex Handl. Trees Kew Pt. i. [Polypet.] (1894) 123.
Aspalathus chamlagu	(Lam.) Kuntze	Revis. Gen. Pl.1: 161 (1891)
Caragana chinensis	Turcz. ex Maxim.	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans9: 470 (1859)
Robinia lucida	Salisb.	Prodr. Stirp. Chap. Allerton: 337 (1796)
Robinia chinensis	Pers.	Syn. Pl.2: 310 (1807)
Robinia flava	Lour.	Fl. Cochinch.: 556 (1790)
Caragana flava	(Lour.) Poir.	J.B.A.M.de Lamarck, Encycl., Suppl. 2: 90 (1811)
Robinia chamlagu	(Lam.) L'Hér.	Stirp. Nov.: 161 (1791)
Caragana sinica var. longipedunculata	C.W.Chang	Acta Phytotax. Sin.17(2): 85 (1979)
Caragana sinica var. megalantha	C.K.Schneid.	Ill. Handb. Laubholzk.2: 97 (1907)
Robinia chamlagu	L'Her.

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
German	chinesischer erbsenstrauch
Japanese	ムレスズメ
Korean	골담초
Chinese	锦鸡儿
Chinese	金雀花
Chinese	土黄芪
Chinese	大绣花针
Chinese	娘娘袜
Chinese	錦鷄兒
Chinese	一种维管植物

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 South-central
  - China Southeast
  - Manchuria
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000186069
UNII	OS5ZP4ZOWW
Tropicos	13057783
KEW	urn:lsid:ipni.org:names:483896-1
The Plant List	ild-32467
Open Tree Of Life	428766
NCBI Taxonomy	403832
IPNI	483896-1
iNaturalist	601640
GBIF	2943171
Freebase	/m/080h9th
EPPO	CRASI
EOL	643742
USDA GRIN	311003
Wikipedia	Caragana_sinica
CMAUP	NPO28914

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

Pest categorisation of Eulecanium giganteum

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A

EFSA J

03-Apr-2024

PMCID:	PMC10988561
doi:	10.2903/j.efsa.2024.8666
PMID:	38576539

E-Stilbenes: General Chemical and Biological Aspects, Potential Pharmacological Activity Based on the Nrf2 Pathway

Mendonça EL, Xavier JA, Fragoso MB, Silva MO, Escodro PB, Oliveira AC, Tucci P, Saso L, Goulart MO

Pharmaceuticals (Basel)

09-Feb-2024

PMCID:	PMC10891666
doi:	10.3390/ph17020232
PMID:	38399446

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

A Systematic Study of Yiqi Qubai Standard Decoction for Treating Vitiligo Based on UPLC-Q-TOF/MS Combined with Chemometrics, Molecular Docking, and Cellular and Zebrafish Assays

Cui L, Ma C, Shi W, Yang C, Wu J, Wu Z, Lou Y, Fan G

Pharmaceuticals (Basel)

11-Dec-2023

PMCID:	PMC10747336
doi:	10.3390/ph16121716
PMID:	38139842

TCM and related active compounds in the treatment of gout: the regulation of signaling pathway and urate transporter

Sun X, Yang L, Sun H, Sun Y, Wei S, Han Y, Wang W, Kong L, Wang X

Front Pharmacol

29-Nov-2023

PMCID:	PMC10716793
doi:	10.3389/fphar.2023.1275974
PMID:	38094893

Alternative Medical Therapy

Jethwa JT

Indian J Orthop

27-Nov-2023

PMCID:	PMC10721595
doi:	10.1007/s43465-023-01035-w
PMID:	38107794

Agrobacterium rhizogenes: paving the road to research and breeding for woody plants

Ying W, Wen G, Xu W, Liu H, Ding W, Zheng L, He Y, Yuan H, Yan D, Cui F, Huang J, Zheng B, Wang X

Front Plant Sci

14-Nov-2023

PMCID:	PMC10682722
doi:	10.3389/fpls.2023.1196561
PMID:	38034586

Discovery of novel tubulin CBSI (R)-9k from the indanone scaffold for the treatment of colorectal cancer

Huo Z, Min D, Zhang S, Tang ML, Sun X

RSC Med Chem

16-Sep-2023

PMCID:	PMC10718523
doi:	10.1039/d3md00337j
PMID:	38107178

Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity

Cely-Veloza W, Kato MJ, Coy-Barrera E

ACS Omega

28-Jul-2023

PMCID:	PMC10413377
doi:	10.1021/acsomega.3c02179
PMID:	37576649

From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds

Isopencu GO, Covaliu-Mierlă CI, Deleanu IM

Plants (Basel)

16-Jul-2023

PMCID:	PMC10386126
doi:	10.3390/plants12142661
PMID:	37514275

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

A specific SNP-based multiplex PCR assay for the simultaneous identification of two biological ingredients for the Chinese patent medicine, Danggui Buxue pill

Liu Y, Yang Y, Zhou Z, Fan J, Diao J, Chao Z, Tian E

Front Pharmacol

11-May-2023

PMCID:	PMC10213767
doi:	10.3389/fphar.2023.1098598
PMID:	37251312

Skin Wound Healing and Anti-Wrinkle-Promoting In Vitro Biological Activities of Caragana sinica Flower Absolute and Its Chemical Composition

Kim MJ, Won KJ, Kim DY, Won YR, Kim NY, Lee DK, Hong BS, Lee HM

Pharmaceuticals (Basel)

03-Feb-2023

PMCID:	PMC9964200
doi:	10.3390/ph16020235
PMID:	37017451

Core Constituents of Caragana sinica Root for Rheumatoid Arthritis Treatment and the Potential Mechanism

Qu B, Wang S, Zhu H, Yin T, Zhou R, Hu W, Lu C

ACS Omega

05-Jan-2023

PMCID:	PMC9851025
doi:	10.1021/acsomega.2c07094
PMID:	36687056

Neurological disorders of COVID-19: insights to applications of natural products from plants and microorganisms

Almasi F, Dang W, Mohammadipanah F, Li N

Arch Pharm Res

28-Nov-2022

PMCID:	PMC9702705
doi:	10.1007/s12272-022-01420-3
PMID:	36441470

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Indanes
(4bR,5R,10R)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol	9890174	Click to see	454.50	unknown	via CMAUP database
5,10-Bis-(4-hydroxy-phenyl)-4b,5,9b,10-tetrahydro-indeno[2,1-a]indene-1,3,6,8-tetraol	57518717	Click to see	454.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
Pallidol	484757	Click to see	454.50	unknown	https://doi.org/10.1016/S0039-9140(01)00375-7 https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1002/CJOC.20040220221 https://doi.org/10.1016/S0040-4020(01)00427-6
> Benzenoids / Phenols / Methoxyphenols
5-(4-Hydroxy-3-methoxyphenyl)pentan-2-one	91206832	Click to see	208.25	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
(+)-Isoampelopsin F	11134199	Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O	454.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
(1R,8R,9S,16S)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol	162890010	Click to see	454.50	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
(1R,8S,9S,16S)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol	101680651	Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O	454.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
(1S,8R,9R,16R)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol	101680650	Click to see	454.50	unknown	via CMAUP database
(1S,8R,9R)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol	46230189	Click to see	454.50	unknown	via CMAUP database
Ampelopsin F	102004746	Click to see	454.50	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol	68171	Click to see	382.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
[(2R)-2,3-dihydroxypropyl] hexacosanoate	124511398	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O	470.80	unknown	https://doi.org/10.1248/CPB.38.432
[(2R)-2,3-dihydroxypropyl] octacosanoate	163065461	Click to see	498.80	unknown	https://doi.org/10.1248/CPB.38.432
[(2R)-2,3-dihydroxypropyl] tetracosanoate	163004763	Click to see	442.70	unknown	https://doi.org/10.1248/CPB.38.432
2,3-Dihydroxypropyl octacosanoate	317842	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O	498.80	unknown	https://doi.org/10.1248/CPB.38.432
2,3-Dihydroxypropyl tetracosanoate	14542801	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCC(CO)O	442.70	unknown	https://doi.org/10.1248/CPB.38.432
Glyceryl hexacosanoate	14542802	Click to see	470.80	unknown	https://doi.org/10.1248/CPB.38.432
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7aS)-7-(acetyloxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	101996850	Click to see	416.40	unknown	via CMAUP database
10-Deoxygeniposidic acid	443353	Click to see	358.34	unknown	via CMAUP database
8-Epideoxyloganic acid	443332	Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O	360.36	unknown	via CMAUP database
Geniposidic Acid	443354	Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO	374.34	unknown	via CMAUP database
Mussaenoside	182423	Click to see	390.40	unknown	via CMAUP database
Shanzhiside Methyl Ester	13892722	Click to see	406.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4R,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[(2S,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid	118855620	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	927.10	unknown	https://doi.org/10.1007/BF02973986
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-4-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid	101629715	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OCC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C	1103.20	unknown	https://doi.org/10.1007/BF02973986
Caraganoside A	73092974	Click to see	1045.20	unknown	https://doi.org/10.1007/BF02973986
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	52940117	Click to see	576.80	unknown	via CMAUP database
Stigmasterol Glucoside	6602508	Click to see	574.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
3-(1H-Indol-3-Yl)-2-(Trimethylazaniumyl)Propanoate	3861164	Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-]	246.30	unknown	https://doi.org/10.1016/S0039-9140(01)00375-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Hypaphorine	442106	Click to see	246.30	unknown	https://doi.org/10.1016/S0039-9140(01)00375-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Propionic Acid	1032	Click to see CCC(=O)O	74.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,4aS,7aS)-7-methylidene-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid	102508537	Click to see	358.34	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Guignardone A	50905842	Click to see	290.40	unknown	via CMAUP database
Guignardone B	50905843	Click to see CC12CCC(C1CC3=C(O2)C4CC(C3=O)(CO4)O)C(C)(C)O	308.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenol	45358120	Click to see	624.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(+-)-Tricholomalide B	44240398	Click to see	348.40	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6 https://doi.org/10.1016/J.BMCL.2011.12.012
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(10R,11S,18S,19S)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol	162952382	Click to see	676.70	unknown	https://doi.org/10.1002/HLCA.200590166
(10R,18R)-3,11,19-tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol	137795509	Click to see C1=CC(=CC=C1C2C3C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(=CC(=C7)O)OC(=C8C9=C3C(=CC(=C9)O)O2)C1=CC=C(C=C1)O)O	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
(10S,11S,18R,19R)-11-(3-hydroxyphenyl)-3,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol	162900000	Click to see	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
(17S,18S)-7,12,14,22-tetrahydroxy-3,18-bis(4-hydroxyphenyl)-4,19-dioxahexacyclo[15.6.1.12,5.011,16.020,24.09,25]pentacosa-1(24),2,5,7,9(25),11(16),12,14,20,22-decaen-10-one	11599596	Click to see	586.50	unknown	https://doi.org/10.1002/HLCA.200590166
[7-(3,5-dihydroxyphenyl)-1-[3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-5-hydroxy-2,6-bis(4-hydroxyphenyl)-2,6,7,8-tetrahydro-1H-cyclopenta[e][1]benzofuran-8-yl]-(4-hydroxyphenyl)methanone	163028507	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC4=C3C(C(O4)C5=CC=C(C=C5)O)C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O)C(=O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O	922.90	unknown	https://doi.org/10.1248/CPB.44.565
11-(3-Hydroxyphenyl)-3,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol	162899999	Click to see	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
3,11,19-Tris(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.12,5.110,13.021,25.09,27.017,26]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-7,15,23-triol	375682	Click to see	678.70	unknown	https://doi.org/10.1248/CPB.38.432 https://doi.org/10.1016/J.BMCL.2011.12.012
4-(3,5-Dihydroxyphenyl)-5,11,19-tris(4-hydroxyphenyl)-6-oxapentacyclo[10.7.0.02,10.03,7.013,18]nonadeca-2(10),3(7),8,13(18),14,16-hexaene-9,15,17-triol	73155211	Click to see	680.70	unknown	https://doi.org/10.1002/HLCA.200590166
5-[(1S,2R,3R,4R)-4-[(2S,3S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,3-bis(4-hydroxyphenyl)cyclopentyl]benzene-1,3-diol	163187069	Click to see C1C(C(C(C1C2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O	923.00	unknown	https://doi.org/10.1248/CPB.44.565
5-[(2R,3R)-7-hydroxy-5-[(2S,3S)-6-hydroxy-2-(3-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol	46890011	Click to see C1=CC(=CC(=C1)O)C2C(C3=C(C=C(C=C3O2)O)C=CC4=CC=C(C=C4)O)C5=CC6=C(C(=C5)O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O	680.70	unknown	via CMAUP database
5-[(2S,3R,4S,5R)-4-[(2S,3S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-7-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]benzene-1,3-diol	44427222	Click to see	924.90	unknown	via CMAUP database
5-[(2S)-4-[(2S)-3-[(2R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]benzene-1,3-diol	364878	Click to see	924.90	unknown	https://doi.org/10.1248/BPB.25.125 https://doi.org/10.1016/S0039-9140(01)00375-7 https://doi.org/10.1016/J.JEP.2005.05.016 https://doi.org/10.1055/S-2006-957996 https://doi.org/10.1248/CPB.44.565
5-[4-[3-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,3-bis(4-hydroxyphenyl)cyclopentyl]benzene-1,3-diol	163055522	Click to see	923.00	unknown	https://doi.org/10.1248/CPB.44.565
5-[4-[3-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]benzene-1,3-diol	500072	Click to see	924.90	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
5-[6-Hydroxy-4-[6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol	366355	Click to see	680.70	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
7,12,14,22-Tetrahydroxy-3,18-bis(4-hydroxyphenyl)-4,19-dioxahexacyclo[15.6.1.12,5.011,16.020,24.09,25]pentacosa-1(24),2,5,7,9(25),11(16),12,14,20,22-decaen-10-one	73024947	Click to see	586.50	unknown	https://doi.org/10.1002/HLCA.200590166
Alpha-Viniferin	196402	Click to see	678.70	unknown	https://doi.org/10.1016/S0039-9140(01)00375-7 https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1248/BPB.25.125 https://doi.org/10.1002/CJOC.20040220221 https://doi.org/10.1055/S-2006-957996 https://doi.org/10.1016/S0040-4020(01)00427-6 https://doi.org/10.1248/CPB.44.565 https://doi.org/10.1248/CPB.38.432
Caraganaphenol A	16145810	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC4=C3C(C(O4)C5=CC=C(C=C5)O)C6=C7C(C(OC7=CC(=C6)O)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O)C(=O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O	922.90	unknown	https://doi.org/10.1248/CPB.44.565
Caraphel A	72754681	Click to see	676.70	unknown	https://doi.org/10.1002/HLCA.200590166
Caraphenol A	484751	Click to see	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
Carasinol B	11309056	Click to see C1=CC(=CC=C1C2C(C(C(O2)C3=CC=C(C=C3)O)C4=C5C(C(OC5=CC(=C4)O)C6=CC=C(C=C6)O)C7=C8C(C(OC8=CC(=C7)O)C9=CC=C(C=C9)O)C1=CC(=CC(=C1)O)O)C1=CC(=CC(=C1)O)O)O	924.90	unknown	via CMAUP database
Carasiphenol C	11964468	Click to see C1=CC(=CC=C1C2C3C(C(C4=C3C=C(C=C4O)O)C5=CC=C(C=C5)O)C6=C2C(=CC7=C6C(C(O7)C8=CC=C(C=C8)O)C9=CC(=CC(=C9)O)O)O)O	680.70	unknown	https://doi.org/10.1002/HLCA.200590166
CID 101692680	101692680	Click to see	922.90	unknown	https://doi.org/10.1248/CPB.44.565
Kobophenol A	484758	Click to see	924.90	unknown	https://doi.org/10.1248/BPB.25.125 https://doi.org/10.1016/S0039-9140(01)00375-7 https://doi.org/10.1002/CJOC.20040220221 https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1055/S-2006-957996 https://doi.org/10.1248/CPB.44.565
Miyabenol C	5388319	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O	680.70	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6 https://doi.org/10.1016/S0039-9140(01)00375-7 https://doi.org/10.1002/CJOC.20040220221 https://doi.org/10.1055/S-2001-17367 https://doi.org/10.1055/S-2006-957996
Miyabenol C	6475924	Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=C6C(C(OC6=CC(=C5)O)C7=CC=C(C=C7)O)C8=CC(=CC(=C8)O)O)O	680.70	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
Stenophyllol B	10794663	Click to see C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C4O)O)C5C(OC6=CC(=CC3=C56)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C2C(=CC(=C9)O)O)O	680.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids / Auronols
Carasinaurone	101767761	Click to see	302.28	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1002/HLCA.200590166
Carpusin	134369	Click to see	302.28	unknown	https://doi.org/10.1002/HLCA.200590166 https://doi.org/10.1016/J.BMCL.2011.12.012
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-Ampelopsin F	484755	Click to see C1=CC(=CC=C1C2C3C24C(C5=C(C4C6=C3C=C(C=C6O)O)C=C(C=C5O)O)C7=CC=C(C=C7)O)O	466.50	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Odoratin	13965473	Click to see	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(1S,2R,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-1-[(R)-(4-hydroxyphenyl)-methoxymethyl]-2,3-dihydro-1H-indene-4,6-diol	162914510	Click to see COC(C1C(C(C2=C1C=C(C=C2O)O)C3=CC(=CC(=C3)O)O)C4=CC=C(C=C4)O)C5=CC=C(C=C5)O	486.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
(1S,2R,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-1-[(S)-(4-hydroxyphenyl)-methoxymethyl]-2,3-dihydro-1H-indene-4,6-diol	162914509	Click to see	486.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012
[(1R,2R,3R)-2-(3,5-dihydroxyphenyl)-4,6-dihydroxy-3-(4-hydroxyphenyl)-2,3-dihydro-1H-inden-1-yl]-(4-hydroxyphenyl)methanone	484754	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(=O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	470.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1016/S0040-4020(01)00427-6
[(1R,2R,3R)-3-(3,5-dihydroxyphenyl)-4,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1H-inden-1-yl]-(4-hydroxyphenyl)methanone	484753	Click to see	470.50	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
[2-(3,5-dihydroxyphenyl)-4,6-dihydroxy-3-(4-hydroxyphenyl)-2,3-dihydro-1H-inden-1-yl]-(4-hydroxyphenyl)methanone	72665145	Click to see C1=CC(=CC=C1C2C(C(C3=C2C(=CC(=C3)O)O)C(=O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O	470.50	unknown	https://doi.org/10.1016/J.BMCL.2011.12.012 https://doi.org/10.1016/S0040-4020(01)00427-6
[3-(3,5-dihydroxyphenyl)-4,6-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1H-inden-1-yl]-(4-hydroxyphenyl)methanone	78191901	Click to see	470.50	unknown	https://doi.org/10.1016/S0040-4020(01)00427-6
Caragasinin A	56950653	Click to see	486.50	unknown	via CMAUP database
Caragasinin B	56950654	Click to see COC(C1C(C(C2=C1C=C(C=C2O)O)C3=CC(=CC(=C3)O)O)C4=CC=C(C=C4)O)C5=CC=C(C=C5)O	486.50	unknown	via CMAUP database
Cis-Resveratrol	1548910	Click to see	228.24	unknown	via CMAUP database
Resveratrol	445154	Click to see	228.24	unknown	via CMAUP database

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.

Caragana sinica

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