Details Top

Internal ID UUID643fd98b4643e061692817
Scientific name Caragana spinosa
Authority (L.) DC.
First published in Prodr. [A. P. de Candolle] 2: 269. 1825 [mid Nov 1825]

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Common names Top

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Language Common/alternative name
Chinese 锦鸡儿
Chinese 多刺锦鸡儿
Chinese 刺锦鸡儿

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Krasnoyarsk
      • Tuva
      • West Siberia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186048
Tropicos 13070666
KEW urn:lsid:ipni.org:names:941350-1
The Plant List ild-32438
Open Tree Of Life 232431
Observations.org 145509
NCBI Taxonomy 626692
IPNI 941350-1
GBIF 2943239
EPPO CRASP
EOL 643720
Elurikkus 730695
USDA GRIN 8946

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 first mitochondrial genome of Calophyllum soulattri Burm.f. Cadorna CA, Pahayo DG, Rey JD Sci Rep 01-Mar-2024
PMCID:PMC10907642
doi:10.1038/s41598-024-55016-6
PMID:38429360
A study on the effect of natural products against the transmission of B.1.1.529 Omicron Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M Virol J 25-Aug-2023
PMCID:PMC10464336
doi:10.1186/s12985-023-02160-6
PMID:37626376
Gastroprotective effects of Caragana ambigua stocks on ethanol‐induced gastric ulcer in rats supported by LC–MS/MS characterization of formononetin and biochanin A Rubab F, Ijaz H, Hussain S, Munir A, Stuppner S, Jakschitz T, Bonn GK, Ishtiaq S J Sci Food Agric 11-Jul-2022
PMCID:PMC9795896
doi:10.1002/jsfa.12064
PMID:35689485
Natural Products for the Prevention and Control of the COVID-19 Pandemic: Sustainable Bioresources Singla RK, He X, Chopra H, Tsagkaris C, Shen L, Kamal MA, Shen B Front Pharmacol 01-Dec-2021
PMCID:PMC8671886
doi:10.3389/fphar.2021.758159
PMID:34925017
Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C Plant Divers 06-Oct-2020
PMCID:PMC7936101
doi:10.1016/j.pld.2020.09.008
PMID:33733011
Computation screening of narcissoside a glycosyloxyflavone for potential novel coronavirus 2019 (COVID-19) inhibitor Dubey K, Dubey R Biomed J 18-May-2020
PMCID:PMC7233213
doi:10.1016/j.bj.2020.05.002
PMID:32426388
Detection Progress of Selected Drugs in TLC Pyka A Biomed Res Int 16-Jan-2014
PMCID:PMC3914296
doi:10.1155/2014/732078
PMID:24551853
Chemical investigation of Caragana spinosa runners D. N. Olennikov, L. M. Tankhaeva, V. V. Partilkhaev Springer Science and Business Media LLC 06-Jan-2012
doi:10.1007/S10600-012-0124-5
New Palaearctic species of the tribe Thalassaphorurini Pomorski, 1998 (Collembola, Onychiuridae) Babenko AB, Chimitova AB, Stebaeva SK Zookeys 02-Sep-2011
PMCID:PMC3175132
doi:10.3897/zookeys.126.1229
PMID:21998539
Flavonoids ofCaragana spinosa G. A. Shpekina Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00605216

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1007/S10600-012-0124-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/S10600-012-0124-5
17-(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-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-012-0124-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/S10600-012-0124-5
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/S10600-012-0124-5
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1007/S10600-012-0124-5
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1007/S10600-012-0124-5
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1007/S10600-012-0124-5
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/S10600-012-0124-5
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1007/S10600-012-0124-5
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/S10600-012-0124-5
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1007/S10600-012-0124-5
Flavan-3,3',4',5,5',7-hexol 1249 Click to see 306.27 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/S10600-012-0124-5
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-012-0124-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1007/BF00605216
https://doi.org/10.1007/S10600-012-0124-5
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/S10600-012-0124-5
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/S10600-012-0124-5
https://doi.org/10.1007/BF00605216
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1007/BF00605216
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1007/S10600-012-0124-5
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1007/S10600-012-0124-5
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13179952 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-012-0124-5
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00605216
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1007/S10600-012-0124-5
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1007/S10600-012-0124-5
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/S10600-012-0124-5
Isoquercitrin 5484006 Click to see 464.40 unknown https://doi.org/10.1007/S10600-012-0124-5
Isorhamnetin 3-robinobioside 6223069 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-012-0124-5
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/S10600-012-0124-5
https://doi.org/10.1007/BF00605216
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1007/BF00605216
https://doi.org/10.1007/S10600-012-0124-5
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1007/S10600-012-0124-5
https://doi.org/10.1007/BF00605216
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1007/S10600-012-0124-5

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