Lysimachia christinae

Details Top

Internal ID UUID643ffd5a286da999520759
Scientific name Lysimachia christinae
Authority Hance
First published in J. Bot. 11: 167 (1873)

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.

Among the Han Chinese, the herb called Jin Qian Cao (the dried whole plant of Lysimachia christinae) is taken as a warm decoction to “promote urination, clear damp‑heat, and relieve painful urinary dysfunction,” as summarized in the WHO monograph on selected medicinal plants (WHO, 2002). The modern pharmacopoeias further note that it is used for jaundice with damp‑heat and for gall‑bladder symptoms and is usually taken as a decoction (State Pharmacopoeia Commission of PRC, 2020). Across southern China’s Guangxi and Guizhou provinces, the same herb—used as a tea or decoction—appears in Zhuang, Miao and Yao herbal practice as a remedy for “naturally moving stones” and “passing painful urine,” with these ethnic uses described in the China ethnobotany literature (Xiao, 2002). In some Anhui communities it is also steeped as a simple hot infusion after fasting to “clear damp heat and benefit urination,” a practice noted in local materia medica (Beijing University of Chinese Medicine, 2009). In each case the plant part is the aerial herb—leaves, stems and flowers—dried and used in water preparations rather than being taken as a powder or smoke.

A concise tea/decoction can be made with about 12–15 g of the dried whole herb (leaves, stems and flowers) simmered in 600–800 mL of water for 20–30 minutes, then cooled and strained. The resulting liquid is split into two daily doses. Some practitioners prefer a gentler infusion for shorter periods and will repeat the tea for several days as needed. As with many diuretic and cholagogue herbs, do not use during pregnancy or if you have known bile‑duct obstruction, and consult a qualified practitioner if you have gallstones, kidney disease or are taking diuretics or anticoagulants (WHO, 2002; PRC Pharmacopoeia, 2020).

Phytochemically, Jin Qian Cao is well known to contain flavonoids (including quercetin, kaempferol and myricetin glycosides), phenolic acids (such as caffeic and chlorogenic acids), coumarins (including scopoletin and esculetin), saponins and terpenoids. These classes fit the herb’s traditional actions in relieving painful urination and supporting gallbladder function (He et al., 2008; Yang et al., 2010). While in vitro work suggests bile‑sequestering and smooth‑muscle‑relaxing activities that could plausibly help stone movement, clinical evidence for single‑herb effectiveness remains limited.

Today the dried herb is widely available from reputable Chinese herbal suppliers and specialty TCM retailers, and it remains a familiar domestic remedy in southern Chinese households. Modern pharmacology explores the flavonoids for gallstone‑related activity, but standardized preparations and clear clinical guidance are still evolving, and most patients in contemporary care use it as part of a multi‑herb formula rather than as a single therapy.

General Uses Top

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Common products:
• Gum/resin ("Jin Qian Cao" gum) produced by the plant, traded as a naturally sourced adhesive/raw material.

Industrial and craft applications:
• Adhesives/coatings: The plant's dried gum resin is used as a natural adhesive base in traditional craft formulations (e.g., bonding paper, wood veneers). Its adhesive properties are attributed to water-soluble polysaccharides and resinous components.
• Scientific/model organism: While not a standard laboratory model, the species serves in botanical research, genetics, and ecology studies. Documented uses include its role in phylogenetic studies within Myrsinoideae and investigations into its resin biosynthesis.

Properties relevant to use:
• Gum resin composition: Contains water-soluble polysaccharides (e.g., arabinose, galactose-rich polymers) contributing to adhesive properties.
• Resin components: Comprises resin acids and terpenoids providing tackiness and water resistance when cured.

Standards and regulation:
• No specific ISO/ASTM/EN standards identified for *L. christinae* gum resin. General adhesive or raw botanical material regulations may apply.

Sustainability and sourcing:
• Collection primarily occurs from wild populations in its native range (China, N. Vietnam). Overharvesting for gum resin poses sustainability risks, necessitating management plans for wild sourcing. No data on cultivation for non-medicinal products.

Synonyms Top

Scientific name Authority First published in
Lysimachia fargesii Franch. J. Bot. (Morot) 9: 463 (1895)
Lysimachia christinae var. intermedia Pamp. Nuovo Giorn. Bot. Ital. n.s., 17: 684 1910
Lysimachia christinae var. pubescens Franch. J. Bot. (Morot) 9: 463 1895
Lysimachia glandulosa R.Knuth Pflanzenr. , IV, 237: 264 (1905)
Lysimachia latronum H.Lév. & Vaniot Bull. Soc. Agric. Sarthe , reimpr., sér. 2, 39: 2 (1904)
Lysimachia legendrei Bonati Bull. Soc. Bot. Genève , sér. 2, 5: 299 (1913 publ. 1914)

Common names Top

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Language Common/alternative name
Chinese 金钱草
Chinese 铜钱草
Chinese 对座草
Chinese 过路黄
Chinese 遍地黄
Chinese 真金草
Chinese 走游草
Chinese 铺地莲

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lysimachia christinae subsp. tanakae (Maxim.) C.M.Hu J. Trop. Subtrop. Bot. 4(3): 15 (1996)
Lysimachia christinae subsp. christinae Unknown

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000442843
KEW urn:lsid:ipni.org:names:701074-1
The Plant List kew-2493137
Open Tree Of Life 157556
NCBI Taxonomy 213255
IPNI 701074-1
GBIF 7290577
USDA GRIN 423466
CMAUP NPO23847

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
Obacunone, a Promising Phytochemical Triterpenoid: Research Progress on Its Pharmacological Activity and Mechanism Zhou Y, Gu J, Li J, Zhang H, Wang M, Li Y, Wang T, Wang J, Shi R Molecules 15-Apr-2024
PMCID:PMC11054759
doi:10.3390/molecules29081791
PMID:38675611
Ethnopharmacology of five flowers herbal tea, a popular traditional beverage in Hong Kong and South China Chan KT, Wu HY, Tin WY, But PP, Cheung SC, Shaw PC J Ethnobiol Ethnomed 15-Mar-2024
PMCID:PMC10943788
doi:10.1186/s13002-024-00674-z
PMID:38491512
Chaihu Shugan prevents cholesterol gallstone formation by ameliorating the microbiota dysbiosis and metabolic disturbance in mice Wang W, Zhang K, Liu B, Zhou T, Tang Y, Li Y Front Pharmacol 31-Jan-2024
PMCID:PMC10866373
doi:10.3389/fphar.2023.1291236
PMID:38357365
Liver metabolomics reveals potential mechanism of Jieduan-Niwan formula against acute-on-chronic liver failure (ACLF) by improving mitochondrial damage and TCA cycle Liang J, Wei X, Hou W, Wang H, Ma R, Gao Y, Du Y, Zhang Q Chin Med 30-Nov-2023
PMCID:PMC10691013
doi:10.1186/s13020-023-00858-x
PMID:38037150
Therapeutic effects of Chinese herbal medicines for treatment of urolithiasis: A review Jiang C, Wang L, Wang Y, Xu R, Yang H, Peng J Chin Herb Med 27-Sep-2023
PMCID:PMC10715892
doi:10.1016/j.chmed.2023.09.001
PMID:38094012
Pathophysiological consequences and treatment strategy of obstructive jaundice Liu JJ, Sun YM, Xu Y, Mei HW, Guo W, Li ZL World J Gastrointest Surg 27-Jul-2023
PMCID:PMC10405123
doi:10.4240/wjgs.v15.i7.1262
PMID:37555128
Dandelion (Taraxacum Genus): A Review of Chemical Constituents and Pharmacological Effects Fan M, Zhang X, Song H, Zhang Y Molecules 27-Jun-2023
PMCID:PMC10343869
doi:10.3390/molecules28135022
PMID:37446683
In vitro evaluation of the composition and acaricidal efficacy of Urtica fissa leaf ethyl acetate extract against Sarcoptes scabiei mites Liao F, Bao T, Tao G, Hu Y, Han C Vet Med (Praha) 24-May-2023
PMCID:PMC10581513
doi:10.17221/6/2023-VETMED
PMID:37982023
Effect of dietary garlic (Allium sativum) on the zootechnical performance and health indicators of aquatic animals: A mini-review Delgado DL, Caceres LL, Gómez SA, Odio AD Vet World 11-May-2023
PMCID:PMC10420702
doi:10.14202/vetworld.2023.965-976
PMID:37576751
The potential of Chinese medicines in the treatment of hyperuricemia Tang J, Gao H, Xu Y, Chen J, Wu B Am J Transl Res 15-Apr-2023
PMCID:PMC10182497
PMID:37193181
Variation of soil physicochemical properties of different vegetation restoration types on subtropical karst area in southern China Xiao C, You R, Zhu N, Mi X, Gao L, Zhou X, Zhou G PLoS One 16-Mar-2023
PMCID:PMC10019609
doi:10.1371/journal.pone.0282620
PMID:36928208
Corydalis saxicola Bunting: A Review of Its Traditional Uses, Phytochemistry, Pharmacology, and Clinical Applications Qin F, Chen Y, Wang FF, Tang SQ, Fang YL Int J Mol Sci 13-Jan-2023
PMCID:PMC9864617
doi:10.3390/ijms24021626
PMID:36675133
A Comprehensive Review on Anti-Inflammatory Response of Flavonoids in Experimentally-Induced Epileptic Seizures Rabidas SS, Prakash C, Tyagi J, Suryavanshi J, Kumar P, Bhattacharya J, Sharma D Brain Sci 05-Jan-2023
PMCID:PMC9856497
doi:10.3390/brainsci13010102
PMID:36672083
Chamomile: A Review of Its Traditional Uses, Chemical Constituents, Pharmacological Activities and Quality Control Studies Dai YL, Li Y, Wang Q, Niu FJ, Li KW, Wang YY, Wang J, Zhou CZ, Gao LN Molecules 23-Dec-2022
PMCID:PMC9822300
doi:10.3390/molecules28010133
PMID:36615326
Exploiting Polyphenol-Mediated Redox Reorientation in Cancer Therapy Li L, Jin P, Guan Y, Luo M, Wang Y, He B, Li B, He K, Cao J, Huang C, Li J, Shen Z Pharmaceuticals (Basel) 12-Dec-2022
PMCID:PMC9787032
doi:10.3390/ph15121540
PMID:36558995

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
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
3-[[(1S,4As,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-2,5-dihydroxycyclohexa-2,5-diene-1,4-dione 9862964 Click to see 344.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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 via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown via CMAUP database
(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 via CMAUP database
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown via CMAUP database
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
(2S,3S,4S,5S,6S)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2S,3R,4S,5R,6R)-4,5,6-trihydroxy-2-methyloxan-3-yl]oxyoxan-3-yl]oxy-5-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-6-methyloxane-3,4-dicarbaldehyde 6325461 Click to see 764.70 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
3-O-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl] 1-O-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] propanedioate 5320846 Click to see 550.40 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
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 via CMAUP database
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1055/S-2006-959773
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257699 Click to see 564.50 unknown via CMAUP database
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 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 via CMAUP database
3-[(2S,5R,6R)-4,5-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44391816 Click to see 740.70 unknown https://doi.org/10.1055/S-2006-959773
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258737 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-959773
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 via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-959773
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> 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 / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-3-(3-hydroxy-4-methoxyphenyl)-1-(2,4,6-trihydroxy-3-methoxyphenyl)prop-2-en-1-one 5321858 Click to see 332.30 unknown via CMAUP database

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