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Chrysosplenium grayanum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440110f760b7032661870
Scientific name Chrysosplenium grayanum
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 23: 248 (1877)

Ethnobotanical Use Top

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General Uses Top

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Common products:
No commercial products are reported for Chrysosplenium grayanum.

Industrial and craft applications:
No industrial or craft uses are documented.

Food and beverages (non-medicinal):
No food or beverage uses are documented.

Colorants and tanning:
No dye or tannin uses are documented.

Wood and fiber:
No wood or fiber uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented.

Properties relevant to use:
Not applicable; no products or properties with established uses are reported for this species.

Standards and regulation:
Not applicable.

Sustainability and sourcing:
Not applicable; no extractive or cultivated product is reported.

Scientific/model-organism use:
The species is occasionally used in environmental science and taxonomy research. It has been employed in studies of microhabitat ecology, wetland vegetation dynamics, and species delimitation within Saxifragaceae, including phylogenetic analyses that contribute to understanding evolutionary relationships and population-level structure. Herbarium specimens and occurrence data are archived in major biodiversity repositories (GBIF; JStor Global Plants), and nomenclatural information is indexed in the International Plant Names Index.

Synonyms Top

Scientific name Authority First published in
Chrysosplenium dickinsii Franch. & Sav. Enum. Pl. Jap. 2: 357 (1878)
Chrysosplenium grayanum var. dickinsii (Franch. & Sav.) Franch. & Sav. Enum. Pl. Jap. 2: 650 1879
Chrysosplenium grayanum var. nipponicum (Franch. & Sav.) Franch. & Sav. Enum. Pl. Jap. 2: 650 1879
Chrysosplenium grayanum var. polysticha Franch. Monogr. Chrysospl. 2: 9 1891
Chrysosplenium nipponicum Franch. & Sav. Enum. Pl. Jap. 2: 356 (1878)

Common names Top

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Language Common/alternative name
Japanese ネコノメソウ
Korean 괭이눈
Chinese 猫眼草

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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No forms added yet.

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
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000603981
Tropicos 29101304
KEW urn:lsid:ipni.org:names:790599-1
The Plant List kew-2720157
Open Tree Of Life 1040364
Observations.org 127208
NCBI Taxonomy 61245
IPNI 790599-1
GBIF 5567424
Freebase /m/0nbhfp0
EPPO CPUGR
EOL 5596366
Elurikkus 545901

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
Diagnostic Evaluation and Preparation of the Reference Information for River Restoration in South Korea Lim CH, Pi JH, Kim AR, Cho HJ, Lee KS, You YH, Lee KH, Kim KD, Moon JS, Lee CS Int J Environ Res Public Health 10-Feb-2021
PMCID:PMC7916817
doi:10.3390/ijerph18041724
PMID:33578983
β-Peltoboykinolic Acid from Astilbe rubra Attenuates TGF-β1-Induced Epithelial-to-Mesenchymal Transitions in Lung Alveolar Epithelial Cells Bang IJ, Kim HR, Jeon Y, Jeong MH, Park YJ, Kwak JH, Chung KH Molecules 15-Jul-2019
PMCID:PMC6680586
doi:10.3390/molecules24142573
PMID:31311194
Novel Flavonoids from Chrysosplenium grayanum Maxim. (Saxifragaceae). Munehisa ARISAWA, Hua BAI, Miwa SHIOJIMA, Toshimitsu HAYASHI, Yasuhiro TEZUKA, Tooru TAGA, Yoshihisa MIWA, Yusuke ITO, Tohru KIKUCHI, Naokata MORITA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.41.571
Chrysograyanone, a novel chromone derivative from Chrysosplenium grayanum MAXIM. Munehisa Arisawa, Miwa shiojima, Hua Bai, Toshimitsu Hayashi, Yasuhiro Tezuka, Tooru Taga, Yoshihisa Miwa, Tohru Kikuchi, Naokata Morita Elsevier BV 12-Feb-2003
doi:10.1016/S0040-4039(00)61104-8
Isolation and identification of a cytotoxic principle from Chrysosplenium grayanum Maxim. (Saxifragaceae) and its antitumor activities. Arisawa M, Bai H, Shimizu S, Koshimura S, Tanaka M, Sasaki T, Morita N Chem Pharm Bull (Tokyo) 01-Dec-1992
doi:10.1248/CPB.40.3274
PMID:1294331
Isolation and cytotoxicity of two new flavonoids from Chrysosplenium grayanum and related flavonols. Arisawa M, Hayashi T, Shimizu M, Morita N, Bai H, Kuze S, Ito Y J Nat Prod 01-May-1991
doi:10.1021/NP50075A029
PMID:1955888

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
Methyl 3,5-dihydroxy-4-methoxybenzoate 5319726 Click to see COC1=C(C=C(C=C1O)C(=O)OC)O 198.17 unknown https://doi.org/10.1021/NP50075A029
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bS,8aS,10R,12aS,14bS)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 133611880 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C 456.70 unknown https://doi.org/10.1248/CPB.40.3274
10-Hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 12314032 Click to see 456.70 unknown https://doi.org/10.1248/CPB.40.3274
Beta-Peltoboykinolic Acid 12016584 Click to see 456.70 unknown https://doi.org/10.1248/CPB.40.3274
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5-Hydroxy-7,2',4'-trimethoxy-3',6'-diketoflavone 44258660 Click to see 358.30 unknown https://doi.org/10.1248/CPB.41.571
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / 3-methoxychromones
2-(5-Hydroxy-3,7-dimethoxy-4-oxochromen-2-yl)-3,5-dimethoxycyclohexa-2,5-diene-1,4-dione 10045780 Click to see 388.30 unknown https://doi.org/10.1248/CPB.41.571
methyl (1S,5R)-1,5-dihydroxy-5-(5-hydroxy-3,7-dimethoxy-4-oxochromen-2-yl)-2-methoxy-4-oxocyclopent-2-ene-1-carboxylate 10002322 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3(C(=O)C=C(C3(C(=O)OC)O)OC)O)O 422.30 unknown https://doi.org/10.1016/S0040-4039(00)61104-8
https://doi.org/10.1248/CPB.41.571
Methyl 1,5-dihydroxy-5-(5-hydroxy-3,7-dimethoxy-4-oxochromen-2-yl)-2-methoxy-4-oxocyclopent-2-ene-1-carboxylate 85088764 Click to see 422.30 unknown https://doi.org/10.1016/S0040-4039(00)61104-8
https://doi.org/10.1248/CPB.41.571
Methyl 1,5-dihydroxy-5-(8-hydroxy-3,6-dimethoxy-4-oxochromen-2-yl)-2-methoxy-4-oxocyclopent-2-ene-1-carboxylate 163192647 Click to see 422.30 unknown https://doi.org/10.1248/CPB.41.571
https://doi.org/10.1016/S0040-4039(00)61104-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-[4,5-dimethoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-hydroxy-3,6,7-trimethoxychromen-4-one 10008104 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC 566.50 unknown https://doi.org/10.1248/CPB.41.571
2-[4,5-Dimethoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-5-hydroxy-3,6,7-trimethoxychromen-4-one 74978515 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC 566.50 unknown https://doi.org/10.1248/CPB.41.571
Brickellin 13871363 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O)OC 404.40 unknown https://doi.org/10.1021/NP50075A029
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown https://doi.org/10.1021/NP50075A029
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1021/NP50075A029
Chrysosplenol E 5315857 Click to see 374.30 unknown https://doi.org/10.1021/NP50075A029
Chrysosplenol F 5491448 Click to see 360.30 unknown https://doi.org/10.1021/NP50075A029
Chrysosplenol G 5315858 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3OC)OC)O)O 374.30 unknown https://doi.org/10.1021/NP50075A029
Chrysosplenoside H 44259889 Click to see 566.50 unknown https://doi.org/10.1248/CPB.41.571
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1021/NP50075A029

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