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Cnidium japonicum

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 UUID64401244a2321045501398
Scientific name Cnidium japonicum
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 3: 60 (1867)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Selinum japonicum (Miq.) Franch. & Sav. Enum. Pl. Jap. 1(1): 186 1873
Oenanthe japonica Nakai in Mori, Enum. Pl. Cor. 272 (1922).

Common names Top

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Language Common/alternative name
Japanese ハマゼリ
Korean 갯사상자
Chinese 滨蛇床
Chinese 濱蛇床

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Ogasawara-Shoto

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000612796
Tropicos 1700368
KEW urn:lsid:ipni.org:names:840454-1
The Plant List kew-2728962
Open Tree Of Life 622361
NCBI Taxonomy 48111
IPNI 840454-1
iNaturalist 639251
GBIF 3638188
EPPO CNJJA
EOL 2890637

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
Evaluation and Comparison of the Antimelanogenic Properties of Different Solvent Fractionated Cnidium japonicum Extracts in B16F10 Murine Melanoma Cells Jo HJ, Oh JH, Karadeniz F, Seo Y, Kong CS Prev Nutr Food Sci 31-Dec-2022
PMCID:PMC9843722
doi:10.3746/pnf.2022.27.4.448
PMID:36721746
Santamarine Shows Anti-Photoaging Properties via Inhibition of MAPK/AP-1 and Stimulation of TGF-β/Smad Signaling in UVA-Irradiated HDFs Oh JH, Kim J, Karadeniz F, Kim HR, Park SY, Seo Y, Kong CS Molecules 11-Jun-2021
PMCID:PMC8230857
doi:10.3390/molecules26123585
PMID:34208202
Culturable Fungal Endophytes Isolated from the Roots of Coastal Plants Inhabiting Korean East Coast Kim H, You YH, Yoon H, Seo Y, Kim YE, Choo YS, Lee IJ, Shin JH, Kim JG Mycobiology 30-Jun-2014
PMCID:PMC4112224
doi:10.5941/MYCO.2014.42.2.100
PMID:25071377
Inhibition of nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophages by Jeju plant extracts Yang EJ, Yim EY, Song G, Kim GO, Hyun CG Interdiscip Toxicol 28-Dec-2009
PMCID:PMC2984114
doi:10.2478/v10102-009-0022-2
PMID:21217861
Antitumor actions of a chromone glucoside cnidimoside A isolated from Cnidium japonicum. Kimura Y, Sumiyoshi M, Taniguchi M, Baba K J Nat Med 01-Jul-2008
doi:10.1007/S11418-008-0242-3
PMID:18418697
Chromone glucosides from Cnidium japonicum Kimiye Baba, Hiromu Kawanishi, Masahiko Taniguchi, Mitsugi Kozawa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90538-7

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
5,7-Dihydroxy-2-methyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl]chromen-4-one 73153615 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)CC=C(C)COC3C(C(C(C(O3)CO)O)O)O)O 438.40 unknown https://doi.org/10.1007/S11418-008-0242-3
Cnidimoside A 21603474 Click to see 438.40 unknown https://doi.org/10.1007/S11418-008-0242-3
https://doi.org/10.1016/S0031-9422(00)90538-7
Cnidimoside B 70682745 Click to see 452.50 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Cnidimol A 102337144 Click to see 276.28 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
2-(1,2-Dihydroxy-1-methylethyl)-2,3-dihydro-4-hydroxy-7-methyl-5H-furo(3,2-g)(1)benzopyran-5-one 21603473 Click to see 292.28 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-(2-Oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl)propan-2-yl 2-methylpropanoate 5315980 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl 2-methylpropanoate 101937463 Click to see CC(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 316.30 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0031-9422(00)90538-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0031-9422(00)90538-7

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