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Ophiorrhiza japonica

Ophiorrhiza japonica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Ophiorrhiza japonica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe541517e6844504118
Scientific name Ophiorrhiza japonica
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 978 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ophiorrhiza acutiloba Hayata Icon. Pl. Formosan. 2: 86 (1912)
Ophiorrhiza cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 13: 177 (1914)
Ophiorrhiza dimorphantha Hayata Icon. Pl. Formosan. 2: 86 (1912)
Ophiorrhiza dimorphantha f. brevistigma Hayata Icon. Pl. Formosan. 2: 87 1912
Ophiorrhiza dimorphantha f. longistigma Hayata Icon. Pl. Formosan. 2: 87 1912
Ophiorrhiza eryei Champ. Hooker's J. Bot. Kew Gard. Misc. 4: 170. 1852 (1852)
Ophiorrhiza japonica var. acutiloba (Hayata) Ohwi Acta Phytotax. Geobot. 7: 195. 1938
Ophiorrhiza japonica var. minor E.H.L.Krause Repert. Spec. Nov. Regni Veg. 12: 489. 1922
Ophiorrhiza japonica var. tashiroi (Maxim.) Ohwi Acta Phytotax. Geobot. 7: 195. 1938
Ophiorrhiza labordei H.Lév. Repert. Spec. Nov. Regni Veg. 13: 177 (1914)
Ophiorrhiza monticola Hayata Icon. Pl. Formosan. 2: 89 (1912)
Ophiorrhiza monticola f. brevistigma Hayata Icon. Pl. Formosan. 2: 89 1912
Ophiorrhiza monticola f. longistigma Hayata Icon. Pl. Formosan. 2: 90 1912
Ophiorrhiza nigricans H.S.Lo Bull. Bot. Res., Harbin 10(2): 53 (1990)
Ophiorrhiza tashiroi Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 32: 489 (1888)
Ophiorrhiza japonica f. plena T.Yamaz. J. Jap. Bot. 79: 269 (2004)

Common names Top

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Language Common/alternative name
nan choâ-kin-chhaú
nan choâ-kin-chháu
Chinese 蛇根草
Chinese 变黑蛇根草
Chinese 散血草
Chinese 日本蛇根草
Chinese 日本蛇根草（蛇根草）
Chinese 猪菜

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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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
      • Hainan
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000257052
Tropicos 50058517
KEW urn:lsid:ipni.org:names:758479-1
The Plant List kew-140419
Open Tree Of Life 394405
Observations.org 360892
NCBI Taxonomy 367363
IPNI 758479-1
iNaturalist 603383
GBIF 5340994
EPPO OPHJA
EOL 1102627
Elurikkus 521101
USDA GRIN 25793

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
Induction of Monoterpenoid Oxindole Alkaloids Production and Related Biosynthetic Gene Expression in Response to Signaling Molecules in Hamelia patens Plant Cultures López-Vázquez AL, Sepúlveda-García EB, Rubio-Rodríguez E, Ponce-Noyola T, Trejo-Tapia G, Barrera-Cortés J, Cerda-García-Rojas CM, Ramos-Valdivia AC Plants (Basel) 27-Mar-2024
PMCID:PMC11013434
doi:10.3390/plants13070966
PMID:38611495
Profiles of Metabolic Genes in Uncaria rhynchophylla and Characterization of the Critical Enzyme Involved in the Biosynthesis of Bioactive Compounds-(iso)Rhynchophylline Yang M, Yao B, Lin R Biomolecules 30-Nov-2022
PMCID:PMC9775700
doi:10.3390/biom12121790
PMID:36551218
Indole-Containing Natural Products 2019–2022: Isolations, Reappraisals, Syntheses, and Biological Activities Umer SM, Solangi M, Khan KM, Saleem RS Molecules 05-Nov-2022
PMCID:PMC9655573
doi:10.3390/molecules27217586
PMID:36364413
The S-Gene YUC6 Pleiotropically Determines Male Mating Type and Pollen Size in Heterostylous Turnera (Passifloraceae): A Novel Neofunctionalization of the YUCCA Gene Family Henning PM, Shore JS, McCubbin AG Plants (Basel) 08-Oct-2022
PMCID:PMC9572539
doi:10.3390/plants11192640
PMID:36235506
Structurally Diverse Metabolites from the Ophiorrhiza japonica Bl. and Their Antioxidant Activities In Vitro and PPARα Agonistic Activities In Silico Bu Q, Jin Y, Xu MJ, Wu L, Liang LF Molecules 19-Aug-2022
PMCID:PMC9412425
doi:10.3390/molecules27165301
PMID:36014541
Total Synthesis of Ophiorrhine A, G and Ophiorrhiside E Featuring a Bioinspired Intramolecular Diels–Alder Cycloaddition Cao W, Dou Y, Kouklovsky C, Vincent G Angew Chem Int Ed Engl 10-Aug-2022
PMCID:PMC9543224
doi:10.1002/anie.202209135
PMID:35869029
Recent studies on chemical constituents of Ophiorrhiza plants Kitajima M J Nat Med 28-Jul-2022
PMCID:PMC9411090
doi:10.1007/s11418-022-01640-3
PMID:35902551
Integrative analysis of transcriptome and metabolome reveals the effect of DNA methylation of chalcone isomerase gene in promoter region on Lithocarpus polystachyus Rehd flavonoids Lin L, Wang S, Zhang J, Song X, Zhang D, Cheng W, Cui M, Long Y, Xing Z Synth Syst Biotechnol 20-May-2022
PMCID:PMC9149025
doi:10.1016/j.synbio.2022.05.003
PMID:35664927
Plants and endophytes – a partnership for the coumarin production through the microbial systems Srinivasa C, Mellappa G, Patil SM, Ramu R, Shreevatsa B, Dharmashekar C, Kollur SP, Syed A, Shivamallu C Mycology 07-Feb-2022
PMCID:PMC9673776
doi:10.1080/21501203.2022.2027537
PMID:36405338
Functional analysis of a dihydroflavonol 4-reductase gene in Ophiorrhiza japonica (OjDFR1) reveals its role in the regulation of anthocyanin Sun W, Zhou N, Feng C, Sun S, Tang M, Tang X, Ju Z, Yi Y PeerJ 20-Oct-2021
PMCID:PMC8541326
doi:10.7717/peerj.12323
PMID:34721993
Traditional Chinese medicine in COVID-19 Lyu M, Fan G, Xiao G, Wang T, Xu D, Gao J, Ge S, Li Q, Ma Y, Zhang H, Wang J, Cui Y, Zhang J, Zhu Y, Zhang B Acta Pharm Sin B 20-Sep-2021
PMCID:PMC8450055
doi:10.1016/j.apsb.2021.09.008
PMID:34567957
LED Lights Promote Growth and Flavonoid Accumulation of Anoectochilus roxburghii and Are Linked to the Enhanced Expression of Several Related Genes Gam DT, Khoi PH, Ngoc PB, Linh LK, Hung NK, Anh PT, Thu NT, Hien NT, Khanh TD, Ha CH Plants (Basel) 12-Oct-2020
PMCID:PMC7599663
doi:10.3390/plants9101344
PMID:33053736
The Chalcone Isomerase Family in Cotton: Whole-Genome Bioinformatic and Expression Analyses of the Gossypium barbadense L. Response to Fusarium Wilt Infection Zu QL, Qu YY, Ni ZY, Zheng K, Chen Q, Chen QJ Genes (Basel) 04-Dec-2019
PMCID:PMC6947653
doi:10.3390/genes10121006
PMID:31817162
Chalcone Isomerase a Key Enzyme for Anthocyanin Biosynthesis in Ophiorrhiza japonica Sun W, Shen H, Xu H, Tang X, Tang M, Ju Z, Yi Y Front Plant Sci 09-Jul-2019
PMCID:PMC6629912
doi:10.3389/fpls.2019.00865
PMID:31338101
Comparison of Strategies to Overcome Drug Resistance: Learning from Various Kingdoms Ogawara H Molecules 18-Jun-2018
PMCID:PMC6100412
doi:10.3390/molecules23061476
PMID:29912169

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Harmala alkaloids
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1248/YAKUSHI1947.87.9_1153
https://doi.org/10.1016/S0040-4039(00)95021-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4S)-3-ethenyl-4-[(6-hydroxy-9H-pyrido[3,4-b]indol-1-yl)methyl]-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 163188336 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3=NC=CC4=C3NC5=C4C=C(C=C5)O 528.50 unknown https://doi.org/10.1248/CPB.34.3064
3-ethenyl-4-(9H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 23757137 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3=NC=CC4=C3NC5=CC=CC=C45 512.50 unknown https://doi.org/10.1248/CPB.34.3064
Carboline metabolite (C26H28N2O10) 139292061 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3=NC=CC4=C3NC5=C4C=C(C=C5)O 528.50 unknown https://doi.org/10.1248/CPB.34.3064
Lyalosidic acid 10391678 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC3=NC=CC4=C3NC5=CC=CC=C45 512.50 unknown https://doi.org/10.1248/CPB.34.3064
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.87.9_1153
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.87.9_1153
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/YAKUSHI1947.87.9_1153
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/0031-9422(88)87030-4
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/0031-9422(88)87030-4
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
17-Ethenyl-18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19-oxa-2,12-diazapentacyclo[14.3.1.02,14.05,13.06,11]icosa-3,5,7,9,11,13-hexaene-20-carboxylic acid 163192292 Click to see C=CC1C2CC3=C4C(=C5C=CC=CC5=N4)C=CN3C(C2C(=O)O)OC1OC6C(C(C(C(O6)CO)O)O)O 512.50 unknown https://doi.org/10.1016/S0040-4039(00)95021-4

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