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Limnocharis flava

Limnocharis flava - 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 UUID64401bf19ae9f959995140
Scientific name Limnocharis flava
Authority (L.) Buchenau
First published in Index Crit. Butom. Alism. Juncag. : 13 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Limnocharis emarginata Humb. & Bonpl. Pl. Aequinoct. 1: 116 (1808)
Limnocharis plumieri Rich. Mém. Mus. Hist. Nat. 1: 370 (1815)
Limnocharis flava var. indica Buchenau Pflanzenr. , IV, 16: 9 (1903)
Alisma flavum L. Sp. Pl. : 343 (1753)
Damasonium flavum Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Damasonium maximum Burm. ex Steud. Nomencl. Bot. , ed. 2, 1: 481 (1840)

Common names Top

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Language Common/alternative name
English yellow velvetleaf
ban biah-biah
bjn patiul
Bengali হলদেপানা
Czech žabníkovka žlutá
Indonesian genjer
Japanese キバナオモダカ
jv genjer
jv gènjèr
mad Ṭong-cènṭongan
Malay pokok keladi senduk
su génjér
Thai ตาลปัตรฤๅษี
Thai ผักพาย
Thai ผักต้นจอง
Thai ตะละปัดฤๅษี
Vietnamese kèo nèo
Vietnamese cù nèo
Chinese 黃花澤瀉
Chinese 黃花藺
Chinese 黄花泽泻
Chinese 黄花蔺

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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northwest
      • Mexico Southeast
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil Southeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000683301
USDA Plants LIFL5
Tropicos 50160232
INPN 735363
KEW urn:lsid:ipni.org:names:58404-1
The Plant List kew-280510
Missouri Botanical Garden 278315
Open Tree Of Life 561070
NCBI Taxonomy 55477
IPNI 58404-1
iNaturalist 283710
GBIF 5328736
Freebase /m/0h3sh2m
EPPO LMNFL
EOL 250023
USDA GRIN 22247
Wikipedia Limnocharis_flava
CMAUP NPO6081
PFAF Limnocharis flava

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
Mining wastewater treatment technologies and resource recovery techniques: A review Matebese F, Mosai AK, Tutu H, Tshentu ZR Heliyon 21-Jan-2024
PMCID:PMC10839889
doi:10.1016/j.heliyon.2024.e24730
PMID:38317979
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Optimizing total ammonia–nitrogen concentration for enhanced microbial fuel cell performance in landfill leachate treatment: a bibliometric analysis and future directions Ishaq A, Said MI, Azman SB, Abdulwahab MF, Jagun ZT Environ Sci Pollut Res Int 15-Jul-2023
PMCID:PMC10404197
doi:10.1007/s11356-023-28580-z
PMID:37454007
Nutritional values of wild edible freshwater macrophytes Zakaria MH, Ramaiya SD, Bidin N, Syed NN, Bujang JS PeerJ 11-Jul-2023
PMCID:PMC10348304
doi:10.7717/peerj.15496
PMID:37456903
Strategies for the Management of Aggressive Invasive Plant Species Lorenzo P, Morais MC Plants (Basel) 28-Jun-2023
PMCID:PMC10346621
doi:10.3390/plants12132482
PMID:37447043
A review on arsenic in the environment: bio-accumulation, remediation, and disposal Patel KS, Pandey PK, Martín-Ramos P, Corns WT, Varol S, Bhattacharya P, Zhu Y RSC Adv 16-May-2023
PMCID:PMC10186335
doi:10.1039/d3ra02018e
PMID:37200696
Molecular Characterization of Resistance to Nicosulfuron in Setaria viridis Cao Y, Lan Y, Huang H, Wei S, Li X, Sun Y, Wang R, Huang Z Int J Mol Sci 12-Apr-2023
PMCID:PMC10138712
doi:10.3390/ijms24087105
PMID:37108267
Responses of aquatic vegetables to biochar amended soil and water environments: a critical review Wang X, Zhao Y, Yao G, Lin Z, Xu L, Jiang Y, Jin Z, Shan S, Ping L RSC Adv 01-Feb-2023
PMCID:PMC9891097
doi:10.1039/d2ra04847g
PMID:36760305
Developmental Morphology and Anatomy Shed Light on Both Parallel and Convergent Evolution of the Umbellate Inflorescence in Monocots, Underlain by a New Variant of Metatopy Martínez-Gómez J, Atluri TA, Rose IJ, Holliday AJ, Strock CF, Lynch JP, Miller WB, Stevenson DW, Specht CD Front Plant Sci 29-Apr-2022
PMCID:PMC9100582
doi:10.3389/fpls.2022.873505
PMID:35574142
Mitragyna Species as Pharmacological Agents: From Abuse to Promising Pharmaceutical Products Ahmad I, Prabowo WC, Arifuddin M, Fadraersada J, Indriyanti N, Herman H, Purwoko RY, Nainu F, Rahmadi A, Paramita S, Kuncoro H, Mita N, Narsa AC, Prasetya F, Ibrahim A, Rijai L, Alam G, Mun’im A, Dej-adisai S Life (Basel) 27-Jan-2022
PMCID:PMC8878704
doi:10.3390/life12020193
PMID:35207481
Heavy Metal Accumulation in Rice and Aquatic Plants Used as Human Food: A General Review Uddin MM, Zakeel MC, Zavahir JS, Marikar FM, Jahan I Toxics 20-Dec-2021
PMCID:PMC8706345
doi:10.3390/toxics9120360
PMID:34941794
New Aspects of Secretory Structures in Five Alismataceae Species: Laticifers or Ducts? Leme FM, Bento JP, Fabiano VS, González JD, Pott VJ, Arruda RD Plants (Basel) 08-Dec-2021
PMCID:PMC8709293
doi:10.3390/plants10122694
PMID:34961164
A review of Fasciolopsis buski distribution and control in Indonesia Ridha MR, Indriyati L, Andiarsa D, Wardhana AH Vet World 26-Oct-2021
PMCID:PMC8654757
doi:10.14202/vetworld.2021.2757-2763
PMID:34903937
Herbicide-Resistant Invasive Plant Species Ludwigia decurrens Walter Kurniadie D, Widianto R, Widayat D, Umiyati U, Nasahi C, Kato-Noguchi H Plants (Basel) 21-Sep-2021
PMCID:PMC8469676
doi:10.3390/plants10091973
PMID:34579505
Fauna associated with Malayan filariasis transmission in Banyuasin, South Sumatra, Indonesia Mulyaningsih B, Umniyati SR, Hadisusanto S, Edyansyah E Vet World 28-Jul-2021
PMCID:PMC8404132
doi:10.14202/vetworld.2021.1954-1959
PMID:34475722

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 acid esters
Methyl 3-phenylpropionate 7643 Click to see COC(=O)CCC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 11130717 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C 320.50 unknown via CMAUP database
(4aalpha)-2-Hydroxy-2beta,5,5,8abeta-tetramethyldecalin-1beta-((R)-3-methylvaleric acid) 11868539 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
Labdanic Acid Methyl Ester 7057547 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)OC 338.50 unknown via CMAUP database
Labdanolic acid 11186394 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol 92812 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
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 via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 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-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(6-O-I(2)-D-xylopyranosyl-I(2)-D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one 102148697 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 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 via CMAUP database
Isoquercetin 5280804 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
Kaempferol-3-O-rutinoside 5318767 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)O)O)O)O)O)O 594.50 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 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)O)O)O)O)O)O)O)O 626.50 unknown via CMAUP database
Rutin 5280805 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)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database

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Collections Top

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