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Trifolium hybridum

Trifolium hybridum - 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 UUID643fdee9c7794259805400
Scientific name Trifolium hybridum
Authority L.
First published in Sp. Pl.: 766 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Trifolium hybridum var. hybridum L.
Amoria hybrida (L.) C.Presl Symb. Bot.1: 47 (1831)
Trifolium elegans subsp. hybridum (L.) Bonnier & Layens Tabl. Syn. Pl. Vasc. France: 78 (1894)

Common names Top

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Language Common/alternative name
English alsike clover
Spanish trebol hibrido
Spanish trebol híbrido
Arabic نفل سويدي
Belarusian Канюшына ружовая
Bulgarian хибридна детелина
Czech jetel zvrhlý
Welsh meillionen fawr-orweddol
Danish aliske-kløver
Danish alsikekløver
Danish alsike-kløver
German gewöhnlicher schwedenklee
German schweden-klee
German schwedenklee
German bastard-klee
German bastardklee
Estonian roosa ristik
Estonian rootsi ristik
Persian شبدر دورگ
Finnish alsikeapila
French trèfle hybride
Irish ailsice
Irish seamair lochlannach
Irish seamair alsike
Upper Sorbian Šwedski dźećel
Icelandic alsikusmári
Icelandic alsíkusmári
Japanese タチオランダゲンゲ
Lithuanian rausvasis dobilas
Macedonian Розова детелина
Norwegian Bokmål alsike
Norwegian Bokmål alsikekløver
Dutch basterdklaver
Dutch bastaardklaver
Norwegian Nynorsk alsike
Norwegian Nynorsk alsikekløver
Polish koniczyna białoróżowa
Russian Клевер розовый
Russian Клевер шведский
Russian Клевер гибридный
Swedish alsikeklöver
Turkish İsveç üçgülü
Ukrainian Конюшина гібридна
Chinese 爱沙苜蓿
Chinese 金花草
Chinese 杂车轴草
Chinese 杂三叶
Chinese 雜種車軸草
Chinese 杂种车轴草
Chinese 砗磲肉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Trifolium hybridum subsp. anatolicum (Boiss.) M.Hossain Notes Roy. Bot. Gard. Edinburgh23: 466 (1961)
Trifolium hybridum subsp. elegans (Savi) Asch. & Graebn. Syn. Mitteleur. Fl.6(2): 496 (1907)
Trifolium hybridum subsp. hybridum L. Unknown

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213009
UNII 0NG564I0YY
Florida Plant Atlas 1799
Flora of Alabama 2082
Canadensys 5921
USDA Plants TRHY
Tropicos 13033929
INPN 127337
Flora of Italy 2610
KEW urn:lsid:ipni.org:names:30240399-2
The Plant List ild-8085
Open Tree Of Life 1066895
Observations.org 7571
NCBI Taxonomy 74517
NBN Atlas NBNSYS0000003246
Nature Serve 2.147285
IPNI 523230-1
iNaturalist 61824
GBIF 6109535
Freebase /m/02vmckm
WisFlora 5270
EPPO TRFHY
EOL 703404
Elurikkus 8000
Calflora (Californian flora) 8083
USDA GRIN 300618
Wikipedia Trifolium_hybridum
CMAUP NPO11206

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
Plant-Associated Bacillus thuringiensis and Bacillus cereus: Inside Agents for Biocontrol and Genetic Recombination in Phytomicrobiome Sorokan A, Gabdrakhmanova V, Kuramshina Z, Khairullin R, Maksimov I Plants (Basel) 30-Nov-2023
PMCID:PMC10707757
doi:10.3390/plants12234037
PMID:38068672
DNA barcoding as new diagnostic tool to lethal plant poisoning in herbivorous mammals Schweikle S, Häser A, Wetters S, Raisin M, Greiner M, Rigbers K, Fischer U, Pietsch K, Suntz M, Nick P PLoS One 15-Nov-2023
PMCID:PMC10650979
doi:10.1371/journal.pone.0292275
PMID:37967132
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Mass Spectrometric Fingerprint Mapping Reveals Species-Specific Differences in Plant Polyphenols and Related Bioactivities Vanhakylä S, Salminen JP Molecules 31-Aug-2023
PMCID:PMC10490256
doi:10.3390/molecules28176388
PMID:37687216
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Edge Effects in the Distribution of Coleoptera in the Forests of the Center of the European Part of Russia Ruchin AB, Egorov LV, Khapugin AA Insects 10-Apr-2023
PMCID:PMC10144564
doi:10.3390/insects14040371
PMID:37103186
Legacy Effects of Phytoremediation on Plant-Associated Prokaryotic Communities in Remediated Subarctic Soil Historically Contaminated with Petroleum Hydrocarbons Papik J, Strejcek M, Musilova L, Guritz R, Leewis MC, Leigh MB, Uhlik O Microbiol Spectr 28-Mar-2023
PMCID:PMC10100700
doi:10.1128/spectrum.04448-22
PMID:36975310
From sequences to species: Charting the phytoplasma classification and taxonomy in the era of taxogenomics Kirdat K, Tiwarekar B, Sathe S, Yadav A Front Microbiol 09-Mar-2023
PMCID:PMC10033645
doi:10.3389/fmicb.2023.1123783
PMID:36970684
Genome survey and genetic characterization of Acacia pachyceras O. Schwartz Habibi N, Al Salameen F, Vyas N, Rahman M, Kumar V, Shajan A, Zakir F, Razzack NA, Al Doaij B Front Plant Sci 16-Feb-2023
PMCID:PMC9979705
doi:10.3389/fpls.2023.1062401
PMID:36875582
The Impact of N.I. Vavilov on the Conservation and Use of Plant Genetic Resources in Scandinavia: A Review Solberg SØ, Loskutov IG, Breian L, Diederichsen A Plants (Basel) 28-Dec-2022
PMCID:PMC9823609
doi:10.3390/plants12010143
PMID:36616272
A Case Study of Photosensitivity Associated with Anaplasma spp. Infection in Cattle Anton A, Solcan G Animals (Basel) 16-Dec-2022
PMCID:PMC9774125
doi:10.3390/ani12243568
PMID:36552488
Inbreeding depression in polyploid species: a meta-analysis Clo J, Kolář F Biol Lett 14-Dec-2022
PMCID:PMC9748776
doi:10.1098/rsbl.2022.0477
PMID:36514955
Endophytic Diaporthe as Promising Leads for the Development of Biopesticides and Biofertilizers for a Sustainable Agriculture Hilário S, Gonçalves MF Microorganisms 12-Dec-2022
PMCID:PMC9784053
doi:10.3390/microorganisms10122453
PMID:36557707
Pest categorisation of Atalodera andina Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Maiorano A, Streissl F, Reignault PL EFSA J 30-Jun-2022
PMCID:PMC9244778
doi:10.2903/j.efsa.2022.7395
PMID:35784818

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 / Naphthacenes
Naphtho[2,1-a]naphthacene 123039 Click to see C1=CC=C2C(=C1)C=CC3=C2C=CC4=CC5=CC6=CC=CC=C6C=C5C=C43 328.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilaurin 10851 Click to see CCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC 639.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(Z)-alpha-ocimene 5463455 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Parkeol 12313974 Click to see CC(CCC=C(C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 44423569 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(=C)C 454.80 unknown via CMAUP database
Cycloneolitsol 101306728 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 454.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24S)-24-Methyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630502 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
24,24-Dimethyllanosta-9(11),25-dien-3beta-ol 102504569 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 454.80 unknown via CMAUP database
4alpha,14alpha-Dimethyl-24-methylene-cholest-9(11)-en-3beta-ol 5283648 Click to see CC1C2CCC3C(=CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C)C2(CCC1O)C 426.70 unknown via CMAUP database
Agrostophyllinol 489917 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24S)-24-Ethyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630504 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C)C(=C)C 454.80 unknown via CMAUP database
(24S)-4alpha,14-Dimethyl-5alpha-stigmasta-9(11),25-dien-3beta-ol 101630497 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(=C)C 440.70 unknown via CMAUP database
4alpha,14-Dimethyl-5alpha-stigmast-9(11)-en-3beta-ol 101630496 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(C)C 442.80 unknown via CMAUP database
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmastanol 241572 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5H-7,4-Methenofuro(3,2-c)oxireno(f)oxacycloundecin-5-one,1a,2,3,7,11,11a-hexahydro-8,11a-dimethyl-, (1aS,7R,11aS)- 497202 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Linderalactone 6450191 Click to see CC1=CCCC2=CC(C3=C(C1)OC=C3C)OC2=O 244.28 unknown via CMAUP database
Pseudoneolinderane 57400551 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Zeylanin 12445041 Click to see CC1=CC2=C(C3C=C(CCC1OC(=O)C)C(=O)O3)C(=CO2)C 302.32 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
2H-10,1a-(Epoxymethano)oxireno(4,5)cyclodeca(1,2-b)furan-12-one, 3,6,10,10a-tetrahydro-5,9-methyl-, (1aS-(1aR*,4E,10R*,10aR*))- 6450227 Click to see CC1=CCCC23C(O2)C(C4=C(C1)OC=C4C)OC3=O 260.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Thamnosmonin 312089 Click to see CC(=C)C(C(C1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)O 276.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1007/BF00567881
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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 https://doi.org/10.1007/BF00567881
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00567881
Populnin 3-O-rhamnopyranoside 90795788 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3,9-Dimethoxypterocarpan 454892 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein(1-) 25201420 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)[O-])O)O 269.23 unknown via CMAUP database

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