Limnanthes douglasii

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Collections

Details Top

Internal ID	UUID6440478800c77604526761
Scientific name	Limnanthes douglasii
Authority	R.Br.
First published in	London Edinburgh Philos. Mag. & J. Sci. 2: 70 (1833)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Floerkea douglasii	Baill.	Hist. Pl. 5: 20 (1873)
Limnanthes howelliana	Abrams	Madroño 6: 27 (1941)

Common names Top

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Filter by language:

Language	Common/alternative name
English	douglas' meadowfoam
English	poached egg plant
Azerbaijani	duqlas limnanthesi
Czech	voďankovec douglasův
Welsh	melynwy
German	douglas-sumpfblume
German	spiegelei-blume
German	spiegeleierblume
Finnish	hilppa
Icelandic	eggjablóm
Dutch	geelwitte moerasbloem
Polish	limnantes douglasa
Swedish	sumpört
Chinese	沼沫花

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Limnanthes douglasii subsp. nivea	(C.T.Mason) C.T.Mason	Madroño 36: 50. 1989
Limnanthes douglasii subsp. ornduffii	E.G.Buxton	Madroño 60: 229 (2013)
Limnanthes douglasii subsp. rosea	(Benth.) C.T.Mason	Madroño 36: 50 (1989)
Limnanthes douglasii subsp. striata	(Jeps.) Morin	J. Bot. Res. Inst. Texas 1: 1017 (2007)
Limnanthes douglasii subsp. sulphurea	(C.T.Mason) C.T.Mason	Madroño 36: 50. 1989

Varieties (abbr. var.) Top

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Name	Authority	First published in
Limnanthes douglasii var. nivea	C.T.Mason	Madroño 36: 50 (1989)
Limnanthes douglasii var. sulphurea	C.T.Mason	Madroño 36: 50 (1989)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Northern Europe
  - Great Britain

Northern America click to expand
- Northwestern U.S.A.
  - Oregon
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001073392
Canadensys	6545
USDA Plants	LIDO2
Tropicos	18500005
INPN	106004
KEW	urn:lsid:ipni.org:names:30052665-2
The Plant List	tro-18500005
Open Tree Of Life	164698
Observations.org	6988
NCBI Taxonomy	28973
NBN Atlas	NHMSYS0000460349
Nature Serve	2.870805
IPNI	30052665-2
iNaturalist	51336
GBIF	5334527
Freebase	/m/05k3py
EPPO	LMADO
EOL	581151
Calflora (Californian flora)	4825
USDA GRIN	22243
Wikipedia	Limnanthes_douglasii

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_036936605.1	dmLimDoug1.0.hap1	Scaffold	UCLA	2024-03-01	36.0x	1.67 Gb

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 Glucosinolate Content and Host-Plant Preference and Suitability in the Small White Butterfly (Lepidoptera: Pieridae) and Comparison with Another Specialist Lepidopteran

Badenes-Pérez FR

Plants (Basel)

29-May-2023

PMCID:	PMC10255426
doi:	10.3390/plants12112148
PMID:	37299126

Eco-Evo-Devo of petal pigmentation patterning

Fairnie AL, Yeo MT, Gatti S, Chan E, Travaglia V, Walker JF, Moyroud E

Essays Biochem

08-Dec-2022

PMCID:	PMC9750854
doi:	10.1042/EBC20220051
PMID:	36205404

The Spectrum of Pharmacological Actions of Syringetin and Its Natural Derivatives—A Summary Review

Chmiel M, Stompor-Gorący M

Nutrients

04-Dec-2022

PMCID:	PMC9739508
doi:	10.3390/nu14235157
PMID:	36501187

A Review of Erucic Acid Production in Brassicaceae Oilseeds: Progress and Prospects for the Genetic Engineering of High and Low-Erucic Acid Rapeseeds (Brassica napus)

Wang P, Xiong X, Zhang X, Wu G, Liu F

Front Plant Sci

11-May-2022

PMCID:	PMC9131074
doi:	10.3389/fpls.2022.899076
PMID:	35645989

Biotechnological approach for improvement of Crambe species as valuable oilseed plants for industrial purposes

Pushkarova N, Yemets A

RSC Adv

02-Mar-2022

PMCID:	PMC8982245
doi:	10.1039/d2ra00422d
PMID:	35424652

Sagan Dalya Tea, a New “Old” Probable Adaptogenic Drug: Metabolic Characterization and Bioactivity Potentials of Rhododendron adamsii Leaves

Olennikov DN, Nikolaev VM, Chirikova NK

Antioxidants (Basel)

27-May-2021

PMCID:	PMC8227344
doi:	10.3390/antiox10060863
PMID:	34072186

Fatty Acids and their Derivatives as Renewable Platform Molecules for the Chemical Industry

Biermann U, Bornscheuer UT, Feussner I, Meier MA, Metzger JO

Angew Chem Int Ed Engl

01-May-2021

PMCID:	PMC8453566
doi:	10.1002/anie.202100778
PMID:	33617111

Co-expressing Eranthis hyemalis lysophosphatidic acid acyltransferase 2 and elongase improves two very long chain polyunsaturated fatty acid production in Brassica carinata

Meesapyodsuk D, Chen Y, Ye S, Chapman RG, Qiu X

Metab Eng Commun

07-Apr-2021

PMCID:	PMC8129929
doi:	10.1016/j.mec.2021.e00171
PMID:	34026531

The Use of Genetic and Gene Technologies in Shaping Modern Rapeseed Cultivars (Brassica napus L.)

Ton LB, Neik TX, Batley J

Genes (Basel)

30-Sep-2020

PMCID:	PMC7600269
doi:	10.3390/genes11101161
PMID:	33008008

A predicted transmembrane region in plant diacylglycerol acyltransferase 2 regulates specificity toward very-long-chain acyl-CoAs

Jeppson S, Mattisson H, Demski K, Lager I

J Biol Chem

01-Sep-2020

PMCID:	PMC7650248
doi:	10.1074/jbc.RA120.013755
PMID:	32873712

Multigene engineering of medium-chain fatty acid biosynthesis in transgenic Arabidopsis thaliana by a Cre/LoxP multigene expression system

Zheng Y, Chen L, Zhu Z, Li D, Zhou P

3 Biotech

17-Jul-2020

PMCID:	PMC7367956
doi:	10.1007/s13205-020-02340-z
PMID:	32714735

Frequency-dependent fitness and reproductive dynamics contribute to habitat segregation in sympatric jewelflowers

Christie K, Strauss SY

Proc Biol Sci

13-May-2020

PMCID:	PMC7287356
doi:	10.1098/rspb.2020.0559
PMID:	32396796

Crambe hispanica Subsp. abyssinica Diacylglycerol Acyltransferase Specificities Towards Diacylglycerols and Acyl-CoA Reveal Combinatorial Effects That Greatly Affect Enzymatic Activity and Specificity

Jeppson S, Demski K, Carlsson AS, Zhu LH, Banaś A, Stymne S, Lager I

Front Plant Sci

12-Nov-2019

PMCID:	PMC6863138
doi:	10.3389/fpls.2019.01442
PMID:	31798607

The impact of reducing fatty acid desaturation on the composition and thermal stability of rapeseed oil

Kaur H, Wang L, Stawniak N, Sloan R, van Erp H, Eastmond P, Bancroft I

Plant Biotechnol J

14-Oct-2019

PMCID:	PMC7061866
doi:	10.1111/pbi.13263
PMID:	31553825

The Conservation of VIT1-Dependent Iron Distribution in Seeds

Eroglu S, Karaca N, Vogel-Mikus K, Kavčič A, Filiz E, Tanyolac B

Front Plant Sci

12-Jul-2019

PMCID:	PMC6640190
doi:	10.3389/fpls.2019.00907
PMID:	31354774

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl henicosa-5,13-dienoate	163019775	Click to see CCCCCCCC=CCCCCCCC=CCCCC(=O)OC	336.60	unknown	https://doi.org/10.1007/BF02668126
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6R)-3-[(1S,4S,6S,10R,12S)-4,12-dimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecan-12-yl]-6-(hydroxymethyl)-6-methyl-1,2-dioxin-3-ol	21778622	Click to see CC12CCC3C(CC3(C)C4(C=CC(OO4)(C)CO)O)C(=C)CCC1O2	350.40	unknown	https://doi.org/10.1021/JA01590A052
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	271605	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,14-dihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	102064900	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)OC5C(C(C(CO5)O)O)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	612.70	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
2,14-dihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-3-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	74379681	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)OC5C(C(C(CO5)O)O)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	612.70	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
25-Deoxycedysterone;25-deoxy-20-ecdysone	4482619	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	464.60	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
Ponasterone A	115127	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	464.60	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-2,14-dihydroxy-10,13-dimethyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	102064901	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(CO5)O)O)O)O)C)C)O)O)O	596.70	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
17-(2,3-dihydroxy-6-methylheptan-2-yl)-2,14-dihydroxy-10,13-dimethyl-3-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	74379682	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(CO5)O)O)O)O)C)C)O)O)O	596.70	unknown	https://doi.org/10.1016/S0031-9422(96)00591-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,2S,3R,4aR,5S,6R,8S,8aR)-5-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-8-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-5,6-dimethylspiro[3,4,4a,6,7,8-hexahydro-2H-naphthalene-1,2'-oxirane]-2-yl] (E)-2-methylbut-2-enoate	102056500	Click to see CC=C(C)C(=O)OC1C(CC2C(C(CC(C2(C13CO3)COC(=O)C)OC(=O)C)C)(C)C4CC5C=COC5O4)O	548.60	unknown	https://doi.org/10.1007/BF02668126
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-2-(3-methoxyphenyl)-N-sulfooxyethanimidothioate	9548725	Click to see COC1=CC=CC(=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	439.50	unknown	https://doi.org/10.1007/BF02028513 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215540/
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(3-methoxyphenyl)-N-sulfooxyethanimidothioate	4479903	Click to see COC1=CC=CC(=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	439.50	unknown	https://doi.org/10.1007/BF02028513 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880616/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215540/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	9830579	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)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1016/0031-9422(75)85127-2
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	122173234	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	https://doi.org/10.1016/0031-9422(75)85127-2
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	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	https://doi.org/10.1016/0031-9422(75)85127-2
Isorhamnetin 3-robinobioside	6223069	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)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1016/0031-9422(75)85127-2
Venoruton	24832108	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	https://doi.org/10.1016/0031-9422(75)85127-2
Vitamin P	5293655	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	https://doi.org/10.1016/0031-9422(75)85127-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	162984008	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C(=C6)OC)O)OC)O)O)O)O)O)O	816.70	unknown	https://doi.org/10.1016/0031-9422(75)85127-2
5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-3-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	163103897	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O)O	788.70	unknown	https://doi.org/10.1016/0031-9422(75)85127-2

Biological Material Top

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Limnanthes douglasii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top