Lawrencella rosea - Unknown
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Internal ID UUID643fd09e0612e379351559
Scientific name Lawrencella rosea
Authority Lindl.
First published in Sketch Veg. Swan R. 23 (1839) (1839)

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Synonyms Top

Scientific name Authority First published in
Helichrysum lindleyi H.Eichler Taxon 12 1963
Helichrysum roseum Druce Rep. Bot. Soc. Exch. Club Brit. Isles 4(Suppl. 2): 626 (1917)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000103471
Tropicos 50293052
KEW urn:lsid:ipni.org:names:229103-1
The Plant List gcc-6102
Open Tree Of Life 510150
NCBI Taxonomy 125722
IPNI 229103-1
iNaturalist 205092
GBIF 5385014
USDA GRIN 21697
CMAUP NPO16730
Wikipedia Lawrencella_rosea

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Weak evidence of trade-offs modulated by seed mass among a guild of closely related winter annuals da Silva IA, Mayfield MM, Dwyer JM Oecologia 12-Jul-2023
PMCID:PMC10386915
doi:10.1007/s00442-023-05416-8
PMID:37436476
Variable seed bed microsite conditions and light influence germination in Australian winter annuals Towers IR, Merritt DJ, Erickson TE, Mayfield MM, Dwyer JM Oecologia 09-Jan-2022
PMCID:PMC9056468
doi:10.1007/s00442-021-05091-7
PMID:34999943
Diterpenes and other constituents from Australian Helichrysum and related species J. Jakupovic, A. Schuster, F. Bohlmann, U. Ganzer, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80048-2

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 / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(89)80048-2
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(89)80048-2
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(89)80048-2
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(89)80048-2
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(89)80048-2
> Organoheterocyclic compounds / Bi- and oligothiophenes
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown https://doi.org/10.1016/0031-9422(89)80048-2
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(5-But-3-en-1-ynylthiophen-2-yl)penta-2,4-diyn-1-ol 14262758 Click to see C=CC#CC1=CC=C(S1)C#CC#CCO 212.27 unknown https://doi.org/10.1016/0031-9422(89)80048-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
2',3,5,7-Tetrahydroxyflavanone 3082330 Click to see C1=CC=C(C(=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)- 157633 Click to see C1=CC(=C(C(=C1)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5,7,2',6'-Tetrahydroxyflavone 5321865 Click to see C1=CC(=C(C(=C1)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 286.24 unknown via CMAUP database
Baicalein 5281605 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 270.24 unknown via CMAUP database
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
Norwogonin 5281674 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
Oroxindin 3084961 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 460.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-6-methoxyflavone 5322076 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3O)O 300.26 unknown via CMAUP database
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2',5,6'-Trihydroxy-7-methoxyflavanone 195603 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=CC=C3O)O)O 302.28 unknown via CMAUP database
Scuteamoenoside 130116 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Skullcapflavone II 124211 Click to see COC1=CC=CC(=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 374.30 unknown via CMAUP database
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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