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Linum salsoloides

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff479a5627500959602
Scientific name Linum salsoloides
Authority Lam.
First published in Encycl. 3: 521 (1792)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

The query specifies preparation methods like teas and tinctures for Linum salsoloides. No verified ethnobotanical sources document such preparations for this exact species. Therefore, I cannot produce the requested paragraph with the required citations and sources.

General Uses Top

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No documented commercial, industrial, or craft uses have been identified for Linum salsoloides in scientific literature or technical sources. This species appears to be primarily of botanical and ecological interest without established applications in commercial or industrial sectors.

Synonyms Top

Scientific name Authority First published in
Linum ortegae Planch. London J. Bot. 7: 184 (1848)
Linum crispum Steud. Nomencl. Bot. 1: 484 (1821)
Linum suffruticosum subsp. ortegae (Planchon) Rivas Goday & Borja ex Rivas Mart. Anales Inst. Bot. Cavanilles 34: 548 (1977 publ. 1978)
Linum tenuifolium subsp. ortegae (Planchon) O.Bolòs & Vigo Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 82 (1974)
Cathartolinum salsoloides Rchb. Handb. Nat. Pfl.-Syst. : 307 (1837)
Linum suffruticosum subsp. salsoloides (Lam.) Rouy Fl. France 4: 71 (1897)
Linum ortegae var. tenuissimum Caball. Anales Jard. Bot. Madrid 4: 425 (1945)
Linum tenuifolium var. ericoides Willk. Flora 34: 609 (1851)
Linum tenuifolium var. salsoloides (Lam.) Paol. Fl. Anal. Italia 2: 250 (1901)
Linum tenuifolium var. ortegae (Planch.) Lacaita Cavanillesia 3: 68 (1930)
Linum tenuifolium subsp. salsoloides (Lam.) Litard. Prodr. Fl. Corse 2(2): 45 (1936)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
  • Europe
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000363321
Tropicos 18700028
KEW urn:lsid:ipni.org:names:544679-1
Open Tree Of Life 7635380
IPNI 544679-1
GBIF 4048547
CMAUP NPO26387

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)!
Title Authors Publication Released IDs
Crispane and crispanone, two compounds from Petroselinum crispum with a new carbon @skeleton Martin H. Spraul, Siegfried Nitz, Friedrich Drawert, Helmut Duddeck, Monika Hiegemannt Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83455-8
Medicinal foodstuffs. XVIII. Phytoestrogens from the aerial part of Petroselinum crispum MIll. (Parsley) and structures of 6"-acetylapiin and a new monoterpene glycoside, petroside. Yoshikawa M, Uemura T, Shimoda H, Kishi A, Kawahara Y, Matsuda H Chem Pharm Bull (Tokyo) 01-Jul-2000
doi:10.1248/CPB.48.1039
PMID:10923837

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 / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl petroselinate 5362717 Click to see 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1-Hydroxy-4,4a-dimethyl-1-propan-2-yl-2,5,6,7,8,8a-hexahydronaphthalen-2-yl) 2-methylbut-2-enoate 163029833 Click to see CC=C(C)C(=O)OC1C=C(C2(CCCCC2C1(C(C)C)O)C)C 320.50 unknown https://doi.org/10.1016/0031-9422(92)83455-8
(1-hydroxy-4,4a-dimethyl-7-oxo-1-propan-2-yl-5,6,8,8a-tetrahydro-2H-naphthalen-2-yl) 2-methylbut-2-enoate 162985179 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(92)83455-8
[(1R,2R,4aR,8aR)-1-hydroxy-4,4a-dimethyl-1-propan-2-yl-2,5,6,7,8,8a-hexahydronaphthalen-2-yl] (Z)-2-methylbut-2-enoate 163029834 Click to see 320.50 unknown https://doi.org/10.1016/0031-9422(92)83455-8
[(1R,2R,4aR,8aR)-1-hydroxy-4,4a-dimethyl-7-oxo-1-propan-2-yl-5,6,8,8a-tetrahydro-2H-naphthalen-2-yl] (Z)-2-methylbut-2-enoate 162985180 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(92)83455-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
p-Mentha-1,3,8-triene 176983 Click to see CC1=CC=C(CC1)C(=C)C 134.22 unknown https://doi.org/10.1016/0031-9422(92)83455-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,2R,3S,4S)-3-hydroxy-4-methyl-1-prop-1-en-2-yl-7-oxabicyclo[2.2.1]heptan-2-yl]oxy]oxane-3,4,5-triol 10569581 Click to see CC(=C)C12CCC(O1)(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)C 346.37 unknown https://doi.org/10.1248/CPB.48.1039
2-(Hydroxymethyl)-6-[(3-hydroxy-4-methyl-1-prop-1-en-2-yl-7-oxabicyclo[2.2.1]heptan-2-yl)oxy]oxane-3,4,5-triol 85188973 Click to see CC(=C)C12CCC(O1)(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)C 346.37 unknown https://doi.org/10.1248/CPB.48.1039
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol 14079044 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1248/CPB.48.1039
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1248/CPB.48.1039
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see 222.24 unknown https://doi.org/10.1248/CPB.48.1039
Myristicin 4276 Click to see 192.21 unknown https://doi.org/10.1248/CPB.48.1039
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1248/CPB.48.1039
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see 300.30 unknown https://doi.org/10.1248/CPB.48.1039
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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 https://doi.org/10.1248/CPB.48.1039
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 https://doi.org/10.1248/CPB.48.1039
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl acetate 85174581 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)OC5C(C(CO5)(CO)O)O)O)O 606.50 unknown https://doi.org/10.1248/CPB.48.1039
6''-Acetylapiin 10531745 Click to see 606.50 unknown https://doi.org/10.1248/CPB.48.1039
7-O-B-D-Glucopyranoside 5378562 Click to see 462.40 unknown https://doi.org/10.1248/CPB.48.1039
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1248/CPB.48.1039
Apiin 5280746 Click to see 564.50 unknown https://doi.org/10.1248/CPB.48.1039
Apioside 5840046 Click to see 564.50 unknown https://doi.org/10.1248/CPB.48.1039
Diosmetin 7-O-beta-D-glucoside 11016019 Click to see 462.40 unknown https://doi.org/10.1248/CPB.48.1039
Luteolin 7-O-(2-(beta-D-apiofuranosyl)-beta-D-glucopyranoside) 101248035 Click to see 580.50 unknown via CMAUP database
Malonylapiin 5280803 Click to see 650.50 unknown via CMAUP database
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1248/CPB.48.1039
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see 270.24 unknown via CMAUP database

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