Sideritis lotsyi - Unknown
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Internal ID UUID643fecd853a8e794836505
Scientific name Sideritis lotsyi
Authority (Pit.) Ceballos & Ortuno
First published in Repert. Spec. Nov. Regni Veg. 19: 276 (1924)

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Synonyms Top

Scientific name Authority First published in
Leucophae lotsyi Pit. Iles Canaries : 314 (1909)
Sideritis lotsyi var. grandifolia Mend.-Heuer Vieraea 3: 135 (1973 publ. 1974)

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Varieties (abbr. var.) Top

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Name Authority First published in
Sideritis lotsyi var. mascaensis Svent. Collect. Bot. (Barcelona) 7: 1154 (1968)

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Distribution (via POWO/KEW) Top

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

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Database ID/link to page
World Flora Online wfo-0000310253
Tropicos 17604901
KEW urn:lsid:ipni.org:names:458987-1
The Plant List kew-191459
Open Tree Of Life 218375
NCBI Taxonomy 403024
IPNI 458987-1
iNaturalist 793724
GBIF 7307604
CMAUP NPO11287

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)!
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Title Authors Publication Released IDs
Medicinal Plants of the Family Lamiaceae in Pain Therapy: A Review Uritu CM, Mihai CT, Stanciu GD, Dodi G, Alexa-Stratulat T, Luca A, Leon-Constantin MM, Stefanescu R, Bild V, Melnic S, Tamba BI Pain Res Manag 08-May-2018
PMCID:PMC5964621
doi:10.1155/2018/7801543
PMID:29854039
A chemotaxonomic study of nine Canarian Sideritis species. Fraga BM, Hernández MG, Fernández C, Santana JM Phytochemistry 01-May-2009
doi:10.1016/J.PHYTOCHEM.2009.05.011
PMID:19535115

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 / Prenol lipids / Diterpenoids
Abietatriene 6432211 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C 270.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4R,9R,10S,13S,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 101615188 Click to see CC1(CCCC2(C1CC(C34C2C=CC(C3)C(C4)(C)O)O)C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
(1R,2S,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 20055664 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown via CMAUP database
(1S,4R,9R,10R,12R,13R,14S)-5,5,9,13-tetramethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane 101285934 Click to see CC1(CCCC2(C1CCC34C2CC5C(C3)C5(C4)C)C)C 272.50 unknown via CMAUP database
(1S,4S,5S,9R,10R,13S,14R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 163015530 Click to see CC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)CO 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
(2-Acetyloxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl hexadecanoate 14487061 Click to see CCCCCCCCCCCCCCCC(=O)OCC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)OC(=O)C)C)C 584.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
[(1R,2S,4S,5S,9R,10S,13R)-2-acetyloxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl hexadecanoate 101526599 Click to see CCCCCCCCCCCCCCCC(=O)OCC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)OC(=O)C)C)C 584.90 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5-(Hydroxymethyl)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecan-2-ol 12444454 Click to see CC1(CCCC2(C1CC(C34C2CC5C(C3)C5(C4)C)O)C)CO 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5-(Hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 13858172 Click to see CC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)CO 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-2,14-diol 163039940 Click to see CC1(CCCC2(C1CC(C34C2C=CC(C3)C(C4)(C)O)O)C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
7-Acetoxy-18-trachylobanol 102239718 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC5C(C3)C5(C4)C)C)(C)CO 346.50 unknown via CMAUP database
ent-Kaurene 11966109 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
ent-Trachylobane 91750049 Click to see CC1(CCCC2(C1CCC34C2CC5C(C3)C5(C4)C)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Kaura-16-ene-7beta,19-diol 7-acetate 101615200 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4)C)(C)CO 346.50 unknown via CMAUP database
Trachinodiol 101306892 Click to see CC1(CCCC2(C1CC(C34C2CC5C(C3)C5(C4)C)O)C)CO 304.50 unknown via CMAUP database
Trachylobane 521405 Click to see CC1(CCCC2(C1CCC34C2CC5C(C3)C5(C4)C)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,4S,5S,9S,10R,12S,13S)-5-(hydroxymethyl)-5,9,13-trimethyltetracyclo[10.2.2.01,10.04,9]hexadecan-13-ol 163032303 Click to see CC1(CCCC2(C1CCC34C2CC(CC3)C(C4)(C)O)C)CO 306.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
5-(Hydroxymethyl)-5,9,13-trimethyltetracyclo[10.2.2.01,10.04,9]hexadecan-13-ol 14109710 Click to see CC1(CCCC2(C1CCC34C2CC(CC3)C(C4)(C)O)C)CO 306.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aS,6aS,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-1,2,5,6,6a,9,10,10b-octahydrobenzo[f]chromen-8-one 15226249 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC(O3)(C)C=C)C)C 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Rhoiptelenol 102304204 Click to see CC1CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1C)C)C)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Akagerine 643662 Click to see CC=C(C=O)C1CC2C3=C(CCN2C)C4=CC=CC=C4N3C(C1)O 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Methyl 3-(3,4-dimethoxyphenyl)prop-2-enoate 94307 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC)OC 222.24 unknown via CMAUP database
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Methyl 3,4-dimethoxycinnamate 766745 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC)OC 222.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011

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