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Sideritis serrata

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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 UUID643fecde79a85811700037
Scientific name Sideritis serrata
Authority Lag.
First published in Gen. Sp. Pl. : 18 (1816)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sideritis spinosa var. serrata (Cav. ex Lag.) Willk. Bot. Zeitung (Berlin) 17: 285 1859
Sideritis incana var. serrata (Cav. ex Lag.) Nyman Consp. Fl. Eur. 584 1881
Sideritis spinosa var. serrata (Lag.) Nyman Consp. Fl. Eur. 583 1881

Common names Top

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Language Common/alternative name
Spanish rabogato

Subspecies (abbr. subsp./ssp.) Top

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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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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-0000310458
Tropicos 17600665
KEW urn:lsid:ipni.org:names:459094-1
The Plant List kew-191654
Open Tree Of Life 6081690
Observations.org 144270
NBN Atlas NBNSYS0000163643
IUCN Red List 162358
IPNI 459094-1
iNaturalist 443681
GBIF 3888771
Elurikkus 434189
USDA GRIN 475169

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
Four new diterpenes from Sideritis serrata Teresa G. de Quesada, Benjamín Rodríguez, Serafín Valverde Elsevier BV 12-Feb-2003
doi:10.1016/0031-9422(75)85120-X
Two new diterpenoid acetates from Sideritis serrata Eleazar M. Escamilla, Benjamín Rodríguez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83202-X

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 / Phenols / Methoxyphenols
7-[5-(2-Hydroxy-5-methoxy-3-methylphenyl)-3-methylpent-3-enyl]-1,2',2',5-tetramethylspiro[bicyclo[3.2.0]heptane-6,5'-oxolane]-3'-ol 162892321 Click to see CC1=CC(=CC(=C1O)CC=C(C)CCC2C3(CCCC3(C24CC(C(O4)(C)C)O)C)C)OC 442.60 unknown https://doi.org/10.1016/0031-9422(80)83202-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4R,8S,9R,10R,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-8,12-diol 102090413 Click to see CC1(CCC(C2(C1CCC34C2CC(C(C3)(C=C4)CO)O)C)O)C 320.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-12-ol 97032112 Click to see CC1(CCCC2(C1CCC34C2CC(C(C3)(C=C4)CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
(1R)-1-[(2S,4aS,4bR,10aS)-2,4a,8,8-tetramethyl-3,4,4b,5,6,7,10,10a-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol 101277418 Click to see CC1(CCCC2C1=CCC3C2(CCC(C3)(C)C(CO)O)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
(1S,2S,4R,9R,10S,13R)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 101277393 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)(C=C4)CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
(8-Acetyloxy-12-hydroxy-5,5,9-trimethyl-13-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methyl acetate 162980872 Click to see CC(=O)OCC12CC3(CCC4C(CCC(C4(C3CC1O)C)OC(=O)C)(C)C)C=C2 404.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
[(1R,4R,8S,9R,10R,12R,13S)-12-acetyloxy-13-(hydroxymethyl)-5,5,9-trimethyl-8-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 8119896 Click to see CC(=O)OC1CCC(C2C1(C3CC(C4(CC3(CC2)C=C4)CO)OC(=O)C)C)(C)C 404.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
[(1R,4R,8S,9R,10R,12R,13S)-8-acetyloxy-12-hydroxy-5,5,9-trimethyl-13-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methyl acetate 162980873 Click to see CC(=O)OCC12CC3(CCC4C(CCC(C4(C3CC1O)C)OC(=O)C)(C)C)C=C2 404.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
[(1R,4R,8S,9R,10R,12R,13S)-8-hydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 45033619 Click to see CC(=O)OC1CC2C3(C(CCC24CC1(C=C4)CO)C(CCC3O)(C)C)C 362.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
[12-Acetyloxy-13-(hydroxymethyl)-5,5,9-trimethyl-8-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 78607622 Click to see CC(=O)OC1CCC(C2C1(C3CC(C4(CC3(CC2)C=C4)CO)OC(=O)C)C)(C)C 404.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
[8-Hydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 163075896 Click to see CC(=O)OC1CC2C3(C(CCC24CC1(C=C4)CO)C(CCC3O)(C)C)C 362.50 unknown https://doi.org/10.1016/0031-9422(80)83202-X
1-(2,4a,8,8-tetramethyl-3,4,4b,5,6,7,10,10a-octahydro-1H-phenanthren-2-yl)ethane-1,2-diol 163020098 Click to see CC1(CCCC2C1=CCC3C2(CCC(C3)(C)C(CO)O)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
13-(Hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-12-ol 162920493 Click to see CC1(CCCC2(C1CCC34C2CC(C(C3)(C=C4)CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
13-(Hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 85362035 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)(C=C4)CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,4R,9R,10S,12R,13S)-13-(hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.01,10.04,9]hexadec-15-en-13-ol 101277423 Click to see CC1(CCCC2(C1CCC34C2CC(C=C3)C(C4)(CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X
13-(Hydroxymethyl)-5,5,9-trimethyltetracyclo[10.2.2.01,10.04,9]hexadec-15-en-13-ol 14488133 Click to see CC1(CCCC2(C1CCC34C2CC(C=C3)C(C4)(CO)O)C)C 304.50 unknown https://doi.org/10.1016/0031-9422(75)85120-X

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