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Sideritis congesta

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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 UUID643fecd095050000744201
Scientific name Sideritis congesta
Authority P.H.Davis & Hub.-Mor.
First published in Kew Bull. 6: 102 (1951)

Description Top

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Synonyms Top

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Common names Top

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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-0000309961
KEW urn:lsid:ipni.org:names:458865-1
The Plant List kew-191175
Open Tree Of Life 6081606
IPNI 458865-1
iNaturalist 940318
GBIF 3891788

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
Composition of the Essential Oil of<i>Sideritis congesta</i>P.H.Davis et Hub.-Mor. N. Kirimer, N. Tabanca, K. H.C. Baser, G. Tümen Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.2001.9699637
Ent-kaurane diterpenoids isolated from Sideritis congesta Gülaçtı Topçu, Abdülselam Ertaş, Mehmet Öztürk, Demet Dinçel, Turgut Kılıç, Belkıs Halfon Elsevier BV 22-May-2011
doi:10.1016/J.PHYTOL.2011.05.001
Essential oil composition of four turkish species of Sideritis Nurten Ezer, Roser Vila, Salvador Cañigueral, Tomas Adzet Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00601-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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4S,5S,6R,9S,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 637194 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
(1R,2S,4S,5S,9R,10S,13R,14S,16R)-5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-ol 12315550 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
(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 https://doi.org/10.1016/J.PHYTOL.2011.05.001
[(1R,2S,4S,5S,6R,9S,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 12442776 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CC4=C)C(CC2C1(C)CO)O)C 362.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
[(1R,2S,4S,5S,6R,9S,10S,13R)-2,6-dihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 11906032 Click to see CC(=O)OCC1(C(CCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)O)C 362.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
[(1R,2S,4S,5S,6S,9R,10S,13R,14S,16R)-2,6-dihydroxy-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl]methyl acetate 163047131 Click to see CC(=O)OCC1(C(CCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)O)C 378.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
[(1R,2S,4S,5S,9R,10S,13R,14R)-14-hydroxy-5-(hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162960701 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(C4)(C)O)C)(C)CO 364.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
[2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 12442775 Click to see CC(=O)OC1CCC2(C3CCC4CC3(CC4=C)C(CC2C1(C)CO)O)C 362.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
[5-(Hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12315547 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,6-diol 12309906 Click to see CC12CCC(C(C1CC(C34C2CCC(C3)C(=C)C4)O)(C)CO)O 320.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
CID 12315541 12315541 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3O)(C)CO)C 304.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
Sideridiol 12315540 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3O)(C)CO)C 304.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
Siderol 12315548 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
Ucriol 12315549 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO 320.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.2001.9699637
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.2001.9699637
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Epicubenol 12046149 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Trichormamide B 118711962 Click to see CCCCCCCC1CC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)N1)C(C)O)CC3=CC=C(C=C3)O)C(C)O)CO)C(C)CC)C)CCC(=O)N)C(C(C)C)O)CCO)C(C(C)C)O)C(C)CC 1446.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.001
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see C12C3C4C1C5(C2C3=C45)O 118.13 unknown https://doi.org/10.1016/0031-9422(95)00601-X

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