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Sideritis infernalis

Sideritis infernalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fecd623e77996808877
Scientific name Sideritis infernalis
Authority Bolle
First published in Bonplandia (Hannover) 8: 286 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Leucophae infernalis Christ Bot. Jahrb. Syst. 9: 140 (1887)

Common names Top

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Language Common/alternative name
Spanish chajorra de adeje

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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No germination or propagation data was added yet.

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-0000310196
Tropicos 17603684
KEW urn:lsid:ipni.org:names:458955-1
The Plant List kew-191405
Open Tree Of Life 218370
Observations.org 129152
NCBI Taxonomy 403022
NBN Atlas NBNSYS0000163626
IUCN Red List 162104
IPNI 458955-1
iNaturalist 443675
GBIF 3890500
Elurikkus 434575
USDA GRIN 475188

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Diterpenes from Sideritis infernalis and S. candicans Braulio M. Fraga, Carlo Bressa, Concepción Fernández, Pedro González, Ricardo Guillermo, Melchor G. Hernández Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2008-0519
Occurrence, Biological Activities and Synthesis of Kaurane Diterpenes and their Glycosides García PA, de Oliveira AB, Batista R Molecules 13-Mar-2007
PMCID:PMC6149336
doi:10.3390/12030455
PMID:17851404
Diterpenes from sideritis infernalis Concepción Fernández, Braulio M. Fraga, Melchor G. Hernández Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84513-6
Distribution of flavonoid aglycones and glycosides in Sideritis species from the canary islands and madeira María I. Gil, Federico Ferreres, Aguedo Marrero, Francisco Tomás-Lorente, Francisco A. Tomas-Barberan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90809-4
Flavonoid aglycones from some canary islands species of sideritis. Fernandez C, Fraga BM, Hernandez MG, Arteaga JM J Nat Prod 01-May-1988
doi:10.1021/NP50057A027
PMID:21401173

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 / Kaurane diterpenoids
(1R,2R,4S,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 101856633 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)C=O)O)C)CO 318.40 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
(1R,2R,4S,5S,9R,10S,13R)-5,14-bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 101856632 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
(1R,2S,4S,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 163009391 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)C=O)O)C)CO 318.40 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 14487053 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)C=O)O)C)CO 318.40 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
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/S0031-9422(00)84513-6
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,15-diol 14239632 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4O)O)C)CO 320.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
5,14-Bis(hydroxymethyl)-5,9-dimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-ol 14239625 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)CO)O)C)CO 336.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
5,14-Bis(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 12315543 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
7beta,19-Dihydroxykaur-15-ene-17-carbaldehyde 14890430 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CC=O)O)C)CO 332.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Candicandiol 20055798 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Candidiol 101316736 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4O)C)CO 304.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Canditriol 20055799 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4O)O)C)CO 320.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
ent-16-Kauren-19-ol 529650 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Epoxysinfernol 118987276 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)CO)O)C)CO 336.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
Sinfernol 183840 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C4)CO)O)C)CO 320.50 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Anemarrhenasaponin I 9810764 Click to see CC1C2C(C(C3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O)OC1(CCC(C)C)O 758.90 unknown https://doi.org/10.1016/S0031-9422(00)84513-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,4S,5S,9R,10S,13R)-2-hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-one 101856627 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=O)C4)O)C)CO 306.40 unknown https://doi.org/10.1515/ZNB-2008-0519
2-Hydroxy-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-one 162846451 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=O)C4)O)C)CO 306.40 unknown https://doi.org/10.1515/ZNB-2008-0519
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl 4-methoxycinnamate 641297 Click to see COC1=CC=C(C=C1)C=CC(=O)OC 192.21 unknown https://doi.org/10.1515/ZNB-2008-0519
Methyl p-methoxycinnamate 92841 Click to see COC1=CC=C(C=C1)C=CC(=O)OC 192.21 unknown https://doi.org/10.1515/ZNB-2008-0519
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)90809-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)90809-4
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)90809-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
CID 45273057 45273057 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C=C(C=C3OC)O 300.30 unknown https://doi.org/10.1021/NP50057A027

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