Sideritis candicans - Unknown
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Internal ID UUID643feccf7fe51471017806
Scientific name Sideritis candicans
Authority Aiton
First published in Hort. Kew. 2: 289 (1789)

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Synonyms Top

Scientific name Authority First published in
Leucophae candicans Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 100 (1845)
Leucophae massoniana Webb & Berthel. Hist. Nat. Iles Canaries 3(2; 3): 101 (1845)
Sideritis candida Salisb. Prodr. Stirp. Chap. Allerton : 79 (1796)
Sideritis massoniana Benth. Labiat. Gen. Spec. : 573 (1834)
Sideritis candicans var. longifolia Lowe Trans. Cambridge Philos. Soc. 6: 535. 1838
Sideritis massoniana f. longifolia (Lowe) Svent Collect. Bot. (Barcelona) 7: 1146 1968
Sideritis candicans var. multiflora (Bornm.) Mend.-Heuer Vieraea 3: 135 (1973 publ. 1974)

Common names Top

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Language Common/alternative name
Arabic فزر أبيض
Portuguese selvageiras
Portuguese selvageira

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Sideritis candicans var. crassifolia Lowe Trans. Cambridge Philos. Soc. 6: 535. 1838

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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-0000309923
Tropicos 17602359
KEW urn:lsid:ipni.org:names:458845-1
The Plant List kew-191139
Open Tree Of Life 762735
NCBI Taxonomy 155236
IPNI 458845-1
iNaturalist 627571
GBIF 7307905
Freebase /m/0w7q29l
EPPO SIECA
USDA GRIN 414399
Wikipedia Sideritis_candicans

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
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
Analyzing factors that influence the folk use and phytonomy of 18 medicinal plants in Navarra Akerreta S, Cavero RY, López V, Calvo MI J Ethnobiol Ethnomed 13-Apr-2007
PMCID:PMC1868015
doi:10.1186/1746-4269-3-16
PMID:17433105
A chemotaxonomical study of Sideritis massoniana taxa Braulio M. Fraga, Melchor G. Hernandez, Jose M.H. Santana, David Terrero, Manuel F. Galvan Elsevier BV 26-Jul-2002
doi:10.1016/0305-1978(95)00067-4
New diterpenes from Sideritis candicans Antonio G. González, Braulio M. Fraga, Melchor G. Hernandez, Javier G. Luis Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)85087-3
Diterpenes from sideritis dendrochahorra and s. cystosiphon Braulio M. Fraga, Melchor G. Hernández, Concepción Fernández, J.M. Arteaga Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84784-6

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
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> 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/10.1016/0305-1978(95)00067-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> 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/10.1515/ZNB-2008-0519
(1R,2R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-ol 101856630 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3O)(C)CO)C 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
(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/10.1515/ZNB-2008-0519
(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/10.1016/0031-9422(73)85087-3
(1R,4S,5S,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-ol 101316736 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4O)C)CO 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
(1S,4S,5S,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 101297703 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO 306.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[(1R,2R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101856626 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4)C)(C)CO 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[(1R,4S,5S,9R,10S,13R,15S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101856629 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)CO)C 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
[5-(Hydroxymethyl)-5,9-dimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163011328 Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)CO)C 346.50 unknown https://doi.org/10.1515/ZNB-2008-0519
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/10.1515/ZNB-2008-0519
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/10.1016/0031-9422(73)85087-3
https://doi.org/10.1515/ZNB-2008-0519
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/10.1515/ZNB-2008-0519
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 14890423 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
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/10.1016/0305-1978(95)00067-4
Candicandiol 20055798 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)CO 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
Candol A 14890424 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4)O)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1016/0305-1978(95)00067-4
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1515/ZNB-2008-0519
https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1016/0305-1978(95)00067-4
ent-16-Kauren-19-ol 529650 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1515/ZNB-2008-0519
https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1016/S0031-9422(00)84784-6
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 https://doi.org/10.1016/0031-9422(73)85087-3
Kaurane-16,19-diol 579830 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO 306.50 unknown https://doi.org/10.1515/ZNB-2008-0519
Sideridiol 12315540 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3O)(C)CO)C 304.50 unknown https://doi.org/10.1515/ZNB-2008-0519
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol 13970287 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC(O3)(C)C=C)C)C 306.50 unknown https://doi.org/10.1016/0305-1978(95)00067-4
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
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 https://doi.org/10.1016/0305-1978(95)00067-4
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
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 https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Anemarrhenasaponin II 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/10.1515/ZNB-2008-0519
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-(5-ethyl-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one 138113837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.011
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[DL-Abu-DL-Val-DL-N(Me)Ala-bAla-DL-OLeu-DL-Pro] 75049028 Click to see CCC1C(=O)NC(C(=O)N(C(C(=O)NCCC(=O)OC(C(=O)N2CCCC2C(=O)N1)CC(C)C)C)C)C(C)C 551.70 unknown https://doi.org/10.1016/0031-9422(73)85087-3
https://doi.org/10.1515/ZNB-2008-0519
> Phenylpropanoids and polyketides / Coumarins and derivatives
Siderin 185740 Click to see CC1=CC(=CC2=C1C(=CC(=O)O2)OC)OC 220.22 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-methoxy-5-methylchromen-2-one 5318268 Click to see CC1=CC(=CC2=C1C(=CC(=O)O2)OC)O 206.19 unknown https://doi.org/10.1016/0305-1978(95)00067-4
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Candidol 44259771 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1016/0031-9422(73)85087-3

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