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Sideritis lasiantha

Sideritis lasiantha - 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 UUID643fecd6ae86d960071809
Scientific name Sideritis lasiantha
Authority Juss. ex Pers.
First published in Syn. Pl. 2: 117 (1806)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sideritis foetens Clemente ex Lag. Gen. Sp. Pl. : 18 (1816)
Sideritis foetens var. rivasgodayi Fern.Casas Anales Inst. Bot. Cavanilles 32: 306 (1975)
Sideritis juncea Cav. ex Willk. & Lange Prodr. Fl. Hispan. 2: 459 (1868)
Sideritis phleoides Lange ex Willk. & Lange Prodr. Fl. Hispan. 2: 459 (1868)

Common names Top

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Language Common/alternative name
Arabic فزر أشعث الأزهار

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000310215
Tropicos 100258798
KEW urn:lsid:ipni.org:names:458969-1
The Plant List kew-191423
Open Tree Of Life 6081642
IPNI 458969-1
iNaturalist 910096
GBIF 3890355
USDA GRIN 475183

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
ent-Kauranoid derivatives from Sideritis moorei. Ghoumari H, Benajiba MH, Azmani A, García-Granados A, Martínez A, Parra A, Rivas F, Socorro O Phytochemistry 01-Jun-2005
doi:10.1016/J.PHYTOCHEM.2005.04.033
PMID:15949828
Diterpenoids from Sideritis foetens Maria C. Garcia-Alvarez, Benjamin Rodriguez Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)91036-7
Products with biological activity obtained from in vitro micropropagated Sideritis foetens A. Garcia-Granados, A. Martinez, M.E. Onorato, A. Parra, M.B. Recondo, F. Rivas, M.L. Arrebola, O. Socorro Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90579-X
The essential oils of some eastern Spain Sideritis Carmen Mateo, Jesús Sanz, José Calderón Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80325-8
Anti-inflammatory and immunomodulating properties of a sterol fraction from Sideritis foetens Clem. Navarro A, De las Heras B, Villar A Biol Pharm Bull 01-May-2001
doi:10.1248/BPB.24.470
PMID:11379762
Immunomodulating properties of the diterpene andalusol. Navarro A, de las Heras B, Villar A Planta Med 01-Apr-2000
doi:10.1055/S-2000-8567
PMID:10821063
Inhibition of NOS-2 expression in macrophages through the inactivation of NF-kappaB by andalusol. de las Heras B, Navarro A, Díaz-Guerra MJ, Bermejo P, Castrillo A, Boscá L, Villar A Br J Pharmacol 01-Oct-1999
PMCID:PMC1571685
doi:10.1038/SJ.BJP.0702844
PMID:10516639
Andalusol, a diterpenoid with anti-inflammatory activity from Siderits foetens Clemen. Navarro A, de las Heras B, Villar AM Z Naturforsch C J Biosci 01-Nov-1997
doi:10.1515/ZNC-1997-11-1219
PMID:9463942

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
(1R,3S,4R,4aR,8S,8aS)-8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,3-diol 162854464 Click to see CC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)CO 322.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
(1R,3S,4R,4aS,8S,8aS)-8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,3-diol 162854463 Click to see CC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)CO 322.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
(1R,3S,4S,4aS,8S,8aR)-8-(Hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)decalin-1,3-diol 188448 Click to see CC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)CO 322.50 unknown https://doi.org/10.1515/ZNC-1997-11-1219
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1571685/
https://doi.org/10.1055/S-2000-8567
https://doi.org/10.1016/J.PHYTOCHEM.2005.04.033
[(1R,3S,4R,4aR,7R,8aR)-3,7-dihydroxy-3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163188820 Click to see CC(=O)OC1CC(C(C2(C1C(C(CC2)O)(C)C)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
[(1R,3S,4R,4aR,7R,8aS)-3,7-dihydroxy-3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163061812 Click to see CC(=O)OC1CC(C(C2(C1C(C(CC2)O)(C)C)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
[(1R,3S,4R,4aR,8S,8aS)-3-hydroxy-8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163033133 Click to see CC(=O)OC1CC(C(C2(C1C(CCC2)(C)CO)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
[(1R,3S,4S,4aR,7R,8aS)-3,7-dihydroxy-3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163061813 Click to see CC(=O)OC1CC(C(C2(C1C(C(CC2)O)(C)C)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
[(1R,3S,4S,4aR,8S,8aS)-3-hydroxy-8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163033132 Click to see CC(=O)OC1CC(C(C2(C1C(CCC2)(C)CO)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
https://doi.org/10.1016/S0031-9422(00)90579-X
[(1S,4aR,5R,6S,8R,8aS)-6,8-dihydroxy-1,4a,6-trimethyl-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 163185269 Click to see CC(=O)OCC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)C 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
[(1S,4aR,5S,6S,8R,8aS)-6,8-dihydroxy-1,4a,6-trimethyl-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 163037703 Click to see CC(=O)OCC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)C 364.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
https://doi.org/10.1016/S0031-9422(00)91036-7
[3-hydroxy-8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163033131 Click to see CC(=O)OC1CC(C(C2(C1C(CCC2)(C)CO)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
https://doi.org/10.1016/S0031-9422(00)91036-7
[3,7-dihydroxy-3,4a,8,8-tetramethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 163061811 Click to see CC(=O)OC1CC(C(C2(C1C(C(CC2)O)(C)C)C)CCC(=C)C=C)(C)O 364.50 unknown https://doi.org/10.1016/S0031-9422(00)91036-7
https://doi.org/10.1016/S0031-9422(00)90579-X
[6,8-dihydroxy-1,4a,6-trimethyl-5-(3-methylidenepent-4-enyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 163037702 Click to see CC(=O)OCC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)C 364.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
https://doi.org/10.1016/S0031-9422(00)91036-7
8-(hydroxymethyl)-3,4a,8-trimethyl-4-(3-methylidenepent-4-enyl)-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,3-diol 14607768 Click to see CC1(CCCC2(C1C(CC(C2CCC(=C)C=C)(C)O)O)C)CO 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.04.033
https://doi.org/10.1016/S0031-9422(00)91036-7
https://doi.org/10.1016/S0031-9422(00)90579-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
[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/S0031-9422(00)90579-X
Siderol 12315548 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)CO)C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Cuminaldehyde 326 Click to see CC(C)C1=CC=C(C=C1)C=O 148.20 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Piperitone 61362 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)80325-8
> 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/S0031-9422(00)90579-X
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol 13970285 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC(O3)(C)C=C)C)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)90579-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/BPB.24.470
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1248/BPB.24.470
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1248/BPB.24.470

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