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Internal ID UUID643fc8ea7efcd757542619
Scientific name Santolina pectinata
Authority Lag.
First published in Gen. Sp. Pl. : 25 (1816)

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Synonyms Top

Scientific name Authority First published in
Santolina rosmarinifolia var. fruticosa Maire
Santolina rosmarinifolia var. subclausa (H.Lindb.) Jahand. & Maire
Santolina rosmarinifolia var. leptocephala (Webb) Pau & Font Quer
Santolina chamaecyparissus subsp. pectinata (Lag.) Bonnier & Layens Bonnier & Layens. 1894. 168 1894
Santolina rosmarinifolia var. pharaonis Maire
Santolina rosmarinifolia subsp. canescens (Lag.) Nyman Nyman, Consp. Fl. Eur. 1879. 369 1879
Santolina rosmarinifolia subsp. pectinata (Lag.) Maire Maire in Jahandiez & Maire, Cat. Pl. Maroc. 1934. 760 1934

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Santolina pectinata subsp. montiberica Riv.-Guerra Syst. Bot. 36(1): 187 (-188) (2011)
Santolina pectinata subsp. pectinata

Varieties (abbr. var.) 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-0000026233
INPN 120799
KEW urn:lsid:ipni.org:names:241984-1
The Plant List gcc-125348
Open Tree Of Life 652088
NCBI Taxonomy 1142027
IPNI 241984-1
GBIF 3125927
CMAUP NPO26151

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)!
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Title Authors Publication Released IDs
Chemical composition, antibacterial and antifungal activities of flowerhead and root essential oils of Santolina chamaecyparissus L., growing wild in Tunisia Bel Hadj Salah-Fatnassi K, Hassayoun F, Cheraif I, Khan S, Jannet HB, Hammami M, Aouni M, Harzallah-Skhiri F Saudi J Biol Sci 26-Mar-2016
PMCID:PMC5415143
doi:10.1016/j.sjbs.2016.03.005
PMID:28490960
Complex distribution patterns, ecology and coexistence of ploidy levels of Allium oleraceum (Alliaceae) in the Czech Republic Duchoslav M, Šafářová L, Krahulec F Ann Bot 01-Apr-2010
PMCID:PMC2859911
doi:10.1093/aob/mcq035
PMID:20363760

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
dimethyl (2S,3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 101630395 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC)C 692.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4S,4aS,6aR,6bS,8aS,12aS,14aR,14bR)-2,3-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 462205 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C 502.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9S,10R,11S,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 93492873 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Bayogenin 12305221 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Medicagenic acid 65048 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1)C)C(=O)O)C 502.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,7abeta)-Hexahydro-2alpha-[(beta-D-glucopyranosyl)oxy]-3beta-(hydroxymethyl)-1H-pyrrolizine-1alpha,7alpha-diol 21576629 Click to see C1CN2C(C(C(C2C1O)O)OC3C(C(C(C(O3)CO)O)O)O)CO 351.35 unknown via CMAUP database
[(8aalpha)-Octahydro-1beta,6alpha,7beta-trihydroxyindolizin]-8alpha-yl beta-D-glucopyranoside 10089286 Click to see C1CN2CC(C(C(C2C1O)OC3C(C(C(C(O3)CO)O)O)O)O)O 351.35 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
6-epi-Castanospermine 184806 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
Castanospermine 54445 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
Rel-(1R,6R,7S,8S,8aS)-octahydroindolizine-1,6,7,8-tetraol 13959480 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
3-Epi-fagomine 10290867 Click to see C1CNC(C(C1O)O)CO 147.17 unknown via CMAUP database
Fagomine 72259 Click to see C1CNC(C(C1O)O)CO 147.17 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines
2-Pyrrolidinemethanol, 3-hydroxy-, (2R,3S)- 11073391 Click to see C1CNC(C1O)CO 117.15 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
(1R,2S,3S,7R,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 21576628 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1R,2S,3S,7S,8R)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 21576627 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1S,2R,3R,7S,7aR)-3-Hydroxymethyl-1,2,7-trihydroxypyrrolizidine 453575 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
(1S,2R,3R,7S,8S)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 14164813 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
3-(Hydroxymethyl)-1,2,7-trihydroxypyrrolizidine 72360 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
3,7a-Diepialexine 189605 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
Australine 442628 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Methoxy-3',4',7-trihydroxyisoflavone 101785462 Click to see COC1=C(C=CC(=C1O)O)C2=COC3=C(C2=O)C=CC(=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown via CMAUP database

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