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Salvia santolinifolia

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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 UUID643febee26a31925137604
Scientific name Salvia santolinifolia
Authority Boiss.
First published in Diagn. Pl. Orient. 5: 13 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pleudia santolinifolia (Boiss.) M.Will, N.Schmalz & Class.-Bockh. Turkish J. Bot. 39: 703 (2015)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000302229
Tropicos 50181866
KEW urn:lsid:ipni.org:names:457181-1
The Plant List kew-183792
Open Tree Of Life 523309
NCBI Taxonomy 392689
IPNI 457181-1
GBIF 3888430

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
Comparison of inhibitory activities of 50 Salvia species against α-Glucosidase Shojaeifard Z, Moheimanian N, Jassbi AR J Diabetes Metab Disord 26-Sep-2023
PMCID:PMC10638318
doi:10.1007/s40200-023-01301-6
PMID:37975136
Changes in Metabolite Profiling and Expression Levels of Key Genes Involved in the Terpenoid Biosynthesis Pathway in Garden Sage (Salvia officinalis) under the Effect of Hydrazine Hydrate Ali M, Abdelkawy AM, Darwish DB, Alatawi HA, Alshehri D, Al-Amrah H, Soudy FA Metabolites 29-Jun-2023
PMCID:PMC10385164
doi:10.3390/metabo13070807
PMID:37512514
Chemical composition, cholinesterase, and α-glucosidase inhibitory activity of the essential oils of some Iranian native Salvia species Gharehbagh HJ, Ebrahimi M, Dabaghian F, Mojtabavi S, Hariri R, Saeedi M, Faramarzi MA, Khanavi M BMC Complement Med Ther 03-Jun-2023
PMCID:PMC10239571
doi:10.1186/s12906-023-04004-w
PMID:37270541
Hyperhydricity in Plant Tissue Culture Polivanova OB, Bedarev VA Plants (Basel) 30-Nov-2022
PMCID:PMC9738826
doi:10.3390/plants11233313
PMID:36501352
Exploration of Lamiaceae in Cardio Vascular Diseases and Functional Foods: Medicine as Food and Food as Medicine Chakrabartty I, Mohanta YK, Nongbet A, Mohanta TK, Mahanta S, Das N, Saravanan M, Sharma N Front Pharmacol 14-Jun-2022
PMCID:PMC9237463
doi:10.3389/fphar.2022.894814
PMID:35774598
Lamiaceae Essential Oils, Phytochemical Profile, Antioxidant, and Biological Activities Ramos da Silva LR, Ferreira OO, Cruz JN, de Jesus Pereira Franco C, Oliveira dos Anjos T, Cascaes MM, Almeida da Costa W, Helena de Aguiar Andrade E, Santana de Oliveira M Evid Based Complement Alternat Med 14-Dec-2021
PMCID:PMC8692021
doi:10.1155/2021/6748052
PMID:34950215
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Natural therapeutics for urinary tract infections—a review Das S 18-Sep-2020
PMCID:PMC7498302
doi:10.1186/s43094-020-00086-2
PMID:33215041
The Health-Benefits and Phytochemical Profile of Salvia apiana and Salvia farinacea var. Victoria Blue Decoctions Afonso AF, Pereira OR, Fernandes ÂS, Calhelha RC, Silva AM, Ferreira IC, Cardoso SM Antioxidants (Basel) 25-Jul-2019
PMCID:PMC6721217
doi:10.3390/antiox8080241
PMID:31349575
Variations in genetic and chemical constituents of Ziziphus spina-christi L. populations grown at various altitudinal zonation up to 2227 m height Moustafa MF, Hesham AE, Quraishi MS, Alrumman SA J Genet Eng Biotechnol 10-Oct-2016
PMCID:PMC6299872
doi:10.1016/j.jgeb.2016.09.001
PMID:30647633
Cytotoxic, Antioxidant and Antimicrobial Activities and Phenolic Contents of Eleven Salvia Species from Iran Firuzi O, Miri R, Asadollahi M, Eslami S, Jassbi AR Iran J Pharm Res 01-Sep-2013
PMCID:PMC3920696
PMID:24523760
Salvicins A and B, new lignans from<i>Salvia santolinifolia</i> Sajid Mehmood, Itrat Fatima, Abdul Malik Informa UK Limited 26-Jun-2011
doi:10.1080/10286020.2011.575781
ChemInform Abstract: Lipoxygenase Inhibitory Lignans from Salvia santolinifolia. S. Mehmood, N. Riaz, Z. Ahmad, N. Afza, A. Malik Wiley 23-Jul-2008
doi:10.1002/CHIN.200833210
New Epoxydammarane Triterpenes from <i>Salvia santolinifolia</i> Zaheer Ahmad, Itrat Fatima, Sajid Mehmood, Rehana Ifzal, Abdul Malik, Nighat Afza Wiley 24-Jan-2008
doi:10.1002/HLCA.200890015
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227

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
3-(4-hydroxy-3,5-dimethoxyphenyl)-6-(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol 13824418 Click to see COC1=CC(=CC(=C1O)OC)C2C3(COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 404.40 unknown https://doi.org/10.1002/CHIN.200833210
3,6-bis(4-hydroxy-3,5-dimethoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol 162852177 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3(CO2)O)C4=CC(=C(C(=C4)OC)O)OC 434.40 unknown https://doi.org/10.1002/CHIN.200833210
8-Hydroxysyringaresinol 145709470 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3(CO2)O)C4=CC(=C(C(=C4)OC)O)OC 434.40 unknown https://doi.org/10.1002/CHIN.200833210
Fraxiresinol 21632950 Click to see COC1=CC(=CC(=C1O)OC)C2C3(COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 404.40 unknown https://doi.org/10.1002/CHIN.200833210
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2S,3R,4R)-4-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl 4-hydroxybutanoate 162885835 Click to see COC1=C(C=CC(=C1)CC2(COC(C2COC(=O)CCCO)C3=CC(=C(C=C3)O)OC)O)O 462.50 unknown https://doi.org/10.1080/10286020.2011.575781
[(2S,3R,4R)-4-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl butanoate 162954811 Click to see CCCC(=O)OCC1C(OCC1(CC2=CC(=C(C=C2)O)OC)O)C3=CC(=C(C=C3)O)OC 446.50 unknown https://doi.org/10.1080/10286020.2011.575781
4-[(2R,3R,4R)-4-[(3,4-dimethoxyphenyl)methyl]-4-hydroxy-3-(hydroxymethyl)oxolan-2-yl]benzene-1,2-diol 162852737 Click to see COC1=C(C=C(C=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)O)O)OC 376.40 unknown https://doi.org/10.1002/CHIN.200833210
4-[4-[(3,4-Dimethoxyphenyl)methyl]-4-hydroxy-3-(hydroxymethyl)oxolan-2-yl]benzene-1,2-diol 74333664 Click to see COC1=C(C=C(C=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)O)O)OC 376.40 unknown https://doi.org/10.1002/CHIN.200833210
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4S,5R,8R,9R,10R,14S,17S)-4-(hydroxymethyl)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-2,3-diol 101838203 Click to see CC1(CCC(O1)C(C)(C)O)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C 490.70 unknown https://doi.org/10.1002/HLCA.200890015
(2R,3R,4S,5R,8R,9R,10R,14S,17S)-4-(hydroxymethyl)-4,8,10,14-tetramethyl-17-[(2S)-2-methyl-5-propan-2-ylideneoxolan-2-yl]-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-2,3-diol 101838204 Click to see CC(=C1CCC(O1)(C)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C 472.70 unknown https://doi.org/10.1002/HLCA.200890015
[(2R,3R,4S,5R,8R,9R,10R,14S,17S)-2-hydroxy-4-(hydroxymethyl)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 3,4-dihydroxybenzoate 101838205 Click to see CC1(CCC(O1)C(C)(C)O)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC(=O)C6=CC(=C(C=C6)O)O)O)C)C)C 626.80 unknown https://doi.org/10.1002/HLCA.200890015
[2-hydroxy-4-(hydroxymethyl)-17-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] 3,4-dihydroxybenzoate 162857116 Click to see CC1(CCC(O1)C(C)(C)O)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC(=O)C6=CC(=C(C=C6)O)O)O)C)C)C 626.80 unknown https://doi.org/10.1002/HLCA.200890015
4-(hydroxymethyl)-17-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,8,10,14-tetramethyl-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-2,3-diol 162904581 Click to see CC1(CCC(O1)C(C)(C)O)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C 490.70 unknown https://doi.org/10.1002/HLCA.200890015
4-(hydroxymethyl)-4,8,10,14-tetramethyl-17-(2-methyl-5-propan-2-ylideneoxolan-2-yl)-2,3,5,6,7,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-2,3-diol 163087974 Click to see CC(=C1CCC(O1)(C)C2CCC3(C2=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C 472.70 unknown https://doi.org/10.1002/HLCA.200890015

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