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Salvia bracteata

Salvia bracteata - 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 UUID643feb9c12782727803969
Scientific name Salvia bracteata
Authority Banks & Sol.
First published in Nat. Hist. Aleppo , ed. 2, 2: 242 (1794)

Description Top

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Synonyms Top

No known synonyms.

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
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000300499
KEW urn:lsid:ipni.org:names:455812-1
The Plant List kew-182184
Open Tree Of Life 6083041
Observations.org 121726
NCBI Taxonomy 1933696
IPNI 455812-1
iNaturalist 513847
GBIF 3883205
Elurikkus 658132

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
Cultural vs. State Borders: Plant Foraging by Hawraman and Mukriyan Kurds in Western Iran Sulaiman N, Salehi F, Prakofjewa J, Cavalleri SA, Ahmed HM, Mattalia G, Rastegar A, Maghsudi M, Amin HM, Rasti A, Hosseini SH, Ghorbani A, Pieroni A, Sõukand R Plants (Basel) 08-Apr-2024
PMCID:PMC11013122
doi:10.3390/plants13071048
PMID:38611576
Essential Oils and Their Main Chemical Components: The Past 20 Years of Preclinical Studies in Melanoma Di Martile M, Garzoli S, Ragno R, Del Bufalo D Cancers (Basel) 16-Sep-2020
PMCID:PMC7565555
doi:10.3390/cancers12092650
PMID:32948083
Synergistic Antifungal, Allelopatic and Anti-Proliferative Potential of Salvia officinalis L., and Thymus vulgaris L. Essential Oils Alexa E, Sumalan RM, Danciu C, Obistioiu D, Negrea M, Poiana MA, Rus C, Radulov I, Pop G, Dehelean C Molecules 16-Jan-2018
PMCID:PMC6017077
doi:10.3390/molecules23010185
PMID:29337923
Phytotherapy and Nutritional Supplements on Breast Cancer Lopes CM, Dourado A, Oliveira R Biomed Res Int 06-Aug-2017
PMCID:PMC5563402
doi:10.1155/2017/7207983
PMID:28845434
Commercial Essential Oils as Potential Antimicrobials to Treat Skin Diseases Orchard A, van Vuuren S Evid Based Complement Alternat Med 04-May-2017
PMCID:PMC5435909
doi:10.1155/2017/4517971
PMID:28546822
An annotated checklist of the scale insects of Iran (Hemiptera, Sternorrhyncha, Coccoidea) with new records and distribution data Moghaddam M Zookeys 23-Sep-2013
PMCID:PMC3804760
doi:10.3897/zookeys.334.5818
PMID:24163586
Diterpenoids from the roots of Salvia bracteata Ayhan Ulubelen, Sevil Öksüz, Ufuk Kolak, Nur Tan, Candan Bozok-Johansson, Cennet Çelik, Hans-Jurgen Kohlbau, Wolfgang Voelter Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00453-7

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
(1S,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-14-one 101006066 Click to see CC(C)C1=C(C=C2C(=C1)C3CC4C2(CO3)C(=O)CCC4(C)C)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
(4aS,10aS)-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene 484400 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)OC 300.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
(4b,8,8-Trimethyl-1,4-dioxo-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl) acetate 162992602 Click to see CC(C)C1=C(C(=O)C2=C(C1=O)CCC3C2(CCCC3(C)C)C)OC(=O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
(4bR,8aR)-1-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-prop-1-en-2-yl-6,7,9,10-tetrahydro-5H-phenanthrene-3,4-dione 10450195 Click to see CC(=C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3(CC2)OC)(C)C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
(4bR,8aR)-3,8a-dimethoxy-4b,8,8-trimethyl-2-prop-1-en-2-yl-6,7,9,10-tetrahydrophenanthrene-1,4,5-trione 163104509 Click to see CC(=C)C1=C(C(=O)C2=C(C1=O)CCC3(C2(C(=O)CCC3(C)C)C)OC)OC 372.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
[(4bS,8aS)-4b,8,8-trimethyl-1,4-dioxo-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl] acetate 162992603 Click to see CC(C)C1=C(C(=O)C2=C(C1=O)CCC3C2(CCCC3(C)C)C)OC(=O)C 358.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
4-Methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-14-one 85160139 Click to see CC(C)C1=C(C=C2C(=C1)C3CC4C2(CO3)C(=O)CCC4(C)C)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 10935937 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Horminone 2751795 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Phenanthrene, 1,2,3,4,4a,9,10,10a-octahydro-6-methoxy-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS-trans)- 627188 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)OC 300.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Salvinolone 11723174 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Sugiol 94162 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3S,4R,5R,6S)-2-[[(1S,4S,6R,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyl-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163040390 Click to see CC1(C2CCC34CC(CCC3C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)C(C4)(CO)O)C 484.60 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[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-carboxylic acid 74081266 Click to see CC1C(C(C(C(O1)OC(=O)C23CCC(CC2C4=CCC5C(C4(CC3)CO)(CCC6C5(CC(C(C6(C)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)(C)C)OC8C(C(C(C(O8)C)OC9C(C(C(CO9)O)OC1C(C(CO1)(CO)O)O)O)O)O)O)O 1237.30 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
methyl (E,6R)-6-[(1R,3R,6S,8S,11R,12S,13S,15R,16R,18R)-6,13-diacetyloxy-18-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoate 162863514 Click to see CC(CCC=C(C)C(=O)OC)C1CC(C2(C1(CC(C34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)O)C)C)OC(=O)C 586.80 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
[(2R,3R,5R,6R,9R,10R,11R,13R,14R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,3,5,6,9-pentahydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 21609792 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC(C3(C2=CC(C4(C3(CC(C(C4)O)O)CO)O)O)O)OC(=O)C)C 536.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 101705 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C)C(C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
Corbisterol 12303924 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C)C(C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Organohalogen compounds / Alkyl halides / Cyclohexyl halides
3-(3-Bromo-4-chloro-4-methylcyclohexyl)-2-methylfuran 23425280 Click to see CC1=C(C=CO1)C2CCC(C(C2)Br)(C)Cl 291.61 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl 14-(furan-3-yl)-4,10-dihydroxy-6,6,13,19-tetramethyl-18-methylidene-16-oxo-5-(3-phenylprop-2-enoyloxy)-2,9,15-trioxapentacyclo[9.6.1.13,7.01,13.010,19]nonadecane-8-carboxylate 162928696 Click to see CC1(C2C(OC3(C2(C(C(C1OC(=O)C=CC4=CC=CC=C4)O)OC56CC(=O)OC(C5(CC3C6=C)C)C7=COC=C7)C)O)C(=O)OC)C 648.70 unknown https://doi.org/10.1016/S0031-9422(99)00453-7
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Marlignan Q 71577007 Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)OC)OCO5)O)OC)OCO3 400.40 unknown https://doi.org/10.1016/S0031-9422(99)00453-7

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