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Stachys lavandulifolia

Stachys lavandulifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Stachys lavandulifolia - 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 UUID643fed63b43d6466541522
Scientific name Stachys lavandulifolia
Authority Vahl
First published in Symb. Bot. 1: 42 (1790)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sideritis calycantha M.Bieb. Fl. Taur.-Caucas. 3: 393 (1819)
Stachys boissieri Kiapell. Zametki Sist. Geogr. Rast. 16: 17. 1951 ; Not. Syst. (Tbilisi)
Stachys calycantha M.Bieb. Fl. Taur.-Caucas. 3: 393 (1819)
Stachys lavandulifolia var. glabrescens R.Bhattacharjee & Hub.-Mor. Notes Roy. Bot. Gard. Edinburgh 33: 283 (1974)
Stachys tomentosa Bunge Labiat. Persic. 71. 1873 (1873)
Stachys zuvandica Rzazade Fl. Azerbaidzhana 7: 611 (1957)
Zietenia lavandulifolia Link Enum. Hort. Berol. Alt. 2: 110 (1822)
Zietenia orientalis Gled. Mém. Acad. Roy. Sci. Hist. (Berlin) 1766: 3 (1766)

Common names Top

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Language Common/alternative name
Azerbaijani ləvəndyarpaq poruq
Polish czyściec lawendolistny
Russian Чистец лавандолистный

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000314187
Tropicos 17604556
KEW urn:lsid:ipni.org:names:459684-1
The Plant List kew-195253
Missouri Botanical Garden 281604
Open Tree Of Life 614050
Observations.org 131577
NCBI Taxonomy 193339
IPNI 459684-1
iNaturalist 549411
GBIF 7306428
Elurikkus 586039
USDA GRIN 407647

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
Edible Herbal Medicines as an Alternative to Common Medication for Sleep Disorders: A Review Article Hosseini A, Mobasheri L, Rakhshandeh H, Rahimi VB, Najafi Z, Askari VR Curr Neuropharmacol 22-Jun-2024
PMCID:PMC10964091
doi:10.2174/1570159X21666230621143944
PMID:37345244
Terminalia arjuna Bark Powder as a Potential Immunomodulator in Labeo rohita: Enhanced Hematological, Adaptive, and Humoral Responses against Bacterial Pathogens and Concordant Liver Histomorphology Meena DK, Das BK, Sahoo AK, Sahu NP, Srivastava PP, Borah S Pathogens 30-Mar-2024
PMCID:PMC11054661
doi:10.3390/pathogens13040295
PMID:38668250
In vitro antimicrobial and antibiofilm screening of eighteen Iranian medicinal plants Hamidi M, Toosi AM, Javadi B, Asili J, Soheili V, Shakeri A BMC Complement Med Ther 28-Mar-2024
PMCID:PMC10976835
doi:10.1186/s12906-024-04437-x
PMID:38549139
Biosynthesis, characterization and study of the application of silver nanoparticle for 4-nitrophenol reduction, and antimicrobial activities Mulu M, Tefera M, Guadie A, Basavaiah K Biotechnol Rep (Amst) 21-Mar-2024
PMCID:PMC10999826
doi:10.1016/j.btre.2024.e00838
PMID:38590717
Evaluation of Habenaria aitchisonii Reichb. for antioxidant, anti-inflammatory, and antinociceptive effects with in vivo and in silico approaches Asiri SA, Shabnam M, Zafar R, Alshehri OM, Alshehri MA, Sadiq A, Mahnashi MH, Jan MS Front Chem 19-Mar-2024
PMCID:PMC10985259
doi:10.3389/fchem.2024.1351827
PMID:38566899
Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 12-Mar-2024
PMCID:PMC10969124
doi:10.3390/foods13060858
PMID:38540848
Conductivity-Based Gas Sensors Using Tamarindus indica Polysaccharide-Capped Gold Nanoparticles for the Detection of Volatile Gases Selvanayakam S, Esakkidurai SP, Kalaiyar S ACS Omega 24-Feb-2024
PMCID:PMC10918775
doi:10.1021/acsomega.3c09137
PMID:38463309
Treating COVID-19 with Medicinal Plants: Is It Even Conceivable? A Comprehensive Review Al-Jamal H, Idriss S, Roufayel R, Abi Khattar Z, Fajloun Z, Sabatier JM Viruses 20-Feb-2024
PMCID:PMC10974729
doi:10.3390/v16030320
PMID:38543686
Oxali-palladium nanoparticle synthesis, characterization, protein binding, and apoptosis induction in colorectal cancer cells Golestannezhad N, Divsalar A, Badalkhani-Khamseh F, Rasouli M, Seyedarabi A, Ghalandari B, Ding X, Goli F, Bekeschus S, Movahedi AA, Moghadam ME J Mater Sci Mater Med 11-Jan-2024
PMCID:PMC10784377
doi:10.1007/s10856-023-06766-8
PMID:38206473
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Therapeutics to Treat Psychiatric and Neurological Disorders: A Promising Perspective from Algerian Traditional Medicine Larit F, León F Plants (Basel) 15-Nov-2023
PMCID:PMC10674704
doi:10.3390/plants12223860
PMID:38005756
Green Synthesis of Metal and Metal Oxide Nanoparticles: A Review of the Principles and Biomedical Applications Radulescu DM, Surdu VA, Ficai A, Ficai D, Grumezescu AM, Andronescu E Int J Mol Sci 20-Oct-2023
PMCID:PMC10607471
doi:10.3390/ijms242015397
PMID:37895077
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
Plant-derived nanomaterials (PDNM): a review on pharmacological potentials against pathogenic microbes, antimicrobial resistance (AMR) and some metabolic diseases Okeke ES, Nweze EJ, Anaduaka EG, Okoye CO, Anosike CA, Joshua PE, Ezeorba TP 3 Biotech 04-Aug-2023
PMCID:PMC10403488
doi:10.1007/s13205-023-03713-w
PMID:37547919
Potent In Vitro and In Vivo Effects of Stachys lavandulifolia Methanolic Extract against Toxoplasma gondii Infection Alanazi AD, Majeed QA, Alnomasy SF, Almohammed HI Trop Med Infect Dis 05-Jul-2023
PMCID:PMC10384536
doi:10.3390/tropicalmed8070355
PMID:37505651

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 / Iridoid O-glycosides
(2R,3R,4R,5S,6R)-2-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163000258 Click to see C1=COC(C2C1C(C=C2CO)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 508.50 unknown https://doi.org/10.1080/14786411003754330
(2S,3R,4S,5S,6R)-2-[[(1S,4aS,5R,7aR)-5-hydroxy-7-(hydroxymethyl)-4a-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162931721 Click to see C1=COC(C2C1(C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 524.50 unknown https://doi.org/10.1080/14786411003754330
2-(Hydroxymethyl)-6-[[7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]oxane-3,4,5-triol 53462670 Click to see C1=COC(C2C1C(C=C2CO)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 508.50 unknown https://doi.org/10.1080/14786411003754330
2-[[4a,5-dihydroxy-7-(hydroxymethyl)-5,7a-dihydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73157015 Click to see C1=COC(C2C1(C(C=C2CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 362.33 unknown https://doi.org/10.1080/14786411003754330
2-[[5-hydroxy-7-(hydroxymethyl)-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 15560475 Click to see C1=COC(C2C1(C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 524.50 unknown https://doi.org/10.1080/14786411003754330
Monomelittoside 11968396 Click to see C1=COC(C2C1(C(C=C2CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 362.33 unknown https://doi.org/10.1080/14786411003754330
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dimethoxyphenyl)prop-2-enoate 163188124 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)OC5C(C(C(CO5)O)O)O)O)O 798.80 unknown https://doi.org/10.1080/14786411003754330
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dimethoxyphenyl)prop-2-enoate 162863833 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)OC5C(C(C(CO5)O)O)O)O)O 798.80 unknown https://doi.org/10.1080/14786411003754330
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 72726475 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1002/HLCA.19880710612
CID 14034195 14034195 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1002/HLCA.19880710612
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74027662 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown https://doi.org/10.1080/14786411003754330
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1080/14786411003754330
Leucosceptoside A 10394343 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown https://doi.org/10.1080/14786411003754330
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1080/14786411003754330

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