Salvia mirzayanii

Details Top

Internal ID UUID643febce0447e314807018
Scientific name Salvia mirzayanii
Authority Rech.f. & Esfand.
First published in Oesterr. Bot. Z. 99: 53 (1952)

Ethnobotanical Use Top

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Synonyms Top

No known synonyms.

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Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301619
Tropicos 100253934
KEW urn:lsid:ipni.org:names:456713-1
The Plant List kew-183217
Open Tree Of Life 5801000
NCBI Taxonomy 1571167
IPNI 456713-1
iNaturalist 1151129
GBIF 3895727
CMAUP NPO24316

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
Effect of different salinity on seed germination, growth parameters and biochemical contents of pumpkin (Cucurbita pepo L.) seeds cultivars Irik HA, Bikmaz G Sci Rep 22-Mar-2024
PMCID:PMC10960046
doi:10.1038/s41598-024-55325-w
PMID:38519514
Integrated transcriptomic and metabolomic analyses elucidate the mechanism of flavonoid biosynthesis in the regulation of mulberry seed germination under salt stress Wang Y, Jiang W, Li C, Wang Z, Lu C, Cheng J, Wei S, Yang J, Yang Q BMC Plant Biol 21-Feb-2024
PMCID:PMC10880279
doi:10.1186/s12870-024-04804-3
PMID:38383312
Effects of Salvia mirzayanii extract administration on hyperglycemia improvement in diabetic rats: The role of GLUT4, PEPCK and G6Pase genes Mahdizadehdehosta R, Shahbazmohammadi H, Moein S, Soltani N, Malekzadeh K, Moein M Heliyon 01-Feb-2024
PMCID:PMC10850551
doi:10.1016/j.heliyon.2024.e25256
PMID:38333789
Volatile Organic Compounds Emitted by Flowers: Ecological Roles, Production by Plants, Extraction, and Identification Lo MM, Benfodda Z, Molinié R, Meffre P Plants (Basel) 31-Jan-2024
PMCID:PMC10857460
doi:10.3390/plants13030417
PMID:38337950
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Antibacterial Efficiency of Tanacetum vulgare Essential Oil against ESKAPE Pathogens and Synergisms with Antibiotics Roman H, Niculescu AG, Lazăr V, Mitache MM Antibiotics (Basel) 17-Nov-2023
PMCID:PMC10669310
doi:10.3390/antibiotics12111635
PMID:37998837
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Nanoparticle-mediated amelioration of drought stress in plants: a systematic review Chandrashekar HK, Singh G, Kaniyassery A, Thorat SA, Nayak R, Murali TS, Muthusamy A 3 Biotech 08-Sep-2023
PMCID:PMC10491566
doi:10.1007/s13205-023-03751-4
PMID:37693636
Evaluating the genotoxicity of salinity stress and secondary products gene manipulation in lime, Citrus aurantifolia, plants Darwish H, Al-Osaimi GS, Al Kashgry NA, Sonbol H, Alayafi AA, Alabdallah NM, Al-Humaid A, Al-Harbi NA, Al-Qahtani SM, Abbas ZK, Darwish DB, Ibrahim MF, Noureldeen A Front Plant Sci 12-Jul-2023
PMCID:PMC10369181
doi:10.3389/fpls.2023.1211595
PMID:37502705
Phytochemical, Morphological, and Physiological Variation in Different Ajowan (Trachyspermum ammi L.) Populations as Affected by Salt Stress, Genotype × Year Interaction and Pollination System Mirniyam G, Rahimmalek M, Arzani A, Yavari P, Sabzalian MR, Ehtemam MH, Szumny A Int J Mol Sci 21-Jun-2023
PMCID:PMC10341850
doi:10.3390/ijms241310438
PMID:37445619
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
Novel antimicrobial/antioxidant Eremurus luteus root gum coating containing rosemary essential oil nanoemulsions for extension of chicken meat shelf life Shahrampour D, Razavi SM Food Sci Nutr 09-Mar-2023
PMCID:PMC10261811
doi:10.1002/fsn3.3295
PMID:37324841
The differential modulation of secondary metabolism induced by a protein hydrolysate and a seaweed extract in tomato plants under salinity Zhang L, Freschi G, Rouphael Y, De Pascale S, Lucini L Front Plant Sci 16-Jan-2023
PMCID:PMC9884811
doi:10.3389/fpls.2022.1072782
PMID:36726679
Advancement in utilization of magnetic catalysts for production of sustainable biofuels Zhang Y, Li W, Wang J, Jin J, Zhang Y, Cheng J, Zhang Q Front Chem 10-Jan-2023
PMCID:PMC9871569
doi:10.3389/fchem.2022.1106426
PMID:36704618
Potential of green synthesized titanium dioxide nanoparticles for enhancing seedling emergence, vigor and tolerance indices and DPPH free radical scavenging in two varieties of soybean under salinity stress Abdalla H, Adarosy MH, Hegazy HS, Abdelhameed RE BMC Plant Biol 02-Dec-2022
PMCID:PMC9716725
doi:10.1186/s12870-022-03945-7
PMID:36460962

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
7-Keto-11c-octadecenoic acid 14861231 Click to see 296.40 unknown via CMAUP database
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.1128
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1002/FFJ.1128
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.1128
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/FFJ.1128
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.1128
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1002/FFJ.1128
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.1128
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1002/FFJ.1128
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1002/FFJ.1128
https://doi.org/10.1002/PTR.3289
Spathulenol 92231 Click to see 220.35 unknown https://doi.org/10.1002/PTR.3289
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.1128
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4aR,5R,6R,8aR)-6-hydroxy-1,4a,6-trimethyl-5-[(E)-3-methyl-5-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162895340 Click to see 418.60 unknown https://doi.org/10.1021/NP970378J
(1R,4aS,5R,6R,8aR)-6-hydroxy-1,4a,6-trimethyl-5-[(E)-3-methyl-5-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 21604147 Click to see 418.60 unknown https://doi.org/10.1021/NP970378J
(1R,4aS,6R)-6-hydroxy-1,4a,6-trimethyl-5-[(E)-3-methyl-5-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 101937331 Click to see 418.60 unknown https://doi.org/10.1021/NP970378J
6-hydroxy-1,4a,6-trimethyl-5-[3-methyl-5-(3-methyl-5-oxo-2H-furan-2-yl)pent-3-enyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 73799282 Click to see 418.60 unknown https://doi.org/10.1021/NP970378J
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1002/FFJ.1128
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone 152430 Click to see 358.30 unknown https://doi.org/10.1515/ZNC-1992-9-1025
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP970378J
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4'-Hydroxywogonin 5322078 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown via CMAUP database
Gardenin A 261859 Click to see 418.40 unknown via CMAUP database
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
Gardenin C 3084507 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 404.40 unknown via CMAUP database
Gardenin D 3080750 Click to see 374.30 unknown via CMAUP database
Gardenin E 3084508 Click to see 390.30 unknown via CMAUP database
Hypolaetin 8,3',4'-trimethyl ether 5316844 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC 344.30 unknown via CMAUP database

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