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Salvia plebeia

Salvia plebeia - 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 UUID643febdf1fe9c385305544
Scientific name Salvia plebeia
Authority R.Br.
First published in Prodr. Fl. Nov. Holland. : 501 (1810)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lumnitzera fastigiata (Roth) Spreng. Syst. Veg., ed. 16 [Sprengel] 2: 687. 1825 [Jan-May 1825]
Mosla virgata Tanaka Bull. Sci. Hort. Inst. Kyushu Imp. Univ. 1: 204 (1925)
Ocimum fastigiatum Roth Nov. Pl. Sp. : 277 (1821)
Ocimum virgatum Thunb. Syst. Nat. ed. 14 : 546 (1784)
Salvia brachiata Roxb. Fl. Ind. 1: 146 1820
Salvia minutiflora Bunge Enum. Pl. China Bor. : 50 (1833)
Salvia plebeia var. latifolia E.Peter Acta Horti Gothob. 9: 141. 1934
Salvia brachiata Roxb. Fl. Ind. 1: 146 (1820)

Common names Top

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Language Common/alternative name
Japanese ユキミソウ
Japanese ミゾコウジュ
Russian Шалфей обыкновенный
szy nipaluma-calahcah
Chinese 癫疙宝草
Chinese 癫疙包草
Chinese 癫肚子苗
Chinese 癫肚皮棵
Chinese 癫蛤蟆草
Chinese 皱皮大菜
Chinese 皱皮草
Chinese 皱皮葱
Chinese 膨胀草
Chinese 蚧肚草
Chinese 赖师草
Chinese 过冬青
Chinese 野猪菜
Chinese 野芥菜
Chinese 隔冬青
Chinese 雪里青
Chinese 青蛙草
Chinese 鱼味草
Chinese 麻鸡婆草
Chinese 黑紫苏
Chinese 节毛鼠尾草
Chinese 凤眼草
Chinese 野芝麻
Chinese 野薄荷
Chinese 臭草
Chinese 山茴香
Chinese 土荆芥
Chinese 荠苎
Chinese 泽泻
Chinese 節毛鼠尾草
Chinese 荔枝草
Chinese 薺薴蛤蟆草
Chinese 賴斷頭草
Chinese 雪见草
Chinese 野茄子
Chinese 劫细
Chinese 土犀角
Chinese 大塔花
Chinese 旋涛草
Chinese 毛苦菜
Chinese 沟香藿
Chinese 波罗子
Chinese 猪婆草
Chinese 猴臂草
Chinese 癫头草
Chinese 癫子草
Chinese 癫格宝草

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Primorye
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Vietnam
    • Malesia
      • Philippines
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301940
UNII L8N3JNG37F
Tropicos 17600604
KEW urn:lsid:ipni.org:names:456965-1
The Plant List kew-183519
Open Tree Of Life 595081
Observations.org 138924
NCBI Taxonomy 424424
IPNI 456965-1
iNaturalist 460320
GBIF 3891879
Freebase /m/0cnyw5h
EPPO SALPL
EOL 2894200
USDA GRIN 423521
Wikipedia Salvia_plebeia

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
Biogenic Salvia species synthesized silver nanoparticles with catalytic, sensing, antimicrobial, and antioxidant properties Ihsan S, Gul H, Jamila N, Khan N, Ullah R, Bari A, Nee TW, Hwang JH, Masood R Heliyon 06-Feb-2024
PMCID:PMC10875438
doi:10.1016/j.heliyon.2024.e25814
PMID:38375246
Cosmosiin Induces Apoptosis in Colorectal Cancer by Inhibiting PD-L1 Expression and Inducing ROS Han JH, Lee EJ, Park W, Choi JG, Ha KT, Chung HS Antioxidants (Basel) 18-Dec-2023
PMCID:PMC10740471
doi:10.3390/antiox12122131
PMID:38136250
Characteristics and phylogenetic analysis of the complete chloroplast genome of Primulina hedyotidea Wen H, Su Y, Xie A, Lin C, Wei W Mitochondrial DNA B Resour 23-Sep-2023
PMCID:PMC10519256
doi:10.1080/23802359.2023.2238932
PMID:37753244
The chemical profiling of Salvia plebeia during different growth periods and the biosynthesis of its main flavonoids ingredients Dai Y, Ye Z, Liu H, Zhu R, Sun L, Li S, Xie G, Zhu Y, Zhao Y, Qin M Front Plant Sci 14-Aug-2023
PMCID:PMC10461478
doi:10.3389/fpls.2023.1228356
PMID:37645462
Urinary Tract Infections Caused by Uropathogenic Escherichia coli: Mechanisms of Infection and Treatment Options Zhou Y, Zhou Z, Zheng L, Gong Z, Li Y, Jin Y, Huang Y, Chi M Int J Mol Sci 23-Jun-2023
PMCID:PMC10341809
doi:10.3390/ijms241310537
PMID:37445714
Current State of Knowledge Regarding WHO High Priority Pathogens—Resistance Mechanisms and Proposed Solutions through Candidates Such as Essential Oils: A Systematic Review Romanescu M, Oprean C, Lombrea A, Badescu B, Teodor A, Constantin GD, Andor M, Folescu R, Muntean D, Danciu C, Dalleur O, Batrina SL, Cretu O, Buda VO Int J Mol Sci 04-Jun-2023
PMCID:PMC10253476
doi:10.3390/ijms24119727
PMID:37298678
Radical oxygen species: an important breakthrough point for botanical drugs to regulate oxidative stress and treat the disorder of glycolipid metabolism Luo M, Zheng Y, Tang S, Gu L, Zhu Y, Ying R, Liu Y, Ma J, Guo R, Gao P, Zhang C Front Pharmacol 12-May-2023
PMCID:PMC10213330
doi:10.3389/fphar.2023.1166178
PMID:37251336
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
The complete chloroplast genome of Elsholtzia fruticosa (D. Don) Rehd. (Labiatae), an ornamental plant with high medicinal value Yu X, Song YR, Zhao ZN Mitochondrial DNA B Resour 28-Feb-2023
PMCID:PMC9980026
doi:10.1080/23802359.2023.2183069
PMID:36876144
Salvia plebeia R.Br. and Rosmarinic Acid Attenuate Dexamethasone-Induced Muscle Atrophy in C2C12 Myotubes Kim JY, Kim HM, Kim JH, Guo S, Lee DH, Lim GM, Kim W, Kim CY Int J Mol Sci 18-Jan-2023
PMCID:PMC9915874
doi:10.3390/ijms24031876
PMID:36768200
Natural Blockers of PD-1/PD-L1 Interaction for the Immunotherapy of Triple-Negative Breast Cancer-Brain Metastasis Nakhjavani M, Shigdar S Cancers (Basel) 19-Dec-2022
PMCID:PMC9777321
doi:10.3390/cancers14246258
PMID:36551742
Salvia plebeia R. Br. Water Extract Ameliorates Hepatic Steatosis in a Non-Alcoholic Fatty Liver Disease Model by Regulating the AMPK Pathway Bae S, Lee YH, Lee J, Park J, Jun W Nutrients 18-Dec-2022
PMCID:PMC9780835
doi:10.3390/nu14245379
PMID:36558538
Belowground seed and bud banks play complementary roles in the potential recruitment of dominant macrophyte communities in a Yangtze River-connected floodplain wetland Chen XS, Huang Y, Cai YH, Hou ZY, Deng ZM, Li F, Zou YA, Xie YH Front Plant Sci 06-Dec-2022
PMCID:PMC9763321
doi:10.3389/fpls.2022.1075496
PMID:36561449
The Molecular Mechanism of Natural Products Activating Wnt/β-Catenin Signaling Pathway for Improving Hair Loss Shin DW Life (Basel) 11-Nov-2022
PMCID:PMC9693075
doi:10.3390/life12111856
PMID:36430990
Targeting matrix metalloproteases: A promising strategy for herbal medicines to treat rheumatoid arthritis Li RL, Duan HX, Liang Q, Huang YL, Wang LY, Zhang Q, Wu CJ, Liu SQ, Peng W Front Immunol 09-Nov-2022
PMCID:PMC9682071
doi:10.3389/fimmu.2022.1046810
PMID:36439173

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 / Dibenzylbutane lignans
[(2R,3R)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]-4-[(12R)-12-methyltetradecanoyl]oxybutyl] (12S)-12-methyltetradecanoate 162915370 Click to see CCC(C)CCCCCCCCCCC(=O)OCC(CC1=CC(=C(C=C1)O)OC)C(CC2=CC(=C(C=C2)O)OC)COC(=O)CCCCCCCCCCC(C)CC 811.20 unknown https://doi.org/10.1016/S0031-9422(00)89701-0
[(2R,3R)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]-4-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxybutyl] (12S)-12-methyltetradecanoate 163188152 Click to see CCC(C)CCCCCCCCCCC(=O)OCC(CC1=CC(=C(C=C1)O)OC)C(CC2=CC(=C(C=C2)O)OC)COC(=O)C=CC3=CC(=C(C=C3)O)OC 763.00 unknown https://doi.org/10.1016/S0031-9422(00)88856-1
[2,3-Bis[(4-hydroxy-3-methoxyphenyl)methyl]-4-(12-methyltetradecanoyloxy)butyl] 12-methyltetradecanoate 162915369 Click to see CCC(C)CCCCCCCCCCC(=O)OCC(CC1=CC(=C(C=C1)O)OC)C(CC2=CC(=C(C=C2)O)OC)COC(=O)CCCCCCCCCCC(C)CC 811.20 unknown https://doi.org/10.1016/S0031-9422(00)89701-0
[2,3-Bis[(4-hydroxy-3-methoxyphenyl)methyl]-4-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]butyl] 12-methyltetradecanoate 162939519 Click to see CCC(C)CCCCCCCCCCC(=O)OCC(CC1=CC(=C(C=C1)O)OC)C(CC2=CC(=C(C=C2)O)OC)COC(=O)C=CC3=CC(=C(C=C3)O)OC 763.00 unknown https://doi.org/10.1016/S0031-9422(00)88856-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 19-oxosteroids
Royleanonic acid 10382993 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C(=O)O)O 346.40 unknown https://doi.org/10.1016/S0308-8146(00)00300-9
> Organoheterocyclic compounds / Naphthopyrans
(1S,7R,9R,10S,12S,14R,15S)-7-(furan-3-yl)-10-hydroxy-9-methyl-6,13,17-trioxapentacyclo[8.8.0.01,15.04,9.012,14]octadec-3-ene-5,16-dione 163186520 Click to see CC12CC(OC(=O)C1=CCC34C2(CC5C(C3C(=O)OC4)O5)O)C6=COC=C6 372.40 unknown https://doi.org/10.1016/S0031-9422(00)81178-4
(1S,7R,9R,10S,14R)-7-(furan-3-yl)-10-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione 162890218 Click to see CC12CC(OC(=O)C1=CCC34C2(CC=CC3C(=O)OC4)O)C5=COC=C5 356.40 unknown https://doi.org/10.1016/S0031-9422(00)81178-4
7-(Furan-3-yl)-10-hydroxy-9-methyl-6,13,17-trioxapentacyclo[8.8.0.01,15.04,9.012,14]octadec-3-ene-5,16-dione 162881609 Click to see CC12CC(OC(=O)C1=CCC34C2(CC5C(C3C(=O)OC4)O5)O)C6=COC=C6 372.40 unknown https://doi.org/10.1016/S0031-9422(00)81178-4
7-(Furan-3-yl)-10-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione 73807349 Click to see CC12CC(OC(=O)C1=CCC34C2(CC=CC3C(=O)OC4)O)C5=COC=C5 356.40 unknown https://doi.org/10.1016/S0031-9422(00)81178-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/0378-8741(85)90026-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/0378-8741(85)90026-1
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1016/S0308-8146(00)00300-9
https://doi.org/10.1016/0378-8741(85)90026-1
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/0378-8741(85)90026-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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/10.1016/S0308-8146(00)00300-9
https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1016/0378-8741(85)90026-1

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