PlantaeDB Logo
Login Sign-up

Elsholtzia splendens

Elsholtzia splendens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID644039221ebe0789160184
Scientific name Elsholtzia splendens
Authority Nakai ex Maekawa
First published in Bot. Mag. (Tokyo) 48: 50 (1934)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Elsholtzia pseudocristata f. miyasiroana (Kitag.) Kitag. J. Jap. Bot. 34: 4 1959
Elsholtzia pseudocristata var. splendens (Nakai ex F.Maek.) Kitag. J. Jap. Bot. 34: 3 1959
Elsholtzia splendens var. miyasiroana Kitag. J. Jap. Bot. 27: 207 1952
Elsholtzia splendens f. miyasiroana (Kitag.) Y.C.Chu in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 962 (1989):.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Korean 꽃향유
Chinese 香薷
Chinese 海州香薷
Chinese 野拔子
Chinese 海洲香薷

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Elsholtzia splendens var. splendens Unknown

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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 Southeast
      • Manchuria
    • Eastern Asia
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000948459
UNII D84389K3OK
Tropicos 17602258
KEW urn:lsid:ipni.org:names:446694-1
The Plant List kew-66808
PFAF Elsholtzia splendens
Open Tree Of Life 844717
NCBI Taxonomy 475396
IPNI 446694-1
iNaturalist 478511
GBIF 7308889
EOL 2893809
USDA GRIN 407673
CMAUP NPO23814

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
Invasive success of star weed (Parthenium hysterophorus L.) through alteration in structural and functional peculiarities Iqbal U, Usman Z, Azam A, Abbas H, Mehmood A, Ahmad KS PeerJ 13-Dec-2023
PMCID:PMC10725175
doi:10.7717/peerj.16609
PMID:38107576
Identification of key genes associated with heart failure based on bioinformatics analysis and screening of traditional Chinese medicines for the prevention and treatment of heart failure Luo X, Wang R, Zhang X, Wen X, Xie W Medicine (Baltimore) 08-Dec-2023
PMCID:PMC10713177
doi:10.1097/MD.0000000000035959
PMID:38065888
Diagnostic validity of premenstrual dysphoric disorder: revisited Naik SS, Nidhi Y, Kumar K, Grover S Front Glob Womens Health 27-Nov-2023
PMCID:PMC10711063
doi:10.3389/fgwh.2023.1181583
PMID:38090047
Achieving abiotic stress tolerance in plants through antioxidative defense mechanisms Mishra N, Jiang C, Chen L, Paul A, Chatterjee A, Shen G Front Plant Sci 02-Jun-2023
PMCID:PMC10272748
doi:10.3389/fpls.2023.1110622
PMID:37332720
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Arbuscular mycorrhizae influence raspberry growth and soil fertility under conventional and organic fertilization Lu Q, Bunn R, Whitney E, Feng Y, DeVetter LW, Tao H Front Microbiol 16-May-2023
PMCID:PMC10227501
doi:10.3389/fmicb.2023.1083319
PMID:37260690
Phytoremediation as an Effective Remedy for Removing Trace Elements from Ecosystems Mocek-Płóciniak A, Mencel J, Zakrzewski W, Roszkowski S Plants (Basel) 14-Apr-2023
PMCID:PMC10141480
doi:10.3390/plants12081653
PMID:37111876
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
Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review Tshikhudo PP, Ntushelo K, Mudau FN Microorganisms 10-Feb-2023
PMCID:PMC9967847
doi:10.3390/microorganisms11020453
PMID:36838418
Elsholtzia ciliata (Thunb.) Hyland: A Review of Phytochemistry and Pharmacology Wang F, Liu X, Chen Y, An Y, Zhao W, Wang L, Tian J, Kong D, Xu Y, Ba Y, Zhou H Molecules 28-Sep-2022
PMCID:PMC9572931
doi:10.3390/molecules27196411
PMID:36234947
Association mapping uncovers maize ZmbZIP107 regulating root system architecture and lead absorption under lead stress Hou F, Liu K, Zhang N, Zou C, Yuan G, Gao S, Zhang M, Pan G, Ma L, Shen Y Front Plant Sci 26-Sep-2022
PMCID:PMC9549328
doi:10.3389/fpls.2022.1015151
PMID:36226300
The potential of mineral weathering of halophilic-endophytic bacteria isolated from Suaeda salsa and Spartina anglica Xi J, Qian K, Shan L, Huang J, Yan Y Arch Microbiol 17-Aug-2022
PMCID:PMC9385829
doi:10.1007/s00203-022-03129-9
PMID:35978053
Comparison of In Vitro and In Planta Heavy Metal Tolerance and Accumulation Potential of Different Armeria maritima Accessions from a Dry Coastal Meadow Purmale L, Jēkabsone A, Andersone-Ozola U, Karlsons A, Osvalde A, Ievinsh G Plants (Basel) 12-Aug-2022
PMCID:PMC9413919
doi:10.3390/plants11162104
PMID:36015407
The Role of Hemicellulose in Cadmium Tolerance in Ramie (Boehmeria nivea (L.) Gaud.) Ma Y, Jie H, Tang Y, Xing H, Jie Y Plants (Basel) 26-Jul-2022
PMCID:PMC9330422
doi:10.3390/plants11151941
PMID:35893645
Antifungal Effects and Active Components of Ligusticum chuanxiong Chen H, Zhao Y, Qin G, Bi Y, Yue G, Zhang M, Chang X, Qiu X, Luo L, Yang C Molecules 19-Jul-2022
PMCID:PMC9320862
doi:10.3390/molecules27144589
PMID:35889462

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Ergoline and derivatives / Clavines and derivatives
(7-methyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinolin-7-ium-9-yl)methanol 46173397 Click to see C[NH+]1CC(=CC2C1CC3=CNC4=CC=CC2=C34)CO 255.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
3-Butenylbenzene 13033 Click to see C=CCCC1=CC=CC=C1 132.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
m-Xylene 7929 Click to see CC1=CC(=CC=C1)C 106.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes
P-Xylene 7809 Click to see CC1=CC=C(C=C1)C 106.16 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol 6992244 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol 11301173 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 304.47 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
5-(113C)methyl-2-(1,3-13C2)propan-2-ylidenecyclohexan-1-one 11665448 Click to see CC1CCC(=C(C)C)C(=O)C1 155.21 unknown via CMAUP database
l-Piperitone 107561 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown via CMAUP database
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Menthone 26447 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown via CMAUP database
p-Menth-3-en-1-ol 11468 Click to see CC(C)C1=CCC(CC1)(C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 45115091 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Zingiberol 5317270 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(S)-(+)-2-butanol 444683 Click to see CCC(C)O 74.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
CID 10487440 10487440 Click to see C=CCC1=CC2=C(C=C1)OCO2 174.14 unknown via CMAUP database
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-Methyl-1-(3-methylfuran-2-yl)butane-2,3-diol 3084495 Click to see CC1=C(OC=C1)CC(C(C)(C)O)O 184.23 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-Furanol, 5-ethenyltetrahydro-5-methyl-2-(1-methylethyl)- 111405 Click to see CC(C)C1(CCC(O1)(C)C=C)O 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Octadecyl ferulate 5320256 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)prop-2-enoate 54710367 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)[O-] 179.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5,5'-dihydroxy-2,2'-bis(4-hydroxyphenyl)-7,7'-dimethoxy-4H,4'H-[6,8'-bichromene]-4,4'-dione 9985405 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC 566.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-hydroxyphenyl)chromen-4-one 13888657 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-methoxyphenyl)chromen-4-one 102115496 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC 566.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-2-(4-hydroxyphenyl)chromen-4-one 102115497 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown via CMAUP database
8,8''-Bisgenkwanin 5316884 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OC 566.50 unknown via CMAUP database
Cupressuflavone 5281609 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 538.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
Apigenin-7-olate 25200950 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 269.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Acacetin-7-O-Beta-D-Galactopyranoside 5480899 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see CC1CC2=C(C=C(C=C2OC1C3=CC(=C(C=C3)O)O)O)O 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-) 25203524 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)[O-] 299.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.