Scientific name	Authority	First published in
Aphanochilus stauntonii	Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 63 (1929)
Elsholtzia stauntonii f. albiflora	H.W.Jen & Y.J.Chang	J. Beijing Forest. Univ. 13(3): 2 (1991)

Common names Top

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Filter by language:

Language	Common/alternative name
Hungarian	kései szálkamenta
Polish	marzymięta chińska
Chinese	香荆芥
Chinese	野拔子
Chinese	华北香薷
Chinese	木香薷
Chinese	山荆芥
Chinese	紫荆芥
Chinese	柴荆芥

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- China
  - China North-central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000948465
Tropicos	17606967
Flora of Italy	12844
KEW	urn:lsid:ipni.org:names:446697-1
The Plant List	kew-66813
Missouri Botanical Garden	281636
Open Tree Of Life	82478
Observations.org	145730
NCBI Taxonomy	41226
IPNI	446697-1
iNaturalist	135427
GBIF	7308883
EPPO	ELHST
EOL	2898772
USDA GRIN	15020
CMAUP	NPO14583

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

Nitrogen Fertilization in a Faba Bean–Wheat Intercropping System Can Alleviate the Autotoxic Effects in Faba Bean

Cen Z, Zheng Y, Guo Y, Yang S, Dong Y

Plants (Basel)

08-Mar-2023

PMCID:	PMC10057412
doi:	10.3390/plants12061232
PMID:	36986921

Genetic Diversity Study on Geographical Populations of the Multipurpose Species Elsholtzia stauntonii Using Transferable Microsatellite Markers

Zhang C, Jia C, Liu X, Zhao H, Hou L, Li M, Cui B, Li Y

Front Plant Sci

12-May-2022

PMCID:	PMC9134938
doi:	10.3389/fpls.2022.903674
PMID:	35646027

Pharmacognostic Study on Elsholtzia ciliata (Thumb.) Hyl: Anatomy, Phytochemistry and Pharmacological Activities

Zhang Q, Porto NM, Guilhon CC, Giorno TB, Alviano DS, Agra MD, Fernandes PD, Boylan F

Pharmaceuticals (Basel)

12-Nov-2021

PMCID:	PMC8620380
doi:	10.3390/ph14111152
PMID:	34832934

Toxicity and Synergistic Effect of Elsholtzia ciliata Essential Oil and Its Main Components against the Adult and Larval Stages of Tribolium castaneum

Liang JY, Xu J, Yang YY, Shao YZ, Zhou F, Wang JL

Foods

16-Mar-2020

PMCID:	PMC7143226
doi:	10.3390/foods9030345
PMID:	32188172

Chemical Compositions and Insecticidal Activities of Alpinia kwangsiensis Essential Oil against Lasioderma serricorne

Wu Y, Zhang WJ, Huang DY, Wang Y, Wei JY, Li ZH, Sun JS, Bai JF, Tian ZF, Wang PJ, Du SS

Molecules

08-Dec-2015

PMCID:	PMC6332138
doi:	10.3390/molecules201219818
PMID:	26670226

Commercialized non-Camellia tea: traditional function and molecular identification

Long P, Cui Z, Wang Y, Zhang C, Zhang N, Li M, Xiao P

Acta Pharm Sin B

24-Mar-2014

PMCID:	PMC4629065
doi:	10.1016/j.apsb.2014.02.006
PMID:	26579387

Subject Index

N/A

01-Jan-2005

PMCID:	PMC7148952
doi:	10.1016/S1572-5995(05)80049-3

Three new c-methylated flavones from Elsholtzia stauntonii.

Zheng S, Kang S, Shen Y, Sun L

Planta Med

01-Mar-1999

doi:	10.1055/S-2006-960459
PMID:	17260252

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,9R)-9-hydroxyoctadec-12-enoic acid	5312848	Click to see CCCCCC=CCCC(CCCCCCCC(=O)O)O	298.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol	57412952	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC	451.60	unknown	via CMAUP database
(1S,4S,5R,7S,8S,9R,10R, 11S,13S,14S,16S,17R)-N-methyl-8,14-dihydroxy-1,16-trimethoxy-4-(methoxymethylene)aconitane	57506227	Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC	421.60	unknown	via CMAUP database
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13R,14S,15R,16R,17S,18R)-8-acetyloxy-11-ethyl-5,14,15-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate	101939155	Click to see CCN1CC2(C3C(C4C1C3(C5CC6(C(CC4(C5C6OC(=O)C7=CC=C(C=C7)OC)OC(=O)C)OC)O)C(C(C2O)O)OC)OC)COC	675.80	unknown	via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-8,18-dihydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate	101939159	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)O)O)OC)COC	571.70	unknown	via CMAUP database
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate	101939158	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC	627.80	unknown	via CMAUP database
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-8-hydroxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate	101622120	Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)O)OC)COC	463.60	unknown	via CMAUP database
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-4-acetyloxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-8-yl] benzoate	101939154	Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OC(=O)C7=CC=CC=C7)OC)COC	567.70	unknown	via CMAUP database
8-Deacetylyunaconitine	101938470	Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)O)OC)OC)O)COC	617.70	unknown	via CMAUP database
CID 11250863	11250863	Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC	659.80	unknown	via CMAUP database
Forestine	101939160	Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)O)OC)OC)COC	601.70	unknown	via CMAUP database
Indaconitine	60208143	Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC	629.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
11alpha-Hydroxyandrosta-1,4-diene-3,17-dione	111337	Click to see CC12CC(C3C(C1CCC2=O)CCC4=CC(=O)C=CC34C)O	300.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(1S)-1-(methylamino)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine	102090481	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C)NC	330.50	unknown	via CMAUP database
Kurchessine	442979	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)C)N(C)C	372.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol	92113	Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 18-hydroxysteroids
[(3S,8R,9S,10R,13R,14S,17S)-3-(dimethylamino)-17-[(1S)-1-(dimethylamino)ethyl]-10-methyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-13-yl]methanol	14543701	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)CO)N(C)C	388.60	unknown	via CMAUP database
Holadysenterine	16742955	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N(C(=O)C)O	390.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Hydrocortisone	5754	Click to see CC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4(C(=O)CO)O)C)O	362.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one	21573748	Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1	327.50	unknown	via CMAUP database
Holanamine	76308534	Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)C=N1	325.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
Holadysine	102093813	Click to see CCC1C(=O)CC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C	329.50	unknown	via CMAUP database
Holarrhimine	15559632	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N	332.50	unknown	via CMAUP database
Irehdiamine B	15560372	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N	330.50	unknown	via CMAUP database
Pregn-5-en-18-ol, 20-amino-3-(methylamino)-, (3beta,20S)-	22214001	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)CO)N	346.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1R,2S,5S,6S,9R,12S,13R,16S,20S)-16-(dimethylamino)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-20-ol	102093825	Click to see CC1C2CCC3C2(CCC4C3C(C=C5C4(CCC(C5)N(C)C)C)O)CN1C	372.60	unknown	via CMAUP database
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one	21573749	Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1C	341.50	unknown	via CMAUP database
(1S,2S,5S,6S,9R,12S,13R,16S,17R,18R,20R)-16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosane-18,20-diol	101529338	Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C	404.60	unknown	via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)-	11225162	Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C	468.70	unknown	via CMAUP database
Conessine	441082	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C	356.60	unknown	via CMAUP database
Holadienine	12310532	Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C	325.50	unknown	via CMAUP database
Holarrhenine	12310556	Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)O	372.60	unknown	via CMAUP database
Isoconessimine	11772257	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1C	342.60	unknown	via CMAUP database
Kurcholessine	20054951	Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C	404.60	unknown	via CMAUP database
N,N-Dimethylconanin-5-en-3alpha-amine	12303833	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C	356.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-ethylcholesta-5,23E-dien-3beta-ol	5283668	Click to see CCC(=CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1R,2S,5S,6S,9R,12S,13R,16S)-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine	12303820	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)CN1	314.50	unknown	via CMAUP database
(1R,2S,5S,6S,9R,12S,13R,16S)-7-hydroxy-N,N,6,13-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine	101529337	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O	358.60	unknown	via CMAUP database
Conessimine	12303831	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1	342.60	unknown	via CMAUP database
Conimin	101686	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1	328.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Azepines
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-4-acetyloxy-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-11-en-8-yl] hexadecanoate	101939156	Click to see CCCCCCCCCCCCCCCC(=O)OC12CC(C3CC(C1C3OC(=O)C)C45C(CCC6(C4CC2C5N=C6)COC)OC)OC	671.90	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Paravallarine	442980	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C(=O)O1	343.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine	76330309	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)C=N1	312.50	unknown	via CMAUP database
Conessidine	22214027	Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C=N1	326.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Muxiangrine III	44258378	Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC(=C(C(=C3)O)O)CC=C(C)C)O	396.40	unknown	https://doi.org/10.1055/S-2006-960459
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Muxiangrine I	44258380	Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC4=C(C(=C3)O)OC(C=C4)(C)C)O	394.40	unknown	https://doi.org/10.1055/S-2006-960459
Muxiangrine II	44258379	Click to see CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC4=C(C(=C3)O)OC(C=C4)(C)C)OC	380.40	unknown	https://doi.org/10.1055/S-2006-960459

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Elsholtzia stauntonii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top