Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Across East and Central Asia, Lycopus lucidus is used most often as an infusion or decoction of the aerial parts to support women’s health and circulation. In traditional Chinese medicine the decoction is taken for conditions involving blood stasis, amenorrhea, dysmenorrhea, and postpartum recovery; the fresh herb is also sometimes made into a poultice for trauma and bruises (He and Hsieh, 2006; National Pharmacopoeia of the People’s Republic of China, 2015). In nearby Korea, aerial parts are simmered and drunk to address menstrual irregularities and subinvolution of the uterus after birth (Jang et al., 2018). In Russian and eastern European practice the related genus Lycopus is used similarly, and Lycopus lucidus itself is listed in Asian pharmacopoeias for these same indications, often emphasizing the whole aboveground plant (Konĕev and Davydova, 2010; PPRC, 2015). As a practical preparation, a mild tea can be made by infusing 1–2 g of dried aerial parts in 200 mL of freshly boiled water for 10–15 minutes; most texts suggest one cup two or three times daily and note caution for pregnancy and for individuals with heavy menstrual bleeding or bleeding disorders due to the herb’s uterine stimulant and vasorelaxant properties. A 1:5 ethanol tincture is made with 20 g of dried aerial parts macerated in 100 mL of 45% ethanol for two weeks, shaking daily; a common dosage is 1–2 mL up to three times daily, again avoiding use in pregnancy unless prescribed. Well‑established phytochemicals in this species—rosmarinic acid, caffeic acid, luteolin‑7‑glucoside and related flavonoids, and essential oils such as α‑ and β‑pinene and limonene—are consistent with documented astringent, anti‑inflammatory, uterine‑tonic, and vasorelaxant activities (He and Hsieh, 2006; Zhang et al., 2015). Lycopus lucidus remains in current Chinese Materia Medica and in some Asian nutraceuticals, and it is the subject of ongoing pharmacological research on its phenolic profile and cardiovascular effects; the decoction and tincture remain in common use where the herb is available (Zheng et al., 2007).

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Phytosalpinx lucida	Lunell	Amer. Midl. Naturalist 5: 2 (1917)
Lycopus lucidus var. typicus	Korsh.	Trudy Imp. S.-Peterburgsk. Bot. Sada 12: 376 (1892)
Lycopus lucidus var. genuinus	Herder	Bull. Soc. Imp. Naturalistes Moscou 61(I): 131 (1885)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	phytosalpinx lucida
Japanese	シロネ
Korean	쉽싸리
mnc	ᠰᡳᠮᡝᠯᡝᠨ ᡧᡠᠩᡴᡝᡵᡳ ᡳᠯᡥᠠ
Russian	Зюзник блестящий
Chinese	泽兰
Chinese	地瓜儿苗
Chinese	地笋
Chinese	地笋（地瓜儿苗）
Chinese	地筍
Chinese	地参
Chinese	提娄
Chinese	地瓜苗

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Lycopus lucidus var. hirtus	(Regel) Makino & Nemoto	Fl. Japan , ed. 2: 1019 (1931)
Lycopus lucidus var. lucidus		Unknown
Lycopus lucidus var. maackianus	Maxim. ex Herder	Bull. Soc. Imp. Naturalistes Moscou 61(I): 131 (1885)

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 click to expand
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Amur
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin
- Siberia
  - Chita
  - Irkutsk
  - Yakutskiya

Europe click to expand
- Southeastern Europe
  - Italy

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000231418
UNII	2237I5787N
Canadensys	16987
Tropicos	17603010
Flora of Italy	10044
KEW	urn:lsid:ipni.org:names:449660-1
The Plant List	kew-115931
Open Tree Of Life	980292
Observations.org	132591
NCBI Taxonomy	516551
IPNI	449660-1
iNaturalist	577962
GBIF	5341460
Freebase	/m/0_v697z
EPPO	LYALU
USDA GRIN	423464
Wikipedia	Lycopus_lucidus
CMAUP	NPO21824

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

Efficacy of probiotics in hair growth and dandruff control: A systematic review and meta-analysis

Yin CS, Minh Nguyen TT, Yi EJ, Zheng S, Bellere AD, Zheng Q, Jin X, Kim M, Park S, Oh S, Yi TH

Heliyon

16-Apr-2024

PMCID:	PMC11064082
doi:	10.1016/j.heliyon.2024.e29539
PMID:	38698995

Liangxue-Qushi-Zhiyang Decoction Ameliorates DNCB-Induced Atopic Dermatitis in Mice through the MAPK Signaling Pathway Based on Network Pharmacology

Zhang L, Zhang H, Niu X, Zhang X, Chen X, Lei S, Ma S, Sun Z

ACS Omega

10-Apr-2024

PMCID:	PMC11044150
doi:	10.1021/acsomega.3c09218
PMID:	38680355

Phosphorylation: new star of pathogenesis and treatment in steatotic liver disease

Lv T, Lou Y, Yan Q, Nie L, Cheng Z, Zhou X

Lipids Health Dis

17-Feb-2024

PMCID:	PMC10873984
doi:	10.1186/s12944-024-02037-9
PMID:	38368351

Traditional Chinese Medicine is Associated with the Reduction in Endpoint Events in Patients with Gouty Arthritis: Cohort Study and Association Rule Analysis

Chen Y, Liu J, Cong C, Li Y, Hu Y

Int J Gen Med

13-Feb-2024

PMCID:	PMC10874188
doi:	10.2147/IJGM.S451097
PMID:	38371521

Chloroplast genome of Ocimum basilicum var. purpurascens Bentham 1830 (Lamiaceae)

Venkatesan A, Balaji R, Tanuja, Parani M

Mitochondrial DNA B Resour

05-Feb-2024

PMCID:	PMC10849003
doi:	10.1080/23802359.2024.2310145
PMID:	38328459

Preparation, Characterization, and Antioxidant Activities of Extracts from Amygdalus persica L. Flowers

Yu Q, Li W, Liang M, Li G, Wu Z, Long J, Yuan C, Mei W, Xia X

Molecules

29-Jan-2024

PMCID:	PMC10856188
doi:	10.3390/molecules29030633
PMID:	38338377

Therapeutic Potential and Mechanisms of Rosmarinic Acid and the Extracts of Lamiaceae Plants for the Treatment of Fibrosis of Various Organs

Boo YC

Antioxidants (Basel)

24-Jan-2024

PMCID:	PMC10886237
doi:	10.3390/antiox13020146
PMID:	38397744

Research Status in the Use of Surface-Enhanced Raman Scattering (SERS) to Detect Pesticide Residues in Foods and Plant-Derived Chinese Herbal Medicines

Chu BY, Lin C, Nie PC, Xia ZY

Int J Anal Chem

12-Jan-2024

PMCID:	PMC10798841
doi:	10.1155/2024/5531430
PMID:	38250173

Convergent application of traditional Chinese medicine and gut microbiota in ameliorate of cirrhosis: a data mining and Mendelian randomization study

Zhou C, Wei J, Yu P, Yang J, Liu T, Jia R, Wang S, Sun P, Yang L, Xiao H

Front Cell Infect Microbiol

06-Nov-2023

PMCID:	PMC10657829
doi:	10.3389/fcimb.2023.1273031
PMID:	38029250

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

A Comprehensive Review of the Pharmacology, Chemistry, Traditional Uses and Quality Control of Star Anise (Illicium verum Hook. F.): An Aromatic Medicinal Plant

Zou Q, Huang Y, Zhang W, Lu C, Yuan J

Molecules

01-Nov-2023

PMCID:	PMC10648513
doi:	10.3390/molecules28217378
PMID:	37959797

The complete chloroplast genome of Ocimum basilicum L. var. basilicum (Lamiaceae) and its phylogenetic analysis

Kirankumar SI, Balaji R, Tanuja, Parani M

Mitochondrial DNA B Resour

30-Oct-2023

PMCID:	PMC10769543
doi:	10.1080/23802359.2023.2275835
PMID:	38188439

Integrative Korean Medicine Treatments for Traumatic Facial Palsy Following Mandibular Fracture: A Case Report and Literature Review

Park H, Lee SH, Lee Y, Choi DJ, Lee J, Jo H, Jung W, Kim SD, Sim HA, Lee YJ, Ha IH

Healthcare (Basel)

14-Sep-2023

PMCID:	PMC10530994
doi:	10.3390/healthcare11182546
PMID:	37761743

Advancements in Diagnostic and Therapeutic Interventions of Non-alcoholic Fatty Liver Disease: A Literature Review

Chaudhry A, Noor J, Batool S, Fatima G, Noor R

Cureus

08-Sep-2023

PMCID:	PMC10560588
doi:	10.7759/cureus.44924
PMID:	37814734

Prebiotics for depression: how does the gut microbiota play a role?

Yang Y, Zhou B, Zhang S, Si L, Liu X, Li F

Front Nutr

06-Jul-2023

PMCID:	PMC10358272
doi:	10.3389/fnut.2023.1206468
PMID:	37485386

Phytochemical Profile Top

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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
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate	44584035	Click to see	299.36	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate	3026	Click to see	278.34	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate	54675866	Click to see C1=CC(=C(C=C1C(=O)O)O)[O-]	153.11	unknown	via CMAUP database
Protocatechuic Acid	72	Click to see	154.12	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 / Phenylpyruvic acid derivatives
3'-O-(8''-Z-Caffeoyl)Rosmarinic Acid	10052949	Click to see	538.50	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonadecane	12401	Click to see	268.50	unknown	via CMAUP database
Pentacosane	12406	Click to see	352.70	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methylpentadecane	15267	Click to see CCCCCCCCCCCCCC(C)C	226.44	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl 14-methylpentadecanoate	21205	Click to see CC(C)CCCCCCCCCCCCC(=O)OC	270.50	unknown	via CMAUP database
Methyl arachidate	14259	Click to see	326.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Octadecanoate	3033836	Click to see	283.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol	6992244	Click to see	128.21	unknown	via CMAUP database
(S)-1-Octen-3-ol	2724898	Click to see CCCCCC(C=C)O	128.21	unknown	via CMAUP database
1-Octen-3-Ol	18827	Click to see	128.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl all-trans-9,12,15-octadecatrienoate	5367462	Click to see	292.50	unknown	via CMAUP database
Methyl linoleate	5284421	Click to see	294.50	unknown	via CMAUP database
Npc92743	176473	Click to see	294.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2E,6E,10E)-6,10-dimethyl-12-(5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal	23424860	Click to see CC1=CC(=O)C=C(C1=O)CC=C(C)CCC=C(C)CCC=C(CCC=C(C)C)C=O	408.60	unknown	via CMAUP database
(2Z,6E,10E)-6,10-dimethyl-12-(5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal	25225126	Click to see	408.60	unknown	via CMAUP database
(2Z,6E,10E)-6,10-dimethyl-12-(5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid	9802458	Click to see CC1=CC(=O)C=C(C1=O)CC=C(C)CCC=C(C)CCC=C(CCC=C(C)C)C(=O)O	424.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(R)-Sargachromenol	51003424	Click to see CC1=CC(=CC2=C1OC(C=C2)(C)CCC=C(C)CCC=C(CCC=C(C)C)C(=O)O)O	424.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,10S,11S,12aS,14bR)-10,11-dihydroxy-12a-(hydroxymethyl)-2,2,6a,6b,9,9-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	3052779	Click to see	650.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E,19E,21Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,21,23-dodecaenyl]-1,3,3-trimethylcyclohexene	10218186	Click to see	534.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aS,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	11897956	Click to see	456.70	unknown	via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45483617	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	45483610	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
3-Epioleanolic acid	11869658	Click to see	456.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(6R)-6-[(3R,5S,7R,9S,10S,13R,14S,17R)-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptanoic acid	53477686	Click to see CC(CCCC(C)C(=O)O)C1CCC2C1(CCC3C2C(CC4C3(CCC(C4)O)C)O)C	434.70	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	576.80	unknown	via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid	18413781	Click to see	258.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,7-Dimethyloct-1-en-3-ol	86748	Click to see	156.26	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(a1-2a)Fruf	11005647	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O	504.40	unknown	via CMAUP database
GlyTouCan:G95076SI	11972400	Click to see	990.90	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole	2758	Click to see	154.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	via CMAUP database
Ethyl Rosmarinate	44437692	Click to see	388.40	unknown	via CMAUP database
Methyl Rosmarinate	6479915	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	via CMAUP database
Rosmarinate	5315615	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	via CMAUP database
Rosmarinic Acid	5281792	Click to see	360.30	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	179.15	unknown	via CMAUP database
Caffeic Acid	689043	Click to see	180.16	unknown	via CMAUP database
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	via CMAUP database
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid	49770232	Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O	364.30	unknown	via CMAUP database

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Lycopus lucidus

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

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