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The first two core requirements—documented ethnobotanical uses with at least three regional citations and a practical preparation—require trustworthy sources. Because no such sources have been provided for Salvia trijuga, an empty response is appropriate.

General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قصعين ثلاثي الآواصر
Chinese	小红参
Chinese	紫丹参
Chinese	三叶鼠尾草
Chinese	三对叶丹参
Chinese	小红丹参

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 click to expand
- China
  - China South-central
  - Tibet

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302518
Tropicos	17606680
KEW	urn:lsid:ipni.org:names:457436-1
The Plant List	kew-184057
Open Tree Of Life	547892
NCBI Taxonomy	342065
IPNI	457436-1
iNaturalist	1231589
GBIF	3885070
Freebase	/m/0ch3sv8
EOL	2894218
Wikipedia	Salvia_trijuga
CMAUP	NPO14979

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

Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach

De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K

In Silico Pharmacol

28-Apr-2023

PMCID:	PMC10141836
doi:	10.1007/s40203-023-00143-7
PMID:	37131867

Development and structure–activity relationships of tanshinones as selective 11β-hydroxysteroid dehydrogenase 1 inhibitors

Deng X, Huang SL, Ren J, Pan ZH, Shen Y, Zhou HF, Zuo ZL, Leng Y, Zhao QS

Nat Prod Bioprospect

22-Sep-2022

PMCID:	PMC9492458
doi:	10.1007/s13659-022-00358-9
PMID:	36131216

The complete chloroplast genome of Vitex trifolia L. (Lamiaceae)

Gentallan Jr. RP, Quiñones KJ, Bartolome MC, Madayag RE, Vera Cruz JR, Cirunay AT, Endonela LE, Borromeo TH, Altoveros NC, Lalusin AG, Alvaran BB, Magtoltol JB, Cejalvo RD

Mitochondrial DNA B Resour

18-Jul-2022

PMCID:	PMC9295813
doi:	10.1080/23802359.2022.2097027
PMID:	35866139

Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China

Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L

J Ethnobiol Ethnomed

23-May-2022

PMCID:	PMC9125852
doi:	10.1186/s13002-022-00532-w
PMID:	35606860

Characterization of the complete chloroplast genome of Salvia trijuga Diels (Lamiaceae)

Du Y, Wang YY, Xiang CL, Yang MQ

Mitochondrial DNA B Resour

20-Oct-2021

PMCID:	PMC8530471
doi:	10.1080/23802359.2021.1991243
PMID:	34693012

Quinonoids: Therapeutic Potential for Lung Cancer Treatment

Ying HZ, Yu CH, Chen HK, Zhang HH, Fang J, Wu F, Yu WY

Biomed Res Int

06-Apr-2020

PMCID:	PMC7166295
doi:	10.1155/2020/2460565
PMID:	32337232

Phylogeny and staminal evolution of Salvia (Lamiaceae, Nepetoideae) in East Asia

Hu GX, Takano A, Drew BT, Liu ED, Soltis DE, Soltis PS, Peng H, Xiang CL

Ann Bot

25-Jun-2018

PMCID:	PMC6153483
doi:	10.1093/aob/mcy104
PMID:	29945172

New Abietane Diterpene Alkaloids Possessing an Oxazole Ring from Salvia trijuga

Tian-Shung Wu, Fu-Wen Lin, Amooru G. Damu

The Japan Institute of Heterocyclic Chemistry

17-Feb-2009

doi:	10.3987/COM-05-10565

Constituents of Salvia trijuga

Hui Yang, Siu-Po Ip, Han-Dong Sun, Chun-Tao Che

Informa UK Limited

14-Aug-2003

doi:	10.1076/PHBI.41.5.375.15938

Diterpenoids from Salvia wiedemannii

G. Topcu, A. Ulubelen

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)83665-8

Trijuganone A and B: Two New Phenanthrenequinones from Roots of Salvia trijuga.

Xuezhao L, Houwei L, Masatake N

Planta Med

01-Feb-1990

doi:	10.1055/S-2006-960892
PMID:	17221374

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
> Benzenoids / Benzene and substituted derivatives / Benzenesulfonic acids and derivatives
Sodium sulfanilate	23664644	Click to see	195.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3-Hydroxybenzoic Acid	7420	Click to see	138.12	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
Protocatechuic Acid	72	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isosalviamine A	86226793	Click to see	287.30	unknown	https://doi.org/10.3987/COM-05-10565
Isosalviamine B	86226794	Click to see	301.30	unknown	https://doi.org/10.3987/COM-05-10565
> Benzenoids / Phenols / Cresols / Ortho cresols
O-Cresol	335	Click to see	108.14	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Lignans, neolignans and related compounds / Furanoid lignans
Fraxiresinol	21632950	Click to see COC1=CC(=CC(=C1O)OC)C2C3(COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	404.40	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid	5282822	Click to see	278.40	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
Linolenic Acid	5280934	Click to see	278.40	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	5321549	Click to see	300.40	unknown	via CMAUP database
Abieta-9(11),8(14),12-trien-12-ol	521330	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1R)-1,6,6-trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11(3aH,11aH)-dione	25181389	Click to see CC1COC2C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	298.40	unknown	via CMAUP database
(S)-6-(Hydroxymethyl)-1,6-dimethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]furan-10,11-dione	9926694	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO	310.30	unknown	via CMAUP database
1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro(1,2-b)furan-10,11-dione	496348	Click to see	296.40	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
2-Hydroxy-4,8-dimethyl-8,9-dihydronaphtho[2,1-f][1]benzofuran-7,11-dione	85607958	Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=C(C=C3)C(=CC(=C4)O)C	294.30	unknown	https://doi.org/10.1055/S-2006-960892
Cryptotanshinone	160254	Click to see	296.40	unknown	https://doi.org/10.1016/0031-9422(91)83665-8 https://doi.org/10.1076/PHBI.41.5.375.15938
Dihydrotanshinone	5316743	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C	278.30	unknown	via CMAUP database
Dihydrotanshinone I	11425923	Click to see	278.30	unknown	via CMAUP database
Methuyl tanshinonate	624381	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC	338.40	unknown	via CMAUP database
Methyl Tanshinonate	14610613	Click to see	338.40	unknown	via CMAUP database
Npc85771	622085	Click to see	292.30	unknown	via CMAUP database
Tanshinone I	114917	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C	276.30	unknown	https://doi.org/10.1016/0031-9422(91)83665-8
Tanshinone IIA	164676	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	294.30	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
Trijuganone B	124416	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC=C4C	280.30	unknown	https://doi.org/10.1055/S-2006-960892
Trijuganone C	164381	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC	340.40	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic Acid	6918774	Click to see	472.70	unknown	via CMAUP database
Euscaphic Acid	471426	Click to see	488.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid	14605533	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O	470.70	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1076/PHBI.41.5.375.15938
Sitogluside	5742590	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	https://doi.org/10.1076/PHBI.41.5.375.15938
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-2-azaniumyl-4-hydroxybutanoate	6971022	Click to see C(CO)C(C(=O)[O-])[NH3+]	119.12	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Sym-homospermidinium(3+)	25245489	Click to see C(CC[NH2+]CCCC[NH3+])C[NH3+]	162.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenol glucoside	9945189	Click to see	326.34	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
D(+)-Glucose	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde	8768	Click to see	138.12	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Dasyclamide	10980024	Click to see	316.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ferulate	54691413	Click to see	193.18	unknown	via CMAUP database
Rosmarinic Acid	5281792	Click to see	360.30	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
Rosmarinic Acid Methyl Ester	3012090	Click to see	374.30	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1076/PHBI.41.5.375.15938
> 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	https://doi.org/10.1076/PHBI.41.5.375.15938

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Salvia trijuga

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

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top