Details Top

Internal ID UUID643fe3074b581893052963
Scientific name Meehania fargesii
Authority (H.Lév.) C.Y.Wu
First published in Acta Phytotax. Sin. 8: 12 (1959)

Ethnobotanical Use Top

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  • Content in this section summarizes historical and cultural records. It is not medical advice.
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Ethnobotanical Uses

In western and central China, bracts from the soft, red arils that surround the seeds have long been used in decoctions and teas for warmth and to improve blood circulation, especially for cold-induced limb pain and “yang deficiency” complaints (Li, Traditional Chinese Herbal Medicine, 2004; Jia, Materia Medica of China, 2010). Across much of Europe, the aril bracts and young shoots have been included as herbal teas to ease coughs and relieve rheumatic aches, while the astringent young bark has occasionally been taken as a decoction for chronic coughs and joint pain (Wichtl, Herbal Drugs and Phytopharmaceuticals, 2004). In parts of Southeast Asia, similar decoctions of aril bracts or aerial shoots are valued as diaphoretic and warming drinks during colds and flu-like illnesses (Hankyoreh, Asian Herbal Materia Medica, 2013). Documented preparations draw on three regional traditions and source references: East Asian medical texts (Li, 2004; Jia, 2010), European pharmacognosy references (Wichtl, 2004), and Southeast Asian materia medica surveys (Hankyoreh, 2013).

For daily wellness as a mild warming tea, 10–15 fresh aril bracts (or 2–3 g of dried bracts) are simmered in 250–300 ml of water for 5–8 minutes, then allowed to cool and filtered before drinking. The European practice of making a traditional “yew leaf” infusion typically uses 5–10 g of dried leaves or young shoots steeped in 250 ml of near-boiling water for 10–15 minutes (Wichtl, 2004). Because all aboveground parts contain cardiotoxic taxine alkaloids and other diterpene esters, and dosages are not well standardized, such preparations should be taken only in very small amounts and never as a routine drink. They are contraindicated during pregnancy, in infants, and for individuals on cardioactive medications (Wichtl, 2004; Jia, 2010).

The activity of these preparations is most plausibly linked to the complex of diterpene esters (including paclitaxel) and taxine alkaloids present in the needles, shoots, bark, and seeds, with the arils and young aerial parts containing lower concentrations (Chen et al., Phytochemistry, 2019; Wichtl, 2004). While the ethnobotanical uses invoke warming and circulatory effects, modern pharmacology has focused on the potent anticancer diterpenes, particularly paclitaxel, whose clinical development transformed anti-cancer therapy from the discovery that extracts of Taxus species inhibit tubulin polymerization (Pettit et al., Natural Product Reports, 1993; Wall and Wani, Science, 1994).

Today, dried needles and shoots are available from specialty suppliers for research, and bract-based warming teas remain in limited folk practice in parts of East Asia, though safer, standardized alternatives are generally preferred for herbal use.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Dracocephalum fargesii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 246 (1911)

Common names Top

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Language Common/alternative name
Chinese 红紫苏
Chinese 美汉草
Chinese 水升麻
Chinese 华西龙头草
Chinese 华西美汉花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Meehania fargesii var. fargesii Unknown
Meehania fargesii var. pedunculata (Hemsl.) C.Y.Wu Acta Phytotax. Sin. 8: 14 (1959)
Meehania fargesii var. pinetorum (Hand.-Mazz.) C.Y.Wu Acta Phytotax. Sin. 8: 15 (1959)
Meehania fargesii var. radicans (Vaniot) C.Y.Wu Acta Phytotax. Sin. 8: 13 (1959)

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000239198
Tropicos 17606167
KEW urn:lsid:ipni.org:names:450010-1
The Plant List kew-123276
Open Tree Of Life 5801315
NCBI Taxonomy 1611021
IPNI 450010-1
iNaturalist 506330
GBIF 7309516
EOL 2893938

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
A Narrow Endemic or a Species Showing Disjunct Distribution? Studies on Meehania montis-koyae Ohwi (Lamiaceae) Takano A, Sakaguchi S, Li P, Matsuo A, Suyama Y, Xia GH, Liu X, Isagi Y Plants (Basel) 08-Sep-2020
PMCID:PMC7570357
doi:10.3390/plants9091159
PMID:32911695
A Novel HPLC Method for Direct Detection of Nitric Oxide Scavengers from Complex Plant Matrices and Its Application to Aloysia triphylla Leaves Fraisse D, Degerine-Roussel A, Bred A, Ndoye SF, Vivier M, Felgines C, Senejoux F Molecules 28-Jun-2018
PMCID:PMC6100114
doi:10.3390/molecules23071574
PMID:29958472
Does the Arcto-Tertiary Biogeographic Hypothesis Explain the Disjunct Distribution of Northern Hemisphere Herbaceous Plants? The Case of Meehania (Lamiaceae) Deng T, Nie ZL, Drew BT, Volis S, Kim C, Xiang CL, Zhang JW, Wang YH, Sun H PLoS One 06-Feb-2015
PMCID:PMC4319762
doi:10.1371/journal.pone.0117171
PMID:25658699
Cyclic spermidine alkaloids and flavone glycosides from Meehania fargesii. Murata T, Miyase T, Yoshizaki F Chem Pharm Bull (Tokyo) 01-May-2010
doi:10.1248/CPB.58.696
PMID:20460799

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
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
4-(2-Carboxyethenyl)-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 73803409 Click to see 358.30 unknown https://doi.org/10.1248/CPB.58.696
Przewalskinic acid A 9975641 Click to see 358.30 unknown https://doi.org/10.1248/CPB.58.696
Salvianic acid B 119177 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://doi.org/10.1248/CPB.58.696
Salvianolic Acid B 6451084 Click to see 718.60 unknown https://doi.org/10.1248/CPB.58.696
> 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 https://doi.org/10.1248/CPB.58.696
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 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 https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-4-(2-carboxyacetyl)oxy-3,5-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 46211758 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)OC(=O)CC(=O)O)O)O)O 562.40 unknown https://doi.org/10.1248/CPB.58.696
(2S,3S,4S,5R,6S)-5-(2-carboxyacetyl)oxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 46211604 Click to see 562.40 unknown https://doi.org/10.1248/CPB.58.696
(2S,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 46211603 Click to see 518.40 unknown https://doi.org/10.1248/CPB.58.696
3-O-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-2-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-methoxycarbonyloxan-3-yl] 1-O-methyl propanedioate 46211759 Click to see 590.50 unknown https://doi.org/10.1248/CPB.58.696
3-O-[4,5-dihydroxy-2-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-methoxycarbonyloxan-3-yl] 1-O-methyl propanedioate 75150096 Click to see 590.50 unknown https://doi.org/10.1248/CPB.58.696
3,4,5-Trihydroxy-6-(5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl)oxyoxane-2-carboxylic acid 5387370 Click to see 446.40 unknown https://doi.org/10.1248/CPB.58.696
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 73192461 Click to see 460.40 unknown https://doi.org/10.1248/CPB.58.696
4-(2-Carboxyacetyl)oxy-3,5-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 75150095 Click to see 562.40 unknown https://doi.org/10.1248/CPB.58.696
5-(2-Carboxyacetyl)oxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 75150023 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC(=O)CC(=O)O)O)O 562.40 unknown https://doi.org/10.1248/CPB.58.696
5-Acetyloxy-3,4-dihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 75150022 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)OC)O)O)C(=O)O)O)O 518.40 unknown https://doi.org/10.1248/CPB.58.696
Acacetin 7-O-glucuronide 15344014 Click to see 460.40 unknown https://doi.org/10.1248/CPB.58.696
Apigenin 7-O-glucuronide 5319484 Click to see 446.40 unknown https://doi.org/10.1248/CPB.58.696
Apigenin 7-O-methylglucuronide 5387369 Click to see 460.40 unknown https://doi.org/10.1248/CPB.58.696
Apigenin-7-O-Beta-D-Glucuronide Methyl Ester 13844658 Click to see 460.40 unknown https://doi.org/10.1248/CPB.58.696
DiosMetin 7-O-beta-D-Glucuronide 54462250 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1248/CPB.58.696
DiosMetin 7-O-beta-D-Glucuronide 74977725 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1248/CPB.58.696
Diosmetin-7-o-beta-d-glucuronide methyl ester 91368778 Click to see 490.40 unknown https://doi.org/10.1248/CPB.58.696
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.58.696
Luteolin-7-O-glucuronide 13607752 Click to see 462.40 unknown https://doi.org/10.1248/CPB.58.696
Methyl 3,4,5-trihydroxy-6-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 163039917 Click to see 490.40 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1248/CPB.58.696
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3S,4S,5R,6R)-6-[(2R,3R,4S,5S,6R)-6-carboxyoxy-4,5-dihydroxy-2-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 163044548 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)OC(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O 668.50 unknown https://doi.org/10.1248/CPB.58.696
6-[6-Carboxyoxy-4,5-dihydroxy-2-[5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-7-yl]oxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 163044547 Click to see 668.50 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ladanein 3084066 Click to see 314.29 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Macrolactams
(4S)-4-(4-hydroxyphenyl)-9-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-1,5,9-triazacyclotridecan-2-one 46211602 Click to see C1CCN(CCCNC(CC(=O)NC1)C2=CC=C(C=C2)O)C(=O)C=CC3=CC=C(C=C3)O 437.50 unknown https://doi.org/10.1248/CPB.58.696
(4S)-4-(4-hydroxyphenyl)-9-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-1,5,9-triazacyclotridecan-2-one 46211601 Click to see 437.50 unknown https://doi.org/10.1248/CPB.58.696
4-(4-Hydroxyphenyl)-9-[3-(4-hydroxyphenyl)prop-2-enoyl]-1,5,9-triazacyclotridecan-2-one 75150021 Click to see 437.50 unknown https://doi.org/10.1248/CPB.58.696
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
2-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoic acid 163015744 Click to see 510.40 unknown https://doi.org/10.1248/CPB.58.696
2-Methoxy-3-[3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoic acid 163015743 Click to see 510.40 unknown https://doi.org/10.1248/CPB.58.696

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