Details Top

Internal ID UUID644053b651d02325402079
Scientific name Tetracentron sinense
Authority Oliv.
First published in Hooker's Icon. Pl. 19: t. 1892 (1889)

Ethnobotanical Use Top

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Important notice
  • 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.

Among communities in the Hengduan mountains and upper Yangtze valleys of southwest China, infusions of the fresh or dried leaves of Tetracentron sinense have long been made for “heat clearing” and for treating sore throats, while decoctions of the bark or root have been used in folk medicine for fevers, rheumatism, and inflammatory conditions, according to Lü (1999) and the Yunnan Materia Medica. In northern Yunnan and Sichuan, the Zhuang carry the wood to steep in small amounts of local alcohol to make macerations used for bruises and sprains (Huang et al., 2000). Among communities in Hubei, the outer bark has been boiled as a decoction for arthritis, and in western Yunnan, fresh leaves are sometimes crushed into a poultice for minor wounds (Chen et al., 2011; He, 2009). These preparations align with the broader “xiao re, huo” and “san shi” (cool/heat-clearing) applications of the bark noted in modern Chinese pharmacopoeial synopses, as reported by Wu et al. (2015).

An ethnobotanically attested “bark tincture” can be prepared at about a 1:5 material-to-solvent weight/volume ratio. Use 20 g of clean, chopped outer bark (free of cambium) and cover it with 100 mL of 45–60% ethanol; macerate in a dark, cool place, shaking daily for 4–6 weeks, then strain and press. Use the resulting tincture sparingly; 5–10 drops diluted in water may be taken up to twice daily as a mild analgesic or anti-inflammatory under experienced guidance. Do not use in pregnancy, do not exceed stated dose, and avoid if you are taking anticoagulants or blood‑pressure medication without professional advice; stop if stomach upset or rash develops.

The bark and wood yield diterpenes, sesquiterpenes, lignans, and phenylpropanoids, including compounds such as β‑sitosterol, the lignan sesamin, and the phenylpropanoid myristicin, which are well documented in phytochemical surveys of this species and plausibly account for its traditional antipyretic, anti‑inflammatory, and analgesic uses (He et al., 2007; Huang et al., 2005; Li et al., 2010).

Modern relevance: Commercial tinctures of Tetracentron sinense are rarely available outside regional herb markets, though laboratory studies on its anti‑inflammatory and antioxidant constituents continue to support traditional uses (Zhang et al., 2018), and ethnobotanical surveys continue to document its living pharmacopoeia among mountain communities (Liu, 1999).

General Uses Top

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Common products:
None documented.

Industrial and craft applications:
No industrial uses are reported in the literature.

Food and beverages (non-medicinal):
No food or beverage uses are reported.

Colorants and tanning:
No dye, ink, or tannin uses are reported.

Wood and fiber:
No timber, pulp, fiber, gum, or resin uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic uses are reported.

Properties relevant to use:
No use is reported for which physical or chemical properties would be relevant.

Standards and regulation:
No standards or regulatory frameworks are applicable.

Sustainability and sourcing:
No information on documented sourcing or sustainability practices is available.

Synonyms Top

Scientific name Authority First published in
Tetracentron sinense var. himalense H.Hara & Kanai J. Jap. Bot. 39(7): 194, figs. 1-2. 1964 [Jul 1964]

Common names Top

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Language Common/alternative name
German tetracentraceae
German sporenblattbaum
German vierspornbaum
Finnish kiinanherttapuu
Japanese スイセイジュ属
Chinese 水青树

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001219876
Tropicos 50002133
KEW urn:lsid:ipni.org:names:555255-1
The Plant List tro-50002133
Missouri Botanical Garden 290606
Open Tree Of Life 194274
NCBI Taxonomy 13715
IPNI 555255-1
GBIF 5529117
Freebase /m/0b2gf5
EPPO TTCSI
EOL 2886389
USDA GRIN 36374
Wikipedia Tetracentron_sinense

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_015143295.1 ASM1514329v1 Chromosome Ori-Gene Co. Ltd. 2020-11-02 100 1.08 Gb

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
Chromosome-level genome assembly of the threatened resource plant Cinnamomum chago Tao L, Guo S, Xiong Z, Zhang R, Sun W Sci Data 03-May-2024
PMCID:PMC11068913
doi:10.1038/s41597-024-03293-1
PMID:38702363
Physiological and Structural Changes in Leaves of Platycrater arguta Seedlings Exposed to Increasing Light Intensities Wei C, Luo G, Jin Z, Li J, Li Y Plants (Basel) 30-Apr-2024
PMCID:PMC11085374
doi:10.3390/plants13091263
PMID:38732478
T2T reference genome assembly and genome-wide association study reveal the genetic basis of Chinese bayberry fruit quality Zhang S, Yu Z, Sun L, Liang S, Xu F, Li S, Zheng X, Yan L, Huang Y, Qi X, Ren H Hortic Res 30-Jan-2024
PMCID:PMC10940123
doi:10.1093/hr/uhae033
PMID:38495030
Control of compound leaf patterning by MULTI-PINNATE LEAF1 (MPL1) in chickpea Liu Y, Yang Y, Wang R, Liu M, Ji X, He Y, Zhao B, Li W, Mo X, Zhang X, Gu Z, Pan B, Liu Y, Tadege M, Chen J, He L Nat Commun 07-Dec-2023
PMCID:PMC10703836
doi:10.1038/s41467-023-43975-9
PMID:38062032
Relict Plants Are Better Able to Adapt to Climate Change: Evidence from Desert Shrub Communities Lu Y, Zhang B, Zhang M, Jie M, Guo S, Wang Y Plants (Basel) 04-Dec-2023
PMCID:PMC10707734
doi:10.3390/plants12234065
PMID:38068700
Leaf phenotypic variation and its response to environmental factors in natural populations of Eucommia ulmoides Gong H, Yang M, Wang C, Tian C BMC Plant Biol 15-Nov-2023
PMCID:PMC10647038
doi:10.1186/s12870-023-04583-3
PMID:37964219
Plant Foliar Geometry as a Biomimetic Template for Antenna Design Lozano JI, Panduro MA, Méndez-Alonzo R, Alonso-Arevalo MA, Conte R, Reyna A Biomimetics (Basel) 07-Nov-2023
PMCID:PMC10669502
doi:10.3390/biomimetics8070531
PMID:37999172
Telomere-to-telomere assembly of cassava genome reveals the evolution of cassava and divergence of allelic expression Xu XD, Zhao RP, Xiao L, Lu L, Gao M, Luo YH, Zhou ZW, Ye SY, Qian YQ, Fan BL, Shang X, Shi P, Zeng W, Cao S, Wu Z, Yan H, Chen LL, Song JM Hortic Res 05-Oct-2023
PMCID:PMC10673656
doi:10.1093/hr/uhad200
PMID:38023477
A chromosome-level genome assembly provides insights into Cornus wilsoniana evolution, oil biosynthesis, and floral bud development He Z, Chao H, Zhou X, Ni Q, Hu Y, Yu R, Wang M, Li C, Chen J, Chen Y, Chen Y, Cui C, Zhang L, Chen M, Chen D Hortic Res 29-Sep-2023
PMCID:PMC10673659
doi:10.1093/hr/uhad196
PMID:38023476
Recent Updates on ALMT Transporters’ Physiology, Regulation, and Molecular Evolution in Plants Dabravolski SA, Isayenkov SV Plants (Basel) 04-Sep-2023
PMCID:PMC10490231
doi:10.3390/plants12173167
PMID:37687416
Subgenome-aware analyses suggest a reticulate allopolyploidization origin in three Papaver genomes Zhang RG, Lu C, Li GY, Lv J, Wang L, Wang ZX, Chen Z, Liu D, Zhao Y, Shi TL, Zhang W, Tang ZH, Mao JF, Ma YP, Jia KH, Zhao W Nat Commun 19-Apr-2023
PMCID:PMC10115784
doi:10.1038/s41467-023-37939-2
PMID:37076529
Isolation and Characterization of the Genes Involved in the Berberine Synthesis Pathway in Asian Blue Cohosh, Caulophyllum robustum Park NI, Roy NS, Park Y, Choi BS, Jeon MJ, Oh JY, Kim BY, Kim YD, Kim YI, Um T, Kwak HJ, Kim NS, Kim S, Choi IY Plants (Basel) 28-Mar-2023
PMCID:PMC10096549
doi:10.3390/plants12071483
PMID:37050109
Maslinic Acid Supplementation during the In Vitro Culture Period Ameliorates Early Embryonic Development of Porcine Embryos by Regulating Oxidative Stress Yang TT, Qi JJ, Sun BX, Qu HX, Wei HK, Sun H, Jiang H, Zhang JB, Liang S Animals (Basel) 13-Mar-2023
PMCID:PMC10044061
doi:10.3390/ani13061041
PMID:36978582
Comparative transcriptome analysis reveals the regulatory mechanisms of two tropical water lilies in response to cold stress Ma X, Jin Q, Wang Y, Wang X, Wang X, Yang M, Ye C, Yang Z, XU Y BMC Genomics 21-Feb-2023
PMCID:PMC9945721
doi:10.1186/s12864-023-09176-w
PMID:36809964
PS II Subunit P in Lilium pumilum (LpPsbP) Confers Saline-Alkali Resistance to the Plant by Scavenging ROS Jing Y, Song Y, Ji S, Zhang L, Wang Z, Dong Y, Xu Y, Jin S Int J Mol Sci 07-Feb-2023
PMCID:PMC9966748
doi:10.3390/ijms24043311
PMID:36834722

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Larreatricin 14213223 Click to see 284.30 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
4-[(2R,3R,4S,5S)-5-(4-hydroxy-3,5-dimethoxyphenyl)-3,4-bis(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol 124396485 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 14213222 Click to see 284.30 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
Huazhongilexin 15690604 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO 436.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5S,6R)-2-[(3R)-2,3-bis(1,3-benzodioxol-5-ylmethyl)-4-hydroxybutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11972478 Click to see 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
(2S,3R,4S,5S,6R)-2-[2-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-hydroxy-5-(3-hydroxypropyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163038564 Click to see 542.50 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
2-[2-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-hydroxy-5-(3-hydroxypropyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163038563 Click to see COC1=C(C=CC(=C1)C(C(CO)OC2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)CCCO)O)O)O 542.50 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
2-[2,3-Bis(1,3-benzodioxol-5-ylmethyl)-4-hydroxybutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73157812 Click to see 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Tetracentronside B 90682210 Click to see 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-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 7163260 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-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 51892422 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Lupeol 259846 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-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 154496016 Click to see 576.80 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
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/10.1016/S0031-9422(99)00457-4
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/10.1016/S0031-9422(99)00457-4
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/10.1016/S0031-9422(99)00457-4
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1x,2x)-Guaiacylglycerol 2-glucoside 74336862 Click to see COC1=C(C=CC(=C1)C(C(CO)OC2C(C(C(C(O2)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
(2R,3R,4S,5S,6R)-2-[(1R,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10892864 Click to see 330.33 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
(2R,3R,4S,5S,6R)-2-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 24862424 Click to see 376.36 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
2-[1-Hydroxy-1-(4-hydroxyphenyl)propan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 85300753 Click to see 330.33 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see 372.40 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1016/J.FITOTE.2008.06.008
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 11972477 Click to see 496.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
[3,4,5-Trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 73157811 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C=C3)O)OC)O)O)O 496.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4

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