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

Description Top

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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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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

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_015143295.1 ASM1514329v1 Chromosome Ori-Gene Co. Ltd. 2020-11-02 100.0x 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
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
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
Wind-dispersed seeds blur phylogeographic breaks: The complex evolutionary history of Populus lasiocarpa around the Sichuan Basin Li X, Ruhsam M, Wang Y, Zhang HY, Fan XY, Zhang L, Wang J, Mao KS Plant Divers 31-Oct-2022
PMCID:PMC10105135
doi:10.1016/j.pld.2022.10.003
PMID:37069930
The Capparis spinosa var. herbacea genome provides the first genomic instrument for a diversity and evolution study of the Capparaceae family Wang L, Fan L, Zhao Z, Zhang Z, Jiang L, Chai M, Tian C Gigascience 30-Oct-2022
PMCID:PMC9618406
doi:10.1093/gigascience/giac106
PMID:36310248
Effect of light intensities on the photosynthesis, growth and physiological performances of two maple species Zhang J, Ge J, Dayananda B, Li J Front Plant Sci 12-Oct-2022
PMCID:PMC9597493
doi:10.3389/fpls.2022.999026
PMID:36311139
A high-quality Buxus austro-yunnanensis (Buxales) genome provides new insights into karyotype evolution in early eudicots Wang Z, Li Y, Sun P, Zhu M, Wang D, Lu Z, Hu H, Xu R, Zhang J, Ma J, Liu J, Yang Y BMC Biol 04-Oct-2022
PMCID:PMC9533543
doi:10.1186/s12915-022-01420-1
PMID:36195948
Involvement of PtPHR1 in phosphates starvation-induced alkaloid biosynthesis in Pinellia ternata (Thunb.) Breit Wang H, Hu J, Li L, Zhang X, Zhang H, Liang Z, Sheng Q, He Y, Hong G Front Plant Sci 10-Aug-2022
PMCID:PMC9400802
doi:10.3389/fpls.2022.914648
PMID:36035724
Chromosome-level genome assembly of the aquatic plant Nymphoides indica reveals transposable element bursts and NBS-LRR gene family expansion shedding light on its invasiveness Yang JS, Qian ZH, Shi T, Li ZZ, Chen JM DNA Res 25-Jun-2022
PMCID:PMC9267246
doi:10.1093/dnares/dsac022
PMID:35751614

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 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
4-[(2S,3S,4R,5R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-3,4-bis(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol 124396485 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
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 14213222 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
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-[(2R,3R)-2,3-bis(1,3-benzodioxol-5-ylmethyl)-4-hydroxybutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 90682210 Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)COC5C(C(C(C(O5)CO)O)O)O 520.50 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
(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 C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)COC5C(C(C(C(O5)CO)O)O)O 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 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-[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 C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)COC5C(C(C(C(O5)CO)O)O)O 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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00457-4
Maslinic Acid 73659 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
Oleanolic Acid 10494 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 https://doi.org/10.1016/S0031-9422(99)00457-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(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 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
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
24-Ethylcholest-5-en-3beta-ol 22012 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 222284 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,2S)-1-(3-Methoxy-4-hydroxyphenyl)-2-(beta-D-glucopyranosyloxy)-1,3-propanediol 24862424 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
(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 CC(C(C1=CC=C(C=C1)O)O)OC2C(C(C(C(O2)CO)O)O)O 330.33 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 CC(C(C1=CC=C(C=C1)O)O)OC2C(C(C(C(O2)CO)O)O)O 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
(Z)-Syringin 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 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
Eleutheroside B 5316860 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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 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 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
[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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