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Tripterospermum chinense

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440465374d3c160520350
Scientific name Tripterospermum chinense
Authority (Migo) Harry Sm.
First published in Grana Palynol. 7: 144 (1967)

Description Top

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Synonyms Top

Scientific name Authority First published in
Crawfurdia chinensis Migo J. Shanghai Sci. Inst. Sect. 3 , 4: 154 (1939)
Tripterospermum carlesii Harry Sm. Notes Roy. Bot. Gard. Edinburgh 26: 246 (1965)
Tripterospermum chinense var. linearifolium X.F.Jin Novon 19: 278 (2009)

Common names Top

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Language Common/alternative name
Chinese 双蝴蝶
Chinese 肺形草
Chinese 雙蝴蝶

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001063738
Tropicos 13802290
KEW urn:lsid:ipni.org:names:371293-1
The Plant List tro-13802290
Open Tree Of Life 66838
NCBI Taxonomy 308429
IPNI 371293-1
GBIF 5596473
EOL 2892770

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
Identification of Gentian-Related Species Based on Two-Dimensional Correlation Spectroscopy (2D-COS) Combined with Residual Neural Network (ResNet) Wu X, Yang X, Cheng Z, Li S, Li X, Zhang H, Diao Y Molecules 26-Jun-2023
PMCID:PMC10343857
doi:10.3390/molecules28135000
PMID:37446662
Variation of soil physicochemical properties of different vegetation restoration types on subtropical karst area in southern China Xiao C, You R, Zhu N, Mi X, Gao L, Zhou X, Zhou G PLoS One 16-Mar-2023
PMCID:PMC10019609
doi:10.1371/journal.pone.0282620
PMID:36928208
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
The linkages of plant, litter and soil C:N:P stoichiometry and nutrient stock in different secondary mixed forest types in the Qinling Mountains, China Pang Y, Tian J, Zhao X, Chao Z, Wang Y, Zhang X, Wang D PeerJ 03-Jun-2020
PMCID:PMC7275688
doi:10.7717/peerj.9274
PMID:32547880
Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J J Ethnobiol Ethnomed 04-May-2017
PMCID:PMC5418811
doi:10.1186/s13002-017-0153-z
PMID:28472968
Flavonoids and Xanthones from Tripterospermum chinense Jing-Jing Fang, Guan Ye Springer Science and Business Media LLC 30-Oct-2008
doi:10.1007/S10600-008-9113-0

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
2,4-Dihydroxy-1,5,6-trimethoxyxanthen-9-one 162973215 Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(O2)C(=CC(=C3OC)O)O)OC 318.28 unknown https://doi.org/10.1007/S10600-008-9113-0
4,5-dihydroxy-1,2-dimethoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 162856389 Click to see COC1=C(C2=C(C(=C1)O)OC3=C(C2=O)C=CC(=C3O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1007/S10600-008-9113-0
4,5-Dihydroxy-1,2-dimethoxy-6-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 162856388 Click to see COC1=C(C2=C(C(=C1)O)OC3=C(C2=O)C=CC(=C3O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1007/S10600-008-9113-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 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/10.1007/S10600-008-9113-0
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/10.1007/S10600-008-9113-0
Epicatechin 72276 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/10.1007/S10600-008-9113-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 6426860 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-008-9113-0
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 4475102 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-008-9113-0
6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 154586125 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-008-9113-0
6-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 14630650 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C4=C(C=C3O)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-008-9113-0
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-008-9113-0
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-008-9113-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
kaempferol-3-O-alpha-L-rhamnoside 15558501 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-008-9113-0
Kaempferol-3-O-rhamnoside 5835713 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1007/S10600-008-9113-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-008-9113-0
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-008-9113-0

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