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Swertia kouitchensis

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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 UUID6440465b06aac350672763
Scientific name Swertia kouitchensis
Authority Franch.
First published in Bull. Soc. Bot. France 46: 320 (1899)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swertia elongata T.N.Ho & S.W.Liu ex J.X.Yang Fl. Tsinling. 1(4): 397 (1983)
Swertia shigucao Z.Y.Zhu Bull. Bot. Res., Harbin 11(4): 63 (1991)

Common names Top

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Language Common/alternative name
Chinese 贵州獐牙菜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Swertia kouitchensis var. jiendeensis (Y.Y.Fang) T.N.Ho Worldwide Monogr. Swertia : 254 (2015)

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001063889
Tropicos 13802899
KEW urn:lsid:ipni.org:names:370953-1
The Plant List tro-13802899
Open Tree Of Life 6069286
NCBI Taxonomy 2831648
IPNI 370953-1
GBIF 5595996
EOL 2892735

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
Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny Yang L, Deng S, Zhu Y, Da Q BMC Plant Biol 28-Mar-2023
PMCID:PMC10044379
doi:10.1186/s12870-023-04183-1
PMID:36977991
Comparative chloroplast genome analyses of 23 species in Swertia L. (Gentianaceae) with implications for its phylogeny Yang L, Li J, Zhou G Front Genet 31-Aug-2022
PMCID:PMC9470856
doi:10.3389/fgene.2022.895146
PMID:36118878
Veratrilla baillonii Franch Ameliorates Diabetic Liver Injury by Alleviating Insulin Resistance in Rats Zhang ZH, Li J, Li J, Ma Z, Huang XJ Front Pharmacol 26-Nov-2021
PMCID:PMC8662784
doi:10.3389/fphar.2021.775563
PMID:34899339
Xanthone Glucosides: Isolation, Bioactivity and Synthesis Huang Q, Wang Y, Wu H, Yuan M, Zheng C, Xu H Molecules 14-Sep-2021
PMCID:PMC8465223
doi:10.3390/molecules26185575
PMID:34577044
Chemistry, Pharmacology and Therapeutic Potential of Swertiamarin – A Promising Natural Lead for New Drug Discovery and Development Muhamad Fadzil NS, Sekar M, Gan SH, Bonam SR, Wu YS, Vaijanathappa J, Ravi S, Lum PT, Dhadde SB Drug Des Devel Ther 21-Jun-2021
PMCID:PMC8233004
doi:10.2147/DDDT.S299753
PMID:34188450
Medicinal Plants with Potential Inhibitory Bioactive Compounds against Coronaviruses Adeleye OA, Bamiro OA, Bakre LG, Odeleye FO, Adebowale MN, Okunye OL, Sodeinde MA, Adebona AC, Menaa F Adv Pharm Bull 30-Jan-2021
PMCID:PMC9012928
doi:10.34172/apb.2022.003
PMID:35517886
Utilization of Swertia chirayita Plant Extracts for Management of Diabetes and Associated Disorders: Present Status, Future Prospects and Limitations Dey P, Singh J, Suluvoy JK, Dilip KJ, Nayak J Nat Prod Bioprospect 28-Oct-2020
PMCID:PMC7648839
doi:10.1007/s13659-020-00277-7
PMID:33118125
Furin: A Potential Therapeutic Target for COVID-19 Wu C, Zheng M, Yang Y, Gu X, Yang K, Li M, Liu Y, Zhang Q, Zhang P, Wang Y, Wang Q, Xu Y, Zhou Y, Zhang Y, Chen L, Li H iScience 05-Oct-2020
PMCID:PMC7534598
doi:10.1016/j.isci.2020.101642
PMID:33043282
Chemical-informatics approach to COVID-19 drug discovery: Exploration of important fragments and data mining based prediction of some hits from natural origins as main protease (Mpro) inhibitors Ghosh K, Amin SA, Gayen S, Jha T J Mol Struct 05-Aug-2020
PMCID:PMC7405777
doi:10.1016/j.molstruc.2020.129026
PMID:32834115
Combating COVID-19 with integrated traditional Chinese and Western medicine in China Ni L, Chen L, Huang X, Han C, Xu J, Zhang H, Luan X, Zhao Y, Xu J, Yuan W, Chen H Acta Pharm Sin B 27-Jun-2020
PMCID:PMC7319939
doi:10.1016/j.apsb.2020.06.009
PMID:32834946
Analysis of therapeutic targets for SARS-CoV-2 and discovery of potential drugs by computational methods Wu C, Liu Y, Yang Y, Zhang P, Zhong W, Wang Y, Wang Q, Xu Y, Li M, Li X, Zheng M, Chen L, Li H Acta Pharm Sin B 27-Feb-2020
PMCID:PMC7102550
doi:10.1016/j.apsb.2020.02.008
PMID:32292689
The Potential of South African Herbal Tisanes, Rooibos and Honeybush in the Management of Type 2 Diabetes Mellitus Ajuwon OR, Ayeleso AO, Adefolaju GA Molecules 05-Dec-2018
PMCID:PMC6321617
doi:10.3390/molecules23123207
PMID:30563087
The Progress of Anti-HBV Constituents from Medicinal Plants in China Geng CA, Chen JJ Nat Prod Bioprospect 05-Jul-2018
PMCID:PMC6102174
doi:10.1007/s13659-018-0178-6
PMID:29978386
Nectary tracks as pollinator manipulators: The pollination ecology of Swertia bimaculata (Gentianaceae) Wang S, Fu W, Du W, Zhang Q, Li Y, Lyu Y, Wang X Ecol Evol 19-Feb-2018
PMCID:PMC5869268
doi:10.1002/ece3.3838
PMID:29607017
Xanthone glycoside constituents of Swertia kouitchensis with α-glucosidase inhibitory activity. Wan LS, Min QX, Wang YL, Yue YD, Chen JC J Nat Prod 26-Jul-2013
doi:10.1021/NP400082G
PMID:23805995

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
1-Hydroxy-2,6-dimethoxy-8-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-9H-xanthen-9-one 72163130 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 582.50 unknown https://doi.org/10.1021/NP400082G
1,2,4,6-tetramethoxy-8-[(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 71745141 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C(=CC(=C5OC)OC)OC 626.60 unknown https://doi.org/10.1021/NP400082G
1,2,5,6-tetramethoxy-8-[(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 71747858 Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=CC(=C3OC)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 626.60 unknown https://doi.org/10.1021/NP400082G
1,8-dihydroxy-4,5-dimethoxy-3-[(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 71745142 Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1021/NP400082G
2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,8-dihydroxy-6-methoxyxanthen-9-one 71745329 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C=C3)OC5=CC(=CC(=C5C4=O)O)OC)O)CO)O)O)O)O)O 582.50 unknown https://doi.org/10.1021/NP400082G
2-hydroxy-1,5,6-trimethoxy-8-[(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 71747857 Click to see COC1=C(C2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C=CC(=C5OC)O)OC 612.50 unknown https://doi.org/10.1021/NP400082G
2,5-dihydroxy-1,6-dimethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 71747859 Click to see COC1=C(C2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(O2)C=CC(=C4OC)O)O 466.40 unknown https://doi.org/10.1021/NP400082G
3,5,8-trimethoxy-1-[(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 71747860 Click to see COC1=C2C(=C(C=C1)OC)OC3=C(C2=O)C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP400082G
8-hydroxy-3,5-dimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 71745144 Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 612.50 unknown https://doi.org/10.1021/NP400082G
8-hydroxy-6-methoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyxanthen-9-one 71745330 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C=C2)OC4=CC(=CC(=C4C3=O)O)OC)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 582.50 unknown https://doi.org/10.1021/NP400082G
Kouitchenside G 71745143 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/NP400082G
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1021/NP400082G
Swertianolin 5281662 Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1021/NP400082G

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