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Swertia macrosperma

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440465a63d34858969883
Scientific name Swertia macrosperma
Authority C.B.Clarke
First published in Fl. Brit. India 4: 123 (1883)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Ophelia macrosperma C.B.Clarke J. Linn. Soc., Bot. 14: 448 (1875)
Swertia randaiensis Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 203 (1911)
Swertia scandens H.Lév. Repert. Spec. Nov. Regni Veg. 12: 188 (1913)

Common names Top

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Language Common/alternative name
Chinese 贵州獐牙菜
Chinese 大籽獐牙菜
Chinese 大籽當藥
Chinese 巒大當藥
Chinese 大籽当药

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 South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001063880
Tropicos 13802890
KEW urn:lsid:ipni.org:names:370972-1
The Plant List tro-13802890
Open Tree Of Life 957040
NCBI Taxonomy 137130
IPNI 370972-1
iNaturalist 702930
GBIF 5595900
EOL 2892737

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
An overview of anti-Hepatitis B virus flavonoids and their mechanisms of action Naderi M, Salavatiha Z, Gogoi U, Mohebbi A Front Cell Infect Microbiol 29-Feb-2024
PMCID:PMC10937540
doi:10.3389/fcimb.2024.1356003
PMID:38487354
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
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
Herbal Medicines Targeting the Improved β-Cell Functions and β-Cell Regeneration for the Management of Diabetes Mellitus Wickramasinghe AS, Kalansuriya P, Attanayake AP Evid Based Complement Alternat Med 14-Jul-2021
PMCID:PMC8298154
doi:10.1155/2021/2920530
PMID:34335803
Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence Linn YH, Ei WW, Myint LM, Lwin KM Virusdisease 14-Jul-2021
PMCID:PMC8473485
doi:10.1007/s13337-021-00714-2
PMID:34631974
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
Natural Products: Review for Their Effects of Anti-HBV Liu X, Ma C, Liu Z, Kang W Biomed Res Int 09-Dec-2020
PMCID:PMC7746453
doi:10.1155/2020/3972390
PMID:33376721
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
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
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Antiviral Evaluation of Herbal Drugs Mukherjee PK Quality Control and Evaluation of Herbal Drugs 21-Jun-2019
PMCID:PMC7149824
doi:10.1016/B978-0-12-813374-3.00016-8
Homology modeling and docking analysis of ßC1 protein encoded by Cotton leaf curl Multan betasatellite with different plant flavonoids Sarwar MW, Riaz A, Nahid N, Al Qahtani A, Ahmed N, Nawaz-Ul-Rehman MS, Younus A, Mubin M Heliyon 07-Mar-2019
PMCID:PMC6407081
doi:10.1016/j.heliyon.2019.e01303
PMID:30899831
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
Hypoglycemic Activity and the Potential Mechanism of the Flavonoid Rich Extract from Sophora tonkinensis Gagnep. in KK-Ay Mice Huang M, Deng S, Han Q, Zhao P, Zhou Q, Zheng S, Ma X, Xu C, Yang J, Yang X Front Pharmacol 05-Sep-2016
PMCID:PMC5011294
doi:10.3389/fphar.2016.00288
PMID:27656144

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aR,6aS,6bR,8aR,10R,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 162942880 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.197600009
(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/10.1002/JCCS.197600009
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1002/JCCS.197600009
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,5-Trihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5857493 Click to see C1=CC(=C2C(=C1O)OC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(89)80400-5
Demethylbellidifolin 5281626 Click to see 260.20 unknown https://doi.org/10.1016/0031-9422(89)80400-5
https://doi.org/10.1080/14786410600906319
Norswertianolin 5281659 Click to see C1=CC(=C2C(=C1O)OC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 422.30 unknown https://doi.org/10.1016/0031-9422(89)80400-5
swertiabisxanthone I 24878847 Click to see C1=CC(=C2C(=C1O)OC3=C(C2=O)C(=C(C(=C3)O)C4=CC(=C5C(=C4O)C(=O)C6=C(C=C(C=C6O5)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O 680.50 unknown https://doi.org/10.1016/0031-9422(89)80400-5
swertiabisxanthone-I 14539914 Click to see C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3O)C4=CC(=C5C(=C4O)C(=O)C6=C(C=C(C=C6O5)O)O)O)O)O 518.40 unknown https://doi.org/10.1016/0031-9422(89)80400-5
> Organoheterocyclic compounds / Pyranopyridines
Gentianine 354616 Click to see C=CC1=CN=CC2=C1CCOC2=O 175.18 unknown https://doi.org/10.1002/JCCS.197600009

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